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TargetPurine nucleoside phosphorylase
LigandBDBM50033666
Substrate/Competitorn/a
Meas. Tech.ChEMBL_162192 (CHEMBL873424)
Ki 10±n/a nM
Citation Beauchamp, LMTuttle, JVRodriguez, MESznaidman, ML Guanine, pyrazolo[3,4-d]pyrimidine, and triazolo[4,5-d]pyrimidine (8-azaguanine) phosphonate acyclic derivatives as inhibitors of purine nucleoside phosphorylase. J Med Chem39:949-56 (1996) [PubMed]  Article
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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  Blast E-value cutoff:
BDBM50033666
n/a
NameBDBM50033666
Synonyms:2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl trihydrogen diphosphate(ACVDP) | Acyclovir Diphosphate | CHEMBL7193 | {[2-(2-Amino-6-oxo-1,6-dihydro-purin-9-ylmethoxy)-ethoxy]-hydroxy-diphosphate
TypeSmall organic molecule
Emp. Form.C8H13N5O9P2
Mol. Mass.385.1644
SMILESNc1nc2n(COCCOP(O)(=O)OP(O)(O)=O)cnc2c(=O)[nH]1
Structure
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