Target
Deoxycytidine kinase
Ligand
BDBM50145605
Substrate
n/a
Meas. Tech.
ChEMBL_53730 (CHEMBL663656)
Ki
360000±n/a nM
Citation
 Palomino, EMeltsner, BRKessel, DHorwitz, JP Synthesis and in vitro evaluation of some modified 4-thiopyrimidine nucleosides for prevention or reversal of AIDS-associated neurological disorders. J Med Chem 33:258-63 (1990) [PubMed]  Article 
Target
Name:
Deoxycytidine kinase
Synonyms:
DCK | DCK_HUMAN
Type:
PROTEIN
Mol. Mass.:
30510.65
Organism:
Homo sapiens (Human)
Description:
ChEMBL_1437135
Residue:
260
Sequence:
MATPPKRSCPSFSASSEGTRIKKISIEGNIAAGKSTFVNILKQLCEDWEVVPEPVARWCNVQSTQDEFEELTMSQKNGGNVLQMMYEKPERWSFTFQTYACLSRIRAQLASLNGKLKDAEKPVLFFERSVYSDRYIFASNLYESECMNETEWTIYQDWHDWMNNQFGQSLELDGIIYLQATPETCLHRIYLRGRNEEQGIPLEYLEKLHYKHESWLLHRTLKTNFDYLQEVPILTLDVNEDFKDKYESLVEKVKEFLSTL
  
Inhibitor
Name:
BDBM50145605
Synonyms:
4-amino-1-[(2R,5S)-5-(hydroxymethyl)tetrahydrofuran-2-yl]pyrimidin-2(1H)-one | CHEMBL853 | DDC | DDCYD | Dideoxycytidine | ZALCITABINE
Type:
Small organic molecule
Emp. Form.:
C9H13N3O3
Mol. Mass.:
211.2178
SMILES:
Nc1ccn([C@H]2CC[C@@H](CO)O2)c(=O)n1 |r|
Structure:
Search PDB for entries with ligand similarity: