Compile Data Set for Download or QSAR

Found 3 hits Enz. Inhib. hit(s) with Target = 'Cell division control protein 45 homolog'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Cell division control protein 45 homolog (Homo sapiens (Human))	BDBM50097530 (CHEMBL168868 | [5-(5-Cyano-1-methyl-pentyl)-1-(1,5...) Show SMILES CC(C)CCCC(C)[C@H]1CC[C@H]2[C@H](CC(O)=O)[C@H](CC[C@]12C)C(C)CCCCC#N Show InChI InChI=1S/C27H47NO2/c1-19(2)10-9-12-21(4)24-13-14-25-23(18-26(29)30)22(15-16-27(24,25)5)20(3)11-7-6-8-17-28/h19-25H,6-16,18H2,1-5H3,(H,29,30)/t20?,21?,22-,23-,24-,25+,27-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	8.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry and Biochemistry Curated by ChEMBL					Assay Description Inhibitory activity tested against human cell division cycle 45-like 2				J Med Chem 44: 834-48 (2001) BindingDB Entry DOI: 10.7270/Q2C82B14
					More data for this Ligand-Target Pair
Cell division control protein 45 homolog (Homo sapiens (Human))	BDBM50097537 (CHEMBL262776 | [5-(5-Cyanomethyl-2-methyl-tetrahyd...) Show SMILES CC(C)CCCC(C)[C@H]1CC[C@H]2[C@H](CC(O)=O)[C@H](CC[C@]12C)[C@@]1(C)CC[C@@H](CC#N)O1 Show InChI InChI=1S/C27H45NO3/c1-18(2)7-6-8-19(3)22-9-10-23-21(17-25(29)30)24(12-14-26(22,23)4)27(5)15-11-20(31-27)13-16-28/h18-24H,6-15,17H2,1-5H3,(H,29,30)/t19?,20-,21-,22+,23-,24-,26+,27+/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	PubMed	n/a	n/a	1.58E+4	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry and Biochemistry Curated by ChEMBL					Assay Description Inhibitory activity tested against human cell division cycle 45-like 2				J Med Chem 44: 834-48 (2001) BindingDB Entry DOI: 10.7270/Q2C82B14
					More data for this Ligand-Target Pair
Cell division control protein 45 homolog (Homo sapiens (Human))	BDBM50097534 (5-[3-(1,5-Dimethyl-hexyl)-3a,6-dimethyl-8-oxo-dode...) Show SMILES CC(C)CCC[C@@H](C)[C@H]1CC[C@H]2[C@@H]3CC(=O)O[C@](C)(CCCCC(O)=O)[C@H]3CC[C@]12C Show InChI InChI=1S/C27H46O4/c1-18(2)9-8-10-19(3)21-12-13-22-20-17-25(30)31-27(5,15-7-6-11-24(28)29)23(20)14-16-26(21,22)4/h18-23H,6-17H2,1-5H3,(H,28,29)/t19-,20+,21-,22+,23+,26-,27-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry and Biochemistry Curated by ChEMBL					Assay Description Inhibitory activity tested against human cell division cycle 45-like 2				J Med Chem 44: 834-48 (2001) BindingDB Entry DOI: 10.7270/Q2C82B14
					More data for this Ligand-Target Pair