Benzimidazole-based DGAT1 inhibitors with a [3.1.0] bicyclohexane carboxylic acid moiety-Reference-Cited by-同舟云学术

Benzimidazole-based DGAT1 inhibitors with a [3.1.0] bicyclohexane carboxylic acid moiety

Published:2019-05 Issue:10 Volume:29 Page:1182-1186
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

He Shuwen,Lai Zhong,Hong Qingmei,Shang Jackie,Reibarkh Mikhail,Kuethe Jeffrey T.,Liu Jian,Guiadeen Deodial,Krikorian Arto D.,Cernak Timothy A.,Dykstra Kevin D.,Sperbeck Donald M.,Wu Zhicai,Yu Yang,Yang Ginger X.,Jian Tianying,Verras Andreas,Sonatore Lisa M.,Wiltsie Judyann,Chung Christine C.,Murphy Beth A.,Gorski Judith N.,Liu Jinqi,Xiao Jianying,Wolff Michael,Tong Sharon X.,Madeira Maria,Karanam Bindhu V.,Shen Dong-Ming,Balkovec James M.,Pinto Shirly,Nargund Ravi P.,DeVita Robert J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference17 articles.

1. Discovery of a Potent and Selective DGAT1 Inhibitor with a Piperidinyl-oxy-cyclohexanecarboxylic Acid Moiety

2. Potent DGAT1 Inhibitors in the Benzimidazole Class with a Pyridyl-oxy-cyclohexanecarboxylic Acid Moiety

3. Über Dehydro‐camphenylsäure resp. Dehydro‐oxycamphenilansäure

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