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TargetThymidine kinase 2, mitochondrial
LigandBDBM50206495
Substrate/Competitorn/a
Meas. Tech.ChEMBL_454745 (CHEMBL886767)
IC50 44000±n/a nM
Citation Ciliberti, NManfredini, SAngusti, ADurini, ESolaroli, NVertuani, SBuzzoni, LBonache, MCBen-Shalom, EKarlsson, ASaada, ABalzarini, J Novel selective human mitochondrial kinase inhibitors: design, synthesis and enzymatic activity. Bioorg Med Chem15:3065-81 (2007) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Thymidine kinase 2, mitochondrial
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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BDBM50206495
n/a
NameBDBM50206495
Synonyms:1-[2'-O-(4-methoxyphenylacetyl)-beta-D-arabinofuranosyl]-5(E)-(2-bromovinyl)uracil | CHEMBL241408
TypeSmall organic molecule
Emp. Form.C20H21BrN2O8
Mol. Mass.497.293
SMILESCOc1ccc(CC(=O)O[C@H]2[C@H](O)[C@@H](CO)O[C@H]2n2cc(C=CBr)c(=O)[nH]c2=O)cc1 |w:22.23|
Structure
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