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Bioactive Enmein-Type ent-Kaurane Diterpenoids from Isodon phyllostachys.
Yang, Jin; Wang, Wei-Guang; Wu, Hai-Yan; Du, Xue; Li, Xiao-Nian; Li, Yan; Pu, Jian-Xin; Sun, Han-Dong.
Afiliación
  • Yang J; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences , Kunming 650201, People's Republic of China.
  • Wang WG; University of Chinese Academy of Sciences , Beijing 100049, People's Republic of China.
  • Wu HY; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences , Kunming 650201, People's Republic of China.
  • Du X; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences , Kunming 650201, People's Republic of China.
  • Li XN; University of Chinese Academy of Sciences , Beijing 100049, People's Republic of China.
  • Li Y; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences , Kunming 650201, People's Republic of China.
  • Pu JX; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences , Kunming 650201, People's Republic of China.
  • Sun HD; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences , Kunming 650201, People's Republic of China.
J Nat Prod ; 79(1): 132-40, 2016 Jan 22.
Article en En | MEDLINE | ID: mdl-26757019
ABSTRACT
Thirty-two enmein-type ent-kaurane diterpenoids, including 13 new compounds, were isolated from the aerial parts of Isodon phyllostachys. Compounds 1 and 2 are the first examples of 3,206,20-diepoxyenmein-type ent-kauranoids, and the structures of these new compounds were established mainly by analyzing NMR and HREIMS data. The absolute configurations of 1 and 8 and the relative configuration of 9 were determined using single-crystal X-ray diffraction. Compounds 11, 15, 20, and 21 were active against five human cancer cell lines (HL-60, SMMC-7721, A-549, MCF-7, and SW-480), with IC50 values ranging from 1.2 to 5.0 µM. Compounds 3, 11, 15, 17, 20, 21, 25, and 29 strongly inhibited NO production in LPS-stimulated RAW264.7 cells, with IC50 values ranging from 0.74 to 4.93 µM.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Medicamentos Herbarios Chinos / Isodon / Diterpenos de Tipo Kaurano / Antineoplásicos Fitogénicos Límite: Animals / Humans Idioma: En Revista: J Nat Prod Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Medicamentos Herbarios Chinos / Isodon / Diterpenos de Tipo Kaurano / Antineoplásicos Fitogénicos Límite: Animals / Humans Idioma: En Revista: J Nat Prod Año: 2016 Tipo del documento: Article