Design, synthesis, in silico molecular docking and biological evaluation of novel oxadiazole based thiazolidine-2,4-diones bis-heterocycles as PPAR-γ agonists-Reference-Cited by-同舟云学术

Design, synthesis, in silico molecular docking and biological evaluation of novel oxadiazole based thiazolidine-2,4-diones bis-heterocycles as PPAR-γ agonists

Published:2014-11 Issue: Volume:87 Page:175-185
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Nazreen Syed,Alam Mohammad Sarwar,Hamid Hinna,Yar Mohammad Shahar,Shafi Syed,Dhulap Abhijeet,Alam Perwez,Pasha M.A.Q.,Bano Sameena,Alam Mohammad Mahboob,Haider Saqlain,Ali Yakub,Kharbanda Chetna,Pillai K.K.

Funder

University Grants Commission, New Delhi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference38 articles.

1. Synthesis, induced-fit docking investigations, and in vitro aldose reductase inhibitory activity of non-carboxylic acid containing 2,4-thiazolidinedione derivatives

2. Thiazolidinediones—Benefits on microvascular complications of type 2 diabetes

3. Novel “Second-Generation” Approaches for the Control of Type 2 Diabetes

4. PPARγ regulates adipose triglyceride lipase in adipocytes in vitro and in vivo

5. Synthesis and biological activity of Benzoxazole containing thiazolidinedione derivatives

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