501-36-0

(e)-5-(2-(4-hydroxyphenyl)ethenyl)-1,3-benzenediol

trans-3,4',5-trihydroxystilbene

(e)-resveratrol

(e)-5-[2-(4-hydroxyphenyl)ethenyl]-1,3-benzenediol

3,4',5-trihydroxystilbene

3,4',5-trihydroxy-stilbene

(e)-5-(p-hydroxystyryl)resorcinol

(e)-5-[2-(4-hydroxyphenyl)ethenyl]-1,3-benzendiol

3,4',5-stilbenetriol

Resveratrol (3,5,4 -trihydroxystilbene) is a polyphenolic phytoalexin. It is a stilbenoid, a derivate of stilbene, and is produced in plants with the help of the enzyme stilbene synthase. It exists as two structural isomers: cis-(Z) and trans-(E), with the trans-isomer shown in the top image. The trans- form can undergo isomerisation to the cis- form when heated or exposed to ultraviolet irradiation. In a 2004 issue of Science, Dr. Sinclair of Harvard University said resveratrol is not an easy molecule to protect from oxidation. It has been claimed that it is readily degraded by exposure to light, heat, and oxygen. However, studies find that Trans-resveratrol undergoes negligible oxidation in normal atmosphere at room temperature. [Wikipedia]

InChI=1S/C14H12O3/c15-12-5-3-10(4-6-12)1-2-11-7-13(16)9-14(17)8-11/h1-9,15-17H/b2-1+

InChIKey=LUKBXSAWLPMMSZ-OWOJBTEDSA-N

resveratrol

obo2:dinto_DB02709

resveratrol

OC1=CC=C(\C=C\C2=CC(O)=CC(O)=C2)C=C1

C14H12O3

5-[(E)-2-(4-hydroxyphenyl)ethenyl]benzene-1,3-diol

PDB:STL

PharmGKB:PA165291843

PubChem Compound:445154

PubChem Substance:46504705

ChemSpider:4880

ChEBI:27881

BindingDB:23926

Wikipedia:http://en.wikipedia.org/wiki/Resveratrol