Feroze Ujjainwalla - Scotch Plains NJ Lin Chu - Scotch Plains NJ Mark T. Goulet - Westfield NJ Bonnie Louridas - Somerset NJ Matthew J. Wyvratt - Mountainside NJ Daniel Warner - Stoneham MA
Assignee:
Merck Co., Inc. - Rahway NJ
International Classification:
A61K 31445
US Classification:
514326, 546193, 546208
Abstract:
Certain novel 4-substituted N-acylated piperidine derivatives are agonists of the human melanocortin receptor(s) and, in particular, are selective agonists of the human melanocortin-4 receptor (MC-4R). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the activation of MC-4R, such as obesity, diabetes, sexual dysfunction, including erectile dysfunction and female sexual dysfunction.
Acylated Piperidine Derivatives As Melanocortin-4 Receptor Agonists
Mark T. Goulet - Lexington MA, US Ravi P. Nargund - East Brunswick NJ, US Feroze Ujjainwalla - Scotch Plains NJ, US Thomas F. Walsh - Watchung NJ, US Daniel Warner - Stoneham MA, US
Certain novel 4-substituted N-acylated piperidine derivatives are agonists of the human melanocortin receptor(s) and, in particular, are selective agonists of the human melanocortin-4 receptor (MC-4R). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the activation of MC-4R, such as obesity, diabetes, sexual dysfunction, including erectile dysfunction and female sexual dysfunction.
Acylated Piperidine Derivatives As Melanocortin-4 Receptor Agonists
Mark T. Goulet - Westfield NJ, US Ravi P. Nargund - East Brunswick NJ, US Iyassu K. Sebhat - New York NY, US Feroze Ujjainwalla - Scotch Plains NJ, US Thomas F. Walsh - Watchung NJ, US Daniel Warner - Stoneham MA, US Zhixiong Ye - Princeton NJ, US Jonathan R. Young - Kendall Park NJ, US Raman K. Bakshi - Edison NJ, US
Certain novel -substituted N-acylated piperidine derivatives are agonists of the human melanocortin receptor(s) and, in particular, are selective agonists of the human melanocortin- receptor (MC-R). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the activation of MC-R, such as obesity, diabetes, sexual dysfunction, including erectile dysfunction and female sexual dysfunction.
Richard B. Toupence - South Plainfield NJ, US John S. Debenham - Scotch Plains NJ, US Mark T. Goulet - Westfield NJ, US Thomas F. Walsh - Watchung NJ, US Shrenik K. Shah - Metuchen NJ, US
Assignee:
Merck & Co., Inc. - Rahway NJ
International Classification:
A61K 31/44 C07D 409/02
US Classification:
514302, 546115
Abstract:
Novel compounds of the structural formula (I) are antagonists and/or inverse agonists of the Cannabinoid-1 (CB1) receptor and are useful in the treatment, prevention and suppression of diseases mediated by the CB1 receptor. The compounds of the present invention are useful as centrally acting drugs in the treatment of psychosis, memory deficits, cognitive disorders, migraine, neuropathy, neuro-inflammatory disorders including multiple sclerosis and Guillain-Barre syndrome and the inflammatory sequelae of viral encephalitis, cerebral vascular accidents, and head trauma, anxiety disorders, stress, epilepsy, Parkinson's disease, movement disorders, and schizophrenia. The compounds are also useful for the treatment of substance abuse disorders, the treatment of obesity or eating disorders, as well as the treatment of asthma, constipation, chronic intestinal pseudo-obstruction, and cirrhosis of the liver.
Diphenyl Cyclopentyl Amides As Cannabinoid-1 Receptor Inverse Agonists
William K. Hagmann - Westfield NJ, US Linus S. Lin - Westfield NJ, US Shrenik K. Shah - Metuchen NJ, US Mark T. Goulet - Westfield NJ, US James P. Jewell - Jersey City NJ, US
Assignee:
Merck & Co., Inc. - Rahway NJ
International Classification:
A61K 31/165
US Classification:
514617, 564161, 514357, 546337
Abstract:
Novel compounds of structural formula (I) are antagonists and/or inverse agonists of the Cannabinoid-1 (CB1) receptor and are useful in the treatment, prevention and suppression of diseases mediated by the CB1 receptor. The compounds of the present invention are useful as psychotropic drugs in the treatment of psychosis, memory deficits, cognitive disorders, migraine, neuropathy, neuro-inflammatory disorders including multiple sclerosis and Guillain-Barre syndrome and the inflammatory sequelae of viral encephalitis, cerebral vascular accidents, and head trauma, anxiety disorders, stress, epilepsy, Parkinsons disease, movement disorders, and schizophrenia. The compounds are also useful for the treatment of substance abuse disorders, the treatment of obesity or eating disorders, as well as, the treatment of asthma, constipation, chronic intestinal pseudo-obstruction, and cirrhosis of the liver.
Mark T. Goulet - Lexington MA, US Feroze Ujjainwalla - Scotch Plains NJ, US Anthony Ogawa - Mountainside NJ, US Derek Von Langen - Scotch Plains NJ, US
Lin Chu - Scotch Plains NJ, US Mark T. Goulet - Westfield NJ, US Feroze Ujjainwalla - Scotch Plains NJ, US Linda Chang - Wayne NJ, US Richard Frenette - Laval, CA Yves Girard - Ile-Bizard, CA Michel Therien - Laval, CA Dwight Macdonald - L'lle-Bizard, CA John H. Hutchinson - LaJolla CA, US
The instant invention provides compounds of formula: (I) which are 5-lipoxygenase activating protein inhibitors: formula (I). Compounds of formula (I) are useful as anti-atherosclerotic, anti-asthmatic, anti-allergic, anti-inflammatory and cyto-protective agents.
Acylated Piperidine Derivatives As Melanocortin-4 Receptor Agonists
Mark T. Goulet - Westfield NJ, US Ravi P. Nargund - East Brunswick NJ, US Feroze Ujjainwalla - Scotch Plains NJ, US Thomas F. Walsh - Watchung NJ, US Daniel Warner - Stoneham MA, US
Assignee:
Merck Sharp & Dohme Corp. - Rahway NJ
International Classification:
C07D 401/06 A61K 31/454 A61K 31/451
US Classification:
546208, 546226, 514326, 514330
Abstract:
Certain novel 4-substituted N-acylated piperidine derivatives are agonists of the human melanocortin receptor(s) and, in particular, are selective agonists of the human melanocortin-4 receptor (MC-4R). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the activation of MC-4R, such as obesity, diabetes, sexual dysfunction, including erectile dysfunction and female sexual dysfunction.
St. Hubert School Windsor Morocco 1956-1960, St. William School Belle River Morocco 1961-1963, Assumption Catholic High School Windsor Morocco 1964-1965
Community:
Angela Nadalin, Bill Reno, Matthew Walczak, Ken Knapp, James Evon, Paul Bachand, Ron Paquette, Maxine Willner, Tony Farah