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Identification of lignans as ATP citrate lyase (ACLY) inhibitors from the roots of Pouzolzia zeylanica.
Li, Jin-Long; Jiang, Jia-Yi; Gu, Shan-Shan; Zhang, Lei; Sun, Yan; Wang, Xue-Han; Li, Dan-Yu; Chen, Zhe-Yu; Jiang, Sheng-Shi; Zhu, Wei-Zhong; Jiang, Hao-Wen; Zhang, Hong-Jie.
Afiliación
  • Li JL; School of Pharmacy, Nantong University, Nantong, People's Republic of China.
  • Jiang JY; School of Chinese Medicine, Hong Kong Baptist University, Kowloon, People's Republic of China.
  • Gu SS; School of Pharmacy, Nantong University, Nantong, People's Republic of China.
  • Zhang L; Department of Pharmacy, Nantong Hospital of Traditional Chinese Medicine, Nantong, People's Republic of China.
  • Sun Y; School of Pharmacy, Nantong University, Nantong, People's Republic of China.
  • Wang XH; Department of Pharmacy, Nantong Hospital of Traditional Chinese Medicine, Nantong, People's Republic of China.
  • Li DY; Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, Hangzhou, People's Republic of China.
  • Chen ZY; School of Chinese Medicine, Hong Kong Baptist University, Kowloon, People's Republic of China.
  • Jiang SS; School of Chinese Medicine, Hong Kong Baptist University, Kowloon, People's Republic of China.
  • Zhu WZ; School of Pharmacy, Nantong University, Nantong, People's Republic of China.
  • Jiang HW; Department of Pharmacy, Nantong Hospital of Traditional Chinese Medicine, Nantong, People's Republic of China.
  • Zhang HJ; School of Pharmacy, Nantong University, Nantong, People's Republic of China.
Nat Prod Res ; 38(10): 1719-1726, 2024 May.
Article en En | MEDLINE | ID: mdl-37265118
A new lignan, named pouzolignan P (1), together with 14 known ones (2 - 15) were isolated from the roots of Pouzolzia zeylanica (L.) Benn. Their structures were deduced based on the detailed spectroscopic analysis. All the isolates were evaluated for their inhibitory activities toward the ATP citrate lyase (ACLY). Among them, four lignans, isopouzolignan K (3), gnemontanins E (5), gnetuhainin I (6), and styraxlignolide D (15) showed excellent ACLY inhibitory effect with IC50 values of 9.06, 0.59, 2.63, and 7.62 µM, respectively. These compounds were further evaluated for their cholesterol-lowing effects on ox-LDL-induced high-cholesterol HepG2 cells. Compound 15 emerges as the most potent ACLY inhibitor, which significantly decreased the TC level in a dose-dependent manner. In addition, molecular docking simulations elucidated that 15 formed a strong hydrogen-bond interaction with Glu599 of ACLY, which was an important site responsible for the enzyme catalytic activity.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: ATP Citrato (pro-S)-Liasa / Lignanos Tipo de estudio: Diagnostic_studies Idioma: En Revista: Nat Prod Res Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: ATP Citrato (pro-S)-Liasa / Lignanos Tipo de estudio: Diagnostic_studies Idioma: En Revista: Nat Prod Res Año: 2024 Tipo del documento: Article