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Target
Pyridoxal kinase
Ligand
BDBM50009722
Substrate
n/a
Meas. Tech.
ChEMBL_1346665 (CHEMBL3253500)
Ki
24000±n/a nM
Citation
 Korytnyk, W; Angelino, N Vitamin B6 antagonists obtained by replacing or modifying the 2-methyl group. J Med Chem 20:745-9 (1977) [PubMed]  Article 
Target
Name:
Pyridoxal kinase
Synonyms:
C21orf124 | C21orf97 | PDXK | PDXK_HUMAN | PKH | PNK | Pyridoxine kinase
Type:
PROTEIN
Mol. Mass.:
35099.40
Organism:
Homo sapiens (Human)
Description:
ChEMBL_103125
Residue:
312
Sequence:
MEEECRVLSIQSHVIRGYVGNRAATFPLQVLGFEIDAVNSVQFSNHTGYAHWKGQVLNSDELQELYEGLRLNNMNKYDYVLTGYTRDKSFLAMVVDIVQELKQQNPRLVYVCDPVLGDKWDGEGSMYVPEDLLPVYKEKVVPLADIITPNQFEAELLSGRKIHSQEEALRVMDMLHSMGPDTVVITSSDLPSPQGSNYLIVLGSQRRRNPAGSVVMERIRMDIRKVDAVFVGTGDLFAAMLLAWTHKHPNNLKVACEKTVSTLHHVLQRTIQCAKAQAGEGVRPSPMQLELRMVQSKRDIEDPEIVVQATVL
  
Inhibitor
Name:
BDBM50009722
Synonyms:
CHEMBL3245250
Type:
Small organic molecule
Emp. Form.:
C7H8ClNO3
Mol. Mass.:
189.596
SMILES:
OCc1cnc(Cl)c(O)c1CO
Structure:
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