BDBM50206485 1-(2'-O-octyl-beta-D-arabinofuranosyl)cytosine::CHEMBL400234

SMILES: CCCCCCCCC(=O)O[C@H]1[C@H](O)[C@@H](CO)O[C@H]1n1ccc(N)nc1=O

InChI Key: InChIKey=ZWFXTBCMBWKCBF-VDNDLQMASA-N

Data: 5 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 5 hits for monomerid = 50206485   

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, cytosolic (Homo sapiens (Human))	BDBM50206485 (1-(2'-O-octyl-beta-D-arabinofuranosyl)cytosine | C...) Show SMILES CCCCCCCCC(=O)O[C@H]1[C@H](O)[C@@H](CO)O[C@H]1n1ccc(N)nc1=O Show InChI InChI=1S/C18H29N3O6/c1-2-3-4-5-6-7-8-14(23)27-16-15(24)12(11-22)26-17(16)21-10-9-13(19)20-18(21)25/h9-10,12,15-17,22,24H,2-8,11H2,1H3,(H2,19,20,25)/t12-,15-,16+,17-/m1/s1	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	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Ferrara Curated by ChEMBL					Assay Description Inhibition of human TK1 assessed as [methyl-3H]dThd phosphorylation				Bioorg Med Chem 15: 3065-81 (2007) Article DOI: 10.1016/j.bmc.2007.01.049 BindingDB Entry DOI: 10.7270/Q29C6Z76
					More data for this Ligand-Target Pair
Thymidine kinase (Human herpesvirus 1 (strain SC16) (HHV-1) (Human h...)	BDBM50206485 (1-(2'-O-octyl-beta-D-arabinofuranosyl)cytosine | C...) Show SMILES CCCCCCCCC(=O)O[C@H]1[C@H](O)[C@@H](CO)O[C@H]1n1ccc(N)nc1=O Show InChI InChI=1S/C18H29N3O6/c1-2-3-4-5-6-7-8-14(23)27-16-15(24)12(11-22)26-17(16)21-10-9-13(19)20-18(21)25/h9-10,12,15-17,22,24H,2-8,11H2,1H3,(H2,19,20,25)/t12-,15-,16+,17-/m1/s1	PDB MMDB B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Ferrara Curated by ChEMBL					Assay Description Inhibition of HSV1 TK assessed as [methyl-3H]dThd phosphorylation				Bioorg Med Chem 15: 3065-81 (2007) Article DOI: 10.1016/j.bmc.2007.01.049 BindingDB Entry DOI: 10.7270/Q29C6Z76
					More data for this Ligand-Target Pair
Thymidine kinase (Varicella-zoster virus (strain Dumas) (HHV-3) (Hum...)	BDBM50206485 (1-(2'-O-octyl-beta-D-arabinofuranosyl)cytosine | C...) Show SMILES CCCCCCCCC(=O)O[C@H]1[C@H](O)[C@@H](CO)O[C@H]1n1ccc(N)nc1=O Show InChI InChI=1S/C18H29N3O6/c1-2-3-4-5-6-7-8-14(23)27-16-15(24)12(11-22)26-17(16)21-10-9-13(19)20-18(21)25/h9-10,12,15-17,22,24H,2-8,11H2,1H3,(H2,19,20,25)/t12-,15-,16+,17-/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Ferrara Curated by ChEMBL					Assay Description Inhibition of VZV TK assessed as [methyl-3H]dThd phosphorylation				Bioorg Med Chem 15: 3065-81 (2007) Article DOI: 10.1016/j.bmc.2007.01.049 BindingDB Entry DOI: 10.7270/Q29C6Z76
					More data for this Ligand-Target Pair
Thymidine kinase, mitochondrial (Homo sapiens (Human))	BDBM50206485 (1-(2'-O-octyl-beta-D-arabinofuranosyl)cytosine | C...) Show SMILES CCCCCCCCC(=O)O[C@H]1[C@H](O)[C@@H](CO)O[C@H]1n1ccc(N)nc1=O Show InChI InChI=1S/C18H29N3O6/c1-2-3-4-5-6-7-8-14(23)27-16-15(24)12(11-22)26-17(16)21-10-9-13(19)20-18(21)25/h9-10,12,15-17,22,24H,2-8,11H2,1H3,(H2,19,20,25)/t12-,15-,16+,17-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Ferrara Curated by ChEMBL					Assay Description Inhibition of human TK2 assessed as [methyl-3H]dThd phosphorylation				Bioorg Med Chem 15: 3065-81 (2007) Article DOI: 10.1016/j.bmc.2007.01.049 BindingDB Entry DOI: 10.7270/Q29C6Z76
					More data for this Ligand-Target Pair
Deoxynucleoside kinase (Drosophila melanogaster)	BDBM50206485 (1-(2'-O-octyl-beta-D-arabinofuranosyl)cytosine | C...) Show SMILES CCCCCCCCC(=O)O[C@H]1[C@H](O)[C@@H](CO)O[C@H]1n1ccc(N)nc1=O Show InChI InChI=1S/C18H29N3O6/c1-2-3-4-5-6-7-8-14(23)27-16-15(24)12(11-22)26-17(16)21-10-9-13(19)20-18(21)25/h9-10,12,15-17,22,24H,2-8,11H2,1H3,(H2,19,20,25)/t12-,15-,16+,17-/m1/s1	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	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Ferrara Curated by ChEMBL					Assay Description Inhibition of Drosophila melanogaster dNK assessed as [methyl-3H]dThd phosphorylation				Bioorg Med Chem 15: 3065-81 (2007) Article DOI: 10.1016/j.bmc.2007.01.049 BindingDB Entry DOI: 10.7270/Q29C6Z76
					More data for this Ligand-Target Pair