Amurensin K
From Infogalactic: the planetary knowledge core
Chemical structure of amurensin K | |
Names | |
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IUPAC name
(1S,6R,7S,11bS)-6-{5-[(7S,8S)-8-(3,5-Dihydroxyphenyl)-4-hydroxy-7-(4-hydroxyphenyl)-7,8-dihydrofuro[3,2-e][1]benzofuran-2-yl]-2-hydroxyphenyl}-1,7-bis(4-hydroxyphenyl)-1,6,7,11b-tetrahydro-2-oxadibenz o[cd,h]azulene-4,8,10-triol
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Identifiers | |
388121-56-0 | |
ChemSpider | 17288573 |
Jmol 3D model | Interactive image |
PubChem | 16131909 |
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Properties | |
C56H40O13 | |
Molar mass | 920.91 g/mol |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
Amurensin K is an oligostilbene. It is a resveratrol tetramer found in Vitis amurensis.[1] Preliminary tests have shown it to be an effective neuraminidase inhibitor against the influenza A virus subtype H1N1.[2]
References
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- ↑ Anti-inflammatory tetramers of resveratrol from the roots of Vitis amurensis and the conformations of the seven-membered ring in some oligostilbenes. Kai-Sheng Huang, Mao Lin, and Gui-Fang Cheng, Phytochemistry, September 2001, Volume 58, Issue 2, Pages 357–362, doi:10.1016/S0031-9422(01)00224-2
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
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