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Filicinic acid based meroterpenoids from Hypericum elodeoides and their anti-Alzheimer's disease effects.
Li, Jing-Dian; He, Shou-Lun; Wang, Guang-Hui; Chen, Jun-Jie; Liu, Xiang-Zhong; Wang, Tian-Qi; Zhou, Mi; Du, Chun-Chun; Chen, Hai-Feng; Tian, Wen-Jing.
Affiliation
  • Li JD; Fujian Provincial Key Laboratory of Innovative Drug Target, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361005, PR China.
  • He SL; Fujian Provincial Key Laboratory of Innovative Drug Target, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361005, PR China.
  • Wang GH; Fujian Provincial Key Laboratory of Innovative Drug Target, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361005, PR China.
  • Chen JJ; Fujian Provincial Key Laboratory of Innovative Drug Target, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361005, PR China.
  • Liu XZ; Fujian Provincial Key Laboratory of Innovative Drug Target, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361005, PR China.
  • Wang TQ; Fujian Provincial Key Laboratory of Innovative Drug Target, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361005, PR China.
  • Zhou M; Fujian Provincial Key Laboratory of Innovative Drug Target, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361005, PR China.
  • Du CC; Fujian Provincial Key Laboratory of Innovative Drug Target, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361005, PR China.
  • Chen HF; Fujian Provincial Key Laboratory of Innovative Drug Target, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361005, PR China. Electronic address: haifeng@xmu.edu.cn.
  • Tian WJ; Fujian Provincial Key Laboratory of Innovative Drug Target, School of Pharmaceutical Sciences, Xiamen University, Xiamen 361005, PR China. Electronic address: tianwj@xmu.edu.cn.
Bioorg Chem ; 153: 107787, 2024 Sep 02.
Article in En | MEDLINE | ID: mdl-39243738
ABSTRACT
(±)-Elodeoidileons A-L (1-12), 12 pairs of previously undescribed filicinic acid based meroterpenoids were isolated from Hypericum elodeoides with unique linear or angular 6/6/6 ring core. Modern spectroscopic techniques, modified Mosher's method and quantum chemical calculations were used to identify the planner structures and configurations of 1-12. Additionally, the potential biosynthetic pathways for 1-12 were anticipated. Moreover, biological activity assessments suggested that 1a, 5a, and 11b could activate Retinoid X receptor-α (RXRα) transcription and enhance the ATP-binding cassette transporter A1 (ABCA1) protein's expression. Fluorescence titration assay suggested that 1a might have a direct interaction with the RXRα-LBD protein, with an estimated Kd value of 5.85 µM. Moreover, molecular docking study confirmed the binding of 1a to RXRα and further validated by cellular thermal shift assay (CETSA). Thus, compound 1a may promote ß-amyloid (Aß) clearance by targeting RXRα and upregulating the expression of the ABCA1 protein, showing promise as anti-Alzheimer's agent.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Bioorg Chem / Bioorganic chem / Bioorganic chemistry Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Bioorg Chem / Bioorganic chem / Bioorganic chemistry Year: 2024 Type: Article