Resveratroloside

Resveratroloside
Names
	Systematic IUPAC name 4-[(E)-2-(3,5-Dihydroxyphenyl)vinyl]phenyl β-D-glucopyranoside
	Other names trans-Resveratrol-4'-O-beta-D-glucopyranoside; (E)-Resveratroloside; 3,5,4'-Trihydroxystilbene-4'-glucoside
Identifiers
CAS Number	38963-95-0;
3D model (JSmol)	Interactive image;
ChemSpider	4479669;
PubChem CID	5322089;
CompTox Dashboard (EPA)	DTXSID60415792 ;
	InChI InChI=1S/C20H22O8/c21-10-16-17(24)18(25)19(26)20(28-16)27-15-5-3-11(4-6-15)1-2-12-7-13(22)9-14(23)8-12/h1-9,16-26H,10H2/b2-1+/t16-,17-,18+,19-,20-/m1/s1 Key: RUOKEYJFAJITAG-CUYWLFDKSA-N; InChI=1/C20H22O8/c21-10-16-17(24)18(25)19(26)20(28-16)27-15-5-3-11(4-6-15)1-2-12-7-13(22)9-14(23)8-12/h1-9,16-26H,10H2/b2-1+/t16-,17-,18+,19-,20-/m1/s1 Key: RUOKEYJFAJITAG-CUYWLFDKBI;
	SMILES C1=CC(=CC=C1/C=C/C2=CC(=CC(=C2)O)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O;
Properties
Chemical formula	C20H22O8
Molar mass	390.388 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Resveratroloside is a stilbenoid glucoside. It can be found in Paeonia lactiflora.[1]

References

Kim, H. J.; Chang, E. J.; Cho, S. H.; Chung, S. K.; Park, H. D.; Choi, S. W. (2002). "Antioxidative activity of resveratrol and its derivatives isolated from seeds of Paeonia lactiflora". Bioscience, Biotechnology, and Biochemistry. 66 (9): 1990–1993. doi:10.1271/bbb.66.1990. PMID 12400706. S2CID 24367582.

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