Sensors for detection of negatively charged phosphate-containing membranes and membrane components

Abstract

This application relates to a method of detecting negatively charged phosphate-containing membranes and membrane components, such as in cell membranes or artificial lipid vesicles, and its use, for example, in detecting apoptosis and bacterial infection.

Claims

1. A method of detecting negatively charged phosphate-containing membrane components comprising: (a) combining a solution of a sample suspected of comprising negatively charged phosphate-containing membrane components with a solution comprising a compound of Formula V, or a metal chelate salt thereof: ##STR00063## wherein L.sup.2 is a linker group selected from C.sub.1-20alkylene, C.sub.2-20alkenylene, C.sub.2-20alkynylene and C.sub.3-10-cycloalkylene, or a combination thereof, each of which is optionally oxo-substituted (O) 1-3 times, and in which 1-3 carbon atoms are optionally replaced with a heteromoiety selected from NH, O, S and Si; and R.sup.3 is selected from ##STR00064## (b) detecting a fluorescence signal; wherein detection of the fluorescence signal in (b) indicates that the sample comprises negatively charged phosphate-containing membrane components.

2. The method of claim 1, wherein the sample is an extract from a bacterial, yeast, insect or mammalian cell line; (b) a bodily sample; or (c) urine, synovial fluid or blood, or any sample that contains or is suspected of comprising negatively charged phosphate-containing membrane components.

3. A compound of Formula V, or a metal chelate salt thereof: ##STR00065## wherein L.sup.2 is a linker group selected from C.sub.1-20alkylene, C.sub.2-20alkenylene, C.sub.2-20alkynylene and C.sub.3-10-cycloalkylene, or a combination thereof, each of which is optionally oxo-substituted (O) 1-3 times, and in which 1-3 carbon atoms are optionally replaced with a heteromoiety selected from NH, O, S and Si; and R.sup.3 is selected from ##STR00066##

4. The compound of claim 3, wherein L.sup.2 is selected from: ##STR00067##

5. The compound of claim 3, wherein the metal is Zn.sup.2+.

6. The compound of claim 5, wherein the compound is ##STR00068## wherein A is a counteranion.

7. The compound of claim 6, wherein A is CF.sub.3SO.sub.3.sup., Cl.sup., Br.sup., I.sup., CH.sub.3COO.sup., HPO.sub.3.sup., HSO.sub.4.sup., SO.sub.4.sup.2 or NO.sub.3.sup..

8. The method of claim 1, wherein the metal is Zn.sup.2+.

9. The method of claim 8, wherein the compound is ##STR00069## wherein A is a counteranion.

10. The method of claim 9, wherein A is CF.sub.3SO.sub.3.sup., Cl.sup., Br.sup., Cl.sup., I.sup., CH.sub.3COO.sup., HPO.sub.3.sup., HSO.sub.4.sup., SO.sub.4.sup.2 or NO.sub.3.sup..

11. The method of claim 2, wherein the mammalian cell line is a human cell line.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) The embodiments of the application will now be described in greater detail with reference to the attached drawings in which:

(2) FIG. 1 shows in panel A an exemplary schematic structure of a sensor compound I, and in panel B the proposed mechanism of detection of negatively charged phospholipids.

(3) FIG. 2 shows the excimer fluorescence enhancement of exemplary compound I-1 upon addition of zwitterionic (PC, PE) and negatively charged (PA, PS, PG, CL) vesicles. Panel A shows the FI.sub.exc of compound I-1 at vesicle concentrations between 0-40 M. Panel B shows the FI.sub.exc of compound I-1 at vesicle concentrations between 0-200 M. Buffer: 50 mM HEPES, 5% DMSO, pH 7.5. [Ia-1]=25 M. .sub.ex/em=350/476 nm.

(4) FIG. 3 shows the FI.sub.exc data for exemplary compounds I-2, I-3, I-4, I-5, and I-6 and compounds II-1, II-4, and II-5 for various vesicles. Panel A shows data at vesicle concentrations from 0 to 40 M. Panel B shows data at vesicle concentrations from 0 to 200 M. Buffer: 50 mM HEPES, 5% DMSO, pH 7.5. [I and II compounds]=25 M. .sub.ex/em=350/476 nm.

(5) FIG. 4 shows the FI for exemplary compounds I-1, I-2, I-3, I-4, I-5, I-6 and PSVue380 for zwitterionic (PE) and negatively charged (PA, PS, PG, CL) vesicles at vesicle concentrations between 0-200 M. Buffer: 50 mM HEPES, 5% DMSO, pH 7.5. [I and II compounds]=25 M, .sub.ex/em=350/476 nm. [PSVue380]=1 M, .sub.ex/em=380/440 nm.

(6) FIG. 5 shows the FI.sub.exc/mon data for exemplary compounds I-1, I-2, I-3, I-4, I-5, I-6 and compounds II-1, II-4, and II-5 for zwitterionic (PE) and negatively charged (PA, PS, PG, CL) vesicles. Panel A shows data at vesicle concentrations from 0 to 40 M. Panel B shows data at vesicle concentrations from 0 to 200 M. Buffer: 50 mM HEPES, 5% DMSO, pH 7.5. [I and II compounds]=25 M, .sub.ex/em=350/476 nm.

(7) FIG. 6 shows in panel A the optimal sensor concentration testing by measuring FI of sensor exemplary compound I-1 with PS and PC vesicles at varying concentrations of exemplary Ia-1. Panel B shows the FI at 25 M of I-1 at different incubation times. Buffer: 50 mM HEPES, 5% DMSO, pH 7.5. .sub.ex/em=350/476 nm.

(8) FIG. 7 shows the FI of exemplary compounds I-1, I-2, I-3, I-4, I-5, I-6 for vesicles containing 5%, 25%, 50%, and 75% PS. Panel A shows results at vesicle concentrations from 0 to 40 M, while panel B shows results at vesicle concentrations from 0 to 200 M. Buffer: 50 mM HEPES, 5% DMSO, pH 7.5. [I compounds]=25 M, .sub.ex/em=350/476 nm.

(9) FIG. 8 shows the FI.sub.exc and FI of exemplary compounds I-11, I-12 and I-9 for zwitterionic (PC, PE) and negatively charged (PA, PS, PG, CL) vesicles. Panel A shows FI.sub.exc of I-11 with all vesicles and short-chain lipids for vesicle concentrations from 0-40 M (left) and 0-200 M (right). Panel B shows FI of I-11 with all vesicles and short-chain lipids for vesicle concentrations from 0-40 M (left) and 0-200 M (right). Panel C shows FI.sub.exc of I-12 with all vesicles and short-chain lipids for vesicle concentrations from 0-40 M (left) and 0-200 M (right). Panel D shows FI of I-12 with all vesicles and short-chain lipids for vesicle concentrations from 0-40 M (left) and 0-200 M (right). Panel E shows FI.sub.exc of I-9 with all vesicles and short-chain lipids for vesicle concentrations from 0-40 M (left) and 0-200 M (right). Panel F shows FI of I-9 with all vesicles and short-chain lipids for vesicle concentrations from 0-40 M (left) and 0-200 M (right). Buffer: 50 mM HEPES, 5% DMSO, pH 7.5. [Ia compounds]=25 M, .sub.ex/em=350/476 nm. (FI.sub.exc=FI.sub.exc vesicle/FI.sub.exc buffer)

(10) FIG. 9 shows FI of exemplary sensor compound I-1 (25 M) upon addition of PS vesicles, in the absence or presence of O-Phospho-L-serine. Panel A shows FI where O-Phospho-L-serine was added before vesicle addition. Panel B shows FI where O-Phospho-L-serine was added after vesicle addition. Buffer: 50 mM HEPES, 5% DMSO, pH 7.5. [Ia-1]=25 M, .sub.ex/em=350/476 nm.

(11) FIG. 10 shows the FI and FI of exemplary metallated I and unmetallated II compounds upon addition of PA vesicles from 0 to 200 M. Panel A shows FI of exemplary compounds I-4, II-4, II-1, I-5, I-1, II-5, PSVue380 and unmetallated PSVue380* with PA vesicles. Panel B shows FI for exemplary compounds I-4, II-4, II-1, I-5, I-1, II-5, PSVue380 and unmetallated PSVue380 with PA vesicles, where metallated compounds I-4, I-5, and I-1 were prepared either as lyophilized powders (denoted as metallated in the figure) or a compound of formula II were combined with a solution containing equimolar amount (except for PSVue380, which was combined with 2 equivalent) of metals salt (denoted as in-situ metalation).

(12) FIG. 11 shows a proof-of-concept E. coli titration. Panel A shows FI and Panel B shows FI of exemplary compound I-1 (10 M) in response to increasing amounts of E. coli K-12 BW25113 cells/mL. Buffer: 50 mM HEPES, pH 7.5, 75 mM NaCl, 0.4% DMSO, .sub.ex/em=350/476 nm.

(13) FIG. 12 shows E. coli K-12 BW25113 cells (10.sup.8 cells/mL; 25 mM HEPES, pH 7.0, 0.4% DMSO; excitation=325/50 nm, emission=447/60 nm, exposure time=30.28 ms) detection using fluorescence microscopy. Panel A shows the average intensity image with exemplary compound I-5. Panel B shows the SRRF intensity image with exemplary compound I-5. Panel C shows the UV image with exemplary sensor compound I-1. Panel D shows the UV image with exemplary compound Ia-6 (30 M). Panel E shows UV image with exemplary compound I-5 (10 M). Panel F shows a petri dish control containing buffer or petri dish with E. coli where exemplary compound Ia-1 (40 M) was added and the plate excited with long wave UV lamp.

(14) FIG. 13 shows Gram-positive bacteria B. subtilis (panel A), B. megaterium (panel B), M. luteus (panel C), and S. epidermidis (panel D) detection using fluorescence microscopy with exemplary compound I-4 (10 M sensor compound, 10.sup.8 cells/mL; 50 mM HEPES, pH 7.5, 75 mM NaCl, 0.4% DMSO; excitation=325/50 nm, emission=447/60 nm, exposure time=30.28 ms).

(15) FIG. 14 shows E. coli K-12 BW25113 cells (10.sup.8 cells/mL; 25 mM HEPES, pH 7.0, 0.4% DMSO; excitation=325/50 nm, emission=447/60 nm, exposure time=30.28 ms) detection using fluorescence microscopy with exemplary compound I-5 in presence of MV4-11 cells. Panel A shows the bright-field image. Panel B shows the UV image. [I-5]=40 M.

(16) FIG. 15 shows the titration curves for B. subtilis (A), B. megaterium (B), M. luteus (C), S. epidermidis (D) (50 mM HEPES, pH 7.5, 75 mM NaCl, 0.4-2.5% DMSO) for exemplary compounds I-1, I-3, I-4, I-8 and I-9. [I compounds]=10 M, .sub.ex/em=350/476 nm.

(17) FIG. 16 shows bacteria flow cytometry results. Panel A shows E. coli K-12 BW25113 cells (10.sup.7 CFU/mL) treated with 40 M POC sensor (exemplary sensor compound I-1). Sample run using UV laser (BD LSR Fortessa X20, emission: 450/50 nm) in 50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5. Panel B shows E. coli K-12 BW25113 cells (10.sup.8 CFU/mL) treated with 40 M POC sensor (exemplary sensor compound I-1). Sample run using UV laser (BD LSR Fortessa X20, emission: 450/50 nm) in 50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5. Panel C shows E. coli K-12 BW25113 cells (10.sup.8 CFU/mL) treated with 40 M Long Cyclam (exemplary sensor compound I-4) sensor. Sample run using UV laser (BD LSR Fortessa X20, emission: 450/50 nm) in 50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5. Panel D shows 40 M POC sensor (exemplary sensor compound I-1) without bacteria. Sample run using UV laser (BD LSR Fortessa X20, emission: 450/50 nm) in 50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5. Panel E shows 40 M Long Cyclam (exemplary sensor compound I-4) without bacteria. Sample run using UV laser (BD LSR Fortessa X20, emission: 450/50 nm) in 50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5.

(18) FIG. 17 shows bacteria flow cytometry results. The left panel shows fluorescence counts of exemplary sensor II-4 without bacteria. The right panel shows fluorescence counts of 1,000 bacteria cells (E. coli or B. subtilis) alone. The middle panel shows the shift of fluorescence counts when both the sensor and 1,000 bacteria cells are present. Gates were set off of unstained control. All samples run using near UV laser (exc: 375 nm, emi: 450/45 nm) and blue laser (exc: 488 nm, emi: 585/42 nm) (BeckmanCoulter, CytoFLEX S) in 50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5.

(19) FIG. 18 shows the FI of exemplary compounds I-1, I-3, I-4 and I-11 for LPS from E. coli O55:B5 (purchased from Sigma-Aldrich). All exemplary compounds are 10 M in 50 mM HEPES, pH 7.5, 75 mM NaCl, 0.4-2.8% DMSO (.sub.ex/em=350/476 nm). LPS was titrated from 10-0.005 M in the same buffer (assuming a MW of 10 kDa). Sensor solutions were prepared from 10 mg/mL DMSO stocks in 50 mM HEPES buffer, pH 7.5, 75 mM NaCl and minimal DMSO (0.4-2.8%) at 20 M The LPS solution was prepared at 20 M in the same buffer without DMSO. The LPS solution was serially diluted 1:1 from 20 M to 0.01 M with buffer in a 96-well plate. In a 384-well black plate, 30 L of sensor was combined with 30 L of analyte (last row contained 30 L buffer), the mixtures were incubated for 10 min away from light, and the fluorescence intensity was recorded at 476 nm (10 nm bandwidth) following excitation at 350 nm (5 nm bandwidth). Fluorescence intensities were used to calculate the excimer emission in response to LPS.

(20) FIG. 19 shows the FI of exemplary compounds I-1, I-3, I-4 and I-11 for LTA from B. subtilis (purchased from Sigma-Aldrich). All exemplary compounds are 10 M in 50 mM HEPES, pH 7.5, 75 mM NaCl, 0.4-2.8% DMSO (.sub.ex/em=350/476 nm). LTA is titrated from 10-0.005 M in the same buffer (assuming a MW of 10 kDa). Sensor solutions were prepared from 10 mg/mL DMSO stocks in 50 mM HEPES buffer, pH 7.5, 75 mM NaCl and minimal DMSO (0.4-2.8%) at 20 M. The LTA solution was prepared at 20 M in the same buffer without DMSO. The LTA solution was serially diluted 1:1 from 20 M to 0.01 M with buffer in a 96-well plate. In a 384-well black plate, 30 L of sensor was combined with 30 L of analyte (last row contained 30 L buffer), the mixtures were incubated for 10 min away from light, and the fluorescence intensity was recorded at 476 nm (10 nm bandwidth) following excitation at 350 nm (5 nm bandwidth). Fluorescence intensities were used to calculate the excimer emission in response to LTA.

(21) FIG. 20 shows mutant bacteria strain fluorimetry results. Panel A shows the fluorimetry results of mutant E. coli strains, including cardiolipin synthase knockouts (clsA, clsB, clsC), LPS synthesis knockout (rfaE) and LPS kinase knockouts (WaaP, waaG) with exemplary compound II-4 (10 M). Panel B shows the fluorimetry results of mutant B. subtilis strains, including cardiolipin synthase knockout (clsA) and CRISPRi-mediated LTA knockout (tagO) with exemplary compound II-4 (10 M). The bacteria were at 10.sup.8 CFUs/mL in buffer (50 mM HEPES, pH 7.5, 75 mM NaCl, 0.4% DMSO). The mixtures were incubated for 10 min away from light, and the fluorescence intensity was recorded at 476 nm (10 nm bandwidth) following excitation at 350 nm (5 nm bandwidth). Fluorescence intensities were used to calculate the excimer emission in response to bacterial strains. Measurements were averaged over two triplicates.

(22) FIG. 21 shows cell apoptosis flow cytometry results. Panel A shows flow cytometry results of untreated (left) and camptothecin (10 M, 7 hr) treated (right) MOLM-13 cells (1.010.sup.6 cells) after treatment with both exemplary compound I-3 (50 M final) and propidium iodide (0.02 g/L). Panel B shows flow cytometry results of untreated (left) and camptothecin (10 M, 7 hr) treated (right) MOLM-13 cells (1.010.sup.6 cells) after treatment with both PSVue380 (90.9 M final) and propidium iodide (0.02 g/L). Gates were set off of single stain samples. All samples run using near UV laser (exc: 375 nm, emi: 450/45 nm) and blue laser (exc: 488 nm, emi: 585/42 nm) (BeckmanCoulter, CytoFLEX S) in 50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5.

DESCRIPTION OF VARIOUS EMBODIMENTS

(I) Definitions

(23) Unless otherwise indicated, the definitions and embodiments described in this and other sections are intended to be applicable to all embodiments and aspects of the present application herein described for which they are suitable as would be understood by a person skilled in the art.

