Patent classifications
C07C381/00
Ketone inhibitors of lysine gingipain
The present invention provides compounds according to Formula I as described herein, and their use for inhibiting the lysine gingipain protease (Kgp) from the bacterium Porphyromonas gingivalis. Also described are gingipain activity probe compounds and methods for assaying gingipain activity are also described, as well as methods for the treatment of disorders associated with P. gingivalis infection, including brain disorders such as Alzheimer's disease.
COMPOUND, ACID GENERATOR, COMPOSITION, CURED PRODUCT, CURED PRODUCT MANUFACTURING METHOD, AND PATTERN COATING MANUFACTURING METHOD
A compound represented by formula (A) exhibits excellent balance between acid generation sensitivity and capability of providing a composition with reduced discoloration.
##STR00001##
In formula (A), R.sup.1, R.sup.11, R.sup.12, R.sup.13, R.sup.14, R.sup.15, R.sup.16, R.sup.17, and n are as defined in the description. R.sup.1 is preferably an optionally substituted aliphatic hydrocarbon group having 1 to 20 carbon atoms or an optionally substituted aromatic hydrocarbon group having 6 to 20 carbon atoms.
Preparation of secondary amines with electrophilic N-linchpin reagents
In one aspect, the present disclosure provides methods of preparing a secondary amine. In some embodiments, the secondary amine comprises two different groups or two identical groups. Also provided herein are compositions for use in the preparation of the secondary amine.
Preparation of secondary amines with electrophilic N-linchpin reagents
In one aspect, the present disclosure provides methods of preparing a secondary amine. In some embodiments, the secondary amine comprises two different groups or two identical groups. Also provided herein are compositions for use in the preparation of the secondary amine.
METHOD FOR SYNTHESIZING D3 DOPAMINE RECEPTOR AGONISTS
An improved method for synthesizing a compound according to formula (I) by reaction of a compound of formula (II) with a sulfinamide according to formula (III). The resultant compound is then reduced and hydrolyzed, and optionally alkylated or arylated to arrive at the compound according to formula (I).
##STR00001##
KETONE INHIBITORS OF LYSINE GINGIPAIN
The present invention provides compounds according to Formula I as described herein, and their use for inhibiting the lysine gingipain protease (Kgp) from the bacterium Porphyromonas gingivalis. Also described are gingipain activity probe compounds and methods for assaying gingipain activity are also described, as well as methods for the treatment of disorders associated with P. gingivalis infection, including brain disorders such as Alzheimer's disease.
KETONE INHIBITORS OF LYSINE GINGIPAIN
The present invention provides compounds according to Formula I as described herein, and their use for inhibiting the lysine gingipain protease (Kgp) from the bacterium Porphyromonas gingivalis. Also described are gingipain activity probe compounds and methods for assaying gingipain activity are also described, as well as methods for the treatment of disorders associated with P. gingivalis infection, including brain disorders such as Alzheimer's disease.
Electrolyte for lithium secondary battery and lithium secondary battery comprising same
The electrolyte for a lithium secondary battery comprises: a lithium salt; a solvent; and a functional additive, wherein the functional additive comprises naphthalen-1-yl sulfurofluoridate, represented by the following formula 1: ##STR00001##
Electrolyte for lithium secondary battery and lithium secondary battery comprising same
The electrolyte for a lithium secondary battery comprises: a lithium salt; a solvent; and a functional additive, wherein the functional additive comprises naphthalen-1-yl sulfurofluoridate, represented by the following formula 1: ##STR00001##
Compounds and compositions for treating conditions associated with NLRP activity
In one aspect, compounds of Formula A, or a pharmaceutically acceptable salt thereof, are featured, or a pharmaceutically acceptable salt thereof, wherein the variables shown in Formula A can be as defined anywhere herein. ##STR00001##