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SMILES: O=C1Cc2cnc3cc(nn3c2-c2cnccc2N1)-c1ccccc1

InChI Key: InChIKey=ITUGUNWECVJZLD-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50308211   

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
Insulin receptor (Homo sapiens (Human))	BDBM50308211 (2-Phenyl-6,8-dihydro-7H-pyrazolo[5',1':2,3]pyrimid...) Show SMILES O=C1Cc2cnc3cc(nn3c2-c2cnccc2N1)-c1ccccc1 Show InChI InChI=1S/C19H13N5O/c25-18-8-13-10-21-17-9-16(12-4-2-1-3-5-12)23-24(17)19(13)14-11-20-7-6-15(14)22-18/h1-7,9-11H,8H2,(H,22,25)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Technische Universitat Braunschweig Curated by ChEMBL					Assay Description Inhibition of INSR assessed as [33Pi] incorporation by microplate scintillation counting in presence of 1 uM ATP				J Med Chem 53: 2433-42 (2010) Article DOI: 10.1021/jm901388c BindingDB Entry DOI: 10.7270/Q24J0G22
					More data for this Ligand-Target Pair
Vascular endothelial growth factor receptor 2 (Homo sapiens (Human))	BDBM50308211 (2-Phenyl-6,8-dihydro-7H-pyrazolo[5',1':2,3]pyrimid...) Show SMILES O=C1Cc2cnc3cc(nn3c2-c2cnccc2N1)-c1ccccc1 Show InChI InChI=1S/C19H13N5O/c25-18-8-13-10-21-17-9-16(12-4-2-1-3-5-12)23-24(17)19(13)14-11-20-7-6-15(14)22-18/h1-7,9-11H,8H2,(H,22,25)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Technische Universitat Braunschweig Curated by ChEMBL					Assay Description Inhibition of VEGFR2 assessed as [33Pi] incorporation by microplate scintillation counting in presence of 1 uM ATP				J Med Chem 53: 2433-42 (2010) Article DOI: 10.1021/jm901388c BindingDB Entry DOI: 10.7270/Q24J0G22
					More data for this Ligand-Target Pair
Serine/threonine-protein kinase PLK1 (Homo sapiens (Human))	BDBM50308211 (2-Phenyl-6,8-dihydro-7H-pyrazolo[5',1':2,3]pyrimid...) Show SMILES O=C1Cc2cnc3cc(nn3c2-c2cnccc2N1)-c1ccccc1 Show InChI InChI=1S/C19H13N5O/c25-18-8-13-10-21-17-9-16(12-4-2-1-3-5-12)23-24(17)19(13)14-11-20-7-6-15(14)22-18/h1-7,9-11H,8H2,(H,22,25)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Technische Universitat Braunschweig Curated by ChEMBL					Assay Description Inhibition of PLK1 assessed as [33Pi] incorporation by microplate scintillation counting in presence of 1 uM ATP				J Med Chem 53: 2433-42 (2010) Article DOI: 10.1021/jm901388c BindingDB Entry DOI: 10.7270/Q24J0G22
					More data for this Ligand-Target Pair