Design, Synthesis, and Structure-Activity Relationships of Bavachinin Analogues as Peroxisome Proliferator-Activated Receptor γ Agonists-Reference-Cited by-同舟云学术

Design, Synthesis, and Structure-Activity Relationships of Bavachinin Analogues as Peroxisome Proliferator-Activated Receptor γ Agonists

Published:2016-12-13 Issue:2 Volume:12 Page:183-193
ISSN:1860-7179
Container-title:ChemMedChem
language:en
Short-container-title:ChemMedChem

Author:

Du Guoxin¹,Zhao Yuanyuan¹,Feng Li¹,Yang Zhuo²,Shi Jiye³,Huang Cheng¹,Li Bo²,Guo Fujiang¹,Zhu Weiliang²,Li Yiming¹

Affiliation:

1. School of Pharmacy; Shanghai University of Traditional Chinese Medicine; 1200 Cailun Road Shanghai 201203 China

2. Key Laboratory of Receptor Research & Drug Discovery and Design Center; Shanghai Institute of Materia Medica, Chinese Academy of Sciences; 555 Zuchongzhi Road Shanghai 201203 China

3. Informatics Department; UCB Pharma; 216 Bath Road Slough SL1 4EN UK

Publisher

Wiley

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics,Molecular Medicine,Drug Discovery,Biochemistry,Pharmacology

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5. Design, Synthesis, and Biological Evaluation of DeuteratedC-Aryl Glycoside as a Potent and Long-Acting Renal Sodium-Dependent Glucose Cotransporter 2 Inhibitor for the Treatment of Type 2 Diabetes

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