Reaction Details |
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Target | Neuraminidase |
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Ligand | BDBM50217942 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1449776 (CHEMBL3378763) |
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IC50 | 96800±n/a nM |
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Citation | Rakers, C; Schwerdtfeger, SM; Mortier, J; Duwe, S; Wolff, T; Wolber, G; Melzig, MF Inhibitory potency of flavonoid derivatives on influenza virus neuraminidase. Bioorg Med Chem Lett24:4312-7 (2014) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Neuraminidase |
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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
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BDBM50217942 |
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n/a |
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Name | BDBM50217942 |
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 |
Type | Small organic molecule |
Emp. Form. | C27H30O16 |
Mol. Mass. | 610.5175 |
SMILES | C[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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