Target
Thymidine kinase
Ligand
BDBM50013075
Substrate
n/a
Meas. Tech.
ChEBML_207840
EC50
15000±n/a nM
Citation
 Focher, FHildebrand, CFreese, SCiarrocchi, GNoonan, TSangalli, SBrown, NSpadari, SWright, G N2-phenyldeoxyguanosine: a novel selective inhibitor of herpes simplex thymidine kinase. J Med Chem 31:1496-500 (1988) [PubMed]  Article 
Target
Name:
Thymidine kinase
Synonyms:
KITH_HHV1S | TK | Thymidine kinase | UL23
Type:
PROTEIN
Mol. Mass.:
40883.42
Organism:
Human herpesvirus 1 (strain SC16) (HHV-1) (Human herpes simplex virus1)
Description:
ChEMBL_213
Residue:
376
Sequence:
MASYPGHQHASAFDQAARSRGHSNRRTALRPRRQQEATEVRPEQKMPTLLRVYIDGPHGMGKTTTTQLLVALGSRDDIVYVPEPMTYWRVLGASETIANIYTTQHRLDQGEISAGDAAVVMTSAQITMGMPYAVTDAVLAPHIGGEAGSSHAPPPALTLIFDRHPIAALLCYPAARYLMGSMTPQAVLAFVALIPPTLPGTNIVLGALPEDRHIDRLAKRQRPGERLDLAMLAAIRRVYGLLANTVRYLQGGGSWREDWGQLSGTAVPPQGAEPQSNAGPRPHIGDTLFTLFRAPELLAPNGDLYNVFAWALDVLAKRLRPMHVFILDYDQSPAGCRDALLQLTSGMIQTHVTTPGSIPTICDLARTFAREMGEAN
  
Inhibitor
Name:
BDBM50013075
Synonyms:
2-(Indan-5-ylamino)-1,9-dihydro-purin-6-one | CHEMBL15985
Type:
Small organic molecule
Emp. Form.:
C14H13N5O
Mol. Mass.:
267.2859
SMILES:
O=c1[nH]c(Nc2ccc3CCCc3c2)nc2nc[nH]c12
Structure:
Search PDB for entries with ligand similarity: