null

SMILES: O=C(CCCCS(=O)(=O)Cc1ccccc1)c1ncc(o1)-c1ccccn1

InChI Key: InChIKey=IPHUIJQTUFWQFI-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 23114   

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
Fatty-acid amide hydrolase 1 (Homo sapiens (Human))	BDBM23114 (5-(phenylmethane)sulfonyl-1-[5-(pyridin-2-yl)-1,3-...) Show SMILES O=C(CCCCS(=O)(=O)Cc1ccccc1)c1ncc(o1)-c1ccccn1 Show InChI InChI=1S/C20H20N2O4S/c23-18(20-22-14-19(26-20)17-10-4-6-12-21-17)11-5-7-13-27(24,25)15-16-8-2-1-3-9-16/h1-4,6,8-10,12,14H,5,7,11,13,15H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Johnson& Johnson Pharmaceutical Research and Development Curated by ChEMBL					Assay Description Inhibition of FAAH				J Med Chem 51: 7327-43 (2009) Article DOI: 10.1021/jm800311k BindingDB Entry DOI: 10.7270/Q2J67HT8
					More data for this Ligand-Target Pair
DNA ligase 1 (Homo sapiens (Human))	BDBM23114 (5-(phenylmethane)sulfonyl-1-[5-(pyridin-2-yl)-1,3-...) Show SMILES O=C(CCCCS(=O)(=O)Cc1ccccc1)c1ncc(o1)-c1ccccn1 Show InChI InChI=1S/C20H20N2O4S/c23-18(20-22-14-19(26-20)17-10-4-6-12-21-17)11-5-7-13-27(24,25)15-16-8-2-1-3-9-16/h1-4,6,8-10,12,14H,5,7,11,13,15H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	>1.00E+4	>-6.82	n/a	n/a	n/a	n/a	n/a	n/a	25
The Scripps Research Institute					Assay Description The inhibition assays were performed by incubating enzyme, 14C-labeled oleamide in reaction buffer at room temperature in the presence of three diffe...				J Med Chem 50: 3359-68 (2007) Article DOI: 10.1021/jm061414r BindingDB Entry DOI: 10.7270/Q2DR2SSH
					More data for this Ligand-Target Pair