Mulberroside A
Names
IUPAC name
3-{(E)-2-[4-(β-D-Glucopyranosyloxy)-2-hydroxyphenyl]ethen-1-yl}-5-hydroxyphenyl β-D-glucopyranoside
Systematic IUPAC name
(12S,13R,14S,15S,16R,4E,82S,83R,84S,85S,86R)-16,86-Bis(hydroxymethyl)-2,7-dioxa-1,8(2)-bis(oxana)-3(1,3),6(1,4)-dibenzenaoctaphan-4-ene-13,14,15,35,62,83,84,85-octol
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C26H32O14/c27-9-17-19(31)21(33)23(35)25(39-17)37-14-4-3-12(16(30)8-14)2-1-11-5-13(29)7-15(6-11)38-26-24(36)22(34)20(32)18(10-28)40-26/h1-8,17-36H,9-10H2/b2-1+/t17-,18-,19-,20-,21+,22+,23-,24-,25-,26-/m1/s1
    Key: HPSWAEGGWLOOKT-VUNDNAJOSA-N
  • C1=CC(=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)O)C=CC3=CC(=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O
Properties
C26H32O14
Molar mass 568.52 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Mulberroside A is a stilbenoid found in Morus alba, the white mulberry.[1] It is the diglucoside of oxyresveratrol.

References

  1. ^ Kim, JK; Kim, M; Cho, SG; Kim, MK; Kim, SW; Lim, YH (2010). "Biotransformation of mulberroside a from Morus alba results in enhancement of tyrosinase inhibition". Journal of Industrial Microbiology & Biotechnology. 37 (6): 631–7. doi:10.1007/s10295-010-0722-9. PMID 20411402. S2CID 21236818.
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