Cannabis Sativa

thcscience_admin
Danielone
Chemical structure of danielone
Names
Preferred IUPAC name
2-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)ethan-1-one
Other names
  • α-Hydroxyacetosyringone
  • 3',5'-Dimethoxy-4'-hydroxy-(2-hydroxy)acetophenone
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
  • InChI=1S/C10H12O5/c1-14-8-3-6(7(12)5-11)4-9(15-2)10(8)13/h3-4,11,13H,5H2,1-2H3 ☒N
    Key: ZTBAPEIDNUHRNC-UHFFFAOYSA-N ☒N
  • InChI=1/C10H12O5/c1-14-8-3-6(7(12)5-11)4-9(15-2)10(8)13/h3-4,11,13H,5H2,1-2H3
    Key: ZTBAPEIDNUHRNC-UHFFFAOYAI
  • COC1=CC(=CC(=C1O)OC)C(=O)CO
Properties
C10H12O5
Molar mass 212.201 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Danielone is a phytoalexin found in the papaya fruit. This compound showed high antifungal activity against Colletotrichum gloesporioides, a pathogenic fungus of papaya.[1] A laboratory synthesis of danielone has been reported.[2]

References[edit]

  1. ^ Echeverri, F.; Torres, F.; Quiñones, W.; Cardona, G.; Archbold, R.; Roldan, J.; Brito, I.; Luis, J. G.; Lahlou, E. H. (1997). "Danielone, a phytoalexin from papaya fruit". Phytochemistry. 44 (2): 255–6. Bibcode:1997PChem..44..255E. doi:10.1016/s0031-9422(96)00418-9. PMID 9004541.
  2. ^ Luis, Javier G.; Andrés, Lucía S. (1999). "Synthesis of Danielone (α-Hydroxyacetosyringone)". Journal of Chemical Research (3): 220–221. doi:10.1039/A808061E.


source: https://en.wikipedia.org/wiki/Danielone

Leave a Reply