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Target
Thymidine kinase, cytosolic
Ligand
BDBM21866
Substrate
n/a
Meas. Tech.
ChEMBL_208011 (CHEMBL816091)
Ki
50±n/a nM
Citation
 Xu, H; Maga, G; Focher, F; Smith, ER; Spadari, S; Gambino, J; Wright, GE Synthesis, properties, and pharmacokinetic studies of N2-phenylguanine derivatives as inhibitors of herpes simplex virus thymidine kinases. J Med Chem 38:49-57 (1995) [PubMed]  Article 
Target
Name:
Thymidine kinase, cytosolic
Synonyms:
KITH_HUMAN | TK1
Type:
PROTEIN
Mol. Mass.:
25476.50
Organism:
Homo sapiens (Human)
Description:
ChEMBL_1333884
Residue:
234
Sequence:
MSCINLPTVLPGSPSKTRGQIQVILGPMFSGKSTELMRRVRRFQIAQYKCLVIKYAKDTRYSSSFCTHDRNTMEALPACLLRDVAQEALGVAVIGIDEGQFFPDIVEFCEAMANAGKTVIVAALDGTFQRKPFGAILNLVPLAESVVKLTAVCMECFREAAYTKRLGTEKEVEVIGGADKYHSVCRLCYFKKASGQPAGPDNKENCPVPGKPGEAVAARKLFAPQQILQCSPAN
  
Inhibitor
Name:
BDBM21866
Synonyms:
2-phenylamino-9-(4-hydroxybutyl)-6-oxopurine | 9-(4-hydroxybutyl)-2-(phenylamino)-6,9-dihydro-3H-purin-6-one | CHEMBL406254 | HBPG
Type:
Small organic molecule
Emp. Form.:
C15H17N5O2
Mol. Mass.:
299.3278
SMILES:
OCCCCn1cnc2c1nc(Nc1ccccc1)[nH]c2=O
Structure:
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