Demethoxylation of curcumin enhances its inhibition on human and rat 17β-hydroxysteroid dehydrogenase 3: QSAR structure-activity relationship and in silico docking analysis-Reference-Cited by-同舟云学术

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Demethoxylation of curcumin enhances its inhibition on human and rat 17β-hydroxysteroid dehydrogenase 3: QSAR structure-activity relationship and in silico docking analysis

Published:2024-04 Issue: Volume:186 Page:114489
ISSN:0278-6915
Container-title:Food and Chemical Toxicology
language:en
Short-container-title:Food and Chemical Toxicology

Author:

Ji Zhongyao,Sang Jianmin,Wang Hong,Xia Miaomiao,Hao Ting,Chen Liping,Lu Han,Wang Shaowei,Yao Ming,Li Linxi,Ge Ren-shan^ORCID

Publisher

Elsevier BV

Reference32 articles.

1. Pharmacology of curcuma longa;Ammon;Planta Med.,1991

2. Bioavailability of curcumin: problems and promises;Anand;Mol. Pharm.,2007

3. Design, synthesis and in vitro evaluation of 4-androstene-3,17-dione/adenosine hybrid compounds as bisubstrate inhibitors of type 3 17beta-hydroxysteroid dehydrogenase;Berube;Med. Chem.,2006

4. Dietary curcumin: correlation between bioavailability and health potential;Dei Cas;Nutrients,2019

5. Identification of a novel series of tetrahydrodibenzazocines as inhibitors of 17beta-hydroxysteroid dehydrogenase type 3;Fink;Bioorg. Med. Chem. Lett,2006

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Targeted Screening of Curcumin Derivatives as Pancreatic Lipase Inhibitors Using Computer-Aided Drug Design;ACS Omega;2024-06-13

2. The role of tetrahydrocurcumin in disease prevention and treatment;Food & Function;2024

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