Gnetucleistol D

Gnetucleistol D
Chemical structure of gnetucleistol D
Names
Preferred IUPAC name
5-[(E)-2-(4-Hydroxy-2-methoxyphenyl)ethen-1-yl]benzene-1,3-diol
Other names
2-methoxyoxyresveratrol
Identifiers
CAS Number
  • 629643-26-1 checkY
3D model (JSmol)
  • Interactive image
ChEMBL
  • ChEMBL219050
ChemSpider
  • 23279071
PubChem CID
  • 44419358
UNII
  • W4XBS7AED8 checkY
CompTox Dashboard (EPA)
  • DTXSID70804092 Edit this at Wikidata
InChI
  • InChI=1S/C15H14O4/c1-19-15-9-12(16)5-4-11(15)3-2-10-6-13(17)8-14(18)7-10/h2-9,16-18H,1H3/b3-2+
    Key: CFQSTARVCGBYNJ-NSCUHMNNSA-N
  • InChI=1/C15H14O4/c1-19-15-9-12(16)5-4-11(15)3-2-10-6-13(17)8-14(18)7-10/h2-9,16-18H,1H3/b3-2+
    Key: CFQSTARVCGBYNJ-NSCUHMNNBH
  • COc2cc(O)ccc2/C=C/c1cc(O)cc(O)c1
Properties
Chemical formula
C15H14O4
Molar mass 258.27 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 D is a stilbenoid found in the Chinese herb Gnetum cleistostachyum.[1]

References

  1. ^ Yao Chun-Suo; Lin Mao; Liu Xin; Wang Ying-Hong (15 August 2003). "Stilbenes from Gnetum cleistostachyum". Acta Chimica Sinica. 61 (8): 1331–1334.
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Hydroxystilbenes and their glycosides (monomeric forms)
Dihydroxylated
  • Pinosylvin
  • 3,4′-Dihydroxystilbene
Trihydroxylated
  • Resveratrol
TetrahydroxylatedO-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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