Synthesis of N-(5-chloro-6-(quinolin-3-yloxy) pyridin-3-yl) benzenesulfonamide derivatives as non-TZD peroxisome proliferator-activated receptor γ (PPARγ) agonist

S Bajare, J Anthony, A Nair, R Marita, A Damre…

Index: Bajare, Swapnil; Anthony, Jessy; Nair, Amrutha; Marita, Rosalind; Damre, Anagha; Patel, Dharmeshkumar; Rao, Chandrika; Sivaramakrishnan; Deka, Nabajyoti European Journal of Medicinal Chemistry, 2012 , vol. 58, p. 355 - 360

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Citation Number: 8

Abstract

The thiazolidinediones (TZDs) are a class of oral antidiabetic drugs that improve insulin sensitivity in patients with type 2 diabetes. Although the mechanism by which the TZDs lower insulin resistance is unclear, they are known to target the peroxisome proliferator-activated receptor γ (PPARγ), a nuclear hormone receptor. Ligands for PPARγ regulate adipocyte production and secretion of fatty acids as well as glucose metabolism, resulting in ...