| Reaction Details |
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 | Report a problem with these data |
| Target | Thymidine kinase 2, mitochondrial |
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| Ligand | BDBM50132291 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | ChEBML_208210 |
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| IC50 | 285000±n/a nM |
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| Citation |  Manfredini, S; Baraldi, PG; Durini, E; Porcu, L; Angusti, A; Vertuani, S; Solaroli, N; De Clercq, E; Karlsson, A; Balzarini, J Design, synthesis and enzymatic activity of highly selective human mitochondrial thymidine kinase inhibitors. Bioorg Med Chem Lett11:1329-32 (2001) [PubMed] |
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| More Info.: | Get all data from this article, Assay Method |
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| Thymidine kinase 2, mitochondrial |
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| Name: | Thymidine kinase 2, mitochondrial |
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| Synonyms: | KITM_HUMAN | TK2 | Thymidine kinase, mitochondrial |
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| Type: | PROTEIN |
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| Mol. Mass.: | 31013.50 |
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| Organism: | Homo sapiens (Human) |
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| Description: | ChEMBL_1333885 |
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| Residue: | 265 |
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| Sequence: | MLLWPLRGWAARALRCFGPGSRGSPASGPGPRRVQRRAWPPDKEQEKEKKSVICVEGNIA
SGKTTCLEFFSNATDVEVLTEPVSKWRNVRGHNPLGLMYHDASRWGLTLQTYVQLTMLDR
HTRPQVSSVRLMERSIHSARYIFVENLYRSGKMPEVDYVVLSEWFDWILRNMDVSVDLIV
YLRTNPETCYQRLKKRCREEEKVIPLEYLEAIHHLHEEWLIKGSLFPMAAPVLVIEADHH
MERMLELFEQNRDRILTPENRKHCP
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| BDBM50132291 |
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| n/a |
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| Name | BDBM50132291 |
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| Synonyms: | 1-((2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)-tetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione | 1-((2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione | 1-((2R,3S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-5-methyl-1H-pyrimidine-2,4-dione | 1-(beta-D-arabinofuranosyl)thymine | 1-beta-D-arabinofuranosylthymine | CHEMBL103283 |
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| Type | Small organic molecule |
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| Emp. Form. | C10H14N2O6 |
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| Mol. Mass. | 258.228 |
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| SMILES | Cc1cn([C@@H]2O[C@H](CO)[C@@H](O)[C@@H]2O)c(=O)[nH]c1=O |r| |
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| Structure | 
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