| Literature DB >> 33374869 |
Hong-Jian Ji1,2,3, Jia-Yuan Li2, Shi-Fei Wu2, Wen-Yong Wu1, Chang-Liang Yao2, Shuai Yao2, Jian-Qing Zhang2, De-An Guo1,2.
Abstract
Twelve compounds, including two new aristolochic acid analogues with a formyloxy moiety (9-10) and 10 known aristolochic acid derivates (1-8 and 11-12), were obtained from the roots of Aristolochiacontorta. Their structures were elucidated using extensive spectroscopic methods. Their cytotoxic activity in human proximal tubular cells HK-2 was evaluated by the MTT method, which has been widely used to assess cell viability. Among these molecules, compounds 3 and 9 were found to be more cytotoxic. Furthermore, molecular modeling was used to evaluate, for the first time, the interactions of compounds 3 and 9 with the target protein organic anionic transporter 1 (OAT1) that plays a key role in mediating aristolochic acid nephropathy. Structure-activity relationships are briefly discussed.Entities:
Keywords: Aristolochia contorta; aristolochic acid; cytotoxicity; molecular docking
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Year: 2020 PMID: 33374869 PMCID: PMC7795626 DOI: 10.3390/molecules26010044
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411