Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/45930
Title: In silico study for the prediction of multiple pharmacological activities of novel hydrazone derivatives
Authors: Rohane, Sachin H
Makwana, Ashlesha G
Keywords: Hydrazone;Molecular docking;Multiple pharmacological activities
Issue Date: Mar-2019
Publisher: NISCAIR-CSIR, India
Abstract: The present studies are aimed to predict multiple pharmacological activities of novel hydrazone derivatives. Molecular docking of compounds 1 to 51 have been performed in Small-Molecule Drug Discovery Suite of Schrödinger. Fifty one compounds have been targeted on seven enzymes viz. 2NSD and 2X22 involved in tuberculosis activity, 4COX and 3LN1 involved in inflammation, 4GCP and 4HL2 involved in bacterial infection and 4WMZ involved in fungal infection. The generated lower energy conformers of all ligands have been docked into generated grid of active site of enzymes by XP precision of docking inside Glide-v7.4. Molecular docking results suggest that the compounds 4, 5, 11, 18, 30, 34, 35, 37, 38, 42, 43, 44, 45, 46 and 47 have good docking score and are predicted to interact with all enzymes. In all fifteen novel hydrazone derivatives have been predicted for multiple pharmacological activities.
Page(s): 387-402
URI: http://nopr.niscair.res.in/handle/123456789/45930
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.58B(03) [March 2019]

Files in This Item:
File Description SizeFormat 
IJCB 58B(3) 387-402.pdf1.31 MBAdobe PDFView/Open


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