| Literature DB >> 30109011 |
Ye Guo1, Pan-Pan Zhou2, Sen-Yan Zhang2, Xiao-Wen Fan1, Yu-Wei Dou1, Xuan-Ling Shi2.
Abstract
AIDS has evolved from a fatal infectious disease to a manageable chronic disease under the treatment of anti-AIDS medications. HIV fusion inhibitors with high activity, low side effects and strong selectivity are promising drugs against HIV. Only one fusion inhibitor is currently approved, thereby highly active long-acting fusion inhibitors need to be developed for long-term AIDS treatment. Here, we synthesised MT-SC22EK (a small HIV fusion inhibitor) derivatives containing 1-2 staples to improve its stability. Antiviral activity studies showed that MT-SC22EK-2 with two staples exhibited potent inhibitory activity against HIV-1 standard strains and Chinese epidemic strains, and at the same time, MT-SC22EK-2 presented strong anti-T20 resistance. Surprisingly, MT-SC22EK-2 possessed excellent protease stability with a half-life of 3665 min. MT-SC22EK-2 is a potential HIV fusion inhibitor considered as a long-acting anti-HIV drug candidate.Entities:
Year: 2018 PMID: 30109011 PMCID: PMC6071707 DOI: 10.1039/c8md00124c
Source DB: PubMed Journal: Medchemcomm ISSN: 2040-2503 Impact factor: 3.597