Reaction Details |
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Target | Purine nucleoside phosphorylase |
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Ligand | BDBM22109 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_162007 (CHEMBL764178) |
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Ki | 0.016±n/a nM |
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Citation | Evans, GB; Furneaux, RH; Lewandowicz, A; Schramm, VL; Tyler, PC Synthesis of second-generation transition state analogues of human purine nucleoside phosphorylase. J Med Chem46:5271-6 (2003) [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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BDBM22109 |
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n/a |
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Name | BDBM22109 |
Synonyms: | 7-{[(3R,4R)-3-hydroxy-4-(hydroxymethyl)pyrrolidin-1-yl]methyl}-1,5-dihydro-4H-pyrrolo[3,2-d]pyrimidin-4-one | 7-{[(3R,4R)-3-hydroxy-4-(hydroxymethyl)pyrrolidin-1-yl]methyl}-1H,4H,5H-pyrrolo[3,2-d]pyrimidin-4-one | CHEMBL1213653 | CHEMBL269864 | DADMe-ImmH,7 |
Type | n/a |
Emp. Form. | C12H16N4O3 |
Mol. Mass. | 264.2804 |
SMILES | OC[C@H]1CN(Cc2c[nH]c3c2nc[nH]c3=O)C[C@@H]1O |r| |
Structure |
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