N-[(2S)-1-[[(2S,3S)-5-[[(2S)-1-[[(2S)-1-amino-4-methyl-1-oxopentan-2-yl]amino]-1-oxopropan-2-yl]amino]-3-hydroxy-5-oxo-1-[(4-thiophen-3-ylphenyl)methoxy]pentan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]pyridine-2-carboxamide

InChIKey	`BIXULWMVWDYEGF-HCFKQQSISA-N`
Compound Name	N-[(2S)-1-[[(2S,3S)-5-[[(2S)-1-[[(2S)-1-amino-4-methyl-1-oxopentan-2-yl]amino]-1-oxopropan-2-yl]amino]-3-hydroxy-5-oxo-1-[(4-thiophen-3-ylphenyl)methoxy]pentan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]pyridine-2-carboxamide
Canonical SMILES	`CC(C)C[C@H](NC(=O)[C@H](C)NC(=O)C[C@H](O)[C@H](COCc1ccc(-c2ccsc2)cc1)NC(=O)[C@@H](NC(=O)c1ccccn1)C(C)C)C(N)=O`
Clinical Status	Data-mined Candidate
Targets (Human+Pathogen)	3
Pfam Stratification	Homologous
Avg pChEMBL	8.99
Source	ChEMBL;BindingDB

2D Structure

Activity Profile

Target	Gene	Organism	Category	Pfam	pChEMBL	Type	Source
P07339	CTSD	Homo sapiens	Human	PF07966 PF00026	8.5	Ki	ChEMBL;BindingDB
P39898	PMI	Plasmodium falciparum (isolate HB3)	Pathogen	PF00026	9.5	Ki	ChEMBL;BindingDB
P46925	PMII	Plasmodium falciparum (isolate HB3)	Pathogen	PF00026	9.0	Ki	ChEMBL;BindingDB