Reaction Details |
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Target | Purine nucleoside phosphorylase |
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Ligand | BDBM50227263 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_153332 (CHEMBL760484) |
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Ki | <5000±n/a nM |
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Citation | Sanghvi, YS; Hanna, NB; Larson, SB; Fujitaki, JM; Willis, RC; Smith, RA; Robins, RK; Revankar, GR Synthesis and evaluation of 5-amino-1-beta-D-ribofuranosyl-1,2,4-triazole-3-carboxamidine and certain related nucleosides as inhibitors of purine nucleoside phosphorylase. J Med Chem31:330-5 (1988) [PubMed] |
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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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BDBM50227263 |
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n/a |
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Name | BDBM50227263 |
Synonyms: | CHEMBL2021376 |
Type | Small organic molecule |
Emp. Form. | C10H14N6O5 |
Mol. Mass. | 298.2554 |
SMILES | Nc1nc2c(O)nc(N)nc2n1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O |r| |
Structure |
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