Amjad Ali - Piscataway NJ, US James M. Balkovec - Martinsville NJ, US Donald W. Graham - Mountainside NJ, US Mark L. Greenlee - Plainfield NJ, US Gayle E. Taylor - Jersey City NJ, US
Assignee:
Merck Sharp & Dohme Corp. - Rahway NJ
International Classification:
A61K 31/56 C07J 5/00
US Classification:
514178, 514179, 552570
Abstract:
The present invention encompasses compounds of Formula (I) or pharmaceutically acceptable salts or hydrates thereof, which are useful as selective glucocorticoid receptor ligands for treating a variety of autoimmune and inflammatory diseases or conditions. Pharmaceutical compositions and methods of use are also included.
Amjad Ali - Freehold NJ, US Joann Bohn - Woodbridge NJ, US Qiaolin Deng - Edison NJ, US Zhijian Lu - Clinton NJ, US Peter J. Sinclair - Scotch Plains NJ, US Gayle E. Taylor - Jersey City NJ, US Christopher F. Thompson - Clark NJ, US Nazia Quraishi - Arlington MA, US
Assignee:
Merck Sharp & Dohme Corp. - Rahway NJ
International Classification:
C07C 261/00 C07C 211/00 A01N 47/10
US Classification:
560115, 560132, 564336, 564337, 514476
Abstract:
Compounds of Formula I, including pharmaceutically acceptable salts of the compounds, are CETP inhibitors, and are useful for raising HDL-cholesterol, reducing LDL-cholesterol, and for treating or preventing atherosclerosis. In the compounds of Formula 1, Aand A2 are each an aromatic ring, a 5-6-membered heterocyclic ring, an aromatic ring fused to a heterocyclic ring, a phenyl ring fused to a heterocyclic ring, or a cycloalkyl ring.
D-Homoandrosta-17-Yl Carbamate Derivatives As Selective Glucocorticoid Receptor Ligands
Amjad Ali - Freehold NJ, US Mark L. Greenlee - Plainfield NJ, US Carol A. McVean - Lansdale PA, US Robert S. Meissner - Schwenksville PA, US Gayle E. Taylor - Jersey City NJ, US
Assignee:
Merck Sharp & Dohme Corp. - Rahway NJ
International Classification:
C07C 261/00
US Classification:
560115, 560 24, 560 27, 560163, 560164
Abstract:
The present invention is directed to D-homoandrosta-17-yl-carbamate derivatives as selective glucocorticoid receptor ligands useful for treating a variety of autoimmune and inflammatory diseases or conditions. Pharmaceutical compositions and methods of use are also included.
Amjad Ali - Freehold NJ, US Zhijian Lu - Clinton NJ, US Peter J. Sinclair - Scotch Plains NJ, US Gayle E. Taylor - Jersey City NJ, US Christopher F. Thompson - Clark NJ, US Cameron J. Smith - Lawrenceville NJ, US Adrian A. Dowst - Hoboken NJ, US Yi-Heng Chen - Whippany NJ, US
Compounds having the structure of Formula (I), including pharmaceutically acceptable salts of the compounds, are CETP inhibitors, and are useful for raising HDL-cholesterol, reducing LDL-cholesterol, and for treating or preventing atherosclerosis. In the compounds of Formula (I), B or Ris a phenyl group which has an ortho amine or aminomethyl substituent which is further substituted, and the other of B or Ris also a cyclic group.
Amjad Ali - Freehold NJ, US Joann Bohn - North Plainfield NJ, US Qiaolin Deng - Edison NJ, US Zhijian Lu - Clinton NJ, US Peter J. Sinclair - Scotch Plains NJ, US Gayle Taylor - Red Bank NJ, US Christopher Thompson - Clark NJ, US Nazia Quraishi - Vienna VA, US
Compounds of Formula I, including pharmaceutically acceptable salts of the compounds, are CETP inhibitors, and are useful for raising HDL-cholesterol, reducing LDL-cholesterol, and for treating or preventing atherosclerosis. In the compounds of Formula 1, Aand A2 are each an aromatic ring, a 5-6-membered heterocyclic ring, an aromatic ring fused to a heterocyclic ring, a phenyl ring fused to a heterocyclic ring, or a cycloalkyl ring.
Amjad Ali - Freehold NJ, US Julianne A. Hunt - Scotch Plains NJ, US Florida Kallashi - Laurence Harbor NJ, US Jennifer Kowalchick - Clark NJ, US Dooseop Kim - Westfield NJ, US Cameron J. Smith - Lawrenceville NJ, US Peter J. Sinclair - Scotch Plains NJ, US Ramzi F. Sweis - Franklin Park NJ, US Gayle E. Taylor - Jersey City NJ, US Christopher F. Thompson - Clark NJ, US Liya Chen - East Brunswick NJ, US Nazia Quraishi - Vienna VA, US
Compounds of Formula I, including pharmaceutically acceptable salts of the compounds, are CETP inhibitors, and are useful for raising HDL-cholesterol, reducing LDL-cholesterol, and for treating or preventing atherosclerosis.
Octahydro-2-H-Naphtho[1,2-F]Indole-4-Carboxamide Derivatives As Selective Glucocorticoid Receptor Modulators
Amjad Ali - Piscataway NJ, US Susan Aster - Teaneck NJ, US James Balkovec - Martinsville NJ, US Donald Graham - Mountainside NJ, US Julianne Hunt - Scotch Plains NJ, US Florida Kallashi - Yonkers NY, US Peter Sinclair - Scotch Plains NJ, US James Tata - Westfield NJ, US Gayle Taylor - Jersey City NJ, US Joung Goulet - Westfield NJ, US
International Classification:
C07D231/54 A61K031/4162
US Classification:
514406000, 548358500
Abstract:
The present invention encompasses compounds of Formula I: or pharmaceutically acceptable salts or hydrates thereof, which are useful as selective glucocorticoid receptor ligands for treating a variety of autoimmune and inflammatory diseases or conditions. Pharmaceutical compositions and methods of use are also included.
Amjad Ali - Freehold NJ, US Joann Napolitano - Woodbridge NJ, US Qiaolin Deng - Edison NJ, US Zhijian Lu - Clinton NJ, US Peter Sinclair - Scotch Plains NJ, US Gayle Taylor - Jersey City NJ, US Christopher Thompson - Clark NJ, US Nazia Quraishi - Arlington MA, US Cameron Smith - Lawrenceville NJ, US Julianne Hunt - Scotch Plains NJ, US Adrian Dowst - Hoboken NJ, US Yi-Heng Chen - Whippany NJ, US Hong Li - Edison NJ, US
International Classification:
A61K 31/421 C07D 263/16
US Classification:
514376000, 548229000
Abstract:
Compounds having the structures of Formula I, including pharmaceutically acceptable salts of the compounds, are CETP inhibitors, and are useful for raising HDL-cholesterol, reducing LDL-cholesterol, and for treating or preventing atherosclerosis: In the compounds of Formula I, B or Ris a phenyl group which has an ortho aryl, heterocyclic, benzoheterocyclic or benzocycloalkyl substituent, and one other position on the 5-membered ring has an aromatic, heterocyclic, cycloalkyl, benzoheterocyclic or benzocycloalkyl substituent connected directly to the ring or attached to the ring through a —CH—.
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