(24) As used in this application and claim(s), the words comprising (and any form of comprising, such as comprise and comprises), having (and any form of having, such as have and has), including (and any form of including, such as include and includes) or containing (and any form of containing, such as contain and contains), are inclusive or open-ended and do not exclude additional, unrecited elements or process steps.

(25) As used in this application and claim(s), the word consisting and its derivatives, are intended to be close ended terms that specify the presence of stated features, elements, components, groups, integers, and/or steps, and also exclude the presence of other unstated features, elements, components, groups, integers and/or steps.

(26) The term consisting essentially of, as used herein, is intended to specify the presence of the stated features, elements, components, groups, integers, and/or steps as well as those that do not materially affect the basic and novel characteristic(s) of these features, elements, components, groups, integers, and/or steps.

(27) The terms about, substantially and approximately as used herein mean a reasonable amount of deviation of the modified term such that the end result is not significantly changed. These terms of degree should be construed as including a deviation of at least 5% of the modified term if this deviation would not negate the meaning of the word it modifies.

(28) As used in this application, the singular forms a, an and the include plural references unless the content clearly dictates otherwise. For example, an embodiment including a compound should be understood to present certain aspects with one compound or two or more additional compounds.

(29) In embodiments comprising an additional or second component, such as an additional or second compound, the second component as used herein is chemically different from the other components or first component. A third component is different from the other, first, and second components, and further enumerated or additional components are similarly different.

(30) The term agent as used herein indicates a compound or mixture of compounds that, when added to a composition, tend to produce a particular effect on the composition's properties.

(31) The term and/or as used herein means that the listed items are present, or used, individually or in combination. In effect, this term means that at least one of or one or more of the listed items is used or present.

(32) The term optionally substituted as used herein refers to no substitution on a referenced group or one or more substitutions on a referenced group where the substituent(s) are selected from halo, CN, C.sub.1-6alkyl, C.sub.2-6alkenyl, C.sub.2-6alkynyl, OH, SH, OC.sub.1-6alkyl, SC.sub.1-6alkyl, NH.sub.2, NHC.sub.1-6alkyl, N(C.sub.1-6alkyl)(C.sub.1-6alkyl), C(O)C.sub.1-6alkyl, C(O)OH, C(O)OC.sub.1-6alkyl, C(O)NH.sub.2, C(O)NHC.sub.1-6alkyl, C(O)N(C.sub.1-6alkyl)(C.sub.1-6alkyl), SO.sub.2C.sub.1-6alkyl, S(O)C.sub.1-6alkyl, C.sub.6-10aryl, heteroaryl, C.sub.3-10cycloalkyl, heterocycloalkyl, C.sub.1-6alkyleneC.sub.6-10aryl, C.sub.1-6alkyleneC.sub.3-10cycloalkyl, C.sub.1-6alkyleneheteroaryl, C.sub.1-6alkyleneheterocycloalkyl, C.sub.1-6alkyleneOH, C.sub.1-6alkyleneOC.sub.1-6alkyl, C.sub.1-6alkyleneSH, C.sub.1-6alkyleneSC.sub.1-6alkyl, C.sub.1-6alkyleneNH.sub.2, C.sub.1-6alkyleneNHC.sub.1-6alkyl and C.sub.1-6alkyleneN(C.sub.1-6alkyl)(C.sub.1-6alkyl), wherein each alkyl, alkenyl, alkynyl, alkylene, aryl, cycloalkyl, heteroaryl and heterocycloalkyl group is optionally fluoro substituted.

(33) The term C.sub.1-nalkyl as used herein means straight or branched chain, saturated alkyl groups containing from one to n carbon atoms and includes (depending on the identity of n) methyl, ethyl, propyl, isopropyl, n-butyl, s-butyl, isobutyl, t-butyl, 2,2-dimethylbutyl, n-pentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, n-hexyl and the like, where the variable n is an integer representing the largest number of carbon atoms in the alkyl radical.

(34) The term C.sub.2-nalkenyl as used herein means straight or branched chain, unsaturated alkyl groups containing from two to n carbon atoms and one to three double bonds, and includes (depending on the identity of n) vinyl, allyl, 2-methylprop-1-enyl, but-1-enyl, but-2-enyl, but-3-enyl, 2-methylbut-1-enyl, 2-methylpent-1-enyl, 4-methylpent-1-enyl, 4-methylpent-2-enyl, 2-methylpent-2-enyl, 4-methylpenta-1,3-dienyl, hexen-1-yl and the like, where the variable n is an integer representing the largest number of carbon atoms in the alkenyl radical.

(35) The term C.sub.2-nalkynyl as used herein means straight or branched chain, unsaturated alkyl groups containing from two to n carbon atoms and one to three triple bonds, and includes (depending on the identity of n) ethynyl, propynyl, 2-methylprop-1-ynyl, but-1-ynyl, but-2-ynyl, but-3-ynyl, 3-methylbut-1-ynyl, 2-methylpent-1-ynyl, 4-methylpent-1-ynyl, 4-methylpent-2-ynyl, 4-methylpent-2-ynyl, penta-1,3-diynyl, hexyn-1-yl and the like, where the variable n is an integer representing the largest number of carbon atoms in the alkynyl radical.

(36) The term cycloalkyl as used herein refers to a monocyclic, bicyclic or polycyclic, carbocylic ring system having 3 to n carbon atoms including (depending on the identity of n), but not limited to, cyclopropyl, cyclopentyl, cyclohexyl, and the like, where the variable n is an integer representing the largest number of carbon atoms in the cycloalkyl radical.

(37) The term C.sub.6-naryl as used herein means a monocyclic, bicyclic or polycyclic, carbocyclic ring system containing from 6 to n carbon atoms and at least one aromatic ring and includes, depending on the identity of n, phenyl, naphthyl, anthracenyl, 1,2-dihydronaphthyl, 1,2,3,4-tetrahydronaphthyl, fluorenyl, indanyl, indenyl and the like, where the variable n is an integer representing the largest number of carbon atoms in the aryl radical.

(38) The term heteroaryl as used herein means a monocyclic or polycyclic ring system containing from 5 to 14 atoms of which one or more, for example 1-8, suitably, 1-6, more suitably 1-5, and more suitably 1-4, of the atoms are a heteromoiety selected from O, S, NH and NC.sub.1-6alkyl, with the remaining atoms being C or CH, said ring system containing at least one aromatic ring. Examples of heteroaryl groups, include, but are not limited to thienyl, imidazolyl, pyridyl, oxazolyl, indolyl, furanyl, benzothienyl, benzofuranyl and the like.

(39) The term bicyclic or polycyclic aryl moiety as used herein refers to a bicyclic or polycyclic conjugated substituted or unsubstituted carbocyclic ring system having two or more rings including, but not limited to, naphthyl, tetrahydronaphthyl, phenanthrenyl, biphenylenyl, indanyl, indenyl, pyrenyl, peryleneyl, tetraceneyl and the like. Non-conjugated or unsaturated rings may also be bonded to or fused to the conjugated ring system.

(40) The term bicyclic or polycyclic heteroaryl moiety as used herein refers to a bicyclic or polycyclic conjugated substituted or unsubstituted carbocyclic ring system having two or more rings containing, of which one or more, for example 1-8, suitably 1-6, more suitably 1-5, and more suitably 1-4, of the atoms are a heteromoiety selected from O, S, NH, NC.sub.1-6alkyl, and C(O), with the remaining atoms being C or CH, said ring system. Examples of heteroaryl moieties, include, but are not limited to substituted carbazoles (9-phenyl-9H-carbazole), 1H-benzo[de]isoquinoline-1,3(2H)-dione, anthra[2,1,9-def:6,5,10-def]diisoquinoline-1,3,8,10(2H,9H)-tetraone and the like. Non-conjugated or unsaturated rings may also be bonded to or fused to the conjugated ring system.

(41) The suffix ene added on to any of the above groups means that the group is divalent, i.e. inserted between two other groups. When the group is a ring system, the two other groups may be located at any location on the ring system, including at adjacent and non-adjacent nodes.

(42) The term oxo-substituted as used herein refers to a carbonyl group (CO) generally replacing a CH.sub.2 moiety.

(43) The term carboxyl as used herein refers to a group of the formula COOH or COO.sup..

(44) The term hydroxyl as used herein refers to a group of the formula OH.

(45) The term amino as used herein refers to an unsubstituted amino group (NH.sub.2) or a primary, secondary or tertiary amino moiety substituted by alkyl or aryl groups. The term amino also includes unsaturated amino groups such as imines, or aromatic amine such as pyridine.

(46) The term halo as used herein means halogen and includes chlorine, bromine, iodine and fluorine.

(47) The term excimer forming fluorophore as used herein refers to a fluorophore compound that can interact with another same or different fluorophore compound to achieve excimer emission, provided that the two such fluorophores can interact together so that a complex is formed between one fluorophore in its excited state (F*) and the other fluorophore (F) in its ground state. The complex formed between F* and F, emits at a longer wavelength that the fluorophore itself.

(48) The term linker moiety as used herein refers to a carbon-based moiety which connects the fluorophore with the metal ion coordinating moiety. The linker moiety may be straight-chained, branched, or cyclic, or a combination of all three, and connects one or more metal ion coordinating moieties with the fluorophore. The linker moiety optionally contains carbonyl, nitrogen and/or other heteroatom functionalities.

(49) The term metal ion coordinating moiety as used herein refers to a moiety which coordinates with a metal ion, for example, a transition metal ion, a lanthanide metal ion or a post-transition metal ion and comprises one or more cyclic or acyclic organic ligands which can coordinate to a metal ion center, for example, amino, amido, carboxyl or hydroxyl groups.

(50) The term metal ion as used herein refers to the positively charged forms or cations of metals.

(51) The term post-transition metal ion as used herein refers to metal ions in Groups IIIB, IVB, VB, and VIB in the periodic table of the elements, and includes, but is not limited to, aluminum, gallium, germanium, indium, tin, antimony etc.

(52) The term lanthanide metal ion as used herein refers to the metal ions with the atomic number from 57 to 71 in the periodic table of the elements, and includes, but is not limited to, terbium, europium, ytterbium etc.

(53) The term binding solution as used herein refers to an aqueous solution containing a compound of the Formula (II) and a suitable metal ion, which optionally forms compounds of the Formula I in solution.

(54) The term negatively charged phosphate-containing membrane components as used herein refers to any compound that comprises a negatively charged phosphate group, and with an overall negative charge, that is found in membrane structures.

(55) The term phospholipid used herein refers to a class of lipids that are a major component of cell membranes. The structure of the phospholipid molecule generally consists of two hydrophobic fatty acid tails and a hydrophilic head comprising a phosphate group. The two components are joined together by a glycerol molecule. The phosphate group can be modified with other neutral or charged organic molecules.

(56) The term vesicle or vesicles as used herein means a supramolecular structure comprising fluid enclosed in a lipid layer or lipid bilayer, either formed naturally in a cell such as during endocytosis or exocytosis, or formed artificially such as in the case of liposomes. A vesicle can further comprise molecules such as proteins and/or peptides.

(57) The term cell membrane or membrane as used herein means the cell wall of a eukaryotic or a prokaryotic cell, where the cell wall comprises a lipid layer or lipid bilayer. The cell membrane or membrane can further comprise other molecules such as proteins and/or peptides.

(58) The term proximal as used herein refers to the spacing between negatively charged phospholipids in, for example a membrane, such that the sites are sufficiently close to allow a bound excimer containing fluorophore compound at one site to interact, overlap or otherwise associate with a bound excimer-forming fluorophore on the other site. In some embodiments, the negatively charged phospholipids may be on two or more separate membranes, cells or vesicles, but are still close enough for interaction with an excimer containing fluorophore compound. In one embodiment, more than one negatively charged phospholipid may be present on the same membrane, cell or vesicle such as the distance between the negatively charged phospholipid sites are close enough for interaction with an excimer containing fluorophore compound. In some embodiments, the distance between negatively charged phospholipid sites may be between 2 and 100 Angstroms, optionally 3 and 50 Angstroms or suitably 5 and 30 Angstroms.

(59) The term subject as used herein refers to any member of the animal kingdom. In one embodiment, the subject is a mammal, such as a human.

(II) Methods of the Application

(60) In some embodiments, the application includes a method of detecting negatively charged phosphate-containing membrane components comprising: (a) combining a solution of a sample suspected of comprising negatively charged phosphate-containing membrane components with a solution comprising a compound of Formula I:

(61) ##STR00007## wherein, W is a fluorophore; V is a linker moiety; Y is a metal ion coordinating moiety; M is a metal cation; and A is a weakly coordinating counter anion; and n is 1, 2 or 3; and (b) detecting a fluorescence signal at a wavelength specific for the fluorophore;
wherein detection of the fluorescence signal in (b) indicates that the sample comprises negatively charged phosphate-containing membrane components.

(62) In some embodiments, W is an excimer forming fluorophore.

(63) In some embodiments, the fluorophore W is an optionally substituted bicyclic or polycyclic aryl or heteroaryl moiety.

(64) In some embodiments, the fluorophore is an unsubstituted or substituted C.sub.10-40-aryl or unsubstituted or substituted C.sub.9-40-heteroaryl. In some embodiments, the fluorophore is unsubstituted or substituted C.sub.10-20-aryl or unsubstituted or substituted C.sub.9-20heteroaryl.

(65) In some embodiments, the fluorophore is an unsubstituted or substituted moiety shown below with any suitable point of attachment to the linker moiety:

(66) ##STR00008##

(67) In some embodiments, the optional substituents on W are selected from halo, carboxyl, hydroxyl, C.sub.1-20alkyl, C.sub.2-20alkenyl, C.sub.2-20alkynyl, C.sub.3-20cycloalkyl, C.sub.1-20alkoxy, NRRC.sub.6-14-aryl, and C.sub.5-14-heteroaryl, wherein R and R are simultaneously or independently H or C.sub.1-6alkyl.

(68) In some embodiments, W is an substituted or unsubstituted

(69) ##STR00009##

(70) In some embodiments, W is unsubstituted.

(71) In some embodiments, the linker moiety is C.sub.1-40alkylene, C.sub.2-40alkenylene, C.sub.2-40alkynylene or C.sub.3-20cycloalkylene, or a combination thereof, each of which is optionally oxo-substituted (O) 1-6 times, optionally 1-3 times, and in which 1-3 carbon atoms are optionally replaced with a heteroatom/heteromoiety selected from NH, O, S and Si.

(72) In some embodiments, the linker moiety is C.sub.1-20alkylene, C.sub.2-20alkenylene, C.sub.2-20alkynylene or C.sub.3-10cycloalkylene, or a combination thereof, each of which is optionally oxo-substituted (O) 1-3 times, and in which 1-3 carbon atoms are optionally replaced with a heteroatom/heteromoiety selected from NH, O, S and Si.

(73) In some embodiments, the linker moiety is selected from

(74) ##STR00010##
wherein , represents the point of attachment to the fluorophore or the metal ion chelate moiety.

(75) In some embodiments, the metal ion coordinating moiety is a multi-dentate moiety comprising amino, carboxyl, hydroxyl, amide, or ether groups, or other heteroatom containing moieties, wherein the heteroatom is O, S, or N.

(76) In some embodiments, the metal ion coordinating moiety is a tri- or tetra-dentate amino group-containing moiety. In some embodiments, the tri- or tetra-dentate amino group-containing moiety is unsubstituted or substituted

(77) ##STR00011##

(78) In some embodiments, the M is any suitable metal ion which coordinates, or otherwise interacts (i.e. through hydrogen bonding, ionic bonding, dipole interactions, metal-ligand interactions etc.) with the metal ion coordinating moiety, and which simultaneously binds to a negatively charged phosphate-containing membrane component (for example, in a cell membrane, a vesicle etc.). In some embodiments, M is a transition metal ion, a lanthanide metal ion or post-transition metal ion. In some embodiments, M is a divalent or trivalent metal cation. In some embodiments, M is Zn(II), Cu(II), Mn(II), Ni(II), Co(III), Fe(II), Cd(II) Al(III) or Fe(III). In some embodiments, M is Al(III) or Ga(III). In some embodiments, M is Tb(III), Eu(III), Nb(III) or Yb(III). In some embodiments, M is Zn(II).

(79) In some embodiments, A is any suitable counter anion for a metal cation that does not prevent the metal cation from interacting with the anionic residues on the phospholipid head group. The anion may or may not dissociate from the metal cation when in aqueous solution. In some embodiments, A is selected from CF.sub.3SO.sub.3.sup. (TfO.sup.), Cl.sup., Br.sup., I.sup., CH.sub.3COO.sup., HPO.sub.3.sup., HSO.sub.4.sup., SO.sub.4.sup.2 and NO.sub.3.sup., and the like.

