BDBM50137353 CHEMBL349154::[((S)-2-Amino-4-methylsulfanyl-butyryl)-hydroxy-amino]-acetic acid

SMILES: CSCC[C@H](N)C(=O)N(O)CC(O)=O

InChI Key: InChIKey=PRVSVAWHKFPRNF-YFKPBYRVSA-N

Data: 2 KI

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50137353   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Methionine Aminopeptidase Type 1 (MetAP1) (Homo sapiens (Human))	BDBM50137353 (CHEMBL349154 | [((S)-2-Amino-4-methylsulfanyl-buty...) Show SMILES CSCC[C@H](N)C(=O)N(O)CC(O)=O Show InChI InChI=1S/C7H14N2O4S/c1-14-3-2-5(8)7(12)9(13)4-6(10)11/h5,13H,2-4,8H2,1H3,(H,10,11)/t5-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	3.90E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Ohio State University Curated by ChEMBL					Assay Description Inhibitory activity of the compound against Methionine aminopeptidase 1				Bioorg Med Chem Lett 14: 77-9 (2003) BindingDB Entry DOI: 10.7270/Q2DV1J90
					More data for this Ligand-Target Pair
Methionine aminopeptidase 2 (Homo sapiens (Human))	BDBM50137353 (CHEMBL349154 | [((S)-2-Amino-4-methylsulfanyl-buty...) Show SMILES CSCC[C@H](N)C(=O)N(O)CC(O)=O Show InChI InChI=1S/C7H14N2O4S/c1-14-3-2-5(8)7(12)9(13)4-6(10)11/h5,13H,2-4,8H2,1H3,(H,10,11)/t5-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	1.30E+6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Ohio State University Curated by ChEMBL					Assay Description Inhibitory activity of the compound against Methionine aminopeptidase 2				Bioorg Med Chem Lett 14: 77-9 (2003) BindingDB Entry DOI: 10.7270/Q2DV1J90
					More data for this Ligand-Target Pair