Reaction Details |
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Target | Purine nucleoside phosphorylase |
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Ligand | BDBM50022253 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_162176 |
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IC50 | 9900±n/a nM |
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Citation | Berry, DA; Gilbertsen, RB; Cook, PD Synthesis of 8-amino-3-deazaguanine via imidazole precursors. Antitumor activity and inhibition of purine nucleoside phosphorylase. J Med Chem29:2034-7 (1986) [PubMed] |
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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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BDBM50022253 |
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n/a |
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Name | BDBM50022253 |
Synonyms: | 2,6-Diamino-1,5-dihydro-imidazo[4,5-c]pyridin-4-one; compound with methanesulfonic acid | CHEMBL61868 |
Type | Small organic molecule |
Emp. Form. | C6H7N5O |
Mol. Mass. | 165.1527 |
SMILES | Nc1nc2c(cc(N)[nH]c2=O)[nH]1 |
Structure |
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