Peter H. Dobbelaar - Morris Plains NJ, US Christopher L. Franklin - Keasbey NJ, US Allan Goodman - Media PA, US Cheng Guo - Schenectady NY, US Peter R. Guzzo - Niskayuna NY, US Mark Hadden - Albany NY, US Shuwen He - Edison NJ, US Alan J. Henderson - Albany NY, US Tianying Jian - Westfield NJ, US Linus S. Lin - Westfield NJ, US Jian Liu - Edison NJ, US Ravi P. Nargund - East Brunswick NJ, US Megan Ruenz - Grayslake IL, US Bruce J. Sargent - Delmar NY, US Iyassu K. Sebhat - Jersey City NJ, US Larry Yet - Albany NY, US
Assignee:
Merck Sharp & Dohme Corp. - Rahway NJ Albany Molecular Research, Inc. - Albany NY
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.
Composition For Producing Chemiluminescent Light Of Controllable Duration
Vilas M. Chopdekar - Edison NJ James R. Schleck - Somerset NJ Cheng Guo - Harrison NJ Amanda J. Hall - Raritan NJ
Assignee:
Jame Fine Chemicals, Inc. - Bound Brook NJ
International Classification:
C09K 300
US Classification:
252700
Abstract:
A chemiluminescent composition comprising an oxalate component comprising polystyrene or homopoly-. alpha. -methylstyrene containing an oxalate ester; an activator component comprising a solution of a peroxide compound and a catalyst in a first solvent; and a fluorescer contained in the oxalate component, activator component, or in both the oxalate component and the activator component. The first solvent is preferably a propylene glycol dialkyl ether. The chemiluminescent composition, when activated, permits light to be produced of controllable duration.
Vilas M. Chopdekar - Edison NJ James R. Schleck - Somerset NJ Vernon A. Brown - Maplewood NJ Cheng Guo - Harrison NJ
Assignee:
Jame Fine Chemicals, Inc. - Bound Brook NJ
International Classification:
C07C 6988
US Classification:
560 68
Abstract:
A process for preparing pure antihistamine tannate compositions. The antihistamine in the form of its free base is contacted with tannic acid in the presence of water for a period of time of about 5 minutes to 4 hours and at a maximum temperature such that not more than about 5 wt. % of the antihistamine tannate will be decomposed. Water is removed from the antihistamine tannate by freeze-drying.
Vilas M. Chopdekar - Edison NJ James R. Schleck - Somerset NJ Cheng Guo - Harrison NJ Amanda J. Hall - Raritan NJ
Assignee:
Jame Fine Chemicals, Inc. - Bound Brook NJ
International Classification:
C09K 300
US Classification:
252700
Abstract:
A chemiluminescent composition comprising an oxalate component comprising an oxalate ester and a solvent, an activator component comprising a peroxide compound and a catalyst and a fluorescer contained in the oxalate component and/or the activator component. The solvent contained in the oxalate component comprises a propylene glycol dihydrocarbyl ether containing one to three propylene moieties and each hydrocarbyl moiety contains up to 8 carbon atoms and is independently selected from the group consisting of straight chain alkyl, branched chain alkyl, cycloalkyl, aryl, alkaryl and aralkyl groups.
Vilas M. Chopdekar - Edison NJ James R. Schleck - Somerset NJ Vernon A. Brown - Maplewood NJ Cheng Guo - Harrison NJ
Assignee:
Jame Fine Chemicals, Inc. - Bound Brook NJ
International Classification:
A61K 31135
US Classification:
514653
Abstract:
Phenylephrine tannate compositions are disclosed wherein the phenylephrine tannate has a minimum purity level of at least 95%. The composition also contains a minor amount of water, but no significant quantities of organic compounds or solvents other than water are present. The phenylephrine tannate will have a density of at least 0. 6 g/cc.
Design And Synthesis Of Novel Disulfide Linker Based Nucleotides As Reversible Terminators For Dna Sequencing By Synthesis
Jingyue Ju - Englewood Cliffs NJ, US Xiaoxu Li - New York NY, US Xin Chen - New York NY, US Zengmin Li - Flushing NY, US Shiv Kumar - Belle Meade NJ, US Shundi Shi - Ozone Park NY, US Cheng Guo - Brooklyn NY, US Jianyi Ren - New York NY, US Minchen Chien - Tenafly NJ, US Chuanjuan Tao - Fort Lee NJ, US Ece Erturk - New York NY, US Sergey Kalachikov - Bronx NY, US James J. Russo - New York NY, US
Assignee:
The Trustees of Columbia University in the City of New York - New York NY
International Classification:
C12Q 1/6869 C07H 19/10 C07H 19/14 C07H 19/20
Abstract:
Disclosed herein, inter alfa, are compounds, compositions, and methods of use thereof in the sequencing of a nucleic acid.
- New York NY, US Xin Chen - Changsha, CN Xiaoxu Li - New York NY, US Zengmin Li - Flushing NY, US Minchen Chien - Tenafly NJ, US Shundi Shi - Ozone Park NY, US Jianyi Ren - Rosemead CA, US Cheng Guo - Brooklyn NY, US Shiv Kumar - Belle Mead NJ, US James Russo - New York NY, US Chuanjuan Tao - Fort Lee NJ, US Steffen Jockusch - New York NY, US Sergey Kalachikov - Bronx NY, US
Assignee:
The Trustees of Columbia University in the City of New York - New York NY
International Classification:
A61K 31/7052 C07H 21/04
Abstract:
Disclosed herein, inter alia, are compounds, compositions, and methods of use thereof in the sequencing a nucleic acid.
Design And Synthesis Of Novel Disulfide Linker Based Nucleotides As Reversible Terminators For Dna Sequencing By Synthesis
- New York NY, US Xiaoxu Li - New York NY, US Xin Chen - New York NY, US Zengmin Li - Flushing NY, US Shiv Kumar - Belle Meade NJ, US Shundi Shi - Ozone Park NY, US Cheng Guo - Brooklyn NY, US Jianyi Ren - New York NY, US Minchen Chien - Tenafly NJ, US Chuanjuan Tao - Fort Lee NJ, US Ece Erturk - New York NY, US Sergey Kalachikov - Bronx NY, US James J. Russo - New York NY, US
Assignee:
The Trustees of Columbia University in the City of New York - New York NY
International Classification:
C12Q 1/6869 C07H 19/10 C07H 19/20 C07H 19/14
Abstract:
Disclosed herein, inter alia, are compounds, compositions, and methods of use thereof in the sequencing of a nucleic acid.
Mar 2008 to Jul 2008China Pharmaceutical University
Aug 2007 to Jan 2008 Research AssistantProf. BopingYe's Lab
Mar 2007 to Aug 2007 Research AssistantSynica Corporation
May 2006 to Aug 2006 Chemical synthesis research internship
Education:
Miami University Aug 2011 to 2000 Ph.D. in BiologyCollege of Life Sciences, China Pharmaceutical University Nanjing, CN Sep 2004 to Jun 2011 B. S. in Biotechnology