Reaction Details |
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Target | Thymidine kinase, cytosolic |
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Ligand | BDBM50118489 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_210617 (CHEMBL811734) |
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IC50 | 33000±n/a nM |
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Citation | Hernández, AI; Balzarini, J; Karlsson, A; Camarasa, MJ; Pérez-Pérez, MJ Acyclic nucleoside analogues as novel inhibitors of human mitochondrial thymidine kinase. J Med Chem45:4254-63 (2002) [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 |
Synonyms: | KITH_HUMAN | TK1 |
Type: | PROTEIN |
Mol. Mass.: | 25476.50 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1333884 |
Residue: | 234 |
Sequence: | MSCINLPTVLPGSPSKTRGQIQVILGPMFSGKSTELMRRVRRFQIAQYKCLVIKYAKDTR
YSSSFCTHDRNTMEALPACLLRDVAQEALGVAVIGIDEGQFFPDIVEFCEAMANAGKTVI
VAALDGTFQRKPFGAILNLVPLAESVVKLTAVCMECFREAAYTKRLGTEKEVEVIGGADK
YHSVCRLCYFKKASGQPAGPDNKENCPVPGKPGEAVAARKLFAPQQILQCSPAN
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BDBM50118489 |
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n/a |
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Name | BDBM50118489 |
Synonyms: | 1-(4-Hydroxy-5-trityloxymethyl-tetrahydro-furan-2-yl)-5-methyl-1H-pyrimidine-2,4-dione | CHEMBL336109 |
Type | Small organic molecule |
Emp. Form. | C29H28N2O5 |
Mol. Mass. | 484.543 |
SMILES | Cc1cn(C2CC(O)C(COC(c3ccccc3)(c3ccccc3)c3ccccc3)O2)c(=O)[nH]c1=O |
Structure |
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