Integrative Biology Journals

Natural Products and Bioprospecting ›› 2024, Vol. 14 ›› Issue (5): 45-45.DOI: 10.1007/s13659-024-00465-9

• ORIGINAL ARTICLES • Previous Articles     Next Articles

Silvaticusins A-D: ent-kaurane diterpenoids and a cyclobutane-containing ent-kaurane dimer from Isodon silvaticus

Qi-Xiu Hai1,2, Kun Hu2, Su-Ping Chen2, Yang-Yang Fu2, Xiao-Nian Li2, Han-Dong Sun2, Hong-Ping He1, Pema-Tenzin Puno2   

  1. 1. College of Chinese Materia Medica and Yunnan Key Laboratory of Southern Medicinal Utilization, Yunnan University of Chinese Medicine, Kunming, 650500, People's Republic of China;
    2. Key Laboratory of Phytochemistry and Natural Medicines, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650201, People's Republic of China
  • Received:2024-06-03 Online:2024-10-14 Published:2024-10-24
  • Contact: Hong-Ping He,E-mail:95431111@qq.com;Pema-Tenzin Puno,E-mail:punopematenzin@mail.kib.ac.cn
  • Supported by:
    This work was financially supported by the National Science Fund for Distinguished Young Scholars (82325047), Second Tibetan Plateau Scientific Expedition and Research (STEP) program (2019QZKK0502), NSFC-Joint Foundation of Yunnan Province (U2002221), and Youth Innovation Promotion Association CAS (2023409).

Silvaticusins A-D: ent-kaurane diterpenoids and a cyclobutane-containing ent-kaurane dimer from Isodon silvaticus

Qi-Xiu Hai1,2, Kun Hu2, Su-Ping Chen2, Yang-Yang Fu2, Xiao-Nian Li2, Han-Dong Sun2, Hong-Ping He1, Pema-Tenzin Puno2   

  1. 1. College of Chinese Materia Medica and Yunnan Key Laboratory of Southern Medicinal Utilization, Yunnan University of Chinese Medicine, Kunming, 650500, People's Republic of China;
    2. Key Laboratory of Phytochemistry and Natural Medicines, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, 650201, People's Republic of China
  • 通讯作者: Hong-Ping He,E-mail:95431111@qq.com;Pema-Tenzin Puno,E-mail:punopematenzin@mail.kib.ac.cn
  • 基金资助:
    This work was financially supported by the National Science Fund for Distinguished Young Scholars (82325047), Second Tibetan Plateau Scientific Expedition and Research (STEP) program (2019QZKK0502), NSFC-Joint Foundation of Yunnan Province (U2002221), and Youth Innovation Promotion Association CAS (2023409).

Abstract: Three new ent-kaurane diterpenoids, silvaticusins A-C (1-3), along with a new ent-kaurane dimer silvaticusin D (4) were isolated from the aerial parts of Isodon silvaticus. The structures of these new compounds were established mainly by comprehensive analysis of their NMR and MS data. The absolute configuration of compounds 1 and 4 were determined using a single-crystal X-ray diffraction and computational methods, respectively. Compounds 2 and 3 were found to exhibit remarkable cytotoxic effects against five human tumor cell lines (HL-60, A-549, SMMC-7721, MDA-MB-231, and SW-480), with IC50 values spanning from 1.27±0.08 to 7.52±0.33 μM.

Key words: Isodon silvaticus, ent-Kaurane diterpenoid, ent-Kaurane dimer, Cyclobutane moiety, Cytotoxicity

摘要: Three new ent-kaurane diterpenoids, silvaticusins A-C (1-3), along with a new ent-kaurane dimer silvaticusin D (4) were isolated from the aerial parts of Isodon silvaticus. The structures of these new compounds were established mainly by comprehensive analysis of their NMR and MS data. The absolute configuration of compounds 1 and 4 were determined using a single-crystal X-ray diffraction and computational methods, respectively. Compounds 2 and 3 were found to exhibit remarkable cytotoxic effects against five human tumor cell lines (HL-60, A-549, SMMC-7721, MDA-MB-231, and SW-480), with IC50 values spanning from 1.27±0.08 to 7.52±0.33 μM.

关键词: Isodon silvaticus, ent-Kaurane diterpenoid, ent-Kaurane dimer, Cyclobutane moiety, Cytotoxicity