(80) In some embodiments, the compound of the Formula I is selected from:

(81) ##STR00012##

(82) In some embodiments, the compound of Formula I-12 has the following structure:

(83) ##STR00013##

(84) In some embodiments, the compound of Formula I-13 has the following structure:

(85) ##STR00014##

(86) In some embodiments, the compound of Formula I-14 has the following structure:

(87) ##STR00015##

(88) In some embodiments, it was found that, when Y is cyclen or cyclam, the method of the application does not require the presence of a metal species in the sensor compounds, Accordingly, in some embodiments, the application includes a method of detecting negatively charged phosphate-containing membrane components comprising: (a) combining a solution of a sample suspected of comprising negatively charged phosphate-containing membrane components with a solution comprising a compound of Formula II:
WVY II wherein, W is a fluorophore; V is a linker moiety; and Y is

(89) ##STR00016## (b) detecting a fluorescence signal at a wavelength specific for the fluorophore;
wherein detection of the fluorescence signal in (b) indicates that the sample comprises negatively charged phosphate-containing membrane components.

(90) In some embodiments, the compounds of Formula I are prepared by reacting a compound of Formula II:
WVY II,
wherein W, V and Y are as defined in Formula I, with a suitable metal ion salt in an organic solvent. In some embodiments, the compounds of Formula I precipitate from the reaction solution and are isolated, for example, by filtration or any other isolation means.

(91) In some embodiments, the compounds of the Formula I are formed in situ, for example by preparing a binding solution of a compound of Formula II and a suitable metal ion salt to form, in solution, compounds of the Formula I. In some embodiments, the binding solution comprises (i) a non-metallated compound of the Formula I; and (ii) a suitable metal ion, for example in the form of a salt. In some embodiments, the components of the binding solution are kept separate until ready for use.

(92) In some embodiments, methods of the application comprise detecting the fluorescence signal using microscopy, flow cytometry and/or fluorometry.

(93) In some embodiments, the fluorescence signal that is detected is at a wavelength specific for fluorescence emitted by an excimer of the fluorophore. In some embodiments the compounds of Formula I bind to negatively charged phosphate-containing membrane components that are in close proximity to each other, resulting in the formation of a [1:1].sub.2 complex of the sensor compound and leading to interaction between the fluorophores and corresponding excimer formation. In some embodiments, the fluorophore excimer formation is accompanied by a decrease in monomer-region fluorescence and the extent of excimer formation is detected and quantified by measuring the decrease in monomer fluorescence. Likewise, excimer formation is accompanied by an increase in fluorescence at the excimer-forming region of a fluorophore and the extent of excimer formation can be detected and quantified by measuring the increase in fluorescence in that region. In some embodiments, ratios of the decrease in monomer-region fluorescence and the increase in fluorescence at the excimer-forming region are calculated to detect and quantify changes at both regions.

(94) In some embodiments, the methods of the disclosure are performed by measuring fluorescence intensity in the excimer and/or monomer regions. In some embodiments, analysis of the fluorescence is performed using fluorescence polarization, as the tertiary complex between proximal negatively charged negatively charged phosphate-containing membrane components and two excimer units limits the tumbling rate of the excimer fluorophore and increase fluorescence polarization and anisotropy values.

(95) It will be understood that the increase in fluorescence intensity depends, for example, on the concentration of the compound of Formula I or II, and the number of negatively charged negatively charged phosphate-containing membrane components in the sample. For quantification, a calibration curve is generated based on the negatively charged phosphate-containing membrane components of known concentration which is used to compare the fluorescence signal from the sample under investigation.

(96) In some embodiments, the relative number of negatively charged phosphate-containing membrane components can be monitored over time to determine, for example, whether this number increases or decreases over time.

(97) In some embodiments, the fluorescence signal that is detected is compared to a control sample that does not comprise the sample and any change in fluorescence signal with the sample compared to the control indicates the presence of negatively charged phospholipids in the sample.

(98) In some embodiments, the fluorescence signal that is detected is compared to a fluorescence signal of one or more control solutions of known quantities of negatively charged phosphate-containing membrane components and detection of a signal having a fluorescence intensity similar to the fluorescence intensity of one of the control solutions indicates that the amount of negatively charged phosphate-containing membrane components in the sample is similar to the amount of negatively charged phosphate-containing membrane components in the control solution.

(99) The sensor compounds of the Formula I and II of the present application and binding solutions and compositions comprising these compounds are useful for detecting negatively charged phosphate-containing membrane components, such as in the form of membranes and/or vesicles. Such detection is useful for a variety of applications, including without limitation, detection of bacterial cells, apoptotic events, mitochondria, as well as phospholipidosis and certain cancers.

(100) In some embodiments, the sample is an extract from a bacterial, yeast, insect or mammalian cell line including human cell lines.

(101) In some embodiments, the sample is a bodily sample, such as urine, synovial fluid or blood, or any sample that contains or is suspected of containing negatively charged phospholipids.

(102) In some embodiments, the methods disclosed herein are performed in solution, such as an aqueous buffer.

(103) In some embodiments, sensor compounds of Formula I or II can also be used for the detection of negatively charged phosphate-containing membrane components that are attached or immobilized by any biological or synthetic means or in fixed cells or live cells.

(104) It will be understood that the above methods can be conducted using a solution or kit, in which a compound of the Formula II and a suitable metal ion are contacted in situ to optionally form the compound of the Formula I in a binding solution. In some embodiments, the binding solution is formed before contact with the sample; for example, a binding solution comprising a compound of the Formula II and a suitable metal ion are combined in an aqueous solution to form the binding solution which is then combined with a sample to detect negatively charged phospholipids. In some embodiments, the binding solution is formed after contact with a sample; for example, an aqueous solution of a sample of a compound of the Formula II is first prepared, followed by addition of a suitable metal ion to form the binding solution. In some embodiments, the kit further comprises reagents for negative and/or positive controls.

(105) In some embodiments, the present application describes a method for detecting negatively charged phosphate-containing membrane components in cell or vesicle membranes.

(106) In some embodiments, the present application describes a method for detecting negatively charged phosphate-containing membrane components in bacterial membranes and/or vesicles.

(107) In some embodiments, the present application describes a method for detecting negatively charged phosphate-containing membrane components in animal cell membranes and/or vesicles.

(108) In some embodiments, the present application describes a method for detecting negatively charged phosphate-containing membrane components in an animal cell undergoing apoptosis.

(109) In some embodiments, the present application describes a method for detecting bacterial infection.

(110) In some embodiments, the negatively charged phosphate-containing membrane components being detected by methods of the present application comprise, at least one of phosphatidic acid, lysophosphatidic acid, cardiolipin, phosphatidylserine, phosphatidylglycerol, di-22:6-bis(monoacylglycerol)phosphate, lipopolysaccharide, and lipoteichoic acid. In some embodiments, the negatively charged phosphate-containing membrane components being detected are negatively charged phospholipids. In some embodiments, the negatively charged phospholipids are selected from a phosphatidylserine (PS), phosphatidic acid (PA), phosphatidylglycine and cardiolipin (CL).

(III) Compounds of the Application

(111) The present application also includes certain novel compounds useful in the sensors of the application. Accordingly, the present application also includes compounds of Formula IV:

(112) ##STR00017##
wherein: L.sup.1 is a linker group selected from C.sub.1-20alkylene, C.sub.2-20alkenylene, C.sub.2-20alkynylene and C.sub.3-10cycloalkylene, or a combination thereof, each of which is optionally oxo-substituted (O) 1-3 times, and in which 1-3 carbon atoms are optionally replaced with a heteromoiety selected from NH, O, S and Si; and R.sup.2 is selected from

(113) ##STR00018##

(114) In some embodiments, L.sup.1 is selected from:

(115) ##STR00019##

(116) The present application also includes compounds of Formula V:

(117) ##STR00020##
wherein L.sup.2 is a linker group selected from C.sub.1-20alkylene, C.sub.2-20alkenylene, C.sub.2-20alkynylene and C.sub.3-10cycloalkylene, or a combination thereof, each of which is optionally oxo-substituted (O) 1-3 times, and in which 1-3 carbon atoms are optionally replaced with a heteromoiety selected from NH, O, S and Si; and R.sup.3 is selected from

(118) ##STR00021##

(119) In some embodiments, L.sup.2 is selected from:

(120) ##STR00022##

(121) The application also includes compounds of Formula IV and V in the form of a metal chelate salt. In some embodiments, the metal is Zn.sup.2+.

EXAMPLES

(122) Materials and Methods:

(123) All reagents and solvents were purchased from Sigma-Aldrich. Silica gel chromatography was performed with Silica Gel 60 (particle size 40-63 m) obtained from EMD. Thin layer chromatography (TLC) plates were obtained from EMD. 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC), 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine (POPE), 1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-(1-rac-glycerol) (sodium salt) (POPG), 1,2-dioleoyl-sn-glycero-3-phospho-L-serine (sodium salt) (DOPS), 1-palmitoyl-2-dioleoyl-sn-glycero-3-phosphate (sodium salt) (POPA), and 1,1,2,2-tetra-(9Z-octadecenoyl) cardiolipin (sodium salt) (TOCL) were purchased from Avanti Polar Lipids (Alabaster, AL). All fluorescence experiments were performed on a Tecan Infinite M1000 using black 384-well plates (Greiner-BioOne 781076). All experiments were conducted in triplicate, in at least two independent trials.

(124) Sensor compounds were diluted from stock solutions to a final concentration of 50 M in 50 mM HEPES, pH 7.5, 10% DMSO, unless otherwise stated.

(125) Care was taken to minimize exposure of compounds to light during synthesis, storage and testing. Molecular sieves were activated by heating to 125 C. under vacuum overnight. NMR spectra were recorded on a Bruker Avance III spectrometer at 23 C., operating at 400 MHz for .sup.1H NMR and 100 MHz for .sup.13C NMR spectroscopy in either CDCl.sub.3 or CD.sub.3CN. Chemical shifts () are reported in parts per million (ppm) referenced to residual isotopic solvent. Coupling constants (J) are reported in Hertz (Hz). High Resolution Mass Spectrometry (HRMS) was performed on an AB/Sciex QStar mass spectrometer with an ESI source, MS/MS and accurate mass capabilities, associated with an Agilent 1100 capillary LC system. Low Resolution Mass Spectrometry (LRMS) was performed on a Waters Micromass ZQ model MM1. UV-vis spectra were collected using a Hewlett Packard 8452A diode array spectrophotometer with 200 L quartz cuvettes. Purifications by prep-HPLC were performed using Atlantis Prep T3 10 m C18 (2) 25019 mm column run at 20 mL/min (preparative) using gradient mixtures of water with 0.1% TFA and 10:1 acetonitrile/water with 0.1% TFA. The crude mixture was injected as a solution 4:1 0.1% TFA in water/acetonitrile. Analysis by rpHPLC was performed using a Phenomex Luna 5 m C18 (2) 1504.60 mm column run at 1.2 mL/min (analytical) using gradient mixtures of 0.1% TFA in water and acetonitrile. Condition (A) started with 0.1% TFA water with a gradient going to 100% acetonitrile over 30 min, followed by 5 min at 100% acetonitrile. Condition (B) started with 0.1% TFA in water with a gradient going to 100% acetonitrile over 50 min, followed by 5 min at 100% acetonitrile. All final compounds were lyophilized from water/acetonitrile after purification by chromatography prior to testing. Titanic solvent was made using 92% DCM, 7% methanol and 1% ammonium hydroxide.

(126) The sensor compounds of Formula I and Ia were prepared as previously described (WO 2015/089639).

(127) Sensor Compound Design and Proposed Mechanism of Detection

(128) Exemplary sensors are comprised of a Zn.sup.2+-coordinated cyclen chelate linked to a pyrene reporter (FIG. 1A). The Zn.sup.2+ centres are hypothesized to bind the negatively charged phospholipid residues (FIG. 1B). When negatively charged phospholipids are found in a lipid bilayer, such as a vesicle or a membrane, they may be found in close proximity, analogous to proximally phosphorylated residues on peptides and proteins. It is hypothesized that the proximity of the phospholipids could facilitate formation of a [1:1].sub.2 complex, where each of the two sensor molecules binds (via the Zn.sup.2+ Lewis acid centre) to one of the neighbouring negatively charged phospholipid head groups, leading to interaction between the pyrene groups and the corresponding excimer formation. This is shown in FIG. 1B.

Synthesis of Sensor Compounds

Example 1: Synthesis of 1,8-bis[(2,2-dipicolylamino)methyl]anthracene (Unmetallated PSVue380)

(129) ##STR00023##

(130) 9,10-bis(chloromethyl)anthracene (100 mg, 0.363 mmol, 1 eq) was dissolved in THF (1 mL) and cooled to 0 C. 2,2-dipicolylamine (0.131 ml, 0.726 mmol, 2 eq) and triethylamine (0.101 ml, 0.726 mmol, 2 eq) were dissolved in THF (1 mL) and added dropwise. The solution was stirred at room temperature for 16 h then filtered. The solvents were removed in vacuo. The residue was dissolved in DCM, washed with brine, dried over Na.sub.2SO.sub.4. After removal of the solvent in vacuo, the residue was purified by flash column chromatography (Hexanes/EtOAc) followed by recrystallization from EtOAc to give the title product (98 mg, 45%) as a pale yellow powder. .sup.1H NMR (400 MHz, CDCl.sub.3) 8.42 (d, J=5 Hz, 2H), 8.39 (dd, J=7 Hz, 4 Hz, 2H), 7.50 (td, J=8 Hz, 2 Hz, 2H), 7.42 (d, J=8 Hz, 2H), 7.28 (d, J=8 Hz, 2H), 7.02 (t, J=5 Hz, 2H), 4.63 (s, 2H), 3.86 (s, 4H). (Data in accordance with the literature: J. Am. Chem. Soc. 2002, 124, 6256-6258).

Example 2: Synthesis of PSVue380

(131) ##STR00024##

(132) To a solution of 1,8-bis[(2,2-dipicolylamino)methyl]anthracene (35 mg, 0.0583 mmol) in DCM (2.1 mL) was added dropwise 116 mM Zn(NO.sub.3).sub.2 in MeOH (1 mL, 0.1166 mmol)). After stirring for 1 h at room temperature, the precipitate was filtered and washed with DCM to give PSVue380 (42 mg, quantitative) as a pale yellow powder. .sup.1H NMR (400 MHz, DMSO-d.sub.6+D.sub.2O) 8.66 (bs, 2H), 8.09 (bs, 2H), 8.00 (bs, 2H), 7.68 (bs, 2H), 7.57 (bs, 2H), 7.28 (bs, 2H), 4.94 (s, 4H), 4.10 (d, 8 Hz, 4H), 3.67 (d, 8 Hz, 4H). .sup.13C NMR (125 MHz, DMSO-d.sub.6+D.sub.2O) 154.7, 148.7, 147.3, 141.8, 140.5, 131.9, 127.5, 126.9, 126.2, 125.9, 124.6, 58.0, 56.9, 55.8.

Example 3: 1-(pyren-1-ylmethyl)-1,4,7,10-tetraazacyclododecane (Non-Metallated II-1)

(133) ##STR00025##

(134) Compound II-1 was prepared in accordance to the following source: Gunning, P. T., Kraskouskaya, D., 2016. Excimer forming compounds. US20160304473 A1.

Example 4: 1-(4-(pyren-1-yl)butyl)-1,4,7,10-tetraazacyclododecane (II-2)

(135) ##STR00026##

(136) Compound II-2 was prepared in accordance to the following source: Gunning, P. T., Kraskouskaya, D., 2016. Excimer forming compounds. US20160304473 A1.

Example 5: tri-tert-butyl 11-(pyren-1-ylmethyl)-1,4,8,11-tetraazacyclotetradecane-1,4,8-tricarboxylate (II-3A)

(137) ##STR00027##

(138) To a solution of 1-pyrenecarboxaldehyde (35 mg, 0.15 mmol) in 1 mL DCE, Boc.sub.3Cyclam (50 mg, 0.10 mmol) was added and stirred together with 4 molecular sieves for 2 h under nitrogen atmosphere. To this solution sodium triacetoxyborohydride (42 mg, 0.2 mmol) was added and the reaction mixture was allowed to stir at ambient temperature over 24 h under nitrogen atmosphere. Subsequently, the reaction mixture was diluted with sodium bicarbonate and extracted with DCM. The extract was purified by flash chromatography with 30% ethyl acetate/hexanes to give the product (63 mg, 88%); 1H NMR (400 MHz, CDCl.sub.3) 8.47 (d, J=9.3 Hz, 1H), 8.21-7.93 (m, 8H), 4.22 (s, 2H), 3.34 (s, 10H), 3.13 (s, 2H), 2.78 (s, 2H), 2.50 (s, 2H), 1.88 (s, 2H), 1.76-1.66 (m, 2H), 1.51-1.17 (m, 27H); .sup.13C NMR (100 MHz, CDCl.sub.3) 155.55, 132.64, 131.33, 130.87, 130.77, 129.71, 128.41, 127.47, 127.10, 125.83, 125.00, 124.83, 124.50, 124.06, 79.67, 79.44, 58.59, 54.24, 53.43, 47.81, 47.07, 29.72, 28.50, 28.46, 28.31; LRMS (ESI+) m/z calc'd for C.sub.42H.sub.58N.sub.4O.sub.6Na [M+Na].sup.+ 737.42, found 737.65.

