Target
Thymidine kinase
Ligand
BDBM50013088
Substrate
n/a
Meas. Tech.
ChEBML_208031
IC50
1300±n/a nM
Citation
 Hildebrand, CSandoli, DFocher, FGambino, JCiarrocchi, GSpadari, SWright, G Structure-activity relationships of N2-substituted guanines as inhibitors of HSV1 and HSV2 thymidine kinases. J Med Chem 33:203-6 (1990) [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:
BDBM50013088
Synonyms:
2-(3,4-Dibromo-phenylamino)-1,9-dihydro-purin-6-one | CHEMBL65438
Type:
Small organic molecule
Emp. Form.:
C11H7Br2N5O
Mol. Mass.:
385.014
SMILES:
Brc1ccc(Nc2nc3nc[nH]c3c(=O)[nH]2)cc1Br
Structure:
Search PDB for entries with ligand similarity: