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摘要:
HIV-1 integrase (IN) is a crucial enzyme in the life cycle of HIV-1 and also a validated target for developing anti-HIV inhibitors. Recent progress in drug design has significantly accelerated the development of anti-AIDS IN inhibitors. A large amount of novel inhibitors that interact specifically with IN were developed along with the expanding and application of methods to drug design. This article reviewed the anti-HIV IN inhibitors discovered by the rational drug design approaches in the recent 5-year.
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来源 :
MINI-REVIEWS IN MEDICINAL CHEMISTRY
ISSN: 1389-5575
年份: 2012
期: 9
卷: 12
页码: 875-889
3 . 8 0 0
JCR@2022
ESI学科: PHARMACOLOGY & TOXICOLOGY;
ESI高被引阀值:174
JCR分区:2
中科院分区:3