Example 6: 1-(pyren-1-ylmethyl)-1,4,8,11-tetraazacyclotetradecane (II-3)

(139) ##STR00028##

(140) To a solution of compound II-3A (108 mg, 0.15 mmol) in 10 mL DCM, 5 mL TFA was added. The reaction mixture was stirred at rt. The progress of the reaction was monitored using MS. The reaction mixture was concentrated down in vacuo and the TFA was azeotroped off in vacuo with MeOH. The crude product was taken up in MeOH and passed through a column packed with Amberlite IRN-78. The solvent was evaporated in vacuo. The mixture was then purified by preparative HPLC. The product was again passed through a column packed with Amberlite IRN-78 to give the product (45 mg, 72%); mp 101-104 C.; .sup.1H NMR (400 MHz, CDCl.sub.3) 8.47 (d, J=9.3 Hz, 1H), 8.18-8.05 (m, 5H), 8.02 (s, 2H), 7.97 (t, J=7.6 Hz, 1H), 4.19 (s, 2H), 2.90-2.79 (m, 6H), 2.78-2.74 (m, 2H), 2.70-2.64 (m, 6H), 2.62-2.57 (m, 2H), 2.56-2.48 (m, 4H), 1.87 (quint, J=5.3 Hz, 2H), 1.60 (quint, J=5.3 Hz, 2H); .sup.13C NMR (100 MHz, CDCl.sub.3) 132.8, 131.2, 130.6, 130.4, 129.5, 128.0, 127.3, 127.0, 126.9, 125.7, 124.9, 124.8, 124.74, 124.72, 124.4, 123.5, 56.8, 54.8, 54.1, 50.3, 48.9, 48.6, 48.3, 47.5, 47.4, 27.9, 26.4; LRMS (ESI+) m/z calc'd for C.sub.27H.sub.35N.sub.4 [M+H].sup.+ 415.29, found 415.20; HRMS (ESI+) m/z calc'd for C.sub.27H.sub.35N.sub.4 [M+H].sup.+ 415.2862, found 415.2854; rpHPLC t.sub.R: condition (A) 12.499 min., condition (B) 19.601 min., purity 99.8% and 96.1% respectively.

Example 7: tri-tert-butyl 11-(4-(pyren-1-yl)butyl)-1,4,8,11-tetraazacyclotetradecane-1,4,8-tricarboxylate (II-4A)

(141) ##STR00029##

(142) To a solution of 4-(pyren-1-yl)butanal (37 mg, 0.14 mmol) in 0.9 mL DCE, Boc.sub.3Cyclam (45 mg, 0.09 mmol) was added and stirred together with 4 molecular sieves for 2 h under nitrogen atmosphere. To this solution sodium triacetoxyborohydride (38 mg, 0.18 mmol) was added and the reaction mixture was allowed to stir at ambient temperature over 24 h under nitrogen atmosphere. Subsequently, the reaction mixture was diluted with sodium bicarbonate and extracted with DCM. The extract was purified by flash chromatography with 35% ethyl acetate/hexanes to give the product (43 mg, 63%); .sup.1H NMR (400 MHz, CDCl.sub.3) 8.29 (d, J=9.3 Hz, 1H), 8.21-7.98 (m, 7H), 7.88 (d, J=7.8 Hz, 1H), 3.46-3.09 (m, 14H), 2.59 (s, 2H), 2.50-2.33 (m, 4H), 1.93-1.74 (m, 4H), 1.73-1.58 (m, 4H), 1.53-1.41 (m, 27H); .sup.13C NMR (100 MHz, CDCl.sub.3) 155.69, 136.80, 131.44, 130.91, 129.80, 128.58, 127.52, 127.24, 127.20, 126.57, 125.81, 125.11, 125.05, 124.86, 124.81, 124.67, 123.40, 79.55, 79.36, 55.42, 48.69, 48.55, 47.30, 46.90, 46.62, 45.69, 33.54, 29.85, 29.72, 28.56, 28.50, 26.79; LRMS (ESI+) m/z calc'd for C.sub.45H.sub.65N.sub.4O.sub.6 [M+H].sup.+ 757.49, found 757.69.

Example 8: Compound II-4

(143) ##STR00030##

(144) To a solution compound II-4A (79 mg, 0.1 mmol) in 15 mL DCM, 1 mL TFA was added. The reaction mixture was stirred at rt. The progress of the reaction was monitored using MS. The reaction mixture was concentrated down in vacuo and the TFA was azeotroped off in vacuo with MeOH. The crude product was taken up in MeOH and passed through a column packed with Amberlite IRN-78. The solvent was evaporated in vacuo. The mixture was then purified by preparative HPLC. The product was again passed through a column packed with Amberlite IRN-78 to give the product (38 mg, 80%); .sup.1H NMR (400 MHz, CDCl.sub.3) 8.30 (d, J=9.3 Hz, 1H), 8.17-8.08 (m, 4H), 8.04-7.95 (m, 3H), 7.88 (d, J=7.8 Hz, 1H), 3.35 (t, J=7.5 Hz, 2H), 2.62 (t, J=5.3 Hz, 2H), 2.59-2.54 (m, 4H), 2.51-2.47 (m, 2H), 2.46-2.41 (m, 4H), 2.40-2.33 (m, 4H), 2.24-2.20 (m, 2H), 1.85 (quint, J=8.1 Hz, 2H), 1.73-1.66 (m, 2H), 1.65-1.59 (m, 2H), 1.59-1.51 (m, 2H); .sup.13C NMR (100 MHz, CDCl.sub.3) 137.1, 131.3, 130.8, 129.6, 128.4, 127.3, 127.2, 127.1, 126.4, 125.6, 124.9, 124.67, 124.65, 124.5, 123.4, 54.6, 54.2, 52.6, 51.2, 49.8, 49.3, 48.5, 47.7, 47.6, 33.4, 30.0, 28.6, 26.4, 26.1; LRMS (ESI+) m/z calc'd for C.sub.30H.sub.40N.sub.4 [M+H].sup.+ 456.33, found 457.32. rpHPLC t.sub.R: condition (A) 13.550 min., condition (B) 21.547 min., purity 99.0% and 98.9% respectively.

Example 9: 1-(pyren-1-yl)-N, N-bis(pyridin-2-ylmethyl)methanamine (II-5)

(145) ##STR00031##

(146) Compound II-5 was prepared in accordance to the following source: Gunning, P. T., Kraskouskaya, D., 2016. Excimer forming compounds. US20160304473 A1.

Example 10: 4-(pyren-1-yl)-N,N-bis(pyridin-2-ylmethyl)butan-1-amine (II-6)

(147) ##STR00032##

(148) Compound II-6 was prepared in accordance to the following source: Gunning, P. T., Kraskouskaya, D., 2016. Excimer forming compounds. US20160304473 A1.

Example 11: 2-(pyren-1-yl)-1-(1,4,7,10-tetraazacyclododecan-1-yl)ethanone (II-7)

(149) ##STR00033##

(150) Compound II-7 was prepared in accordance to the following source: Gunning, P. T., Kraskouskaya, D., 2016. Excimer forming compounds. US20160304473 A1.

Example 12: tri-tert-butyl 10-(4-(pyren-1-yl)butanoyl)-1,4,7,10-tetraazacyclododecane-1,4,7-tricarboxylate (II-8A)

(151) ##STR00034##

(152) To a solution of 1-pyrenebutyric acid (48.8 mg, 0.169 mmol) in 1 mL DMF was added Boc.sub.3Cyclen (80 mg, 0.169 mmol) and TBTU (87 mg, 0.271 mmol) and the reaction mixture was stirred for 30 min at rt. DIPEA (103 L, 0.592 mmol) was then added to this reaction mixture and stirred at rt for 16 h. Subsequently, the mixture was diluted with water and extracted with dichloromethane. The combined organic phases were dried over sodium sulfate and concentrated. The crude product was purified by flash chromatography with 30% ethyl acetate/hexanes to give the product (93 mg, 74%); .sup.1H NMR (400 MHz, CDCl.sub.3) 8.35 (d, J=9.2 Hz, 1H), 8.19-8.09 (m, 4H), 8.01 (s, 2H), 7.98 (t, J=7.6 Hz, 1H), 7.88 (d, J=7.8 Hz, 1H), 3.80-3.19 (m, 16H), 2.50 (bs, 2H), 2.24 (p, J=7.0 Hz, 2H), 2.05 (s, 2H), 1.48 (s, 9H), 1.42 (s, 18H); .sup.13C NMR (100 MHz, CDCl.sub.3) 171.1, 155.4, 136.1, 131.4, 130.9, 129.9, 128.8, 127.5, 127.3, 127.2, 126.6, 125.8, 125.1, 125.0, 124.8, 124.8, 124.7, 123.5, 80.3, 80.3, 80.1, 60.4, 51.4, 49.7, 33.1, 28.5, 28.4, 27.1, 21.0, 14.2; LRMS (ESI+) m/z calc'd for C.sub.43H.sub.58N.sub.4O.sub.7Na [M+Na].sup.+ 751.42, found 751.42.

Example 13: 4-(pyren-1-yl)-1-(1,4,7,10-tetraazacyclododecan-1-yl)butan-1-one (II-8)

(153) ##STR00035##

(154) To a solution of compound II-8A (102 mg, 0.14 mmol) in 10 mL DCM, 5 mL TFA was added. The reaction mixture was stirred at rt. The progress of the reaction was monitored using MS. The reaction mixture was concentrated down in vacuo and the TFA was azeotroped off in vacuo with MeOH. The crude product was taken up in MeOH and passed through a column packed with Amberlite IRN-78. The solvent was evaporated in vacuo. The mixture was then purified by preparative HPLC. The product was again passed through a column packed with Amberlite IRN-78 to give the product (49 mg, 79%); mp 83-86 C.; .sup.1H NMR (400 MHz, CD.sub.3OD) 8.31 (d, J=9.3 Hz, 1H), 8.15-8.10 (m, 2H), 8.09-8.04 (m, 2H), 8.01-7.91 (m, 3H), 7.84 (d, J=7.8 Hz, 1H), 3.60-3.53 (m, 4H), 3.36-3.29 (m, 2H), 3.10 (br, 10H), 3.00 (br, 2H), 2.53 (t, J=7.3 Hz, 2H), 2.08 (quint, J=7.7 Hz, 2H); .sup.13C NMR (100 MHz, CD.sub.3OD) 175.3, 136.1, 131.4, 130.9, 129.9, 128.6, 127.2, 127.1, 127.0, 126.3, 125.7, 124.8, 124.7, 124.6, 124.6, 124.5, 123.2, 48.3, 47.3, 46.7, 44.8, 43.9, 32.3, 32.0, 26.8; LRMS (ESI+) m/z calc'd for C.sub.28H.sub.35N.sub.4O [M+H].sup.+ 443.28, found 444.22; HRMS (ESI+) m/z calc'd for C.sub.28H.sub.35N.sub.4O [M+H].sup.+ 443.2811, found 443.2815; rpHPLC t.sub.R: condition (A) 13.382 min., condition (B) 19.843 min., purity 100.0% and 99.8% respectively.

Example 14: 2-(p-tolyl)ethene-1,1,2-triyl)tribenzene (II-9A)

(155) ##STR00036##

(156) 2-Bromo-1,1,2-triphenylethylene (300 mg, 0.895 mmol) 4-methylphenylboronic acid (146 mg, 1.07 mmol), tetrabutylammonium bromide (14.4 mg, 0.0447 mmol), and tetrakis(triphenylphosphine)palladium(0) (103 mg, 0.0895 mmol) were transferred into a rbf under argon. The reagents were dissolved in 9 mL of THF, and then 0.2 mL of 2 M potassium carbonate (2 mmol) was injected into the rbf. The solution was stirred in an oil bath at 100 C. for 16 h. The solvent was evaporated and the residue was extracted with chloroform and brine. The organic layers were combined and dried with anhydrous magnesium sulfate. The crude product was purified by column chromotography using 4:1 DCM/Hexanes as eluent (267 mg, 86%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.21-7.03 (m, 15H), 6.96 (s, 4H), 2.31 (s, 3H).

Example 15: (2-(4-(bromomethyl)phenyl)ethene-1,1,2-triyl)tribenzene (II-9B)

(157) ##STR00037##

(158) A solution of II-9A (160 mg, 0.462 mmol), N-bromosuccinimide (90.4 mg, 0.508 mmol) and benzoyl peroxide (11.2 mg, 0.0462 mmol) were dissolved in 2.5 mL of chloroform. The solution was refluxed for 14 h. The mixture was extracted with dichloromethane and water. The organic layers were combined, dried with magnesium sulfate and concentrated down in vacuo. The crude product was purified by column chromotography using 5% ethyl acetate in hexanes as eluent to give the product as a white solid (145 mg, 74%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.23-7.06 (m, 19H), 4.46 (s, 2H).

Example 16: tri-tert-butyl 10-(4-(1,2,2-triphenylvinyl)benzyl)-1,4,7,10-tetraazacyclododecane-1,4,7-tricarboxylate (II-9C)

(159) ##STR00038##

(160) A solution of II-9B (145 mg, 0.341 mmol), Boc.sub.3Cyclen (201 mg, 0.426 mmol) and potassium carbonate (236 mg, 1.7 mmol) was dissolved in 3.5 mL acetonitrile and refluxed overnight. The solution was concentrated down in vacuo and the residue was extracted with dichloromethane and water. The organic layer was washed with brine and dried with magnesium sulfate. The solvent was concentrated down in vacuo and purified by flash chromatography using ethyl acetate/hexanes (2:1) as eluent to give the product (176 mg, 87%). .sup.1H NMR (400 MHz, CDCl.sub.3) 7.16-6.96 (m, 19H), 3.65 (s, 2H), 3.61-3.52 (m, 4H), 3.44-3.03 (m, 8H), 1.51-1.45 (br, 28H). LRMS (ESI+) m/z calc'd for C.sub.50H.sub.65N.sub.4O.sub.6 [M+H].sup.+ 818.09, found 817.86.

Example 17: 1-(4-(1,2,2-triphenylvinyl)benzyl)-1,4,7,10-tetraazacyclododecane (II-9)

(161) ##STR00039##

(162) To a solution of II-9C (176 mg, 0.215 mmol) in 2 mL DCM, 0.72 mL TFA was added. The reaction mixture was stirred at rt overnight. The progress of the reaction was monitored using MS. The reaction mixture was concentrated down in vacuo and the TFA was azeotroped off in vacuo with MeOH. The crude product was taken up in MeOH and passed through a column packed with Amberlite IRN-78. The solvent was evaporated in vacuo. The mixture was then purified by preparative HPLC. The product was again passed through a column packed with Amberlite IRN-78 to give the product (82 mg, 86%); .sup.1H NMR (400 MHz, CDCl.sub.3) 7.14-7.07 (m, 9H), 7.07-7.00 (m, 8H), 7.00-6.95 (m, 2H), 3.57 (s, 2H), 2.80 (t, J=6.6, 3.7 Hz, 4H), 2.67 (t, J=5.0 Hz, 4H), 2.57 (t, J=7.1, 4.4, 3.6 Hz, 8H). LRMS (ESI+) m/z calc'd for C.sub.35H.sub.41N.sub.4 [M+H].sup.+ 517.74, found 517.50; rpHPLC t.sub.R: condition (A) 16.241 min., condition (B) 26.261 min., purity 98.6% and 97.5% respectively.

Example 18: 1-(pyridin-2-yl)-N-(pyridin-2-ylmethyl)-N-(3-(1,2,2-triphenylvinyl)benzyl)methanamine (II-10)

(163) ##STR00040##

(164) A mixture of II-9B (151 mg, 0.356 mmol), bis(2-pyridylmethyl)amine (106 mg, 0.534 mmol) and K.sub.2CO.sub.3 (246 mg, 178 mmol) in acetonitrile (3.6 mL) was added together under Nitrogen atmosphere, and refluxed overnight. After, the solution was concentrated down in vacuo, followed by dissolving the residue in DCM and extracted with water and brine. The combined organic layers were dried with magnesium sulfate and concentrated in vacuo. The mixture was then purified by preparative HPLC. The product was passed through a column packed with Amberlite IRN-78 to give the product (79 mg, 41%). .sup.1H NMR (400 MHz, CD.sub.3CN-d3) 8.49 (dt, J=4.9, 1.2 Hz, 2H), 7.70 (td, J=7.7, 1.8 Hz, 2H), 7.51 (d, J=7.8 Hz, 2H), 7.23-7.09 (m, 10H), 7.07-6.97 (m, 11H), 3.71 (s, 4H), 3.57 (s, 2H); .sup.13C NMR (101 MHz, CD.sub.3CN-d3) 148.82, 136.34, 130.89, 130.87, 130.75, 128.31, 127.71, 127.70, 127.64, 126.46, 122.77, 121.98, 117.30, 59.52. HRMS (ESI+) m/z calc'd for C.sub.39H.sub.34N.sub.3 [M+H].sup.+ 544.2747, found 544.2752.

