Reaction Details |
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Target | Neuraminidase |
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Ligand | BDBM50165355 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_305719 (CHEMBL829392) |
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IC50 | 2.48±n/a nM |
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Citation | Macdonald, SJ; Cameron, R; Demaine, DA; Fenton, RJ; Foster, G; Gower, D; Hamblin, JN; Hamilton, S; Hart, GJ; Hill, AP; Inglis, GG; Jin, B; Jones, HT; McConnell, DB; McKimm-Breschkin, J; Mills, G; Nguyen, V; Owens, IJ; Parry, N; Shanahan, SE; Smith, D; Watson, KG; Wu, WY; Tucker, SP Dimeric zanamivir conjugates with various linking groups are potent, long-lasting inhibitors of influenza neuraminidase including H5N1 avian influenza. J Med Chem48:2964-71 (2005) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Neuraminidase |
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Name: | Neuraminidase |
Synonyms: | Influenza A Virus Neuraminidase | NA | NRAM_I34A1 | Neuraminidase | Neuraminidase A |
Type: | Enzyme |
Mol. Mass.: | 50124.14 |
Organism: | Influenza A virus (A/Puerto Rico/8/34/Mount Sinai(H1N1)) |
Description: | P03468 |
Residue: | 454 |
Sequence: | MNPNQKIITIGSICLVVGLISLILQIGNIISIWISHSIQTGSQNHTGICNQNIITYKNST
WVKDTTSVILTGNSSLCPIRGWAIYSKDNSIRIGSKGDVFVIREPFISCSHLECRTFFLT
QGALLNDKHSNGTVKDRSPYRALMSCPVGEAPSPYNSRFESVAWSASACHDGMGWLTIGI
SGPDNGAVAVLKYNGIITETIKSWRKKILRTQESECACVNGSCFTIMTDGPSDGLASYKI
FKIEKGKVTKSIELNAPNSHYEECSCYPDTGKVMCVCRDNWHGSNRPWVSFDQNLDYQIG
YICSGVFGDNPRPEDGTGSCGPVYVDGANGVKGFSYRYGNGVWIGRTKSHSSRHGFEMIW
DPNGWTETDSKFSVRQDVVAMTDWSGYSGSFVQHPELTGLDCMRPCFWVELIRGRPKEKT
IWTSASSISFCGVNSDTVDWSWPDGAELPFSIDK
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BDBM50165355 |
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n/a |
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Name | BDBM50165355 |
Synonyms: | (2R,4S)-3-(acetylamino)-4-{[(E)-amino(imino)methyl]amino}-2-[(1R,2R)-1,2,3-trihydroxypropyl]-3,4-dihydro-2H-pyran-6-carboxylic acid | CHEMBL193303 |
Type | Small organic molecule |
Emp. Form. | C12H20N4O7 |
Mol. Mass. | 332.3098 |
SMILES | [#6]-[#6](=O)-[#7]-[#6]-1-[#6@H](-[#6]=[#6](-[#8]-[#6@H]-1-[#6@H](-[#8])-[#6](-[#8])-[#6]-[#8])-[#6](-[#8])=O)\[#7]=[#6](\[#7])-[#7] |c:6| |
Structure |
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