Molecule Details
InChIKeySVOHWMZXBFVEHY-DQDWUXFNSA-N
Compound Name2-[2-(2-{4-[7-(3-{1-[1-(1-Methoxycarbonyl-2-methyl-propylcarbamoyl)-3-methyl-butylcarbamoyl]-2-methyl-propylcarbamoyl}-propoxy)-naphthalen-2-yloxy]-butyrylamino}-3-methyl-butyrylamino)-4-methyl-pentanoylamino]-3-methyl-butyric acid methyl ester; Dihydrate
Canonical SMILESCOC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)CCCOc1ccc2ccc(OCCCC(=O)N[C@H](C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](C(=O)OC)C(C)C)C(C)C)cc2c1)C(C)C)C(C)C
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)3
Pfam Stratification Homologous
Avg pChEMBL6.25
SourceBindingDB;ChEMBL
2D Structure
2D structure
Activity Profile
Target Activities (3)
Target Gene Organism Category Pfam pChEMBL Type Source
P04585 gag-pol Human immunodeficiency virus type 1 group M subtype B (isolate HXB2) Pathogen PF00540 PF19317 PF00552 PF02022 PF00075 PF00665 PF00077 PF00078 PF06815 PF06817 PF00098 6.2 Ki BindingDB
Q72874 pol Human immunodeficiency virus type 1 Pathogen PF00077 6.2 Ki ChEMBL
Q9YQ12 protease Human immunodeficiency virus type 1 Pathogen PF00077 6.2 Ki ChEMBL;BindingDB