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SMILES: COc1ccc(cc1OC1CCCC1)C(=O)Nc1ccccc1Br

InChI Key: InChIKey=PLZLWHQWKGKDDM-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50041845   

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)	BDBM50041845 (CHEMBL296700 | N-(2-Bromo-phenyl)-3-cyclopentyloxy...) Show SMILES COc1ccc(cc1OC1CCCC1)C(=O)Nc1ccccc1Br Show InChI InChI=1S/C19H20BrNO3/c1-23-17-11-10-13(12-18(17)24-14-6-2-3-7-14)19(22)21-16-9-5-4-8-15(16)20/h4-5,8-12,14H,2-3,6-7H2,1H3,(H,21,22)	UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	130	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))	BDBM50041845 (CHEMBL296700 | N-(2-Bromo-phenyl)-3-cyclopentyloxy...) Show SMILES COc1ccc(cc1OC1CCCC1)C(=O)Nc1ccccc1Br Show InChI InChI=1S/C19H20BrNO3/c1-23-17-11-10-13(12-18(17)24-14-6-2-3-7-14)19(22)21-16-9-5-4-8-15(16)20/h4-5,8-12,14H,2-3,6-7H2,1H3,(H,21,22)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+6	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