Reaction Details |
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Target | Purine nucleoside phosphorylase |
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Ligand | BDBM50280445 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_162191 (CHEMBL766711) |
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Ki | 1.8±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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BDBM50280445 |
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n/a |
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Name | BDBM50280445 |
Synonyms: | (E)-2-{2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methyl]phenyl}-1-fluorovinylphosphonate |
Type | Small organic molecule |
Emp. Form. | C14H11FN5O4P |
Mol. Mass. | 363.2415 |
SMILES | Nc1nc2n(Cc3ccccc3C=C(F)P([O-])([O-])=O)cnc2c(=O)[nH]1 |w:12.12| |
Structure |
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