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Abstract：
A series of potential HIV-1 integrase inhibitors based on 5-chloro-2-hydroxy-3-triazolylbenzoic acid scaffold was designed and synthesized. Some of these compounds exhibit potent inhibitory activities at micromolar concentrations against HIV-1 integrase in the 3＇-end processing and the strand transfer step.
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MEDICINAL CHEMISTRY RESEARCH
ISSN： 1054-2523
Year： 2015
Issue： 7
Volume： 24
Page： 2950-2959
2 . 6 0 0
JCR@2022
ESI Discipline： PHARMACOLOGY & TOXICOLOGY;
ESI HC Threshold：182
JCR Journal Grade：3
CAS Journal Grade：4
Cited Count：
WoS CC Cited Count： 3
SCOPUS Cited Count： 4
ESI Highly Cited Papers on the List： 0 Unfold All
WanFang Cited Count：
Chinese Cited Count：
30 Days PV： 8
Affiliated Colleges：
