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TargetNeuraminidase
LigandBDBM50217942
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1449776 (CHEMBL3378763)
IC50 96800±n/a nM
Citation Rakers, CSchwerdtfeger, SMMortier, JDuwe, SWolff, TWolber, GMelzig, MF Inhibitory potency of flavonoid derivatives on influenza virus neuraminidase. Bioorg Med Chem Lett24:4312-7 (2014) [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:
BDBM50217942
n/a
NameBDBM50217942
Synonyms:2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl 6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside | 3-Rhamnoglucosylquercetin | 3-Rutinosyl quercetin | CHEMBL226335 | cid_5280805 | rutin
TypeSmall organic molecule
Emp. Form.C27H30O16
Mol. Mass.610.5175
SMILESC[C@@H]1O[C@@H](OC[C@H]2O[C@@H](Oc3c(O)c4c(cc(O)cc4=O)oc3-c3ccc(O)c(O)c3)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1O |r|
Structure
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