Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/58193
Title: Synthesis and structural confirmation on selective N-alkylation of (Z)-5-((5-chloro- 1H-indol-3-yl)methylene)thiazolidine-2,4-dione analogues with their molecular docking studies
Authors: Sreenatha, Vasappanavara
Prasad, Karnam Jayarampillai Rajendra
Keywords: Selective N-alkylation;2D NMR;Molecular docking studies;ADME studies;T2DM
Issue Date: Sep-2021
Publisher: NIScPR-CSIR, India
Abstract: In the present investigation, a series of novel (Z)-5-((5-chloro-1H-indol-3-yl)methylene)thiazolidine-2,4-dione analogues have been designed and synthesized in good yields with the objective of selective N-alkylation at thiazolidine 2,4-dione ring in competence with indole ring under basic conditions in the presence of aprotic solvent dimethylformamide (DMF). The newly synthesized compounds have been characterized by spectral data (IR, 1H and 13C NMR, NOE, NOESY, 1H-1H-COSY and LC-MS). Further, molecular docking and ADME studies have revealed that the newly synthesized compounds have very good docking score against antidiabetic and anti-inflammation activities (PPARy and COX-2) as compared with standard rosiglitazone.
Page(s): 1264-1271
URI: http://nopr.niscair.res.in/handle/123456789/58193
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.60B(09) [September 2021]

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