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PMID: 23405965 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Indolizine derivatives as HIV-1 VIF-ElonginC interaction inhibitors.

Chemical biology & drug design ·Vol. 81 ·No. 6 ·2013-06-00 ·Pages 730-41

Huang W, Zuo T, Luo X, Jin H, Liu Z, Yang Z, Yu X, Zhang L, Zhang L

Abstract

Compound 1 (VEC-5) was identified as a potent small-molecular HIV-1 viron infectivity factor inhibitor that targets the viron infectivity factor-ElonginC interaction. A structure-activity relationship study was carried out to develop compounds with improved efficacy against HIV-1 and 49 indolizine derivatives of three categories were designed and synthesized. We found that five compounds exhibited promising anti-HIV-1 activity, and the most active compound 2g had an IC50 value of 11.0 μm. These results provide new information to develop highly potent small-molecule HIV-1 viron infectivity factor inhibitors.

MeSH Terms
Anti-HIV Agents/chemistry,metabolism,pharmacology Elongin HIV-1/drug effects,metabolism Humans Indolizines/chemistry,metabolism,pharmacology Protein Binding/drug effects Structure-Activity Relationship Transcription Factors/antagonists & inhibitors,metabolism vif Gene Products, Human Immunodeficiency Virus/antagonists & inhibitors,metabolism
Chemicals
Anti-HIV Agents Elongin Indolizines Transcription Factors ethyl 3-(2-naphthoyl)-7-isonicotinoylindolizine-1-carboxylate vif Gene Products, Human Immunodeficiency Virus indolizine
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Huang Wenlin
State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing 100191, China.
Zuo Tao
Luo Xiao
Jin Hongwei
Liu Zhenming
Yang Zhenjun
Yu Xianghui
Zhang Liangren
Zhang Lihe
Article Info
Journal
Chemical biology & drug design
Abbr.
Chem Biol Drug Des
ISSN
1747-0285
Published
2013-06-00
Pages
730-41
Language
English
Region
England
NLM ID
101262549
Subset
IM
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