null

SMILES: CC(C)[C@@H]1COC(=O)N1CC(=O)Nc1nc(C)c(s1)-c1ccc(N)cc1

InChI Key: InChIKey=JJSJJDRYTQMCBL-AWEZNQCLSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50436480   

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
Cytochrome P450 2D6 (Homo sapiens (Human))	BDBM50436480 (CHEMBL2397306) Show SMILES CC(C)[C@@H]1COC(=O)N1CC(=O)Nc1nc(C)c(s1)-c1ccc(N)cc1 |r| Show InChI InChI=1S/C18H22N4O3S/c1-10(2)14-9-25-18(24)22(14)8-15(23)21-17-20-11(3)16(26-17)12-4-6-13(19)7-5-12/h4-7,10,14H,8-9,19H2,1-3H3,(H,20,21,23)/t14-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Boehringer Ingelheim (Canada) Ltd. Curated by ChEMBL					Assay Description Inhibition of CYP2D6 (unknown origin)				Bioorg Med Chem Lett 23: 3841-7 (2013) Article DOI: 10.1016/j.bmcl.2013.04.077 BindingDB Entry DOI: 10.7270/Q2BG2QCX
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50436480 (CHEMBL2397306) Show SMILES CC(C)[C@@H]1COC(=O)N1CC(=O)Nc1nc(C)c(s1)-c1ccc(N)cc1 |r| Show InChI InChI=1S/C18H22N4O3S/c1-10(2)14-9-25-18(24)22(14)8-15(23)21-17-20-11(3)16(26-17)12-4-6-13(19)7-5-12/h4-7,10,14H,8-9,19H2,1-3H3,(H,20,21,23)/t14-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Boehringer Ingelheim (Canada) Ltd. Curated by ChEMBL					Assay Description Inhibition of CYP3A4 (unknown origin)				Bioorg Med Chem Lett 23: 3841-7 (2013) Article DOI: 10.1016/j.bmcl.2013.04.077 BindingDB Entry DOI: 10.7270/Q2BG2QCX
					More data for this Ligand-Target Pair