Patent classifications
C07D515/08
MACROCYCLIC SULFONYLAMIDE DERIVATIVES USEFUL AS NLRP3 INHIBITORS
The present invention relates to macrocyclic compounds, such as macrocyclic sulfonyl amides. The present invention further relates to associated salts, solvates, prodrugs and pharmaceutical compositions, and to the use of such compounds in the treatment and prevention of medical disorders and diseases, most especially by NLRP.sub.3 inhibition.
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MACROCYCLIC SULFONYLAMIDE DERIVATIVES USEFUL AS NLRP3 INHIBITORS
The present invention relates to macrocyclic compounds, such as macrocyclic sulfonyl amides. The present invention further relates to associated salts, solvates, prodrugs and pharmaceutical compositions, and to the use of such compounds in the treatment and prevention of medical disorders and diseases, most especially by NLRP.sub.3 inhibition.
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CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR MODULATING AGENTS
- Alexander Russell Abela ,
- Sunny Abraham ,
- Corey Don ANDERSON ,
- Vijayalaksmi Arumugam ,
- Jaclyn CHAU ,
- Jeremy CLEMENS ,
- Thomas Cleveland ,
- Timothy A. DWIGHT ,
- Bryan A. Frieman ,
- Peter Grootenhuis ,
- Sara Sabina Hadida Ruah ,
- Yoshihiro ISHIHARA ,
- Paul KRENITSKY ,
- Jason McCartney ,
- Vito Melillo ,
- Mark Thomas MILLER ,
- Alina SILINA ,
- Johnny Uy ,
- Jinglan Zhou
Compound (I), deuterated derivatives, and pharmaceutically acceptable salts of any of the foregoing are disclosed. Methods of treating cystic fibrosis using these compounds are also disclosed.
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CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR MODULATING AGENTS
- Alexander Russell Abela ,
- Sunny Abraham ,
- Corey Don ANDERSON ,
- Vijayalaksmi Arumugam ,
- Jaclyn CHAU ,
- Jeremy CLEMENS ,
- Thomas Cleveland ,
- Timothy A. DWIGHT ,
- Bryan A. Frieman ,
- Peter Grootenhuis ,
- Sara Sabina Hadida Ruah ,
- Yoshihiro ISHIHARA ,
- Paul KRENITSKY ,
- Jason McCartney ,
- Vito Melillo ,
- Mark Thomas MILLER ,
- Alina SILINA ,
- Johnny Uy ,
- Jinglan Zhou
Compound (I), deuterated derivatives, and pharmaceutically acceptable salts of any of the foregoing are disclosed. Methods of treating cystic fibrosis using these compounds are also disclosed.
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INHIBITORS OF HEPATITIS B VIRUS
The present invention relates to compounds that are inhibitors of hepatitis B virus (HBV). Compounds of this invention are useful alone or in combination with other agents for treating, ameliorating, preventing or curing HBV infection and related conditions. The present invention also relates to pharmaceutical compositions containing the compounds.
INHIBITORS OF HEPATITIS B VIRUS
The present invention relates to compounds that are inhibitors of hepatitis B virus (HBV). Compounds of this invention are useful alone or in combination with other agents for treating, ameliorating, preventing or curing HBV infection and related conditions. The present invention also relates to pharmaceutical compositions containing the compounds.
Modulators of Alpha-4-beta-7 Integrin and MAdCAM
The instant disclosure describes novel modulators of alpha α4β7 and/or MAdCAM and their use for the treatment of diseases and conditions associated with their biological function. Further described herein are methods of treating diseases or conditions associated with α4β7 and/or MAdCAM.
Modulators of Alpha-4-beta-7 Integrin and MAdCAM
The instant disclosure describes novel modulators of alpha α4β7 and/or MAdCAM and their use for the treatment of diseases and conditions associated with their biological function. Further described herein are methods of treating diseases or conditions associated with α4β7 and/or MAdCAM.
Tricyclic inhibitors of Hepatitis B virus
The present invention relates to compounds that are inhibitors of hepatitis B virus (HBV). Compounds of this invention are useful alone or in combination with other agents for treating, ameliorating, preventing or curing HBV infection and related conditions. The present invention also relates to pharmaceutical compositions containing the compounds.
Tricyclic inhibitors of Hepatitis B virus
The present invention relates to compounds that are inhibitors of hepatitis B virus (HBV). Compounds of this invention are useful alone or in combination with other agents for treating, ameliorating, preventing or curing HBV infection and related conditions. The present invention also relates to pharmaceutical compositions containing the compounds.