Methods and compositions for treating disease caused by infectious agents, particularly tuberculosis. In particular, methods and compositions comprising substituted ethylene diamines for the treatment of infectious diseases are provided. In one embodiment, these methods and compositions are used for the treatment of mycobacterial infections, including, but not limited to, tuberculosis. In certain embodiments, the present invention comprises compositions comprising novel substituted ethylene diamine compounds further comprising antitubercular agents such as rifampicin, isoniazid, pyrazinamide and ethambutol.
Novel Cyclic Azabenzimidazole Derivatives Useful As Anti-Diabetic Agents
Rajan Anand - Fanwood NJ, US James M. Apgar - Highland Park NJ, US Tesfaye Biftu - Freehold NJ, US Ping Chen - Edison NJ, US Lin Chu - Scotch Plains NJ, US Vincent J. Colandrea - North Brunswick NJ, US Guizhen Dong - Dayton NJ, US James F. Dropinski - Colts Neck NJ, US Danqing Feng - Green Brook NJ, US Jacqueline D. Hicks - Scotch Plains NJ, US Jinlong Jiang - Scotch Plains NJ, US Alexander J. Kim - Morganville NJ, US Kenneth J. Leavitt - Plainsboro NJ, US Bing Li - Towaco NJ, US Xiaoxia Qian - New York NY, US Iyassu Sebhat - Jersey City NJ, US Lan Wei - Berkeley Heights NJ, US Robert R. Wilkening - Maplewood NJ, US Zhicai Wu - Montvale NJ, US
Novel compounds of structural formula (I) are activators of AMP-protein kinase and are useful in the treatment, prevention and suppression of diseases mediated by the AMPK-activated protein kinase. The compounds of the present invention are useful in the treatment of Type 2 diabetes, hyperglycemia, metabolic syndrome, obesity, hypercholesterolemia, and hypertension.
Substituted Seven-Membered Heterocyclic Compounds As Dipeptidyl Peptidase-Iv Inhibitors For The Treatment Of Diabetes
Jacqueline D. Hicks - Scotch Plains NJ, US Tesfaye Biftu - Freehold NJ, US Ping Chen - Edison NJ, US Xiaoxia Qian - New York NY, US Robert R. Wilkening - Maplewood NJ, US
The present invention is directed to novel amino-substituted seven-membered heterocyclic compounds of structural formula (I) which are inhibitors of the dipeptidyl peptidase-IV enzyme and which are useful in the treatment or prevention of diseases in which the dipeptidyl peptidase-IV enzyme is involved, such as diabetes and particularly Type 2 diabetes. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which the dipeptidyl peptidase-IV enzyme is involved.
Novel Crystalline Forms Of A Dipeptidyl Peptidase-Iv Inhibitor
Novel crystalline forms of (2R,3S,5R)-2-(2,5-Difluorophenyl)-5-[2-(methylsulfonyl)-2,6-dihydropyrrolo[3,4-c]pyrazol-5(4H)-yl]tetrahydro-2H-pyran-3-amine are potent inhibitors of dipeptidyl peptidase-IV and are useful for the treatment of non-insulin dependent (Type 2) diabetes mellitus. The invention also relates to pharmaceutical compositions containing these novel forms, processes to prepare these forms and their pharmaceutical compositions as well as uses thereof for the treatment of Type 2 diabetes.
Charles G. Caldwell - Scotch Plains NJ Ping Chen - Old Bridge NJ Philippe L. Durette - New Providence NJ Paul Finke - Milltown NJ Jeffrey Hale - Westfield NJ Edward Holson - New York NY Ihor Kopka - Millburn NJ Malcolm MacCoss - Freehold NJ Laura Meurer - Scotch Plains NJ Sander G. Mills - Woodbridge NJ Albert Robichaud - Stirling NJ
Assignee:
Merck & Co., Inc. - Rahway NJ
International Classification:
A61K 3141 C07D25704 C07D27110
US Classification:
514364
Abstract:
The present invention is directed to certain novel compounds represented by structural formula I: ##STR1## or a pharmaceutically acceptable salt thereof, wherein R. sup. 3, R. sup. 6, R. sup. 7, R. sup. 8, R. sup. 11, R. sup. 12, R. sup. 13, A, Q, W, X, Y, Z and n are defined herein. The invention is also concerned with pharmaceutical formulations comprising these novel compounds as active ingredients and the use of the novel compounds and their formulations in the treatment of certain disorders. The compounds of this invention are tachykinin receptor antagonists and are useful in the treatment of inflammatory diseases, pain or migraine, asthma and emesis.
Heteroaryl Pyrrolidine And Piperidine Orexin Receptor Agonists
- Rahway NJ, US Ping Chen - Edison NJ, US Dane James Clausen - Rahway NJ, US Jinsong Hao - Belle Mead NJ, US Dipannita Kalyani - Union NJ, US Michael T. Rudd - Collegeville PA, US Shawn P. Walsh - Bridgewater NJ, US Lan Wei - Berkeley Heights NJ, US Dexi Yang - Livingston NJ, US
The present invention is directed to heteroaryl pyrrolidine and piperidine compounds which are agonists of orexin receptors. The present invention is also directed to uses of the compounds described herein in the potential treatment or prevention of neurological and psychiatric disorders and diseases in which orexin receptors are involved. The present invention is also directed to compositions comprising these compounds. The present invention is also directed to uses of these compositions in the potential prevention or treatment of such diseases in which orexin receptors are involved.
