Synthesis and structure–activity relationships of 2-aryl-4-oxazolylmethoxy benzylglycines and 2-aryl-4-thiazolylmethoxy benzylglycines as novel, potent PPARα selective activators- PPARα and PPARγ selectivity modulation-Reference-Cited by-同舟云学术

Synthesis and structure–activity relationships of 2-aryl-4-oxazolylmethoxy benzylglycines and 2-aryl-4-thiazolylmethoxy benzylglycines as novel, potent PPARα selective activators- PPARα and PPARγ selectivity modulation

Published:2010-05 Issue:9 Volume:20 Page:2933-2937
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Ye Xiang-Yang,Chen Stephanie,Zhang Hao,Locke Kenneth T.,O’Malley Kevin,Zhang Litao,Srivastava Raijit,Miao Bowman,Meyers Daniel,Monshizadegan Hossain,Search Debra,Grimm Denise,Zhang Rongan,Lippy Jonathan,Twamley Celeste,Muckelbauer Jodi K.,Chang Chiehying,An Yongmi,Hosagrahara Vinayak,Zhang Lisa,Yang T.-J.,Mukherjee Ranjan,Cheng Peter T.W.,Tino Joseph A.

Publisher

Elsevier BV

Subject

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

Reference37 articles.

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5. Nuclear Hormone Receptor Modulators for the Treatment of Diabetes and Dyslipidemia

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