Design, synthesis and antitumor activity of pentacyclic triterpenoid ursolic acid derivatives and oleanolic acid derivatives based on multi-target

IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED Journal of Asian Natural Products Research Pub Date : 2025-10-03 DOI:10.1080/10286020.2025.2473635
Jun-Jiao Ma , Liang-Feng Zhang , Dong-Ping Xu , Zan Wang , Yan-Qiu Meng
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Abstract

Totally twelve inhibitors of Survivin and Sp1 based on ursolic acid (UA) derivatives and oleanolic acid (OA) derivatives were designed and synthesized with modification at C-2, C-3 and C-28 of UA and OA. Their structures were confirmed by HRMS,1H NMR and 13C NMR. In vitro activity assay showed that these compounds can inhibit cell proliferation of HeLa, SKOV3, BGC-823 and HT1080 cells, especially compounds IV and X showed better inhibitory activity on these tumor cells than that of the positive control drug Gefitinib and similar to Vp-16. Mechanistically, selected compound may inhibit the proliferation of SKOV3 cells and trigger apoptosis by activating Sp1 to inhibit Survivin protein expression, which may be promising leading compounds for cancer therapy.
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基于多靶点的五环三萜熊果酸衍生物和齐墩果酸衍生物的设计、合成及其抗肿瘤活性。
以熊果酸(UA)衍生物和齐墩果酸(OA)衍生物为基础,分别在UA和OA的C-2、C-3和C-28位点进行修饰,设计合成了12种Survivin和Sp1抑制剂。它们的结构经HRMS、1H NMR和13C NMR确证。体外活性测定表明,这些化合物均能抑制HeLa、SKOV3、BGC-823和HT1080细胞的增殖,特别是化合物IV和X对这些肿瘤细胞的抑制活性优于阳性对照药物吉非替尼,且与Vp-16相似。从机制上讲,所选化合物可能通过激活Sp1抑制Survivin蛋白表达,抑制SKOV3细胞的增殖并引发细胞凋亡,这可能是有希望用于癌症治疗的先导化合物。
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来源期刊
CiteScore
3.20
自引率
5.90%
发文量
47
审稿时长
2.3 months
期刊介绍: The Journal of Asian Natural Products Research (JANPR) publishes chemical and pharmaceutical studies in the English language in the field of natural product research on Asian ethnic medicine. The journal publishes work from scientists in Asian countries, e.g. China, Japan, Korea and India, including contributions from other countries concerning natural products of Asia. The journal is chemistry-orientated. Major fields covered are: isolation and structural elucidation of natural constituents (including those for non-medical uses), synthesis and transformation (including biosynthesis and biotransformation) of natural products, pharmacognosy, and allied topics. Biological evaluation of crude extracts are acceptable only as supporting data for pure isolates with well-characterized structures. All published research articles in this journal have undergone rigorous peer review, based on initial editor screening and anonymized refereeing by at least two expert referees.
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