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TargetNeuraminidase
LigandBDBM7462
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1449777 (CHEMBL3378764)
IC50 42200±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:
BDBM7462
n/a
NameBDBM7462
Synonyms:3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one | 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-chromen-4-one | CHEMBL150 | Kaempferol (18) | Kaempferol (Kmp) | cid_5280863 | kaempferol
TypeSmall organic molecule
Emp. Form.C15H10O6
Mol. Mass.286.2363
SMILESOc1ccc(cc1)-c1oc2cc(O)cc(O)c2c(=O)c1O
Structure
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