Crystal structure of the complex of mutant HIV-1 protease (A71V, V82T, I84V) with a hydroxyethylamine peptidomimetic inhibitor BOC-PHE-PSI[R-CH(OH)CH2NH]-PHE-GLU-PHE-NH2

NIAID Data Ecosystem10

Inactivation of Human Immunodeficiency Virus Type 1 by Porphyrins

抗HIV药物

病毒灭活机制

We have evaluated the anti-human immunodeficiency virus (HIV) activity of a series of natural and synthetic porphyrins to identify compounds that could potentially be used as microbicides to provide a

PubMed Central40

HIV-1 Protease WT (NL4-3) in Complex with LR4-44

HIV-1蛋白酶抑制剂

艾滋病药物设计

HIV-1 Protease WT (NL4-3) in Complex with LR4-44 Descriptor: (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl {(2S,3R)-1-(3,5-difluorophenyl)-3-hydroxy-4-[{4-[(1S)-1-hydroxyethyl]benzene-1-sulfonyl}(2-meth

Protein Data Bank Japan2026-01-07 更新10

I50V HIV-1 protease in complex with an amino decorated pyrrolidine-based inhibitor

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