Merck Sharp + Dohme Corp.

Merck + Co., Inc.

Albany Molecular Research, Inc.

Mochida Paraceuticals Co., Ltd.

Mochida Pharmaceutical Co., Ltd.

Tianying Jian

Liangqin Guo

Ting Zhang

Ravi P Nargund

Jian Liu

Shuwen He

Deping Wang

Philippe G Nantermet

Mark E Layton

Thomas J Greshock

Ronald M Kim

Harold B Wood

Dongfang Meng

Anthony J Roecker

Rajan Anand

James J Mulhearn

Walter Won

Gang Zhou

Meng Yang

Amjad Ali

Sung-Sau So

Peter Guzzo

Feroze Ujjainwalla

Robert R Wilkening

Iyassu Sebhat

Christopher S Burgey

John S Debenham

Jonathan R Young

Shawn P Walsh

Alan W Hruza

Bing Li

Rongze Kuang

Linus S Lin

Anthony K Ogawa

Zhixiong Ye

Richard Berger

Manuel De Lera Ruiz

Yi-Heng Chen

Michael J Kelly, Iii

Jiayi Xu

Dexi Yang

Lan Wei

Jacqueline D Hicks

John E Stelmach

Bruce Sargent

Dann LeRoy Parker, Jr

Hong Li

Alan John Henderson

Robert Kevin Orr

Edward C Sherer

Christopher L Franklin

Kenneth Ellsworth

Mark Hadden

Bart Harper

Iyassu K Sebhat

Jun Wang

Allan James Goodman

Louis-Charles Campeau

Jane Yang Wu

Matthew Lombardo

Cheng Guo

Sunita V Dewnani

Wenlang Fu

Yingjie Lai

Larry Yet

Isao Sakurada

Peter Nizner

Daniel A Tatosian

Peter H Dobbelaar

Megan Ruenz

Dann L Parker

Michael J Iii Kelly

The present invention provides a compound of Formula (I) and pharmaceutical compositions comprising one or more said compounds, and methods for using said compounds for treating or preventing thromboses, embolisms, hypercoagulability or fibrotic changes. The compounds are selective Factor XI activation inhibitors.

Factor XI activation inhibitors

Disclosed are compounds of Formula A, or a salt thereof: Formula (A), wherein: Het, Q and Rto Rare defined herein, which compounds have properties for blocking Na1.7 ion channels found in peripheral and sympathetic neurons. Also described are pharmaceutical formulations comprising the compounds of Formula A or their salts, and methods of treating cough, itch, acute pain and neuropathic pain disorders using the same. 

Diamino-alkylamino-linked arylsulfonamide compounds with selective activity in voltage-gated sodium channels

Disclosed are compounds of Formula A, or a salt thereof, where Q, X, R1 and R2 are as defined herein, which compounds have properties for inhibiting Na1.7 ion channels found in peripheral and sympathetic neurons. Also described are pharmaceutical formulations comprising the compounds of Formula A or their salts, and methods of treating pain (acute, post-operative, neuropathic), or cough or itch disorders using the same. 

The present invention provides a compound of Formula I and pharmaceutical compositions comprising one or more said compounds, and methods for using said compounds for treating or preventing unstable angina, refractory angina, myocardial infarction, transient ischemic attacks, atrial fibrillation, thrombotic stroke, embolic stroke, deep vein thrombosis, disseminated intravascular coagulation, ocular build up of fibrin, and reocclusion or restenosis of recanalized vessels. The compounds are selective Factor IXa inhibitors. 

Factor IXa inhibitors

The present invention provides a compound of Formula I, and pharmaceutical compositions comprising one or more said compounds, and methods for using said compounds for treating or preventing unstable angina, refractory angina, myocardial infarction, transient ischemic attacks, atrial fibrillation, thrombotic stroke, embolic stroke, deep vein thrombosis, disseminated intravascular coagulation, ocular build up of fibrin, and reocclusion or restenosis of recanalized vessels. The compounds are selective Factor IXa inhibitors. 

Certain novel N-acylated spiropiperidine derivatives are ligands of the human melanocortin receptor(s) and, in particular, are selective ligands 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 modulation of MC-4R, such as obesity, diabetes, nicotine addiction, alcoholism, sexual dysfunction, including erectile dysfunction and female sexual dysfunction.

Acylated spiropiperidine derivatives as melanocortin-4 receptor modulators

Certain novel substituted imidazoles are ligands of the human bombesin receptor and, in particular, are selective ligands of the human bombesin receptor subtype-3 (BRS-3). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the modulation of BRS-3, such as obesity, and diabetes.

Substituted imidazoles as bombesin receptor subtype-3 modulators

Certain novel N-acylated spiropiperidine 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 spiropiperidine derivatives as melanocortin-4 receptor agonists

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Westfield, NJ, United States of America

Tianying Jian