Reaction Details |
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Target | Thymidine kinase 2, mitochondrial |
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Ligand | BDBM50206507 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_454745 (CHEMBL886767) |
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IC50 | 3800±n/a nM |
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Citation | Ciliberti, N; Manfredini, S; Angusti, A; Durini, E; Solaroli, N; Vertuani, S; Buzzoni, L; Bonache, MC; Ben-Shalom, E; Karlsson, A; Saada, A; Balzarini, J Novel selective human mitochondrial kinase inhibitors: design, synthesis and enzymatic activity. Bioorg Med Chem15:3065-81 (2007) [PubMed] Article |
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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 |
Synonyms: | KITM_HUMAN | TK2 | Thymidine kinase, mitochondrial |
Type: | PROTEIN |
Mol. Mass.: | 31013.50 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1333885 |
Residue: | 265 |
Sequence: | MLLWPLRGWAARALRCFGPGSRGSPASGPGPRRVQRRAWPPDKEQEKEKKSVICVEGNIA
SGKTTCLEFFSNATDVEVLTEPVSKWRNVRGHNPLGLMYHDASRWGLTLQTYVQLTMLDR
HTRPQVSSVRLMERSIHSARYIFVENLYRSGKMPEVDYVVLSEWFDWILRNMDVSVDLIV
YLRTNPETCYQRLKKRCREEEKVIPLEYLEAIHHLHEEWLIKGSLFPMAAPVLVIEADHH
MERMLELFEQNRDRILTPENRKHCP
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BDBM50206507 |
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n/a |
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Name | BDBM50206507 |
Synonyms: | 1-[2'-O-(N-Boc-12-aminododecanoyl)-beta-D-arabinofuranosyl]-5(E)-(2-bromovinyl)uracil | CHEMBL400232 |
Type | Small organic molecule |
Emp. Form. | C28H44BrN3O9 |
Mol. Mass. | 646.568 |
SMILES | CC(C)(C)OC(=O)NCCCCCCCCCCCC(=O)O[C@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cc(C=CBr)c(=O)[nH]c1=O |w:34.35| |
Structure |
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