Example 19: 2-(bromomethyl)-6-((4-(pyren-1-yl)butoxy)methyl)pyridine (II-11A)

(165) ##STR00041##

(166) To a stirred solution of 1-pyrenebutanol (442 mg, 1.61 mmol) in 16.1 mL dry THF (0.1 M) in an ice bath was added 95% NaH (407 mg, 16.1 mmol) under an Nitrogen atmosphere. The reaction flask was removed from the ice bath after 30 min and allowed to return to room temperature. After, 2,6-bis(bromomethyl)pyridine (1.07 g, 4.07 mmol) was added and the flask was stirred at ambient temperature for 4 h under an Nitrogen atmosphere. Subsequently, the reaction mixture was quenched with methanol and concentrated by evaporation. The organic layer was extracted in DCM and NaHCO.sub.3(aq) and dried with excess sodium sulfate. The extract was filtered and concentrated by evaporation. The crude material was purified by flash chromatography was performed (20% ethyl acetate in hexanes) to afford the product as a white powder (502 mg, 68%). .sup.1H NMR (400 MHz, CH.sub.2Cl.sub.2-d.sub.2) 8.32 (d, J=9.0 Hz, 1H), 8.23-7.95 (m, 7H), 7.92 (d, J=8.0 Hz, 1H), 7.66 (t, J=8.0 Hz, 1H), 7.38-7.27 (m, 2H), 4.59 (s, 2H), 4.51 (s, 2H), 3.65 (t, J=6.0 Hz, 2H), 3.45-3.36 (m, 2H), 2.05-1.93 (m, 2H), 1.90-1.78 (m, 2H); LRMS (ESI+) m/z calc'd for C.sub.27H.sub.25BrNO [M+H].sup.+ 459.41, found 460.38.

Example 20: 1-amino-3-(((6-((4-(pyren-1-yl)butoxy)methyl)pyridin-2-yl)methyl)amino)propan-2-ol (II-11B)

(167) ##STR00042##

(168) To a stirred solution of II-11A (270 mg, 0.589 mmol) in 2.4 mL DMF was added 1,3-diamino-2-propanol (531 mg, 5.89 mmol) and potassium carbonate (244 mg, 1.77 mmol). The reaction was stirred at ambient temperature for 1 hr under an Nitrogen atmosphere. The reaction mixture was filtered and concentrated by evaporation. The crude material was purified by flash chromatography (14% MeOH, 85% DCM, 1% NH.sub.4OH) to afford compound II-11B as a brown oil (202 mg, 73%). .sup.1H NMR (400 MHz, CH.sub.2Cl.sub.2-d.sub.2) 8.28 (d, J=9.0 Hz, 1H), 8.15 (d, J=8.0 Hz, 2H), 8.14-7.91 (m, 5H), 7.86 (d, J=8.0 Hz, 1H), 7.55 (t, J=8.0 Hz, 1H), 7.22 (d, J=8.0 Hz, 1H), 7.10 (d, J=8.0 Hz, 1H), 4.54 (s, 2H), 3.82 (d, J=3.0 Hz, 2H), 3.71 (s, 2H), 3.58 (s, 1H), 3.42-3.30 (m, 2H), 2.83 (dd, J=12.0, 3.0 Hz, 1H), 2.73-2.61 (m, 2H), 2.55 (dd, J=12.0, 8.0 Hz, 1H), 1.98-1.89 (m, 1H), 1.87-1.73 (m, 2H), 1.30 (d, J=12.0 Hz, 1H), 0.95-0.83 (m, 1H); LRMS (ESI+) m/z calc'd for C.sub.30H.sub.34N.sub.3O.sub.2 [M+H].sup.+ 468.26, found 468.36.

Example 21: 1-(bis(pyridin-2-ylmethyl)amino)-3-(((6-((4-(pyren-1-yl)butoxy)methyl)pyridin-2-yl)methyl)(pyridin-2-ylmethyl)amino)propan-2-ol (II-11)

(169) ##STR00043##

(170) To a stirred solution of compound II-11B (200 mg, 0.428 mmol, 1 equiv.) in 10 mL 1,2-dichloroethane (DCE, 0.04 M) was added 2-pyridinecarboxaldehyde (0.407 mL, 4.28 mmol, 10 equiv.) and 20-30 molecular sieves under an Nitrogen atmosphere. After, Na(OAc).sub.3BH (952 mg, 4.49 mmol, 10.5 equiv.) was added and the reaction was left stirring overnight at ambient temperature. The reaction mixture was quenched using saturated sodium bicarbonate, extracted in DCM and NaHCO.sub.3(aq), and dried with excess magnesium sulfate. The extract was filtered and concentrated by evaporation. The crude material was purified by flash chromatography (93% DCM, 6% MeOH, 1% NH.sub.4OH) to afford the compound as a brown oil (125 mg, 40%). .sup.1H NMR (400 MHz, CD.sub.3CN) 8.44-8.36 (m, 3H), 8.31 (d, J=9.5 Hz, 1H), 8.19 (dd, J=7.5, 1.5 Hz, 2H), 8.13 (d, J=8.0 Hz, 1H), 8.09 (d, J=9.5 Hz, 1H), 8.05 (d, J=1.0 Hz, 2H), 8.01 (t, J=7.5 Hz, 1H), 7.89 (d, J=8.0 Hz, 1H), 7.63-7.53 (m, 4H), 7.31 (t, J=8.0 Hz, 3H), 7.20 (dd, J=7.5, 3.0 Hz, 2H), 7.10 (dd, J=6.5, 5.0 Hz, 3H), 4.64 (s, 1H), 4.47 (s, 2H), 3.86-3.65 (m, 9H), 3.57 (t, J=6.5 Hz, 2H), 3.34 (t, J=8.0 Hz, 2H), 2.53 (dd, J=13.0, 3.0 Hz, 2H), 2.39 (ddd, J=13.0 7.5, 3.0 Hz, 2H), 1.92-1.83 (m, 2H), 1.80-1.70 (m, 2H). .sup.13C NMR (101 MHz, CD.sub.2Cl.sub.2) 159.57, 158.82, 158.13, 148.73, 148.33, 136.96, 136.65, 136.35, 136.04, 131.29, 130.79, 129.59, 128.47, 127.35, 127.18, 126.93, 126.32, 125.68, 124.84, 124.80, 124.66, 124.64, 124.50, 123.38, 122.82, 121.92, 121.69, 121.25, 120.22, 119.13, 73.64, 70.67, 67.08, 64.08, 60.62, 60.53, 58.90, 33.07, 29.68, 28.36. HRMS (ESI+): m/z: calc'd for C.sub.48H.sub.49N.sub.6O.sub.2: 741.3917; found: 741.3916.

Example 22: Compound II-12A

(171) ##STR00044##

(172) This compound was prepared according to the following source: Kawasaki, A., Kobashi, T., Koike, T., Takahagi, M., 2004. Method for labelling phosphorylated peptides, complex compounds used in the methods, process for producing the same, and their intermediates. EP1455189 A1.

Example 23: Compound II-12B

(173) ##STR00045##

(174) This compound was prepared according to the following source: Kawasaki, A., Kobashi, T., Koike, T., Takahagi, M., 2004. Method for labelling phosphorylated peptides, complex compounds used in the methods, process for producing the same, and their intermediates. EP1455189 A1.

Example 24: Compound II-12C

(175) ##STR00046##

(176) This compound was prepared according to the following source: Kawasaki, A., Kobashi, T., Koike, T., Takahagi, M., 2004. Method for labelling phosphorylated peptides, complex compounds used in the methods, process for producing the same, and their intermediates. EP1455189 A1.

Example 25: 2-(((3-(bis(pyridin-2-ylmethyl)amino)-2-hydroxypropyl)(pyridin-2-ylmethyl)amino)methyl)-N-(2-(3-(pyren-1-yl)propanamido)ethyl)isonicotinamide (II-12)

(177) ##STR00047##

(178) A solution of 1-pyrenebutyric acid (55.5 g, 0.192 mmol), I-12C (104 mg, 0.192 mmol) and DMAP (47 mg, 0.385 mmol) in DCM (11 mL) was stirred under an argon atmosphere. EDC (73.7 mg, 0.385 mmol) was separately dissolved in DCM (1.5 mL) and added. The solution was stirred at ambient temperature overnight. The solution was extracted with water and dried with anhydrous Magnesium sulfate. The product was concentrated down in vacuo and the crude product purified by preparative TLC using DCM/MeOH/NH.sub.4OH 91:8:1 as the eluent to yield the product as a yellow oil. .sup.1H NMR (400 MHz, CDCl.sub.3) 8.84 (s, 1H), 8.35 (t, J=5.0 Hz, 2H), 8.12 (d, J=10.5 Hz, 1H), 8.02 (dd, J=16.0, 8.0 Hz, 2H), 7.93 (d, J=8.5 Hz, 2H), 7.91-7.80 (m, 4H), 7.68 (d, J=8.0 Hz, 1H), 7.53-7.36 (m, 3H), 7.29-7.11 (m, 4H), 7.05-6.93 (m, 3H), 6.88 (t, 5.0 Hz, 1H), 3.88-3.59 (m, 9H), 3.48-3.41 (m, 2H), 3.41-3.33 (m, 2H), 3.20 (t, J=7.5 Hz, 2H), 2.50 (dd, J=13.0, 3.5 Hz, 2H), 2.41 (dd, J=13.0, 8.0 Hz, 2H), 2.22 (t, J=7.0 Hz, 2H), 2.13-1.97 (m, 2H). LRMS (ESI+) m/z calc'd for C.sub.50H.sub.50N.sub.8O.sub.3Na [M+Na].sup.+ 833.99, found 833.86.

Example 26: Compound II-13A

(179) ##STR00048##

(180) This compound was prepared according to the following source: Kawasaki, A., Kobashi, T., Koike, T., Takahagi, M., 2004. Method for labelling phosphorylated peptides, complex compounds used in the methods, process for producing the same, and their intermediates. EP1455189 A1.

Example 27: Compound II-13B

(181) ##STR00049##

(182) This compound was prepared according to the following source: Kawasaki, A., Kobashi, T., Koike, T., Takahagi, M., 2004. Method for labelling phosphorylated peptides, complex compounds used in the methods, process for producing the same, and their intermediates. EP1455189 A1.

Example 28: 1-(bis(pyridin-2-ylmethyl)amino)-3-(((6-((4-(pyren-1-yl)butyl)amino)pyridin-2-yl)methyl)(pyridin-2-ylmethyl)amino)propan-2-ol (II-13)

(183) ##STR00050##

(184) A solution of precursor II-13B (181 mg, 0.385 mmol) dissolved in DCE (2 mL) was transferred into a solution of 4-(pyren-1-yl)butanal (157 mg, 0.578 mmol) in DCE (2 mL). To this solution was added acetic acid (66.2 L, 1.16 mmol), followed by addition of powdered NaBH(OAc).sub.3 (245 mg, 1.16 mmol) in one portion under nitrogen at ambient temperature, and stirred overnight. The mixture was diluted with DCM and quenched with concentrated NH.sub.4OH in water. The two layers were separated, and the aqueous layer was extracted with DCM (10 mL2). The combined organic layers were washed 3 times with water and brine and dried using magnesium sulfate. The crude was purified with the use of preparative HPLC (0.1% TFA in 100% water to 100% ACN gradient). The collected fractions were lyophilized from ACN/Water to give the product (16 mg, 6%). .sup.1H NMR (400 MHz, CDCl.sub.3) 8.71 (d, J=5.5 Hz, 2H), 8.66 (d, J=5.5 Hz, 1H), 8.21 (d, J=9.0 Hz, 1H), 8.19-8.13 (m, 2H), 8.11 (d, J=7.5 Hz, 1H), 8.09-8.04 (m, 2H), 8.04-7.94 (m, 4H), 7.89-7.79 (m, 2H), 7.75 (d, J=8.0 Hz, 2H), 7.68 (d, J=5.5 Hz, 2H), 7.46 (t, J=6.0 Hz, 2H), 7.33-7.22 (m, 1H), 7.16 (dd, J=8.5, 5.5 Hz, 1H), 6.89 (d, J=8.5 Hz, 1H), 4.33-4.11 (m, 8H), 4.07 (d, J=15.0 Hz, 2H), 3.35 (dd, J=9.0, 6.0 Hz, 3H), 3.17-3.07 (m, 2H), 2.74-2.50 (m, 2H), 2.03-1.89 (m, 2H), 1.85-1.72 (m, 2H). .sup.13C NMR (101 MHz, CDCl.sub.3) 153.32, 153.22, 145.52, 143.83, 143.55, 143.15, 142.71, 136.39, 135.80, 131.31, 130.74, 129.73, 128.47, 127.48, 127.27, 127.00, 126.71, 126.42, 126.04, 125.97, 125.79, 125.04, 124.86, 124.81, 124.67, 123.26, 121.36, 64.67, 59.54, 58.40, 56.65, 54.14, 42.84, 32.89, 28.84, 27.81. LRMS (ESI+) m/z calc'd for C.sub.47H.sub.47N.sub.7ONa [M+Na].sup.+ 748.93, found 748.70. HRMS (ESI+): m/z: calc'd for C.sub.47H.sub.48N.sub.7O [M+H]+: 726.3915, found: 726.3906.

Example 29: N-(6-(((3-(bis(pyridin-2-ylmethyl)amino)-2-hydroxypropyl)(pyridin-2-ylmethyl)amino)methyl)pyridin-2-yl)-4-(pyren-1-yl)butanamide (II-14)

(185) ##STR00051##

(186) To a solution of 1-pyrenebutyric acid (73 mg, 0.253 mmol) in DCM (2.5 mL), DMAP (4.94 mg, 0.0404 mmol) and triethylamine (35.2 L, 0.253 mmol) were added at ambient temperature. A solution of II-13B (95 mg, 0.202 mmol) in DCM (2.5 mL) was added dropwise at ambient temperature. EDC (48 mg, 0.253 mmol) was then added and the reaction was refluxed overnight. Afterwards, the reaction was allowed to stir for another 24 h at ambient temperature. The obtained reaction mixture extracted with DCM and water. The combined organic layers were washed 3 times with water and brine and dried using magnesium sulfate. The crude product was purified by column chromatography (DCM:MeOH:NH.sub.4OH 93:6:1) to obtain a yellow oil. .sup.1H NMR (400 MHz, CD.sub.3CN) 9.04 (s, 1H), 8.71 (dd, J=10.8, 5.5 Hz, 4H), 8.53 (d, J=8.4 Hz, 1H), 8.45 (dd, J=4.5, 1.0 Hz, 1H), 8.37 (d, J=9.5 Hz, 1H), 8.32 (td, J=8.0, 1.5 Hz, 2H), 8.25 (td, J=8.0, 1.5 Hz, 1H), 8.21 (d, J=7.5 Hz, 2H), 8.15 (dd, J=11.5, 8.5 Hz, 2H), 8.07 (s, 2H), 8.03 (t, J=8.0 Hz, 1H), 7.94 (d, J=8.0 Hz, 1H), 7.85-7.63 (m, 6H), 4.35-4.00 (m, 8H), 3.42 (t, J=7.0 Hz, 2H), 2.71 (dd, J=14.0, 2.0 Hz, 1H), 2.64 (t, J=7.0 Hz, 2H), 2.59 (d, J=14.0 Hz, 1H), 2.48 (dd, J=14.0, 10.0 Hz, 1H), 2.37 (dd, J=14.0, 9.5 Hz, 1H), 2.28-2.16 (m, 2H), 2.00 (d, J=5.0 Hz, 1H), 1.97 (p, J=2.5 Hz, 1H). LRMS (ESI+): m/z: calcd for C.sub.47H.sub.46N.sub.7O.sub.2: 740.93; found: 740.71. HRMS (ESI+): m/z: calc'd for C.sub.47H.sub.46N.sub.7O.sub.2: 740.3708; found: 740.3711.