Novel Substituted Piperazine Amide Compounds As Indoleamine 2,3-Dioxygenase (Ido) Inhibitors
Dane CLAUSEN - Kenilworth NJ, US Ping CHEN - Kenilworth NJ, US Xavier FRADERA - Boston MA, US Liangqin GUO - Kenilworth NJ, US Yongxin HAN - Boston MA, US Shuwen HE - Fanwood NJ, US Xianhai HUANG - Warren NJ, US Joseph KOZLOWSKI - Princeton NJ, US Guoqing LI - Kenilworth NJ, US Theodore A. MARTINOT - Southborough MA, US Alexander PASTERNAK - Boston MA, US Andreas VERRAS - New York NY, US Li XIAO - Kenilworth NJ, US Wensheng YU - Kenilworth NJ, US Rui ZHANG - Kenilworth NJ, US - Rahway NJ, US
Disclosed herein are compounds of formula (I) which are inhibitors of an IDO enzyme: (I). Also disclosed herein are uses of the compounds in the potential treatment or prevention of an IDO-associated disease or disorder. Also disclosed herein are compositions comprising these compounds. Further disclosed herein are uses of the compositions in the potential treatment or prevention of an IDO-associated disease or disorder.
Novel Arylalkyl Pyrazole Compounds As Indoleamine 2,3-Dioxygenase Inhibitors
- Rahway NJ, US Ping Chen - Edison NJ, US Xavier Fradera - Brookline MA, US Liangqin Guo - Monroe NJ, US Yongxin Han - Needham MA, US Shuwen He - Fanwood NJ, US Jongwon Lim - Lexington MA, US Theodore A. Martinot - Southborough MA, US Alexander Pasternak - Jamaica Plain MA, US Li Xiao - Cranbury NJ, US Wensheng Yu - Edison NJ, US
Assignee:
Merck Sharp & Dohme Corp. - Rahway NJ
International Classification:
C07D 413/14 C07D 401/06 C07D 401/14 C07D 413/06
Abstract:
Disclosed herein are compounds of formula (I) which are inhibitors of an IDO enzyme: Also disclosed herein are uses of the compounds in the potential treatment or prevention of an IDO-associated disease or disorder. Also disclosed herein are compositions comprising these compounds. Further disclosed herein are uses of the compositions in the potential treatment or prevention of an IDO-associated disease or disorder.
Mar 2011 to Present Product controller, Middle OfficeCITCO Fund Services Ltd
Sep 2007 to Mar 2011 Manager, P&L Analytical / ValuationBank of New York Mellon, NJ New York, NY Nov 2005 to Aug 2007 Analyst II, Global Asset Management
Education:
Temple University, Fox Business School Philadelphia, PA May 2005 Master in FinancePhiladelphia University Philadelphia, PA May 2003 Bachelor in Computer & Information Science
Medicine Doctors
Dr. Ping Chen, Towson MD - DMD (Doctor of Dental Medicine)
Southeastern Integrated MedicalSoutheast Integrated Medical Rehabilitation Medicine 1315 NW 21 Ave STE 2, Chiefland, FL 32626 3524931655 (phone), 3524908641 (fax)
Languages:
English
Description:
Ms. Chen works in Chiefland, FL and specializes in Physical Medicine & Rehabilitation. Ms. Chen is affiliated with UF Health Shands Rehabilitation Hospital.
"Being anti-America is work, living in America is life". This phrase h...
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13m 13s
Chen Ping - Three Prospects of China-US Trade...
Chen Ping, he described the current situation of China-US trade war. *...
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7m 22s
Land of Big Numbers with Te-Ping Chen and Cha...
Join the Asian American Writers' Workshop for the official launch of T...
Duration:
1h 9m 49s
Ping Chen Interview
Dr. Ping Chen, PhD, is a research grant recipient from Regenerative Me...
Duration:
2m 12s
(Full Audiobook) Land of Big Numbers by Te Pi...
(Full Audiobook) Land of Big Numbers by Te Ping Chen - Great Novel A d...
Duration:
6h 37m 22s
Te-Ping Chen, in conversation with Jiayang Fa...
(2/09/21) Gripping and compassionate, Land of Big Numbers traces the j...
Duration:
54m 29s
Googleplus
Ping Chen
Work:
Google, Inc - Software Engineer (2006) America Online
Education:
University of California, Irvine
Relationship:
Married
About:
I love building cool stuff, but I love taking photos even more :) Other hobbies include food and travel Disclaimer: The views expressed by me are mine (all mine!) and not my employer's.
Bragging Rights:
Climbed down 71 flights of stairs in Taipei 101 building