Synthesis and biological evaluation of 3,5-diaryl isoxazoline/isoxazole linked 2,3-dihydroquinazolinone hybrids as anticancer agents

Eur J Med Chem. 2011 Feb;46(2):691-703. doi: 10.1016/j.ejmech.2010.12.004.

Ahmed Kamal ¹, E Vijaya Bharathi, J Surendranadha Reddy, M Janaki Ramaiah, D Dastagiri, M Kashi Reddy, A Viswanath, T Lakshminarayan Reddy, T Basha Shaik, S N C V L Pushpavalli, Manika Pal Bhadra

Affiliations

Affiliation

1 Division of Organic Chemistry, Indian Institute of Chemical Technology, Tarnaka, Hyderabad 500607, India. ahmedkamal@iict.res.in

PMID: 21194809 DOI: 10.1016/j.ejmech.2010.12.004

Abstract

A series of new 3,5-diaryl isoxazoline/isoxazole linked 2,3-dihydro quinazolinone hybrids with different linker architectures have been designed and synthesized. These compounds have been evaluated for their Anticancer activity. One of the compounds 4c amongst this series has shown promising Anticancer activity. Further some detailed biological assays relating to the cell cycle aspects and tubulin depolymerization activity have been examined with a view to understand the mechanism of action of this conjugate.

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