Pterostilbene

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Pterostilbene
200px
Names
IUPAC name
4-[(E)-2-(3,5-Dimethoxyphenyl)ethenyl]phenol
Other names
3',5'-Dimethoxy-4-stilbenol
3,5-Dimethoxy-4'-hydroxy-E-stilbene
3',5'-dimethoxy-resveratrol
Identifiers
537-42-8 N
ChEBI CHEBI:8630 N
ChEMBL ChEMBL83527 YesY
ChemSpider 4445042 YesY
2681
Jmol 3D model Interactive image
PubChem 5281727
  • InChI=1S/C16H16O3/c1-18-15-9-13(10-16(11-15)19-2)4-3-12-5-7-14(17)8-6-12/h3-11,17H,1-2H3/b4-3+ YesY
    Key: VLEUZFDZJKSGMX-ONEGZZNKSA-N YesY
  • InChI=1S/C16H16O3/c1-18-15-9-13(10-16(11-15)19-2)4-3-12-5-7-14(17)8-6-12/h3-11,17H,1-2H3/b4-3+
    Key: VLEUZFDZJKSGMX-ONEGZZNKBK
  • Key: VLEUZFDZJKSGMX-ONEGZZNKSA-N
  • O(c1cc(cc(OC)c1)\C=C\c2ccc(O)cc2)C
Properties
C16H16O3
Molar mass 256.296 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).
N verify (what is YesYN ?)
Infobox references

Pterostilbene is a stilbenoid chemically related to resveratrol. In plants, it serves a defensive phytoalexin role.[1]

Natural occurrences

Pterostilbene is found in almonds,[2] various Vaccinium berries[3] and grape leaves and vines.[1][4]

While resveratrol is under research for its potential properties from consuming wine and other foods or beverages, pterostilbene is not found in wine.[5]

Basic research

The possible biological effects of pterostilbene are being examined in basic research involving laboratory models of several disorders, including age-related cognitive decline.[6]

See also

References

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