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New ent-kaurene and germacrene derivatives from Mesona procumbens Hemseley and their biological activity.
Ganzon, Jerome G; Liaw, Chia-Ching; Lin, Yu-Chi; Lin, Zhi-Hu; Wang, Chang-Hung; Chen, Che-Yi; Chuang, Kuo-Hsiang; Kuo, Yao-Haur.
Afiliação
  • Ganzon JG; Division of Chinese Materia Medica Development, National Research Institute of Chinese Medicine, Taipei, Taiwan.
  • Liaw CC; Division of Chinese Materia Medica Development, National Research Institute of Chinese Medicine, Taipei, Taiwan.
  • Lin YC; Department of Biochemical Science and Technology, National Chiayi University, Chiayi, Taiwan.
  • Lin ZH; Division of Chinese Materia Medica Development, National Research Institute of Chinese Medicine, Taipei, Taiwan.
  • Wang CH; Division of Chinese Materia Medica Development, National Research Institute of Chinese Medicine, Taipei, Taiwan.
  • Chen CY; Ph.D. Program in Clinical Drug Development of Herbal Medicine, Taipei Medical University, Taipei, Taiwan.
  • Chuang KH; Ph.D. Program in Clinical Drug Development of Herbal Medicine, Taipei Medical University, Taipei, Taiwan.
  • Kuo YH; Ph.D. Program in Clinical Drug Development of Herbal Medicine, Taipei Medical University, Taipei, Taiwan.
Nat Prod Res ; 37(13): 2172-2180, 2023 Jul.
Article em En | MEDLINE | ID: mdl-35105219
Mesona procumbens Hemseley is a well-known traditional herbal medicine used for heat-related ailments. In Taiwan, boiled extracts of M. procumbens are also used as desserts called grass jelly. In this study, the hexane extract from 75% EtOH of M. procumbens showed potent activities on inhibition of E. coli ß-glucuronidase (eßG) and NO production and cytotoxicity against MCF-7 and HepG2 cancer cell lines. Furthermore, using various flash columns and HPLC chromatography on the bioactive layer led to the isolation of twelve compounds (1-12), including a new ent-kaurene, mesokaurol A (1), and a new germacrene derivative, mesogermapene A (2). Their structures were elucidated by extensive spectroscopic analyses, especially 2 D NMR and mass data. Biological assays showed that compound 9 (linolenic acid) had specific activity on inhibition of eßG (68.27%) at 100 µg/mL but was non-inhibitory to human ß-glucuronidase. Compound 1 possessed significant cytotoxicity against MCF-7 (EC50 = 9.76 µM) and HepG2 (EC50 = 8.64 µM) cancer cell lines.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Lamiaceae / Diterpenos do Tipo Caurano Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Lamiaceae / Diterpenos do Tipo Caurano Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article