Anti-invasive and cytotoxic evaluation of a (+)-pinoresinol-based semisynthetic library against glioblastoma.

IF 2.7 4区 化学 Q2 CHEMISTRY, ORGANIC
Beilstein Journal of Organic Chemistry Pub Date : 2026-05-11 eCollection Date: 2026-01-01 DOI:10.3762/bjoc.22.54
Chen Zhang, Kah Yean Lum, Jonathan M White, Paul I Forster, Nicholas Booth, Sunita A Ramesh, Rohan A Davis
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引用次数: 0

Abstract

The Australian endemic plant genus Eremophila has long been recognized for its unique chemical diversity, with numerous novel and bioactive compounds reported. In this study, we chemically investigated the seeds of Eremophila maculata for the first time, which led to the isolation and characterization of two known plant metabolites, (+)-salicifoliol and (+)-pinoresinol. Due to the reported biological properties of the lignan natural product (+)-pinoresinol and its high abundance from the seeds of E. maculata, we synthesized five analogues for biological evaluations. Preliminary cytotoxicity evaluations of the semisynthetic pinoresinol-based library against two human glioblastoma cell lines, U251MG and KNS42, showed (+)-4,4'-di(3,3-dimethylbutanoyl)pinoresinol had slight cytotoxicity at 10 µM. A transwell anti-invasive assay on the same compound showed a reduction in the invasion of adult U251MG cells by 50% and pediatric KNS42 cells by 30%, with IC50 values of 0.26 and 0.40 µM, respectively.

(+)-松脂醇基半合成文库抗胶质母细胞瘤侵袭性及细胞毒性评价。
澳大利亚特有植物Eremophila因其独特的化学多样性而长期受到认可,报道了许多新的生物活性化合物。在这项研究中,我们首次对Eremophila maculata的种子进行化学研究,从而分离和鉴定了两种已知的植物代谢产物,(+)-水杨酸油醇和(+)-松脂醇。由于木脂素天然产物(+)-松脂醇的生物学特性和其在黄斑藤种子中的高丰度,我们合成了五个类似物进行生物学评价。半合成松脂醇文库对两种人胶质母细胞瘤细胞系U251MG和KNS42的细胞毒性初步评价显示,(+)-4,4′-二(3,3-二甲基丁醇)松脂醇在10µM时具有轻微的细胞毒性。transwell抗侵袭实验显示,该化合物对成人U251MG细胞的侵袭减少了50%,对儿童KNS42细胞的侵袭减少了30%,IC50值分别为0.26和0.40µM。
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来源期刊
CiteScore
4.90
自引率
3.70%
发文量
167
审稿时长
1.4 months
期刊介绍: The Beilstein Journal of Organic Chemistry is an international, peer-reviewed, Open Access journal. It provides a unique platform for rapid publication without any charges (free for author and reader) – Platinum Open Access. The content is freely accessible 365 days a year to any user worldwide. Articles are available online immediately upon publication and are publicly archived in all major repositories. In addition, it provides a platform for publishing thematic issues (theme-based collections of articles) on topical issues in organic chemistry. The journal publishes high quality research and reviews in all areas of organic chemistry, including organic synthesis, organic reactions, natural product chemistry, structural investigations, supramolecular chemistry and chemical biology.
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