Gnetucleistol E

Gnetucleistol E
Chemical structure of gnetucleistol E
Names
IUPAC name
5-[2-(3,4-dimethoxyphenyl)ethenyl]benzene-1,3-diol
Other names
3-methoxy-isorhapontigenin
Identifiers
CAS Number
  • 629643-27-2
3D model (JSmol)
  • Interactive image
ChemSpider
  • 23333675
PubChem CID
  • 53395175
CompTox Dashboard (EPA)
  • DTXSID00694084 Edit this at Wikidata
InChI
  • InChI=1S/C16H16O4/c1-19-15-6-5-11(9-16(15)20-2)3-4-12-7-13(17)10-14(18)8-12/h3-10,17-18H,1-2H3/b4-3+
    Key: WHKSEHKYYXHCTA-ONEGZZNKSA-N
  • InChI=1/C16H16O4/c1-19-15-6-5-11(9-16(15)20-2)3-4-12-7-13(17)10-14(18)8-12/h3-10,17-18H,1-2H3/b4-3+
    Key: WHKSEHKYYXHCTA-ONEGZZNKBB
  • COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)O)O)OC
Properties
Chemical formula
C16H16O4
Molar mass 272.29 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Chemical compound

Gnetucleistol E is a stilbenoid found in the Chinese herb Gnetum cleistostachyum.[1]

References

  1. ^ Stilbenes from Gnetum cleistostachyum. Yao Chun-Suo, Lin Mao, Liu Xin and Wangy Ying-Hong, Huaxue xuebao, 2003, vol. 61, no 8, pages 1331-1334, INIST 15332136original article
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Hydroxystilbenes and their glycosides (monomeric forms)
Dihydroxylated
  • Pinosylvin
  • 3,4′-Dihydroxystilbene
Trihydroxylated
  • Resveratrol
Tetrahydroxylated
O-methylated
Combretastatins
carboxylatedother acylationsGlycosides
of resveratrol
of rhapontigenin
  • Rhapontigenin 3-O-rutinoside
    • 4'-Methoxy-(E)-resveratrol 3-O-rutinoside
  • Rhaponticin (Rhapontigenin glucoside)
Oligomeric forms


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