Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/60510
metadata.dc.identifier.doi: https://doi.org/10.56042/ijc.v61i9.66345
Title: DMAP-catalysed synthesis, antibacterial activity evaluation, cytotoxicity and docking studies of some heterocyclic molecules bearing sulfonamide moiety
Authors: Naaz, Farha
Srivastava, Ritika
Yadav, Madhu
Singh, Vishal K
Mishra, Richa
Chaurasia, Himani
Singh, Ramendra K
Keywords: DMAP;sulfonamides;antibacterial activity;molecular docking;peptide deformylase inhibitor
Issue Date: Sep-2022
Publisher: NIScPR-CSIR,India
Abstract: DMAP has been shown to be a highly efficient nucleophilic catalyst when compared to triethylamine and pyridine using acetonitrile as solvent for the synthesis of a series of novel N- heterocyclic sulfonamide derivatives. The influence of the reaction parameters, like choice of solvent, catalyst, amount of catalyst and reaction time on product yield has been studied. Antibacterial screening involving a range of sulfonamide analogues as new peptide deformylase (PDF) inhibitors have been focused. The molecules show significant antibacterial activity (MIC value 6.2 − 3.1 μg/mL) against B. subtilis, S. pyrogenes, P. vulgaris and P. mirabilis. Potential in silico docking studies have been in conjugation with in vitro antibacterial results. Molecular docking of all compounds with PDF enzyme (PDB code: 1G2A) explain how certain moieties play significant roles in increasing the binding interactions and stabilizing the protein-ligand complexes. The compounds also confirm low extent of cytotoxicity when tested on HEL and HeLa cell lines.
Page(s): 951-960
ISSN: 2583-1321 (Online); 0019-5103 (Print)
Appears in Collections:IJC Vol.61(09) [Sep 2022]

Files in This Item:
File Description SizeFormat 
IJC 61(9) 951-960.pdfMain Article405.6 kBAdobe PDFView/Open
IJC 61(9) 951-960 Suppl_Data.pdfSupplementary Data537.77 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.