BDBM50352163 CHEMBL1824792

SMILES: CC[C@H](CO)NCc1ccc(cc1)[N+]([O-])=O

InChI Key: InChIKey=ULCNJCXXUJYDEK-SNVBAGLBSA-N

Data: 1 KI  1 IC50

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 = 50352163   

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
Glutathione reductase (GR) (Homo sapiens (Human))	BDBM50352163 (CHEMBL1824792) Show SMILES CC[C@H](CO)NCc1ccc(cc1)[N+]([O-])=O |r| Show InChI InChI=1S/C11H16N2O3/c1-2-10(8-14)12-7-9-3-5-11(6-4-9)13(15)16/h3-6,10,12,14H,2,7-8H2,1H3/t10-/m1/s1	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	4.57E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Batman University Curated by ChEMBL					Assay Description Competitive inhibition of human erythrocyte Glutathione reductase using GSSG substrate by Lineweaver-Burk plot analysis				Bioorg Med Chem Lett 21: 5398-402 (2011) Article DOI: 10.1016/j.bmcl.2011.07.002 BindingDB Entry DOI: 10.7270/Q2V69KKH
					More data for this Ligand-Target Pair
Glutathione reductase (GR) (Homo sapiens (Human))	BDBM50352163 (CHEMBL1824792) Show SMILES CC[C@H](CO)NCc1ccc(cc1)[N+]([O-])=O |r| Show InChI InChI=1S/C11H16N2O3/c1-2-10(8-14)12-7-9-3-5-11(6-4-9)13(15)16/h3-6,10,12,14H,2,7-8H2,1H3/t10-/m1/s1	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.33E+4	n/a	n/a	n/a	n/a	n/a	n/a
Batman University Curated by ChEMBL					Assay Description Inhibition of human erythrocyte Glutathione reductase				Bioorg Med Chem Lett 21: 5398-402 (2011) Article DOI: 10.1016/j.bmcl.2011.07.002 BindingDB Entry DOI: 10.7270/Q2V69KKH
					More data for this Ligand-Target Pair