BDBM50137354 CHEMBL164406::[((R)-2-Amino-propionyl)-hydroxy-amino]-acetic acid

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

InChI Key: InChIKey=YULAFRXRGVGOAA-GSVOUGTGSA-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 = 50137354   

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))	BDBM50137354 (CHEMBL164406 | [((R)-2-Amino-propionyl)-hydroxy-am...) Show SMILES C[C@@H](N)C(=O)N(O)CC(O)=O Show InChI InChI=1S/C5H10N2O4/c1-3(6)5(10)7(11)2-4(8)9/h3,11H,2,6H2,1H3,(H,8,9)/t3-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	1.80E+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))	BDBM50137354 (CHEMBL164406 | [((R)-2-Amino-propionyl)-hydroxy-am...) Show SMILES C[C@@H](N)C(=O)N(O)CC(O)=O Show InChI InChI=1S/C5H10N2O4/c1-3(6)5(10)7(11)2-4(8)9/h3,11H,2,6H2,1H3,(H,8,9)/t3-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	6.00E+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 2				Bioorg Med Chem Lett 14: 77-9 (2003) BindingDB Entry DOI: 10.7270/Q2DV1J90
					More data for this Ligand-Target Pair