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TargetNeuraminidase
LigandBDBM50049395
Substrate/Competitorn/a
Meas. Tech.ChEMBL_514314 (CHEMBL979144)
IC50 46300±n/a nM
Citation Liu, ALWang, HDLee, SMWang, YTDu, GH Structure-activity relationship of flavonoids as influenza virus neuraminidase inhibitors and their in vitro anti-viral activities. Bioorg Med Chem16:7141-7 (2008) [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:
BDBM50049395
n/a
NameBDBM50049395
Synonyms:5,7,4'-Trihydroxy-6-methoxyflavone | 5,7-Dihydroxy-2-(4-hydroxy-phenyl)-6-methoxy-chromen-4-one | 5,7-dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-4H-chromen-4-one | 6-methoxy apigenin | 6-methoxyapigenin | CHEMBL293776 | Hispidulin | NSC-122415 | TCMDC-123942 | cid_5281628 | dinatin
TypeSmall organic molecule
Emp. Form.C16H12O6
Mol. Mass.300.2629
SMILESCOc1c(O)cc2oc(cc(=O)c2c1O)-c1ccc(O)cc1
Structure
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