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.
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 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—.
Niacin Receptor Agonists, Compositions Containing Such Compounds And Methods Of Treatment
Steven Colletti - Princeton Junction NJ, US Richard Beresis - Matawan NJ, US Weichun Chen - Livingston NJ, US James Tata - Westfield NJ, US Hong Shen - West Windsor NJ, US Daria Marley - Hoboken NJ, US Qiaolin Deng - Edison NJ, US Jessica Frie - Princeton NJ, US
The present invention relates to niacin receptor agonists of formula: (I); as well as pharmaceutically acceptable salts and solvates. The compounds are useful for treating dyslipidemias, and in particular, reducing serum LDL, VLDL and triglycerides, and raising HDL levels. Pharmaceutical compositions and methods of treatment are also included.
Amjad Ali - Freehold NJ, US Joann M. Napolitano - 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 Cameron J. Smith - Lawrenceville NJ, US Julianne A. Hunt - Scotch Palins NJ, US Adrian A. Dowst - Hoboken NJ, US Yi-Heng Chen - Whippany NJ, US Hong Li - Edison NJ, US
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—.
Amjad ALI - Freehold NJ, US Joann M. Napolitano - 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 Cameron J. Smith - Lawrenceville NJ, US Julianne A. Hunt - Scotch Plains NJ, US Adrian A. Dowst - Hoboken NJ, US Yi-Heng Chen - Whippany NJ, US Hong Li - Edison NJ, US
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—.
9-Substituted Amino Triazolo Quinazoline Derivatives As Adenosine Receptor Antagonists, Pharmaceutical Compositions And Their Use
- Rahway NJ, US Amjad Ali - Freehold NJ, US Jared Cumming - Winchester MA, US Duane DeMong - Hanover MA, US Qiaolin Deng - Edison NJ, US Thomas H. Graham - Somerville MA, US Elisabeth Hennessy - Weston MA, US Andrew J. Hoover - Boston MA, US Ping Liu - Westfield NJ, US Kun Liu - Needham MA, US Umar Faruk Mansoor - Hopkinton MA, US Jianping Pan - Monmouth Junction NJ, US Christopher W. Plummer - Cranford NJ, US Aaron Sather - Melrose MA, US Uma Swaminathan - Auburndale MA, US Huijun Wang - Westfield NJ, US Yonglian Zhang - East Brunswick NJ, US
Assignee:
Merck Sharp & Dohme Corp. - Rahway NJ
International Classification:
C07D 487/04
Abstract:
In its many embodiments, the present invention provides certain 9-substituted amino triazolo quinazoline compounds of the structural Formula (I):and pharmaceutically acceptable salts thereof, wherein, ring A, Rand Rare as defined herein, pharmaceutical compositions comprising one or more such compounds (alone and in combination with one or more other therapeutically active agents), and methods for their preparation and use, alone and in combination with other therapeutic agents, as antagonists of A2a and/or A2b receptors, and in the treatment of a variety of diseases, conditions, or disorders that are mediated, at least in part, by the adenosine A2a receptor and/or the adenosine A2b receptor.
- Rahway NJ, US Chunhui Huang - Arlington MA, US Zhiqiang Yang - Westfield NJ, US Lin Yan - East Brunswick NJ, US Songnian Lin - Holmdel NJ, US Pei Huo - Millburn NJ, US Qiaolin Deng - Edison NJ, US Elisabetta Bianchi - Pomezia, IT Federica Orvieto - Pomezia, IT
Insulin-incretin conjugates comprising a peptide having agonist activity at the glucagon-like 1 (GLP-1) receptor, the glucagon (GCG) receptor, and/or the gastric inhibitory protein (GIP) receptor conjugated to an insulin molecule having agonist activity at the insulin receptor and use of the conjugates for treatment of metabolic diseases, for example, Type 2 diabetes, are described.