Patent classifications
C07D209/02
TEAD inhibitors and uses thereof
The present invention provides compounds, compositions thereof, and methods of using the same.
COMPOSITIONS AND METHODS FOR MODULAR CONTROL OF BIOORTHOGONAL LIGATION
The present invention provides a compound having the structure:
##STR00001## wherein R.sub.1 is H or a protecting group; R.sub.2 and R.sub.3 are each independently H, halo, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl, C.sub.2-C.sub.6 alkynyl, C.sub.1-C.sub.6 alkyl-C(O)NHR.sub.6, C.sub.1-C.sub.6 alkyl-C(O)OR.sub.6, wherein R.sub.6 is H, C.sub.1-C.sub.6 alkyl, C.sub.2-C.sub.6 alkenyl or C.sub.2-C.sub.6 alkynyl, or R.sub.2 and R.sub.3 combine to form a 3-7 membered cycloalkyl, heterocycloalkyl, aryl or heteroaryl ring; and R.sub.4 and R.sub.5 are each independently halo.
Bisamide sarcomere activating compounds and uses thereof
- Luke Ashcraft ,
- Alessandro Boezio ,
- John Butler ,
- Aroop CHANDRA ,
- Chihyuan Chuang ,
- Scott E. Collibee ,
- Mikkel V. Debenedetto ,
- Vincent Dimassa ,
- Russell Graceffa ,
- Justin Malinowski ,
- David Moebius ,
- Bradley Paul Morgan ,
- Joshua Payette ,
- Antonio ROMERO ,
- David St. Jean, Jr. ,
- Richard Vargas ,
- John Yeoman ,
- Hanmo Zhang ,
- Alan Cheng ,
- Felix Gonzalez Lopez De Turiso ,
- Michael Garrett Johnson
The present invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising a compound of the invention, a method for manufacturing compounds of the invention and therapeutic uses thereof. ##STR00001##
Bisamide sarcomere activating compounds and uses thereof
- Luke Ashcraft ,
- Alessandro Boezio ,
- John Butler ,
- Aroop CHANDRA ,
- Chihyuan Chuang ,
- Scott E. Collibee ,
- Mikkel V. Debenedetto ,
- Vincent Dimassa ,
- Russell Graceffa ,
- Justin Malinowski ,
- David Moebius ,
- Bradley Paul Morgan ,
- Joshua Payette ,
- Antonio ROMERO ,
- David St. Jean, Jr. ,
- Richard Vargas ,
- John Yeoman ,
- Hanmo Zhang ,
- Alan Cheng ,
- Felix Gonzalez Lopez De Turiso ,
- Michael Garrett Johnson
The present invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising a compound of the invention, a method for manufacturing compounds of the invention and therapeutic uses thereof. ##STR00001##
Polycyclic compound acting as IDO inhibitor and/or IDO-HDAC dual inhibitor
Compounds as IDO inhibitors and/or dual inhibitors of IDO-HDAC are described. Specifically, the compounds represented by the following formula (I) are described, wherein each group is defined as described in the specification. The compounds have IDO inhibitory activity or IDO-HDAC dual inhibitory activity and can be used for preventing or treating diseases associated with IDO and/or IDO-HDAC activity or expression levels. At the same time, the compounds of the present invention can be combined with an anti-tumor antibody such as PD-1 and PD-L1, and such a combination can greatly increase the anti-tumor response rate of the antibody and broaden the types of tumors to be treated. ##STR00001##
Therapeutic compounds and methods of use thereof
The invention provides compounds having the general Formula (I); ##STR00001##
and pharmaceutically acceptable salts thereof; wherein the variables R.sup.A, R.sup.AA, subscript n, subscript q, ring A, X.sup.2, L, subscript m, X.sup.1, R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, D and E have the meaning as described herein, and compositions containing such compounds and methods for using such compounds and compositions.
Therapeutic compounds and methods of use thereof
The invention provides compounds having the general Formula (I); ##STR00001##
and pharmaceutically acceptable salts thereof; wherein the variables R.sup.A, R.sup.AA, subscript n, subscript q, ring A, X.sup.2, L, subscript m, X.sup.1, R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, D and E have the meaning as described herein, and compositions containing such compounds and methods for using such compounds and compositions.
PREPARATION AND USE OF (+)-1-(3,4-DICHLOROPHENYL)-3-AZABICYCLO[3.1.0]HEXANE IN THE TREATMENT OF CONDITIONS AFFECTED BY MONOAMINE NEUROTRANSMITTERS
The present invention relates to (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane and pharmaceutically acceptable active salts, polymorphs, glycosylated derivatives, metabolites, solvates, hydrates, and/or prodrugs of (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane and their use alone or in combination with additional psychotherapeutic compositions in the treatment of conditions affected by monoamine neurotransmitters, including treatment of refractory individuals.
PREPARATION AND USE OF (+)-1-(3,4-DICHLOROPHENYL)-3-AZABICYCLO[3.1.0]HEXANE IN THE TREATMENT OF CONDITIONS AFFECTED BY MONOAMINE NEUROTRANSMITTERS
The present invention relates to (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane and pharmaceutically acceptable active salts, polymorphs, glycosylated derivatives, metabolites, solvates, hydrates, and/or prodrugs of (+)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane and their use alone or in combination with additional psychotherapeutic compositions in the treatment of conditions affected by monoamine neurotransmitters, including treatment of refractory individuals.
THERAPEUTIC COMPOUNDS AND METHODS OF USE THEREOF
The invention provides compounds having the general Formula (I);
##STR00001##
and pharmaceutically acceptable salts thereof; wherein the variables R.sup.A, R.sup.AA, subscript n, subscript q, ring A, X.sup.2, L, subscript m, X.sup.1, R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, D and E have the meaning as described herein, and compositions containing such compounds and methods for using such compounds and compositions.