null

SMILES: COc1ccc(cc1OC1CCCC1)C(=O)Nc1ccccc1[N+]([O-])=O

InChI Key: InChIKey=IAXYKIKFJWCHNY-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50041851   

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
3',5'-cyclic-AMP phosphodiesterase (Sus scrofa)	BDBM50041851 (3-Cyclopentyloxy-4-methoxy-N-(2-nitro-phenyl)-benz...) Show SMILES COc1ccc(cc1OC1CCCC1)C(=O)Nc1ccccc1[N+]([O-])=O Show InChI InChI=1S/C19H20N2O5/c1-25-17-11-10-13(12-18(17)26-14-6-2-3-7-14)19(22)20-15-8-4-5-9-16(15)21(23)24/h4-5,8-12,14H,2-3,6-7H2,1H3,(H,20,22)	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	250	n/a	n/a	n/a	n/a	n/a	n/a
Rhône-Poulenc Rorer Central Research Curated by ChEMBL					Assay Description Inhibitory potency against pig aortic PDE IV				J Med Chem 37: 1696-703 (1994) BindingDB Entry DOI: 10.7270/Q2CF9P5F
					More data for this Ligand-Target Pair
cGMP-specific 3',5'-cyclic phosphodiesterase (Homo sapiens (Human))	BDBM50041851 (3-Cyclopentyloxy-4-methoxy-N-(2-nitro-phenyl)-benz...) Show SMILES COc1ccc(cc1OC1CCCC1)C(=O)Nc1ccccc1[N+]([O-])=O Show InChI InChI=1S/C19H20N2O5/c1-25-17-11-10-13(12-18(17)26-14-6-2-3-7-14)19(22)20-15-8-4-5-9-16(15)21(23)24/h4-5,8-12,14H,2-3,6-7H2,1H3,(H,20,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	n/a	n/a	6.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Rhône-Poulenc Rorer Central Research Curated by ChEMBL					Assay Description Inhibitory potency against pig aortic PDE V.				J Med Chem 37: 1696-703 (1994) BindingDB Entry DOI: 10.7270/Q2CF9P5F
					More data for this Ligand-Target Pair