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Two new pregnane alkaloids from Pachysandra terminalis Sieb. et Zucc. and their cytotoxic activities.
Wu, Ying; Rui, Yun; Ding, Chao; Liu, Chenwang; Zheng, Dan; Zhang, Zilong; Li, Yuze; Song, Xiaomei; Zhang, Dongdong.
Affiliation
  • Wu Y; Shaanxi Key Laboratory of Research and Application of Taibai Qi Yao, School of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, P.R. China.
  • Rui Y; Library of SHUTCM, School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, P.R. China.
  • Ding C; Shaanxi Key Laboratory of Research and Application of Taibai Qi Yao, School of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, P.R. China.
  • Liu C; Shaanxi Key Laboratory of Research and Application of Taibai Qi Yao, School of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, P.R. China.
  • Zheng D; Center for Translational Medicine, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Sixth People's Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, P.R. China.
  • Zhang Z; Library of SHUTCM, School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, P.R. China.
  • Li Y; Shaanxi Key Laboratory of Research and Application of Taibai Qi Yao, School of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, P.R. China.
  • Song X; Shaanxi Key Laboratory of Research and Application of Taibai Qi Yao, School of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, P.R. China.
  • Zhang D; Shaanxi Key Laboratory of Research and Application of Taibai Qi Yao, School of Pharmacy, Shaanxi University of Chinese Medicine, Xianyang, P.R. China.
Nat Prod Res ; : 1-7, 2024 Jul 09.
Article de En | MEDLINE | ID: mdl-38980258
ABSTRACT
Pactermines E and F (1 and 2), two new pregnane alkaloids were isolated from the whole plant of Pachysandra terminalis Sieb. et Zucc. Their structures were determined by physicochemical properties and spectroscopic methods including 1D, 2D NMR, IR, HR-ESI-MS data. Cytotoxic activities against three human cancer A549, HCT116 and SW620 cell lines of the isolated compounds were evaluated by CCK8 method. However, all compounds showed no significant activity against the three cancer cells (IC50>100 µM) except for compound 1, which showed inhibitory effects against HCT116 cells with IC50 values of 84.6 µM.
Mots clés

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Nat Prod Res Année: 2024 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Langue: En Journal: Nat Prod Res Année: 2024 Type de document: Article