Your browser doesn't support javascript.
loading
Biosynthesis of (2-nitroethyl)benzene and (Z)- and (E)-(2-nitroethenyl)benzenes from (Z)- and (E)-phenylacetaldoximes and phenylacetonitrile; defense allomone of Eutrichodesmus elegans and Eutrichodesmus armatus (Polydesmida: Haplodesmidae).
Kuwahara, Yasumasa; Ichiki, Yayoi; Morita, Masashi; Tanabe, Tsutomu; Asano, Yasuhisa.
Afiliación
  • Kuwahara Y; Asano Active Enzyme Molecular Project, JST, ERATO, Kyoto Branch, Kyoto, Kyoto 602-0841, Japan.
  • Ichiki Y; Asano Active Enzyme Molecular Project, JST, ERATO, 5180 Kurokawa, Imizu, Toyama 939-0398, Japan.
  • Morita M; Asano Active Enzyme Molecular Project, JST, ERATO, Kyoto Branch, Kyoto, Kyoto 602-0841, Japan.
  • Tanabe T; Asano Active Enzyme Molecular Project, JST, ERATO, 5180 Kurokawa, Imizu, Toyama 939-0398, Japan.
  • Asano Y; Asano Active Enzyme Molecular Project, JST, ERATO, Kyoto Branch, Kyoto, Kyoto 602-0841, Japan.
J Pestic Sci ; 43(4): 240-247, 2018 Nov 20.
Article en En | MEDLINE | ID: mdl-30479544
ABSTRACT
The defense allomones of two haplodesmid millipedes, Eutrichodesmus elegans and E. armatus (Polydesmida Haplodesmidae), are known as a mixture of the following three nitro compounds (2-nitroethyl)benzene and (Z)- and (E)-(2-nitroethenyl)benzenes. Administrations of a mixture of 2H-labeled (Z)- and (E)-phenylacetaldoximes and of 2H-labeled phenylacetonitrile as precursors resulted in the same production of three 2H-labeled nitro compounds, [2'-nitroethyl][2,3,4,5,6-2H5]benzene and [(Z)- and (E)-2'-nitroethenyl][2,3,4,5,6-2H5]benzenes, in both species. Oxime administration at an appropriate dose resulted in the production of three nitro compounds with similar natural ratios more effectively than nitrile administration. Conversion from oximes to nitrile and vice versa was evidenced during administration. Occurrences of three precursors (Z- and E-oximes and nitrile) were detected sporadically in millipede extracts by selected ion chromatography.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Pestic Sci Año: 2018 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Pestic Sci Año: 2018 Tipo del documento: Article