Abstract |
Agaritine, or beta-N-[gamma-L(+)-glutamyl]-4-hydroxymethylphenylhydrazine, is a Chinese herbal medicine, known having the antiviral and anticancer function. However, so far no reports whatsoever have been made for its potential as an anti-HIV agent. It was observed by docking experiments for more than 9,000 compounds extracted from various Chinese medicines that the compound agaritine distinguished itself from all the others in binding to the HIV protease with the most favorable free energy. Based on this, a series of derivatives were generated by modifying agaritine. It has been observed thru an extensive docking study that some of agaritine derivatives had markedly stronger binding interaction with the HIV protease than agaritine, suggesting that these derivatives might be good candidates for developing drugs for AIDS therapy.
|
Authors | Wei-Na Gao, Dong-Qing Wei, Yun Li, Hui Gao, Wei-Ren Xu, Ai-Xiu Li, Kuo-Chen Chou |
Journal | Medicinal chemistry (Shariqah (United Arab Emirates))
(Med Chem)
Vol. 3
Issue 3
Pg. 221-6
(May 2007)
ISSN: 1573-4064 [Print] Netherlands |
PMID | 17504192
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- HIV Protease Inhibitors
- Phenylhydrazines
- HIV Protease
- agaritine
|
Topics |
- Computer Simulation
- HIV Protease
(metabolism)
- HIV Protease Inhibitors
(chemistry)
- Humans
- Phenylhydrazines
(chemistry, pharmacology)
- Protein Binding
- Structure-Activity Relationship
- Thermodynamics
|