Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/660
Title: Structural feature indenture for estrogen analogs as anticancer agents: De novo and Hansch Approach
Authors: Gupta, Arun Kumar
Jain, Anurekha
Jain, Avijeet
Joshi, Anirudh
Revathi, S
Keywords: Estrogen analogs
Hansch approach
Fujita-Ban analysis
QSAR
Antiproliferative activity
Anticancer agents
Issue Date: Jul-2007
Publisher: CSIR
Abstract: Quantitative structure activity relationships have been performed on a series of twenty-six compounds of estrogen derivatives, for their anti-proliferative activity, in order to understand the essential structural requirement for inhibition of proliferation in estrogen dependent MCF-7 human breast cancer cells. The quantitative models derived for the study illustrates the significance of the β-hydroxy group at 17th position for the drug–enzyme interaction and allowed hydrogen-bonding interaction to estrogenic receptor in optimal manner (free rotation) as compared to oxo group (restricted orientation). The results of the study also reveal the necessity of sulfonamide moiety at 3rd position of estrogen. Additionally, presence of smaller substituents at 2nd position will be conducive for the activity.
Description: 1148-1153
URI: http://hdl.handle.net/123456789/660
ISSN: 0376-4699
Appears in Collections:IJC-B Vol.46B(07) [July 2007]

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