Reaction Details |
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Target | IAG-nucleoside hydrolase |
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Ligand | BDBM50260485 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_531315 (CHEMBL989727) |
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Ki | 1283000±n/a nM |
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Citation | Goeminne, A; McNaughton, M; Bal, G; Surpateanu, G; Van Der Veken, P; De Prol, S; Versées, W; Steyaert, J; Haemers, A; Augustyns, K Synthesis and biochemical evaluation of guanidino-alkyl-ribitol derivatives as nucleoside hydrolase inhibitors. Eur J Med Chem43:315-26 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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IAG-nucleoside hydrolase |
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Name: | IAG-nucleoside hydrolase |
Synonyms: | n/a |
Type: | PROTEIN |
Mol. Mass.: | 36316.77 |
Organism: | Trypanosoma vivax |
Description: | ChEMBL_531315 |
Residue: | 327 |
Sequence: | MAKNVVLDHDGNLDDFVAMVLLASNTEKVRLIGALCTDADCFVENGFNVTGKIMCLMHNN
MNLPLFPIGKSAATAVNPFPKEWRCLAKNMDDMPILNIPENVELWDKIKAENEKYEGQQL
LADLVMNSEEKVTICVTGPLSNVAWCIDKYGEKFTSKVEECVIMGGAVDVRGNVFLPSTD
GTAEWNIYWDPASAKTVFGCPGLRRIMFSLDSTNTVPVRSPYVQRFGEQTNFLLSILVGT
MWAMCTHCELLRDGDGYYAWDALTAAYVVDQKVANVDPVPIDVVVDKQPNEGATVRTDAE
KYPLTFVARNPEAEFFLDMLLRSARAC
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BDBM50260485 |
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n/a |
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Name | BDBM50260485 |
Synonyms: | 2,5-Anhydro-1-deoxy-1-(trimethylammonio)-D-allitol iodide | CHEMBL495460 |
Type | Small organic molecule |
Emp. Form. | C9H20NO4 |
Mol. Mass. | 206.2589 |
SMILES | C[N+](C)(C)C[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O |r| |
Structure |
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