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TargetNeuraminidase
LigandBDBM4994
Substrate/Competitorn/a
Meas. Tech.NA Inhibition Assay
IC50 170±n/a nM
Citation Liu, YZhang, LGong, JFang, HLiu, ADu, GXu, W Design, synthesis, and biological activity of thiazole derivatives as novel influenza neuraminidase inhibitors. J Enzyme Inhib Med Chem26:506-13 (2011) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Neuraminidase
Name:Neuraminidase
Synonyms:NA | NRAM_I82A7 | Neuraminidase (NA)
Type:Enzyme
Mol. Mass.:49917.65
Organism:Influenza A virus H3N2
Description:Q67344
Residue:446
Sequence:
MQIAILVTTVTLHFNQYECDSLADNQVMPCEPIIIERNITEIIYLTNTTIEKEICPKLME
YRNWSRPQCKITGFAPFSKDNSIRLSAGGDIWVTREPYVSCDPGKCYQFALGQGTTLDNK
HSNDTIHDRIPHRTLLMNELGVPFHLGTRQVCIAWSSSSCHDGKAWLHVCVTGDDKNATA
SFIYDGRLVDSMGSWSQNILRTQESECVCINGTCTVVMTDGSASGRADTRILFIEEGKIV
HISPLSGSAQHVEECSCYPRYPSVRCICRDNWKGSNRPIVDINIKDYSIDSRYVCSGLVG
DTPRNNDRSSSSDCKNPNNDKGNHGVKGWAFDDGNDVWMGRTISKDSRSGYETFKVIDGW
STPNSKSQINRQVIVDRDNRSGYSGIFSVESKGCINRCFYVELIRGRKQETRVWWTSSSI
VVFCGTSGTYGKGSWPDGANINFMPI
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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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