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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/45441
Title: Probing the origin of estrogen receptor alpha inhibition: Via large-scale QSAR study
Authors: Naravut Suvannang
Likit Preeyanon
Aijaz Ahmad Malik
Nalini Schaduangrat
Watshara Shoombuatong
Apilak Worachartcheewan
Tanawut Tantimongcolwat
Chanin Nantasenamat
Mahidol University
Keywords: Chemical Engineering;Chemistry
Issue Date: 1-Jan-2018
Citation: RSC Advances. Vol.8, No.21 (2018), 11344-11356
Abstract: © 2018 The Royal Society of Chemistry. Estrogen is an important component for the sustenance of normal physiological functions of the mammary glands, particularly for growth and differentiation. Approximately, two-thirds of breast cancers are positive for estrogen receptor (ERs), which is a predisposing factor for the growth of breast cancer cells. As such, ERα represents a lucrative therapeutic target for breast cancer that has attracted wide interest in the search for inhibitory agents. However, the conventional laboratory processes are cost- and time-consuming. Thus, it is highly desirable to develop alternative methods such as quantitative structure-activity relationship (QSAR) models for predicting ER-mediated endocrine agitation as to simplify their prioritization for future screening. In this study, we compiled and curated a large, non-redundant data set of 1231 compounds with ERα inhibitory activity (pIC50). Using comprehensive validation tests, it was clearly observed that the model utilizing the substructure count as descriptors, performed well considering two objectives: using less descriptors for model development and achieving high predictive performance (RTr2 = 0.94, QCV2 = 0.73, and QExt2 = 0.73). It is anticipated that our proposed QSAR model may become a useful high-throughput tool for identifying novel inhibitors against ERα.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85044628264&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/45441
ISSN: 20462069
Appears in Collections:Scopus 2018

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