Methyl N-[(1S)-1-[[[(3S)-3-benzyl-3-hydroxy-4-[[(1S,2R)-2-hydroxyindan-1-yl]amino]-4-oxo-butyl]-[[4-(3-pyridyl)phenyl]methyl]amino]carbamoyl]-2,2-dimethyl-propyl]carbamate

InChIKey	`DEWMMLXUMBSCSB-UKVDXBKXSA-N`
Compound Name	Methyl N-[(1S)-1-[[[(3S)-3-benzyl-3-hydroxy-4-[[(1S,2R)-2-hydroxyindan-1-yl]amino]-4-oxo-butyl]-[[4-(3-pyridyl)phenyl]methyl]amino]carbamoyl]-2,2-dimethyl-propyl]carbamate
Canonical SMILES	`COC(=O)N[C@H](C(=O)NN(CC[C@@](O)(Cc1ccccc1)C(=O)N[C@H]1c2ccccc2C[C@H]1O)Cc1ccc(-c2cccnc2)cc1)C(C)(C)C`
Clinical Status	Data-mined Candidate
Targets (Human+Pathogen)	2
Pfam Stratification	Homologous
Avg pChEMBL	8.36
Source	BindingDB;ChEMBL

2D Structure

Activity Profile

Target	Gene	Organism	Category	Pfam	pChEMBL	Type	Source
Q9YQ12	protease	Human immunodeficiency virus type 1	Pathogen	PF00077	8.9	Ki	ChEMBL;BindingDB
Q72874	pol	Human immunodeficiency virus type 1	Pathogen	PF00077	7.8	Ki	ChEMBL