Example 30: 5-(diethylamino)-2-formylphenyl trifluoromethanesulfonate (II-15A)

(187) ##STR00052##

(188) A solution of 4-(diethylamino)salicylaldehyde (300 mg, 1.55 mmol) in 21 mL of DCM, was added pyridine (0.251 mL, 3.1 mmol) and trifluoromethanesulfonic acid (0.495 mL, 2.94 mmol) under a nitrogen atmosphere at 0 C. The reaction mixture was stirred for 4 h, and then quenched with water. This mixture was washed further with water and extracted with DCM, before being dried with magnesium sulfate and filtered. The resultant solution was evaporated down in vacuo. The crude was then purified via flash chromatography (8:1 Hexane/EtOAc) to obtain a white powder (336 mg, 66.7%). .sup.1H NMR (400 MHz, CDCl.sub.3) 9.91 (s, 1H), 7.74 (d, J=9.0 Hz, 1H), 6.64 (dd, J=9.0, 2.5 Hz, 1H), 6.42 (d, J=2.5 Hz, 1H), 3.42 (q, J=7.0 Hz, 1H), 1.21 (t, J=7.0 Hz, 1H). .sup.13C NMR (100 MHz, CDCl.sub.3) 184.50, 152.96, 152.19, 132.21, 120.11, 116.92, 115.78, 110.24, 102.96, 44.92, 11.96. .sup.19F NMR (376 MHz, CDCl.sub.3) 5-74.32 (s). LRMS (ESI+) m/z calc'd C.sub.12H.sub.15F.sub.3NO.sub.4S [M+H].sup.+ 326.06, found 326.23.

Example 31: N,N-bis(pyridin-2-ylmethyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)propan-1-amine (II-15B)

(189) ##STR00053##

(190) A microwave vial charged with bis(2-pyridylmethyl)amine, 3-bromopropylboronic acid pinacol ester and K2CO3 in MeCN, was stirred at 60 C. for 24 hours. The reaction mixture was extracted with water and ethyl acetate. The combined organic phases were dried with sodium sulfate and concentrated down in vacuo to give the crude material. The crude was then purified via flash chromatography (Hexane/EtOAc) to obtain a white powder (177 mg, 48%). .sup.1H NMR (400 MHz, CDCl.sub.3) 8.44 (d, J=4.5 Hz, 2H), 7.59 (t, J=7.5 Hz, 2H), 7.52 (d, J=7.5 Hz, 2H), 7.07 (t, J=6.0 Hz, 2H), 3.75 (s, 4H), 2.45 (t, J=7.5 Hz, 2H), 1.62 (p, J=8.0 Hz, 2H), 1.13 (s, 12H), 0.69 (t, J=8.0 Hz, 2H). .sup.13C NMR (101 MHz, CDCl.sub.3) 160.10, 148.63, 136.18, 122.56, 121.58, 82.74, 74.71, 60.19, 56.48, 24.69, 24.58, 21.35. LRMS (ESI+) m/z calc'd C.sub.21H.sub.30BN.sub.3O.sub.2Na [M+Na].sup.+ 390.29, found 390.49.

Example 32: 2-(3-(bis(pyridin-2-ylmethyl)amino)propyl)-4-(diethylamino)benzaldehyde (II-15C)

(191) ##STR00054##

(192) To a stirred solution of II-15A (100 mg, 0.307 mmol) in 1.1 mL THF was added II-15B (169 mg, 0.461 mmol), 3 M NaOH (0.3 mL, 0.896 mmol), and 1,1-bis-(diphenylphosphinoferrocene)Pd (45 mg, 0.0614 mmol). The reaction mixture was heated at 100 C. for 2 h. After cooling to room temperature, the solution was concentrated down in vacuo. The residue with ethyl acetate and water. The organic layer was dried with magnesium sulfate and evaporated. The crude material was purified by preparative TLC (3% MeOH in DCM) to give the product (49.2 mg, 38.4%). LRMS (ESI+) m/z calc'd C.sub.26H.sub.32N.sub.4ONa [M+Na].sup.+ 439.56, found 439.44.

Example 33: (E)-2-(benzo[d]thiazol-2-yl)-3-(2-(3-(bis(pyridin-2-ylmethyl)amino)propyl)-4-(diethylamino)phenyl)acrylonitrile (II-15)

(193) ##STR00055##

(194) To a stirred solution of II-15C (49.2 mg, 0.118 mmol) in 1.2 mL EtOH was added benzothiazole-2-acetonitrile (20.6 mg, 0.118 mmol) under an nitrogen atmosphere. After, piperidine (11.7 uL, 0.118 mmol) was added and the reaction was left stirring overnight at ambient temperature. The resultant mixture was washed with 0.1% HCl, and the crude extracted via DCM, before being dried with magnesium sulfate and filtered. The resultant solution was evaporated in vacuo. The crude was purified with the use of preparative HPLC (0.1% TFA in 100% water to 100% ACN gradient). The collected fractions were lyophilized from ACN/Water to give the product (29 mg, 43%). .sup.1H NMR (400 MHz, MeOH-d.sub.4) 8.36 (d, J=4.5 Hz, 2H), 8.31 (d, J=9.0 Hz, 1H), 8.29 (s, 1H), 7.89 (d, J=8.0 Hz, 1H), 7.86 (d, J=8.0 Hz, 1H), 7.67 (td, J=7.5, 1.5 Hz, 2H), 7.60 (d, J=8.0 Hz, 2H), 7.49 (t, J=7.2 Hz, 1H), 7.41 (t, J=7.6 Hz, 1H), 7.18-7.13 (m, 2H), 6.64 (dd, J=9.0, 2.5 Hz, 1H), 6.50 (d, J=2.5 Hz, 1H), 3.82 (s, 4H), 3.45 (q, J=7.0 Hz, 4H), 2.79 (t, J=8.0 Hz, 3H), 2.66 (t, J=8.0 Hz, 3H), 1.93-1.77 (m, 3H), 1.19 (t, J=7.0 Hz, 6H). .sup.13C NMR (100 MHz, MeOH-d.sub.4) 165.54, 159.04, 153.47, 151.04, 147.98, 147.27, 144.23, 137.24, 134.07, 130.41, 126.49, 123.40, 122.35, 122.19, 121.36, 117.19, 111.90, 109.60, 96.36, 59.91, 53.73, 44.21, 31.59, 29.50, 11.80. HRMS (ESI+): m/z: calc'd for C.sub.35H.sub.37N.sub.6S [M+H].sup.+ 573.2795; found: 573.2786.

Example 34: 4-(diethylamino)-2-(3-oxopropyl)benzaldehyde (II-16A)

(195) ##STR00056##

(196) In a microwave vial, allyl alcohol (0.0136 mL, 0.2 mmol) was added to a mixture of II-15A (78.1 mg, 0.24 mmol), palladium acetate (2.25 mg, 0.01 mmol), sodium bicarbonate (33.6 mg, 0.4 mmol) and tetrabutylammonium bromide (200 mg, 0.62 mmol) under a nitrogen atmosphere, and heated at 110 C. for 3 h. The resultant mixture was washed with cold aqueous 0.1 M HCl, extracted with DCM, and dried with magnesium sulfate. The resultant solution was evaporated in vacuo. The crude was purified via flash column chromatography (7:3 hexane/EtOAc) to give 2 as a yellow solid (10 mg, 21.4%). .sup.1H NMR (400 MHz, CD.sub.2Cl.sub.2): 9.85 (1H, t, J=1.5 Hz), 9.82 (1H, s), 7.60 (1H, d, J=9.0 Hz), 7.28 (s, CDCl.sub.3), 6.59 (1H, dd, J=9.0, 3.0 Hz), 6.49 (2H, d, J=3.0 Hz), 3.45 (4H, q, J=8.0 Hz), 3.32 (2H, t, J=7.5 Hz), 2.81 (2H, td, J=7.5, 1.5 Hz), 1.24 (6H, t, J=7.0 Hz); .sup.13C NMR (100 MHz, CD.sub.2Cl.sub.2): 202.05, 190.26, 137.98, 113.05, 108.59, 77.01, 45.09, 44.61, 29.71, 26.93, 12.53. LRMS (ESI+) m/z calc'd C.sub.14H.sub.19NO.sub.2Na [M+Na].sup.+ 256.30, found 256.32.

Example 35: tri-tert-butyl 10-(3-(5-(diethylamino)-2-formylphenyl)propyl)-1,4,7,10-tetraazacyclododecane-1,4,7-tricarboxylate (II-16B)

(197) ##STR00057##

(198) A solution of II-16A (29.2 mg, 0.125 mmol) in 0.5 ml of DCE was added to a solution of Boc.sub.3cyclen (47.3 mg, 0.1 mmol) in 0.5 mL of DCE in a rbf at 0 C., and stirred together with 4 molecular sieves for 2 h under nitrogen atmosphere. Sodium triacetoxyborohydride (31.8 mg, 0.15 mmol) in 0.2 mL of DCE was then added, and the reaction stirred for 24 h at rt. The resultant mixture was washed with water, extracted with DCM, and dried under magnesium sulfate. The solution was evaporated down in vacuo. The crude was purified by flash chromatography (1:1 Hexane/EtOAc) to give an orange solid (50 mg, 58%). .sup.1H NMR (400 MHz, CD.sub.2Cl.sub.2): 9.87 (1H, s), 7.64 (1H, d, J=8.8 Hz), 6.58 (1H, dd) 6.43 (1H, d, J=8.8 Hz), 3.6-2.6 (16H, m), 1.60 (4H, s), 1.48 (9H, s), 1.45 (18H, s), 1.30-1.22 (6H, m). .sup.13C NMR (100 MHz, CD.sub.2Cl.sub.2): 189.93, 151.34, 112.28, 108.55, 79.19, 77.01, 44.54, 29.71, 28.72, 28.51, 12.59. LMRS (ESI+) m/z calc'd C.sub.37H.sub.64N.sub.5O.sub.7 [M+H].sup.+ 690.95, found 690.64.

Example 36: tri-tert-butyl (E)-10-(3-(2-(2-(benzo[d]thiazol-2-yl)-2-cyanovinyl)-5-(diethylamino)phenyl)propyl)-1,4,7,10-tetraazacyclododecane-1,4,7-tricarboxylate (II-16C)

(199) ##STR00058##

(200) To a stirred solution of II-16B (50 mg, 0.0725 mmol) in 1 mL EtOH was added benzothiazole-2-acetonitrile (13.9 mg, 0.0798 mmol) under a nitrogen atmosphere. After, piperidine (21.5 uL, 0.217 mmol) was added and the reaction was left stirring overnight at ambient temperature. The resultant mixture was washed with 0.1% HCl, and the crude extracted via DCM, before being dried with magnesium sulfate and filtered. The resultant solution was evaporated in vacuo. The crude material was purified by flash chromatography (7:3 Hexane/EtOAc) to give a red solid (30 mg, 48.9%). .sup.1H NMR (400 MHz, CD.sub.2Cl.sub.2): 8.45-6.4 (15H), 4.15 (2H, q, J=7.2 Hz), 3.54-3.15 (21H, m), 1.48-1.42 (28H, m), 1.31-1.26 (34H, m) 0.94-0.81 (21H, m). LMRS (ESI+) m/z calc'd C.sub.46H.sub.68N.sub.7O.sub.6S [M+H].sup.+ 847.15, found 846.75.

Example 37: (E)-3-(2-(3-(1,4,7,10-tetraazacyclododecan-1-yl)propyl)-4-(diethylamino)phenyl)-2-(benzo[d]thiazol-2-yl)acrylonitrile (II-16)

(201) ##STR00059##

(202) 85% wt Phosphoric Acid (0.0592 ml, 1.02 mmol) was added to II-16C (30 mg, 0.0355 mmol) in 0.3 mL of DCM under N.sub.2, and the reaction was stirred overnight at rt. The solution was cooled to 0 C., and 1 mL of water was added. The reaction was then quenched with 2M NaOH, and resultant mixture was filtered to give a red precipitate. The crude was purified with the use of preparative HPLC (0.1% TFA in 100% water to 100% ACN gradient). The collected fractions were lyophilized from ACN/Water to give II-16 as a red crystal (1 mg, 5%); LRMS (ESI+) m/z calc'd for C.sub.31H.sub.44N.sub.7S [M+H].sup.+ 546.80, found 546.54.

Example 38: Compound II-17

(203) ##STR00060##

Example 39: N,N-bis(pyridin-2-ylmethyl)pyrene-1-carboxamide (II-18)

(204) ##STR00061##

(205) To a solution of 1-pyrenecarboxylic acid (50 mg, 0.2 mmol) in DCM (2 mL) was added oxalyl chloride (51.5 L, 0.6 mmol). One drop of DMF was also injected as a catalyst. The resulting mixture was stirred at room temperature for 4 h. Evaporation of the volatiles yielded pyrene-1-carbonyl chloride. The product was dissolved in DCM (1 mL) and was added dropwise to the solution of DPA (183 L, 1.02 mmol) in DCM (2.5 mL). The resulting solution was stirred at room temperature for 3 h. The reaction mixture was washed with distilled water, evaporated, and concentrated to dryness to afford the product as a yellowish oil. 1H NMR (400 MHz, DMSO-d.sub.6) 8.72 (dt, J=5, 1.5 Hz, 1H), 8.54-8.48 (m, 1H), 8.44-8.02 (m, 9H), 7.90 (td, J=8, 2 Hz, 1H), 7.65 (td, J=8, 2 Hz, 1H), 7.57 (d, J=8 Hz, 1H), 7.41 (ddd, J=8, 5, 1 Hz, 1H), 7.24 (ddd, J=8, 5, 1 Hz, 1H), 7.11 (d, J=8 Hz, 1H), 5.24 (s, 1H), 4.74 (s, 1H), 4.51 (d, J=14 Hz, 2H). .sup.13C NMR (100 MHz, DMSO-d.sub.6) 171.41, 157.38, 156.58, 149.77, 149.75, 137.43, 137.25, 131.81, 131.41, 131.17, 130.78, 128.80, 128.51, 127.64, 127.44, 127.11, 126.25, 126.08, 125.05, 124.89, 124.47, 124.12, 124.08, 123.03, 122.98, 122.71, 122.20, 54.48, 50.33. LRMS (ESI+) m/z calc'd for C.sub.29H.sub.21N.sub.3ONa [M+Na].sup.+ 450.50, found 450.41.

Example 40: Compound II-19

(206) ##STR00062##

Example 41: Formation of Zinc Chelates (Compounds of Formula I)

(207) To a solution of the compound of Formula II (1 equivalent) in ACN was added Zn(OTf).sub.2 (1 equivalent). After stirring for 2 h at room temperature, distilled water was added and the solution was lyophilized to give the compounds of Formula I.

Example 42 Lipid Detection

Example 42.1 Vesicle Preparation

(208) Small Unilamellar Vesicles (SUVs) were prepared by the extrusion method. Appropriate amounts of lipid in the desired proportions were weighed out to create 10 mM liposome suspensions. The lipids were then dissolved in a minimum amount of chloroform and vortexed to ensure thorough mixing. The excess solvent was then dried off under a gentle stream of nitrogen and allowed to dry overnight in a vacuum dessicator to remove any remaining traces of solvent. The resulting lipid film was then hydrated with 2 mL of HEPES buffer (50 mM HEPES, pH 7.5) for 1 h. The sample was then subjected to five cycles of freeze-thaw-vortex, cycling between liquid nitrogen and a 60 C. water bath. The resulting suspension of multilamellar vesicles (MLVs) was then extruded 25 times through a 0.1 m polycarbonate membrane installed in a mini-extruder (Avanti Polar Lipids, Alabaster, AL) to form SUV.

