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TargetNeuraminidase
LigandBDBM50165355
Substrate/Competitorn/a
Meas. Tech.ChEMBL_305719 (CHEMBL829392)
IC50 2.48±n/a nM
Citation Macdonald, SJCameron, RDemaine, DAFenton, RJFoster, GGower, DHamblin, JNHamilton, SHart, GJHill, APInglis, GGJin, BJones, HTMcConnell, DBMcKimm-Breschkin, JMills, GNguyen, VOwens, IJParry, NShanahan, SESmith, DWatson, KGWu, WYTucker, 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
More Info.:Get all data from this article,  Assay Method
 
Neuraminidase
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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50165355
n/a
NameBDBM50165355
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
TypeSmall 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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