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SMILES: Cc1cn(CCOCCOC(c2ccccc2)(c2ccccc2)c2ccncc2)c(=O)[nH]c1=O

InChI Key: InChIKey=FALXHDVQJVMXGK-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50200991   

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
Thymidine kinase 2, mitochondrial (Homo sapiens (Human))	BDBM50200991 (1-[2-[2-[1,1-(diphenyl)-1-(4-pyridyl)methoxy]ethox...) Show SMILES Cc1cn(CCOCCOC(c2ccccc2)(c2ccccc2)c2ccncc2)c(=O)[nH]c1=O Show InChI InChI=1S/C27H27N3O4/c1-21-20-30(26(32)29-25(21)31)16-17-33-18-19-34-27(22-8-4-2-5-9-22,23-10-6-3-7-11-23)24-12-14-28-15-13-24/h2-15,20H,16-19H2,1H3,(H,29,31,32)	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Química Médica (C.S.I.C.) Curated by ChEMBL					Assay Description Inhibition of [3H]methyl dThd phosphorylation by TK2				J Med Chem 49: 7766-73 (2006) Article DOI: 10.1021/jm0610550 BindingDB Entry DOI: 10.7270/Q2K073XW
					More data for this Ligand-Target Pair
Thymidine kinase (Human herpesvirus 1 (strain SC16) (HHV-1) (Human h...)	BDBM50200991 (1-[2-[2-[1,1-(diphenyl)-1-(4-pyridyl)methoxy]ethox...) Show SMILES Cc1cn(CCOCCOC(c2ccccc2)(c2ccccc2)c2ccncc2)c(=O)[nH]c1=O Show InChI InChI=1S/C27H27N3O4/c1-21-20-30(26(32)29-25(21)31)16-17-33-18-19-34-27(22-8-4-2-5-9-22,23-10-6-3-7-11-23)24-12-14-28-15-13-24/h2-15,20H,16-19H2,1H3,(H,29,31,32)	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Química Médica (C.S.I.C.) Curated by ChEMBL					Assay Description Inhibition of [3H]methyl dThd phosphorylation by HSV1 TK				J Med Chem 49: 7766-73 (2006) Article DOI: 10.1021/jm0610550 BindingDB Entry DOI: 10.7270/Q2K073XW
					More data for this Ligand-Target Pair
Deoxynucleoside kinase (Drosophila melanogaster)	BDBM50200991 (1-[2-[2-[1,1-(diphenyl)-1-(4-pyridyl)methoxy]ethox...) Show SMILES Cc1cn(CCOCCOC(c2ccccc2)(c2ccccc2)c2ccncc2)c(=O)[nH]c1=O Show InChI InChI=1S/C27H27N3O4/c1-21-20-30(26(32)29-25(21)31)16-17-33-18-19-34-27(22-8-4-2-5-9-22,23-10-6-3-7-11-23)24-12-14-28-15-13-24/h2-15,20H,16-19H2,1H3,(H,29,31,32)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Química Médica (C.S.I.C.) Curated by ChEMBL					Assay Description Inhibition of [3H]methyl dThd phosphorylation by Drosophila melanogaster dNK				J Med Chem 49: 7766-73 (2006) Article DOI: 10.1021/jm0610550 BindingDB Entry DOI: 10.7270/Q2K073XW
					More data for this Ligand-Target Pair