Kadsurin
Names
Preferred IUPAC name
(6R,7R,8R)-1,2,3,13-Tetramethoxy-6,7-dimethyl-5,6,7,8-tetrahydro-11H-benzo[3,4]cycloocta[1,2-f][1,3]benzodioxol-8-yl acetate
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
  • InChI=1S/C25H30O8/c1-12-8-15-9-17(27-4)22(28-5)24(29-6)19(15)20-16(21(13(12)2)33-14(3)26)10-18-23(25(20)30-7)32-11-31-18/h9-10,12-13,21H,8,11H2,1-7H3/t12-,13-,21-/m1/s1
    Key: QUGMSTJBNZWXQS-SQHYZVFZSA-N
  • InChI=1/C25H30O8/c1-12-8-15-9-17(27-4)22(28-5)24(29-6)19(15)20-16(21(13(12)2)33-14(3)26)10-18-23(25(20)30-7)32-11-31-18/h9-10,12-13,21H,8,11H2,1-7H3/t12-,13-,21-/m1/s1
    Key: QUGMSTJBNZWXQS-SQHYZVFZBD
  • C[C@@H]1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3[C@@H]([C@@H]1C)OC(=O)C)OCO4)OC)OC)OC)OC
Properties
C25H30O8
Molar mass 458.507 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

Kadsurin is a bioactive isolate of Kadsura.[1]

References

  1. ↑ Yang, X. W.; Hattori, M; Namba, T; Chen, D. F.; Xu, G. J. (1992). "Anti-lipid peroxidative effect of an extract of the stems of Kadsura heteroclita and its major constituent, kadsurin, in mice". Chemical & Pharmaceutical Bulletin. 40 (2): 406–9. doi:10.1248/cpb.40.406. PMID 1606637.


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