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TargetNeuraminidase
LigandBDBM50485138
Substrate/Competitorn/a
Meas. Tech.ChEMBL_819002 (CHEMBL2034234)
IC50>346000±n/a nM
Citation Dao, TTDang, TTNguyen, PHKim, EThuong, PTOh, WK Xanthones from Polygala karensium inhibit neuraminidases from influenza A viruses. Bioorg Med Chem Lett22:3688-92 (2012) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Neuraminidase
Name:Neuraminidase
Synonyms:NA | NRAM_I33A0
Type:PROTEIN
Mol. Mass.:49687.56
Organism:Influenza A virus
Description:ChEMBL_1347422
Residue:453
Sequence:
MNPNQKIITIGSICMVVGIISLILQIGNIISIWISHSIQTGNQNHTGICNQGIITYNVVA
GQDSTSVILTGNSSLCPIRGWAIHSKDNGIRIGSKGDVFVIREPFISCSHLECRTFFLTQ
GALLNDKHSNGTVKDRSPYRALMSCPVGEAPSPYNSRFESVAWSASACHDGMGWLTIGIS
GPDNGAVAVLKYNGIITETIKSWRKKILRTQESECTCVNGSCFTIMTDGPSNGLASYKIF
KIEKGKVTKSIELNAPNSHYEECSCYPDTGKVMCVCRDNWHGSNRPWVSFDQNLDYQIGY
ICSGVFGDNPRPKDGPGSCGPVSADGANGVKGFSYRYGNGVWIGRTKSDSSRHGFEMIWD
PNGWTETDSRFSVRQDVVAMTDRSGYSGSFVQHPELTGLDCMRPCFWVELIRGRPEEETI
WTSGSIISFCGVNSDTVDWSWPDGAELPFTIDK
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  Blast E-value cutoff:
BDBM50485138
n/a
NameBDBM50485138
Synonyms:CHEMBL2029864
TypeSmall organic molecule
Emp. Form.C15H12O6
Mol. Mass.288.2522
SMILESCOc1c(O)cc2oc3cc(O)ccc3c(=O)c2c1OC
Structure
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