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TargetThymidine kinase
LigandBDBM50101064
Substrate/Competitorn/a
Meas. Tech.ChEBML_210614
IC50 1.4±n/a nM
Citation Martin, JALambert, RWMerrett, JHParkes, KEThomas, GJBaker, SJBushnell, DJCansfield, JEDunsdon, SJFreeman, ACHopkins, RAJohns, IRKeech, ESimmonite, HWalmsley, AWong Kai-In, PHolland, M Nucleoside analogues as highly potent and selective inhibitors of herpes simplex virus thymidine kinase. Bioorg Med Chem Lett11:1655-8 (2001) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Thymidine kinase
Name:Thymidine kinase
Synonyms:n/a
Type:PROTEIN
Mol. Mass.:40396.73
Organism:Human herpesvirus 2
Description:ChEMBL_474155
Residue:376
Sequence:
MASHAGQQHAPAFGQAARASGPTDGRAASRPSHRQGASGARGDPELPTLLRVYIDGPHGV
GKTTTSAQLMEALGPRDNIVYVPEPMTYWQVLGASETLTNIYNTQHRLDRGEISAGEAAV
VMTSAQITMSTPYAATDAVLAPHIGGEAVGPQAPPPALTLVFDRHPIASLLCYPAARYLM
GSMTPQAVLAFVALMPPTAPGTNLVLGVLPEAEHADRLARRQRPGERLDLAMLSAIRRVY
DLLANTVRYLQRGGRWREDWGRLTGVAAATPRPDPEDGAGSLPRIEDTLFALFRVPELLA
PNGDLYHIFAWVLDVLADRLLPMHLFVLDYDQSPVGCRDALLRLTAGMIPTRVTTAGSIA
EIRDLARTFAREVGGV
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  Blast E-value cutoff:
BDBM50101064
n/a
NameBDBM50101064
Synonyms:9H-Thioxanthene-9-carboxylic acid [(2R,3S,5R)-5-(5-ethyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-3-hydroxy-tetrahydro-furan-2-ylmethyl]-amide | CHEMBL288569
TypeSmall organic molecule
Emp. Form.C25H25N3O5S
Mol. Mass.479.548
SMILESCCc1cn([C@H]2C[C@H](O)[C@@H](CNC(=O)C3c4ccccc4Sc4ccccc34)O2)c(=O)[nH]c1=O
Structure
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