Example 42.2 Serial Dilution Vesicle Fluorescence Intensity Experiments

(209) 10 mM stock solutions of vesicles were diluted separately to 400 M and 80 M in pH 7.5, 50 mM HEPES buffer. Two concentration ranges were prepared through serial dilutions (400-42 M, 4:5 dilution; 80-4 M, 3:4 dilution). The sensors were dissolved to a concentration of 50 M (from 800 M stock solutions in 100% DMSO) in 50 mM HEPES, pH 7.5, 10% DMSO buffer. 30 L of the vesicle solutions were combined with 30 L of sensor solutions, the mixtures were incubated for 10 min away from light, and the fluorescence intensity was recorded at 476 nm (10 nm bandwidth) following excitation at 350 nm. For the monomer of sensor compounds, emission at 376 nm (10 nm bandwidth) was measured following excitation at 350 nm (5 nm bandwidth). Fluorescence intensities measured were used to calculate the following parameters: FI.sub.exc, FI.sub.exc, FI.sub.mon, FI.sub.mon, FI.sub.exc/mon and FI. The following equations were used for the calculations:

(210) $\begin{array}{cc}{\mathrm{FI}}_{\mathrm{exc}}=\frac{{\mathrm{FI}}_{\mathrm{exc}\mathrm{sensor}+\mathrm{vesicle}}}{{\mathrm{FI}}_{\mathrm{exc}\mathrm{sensor}}}& \mathrm{Equation}1\end{array}$$\begin{array}{cc}{\mathrm{FI}}_{\mathrm{exc}}=\frac{{\mathrm{FI}}_{\mathrm{exc}\mathrm{vesicle}}}{{\mathrm{FI}}_{\mathrm{exc}100\%\mathrm{PC}}}& \mathrm{Equation}2\end{array}$$\begin{array}{cc}{\mathrm{FI}}_{\mathrm{mon}}=\frac{{\mathrm{FI}}_{\mathrm{mon}\mathrm{sensor}+\mathrm{vesicle}}}{{\mathrm{FI}}_{\mathrm{mon}\mathrm{sensor}}}& \mathrm{Equation}3\end{array}$$\begin{array}{cc}{\mathrm{FI}}_{\mathrm{exc}/\mathrm{mon}}=\frac{{\mathrm{FI}}_{\mathrm{exc}}}{{\mathrm{FI}}_{\mathrm{mon}}}& \mathrm{Equation}4\end{array}$$\begin{array}{cc}{\mathrm{FI}}_{\mathrm{mon}}=\frac{{\mathrm{FI}}_{\mathrm{mon}\mathrm{vesicle}}}{{\mathrm{FI}}_{\mathrm{mon}100\%\mathrm{PC}}}& \mathrm{Equation}5\end{array}$$\begin{array}{cc}\mathrm{FI}=\frac{{\mathrm{FI}}_{\mathrm{exc}}}{{\mathrm{FI}}_{\mathrm{mon}}}.& \mathrm{Equation}6\end{array}$

(211) To evaluate the potential of exemplary sensors of the application for selective detection of negatively charged phospholipids within biological and artificial lipid membrane structures, sensor compounds II were screened against small unilamellar vesicles, composed of (unless otherwise stated) 50% (mol) POPC (PC) and 50% of POPE (PE), DOPS (PS), POPG (PG), POPA (PA) or TOCL (CL). Of these, PC and PE represented the zwitterionic vesicles; PS (1), PA (1), PG (1) and CL (2) represented the negatively charged vesicles. The commercially available sensor for the detection of negatively charged membranes, PSVue 380, was tested alongside sensors compounds Ia to allow direct comparison of the sensitivity and selectivity profiles.

(212) The initial proof-of-concept experiment was conducted to probe whether compound I-1 selectively detected negatively charged vesicles over the zwitterionic vesicles. Compound I-1 (25 M) was incubated with or without zwitterionic PC or PE vesicles, or negatively charged PS, PG, PA, or CL vesicles (2-200 M) in 50 mM HEPES, pH 7.5, 5% DMSO, and fluorescence intensity corresponding to excimer emission (476 nm) was measured. The fluorescence enhancement of the excimer (FI.sub.exc) species in the presence of vesicles was calculated using equation 1, which is defined as the ratio of the emission intensities of the sensor-vesicle sample and the sensor alone.

(213) FIG. 2 panels A and B show that sensor compound I-1 selectively detected all negatively charged vesicles (FI.sub.exc5) over the two zwitterionic vesicles (FI.sub.exc1) at different vesicle concentrations. PA vesicles were detected best, with FI values reaching 20 at 50 M PA vesicle concentration, closely followed by CL, and further by PS and PG. While not wishing to be limited by theory, higher sensitivity to PA and CL vesicles could be attributed to the higher negative charge associated with these lipids: the head group of PA contains a phosphate-monoester (as compared to the phosphate-diester in CL, PG and PS) affording a doubly-ionizable phosphate group, while CL contains two phosphate-diester groups per lipid molecule (PA, PG, and PS contain one). Additionally, while not wishing to be limited by theory, the phosphate-monoester of PA is less sterically hindered, which could facilitate more optimal binding of the sensor molecules. A linear response was, on average, observed from 2 to 40 M vesicles (50 M for PA) (panel A), followed by a gradual decrease in signal at higher vesicle concentration (panel B). The observed decrease is consistent with the proposed [1:1].sub.2 sensing mechanism of the sensor compounds; the excimer-emitting [1:1].sub.2 complex dissociates in favour of forming monomer-emitting [1:1].sub.2 complexes. The zwitterionic PC and PE vesicles were not detected, with an excimer signal almost identical to that of the sensor alone. This is consistent with the proposed sensing mechanism (FIG. 1B), which relies on the coordinative interaction between the negatively charged phospholipid head group and the Lewis acid Zn.sup.2+ of the sensors.

(214) Following the validation that the sensor compound I-1 is suitable for the selective detection of vesicles containing negatively charged lipids, the remaining exemplary sensors compounds of Formula I were investigated with the goal of identifying a sensor derivative which would afford maximum sensitivity and selectivity for negatively charged vesicles. For each sensor, monomer (376 nm) and excimer (476 nm) emission intensities (FI.sub.mon and FI.sub.exc, respectively) were recorded, and were used to calculate the following parameters: FI.sub.exc (hereon referred to as FI; Equation 1); FI.sub.exc (hereon referred to as FI; Equation 2); FI.sub.mon (Equation 3); FI.sub.exc/mon (Equation 4); FI.sub.mon (Equation 5) and FI (Equation 6). FI parameter was used to provide an unbiased quantification of sensors' selectivity for negatively charged over zwitterionic vesicles by expressing the signal as a ratio of the FI of each vesicle to the FI of a zwitterionic PC vesicle, (Equation 2).

(215) FIG. 3 shows FI values of compounds I-1, I-2, I-3, I-4, I-5, I-6, and compounds II-1, II-4, and II-5 (Panel A for vesicle concentrations 0 to 40 M, Panel B for vesicle concentration 0-200 M). FIG. 4 shows the FI values for compounds I-2, I-3, I-4, I-5, I-6 and PSVue380. FIG. 5 shows FI.sub.exc/mon of I-1, I-2, I-3, I-4, I-5, I-6 and compounds II-1, II-4, and II-5 (Panel A for vesicle concentrations 0 to 40 M, Panel B for vesicle concentration 0-200 M).

(216) All compounds of Formula I and PSVue380 tested detected negatively charged, but not zwitterionic vesicles. All sensor compounds of Formula I exhibited a signal decrease in the presence of excess vesicles, suggesting that they operate by the same [1:1].sub.2 mechanism described above. On the other hand, PSVue380 did not exhibit this signal decrease highlighting the difference in the sensing mechanisms. The increasing vesicle concentration is associated with a greater enhancement in excimer signal, as compared to that of monomer. As shown in FIG. 5, DPA-containing sensors such as compound I-6 exhibit very low FI.sub.exc/mon, which, without wishing to be limited by theory, is attributed to analyte-mediated de-quenching of sensor fluorescence, where the monomer emission is affected to a greater extent. Thus, in further evaluating sensors' potency, only FI parameter, which does not factor in monomer emission was used. Of the seven sensors tested, compound I-6 displayed the lowest FI values (FIG. 4) for the negatively charged vesicles: the change in excimer fluorescence of I-6 in response to 100% PC vesicles (FI) approached 7 (FIG. 4) resulting in the lower observed FI values as compared to other sensors. While not wishing to be limited by theory, significant excimer formation of sensor 6 (compound I-6) in the presence of zwitterionic PC could be rationalized by the higher hydrophobicity of this sensor (contains a DPA group and a hydrophobic butyl linker) as compared to the other Ia compounds tested. With this notable PC detection, sensor compound I-6 was concluded to be sub-optimal for the selective detection of negatively charged vesicles. All exemplary sensor compounds for Formula I, and in particular sensor compounds I-3, but not PSVue380, detected PA and CL vesicles to a greater extent (sensor compound I-3-PA FI25) than PS and PG vesicles. As mentioned above, while not wishing to be limited by theory, this may be attributed to the higher negative charge found in the PA and CL lipids as compared to their PS and PG counterparts. Surprisingly, PSVue 380 does not appear to be sensitive to the higher negative charge of the PA and CL lipids. In previous studies by Smith et. al, it was shown that PSVue 380 only detected PS as part of the vesicles, and not in its free monomeric form, suggesting that the sensing mechanism of PSVue 380 could require formation of a [2:1] lipid-sensor complex, with each of the two Zn.sup.2+ centres interacting with a single phosphate group. It is likely that the conformational constraint imposed via formation of a [2:1] complex prohibits the further coordinative interaction offered through the additional negative charge in PA and CL. While not wishing to be limited by theory, significant selectivity of sensor 3 (compound I-3) for PA but not CL, may be attributed to the unique conformation of this sensor which translates into improved binding to the phosphate mono-ester as compared to the phosphate-diesters of the CL, PG, and PS.

(217) PSVue380 displayed the smallest linear response (2-10 M), reaching full saturation >20 M vesicles (FIG. 4). At 25 M of sensor compounds I, a linear response is observed from 2 to a minimum of 40 M vesicles (FIGS. 2A, 3A, and 5A); by increasing sensor compounds I concentration to 50 M a linear response from 5 to 200 M can be achieved (FIG. 6A). Since the use of higher PSVue380 concentrations leads to reduced sensitivity, it was proposed that exemplary sensors can be particularly useful in applications where quantification of negatively charged lipids over large concentration ranges is of interest. Table 1 summarizes the FI for each vesicle-sensor combination at 5 and 20 M vesicle concentrations, and allows more detailed comparison of sensors' performance. To facilitate visual comparison, within each row corresponding to a particular vesicle, the FI for each sensor were ranked from lowest (light grey) to highest (dark grey). Notably sensors I-3 and I-4 are superior to PSVue380 at sensing PA. Sensitivity comparable to that of PSVue380 is also observed for the detection of 5 M PS vesicles by sensors I-3 and I-4, and 20 M CL vesicles by sensors I-4 and I-5. Sensor I-4, a butyl linker-containing cyclam, appeared to have most optimal sensing selectivity and afforded comparable or superior (as compared to PSVue380) detection of negatively charged vesicles, especially at low (5 M) vesicle concentration. The higher the FI, the more sensitive a sensor compound is to the type of vesicle. It is evident from the overall examination of Table 1 that PSVue380 is overall more sensitive than compounds Ia, with one notable exception: sensors compounds I-3 and I-4 are superior to PSVue380 at sensing PA. Sensitivity comparable to that of PSVue380 is also observed for the detection of 5 M PS vesicles by sensors compounds I-3 and I-4, and 20 M CL vesicles by sensors compounds I-4 and I-5. Sensor I-4, butyl linker-containing cyclam, appeared to have most optimal sensing selectivity and afforded comparable or superior (as compared to PSVue380) detection of negatively charged vesicles, especially at low (5 M) vesicle concentration. Overall, cyclam-containing sensor compounds I-3 and I-4, and a methyl-linker DPA sensor compound I-5 appeared to be most optimal for the use in the detection of negatively charged vesicles.

(218) TABLE-US-00001 TABLE 1 Summary of FI of all sensor compounds for all vesicles tested Vesicle 1-1 1-2 1-3 1-4 1-5 1-6 PSVue380 5 M PE 1 1.1 1 1 0.9 1 1.1 PG 2.6 2.5 2.4 3.4 1.7 1.8 3.9 CL 3.3 4.4 4.1 5.9 5 2.7 10.3 33% CL 2.8 3 2.4 3.9 2.5 1.9 5.3 5% PS 1.3 1.6 1.8 2.2 1.4 1.6 2.6 25% PS 1.5 1.8 2.2 2.9 1.9 2.1 3.3 PS 2.6 2.8 3.5 4.5 2.9 2.9 4 75% PS 3.3 4.2 6.5 7.1 5.4 4.5 6.1 PA 2.9 4.3 7.7 7.3 4.4 4.4 4.9 20 M PE 1 1.6 1 1.3 1 1 1.1 PG 5.4 5.5 6.2 7.7 3.9 2.7 10.2 CL 10.6 12 10.2 16.3 15.9 4.3 15.3 33% CL 6.6 7.2 6 9.2 7.9 3.1 15.4 5% PS 2.2 3.1 3.5 3.9 2.6 2.4 7.4 25% PS 2.9 4.3 5.3 5.6 4 3 10.8 PS 6.6 7.6 9.8 10.3 8.8 4.8 16 75% PS 9.4 11.7 15.6 16.7 16.7 7.5 17.4 PA 9.5 12.3 23.2 21.7 14.1 6.9 11.4

(219) Since early apoptosis could potentially be detected via sensing of the PS-enriched outer membrane of a mammalian cell during early apoptosis, the sensitivity of PS detection by compounds of the Formula Ia was addressed.

(220) It is estimated that a mammalian cell membrane is composed of 10% PS, with the majority located on the inner leaflet in the healthy state. However, during the early stages of apoptosis, this asymmetry is lost and PS becomes symmetrically distributed resulting in 5% of PS externalized to the outer leaflet. To address if compounds of this application could potentially be used for the detection of the PS externalization event during apoptosis, the exemplary sensors were screened against PC vesicles containing biologically-relevant levels of PS (5 and 25% PS, corresponding to 2.5 and 12.5% of PS exposed to solution; assuming that approximately half of the lipid head groups will be exposed to the interior of the vesicle). The resulting FI for vesicle concentrations up to 40 M are presented in FIG. 7 and Table 1 (FI for vesicle concentrations up to 200 M is presented in FIG. 4). It can be seen that sensor compounds I-3 and I-4 efficiently detected these PS vesicles. Additionally, as can be seen from Table 1, the signals for compounds of Formula Ia are proportional to the amount of PS present in the vesicles. Collectively, these data suggest that sensor compounds I-3 and I-4 are suitable candidates for further exploring their utility in the detection of apoptosis.

Example 42.3: Testing of Further Exemplary Sensors

(221) FIG. 8 shows the FI.sub.exc and FI.sub.exc/mon for compounds I-11, I-12 and I-9 with all vesicles (zwitterionic PC and PE and negatively charged PA, PG, CL and PS) and short-chain lipid controls (DHPC & DHPS). As evident in FIG. 8A, sensor compound I-11 selectively detected all negatively charged vesicles, with FI.sub.exc50 and above (up to 150) over zwitterionic ones (FI.sub.exc3). As evident in FIG. 8C, sensor compound I-12 selectively detected all negatively charged vesicles, with FI.sub.exc20 and above (up to 80) over zwitterionic ones (FI.sub.exc2). As evident in FIG. 8E, sensor compound I-9 detected the negatively charged vesicles with FI.sub.exc3 and above (up to 10). However, the FI.sub.exc for zwitterionic vesicles was around 1, indicating that the enhancement in signal for the negatively charged vesicles as compared to the zwitterionic vesicles was low evident by the low FI.sub.exc/mon values as observed in FIG. 8F. Thus, sensor compound I-9 was concluded to be sub-optimal for the detection of negatively charged phospholipids.

Example 42.4: Phosphoserine Competition Experiments

(222) To probe whether the sensors were directly binding to the negatively charged phospholipid head groups, phosphoserine competition experiments were performed with sensor compound I-1. Briefly, it was hypothesized that if the sensing mechanism necessitates direct binding of the sensor to the phospholipid head groups, phosphoserine added to the sensor-vesicle solution would compete for binding to the sensor (yet not induce an excimer signal as demonstrated in FIG. 9), which would lead to a decrease of the excimer signal. Vesicle fluorescence intensity experiments were performed in the absence or presence of phosphoserine, where phosphoserine was added to sensor either before or after combining with vesicles.

(223) PS vesicles were prepared from stock solutions from 400-40 M in 20 M intervals in pH 7.5, 50 mM HEPES. Phosphoserine Absent: PS vesicles were combined in equal volumes with 50 M of sensor 1 (compound I-1) in pH 7.5, 50 mm HEPES, 10% DMSO and incubated for 10 min away from light, and the fluorescence intensity at 476 nm was measured after excitation at 350 nm. Phosphoserine Addition Before: A second trial was similarly performed, except sensor compound I-1 was pre-incubated with O-Phospho-L-serine (4:1 phosphoserine:sensor) for 5 min, and was then combined with PS vesicles, followed by fluorescence intensity measurements. Phosphoserine Addition After: A third trial was also performed where sensor and PS vesicles were combined as described previously, and the fluorescence intensity was measured. Following this, O-Phospho-L-serine was added (4:1 Phosphoserine:sensor) and fluorescence intensity was again measured.

(224) In both experimental setups, the excimer signal was decreased compared to control in the presence of phosphoserine (shown in FIG. 9), supporting sensors' direct interaction with negatively charged phospholipid head groups.

Example 42.5 Zinc Metalation Fluorescence Experiments

(225) To ascertain whether the sensing mechanism is metal-dependent, selected experiments from Example 1.1 were repeated against all vesicles using compounds III-1, II-4 and II-5, corresponding to the unmetallated counterparts of compounds I-1, I-4 and I-5 respectively. Vesicle fluorescence intensity experiments were performed in the absence or presence of zinc(II) (trifluoromethanesulfonate salt). Unmetallated PSVue380 (PSVue380*) was also included for reference.

(226) All glassware was treated with 0.1 M HCl overnight, rinsed three times with MilliQ water, and oven dried. Absence of Zinc: the same procedure described for the serial dilution vesicle fluorescence intensity experiments was performed with compounds I-1, I-4, and I-5, along with their unmetallated counterparts (compounds II-1, II-4, and II-5), where sensors were combined with PA vesicles. Presence of Zinc: A second procedure with the unmetallated sensor compounds II-1, II-4 and II-5 was performed where zinc (II) trifluoromethanesulfonate was added (1 equivalent). The sensor-zinc solutions were then combined with PA vesicles, prepared as described above, incubated as described above and the fluorescence emission intensity was then measured as described above.

