新型山酮衍生物的抗炎活性

Darakhshan Parveen, Amrita Parle, Rajnish Srivastava
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引用次数: 0

摘要

由于癌症、代谢紊乱、衰老、神经退行性疾病等许多疾病都是通过炎症表现出来的,因此总是需要更好的抗炎药物。Xanthones是一种独特的支架,其核心结构为9h - xanthen -9- 1,具有抗炎活性。本研究工作包括从理论上设计30个3-氨基烷氧基山酮衍生物,对其理化性质进行评价,并与COX-1受体进行分子对接。其中,光晕取代苯基衍生物LIG12、LIG23和LIG30、苯胺取代苯基衍生物LIG7和邻硝基取代苯基衍生物LIG27的对接分数最高。LIG7、LIG12、LIG23、LIG27和LIG30的对接分数分别为-10.6、-10.7、-10.7、-10.8和-10.5 kcal/mol。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Anti-inflammatory activity of novel xanthone derivatives
As many diseases such as cancer, metabolic disorders, aging, and neurodegenerative diseases present themselves via inflammation,there is always a need to have better anti-inflammatory drugs. Xanthones, a unique scaffold with a 9H-Xanthen-9-one core structure possesses anti-inflammatory activity. This research work comprised of theoretically designing thirty 3-aminoalkoxy derivatives of xanthone, estimation of physicochemical properties and their Molecular Docking with COX-1 receptor. The best docking scores are possessed by LIG12, LIG23 and LIG30 which were halo substituted phenyl derivatives, LIG7 which had an anilino substitution and LIG27 which had ortho-nitro phenyl substituted derivative. The docking scores of LIG7, LIG12, LIG23, LIG27 and LIG30 were found to be -10.6, -10.7, -10.7, -10.8 and -10.5 kcal/mol.
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