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针对一系列螺环氧化吲哚衍生物对结肠癌细胞系HCT - 116的抗癌活性的定量构效关系及药物代谢动力学预测研究。

Quantitative structure-activity relationship and ADME prediction studies on series of spirooxindoles derivatives for -cancer activity against colon cancer cell line HCT-116.

作者信息

Kaur Sukhmeet, Kaur Jasneet, Zarger Bilal Ahmad, Islam Nasarul, Mir Nazirah

机构信息

P.G. Department of Chemistry, Khalsa College, Amritsar, India.

College of Pharmacy, Cihan University-Erbil, Kurdistan Region, Iraq.

出版信息

Heliyon. 2024 Aug 8;10(16):e35897. doi: 10.1016/j.heliyon.2024.e35897. eCollection 2024 Aug 30.

DOI:10.1016/j.heliyon.2024.e35897
PMID:39224319
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11367057/
Abstract

Forty-one derivatives of spirooxindoles, active against HCT-116 colon cancer cells, underwent pharmacophore-based 3D-QSAR analysis to understand their correlation with anti-cancer activity. The study identified a seven-point pharmacophore model (ADHHRRR1) and QSAR models, offering insights for lead optimization and novel analogue design, thus advancing anti-cancer drug discovery. This research underscores the value of molecular modeling in elucidating structure-activity relationships and enhancing drug development efforts.

摘要

41种对HCT-116结肠癌细胞有活性的螺环氧化吲哚衍生物进行了基于药效团的3D-QSAR分析,以了解它们与抗癌活性的相关性。该研究确定了一个七点药效团模型(ADHHRRR1)和QSAR模型,为先导优化和新型类似物设计提供了见解,从而推动了抗癌药物的发现。这项研究强调了分子建模在阐明构效关系和加强药物开发工作方面的价值。

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