BDBM50286492 2-(4-Amino-cyclohexyl)-5-cyclopropyl-7-(2,6-dimethyl-pyridin-4-yl)-6,8-difluoro-2,5-dihydro-pyrazolo[4,3-c]quinolin-3-one::CHEMBL132098

SMILES: Cc1cc(cc(C)n1)-c1c(F)cc2c3nn([C@@H]4CC[C@H](N)CC4)c(=O)c3cn(C3CC3)c2c1F

InChI Key: InChIKey=DSDIBKDSIAQRAN-MAEOIBBWSA-N

Data: 2 EC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50286492   

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
DNA topoisomerase II (Homo sapiens (Human))	BDBM50286492 (2-(4-Amino-cyclohexyl)-5-cyclopropyl-7-(2,6-dimeth...) Show SMILES Cc1cc(cc(C)n1)-c1c(F)cc2c3nn([C@@H]4CC[C@H](N)CC4)c(=O)c3cn(C3CC3)c2c1F |wU:16.16,19.20,(1.59,-7.35,;2.95,-8.14,;4.28,-7.37,;5.63,-8.14,;5.63,-9.68,;4.3,-10.45,;4.3,-11.99,;2.95,-9.68,;6.96,-7.37,;6.96,-5.83,;5.61,-5.06,;8.29,-5.06,;9.62,-5.83,;10.95,-5.06,;11.28,-3.55,;12.79,-3.39,;13.56,-2.05,;15.1,-2.05,;15.87,-.73,;15.1,.61,;15.87,1.94,;13.56,.61,;12.77,-.73,;13.45,-4.78,;14.94,-5.09,;12.28,-5.83,;12.28,-7.37,;10.95,-8.14,;10.95,-9.68,;10.18,-11.02,;11.72,-11.01,;9.62,-7.37,;8.29,-8.14,;8.29,-9.68,)| Show InChI InChI=1S/C26H27F2N5O/c1-13-9-15(10-14(2)30-13)22-21(27)11-19-24-20(12-32(17-7-8-17)25(19)23(22)28)26(34)33(31-24)18-5-3-16(29)4-6-18/h9-12,16-18H,3-8,29H2,1-2H3/t16-,18+	PDB KEGG UniProtKB/SwissProt antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	n/a	n/a	500	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested for topoisomerase II inhibition in purified HeLa cells by SDS/K+ precipitation method				Bioorg Med Chem Lett 5: 405-410 (1995) Article DOI: 10.1016/0960-894X(95)00044-T BindingDB Entry DOI: 10.7270/Q2CZ37N7
					More data for this Ligand-Target Pair
DNA topoisomerase II (Homo sapiens (Human))	BDBM50286492 (2-(4-Amino-cyclohexyl)-5-cyclopropyl-7-(2,6-dimeth...) Show SMILES Cc1cc(cc(C)n1)-c1c(F)cc2c3nn([C@@H]4CC[C@H](N)CC4)c(=O)c3cn(C3CC3)c2c1F |wU:16.16,19.20,(1.59,-7.35,;2.95,-8.14,;4.28,-7.37,;5.63,-8.14,;5.63,-9.68,;4.3,-10.45,;4.3,-11.99,;2.95,-9.68,;6.96,-7.37,;6.96,-5.83,;5.61,-5.06,;8.29,-5.06,;9.62,-5.83,;10.95,-5.06,;11.28,-3.55,;12.79,-3.39,;13.56,-2.05,;15.1,-2.05,;15.87,-.73,;15.1,.61,;15.87,1.94,;13.56,.61,;12.77,-.73,;13.45,-4.78,;14.94,-5.09,;12.28,-5.83,;12.28,-7.37,;10.95,-8.14,;10.95,-9.68,;10.18,-11.02,;11.72,-11.01,;9.62,-7.37,;8.29,-8.14,;8.29,-9.68,)| Show InChI InChI=1S/C26H27F2N5O/c1-13-9-15(10-14(2)30-13)22-21(27)11-19-24-20(12-32(17-7-8-17)25(19)23(22)28)26(34)33(31-24)18-5-3-16(29)4-6-18/h9-12,16-18H,3-8,29H2,1-2H3/t16-,18+	PDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of calf thymus DNA/ethidium bromide complex formation.				Bioorg Med Chem Lett 5: 405-410 (1995) Article DOI: 10.1016/0960-894X(95)00044-T BindingDB Entry DOI: 10.7270/Q2CZ37N7
					More data for this Ligand-Target Pair