New Serratane Triterpenoid and Musashi2 inhibitors from Huperzia serrata.

IF 2.1 4区 医学 Q3 CHEMISTRY, MEDICINAL
Planta medica Pub Date : 2026-07-06 DOI:10.1055/a-2900-3049
Tamara Balsiger, Malik Rakhmanov, Alessandro Prescimone, Annalena Kaiser, Kim-Dung Huynh, Andreas Papassotiropoulos, Robin Teufel, Attila Stetak, Eliane Garo
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Abstract

Abstract: Forgetting and memory formation are 2 distinct processes, both essential for the survival of humans and other animals. The protein Musashi2 (MSI2) was recently discovered as a key regulator of forgetting in the model organism Caenorhabditis elegans, making it an attractive therapeutic target for drug discovery and development.

Abstract: Here, we report a fluorescence polarization assay-based screening campaign aimed at identifying MSI2 inhibitors from 2,844 plant extracts. The dichloromethane extract of the aerial parts of Huperzia serrata, a plant traditionally used in Chinese medicine for the treatment of memory dysfunction, was identified as a hit and subsequently subjected to HPLC-based activity profiling. Scale-up isolation identified fatty acids, namely linoleic acid (11: ) and palmitoleic acid (12: ), both eluting within the main active window. As other fractions also seem to display activity, although weaker, their minor constituents were also investigated, revealing 1 new serratane triterpenoid (1: ) and 7 known serratene triterpenoids 2: -8: , their biosynthetic precursor α-onocerin (9: ), as well as an abietane diterpene (10: ). The absolute configuration of compound 1: was established by X-ray crystallography. All isolated compounds were evaluated for their activity, revealing that linoleic acid (11: ) and palmitoleic acid (12: ) inhibited MSI2 with IC50 values of 14.6 and 23.1 µM, respectively, while compound 10: only showed moderate activity (IC50 of 34.4 µM).

新Serratane三萜和Musashi2抑制剂。
摘要:遗忘和记忆形成是两个截然不同的过程,对人类和其他动物的生存都至关重要。蛋白Musashi2 (MSI2)最近被发现是模式生物秀丽隐杆线虫中遗忘的关键调节因子,使其成为药物发现和开发的一个有吸引力的治疗靶点。摘要:本文报道了一项基于荧光偏振分析的筛选活动,旨在从2,844种植物提取物中鉴定MSI2抑制剂。胡柏属(Huperzia serrata)是一种传统中药用于治疗记忆功能障碍的植物,其地上部分的二氯甲烷提取物被确定为一种打击,随后进行了基于高效液相色谱(hplc)的活性分析。放大分离鉴定出脂肪酸,即亚油酸(11%)和棕榈油酸(12%),两者都在主活性窗口内洗脱。由于其他部分似乎也显示出活性,虽然较弱,它们的次要成分也进行了研究,揭示了1个新的serratene三萜(1:)和7个已知的serratene三萜(2:-8:),它们的生物合成前体α-onocerin(9:),以及abietane二萜(10:)。用x射线晶体学方法确定了化合物1的绝对构型。结果表明,亚油酸(11∶)和棕榈油酸(12∶)抑制MSI2的IC50值分别为14.6和23.1µM,而化合物10∶仅具有中等活性(IC50值为34.4µM)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Planta medica
Planta medica 医学-药学
CiteScore
5.10
自引率
3.70%
发文量
101
审稿时长
1.8 months
期刊介绍: Planta Medica is one of the leading international journals in the field of natural products – including marine organisms, fungi as well as micro-organisms – and medicinal plants. Planta Medica accepts original research papers, reviews, minireviews and perspectives from researchers worldwide. The journal publishes 18 issues per year. The following areas of medicinal plants and natural product research are covered: -Biological and Pharmacological Activities -Natural Product Chemistry & Analytical Studies -Pharmacokinetic Investigations -Formulation and Delivery Systems of Natural Products. The journal explicitly encourages the submission of chemically characterized extracts.
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