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Guided Discovery of Antidiabetic Sesquiterpenoids From <i>Lindera Aggregate</i> by Activity Labeled Molecular Networking

Jinqian YuKey Laboratory for Natural Active Pharmaceutical Constituents Research in Universities of Shandong Province, School of Pharmaceutical Sciences Qilu University of Technology (Shandong Academy of Sciences) Jinan ChinaLei ZhaoChemical Technology Research Institute of Shandong Qingdao University of Science and Technology Jinan P. R. ChinaG.A.S. PremakumaraDepartment of Basic Science &amp; Social Science for Nursing University of Colombo Sri LankaYingjian GuoKey Laboratory for Natural Active Pharmaceutical Constituents Research in Universities of Shandong Province, School of Pharmaceutical Sciences Qilu University of Technology (Shandong Academy of Sciences) Jinan ChinaTao YueChemical Technology Research Institute of Shandong Qingdao University of Science and Technology Jinan P. R. ChinaSagdullaev Shamansur ShaksaidovichS. Yu. Yunusov Institute of the Chemistry of Plant Substances Academy of Sciences of the Republic of Uzbekistan Tashkent UzbekistanXiao WangKey Laboratory for Natural Active Pharmaceutical Constituents Research in Universities of Shandong Province, School of Pharmaceutical Sciences Qilu University of Technology (Shandong Academy of Sciences) Jinan China
Phytochemical Analysisjournal2025en
ABI

Аннотация

INTRODUCTION: The roots of Lindera aggregata (Sims) Kosterm named "Wuyao" in Chinese, showed significant antidiabetic bioactivity detected by the insulin resistance HepG2 cells. However, efficient identification of the new antidiabetic compounds has been lacking. OBJECTIVE: To develop a guided discovery strategy for new antidiabetic compounds from L. aggregate with activity labeled molecular networking (ALMN). METHODOLOGY: The constructed ALMN could clearly visualize the activities and the structure nodes, which can facilitate the annotation of the active candidates. RESULTS: Eight new sesquiterpenoids (1-8) were obtained from the roots of Lindera aggregate according to the ALMN workflow showed antidiabetic activity. As for the new compounds, 1 was characteristic of 15-nor-lindenane type, which was reported for the first time, 2 and 3 of aconitane type, 4 of germarane type, 5-8 of eudesmane type sesquiterpenes. CONCLUSION: As results indicated, all the eight compounds showed significant antidiabetic effects, which were consistent with the obtained activity annotations by ALMN. The mechanism of the antidiabetic activity for 1-8 were further delved via Akt/GSK3β signal pathway, which can be observed as potential agents against the insulin resistance for the insulin resistance Type II diabetes.

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