Jump to content

Amurensin K

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by DePiep (talk | contribs) at 19:26, 7 July 2015 (Chembox: rm/replace deprecated params. Fix unknown parameters (via AWB script)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Amurensin K
Chemical structure of amurensin K
Names
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
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C56H40O13/c57-30-8-1-25(2-9-30)47-49(38-20-36(63)22-45-51(38)53(39-19-35(62)21-42(65)50(39)47)55(68-45)27-5-12-32(59)13-6-27)37-17-28(7-14-41(37)64)44-23-40-52-46(24-43(66)56(40)67-44)69-54(26-3-10-31(58)11-4-26)48(52)29-15-33(60)18-34(61)16-29/h1-24,47-49,53-55,57-66H/t47-,48+,49+,53+,54-,55-/m1/s1
    Key: KYCWATKXJOSHQR-KPXHRNBCSA-N
  • C1=CC(=CC=C1[C@@H]2[C@H](C3=CC(=CC4=C3[C@@H]([C@H](O4)C5=CC=C(C=C5)O)C6=CC(=CC(=C26)O)O)O)C7=C(C=CC(=C7)C8=CC9=C1[C@@H]([C@H](OC1=CC(=C9O8)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O)O
Properties
C56H40O13
Molar mass 920.91 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Amurensin K is an oligostilbene. It is a resveratrol tetramer found in Vitis amurensis.[1]

References

  1. ^ 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

Template:Natural phenol-stub