(227) FIG. 10A shows the FI of exemplary metallated compounds I, unmetallated compounds II, and metallated and unmetallated PSVue380 at various vesicle concentrations. As the proposed sensing mechanism relies on the coordinative interaction between the chelated Zn.sup.2+ and the negatively charged phospholipid head group (FIG. 1), it was expected that unmetallated sensors would not bind, and therefore, not detect the negatively charged vesicles. Representative results with PA vesicles are shown in FIG. 10. As expected, compound II-5 (and PSVue380*) lost their ability to sense PA in the absence of Zn.sup.2+. The unmetallated cyclen and cyclam sensors compound II-1 and II-4 not only retained their ability to detect PA in the absence of Zn.sup.2+, but sensor compound II-1 also outperformed its metallated counterpart.

(228) The ability of cyclen and cyclam, but not DPA sensors, to detect negatively charged vesicles in both, metallated and unmetallated sensor states warranted further investigation. In order to rule out the possibility that this result was an artifact of unmetallated cyclen and cyclam sensors undergoing in situ metalation with trace metal present in the buffers or plastics, whereas DPA, owing to its lower affinity to Zn.sup.2+ (DPA Kd=70 nM in 0.1 M KNO.sub.3, Cyclen Kd=0.63 fM in 0.1 M NaNO.sub.3, Cyclam Kd=3.2 fM 0.5 M KNO.sub.3; all at 25 C.), may fail to form metal complexes in situ. Although it was unlikely that trace metal could fully recover and further improve the sensing ability of sensors. In an effort to eliminate this possibility, all glassware was acid-treated and all buffers were chelex-treated to remove any metals, and the screens were repeated with PA vesicles. For these experiments, original non-normalized FI.sub.exc values were analyzed. As can be seen from FIG. 10B, unmetallated (square) and metallated (circle) sensors II-1 and II-4 showed comparable responses to increasing PA vesicle concentrations. The difference originally observed in FI between the unmetallated (II-1) and metallated sensor 1 (I-1) in fact originated from the difference in their background sensor signal which was used to normalize the FI values in the FI calculation (FIG. 10B, Inset). On the other hand, unmetallated DPA sensor II-5 and PSVue380* did not respond to the increasing concentrations of PA vesicles (FIG. 10B, flat line with square markers). To eliminate the possibility that DPA sensors could not undergo in situ metalation with trace metal, equimolar amount of Zn.sup.2+ (25 M, trifluoromethanesulfonate salt) was added exogenously to all sensor-vesicle solutions. As expected, both DPA sensors' signal was restored to the levels of metallated sensors (FIG. 10B, triangle). Collectively, this data suggested that the sensing ability of unmetallated cyclen and cyclam sensors II-1 and II-5 was likely not an artifact of in situ metalation with trace metal. It is proposed that cyclen and cyclam sensors could potentially operate by both, a metal-independent and metal-dependent mechanisms, where in the former, cyclen and cyclam chelates are found in their doubly protonated states (cyclen pKa's=10.97, 8.97; cyclam pKa's=11.29, 10.19) and interact with the negatively charged phospholipid head group via electrostatic and hydrogen-bonding interactions. Consistent with this hypothesis is the lower potential of protonation in unmetallated DPA sensors (pKa's=7.30, 2.60, 1.12), which translates into their inability for forming significant electrostatic and hydrogen-bonding interactions with PA head groups. It is unlikely that cyclen and cyclam sensors operate in a chelate-independent mechanism, as consistent selectivity for negatively charged vesicles was demonstrated.

Example 43: Bacterial Detection

(229) General

(230) E. coli K-12 BW25113 cells were grown overnight in M9 minimal media and then harvested the following morning. Cells were then washed (spun at 5000 rpm for 10 min/wash) three times in buffer (50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5). Cell concentrations were then determined using OD600 and cell samples were diluted to the appropriate concentrations. Fluorescence microscopy experiments were performed with an Olympus IX81 Inverted TIRF microscope with an X-Cite 120Q excitation light source using maximum power. For all experiments, the excitation filter was 325/50 nm, the emission filter was 447/60 nm and exposure time was set to 30.28 ms.

(231) FIG. 11 shows a proof-of-concept E. coli titration panel A shows FI and panel B shows FI of compound I-1 (10 M) in response to increasing amounts of E. coli K-12 BW25113 cells/mL (50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5). Results clearly indicate that compound I-1 is capable of sensing increasing amounts of bacteria.

Example 43.1 Fluorescence Microscopy Experiments with Bacteria

(232) Coverslips were coated in Poly-L-Lysine (0.1 mg/mL) overnight. Bacteria samples were added onto the Poly-L-Lysine coated coverslip and left to stick for 5 minutes. The bacteria were first visualized in bright field and then auto-fluorescence was recorded with UV excitation. Sensors were added on top of the bacteria at appropriate concentrations and fluorescence emission was captured.

(233) FIG. 12 shows Gram-negative bacteria E. coli K-12 BW25113 cells (10.sup.8 cells/mL; 25 mM HEPES, pH 7.0, 0.4% DMSO; excitation=325/50 nm, emission=447/60 nm, exposure time=30.28 ms) detection using fluorescence microscopy. Panel A shows the average intensity image with compound I-5. Panel B shows the SRRF intensity image with compound I-5. Panel C shows the average intensity image with sensor compound I-1. Panel D shows the average intensity image with compound I-6 (30 M). Panel E shows the average intensity image with compound I-5 (10 M). Panel F shows a petri dish control with buffer or petri dish with E. coli where compound I-1 (40 M) was added and the plate excited with long wave UV lamp.

(234) FIG. 13 shows Gram-positive bacteria B. subtilis (panel A), B. megaterium (panel B), M. luteus (panel C), and S. epidermidis (panel D) detection using fluorescence microscopy with compound I-4 (10 M sensor compound, 10.sup.8 cells/mL; 50 mM HEPES, pH 7.5, 75 mM NaCl, 0.4% DMSO; excitation=325/50 nm, emission=447/60 nm, exposure time=30.28 ms).

(235) The results demonstrate that exemplary sensor compounds I are capable of detecting both Gram-positive and Gram-negative bacteria.

Example 43.2 Fluorescence Microscopy Experiments with Bacteria and Mammalian Cells

(236) MV4-11 mammalian cells and bacteria samples were both added to a microscope chamber slide and left to incubate for 5 minutes. Visualization was performed first in bright field and then auto-fluorescence was recorded with UV excitation. Sensors were then added into the chamber at appropriate concentrations and fluorescence emission was captured.

(237) FIG. 14 shows E. coli K-12 BW25113 cells (10.sup.8 cells/mL; 25 mM HEPES, pH 7.0, 0.4% DMSO; excitation=325/50 nm, emission=447/60 nm, exposure time=30.28 ms) detection using fluorescence microscopy with compound I-5 in presence of MV4-11 cells. Panel A shows the bright-field image. Panel B shows the UV image. These results suggest that bacterial cells are detected more readily than mammalian MV4-11 cells.

Example 43.3 Fluorescence Titrations with Bacteria

(238) Bacteria samples were titrated from 10.sup.8-10.sup.10 cells/mL in a large-volume 12 well plate. Bacteria samples were added to black 384-well plates in triplicate. Sensors ([Final]=10 M; 50 mM HEPES, pH 7.5, 75 mM NaCl, 0.4% DMSO) were added to each bacteria sample, and were incubated for 10 minutes prior to reading fluorescence intensity (ex/em=350/476 nm, excitation bandwidth=5 nm, emission bandwidth=10 nm).

(239) A proof-of-concept titration experiment was performed with compounds I-1, I-3, I-4, I-8 and I-9. FIG. 15 shows the titration curves for B. subtilis (A), B. megaterium (B), M. luteus (C), S. epidermidis (D) (50 mM HEPES, pH 7.5, 75 mM NaCl, 0.4-2.5% DMSO). The results suggest that these sensors can detect Gram-positive bacteria using a fluorometer in a bulk solution without bacterial immobilization.

Example 43.4 Bacteria Flow Cytometry Experiments

(240) Bacteria samples (500 L) were treated with 40 uM sensor (POC Sensor compound Ia-1 & Long Cyclam Sensor compound I-6). Samples were run at the Flow Cytometry Facility, Medical Sciences Building, University of Toronto, on a BD LSR Fortessa X20 using the UV laser (emission: 450/50 nm) with low flow rate (15 uL sample/min) for 2 min.

(241) FIG. 16 shows bacteria flow cytometry results. Panel A shows E. coli K-12 BW25113 cells (10.sup.7 CFU/mL) treated with 40 uM POC sensor (Sensor compound I-1). Sample run using UV laser (BD LSR Fortessa X20, emission: 450/50 nm) in 50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5. Panel B shows E. coli K-12 BW25113 cells (10.sup.8 CFU/mL) treated with 40 M POC sensor (Sensor compound I-1). Sample run using UV laser (BD LSR Fortessa X20, emission: 450/50 nm) in 50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5. Panel C shows E. coli K-12 BW25113 cells (10.sup.7 CFU/mL) treated with 40 M POC (Sensor compound I-1). Sample run using UV laser (BD LSR Fortessa X20, emission: 450/50 nm) in 50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5. Panel D shows E. coli K-12 BW25113 cells (10.sup.8 CFU/mL) treated with 40 uM Long Cyclam (Sensor compound I-6) sensor. Sample run using UV laser (BD LSR Fortessa X20, emission: 450/50 nm) in 50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5. Panel E shows 40 M POC sensor (Sensor compound I-1) without bacteria. Sample run using UV laser (BD LSR Fortessa X20, emission: 450/50 nm) in 50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5. These results demonstrate that these sensors are suitable for the detection of bacteria using a flow cytometer.

(242) FIG. 17 shows bacteria flow cytometry results. The left panel shows fluorescence counts of exemplary sensor II-4 without bacteria. The right panel shows fluorescence counts of 1,000 bacteria cells (E. coli or B. subtilis) alone. The middle panel shows the shift of fluorescence counts when both the sensor and 1,000 bacteria cells are present. Gates were set off of unstained control. All samples run using near UV laser (exc: 375 nm, emi: 450/45 nm) and blue laser (exc: 488 nm, emi: 585/42 nm) (BeckmanCoulter, CytoFLEX S) in 50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5.

Example 44: LPS Detection

(243) FIG. 18 shows the FI of exemplary compounds I-1, I-3, I-4 and I-11 for LPS from E. coli O55:B5 (purchased from Sigma-Aldrich). All exemplary compounds were 10 M in 50 mM HEPES, pH 7.5, 75 mM NaCl, 0.4-2.8% DMSO (.sub.ex/em=350/476 nm). LPS was titrated from 10-0.005 M in the same buffer (assuming a MW of 10 kDa). Sensor solutions were prepared from 10 mg/mL DMSO stocks in 50 mM HEPES buffer, pH 7.5, 75 mM NaCl and minimal DMSO (0.4-2.8%) at 20 M. The LPS solution was prepared at 20 M in the same buffer without DMSO. The LPS solution was serially diluted 1:1 from 20 M to 0.01 M with buffer in a 96-well plate. In a 384-well black plate, 30 L of sensor was combined with 30 L of analyte (last row contained 30 L buffer), the mixtures were incubated for 10 min away from light, and the fluorescence intensity was recorded at 476 nm (10 nm bandwidth) following excitation at 350 nm (5 nm bandwidth). Fluorescence intensities were used to calculate the excimer emission in response to LPS.

Example 45: LTA Detection

(244) FIG. 19 shows the FI of exemplary compounds I-1, I-3, I-4 and I-11 for LTA from B. subtilus (purchased from Sigma-Aldrich). All exemplary compounds were 10 M in 50 mM HEPES, pH 7.5, 75 mM NaCl, 0.4-2.8% DMSO (.sub.ex/em=350/476 nm). LTA is titrated from 10-0.005 M in the same buffer (assuming a MW of 10 kDa). Sensor solutions were prepared from 10 mg/mL DMSO stocks in 50 mM HEPES buffer, pH 7.5, 75 mM NaCl and minimal DMSO (0.4-2.8%) at 20 M. The LTA solution was prepared at 20 M in the same buffer without DMSO. The LTA solution was serially diluted 1:1 from 20 M to 0.01 M with buffer in a 96-well plate. In a 384-well black plate, 30 L of sensor was combined with 30 L of analyte (last row contained 30 L buffer), the mixtures were incubated for 10 min away from light, and the fluorescence intensity was recorded at 476 nm (10 nm bandwidth) following excitation at 350 nm (5 nm bandwidth). Fluorescence intensities were used to calculate the excimer emission in response to LTA.

Example 46: Bacteria Mutant Strain Knockout Detection

(245) FIG. 20 shows mutant bacteria strain fluorimetry results. Panel A shows the fluorimetry results of WT and mutant E. coli strains, including cardiolipin synthase knockouts (clsA, clsB, clsC), LPS synthesis knockout (rfaE) and LPS kinase knockouts (WaaP, waaG) with exemplary compound II-4 (10 M). Panel B shows the fluorimetry results of WT and mutant B. subtilis strains, including cardiolipin synthase knockout (clsA) and CRISPRi-mediated LTA knockout (tagO) with exemplary compound II-4 (10 M). The bacteria were at 10.sup.8 CFUs/mL in buffer (50 mM HEPES, pH 7.5, 75 mM NaCl, 0.4% DMSO). The mixtures were incubated for 10 min away from light, and the fluorescence intensity was recorded at 476 nm (10 nm bandwidth) following excitation at 350 nm (5 nm bandwidth). Fluorescence intensities were used to calculate the excimer emission in response to bacterial strains. Measurements were averaged over two triplicates.

(246) The results of fluorimetry experiments with mutant bacteria strains show insight into the mechanism of action of the cyclen and cyclam-based sensors. Compared to the WT strains, exemplary compound II-4 showed the least changes in fluorescence, but a general decrease in fluorescence fold intensity for the E. coli strains, and no changes for B. subtilis strains. However, exemplary compounds II-3 and II-5 show that for E. coli strains, knocking out the cardiolipin synthases has the greatest effect on fluorescence fold, while the LPS kinases show little to no change. These results suggest that the mechanism of binding of the sensors towards the model gram-negative strain is membrane-dependent. Additionally, the LPS synthesis knockout (rfaE) also showed fluorescence fold changes across all three sensors, presumably due to the knockout greatly disrupting the natural morphology of the bacterial membrane. For the gram-positive B. subtilis mutant strains, no clear trend could be seen. However, the fact that compound II-4 showed no fluorescence fold change against the three strains suggests that the mechanism might not be membrane-dependent, but partially or separately entirely. These results coincide with fluorescence microscopy, where E. coli cells were stained brightly on the membrane (FIG. 12), while B. subtilis cells were stained on distinct foci on or within the cells (FIG. 13).

Example 47: Apoptosis Detection

(247) MOLM-13 cells were cultured in Roswell Park Memorial Institute (RPMI)-1640 Medium supplemented with 10% FCS and 1% antibiotic/antimycotic (Gibco, cat. 15240062).

(248) FIG. 21 shows apoptosis flow cytometry results. MOLM-13 cells were cultured to a density of 5.010.sup.5 cells/mL in regular media and transferred to 6-well tissue culture treated plates (1.010.sup.6 cells/well). Treated Cells. Camptothecin (100 L of 210 M camptothecin in media) was added to a final concentration of 10 M (1% DMSO final). Untreated Cells. DMSO Vehicle (100 L DMSO in media) was added (1% DMSO final). All cells were then incubated at 37 C. for 7 hrs. Cells were then washed once with HEPES buffer (50 mM HEPES, 75 mM NaCl, 1% BSA, 0.4% DMSO, pH 7.5) and then re-suspended in HEPES buffer for staining. Cell samples were then treated simultaneously with either 1) exemplary compound I-3 (in HEPES buffer, final concentration of 50 M), and propidium iodide (0.02 g/L) or 2) PSVue380 (in HEPES buffer, final concentration of 90.9 M as previously reported.sup.39) and propidium iodide (0.02 g/L). Samples were then incubated for 15 min away from light at 37 C. and were then analyzed by flow cytometry (CytoFLEX S, BeckmanCoulter) using the near UV laser (exc: 375 nm, emi: 450/45 nm) and blue laser (exc: 488 nm, emi: 585/42 nm). Gates were set off of single stain samples. Results demonstrate that for camptothecin treated cells, exemplary compound I-3 detects a population of cells, undetected by the dead cell stain propidium iodide. These cells are likely early apoptotic cells, as a similar population of cells is detected by PSVue380, which has been shown to detect early apoptotic cells under similar conditions..sup.39

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