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Current Microwave Chemistry

Editor-in-Chief

ISSN (Print): 2213-3356
ISSN (Online): 2213-3364

Research Article

Design, Microwave Assisted Organic Synthesis and Molecular Docking Studies of Some 4 - (3H)-Quinazolinone Derivatives as Inhibitors of Colchicine- Binding Site of Tubulin

Author(s): Rakesh D. Amrutkar* and Mahendra S. Ranawat

Volume 5, Issue 3, 2018

Page: [198 - 205] Pages: 8

DOI: 10.2174/2213335605666181024142317

Price: $65

Abstract

Background: Currently, new chemical entities developed as anticancer agents against tubulin as a protein target. The present work, a quinazoline derivatives were used to design and synthesized by microwave irradiation as an anticancer agent through selective inhibitors of colchicinebinding site of tubulin by the molecular docking of quinazoline derivatives using Schrödinger, LLC, New York, NY, 2017.

Methods: Seven of quinazoline derivatives were docked into colchicine-binding site of tubulin with PDB code 5OSK.

Results: The interaction was evaluated based on the re-ranked score comparison between quinazoline derivatives with 3,4-dihydroquinazolin-2(1H)-one. The title compounds show similar type of hydrogen bond interaction; however, the compound 4a with good binding energy and RMSD interacted with THR: A179 and LYS B: 352 through NH and CO of acetamido group.

Keywords: 4-(3H)-quinazolinone, colchicine-binding site of tubulin, molecular docking, organic synthesis, 2(1H).

Graphical Abstract

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