来自 Glycosmis lanceolata (Blume) D.Dietr. 的三种新的吖啶酮生物碱及其对肿瘤细胞系的细胞毒性作用。

IF 1.6 3区化学 Q3 CHEMISTRY, APPLIED

Natural Product Research Pub Date : 2025-07-03 DOI:10.1080/14786419.2024.2306175

Chihiro Ito , Takuya Matsui , Ami Sato , Nisjiri Ruangrungsi , Masataka Itoigawa

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引用次数: 0

摘要

我们从泰国采集的 Glycosmis lanceolata (Blume) D.Dietr. 树枝的丙酮提取物中分离并阐明了三种新的吖啶酮生物碱（glycomontamine A (1)、B (2)和 C (3)）以及三种已知化合物（glycofoline、kokusaginine 和 dictamnine）。用人肺腺癌细胞株 A549、乳腺癌细胞株 T47D、宫颈上皮样癌细胞株 Hela、急性淋巴性白血病 B 细胞株 NALM-6 和人真皮成纤维细胞对这些化合物进行了细胞活力检测。用化合物 1 处理过的 Hela 细胞（IC50 值为 17.6 μM）和用化合物 2 处理过的 T47D 细胞（IC50 值为 17.4 μM）的存活率呈剂量依赖性下降。这两种化合物对 NALM-6 细胞也有细胞毒性（IC50 分别为 16.5 和 9.3 μM）。此外，化合物 1 会降低 Hela 细胞的线粒体膜电位，而化合物 2 则不会改变 T47D 细胞的线粒体膜电位。

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Three new acridone alkaloids from Glycosmis lanceolata (Blume) D.Dietr. and their cytotoxic effects on tumour cell lines

We separated and structurally elucidated three new acridone alkaloids (glycomontamine A (1), B (2), and C (3)), together with three known compounds (glycofoline, kokusaginine and dictamnine) from the acetone extract of Glycosmis lanceolata (Blume) D.Dietr. branches collected in Thailand. The compounds were assayed for cell viability using human lung adenocarcinoma cell line A549, breast adenocarcinoma cell line T47D, cervix epithelioid carcinoma cell line Hela, acute lymphoid leukaemia B cell line NALM-6, and human dermal fibroblasts. The viability of Hela cells treated with compound 1 (IC₅₀ 17.6 μM) and T47D cells treated with compound 2 (IC₅₀ 17.4 μM) decreased dose-dependently. Both compounds also showed cytotoxicity against NALM-6 cells (IC₅₀ 16.5 and 9.3 μM). Additionally, compound 1 decreased the mitochondrial membrane potential of Hela cells, whereas compound 2 did not change the mitochondrial membrane potential in T47D cells.

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来源期刊

Natural Product Research 化学-医药化学

CiteScore

5.10

自引率

9.10%

发文量

605

审稿时长

2.1 months

期刊介绍： The aim of Natural Product Research is to publish important contributions in the field of natural product chemistry. The journal covers all aspects of research in the chemistry and biochemistry of naturally occurring compounds. The communications include coverage of work on natural substances of land and sea and of plants, microbes and animals. Discussions of structure elucidation, synthesis and experimental biosynthesis of natural products as well as developments of methods in these areas are welcomed in the journal. Finally, research papers in fields on the chemistry-biology boundary, eg. fermentation chemistry, plant tissue culture investigations etc., are accepted into the journal. Natural Product Research issues will be subtitled either ""Part A - Synthesis and Structure"" or ""Part B - Bioactive Natural Products"". for details on this , see the forthcoming articles section. All manuscript submissions are subject to initial appraisal by the Editor, and, if found suitable for further consideration, to peer review by independent, anonymous expert referees. All peer review is single blind and submission is online via ScholarOne Manuscripts.