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SMILES: Nc1cc2nc(N)c(cc2cn1)-c1c(Cl)cccc1Cl

InChI Key: InChIKey=RFCMDTOLDNJWEN-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 4607   

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
Fibroblast growth factor receptor 1 (Homo sapiens (Human))	BDBM4607 (1,6-naphthyridine deriv. 9 | 3-(2,6-dichlorophenyl...) Show SMILES Nc1cc2nc(N)c(cc2cn1)-c1c(Cl)cccc1Cl |(-5.57,-1.95,;-4.23,-1.18,;-2.9,-1.95,;-1.57,-1.18,;-.23,-2.01,;1.1,-1.24,;2.43,-2.01,;1.1,.3,;-.23,1.07,;-1.57,.36,;-2.9,1.13,;-4.23,.36,;2.43,1.07,;3.78,.32,;3.78,-1.22,;5.1,1.11,;5.08,2.65,;3.73,3.4,;2.41,2.61,;1.08,3.38,)| Show InChI InChI=1S/C14H10Cl2N4/c15-9-2-1-3-10(16)13(9)8-4-7-6-19-12(17)5-11(7)20-14(8)18/h1-6H,(H2,17,19)(H2,18,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	2.80E+3	n/a	n/a	n/a	n/a	7.4	25
University of Auckland					Assay Description IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...				J Med Chem 43: 4200-11 (2000) Article DOI: 10.1021/jm000161d BindingDB Entry DOI: 10.7270/Q2JW8C3G
					More data for this Ligand-Target Pair
Proto-oncogene tyrosine-protein kinase Src (Homo sapiens (Human))	BDBM4607 (1,6-naphthyridine deriv. 9 | 3-(2,6-dichlorophenyl...) Show SMILES Nc1cc2nc(N)c(cc2cn1)-c1c(Cl)cccc1Cl |(-5.57,-1.95,;-4.23,-1.18,;-2.9,-1.95,;-1.57,-1.18,;-.23,-2.01,;1.1,-1.24,;2.43,-2.01,;1.1,.3,;-.23,1.07,;-1.57,.36,;-2.9,1.13,;-4.23,.36,;2.43,1.07,;3.78,.32,;3.78,-1.22,;5.1,1.11,;5.08,2.65,;3.73,3.4,;2.41,2.61,;1.08,3.38,)| Show InChI InChI=1S/C14H10Cl2N4/c15-9-2-1-3-10(16)13(9)8-4-7-6-19-12(17)5-11(7)20-14(8)18/h1-6H,(H2,17,19)(H2,18,20)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	680	n/a	n/a	n/a	n/a	n/a	n/a
University of Auckland					Assay Description IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...				J Med Chem 43: 4200-11 (2000) Article DOI: 10.1021/jm000161d BindingDB Entry DOI: 10.7270/Q2JW8C3G
					More data for this Ligand-Target Pair
Platelet-derived growth factor receptor beta (Homo sapiens (Human))	BDBM4607 (1,6-naphthyridine deriv. 9 | 3-(2,6-dichlorophenyl...) Show SMILES Nc1cc2nc(N)c(cc2cn1)-c1c(Cl)cccc1Cl |(-5.57,-1.95,;-4.23,-1.18,;-2.9,-1.95,;-1.57,-1.18,;-.23,-2.01,;1.1,-1.24,;2.43,-2.01,;1.1,.3,;-.23,1.07,;-1.57,.36,;-2.9,1.13,;-4.23,.36,;2.43,1.07,;3.78,.32,;3.78,-1.22,;5.1,1.11,;5.08,2.65,;3.73,3.4,;2.41,2.61,;1.08,3.38,)| Show InChI InChI=1S/C14H10Cl2N4/c15-9-2-1-3-10(16)13(9)8-4-7-6-19-12(17)5-11(7)20-14(8)18/h1-6H,(H2,17,19)(H2,18,20)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	3.50E+4	n/a	n/a	n/a	n/a	7.4	25
University of Auckland					Assay Description IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...				J Med Chem 43: 4200-11 (2000) Article DOI: 10.1021/jm000161d BindingDB Entry DOI: 10.7270/Q2JW8C3G
					More data for this Ligand-Target Pair