Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/7404
Title: Synthesis, biological evaluation and molecular docking of aryl hydrazines and hydrazides for anticancer activity
Authors: Gohil, Vikrantsinh M
Agrawal, Satyam K
Saxena, Ajit K
Garg, Divita
Gopimohan, C
Bhutani, Kamlesh K
Keywords: Anticancer activity
Aryl hydrazides
Aryl hydrazines
Molecular docking
Issue Date: Mar-2010
Publisher: CSIR
Abstract: Aryl hydrazine and hydrazide analogues were synthesized based on p-tolyl hydrazine, isolated as a breakdown product of a secondary metabolite from the mushroom, Agaricus bisporus, and tested to be highly active molecule than 5-fluorouracil in in vitro anticancer studies. The synthesized analogues were tested for anticancer activity using NCI protocol. Anolgues 12 and 15 emerged as molecules with significant in vitro anticancer activity. Molecular docking study revealed the binding orientations of aryl hydrazines and hydrazides analogues in the active sites of thymidylate synthase.
Description: 265-268
URI: http://hdl.handle.net/123456789/7404
ISSN: 0975-1009 (Online); 0019-5189 (Print)
Appears in Collections:IJEB Vol.48(03) [March 2010]

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