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Rosarin

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Rosarin
Names
IUPAC name (2E)-3-Phenylprop-2-en-1-yl α-L-arabinofuranosyl-(1→6)-β-D-glucopyranoside
Systematic IUPAC name (2R,3S,4S,5R,6R)-2-({oxy}methyl)-6-{oxy}oxane-3,4,5-triol
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C20H28O10/c21-9-12-14(22)17(25)20(29-12)28-10-13-15(23)16(24)18(26)19(30-13)27-8-4-7-11-5-2-1-3-6-11/h1-7,12-26H,8-10H2/b7-4+/t12-,13+,14-,15+,16-,17+,18+,19+,20+/m0/s1Key: IEBFEMIXXHIISM-YZOUKVLTSA-N
  • InChI=1/C20H28O10/c21-9-12-14(22)17(25)20(29-12)28-10-13-15(23)16(24)18(26)19(30-13)27-8-4-7-11-5-2-1-3-6-11/h1-7,12-26H,8-10H2/b7-4+/t12-,13+,14-,15+,16-,17+,18+,19+,20+/m0/s1Key: IEBFEMIXXHIISM-YZOUKVLTBR
SMILES
  • C1=CC=C(C=C1)/C=C/CO2((((O2)CO3(((O3)CO)O)O)O)O)O
Properties
Chemical formula C20H28O10
Molar mass 428.434 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Rosarin is a cinnamyl alcohol glycoside isolated from Rhodiola rosea.

References

  1. Mudge, E.; Lopes-Lutz, D.; Brown, P. N.; Schieber, A. (2013). "Purification of Phenylalkanoids and monoterpene glycosides from Rhodiola rosea L. Roots by high-speed counter-current chromatography". Phytochemical Analysis. 24 (2): 129–134. doi:10.1002/pca.2391. PMID 22811209.
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