Reaction Details |
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Target | Purine nucleoside phosphorylase |
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Ligand | BDBM50195595 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_414098 (CHEMBL908314) |
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Ki | 30.6±n/a nM |
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Citation | Semeraro, T; Lossani, A; Botta, M; Ghiron, C; Alvarez, R; Manetti, F; Mugnaini, C; Valensin, S; Focher, F; Corelli, F Simplified analogues of immucillin-G retain potent human purine nucleoside phosphorylase inhibitory activity. J Med Chem49:6037-45 (2006) [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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BDBM50195595 |
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n/a |
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Name | BDBM50195595 |
Synonyms: | 2-amino-1,5-dihydro-7-[[[N-[2-(hydroxy)ethyl]-N-methyl]amino]methyl]-4H-pyrrolo[3,2-d]pyrimidin-4-one diacetate |
Type | Small organic molecule |
Emp. Form. | C10H15N5O2 |
Mol. Mass. | 237.2584 |
SMILES | CN(CCO)Cc1c[nH]c2c1nc(N)[nH]c2=O |
Structure |
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