Liriodenine

Liriodenine
Names
IUPAC name
4,5,6,6a-Tetradehydro-12-nor-2′H-[1,3]dioxolo[4′,5′:1,2]aporphin-7-one
Systematic IUPAC name
2H,8H-Benzo[g][1,3]benzodioxolo[6,5,4-de]quinolin-8-one
Identifiers
CAS Number
  • 475-75-2 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:70649
ChemSpider
  • 9738
KEGG
  • C09567
PubChem CID
  • 10144
UNII
  • E134R7X4O9 checkY
CompTox Dashboard (EPA)
  • DTXSID40197165 Edit this at Wikidata
InChI
  • InChI=1S/C17H9NO3/c19-16-11-4-2-1-3-10(11)14-13-9(5-6-18-15(13)16)7-12-17(14)21-8-20-12/h1-7H,8H2
    Key: MUMCCPUVOAUBAN-UHFFFAOYSA-N
  • InChI=1/C17H9NO3/c19-16-11-4-2-1-3-10(11)14-13-9(5-6-18-15(13)16)7-12-17(14)21-8-20-12/h1-7H,8H2
    Key: MUMCCPUVOAUBAN-UHFFFAOYAX
  • C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53
Properties
Chemical formula
 C17H9NO3
Molar mass 275.263 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
Chemical compound

Liriodenine is a bio-active isolate of the Chinese medicinal herb Zanthoxylum nitidum. It was isolated for the first time, at least with the name liriodenine, from the heartwood of Liriodendron tulipifera, the common yellow poplar of the south-eastern USA. It is found in very many other plants, notably in Annona cherimolia and Annona muricata, widely cultivated for their edible fruit.[1]

References

  1. ^ Chen, ZF; Liu, YC; Peng, Y; Hong, X; Wang, HH; Zhang, MM; Liang, H (February 2012). "Synthesis, characterization, and in vitro antitumor properties of gold(III) compounds with the traditional Chinese medicine (TCM) active ingredient liriodenine". Journal of Biological Inorganic Chemistry. 17 (2): 247–61. doi:10.1007/s00775-011-0846-z. PMID 21960256. S2CID 254085779.
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