Issue 5, 2011

Synthesis, in silico screening and bioevaluation of dispiro-cycloalkanones as antitubercular and mycobacterialNAD+-dependent DNA ligase inhibitors

Abstract

A series of dispiro-cycloalkanones were synthesized using the “Corey Chaykovsky” reaction of α,α′-(E,E)-bis(benzylidene)-cycloalkanones/methanone in good yields. The compounds were evaluated for their in vitro antituberculosis activity against M. tuberculosis H37Rv and screened in silico. Some selected compounds were screened for mycobacterial NAD+-dependent DNA ligase inhibitory activity. Two of the compounds showed good in vitro antitubercular and NAD+-dependent DNA ligase inhibitory activity along with good correlation to in silico results.

Graphical abstract: Synthesis, in silico screening and bioevaluation of dispiro-cycloalkanones as antitubercular and mycobacterial NAD+-dependent DNA ligase inhibitors

Supplementary files

Article information

Article type
Concise Article
Submitted
01 Dec 2010
Accepted
21 Jan 2011
First published
28 Feb 2011

Med. Chem. Commun., 2011,2, 378-384

Synthesis, in silico screening and bioevaluation of dispiro-cycloalkanones as antitubercular and mycobacterial NAD+-dependent DNA ligase inhibitors

R. P. Tripathi, J. Pandey, V. Kukshal, A. Ajay, M. Mishra, D. Dube, D. Chopra, R. Dwivedi, V. Chaturvedi and R. Ramachandran, Med. Chem. Commun., 2011, 2, 378 DOI: 10.1039/C0MD00246A

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