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Cytotoxic Aporphine Alkaloids from Leaves and Twigs of Pseuduvaria trimera (Craib)

机译:假单胞菌叶片和细枝的细胞毒性紫花碱生物碱(蟹)

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摘要

From ethyl acetate-methanol extracts of leaves and twigs of Pseuduvaria trimera a new aporphine alkaloid; 8-hydroxy-1,4,5-trimethoxy-7-oxoaporphine or 8-hydroxyartabonatine C (>1) was isolated, together with the known 1,2,3-trimethoxy-4,5-dioxo-6a,7-dehydroaporphine (ouregidione, >2). Their structures were elucidated by a combination of spectral methods; mainly 2D NMR; IR and MS. Compounds >1 and >2 exhibited cytotoxic activity with IC50 values of 26.36 ± 5.18 μM and 12.88 ± 2.49 μM, respectively, for human hepatocellular carcinoma HepG2 cells, and 64.75 ± 4.45 and 67.06 ± 3.5 μM, respectively, for human breast cancer MDA-MB231 cells. Both compounds displayed anti-cancer activity but less than that of doxorubicin; a conventional chemotherapeutic drug, the IC50 levels of which were 2.21 ± 1.72 and 1.83 ± 0.09 μM for HepG2 and MDA-MB231 cells, respectively.
机译:从三叶假单胞菌的叶和嫩枝的乙酸乙酯-甲醇提取物中提取一种新的阿芬吗啡生物碱;分离出8-羟基-1,4,5-三甲氧基-7-氧杂卟啉或8-羟基青蒿素C(> 1 ),以及已知的1,2,3-三甲氧基-4,5-二氧杂-6a,7-dehydroaporphine(ouregidione,> 2 )。结合光谱方法阐明了它们的结构。主要是2D NMR;红外和质谱。化合物> 1 和> 2 表现出细胞毒活性,对人肝癌HepG2细胞的IC50值分别为26.36±5.18μM和12.88±2.49μM,以及64.75±4.45和67.06对于人乳腺癌MDA-MB231细胞,分别为±3.5μM。两种化合物均显示出抗癌活性,但低于阿霉素。常规化疗药物,HepG2细胞和MDA-MB231细胞的IC50水平分别为2.21±1.72和1.83±0.09μM。

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