Reaction Details |
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Target | Purine nucleoside phosphorylase |
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Ligand | BDBM50122724 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_162009 (CHEMBL764180) |
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Ki | 0.096±n/a nM |
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Citation | Evans, GB; Furneaux, RH; Gainsford, GJ; Hanson, JC; Kicska, GA; Sauve, AA; Schramm, VL; Tyler, PC 8-Aza-immucillins as transition-state analogue inhibitors of purine nucleoside phosphorylase and nucleoside hydrolases. J Med Chem46:155-60 (2002) [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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BDBM50122724 |
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n/a |
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Name | BDBM50122724 |
Synonyms: | 4-Amino-5-(3,4-dihydroxy-5-hydroxymethyl-pyrrolidin-2-yl)-2H-pyrazole-3-carboxylic acid amide | CHEMBL41949 |
Type | Small organic molecule |
Emp. Form. | C9H15N5O4 |
Mol. Mass. | 257.2465 |
SMILES | NC(=O)c1[nH]nc(C2N[C@H](CO)[C@H](O)[C@@H]2O)c1N |
Structure |
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