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TargetNeuraminidase
LigandBDBM5014
Substrate/CompetitorBDBM4702
Meas. Tech.Neuraminidase Inhibition Assay
IC50 2300±n/a nM
Citation Lew, WWu, HMendel, DBEscarpe, PAChen, XLaver, WGGraves, BJKim, CU A new series of C3-aza carbocyclic influenza neuraminidase inhibitors: synthesis and inhibitory activity. Bioorg Med Chem Lett8:3321-4 (1998) [PubMed]  Article
More Info.:Get all data from this article,   Solution Info,  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
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  Blast E-value cutoff:
BDBM5014
BDBM4702
NameBDBM5014
Synonyms:(3R,4R,5S)-5-amino-4-acetamido-2-methyl-3-(pentan-3-yloxy)cyclohex-1-ene-1-carboxylic acid | C2-Substituted Carbocyclic Analogue 4 | Carbocyclic Analogue 64
TypeSmall organic molecule
Emp. Form.C15H26N2O4
Mol. Mass.298.3779
SMILESCCC(CC)O[C@H]1[C@H](NC(C)=O)[C@@H](N)CC(C(O)=O)=C1C |r,c:18|
Structure
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