tert-butyl N-[(1S)-1-[[(1R)-2-[[(1S)-1-(hex-5-enylsulfonylcarbamoyl)butyl]amino]-1-[4-[(7-methoxy-2-phenyl-4-quinolyl)oxy]-3-vinyl-phenyl]-2-oxo-ethyl]carbamoyl]-2,2-dimethyl-propyl]carbamate

InChIKey	`GBVSVJQQQRTYIH-FAZLVCDOSA-N`
Compound Name	tert-butyl N-[(1S)-1-[[(1R)-2-[[(1S)-1-(hex-5-enylsulfonylcarbamoyl)butyl]amino]-1-[4-[(7-methoxy-2-phenyl-4-quinolyl)oxy]-3-vinyl-phenyl]-2-oxo-ethyl]carbamoyl]-2,2-dimethyl-propyl]carbamate
Canonical SMILES	`C=CCCCCS(=O)(=O)NC(=O)[C@H](CCC)NC(=O)[C@H](NC(=O)[C@@H](NC(=O)OC(C)(C)C)C(C)(C)C)c1ccc(Oc2cc(-c3ccccc3)nc3cc(OC)ccc23)c(C=C)c1`
Clinical Status	Data-mined Candidate
Targets (Human+Pathogen)	2
Pfam Stratification	Homologous
Avg pChEMBL	6.43
Source	ChEMBL;BindingDB

2D Structure

Activity Profile

Target	Gene	Organism	Category	Pfam	pChEMBL	Type	Source
Q0ZMF1	NS3	Hepatitis C virus genotype 1b	Pathogen	PF02907	6.6	Ki	ChEMBL;BindingDB
C1KIQ2		Hepacivirus hominis	Pathogen	PF02907	6.3	Ki	ChEMBL