Ailanthone
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.208.660
  • InChI=1S/C20H24O7/c1-8-4-12(21)16(24)18(3)10(8)5-13-19-7-26-20(25,17(18)19)15(23)9(2)11(19)6-14(22)27-13/h4,10-11,13,15-17,23-25H,2,5-7H2,1,3H3/t10-,11-,13+,15+,16+,17+,18+,19+,20-/m0/s1
    Key: WBBVXGHSWZIJST-RLQYZCPESA-N
  • InChI=1/C20H24O7/c1-8-4-12(21)16(24)18(3)10(8)5-13-19-7-26-20(25,17(18)19)15(23)9(2)11(19)6-14(22)27-13/h4,10-11,13,15-17,23-25H,2,5-7H2,1,3H3/t10-,11-,13+,15+,16+,17+,18+,19+,20-/m0/s1
    Key: WBBVXGHSWZIJST-RLQYZCPEBG
  • CC1=CC(=O)[C@H]([C@]2([C@H]1C[C@@H]3[C@]45[C@@H]2[C@]([C@@H](C(=C)[C@@H]4CC(=O)O3)O)(OC5)O)C)O
Properties
C20H24O7
Molar mass 376.405 g·mol−1
Density 1.47 g/cm3
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Ailanthone is an allelopathic chemical that is produced by the Ailanthus altissima tree which inhibits the growth of other plants.[1]

References

  1. ↑ Heisy, Rod M. (February 1996). "Identification of an Allelopathic Compound from Ailanthus altissima (Simaroubaceae) and Characterization of its Herbicidal Activity". American Journal of Botany. 83 (2): 192–200. doi:10.2307/2445938. JSTOR 2445938.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.