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TargetNeuraminidase
LigandBDBM50037587
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1438031 (CHEMBL3387278)
IC50 31±n/a nM
Citation Hong, BTChen, CLFang, JMTsai, KCWang, SYHuang, WICheng, YSWong, CH Oseltamivir hydroxamate and acyl sulfonamide derivatives as influenza neuraminidase inhibitors. Bioorg Med Chem22:6647-54 (2015) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Neuraminidase
Name:Neuraminidase
Synonyms:NA | NRAM_I77AB | Neuraminidase
Type:PROTEIN
Mol. Mass.:51863.92
Organism:Influenza A virus (strain A/USSR/90/1977 H1N1)
Description:ChEMBL_109720
Residue:470
Sequence:
MNPNQKIITIGSICMAIGIISLILQIGNIISIWVSHSIQTGSQNHTGICNQRIITYENST
WVNQTYVNISNTNVVAGKDTTSMTLAGNSSLCPIRGWAIYSKDNSIRIGSKGDVFVIREP
FISCSHLECRTFFLTQGALLNDKHSNGTVKDRSPYRALMSCPIGEAPSPYNSRFESVAWS
ASACHDGMGWLTIGISGPDDGAVAVLKYNGIITETIKSWRKQILRTQESECVCVNGSCFT
IMTDGPSDGPASYRIFKIEKGKITKSIELDAPNSHYEECSCYPDTGTVMCVCRDNWHGSN
RPWVSFNQNLDYQIGYICSGVFGDNPRPKDGKGSCDPVNVDGADGVKGFSYRYGNGVWIG
RTKSNSSRKGFEMIWDPNGWTDTDSNFLVKQDVVAMTDWSGYSGSFVQHPELTGLDCMRP
CFWVELIRGRPREKTTIWTSGSSISFCGVNSDTVNWSWPDGAELPFTIDK
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50037587
n/a
NameBDBM50037587
Synonyms:CHEMBL3357202
TypeSmall organic molecule
Emp. Form.C21H31N3O4
Mol. Mass.389.4885
SMILESCCC(CC)O[C@@H]1C=C(C[C@H](N)[C@H]1NC(C)=O)C(=O)NOCc1ccccc1 |r,c:7|
Structure
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