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Prenylated Acetophenone Derivatives from the Leaves of Acronychia pedunculata and Their Anti-proliferative Activities.
Yang, Zhen-Zhen; Li, Ni-Ping; Lv, Li-Xia; Li, Yi-Yi; Ge, Ge; Zhuo, Yue; Wang, Qi; Gu, Ji-Hong; Wu, Yan.
Affiliation
  • Yang ZZ; Guangzhou University of Chinese Medicine, Science and Technology Innovation Center, 232 Outer Ring East Road, Guangzhou, CHINA.
  • Li NP; Jinan University, State Key Laboratory of Bioactive Molecules and Druggability Assessment, 601 West Huangpu Avenue, Guangzhou, CHINA.
  • Lv LX; Guangzhou University of Chinese Medicine, Science and Technology Innovation Center, 232 Outer Ring East Road, Guangzhou, CHINA.
  • Li YY; Jinan University, State Key Laboratory of Bioactive Molecules and Druggability Assessment, 601 West Huangpu Avenue, Guangzhou, CHINA.
  • Ge G; Shenzhen Technology University, College of Pharmacy, 3002 Lantian Road, Pingshan District, 518118, shenzhen, CHINA.
  • Zhuo Y; Guangzhou University of Chinese Medicine, Science and Technology Innovation Center, 232 Outer Ring East Road District, Guangzhou, CHINA.
  • Wang Q; Guangzhou University of Chinese Medicine, Science and Technology Innovation Center, 232 Outer Ring East Road, Guangzhou, CHINA.
  • Gu JH; Guangzhou University of Chinese Medicine, Science and Technology Innovation Center, 232 Outer Ring East Road, Guangzhou, CHINA.
  • Wu Y; Shenzhen Technology University, College of Pharmacy, 3002 Lantian Road, Pingshan District, 518118, shenzhen, CHINA.
Chem Biodivers ; : e202401027, 2024 Jul 29.
Article in En | MEDLINE | ID: mdl-39073310
ABSTRACT
Four new prenylated acetophenone derivatives, including one acetophenone dimer [acronyrone D (1)] and three acetophenone monomers [acronyrones E-G (2-4)], along with seven known analogues (5-11) were obtained from the leaves of Acronychia pedunculata. Their structures and absolute configurations were established by analysis of HRMS and NMR data, single crystal X-ray diffraction studies and quantum chemical calculations. In addition, the isolates were tested for their anti-proliferative acivity against HCT-116, RKO and SW480 cancer cell lines. Remarkably, compound 5 exhibited significant anti-proliferative effects on the three cell lines, with IC50 values ranging from 0.24 to 5.3 µM.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chem Biodivers Journal subject: BIOQUIMICA / QUIMICA Year: 2024 Type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Chem Biodivers Journal subject: BIOQUIMICA / QUIMICA Year: 2024 Type: Article Affiliation country: China