Cannabis Ruderalis

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Eusiderin
Chemical structure of eusiderin
Names
Preferred IUPAC name
(2R,3R)-5-Methoxy-3-methyl-7-(prop-2-en-1-yl)-2-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,4-benzodioxine
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C22H26O6/c1-7-8-14-9-16(23-3)22-19(10-14)28-20(13(2)27-22)15-11-17(24-4)21(26-6)18(12-15)25-5/h7,9-13,20H,1,8H2,2-6H3/t13-,20+/m1/s1 ☒N
    Key: BVNKWNRETUIZFZ-XCLFUZPHSA-N ☒N
  • InChI=1/C22H26O6/c1-7-8-14-9-16(23-3)22-19(10-14)28-20(13(2)27-22)15-11-17(24-4)21(26-6)18(12-15)25-5/h7,9-13,20H,1,8H2,2-6H3/t13-,20+/m1/s1
    Key: BVNKWNRETUIZFZ-XCLFUZPHBF
  • O1c3c(O[C@@H]([C@H]1c2cc(OC)c(OC)c(OC)c2)C)c(OC)cc(c3)C\C=C
Properties
C22H26O6
Molar mass 386.42 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Eusiderin is a neolignan found in Virola sp[1] and Aniba sp.[2]

References[edit]

  1. ^ Eusiderins and 1,3-diarylpropanes from Virola species. Joāo B. Fernandes, M.Nilce de S. Ribeiro, Otto R. Gottlieb and Hugo E. Gottlieb, Phytochemistry, Volume 19, Issue 7, 1980, Pages 1523-1525, doi:10.1016/0031-9422(80)80209-3
  2. ^ Eusiderins and other neolignans from an Aniba species. Silvia M.C. Dias, Joāo B. Fernandes, José G.S. Maia, Otto R. Gottlieb and Hugo E. Gottlieb, Phytochemistry, Volume 25, Issue 1, 23 December 1985, Pages 213-217, doi:10.1016/S0031-9422(00)94531-X


source: https://en.wikipedia.org/wiki/Eusiderin

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