null

SMILES: O=C(Cc1ccc(cc1)-n1cnnn1)N1CCC(CC1)\C=C\c1ccc2C(=O)OCc2c1

InChI Key: InChIKey=BBMPBQFKQLZBBW-OWOJBTEDSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50163364   

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
ATP-sensitive inward rectifier potassium channel 1 (Rattus norvegicus (Rat))	BDBM50163364 (CHEMBL3794510) Show SMILES O=C(Cc1ccc(cc1)-n1cnnn1)N1CCC(CC1)\C=C\c1ccc2C(=O)OCc2c1 Show InChI InChI=1S/C24H23N5O3/c30-23(14-19-3-6-21(7-4-19)29-16-25-26-27-29)28-11-9-17(10-12-28)1-2-18-5-8-22-20(13-18)15-32-24(22)31/h1-8,13,16-17H,9-12,14-15H2/b2-1+	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	180	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Inhibition of rat ROMK expressed in HEK293 cells after 30 mins by [86Rb+] flux functional assay				Bioorg Med Chem Lett 26: 2339-43 (2016) BindingDB Entry DOI: 10.7270/Q2668G3Q
					More data for this Ligand-Target Pair
1,3-beta-glucan synthase component GSC2 (Saccharomyces cerevisiae)	BDBM50163364 (CHEMBL3794510) Show SMILES O=C(Cc1ccc(cc1)-n1cnnn1)N1CCC(CC1)\C=C\c1ccc2C(=O)OCc2c1 Show InChI InChI=1S/C24H23N5O3/c30-23(14-19-3-6-21(7-4-19)29-16-25-26-27-29)28-11-9-17(10-12-28)1-2-18-5-8-22-20(13-18)15-32-24(22)31/h1-8,13,16-17H,9-12,14-15H2/b2-1+	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Displacement of [35S]-MK499 from human ERG expressed in HEK293 cells				Bioorg Med Chem Lett 26: 2339-43 (2016) BindingDB Entry DOI: 10.7270/Q2668G3Q
					More data for this Ligand-Target Pair