Target
Thymidine kinase
Ligand
BDBM50206489
Substrate
n/a
Meas. Tech.
ChEMBL_454748 (CHEMBL886771)
IC50
>500000±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 Chem 15:3065-81 (2007) [PubMed]  Article 
Target
Name:
Thymidine kinase
Synonyms:
KITH_VZVD | TK
Type:
PROTEIN
Mol. Mass.:
37819.99
Organism:
Varicella-zoster virus (strain Dumas) (HHV-3) (Human herpesvirus 3)
Description:
ChEMBL_444706
Residue:
341
Sequence:
MSTDKTDVKMGVLRIYLDGAYGIGKTTAAEEFLHHFAITPNRILLIGEPLSYWRNLAGEDAICGIYGTQTRRLNGDVSPEDAQRLTAHFQSLFCSPHAIMHAKISALMDTSTSDLVQVNKEPYKIMLSDRHPIASTICFPLSRYLVGDMSPAALPGLLFTLPAEPPGTNLVVCTVSLPSHLSRVSKRARPGETVNLPFVMVLRNVYIMLINTIIFLKTNNWHAGWNTLSFCNDVFKQKLQKSECIKLREVPGIEDTLFAVLKLPELCGEFGNILPLWAWGMETLSNCSRSMSPFVLSLEQTPQHAAQELKTLLPQMTPANMSSGAWNILKELVNAVQDNTS
  
Inhibitor
Name:
BDBM50206489
Synonyms:
CHEMBL241196 | N3-octyl-1-(beta-D-arabinofuranosyl)thymine
Type:
Small organic molecule
Emp. Form.:
C18H30N2O6
Mol. Mass.:
370.4406
SMILES:
CCCCCCCCn1c(=O)c(C)cn([C@@H]2O[C@H](CO)[C@@H](O)[C@@H]2O)c1=O
Structure:
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