BDBM50352162 NITROBENZENE

SMILES: [O-][N+](=O)c1ccccc1

InChI Key: InChIKey=LQNUZADURLCDLV-UHFFFAOYSA-N

Data: 1 KI  1 IC50

PDB links: 4 PDB IDs match this monomer.

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50352162   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Glutathione reductase (GR) (Homo sapiens (Human))	BDBM50352162 (NITROBENZENE) Show SMILES [O-][N+](=O)c1ccccc1 Show InChI InChI=1S/C6H5NO2/c8-7(9)6-4-2-1-3-5-6/h1-5H	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	Purchase CHEBI KEGG MMDB PC cid PC sid PDB UniChem Patents	Article PubMed	2.74E+5	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))	BDBM50352162 (NITROBENZENE) Show SMILES [O-][N+](=O)c1ccccc1 Show InChI InChI=1S/C6H5NO2/c8-7(9)6-4-2-1-3-5-6/h1-5H	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar	Purchase CHEBI KEGG MMDB PC cid PC sid PDB UniChem Patents	Article PubMed	n/a	n/a	5.47E+5	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