| Reaction Details |
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 | Report a problem with these data |
| Target | Thymidine kinase, cytosolic |
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| Ligand | BDBM50132254 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEMBL_210613 (CHEMBL816579) |
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| IC50 | >500000±n/a nM |
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| Citation |  Hernández, AI; Balzarini, J; Rodríguez-Barrios, F; San-Félix, A; Karlsson, A; Gago, F; Camarasa, MJ; Pérez-Pérez, MJ Improving the selectivity of acyclic nucleoside analogues as inhibitors of human mitochondrial thymidine kinase: replacement of a triphenylmethoxy moiety with substituted amines and carboxamides. Bioorg Med Chem Lett13:3027-30 (2003) [PubMed] |
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| More Info.: | Get all data from this article, Assay Method |
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| Thymidine kinase, cytosolic |
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| Name: | Thymidine kinase, cytosolic |
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| Synonyms: | KITH_HUMAN | TK1 |
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| Type: | PROTEIN |
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| Mol. Mass.: | 25476.50 |
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| Organism: | Homo sapiens (Human) |
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| Description: | ChEMBL_1333884 |
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| Residue: | 234 |
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| Sequence: | MSCINLPTVLPGSPSKTRGQIQVILGPMFSGKSTELMRRVRRFQIAQYKCLVIKYAKDTR
YSSSFCTHDRNTMEALPACLLRDVAQEALGVAVIGIDEGQFFPDIVEFCEAMANAGKTVI
VAALDGTFQRKPFGAILNLVPLAESVVKLTAVCMECFREAAYTKRLGTEKEVEVIGGADK
YHSVCRLCYFKKASGQPAGPDNKENCPVPGKPGEAVAARKLFAPQQILQCSPAN
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| BDBM50132254 |
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| n/a |
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| Name | BDBM50132254 |
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| Synonyms: | 5-Methyl-1-[4-(4-methyl-piperazin-1-yl)-but-2-enyl]-1H-pyrimidine-2,4-dione | CHEMBL321097 |
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| Type | Small organic molecule |
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| Emp. Form. | C14H22N4O2 |
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| Mol. Mass. | 278.3501 |
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| SMILES | CN1CCN(C\C=C/Cn2cc(C)c(=O)[nH]c2=O)CC1 |
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| Structure | 
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