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TargetPurine nucleoside phosphorylase
LigandBDBM50022253
Substrate/Competitorn/a
Meas. Tech.ChEBML_162176
IC50 9900±n/a nM
Citation Berry, DAGilbertsen, RBCook, PD Synthesis of 8-amino-3-deazaguanine via imidazole precursors. Antitumor activity and inhibition of purine nucleoside phosphorylase. J Med Chem29:2034-7 (1986) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Purine nucleoside phosphorylase
Name:Purine nucleoside phosphorylase
Synonyms:Inosine phosphorylase | Inosine-guanosine phosphorylase | NP | PNP | PNPH_HUMAN | Purine nucleoside phosphorylase (PNPase)
Type:Enzyme
Mol. Mass.:32119.53
Organism:Homo sapiens (Human)
Description:n/a
Residue:289
Sequence:
MENGYTYEDYKNTAEWLLSHTKHRPQVAIICGSGLGGLTDKLTQAQIFDYGEIPNFPRST
VPGHAGRLVFGFLNGRACVMMQGRFHMYEGYPLWKVTFPVRVFHLLGVDTLVVTNAAGGL
NPKFEVGDIMLIRDHINLPGFSGQNPLRGPNDERFGDRFPAMSDAYDRTMRQRALSTWKQ
MGEQRELQEGTYVMVAGPSFETVAECRVLQKLGADAVGMSTVPEVIVARHCGLRVFGFSL
ITNKVIMDYESLEKANHEEVLAAGKQAAQKLEQFVSILMASIPLPDKAS
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BDBM50022253
n/a
NameBDBM50022253
Synonyms:2,6-Diamino-1,5-dihydro-imidazo[4,5-c]pyridin-4-one; compound with methanesulfonic acid | CHEMBL61868
TypeSmall organic molecule
Emp. Form.C6H7N5O
Mol. Mass.165.1527
SMILESNc1nc2c(cc(N)[nH]c2=O)[nH]1
Structure
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