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Phytotoxic and Nematicidal Components of Lavandula luisieri.
Julio, Luis F; Barrero, Alejandro F; Herrador del Pino, M Mar; Arteaga, Jesús F; Burillo, Jesús; Andres, Maria Fe; Díaz, Carmen E; González-Coloma, Azucena.
Afiliação
  • Julio LF; Instituto de Ciencias Agrarias, Consejo Superior de Investigaciones Científicas , Serrano 115-bis, 28006 Madrid, Spain.
  • Barrero AF; Departamento de Química Orgánica, Instituto de Biotecnología, Universidad de Granada , Campus de Fuente Nueva, s/n, 18071 Granada, Spain.
  • Herrador del Pino MM; Departamento de Química Orgánica, Instituto de Biotecnología, Universidad de Granada , Campus de Fuente Nueva, s/n, 18071 Granada, Spain.
  • Arteaga JF; CIQSO, Center for Research in Sustainable Chemistry and Department of Chemical Engineering, Physical Chemistry, and Organic Chemistry, Facultad de Ciencias Experimentales, Universidad de Huelva , Campus el Carmen, 21071 Huelva, Spain.
  • Burillo J; Departamento de Ciencia, Tecnología y Universidad, Centro de Investigación y Tecnología Agroalimentaria de Aragón, Gobierno de Aragón , Avenida Montañana, 930, Zaragoza, Spain.
  • Andres MF; Instituto de Ciencias Agrarias, Consejo Superior de Investigaciones Científicas , Serrano 115-bis, 28006 Madrid, Spain.
  • Díaz CE; Instituto de Productos Naturales y Agrobiología, Consejo Superior de Investigaciones Científicas , Avenida Astrofísico F. Sánchez, 3, 38206 La Laguna, Tenerife, Spain.
  • González-Coloma A; Instituto de Ciencias Agrarias, Consejo Superior de Investigaciones Científicas , Serrano 115-bis, 28006 Madrid, Spain.
J Nat Prod ; 79(2): 261-6, 2016 Feb 26.
Article em En | MEDLINE | ID: mdl-26797293
ABSTRACT
Several preparations were obtained from the aerial parts of predomesticated Lavandula luisieri, including the essential oil and ethanolic, hexane, and ethyl acetate extractives. Additionally, pilot plant vapor pressure extraction was carried out at a pressure range of 0.5-1.0 bar to give a vapor pressure oil and an aqueous residue. A chemical study of the hexane extract led to the isolation of six necrodane derivatives (1, 2, and 4-7), with four of these (1, 2, 5, and 7) being new, as well as camphor, a cadinane sesquiterpene (9), tormentic acid, and ursolic acid. The EtOAc and EtOH extracts contained a mixture of phenolic compounds with rosmarinic acid being the major component. Workup of the aqueous residue resulted in the isolation of the necrodane 3 and (1R*,2S*,4R*)-p-menth-5-ene-1,2,8-triol (8), both new natural compounds. The structures of the new compounds were established based on their spectroscopic data. The phytotoxic and nematicidal activities of these compounds were evaluated.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Terpenos / Antinematódeos Limite: Animals País/Região como assunto: Europa Idioma: En Revista: J Nat Prod Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Espanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Terpenos / Antinematódeos Limite: Animals País/Região como assunto: Europa Idioma: En Revista: J Nat Prod Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Espanha