BDBM50155213 1-(5-Cyclobutyl-thiazol-2-yl)-3-isoquinolin-8-yl-urea::CHEMBL186342

SMILES: O=C(Nc1ncc(s1)C1CCC1)Nc1cccc2ccncc12

InChI Key: InChIKey=MEWQZVRRNOXYMJ-UHFFFAOYSA-N

Data: 2 IC50

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 = 50155213   

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
Cyclin-dependent-like kinase 5 (Homo sapiens (Human))	BDBM50155213 (1-(5-Cyclobutyl-thiazol-2-yl)-3-isoquinolin-8-yl-u...) Show SMILES O=C(Nc1ncc(s1)C1CCC1)Nc1cccc2ccncc12 Show InChI InChI=1S/C17H16N4OS/c22-16(21-17-19-10-15(23-17)12-4-1-5-12)20-14-6-2-3-11-7-8-18-9-13(11)14/h2-3,6-10,12H,1,4-5H2,(H2,19,20,21,22)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Concentration required for inhibition of cyclin-dependent kinase 5 was measured by scintillation proximity assay				Bioorg Med Chem Lett 14: 5521-5 (2004) Article DOI: 10.1016/j.bmcl.2004.09.006 BindingDB Entry DOI: 10.7270/Q2D50MFB
					More data for this Ligand-Target Pair
CDK2/CycE (Homo sapiens (Human))	BDBM50155213 (1-(5-Cyclobutyl-thiazol-2-yl)-3-isoquinolin-8-yl-u...) Show SMILES O=C(Nc1ncc(s1)C1CCC1)Nc1cccc2ccncc12 Show InChI InChI=1S/C17H16N4OS/c22-16(21-17-19-10-15(23-17)12-4-1-5-12)20-14-6-2-3-11-7-8-18-9-13(11)14/h2-3,6-10,12H,1,4-5H2,(H2,19,20,21,22)	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	55	n/a	n/a	n/a	n/a	n/a	n/a
Pfizer Global Research and Development Curated by ChEMBL					Assay Description Concentration required for inhibition of cyclin dependant kinase 2-cyclin E was measured by scintillation proximity assay				Bioorg Med Chem Lett 14: 5521-5 (2004) Article DOI: 10.1016/j.bmcl.2004.09.006 BindingDB Entry DOI: 10.7270/Q2D50MFB
					More data for this Ligand-Target Pair