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TargetNeuraminidase
LigandBDBM4994
Substrate/Competitorn/a
Meas. Tech.ChEMBL_709671
IC50 3.7±n/a nM
Citation Govorkova EAIlyushina NAMcClaren JLNaipospos TSDouangngeun BWebster RG Susceptibility of highly pathogenic H5N1 influenza viruses to the neuraminidase inhibitor oseltamivir differs in vitro and in a mouse model. Antimicrob Agents Chemother 53:3088-96 (2009) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Neuraminidase
Name:Neuraminidase
Synonyms:n/a
Type:PROTEIN
Mol. Mass.:49064.69
Organism:Influenza A virus
Description:ChEMBL_709401
Residue:449
Sequence:
MNPNQKIITIGSICMVIGMVSLMLQIGNMISIWLSHSIQTGNQHQAESISNNNLLTENAV
ASVTLAGNSSLCPIRGWAVHSKDNSIRIGSKGDVFVIREPFISCSHLECRTFFLTQGALL
NDKHSNGTVKDRSPHRTLMSCPVGEAPSPYNSRFESVAWSASACHDGISWLTIGISGPDN
GAVAVLKYNGIITDTIKSWRNNILRTQESECACVNGSCFTVMTDGPSNGQASYKIFKMEK
GKVVKSVELDAPNYHYEECSCYPDAGEITCVCRDNWHGSNRPWVSFNQNLEYQIGYICSG
VFGDNPRPNDGTGSCGPMSPNGAYGVKGFSFKYGNGVWIGRTKSTNSRSGFEMIWDPNGW
TGTDSSFSVKQDIVAITDWSGYSGSFVQHPELTGLDCIRPCFWVELIRGRPKESTIWTSG
SSISFCGVNGDTVSWSWPDGAELPFIIDK
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  Blast E-value cutoff:
BDBM4994
n/a
NameBDBM4994
Synonyms:(3R,4R,5S)-5-amino-4-acetamido-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylic acid | CHEMBL674 | GS4071 | Oseltamivir carboxylate
TypeSmall organic molecule
Emp. Form.C14H24N2O4
Mol. Mass.284.3514
SMILESCCC(CC)O[C@@H]1C=C(C[C@H](N)[C@H]1NC(C)=O)C(O)=O |r,c:7|
Structure
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