Reaction Details |
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Target | Purine nucleoside phosphorylase |
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Ligand | BDBM50280448 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_162191 (CHEMBL766711) |
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Ki | 1.3±n/a nM |
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Citation | Halazy, S; Eggenspiller, A; Ehrhard, A; Danzin, C Phosphonate derivatives of N9-benzylguanine: a new class of potent purine nucleoside phosphorylase inhibitors Bioorg Med Chem Lett2:407-410 (1992) 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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BDBM50280448 |
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n/a |
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Name | BDBM50280448 |
Synonyms: | 2-{2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methyl]phenyl}-1,1,2-trifluoroethylphosphonate |
Type | Small organic molecule |
Emp. Form. | C14H11F3N5O4P |
Mol. Mass. | 401.2383 |
SMILES | Nc1nc2n(Cc3ccccc3C(F)C(F)(F)P([O-])([O-])=O)cnc2c(=O)[nH]1 |
Structure |
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