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Rubesanolides F and G: Two Novel Lactone-Type Norditerpenoids from Isodon rubescens.
He, Kang; Zou, Juan; Wang, Yu-Xue; Zhao, Chen-Liang; Ye, Jiang-Hai; Zhang, Jing-Jie; Pan, Lu-Tai; Zhang, Hong-Jie.
Afiliación
  • He K; The Key Laboratory of Miao Medicine of Guizhou Province, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China.
  • Zou J; The Key Laboratory of Miao Medicine of Guizhou Province, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China.
  • Wang YX; The Key Laboratory of Miao Medicine of Guizhou Province, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China.
  • Zhao CL; The Key Laboratory of Miao Medicine of Guizhou Province, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China.
  • Ye JH; School of Chinese Medicine, Hong Kong Baptist University, Kowloon, Hong Kong, China.
  • Zhang JJ; The Key Laboratory of Miao Medicine of Guizhou Province, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China.
  • Pan LT; The Key Laboratory of Miao Medicine of Guizhou Province, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China.
  • Zhang HJ; The Key Laboratory of Miao Medicine of Guizhou Province, Guizhou University of Traditional Chinese Medicine, Guiyang 550025, China.
Molecules ; 26(13)2021 Jun 24.
Article en En | MEDLINE | ID: mdl-34202760
ABSTRACT
A phytochemical investigation of the leaves of the medicinal plant Isodon rubescens led to the isolation of the two new degraded abietane lactone diterpenoids rubesanolides F (1) and G (2). Their structures were elucidated based on the analyses of the HRESIMS and 1D/2D NMR spectral data, and their absolute configurations were determined by ECD spectrum calculations and X-ray single crystal diffraction methods. Compounds 1 and 2, with a unique γ-lactone subgroup between C-8 and C-20, were found to form a carbonyl carbon at C-13 by removal of the isopropyl group in an abietane diterpene skeleton. Rubesanolide G (2) is a rare case of abietane that possesses a cis-fused configuration between rings B and C. The two isolates were evaluated for their biological activities against two cancer cell lines (A549 and HL60), three fungal strains (Candida alba, Aspergillus niger and Rhizopus nigricans) and three bacterial strains (Escherichia coli, Staphylococcus aureus and Bacillus subtilis).
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Bacterias / Hojas de la Planta / Isodon / Abietanos / Hongos / Lactonas / Antiinfecciosos / Neoplasias / Antineoplásicos Fitogénicos Idioma: En Revista: Molecules Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Bacterias / Hojas de la Planta / Isodon / Abietanos / Hongos / Lactonas / Antiinfecciosos / Neoplasias / Antineoplásicos Fitogénicos Idioma: En Revista: Molecules Año: 2021 Tipo del documento: Article País de afiliación: China