BDBM50206497 1-[2'-O-(4-aminobutanoyl)-beta-D-arabinofuranosyl]-5(E)-(2-bromovinyl)uracil::CHEMBL400233

SMILES: NCCCC(=O)O[C@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cc(C=CBr)c(=O)[nH]c1=O

InChI Key: InChIKey=IQCSJPCYLWAYFM-SGESHTKJSA-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 = 50206497   

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, mitochondrial (Homo sapiens (Human))	BDBM50206497 (1-[2'-O-(4-aminobutanoyl)-beta-D-arabinofuranosyl]...) Show SMILES NCCCC(=O)O[C@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cc(C=CBr)c(=O)[nH]c1=O |w:19.20| Show InChI InChI=1S/C15H20BrN3O7/c16-4-3-8-6-19(15(24)18-13(8)23)14-12(11(22)9(7-20)25-14)26-10(21)2-1-5-17/h3-4,6,9,11-12,14,20,22H,1-2,5,7,17H2,(H,18,23,24)/t9-,11-,12+,14-/m1/s1	Reactome pathway KEGG UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.87E+5	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
Thymidine kinase, cytosolic (Homo sapiens (Human))	BDBM50206497 (1-[2'-O-(4-aminobutanoyl)-beta-D-arabinofuranosyl]...) Show SMILES NCCCC(=O)O[C@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cc(C=CBr)c(=O)[nH]c1=O |w:19.20| Show InChI InChI=1S/C15H20BrN3O7/c16-4-3-8-6-19(15(24)18-13(8)23)14-12(11(22)9(7-20)25-14)26-10(21)2-1-5-17/h3-4,6,9,11-12,14,20,22H,1-2,5,7,17H2,(H,18,23,24)/t9-,11-,12+,14-/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	>5.00E+5	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...)	BDBM50206497 (1-[2'-O-(4-aminobutanoyl)-beta-D-arabinofuranosyl]...) Show SMILES NCCCC(=O)O[C@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cc(C=CBr)c(=O)[nH]c1=O |w:19.20| Show InChI InChI=1S/C15H20BrN3O7/c16-4-3-8-6-19(15(24)18-13(8)23)14-12(11(22)9(7-20)25-14)26-10(21)2-1-5-17/h3-4,6,9,11-12,14,20,22H,1-2,5,7,17H2,(H,18,23,24)/t9-,11-,12+,14-/m1/s1	PDB MMDB B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.70E+4	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...)	BDBM50206497 (1-[2'-O-(4-aminobutanoyl)-beta-D-arabinofuranosyl]...) Show SMILES NCCCC(=O)O[C@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cc(C=CBr)c(=O)[nH]c1=O |w:19.20| Show InChI InChI=1S/C15H20BrN3O7/c16-4-3-8-6-19(15(24)18-13(8)23)14-12(11(22)9(7-20)25-14)26-10(21)2-1-5-17/h3-4,6,9,11-12,14,20,22H,1-2,5,7,17H2,(H,18,23,24)/t9-,11-,12+,14-/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.60E+3	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
Deoxynucleoside kinase (Drosophila melanogaster)	BDBM50206497 (1-[2'-O-(4-aminobutanoyl)-beta-D-arabinofuranosyl]...) Show SMILES NCCCC(=O)O[C@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cc(C=CBr)c(=O)[nH]c1=O |w:19.20| Show InChI InChI=1S/C15H20BrN3O7/c16-4-3-8-6-19(15(24)18-13(8)23)14-12(11(22)9(7-20)25-14)26-10(21)2-1-5-17/h3-4,6,9,11-12,14,20,22H,1-2,5,7,17H2,(H,18,23,24)/t9-,11-,12+,14-/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	1.60E+5	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