Reaction Details |
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Target | Purine nucleoside phosphorylase |
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Ligand | BDBM50382672 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_816905 (CHEMBL2026248) |
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Ki | 12±n/a nM |
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Citation | Rejman, D; Panova, N; Klener, P; Maswabi, B; Pohl, R; Rosenberg, I N-phosphonocarbonylpyrrolidine derivatives of guanine: a new class of bi-substrate inhibitors of human purine nucleoside phosphorylase. J Med Chem55:1612-21 (2012) [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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BDBM50382672 |
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n/a |
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Name | BDBM50382672 |
Synonyms: | CHEMBL2024005 |
Type | Small organic molecule |
Emp. Form. | C10H13N6O6P |
Mol. Mass. | 344.2206 |
SMILES | Nc1nc2n(cnc2c(=O)[nH]1)[C@@H]1CN(C[C@@H]1O)C(=O)P(O)(O)=O |r| |
Structure |
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