Reaction Details |
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Target | Purine nucleoside phosphorylase |
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Ligand | BDBM50049958 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_162192 (CHEMBL873424) |
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Ki | 550±n/a nM |
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Citation | Beauchamp, LM; Tuttle, JV; Rodriguez, ME; Sznaidman, 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 |
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More Info.: | Get all data from this article, Assay Method |
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Purine nucleoside phosphorylase |
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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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BDBM50049958 |
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n/a |
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Name | BDBM50049958 |
Synonyms: | CHEMBL172306 | [5-(5-Amino-7-oxo-6,7-dihydro-[1,2,3]triazolo[4,5-d]pyrimidin-2-ylmethoxy)-pentyl]-phosphonic acid |
Type | Small organic molecule |
Emp. Form. | C10H17N6O5P |
Mol. Mass. | 332.2529 |
SMILES | Nc1nc2nn(COCCCCCP(O)(O)=O)nc2c(=O)[nH]1 |
Structure |
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