Reaction Details |
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Target | Purine nucleoside phosphorylase |
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Ligand | BDBM50046867 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_153329 (CHEMBL760481) |
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Ki | 15000±n/a nM |
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Citation | Chern, JW; Lee, HY; Chen, CS; Shewach, DS; Daddona, PE; Townsend, LB Nucleosides. 5. Synthesis of guanine and formycin B derivatives as potential inhibitors of purine nucleoside phosphorylase. J Med Chem36:1024-31 (1993) [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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BDBM50046867 |
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n/a |
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Name | BDBM50046867 |
Synonyms: | 2-Amino-9-(2-iodo-ethoxymethyl)-1,9-dihydro-purin-6-one | CHEMBL274150 |
Type | Small organic molecule |
Emp. Form. | C8H10IN5O2 |
Mol. Mass. | 335.1018 |
SMILES | Nc1nc2n(COCCI)cnc2c(=O)[nH]1 |
Structure |
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