HIV-1 Protease WT (NL4-3) with Inhibitor NR01-141
收藏NIAID Data Ecosystem2026-05-10 收录
数据链接:
官方服务:
资源简介:
HIV-1 Protease WT (NL4-3) with Inhibitor NR01-141
应用场景:
创建时间:
2026-01-07
相关数据集
HIV-1 protease in complex with an isobutyl decorated oligoamine (symmetric binding mode)
HIV-1 protease in complex with an isobutyl decorated oligoamine (symmetric binding mode) Descriptor: CHLORIDE ION, N,N'-(iminodiethane-2,1-diyl)bis[4-amino-N-(2-methylpropyl)benzenesulfonamide], Prote
Protein Data Bank Japan2023-11-01 更新50
CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH PETT-1 (PETT131A94)
CRYSTAL STRUCTURE OF HIV-1 REVERSE TRANSCRIPTASE IN COMPLEX WITH PETT-1 (PETT131A94)
NIAID Data Ecosystem30
Design and Development of Highly Potent HIV‑1 Protease Inhibitors with a Crown-Like Oxotricyclic Core as the P2-Ligand To Combat Multidrug-Resistant HIV Variants
Design, synthesis, and evaluation of a new class of exceptionally potent HIV-1 protease inhibitors are reported. Inhibitor 5 displayed superior antiviral activity and drug-resistance profiles. In fact
Figshare2017-04-18 更新30
Design of HIV‑1 Protease Inhibitors with Amino-bis-tetrahydrofuran Derivatives as P2-Ligands to Enhance Backbone-Binding Interactions: Synthesis, Biological Evaluation, and Protein–Ligand X‑ray Studies
Structure-based design, synthesis, and biological evaluation of a series of very potent HIV-1 protease inhibitors are described. In an effort to improve backbone ligand–binding site interactions, we h
NIAID Data Ecosystem40
Structure of HIV1 protease and hh1_173_3a complex.
Structure of HIV1 protease and hh1_173_3a complex. Descriptor: (3S)-TETRAHYDROFURAN-3-YL (1R)-3-{(2R)-4-[(1S,3S)-3-(2-AMINO-2-OXOETHYL)-2,3-DIHYDRO-1H-INDEN-1-YL]-2-BENZYL-3-OXO-2,3-DIHYDRO-1H-PYRROL-
Protein Data Bank Japan2023-08-23 更新30



