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Contents

   



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1 See also  




2 References  













Nothoapiole







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From Wikipedia, the free encyclopedia
  

Nothoapiole
Names
Preferred IUPAC name

4,5,7-Trimethoxy-6-(prop-2-en-1-yl)-2H-1,3-benzodioxole

Other names

2,3,6-Trimethoxy,4,5-methylenedioxy-allylbenzene; 1,3-Benzodioxole, 4,5,7-trimethoxy-6-(2-propen-1-yl)-

Identifiers

CAS Number

3D model (JSmol)
ChemSpider

PubChem CID

CompTox Dashboard (EPA)

  • InChI=1S/C13H16O5/c1-5-6-8-9(14-2)11(16-4)13-12(10(8)15-3)17-7-18-13/h5H,1,6-7H2,2-4H3 checkY

    Key: IWGPXDGGZYMDJF-UHFFFAOYSA-N checkY

  • InChI=1S/C13H16O5/c1-5-6-8-9(14-2)11(16-4)13-12(10(8)15-3)17-7-18-13/h5H,1,6-7H2,2-4H3

  • COC1=C(C(=C(C2=C1OCO2)OC)OC)CC=C

Properties

Chemical formula

 C13H16O5
Molar mass 252.266 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

Nothoapiole is a phenylpropene, a natural organic compound present in the essential oilofPerilla frutescens from Jeju IslandinKorea[1] and the major component of the essential oil obtained from the roots of Pleurospermum angelicoides Benth.[2] It is also found in the essential oil of black caraway (Carum bulbocastanum) fruits[3] and Carum nigrum.[4]

This highly oxygenated phenylpropanoid, previously reported in a few Carum species, is structurally and biogenetically related to myristicin, apiole and dillapiole.[5][6]

See also[edit]

References[edit]

  1. ^ Ito, Michiho; Toyoda, Mariko; Yuba, Akiko; Honda, Gisho (1999). "Genetic Analysis of Nothoapiol Formation in Perilla frutescens". Biological & Pharmaceutical Bulletin. 22 (6): 598–601. doi:10.1248/bpb.22.598. PMID 10408233.
  • ^ http://www.acgpubs.org/RNP/2015/Volume9/Issue%201/67-RNP-EO_1202-015.pdf [bare URL PDF]
  • ^ Journal of the Science of Food and Agriculture Volume 90, Issue 3, pages 385–390, February 2010
  • ^ Singh, Gurdip; Marimuthu, Palanisamy; De Heluani, Carola S.; Catalan, Cesar A. N. (2006). "Antioxidant and Biocidal Activities of Carum nigrum(Seed) Essential Oil, Oleoresin, and Their Selected Components†". Journal of Agricultural and Food Chemistry. 54 (1): 174–81. doi:10.1021/jf0518610. hdl:11336/99544. PMID 16390196.
  • ^ H. Laouer; E.K. Meriem; S. Prado; N. Baldovini (2009). "An antibacterial and antifungal phenylpropanoid from Carum montanum (Coss. et Dur.) Benth. et Hook". Phytother. Res. 23 (12): 1726–1730. doi:10.1002/ptr.2820. PMID 19370550. S2CID 2668369.
  • ^ M. Ito; M. Toyoda; A. Yuba; G. Honda (1999). "Genetic analysis of nothoapiole formation in Perilla frutescens". Biol. Pharm. Bull. 22 (6): 598–601. doi:10.1248/bpb.22.598. PMID 10408233.

    • Retrieved from "https://en.wikipedia.org/w/index.php?title=Nothoapiole&oldid=1170159979"
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    ●Phenylpropenes
     ●O-methylated phenylpropanoids
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