Molecule Details
InChIKeyOFAZWNGNAATRSH-GWCXRDAXSA-N
Compound NameN~2~-[(2R,4S,5S)-5-{[N-{[(3,5-Dimethyl-1H-pyrazol-1-YL)methoxy]carbonyl}-3-(methylsulfonyl)-L-alanyl]amino}-4-hydroxy-2,7-dimethyloctanoyl]-N-isobutyl-L-valinamide
Canonical SMILESCc1cc(C)n(COC(=O)N[C@@H](CS(C)(=O)=O)C(=O)N[C@@H](CC(C)C)[C@@H](O)C[C@@H](C)C(=O)N[C@H](C(=O)NCC(C)C)C(C)C)n1
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)3
Pfam Stratification Homologous
Avg pChEMBL7.62
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (3)
Target Gene Organism Category Pfam pChEMBL Type Source
P56817 BACE1 Homo sapiens Human PF00026 9.5 Ki ChEMBL;BindingDB
P07339 CTSD Homo sapiens Human PF07966 PF00026 6.9 Ki ChEMBL;BindingDB
Q9Y5Z0 BACE2 Homo sapiens Human PF00026 6.5 Ki ChEMBL;BindingDB