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Cytotoxic activity of acyl phloroglucinols isolated from the leaves of Eucalyptus cinerea F. Muell. ex Benth. cultivated in Egypt

机译:从灰桉桉叶片分离的酰基间苯三酚的细胞毒活性。前Benth。在埃及种植

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摘要

Two acyl phloroglucinol compounds namely; Sideroxylonal B (1) and Macrocarpal A (2) were isolated from the Sideroxylonal-Rich Extract (SRE) of the juvenile leaves of Eucalyptus cinerea; F. Muell. ex Benth cultivated in Egypt. Identification of the isolated compounds was established on the basis of physico-chemical properties and spectral analysis (1D & 2D NMR). The two compounds were isolated for the first time from this species. The SRE alongside with the isolated compounds were tested against three human cancer cell lines; MCF7 (breast carcinoma cell line), HEP2 (laryngeal carcinoma), CaCo (colonic adenocarcinoma) and one type of normal human cell line;10 FS (fibroblast cells). The SRE, (1), and (2) showed cytotoxic activity with IC50 13.6 ± 0.62, 7.2 ± 0.5, 14.8 ± 0.55 μg mL−1 against HEP2 respectively, 11.6 ± 0.47, 4 ± 0.36, 11.4 ± 0.45 μg mL−1 against CaCo, respectively, and 8.6 ± 0.29, 4.4 ± 0.25, and 7.8 ± 0.3 μg mL−1 against MCF7, respectively. Meanwhile, the (SRE) together with (1) and (2) exhibited low cytotoxicity against normal cell line 10 FS, with IC50 55.4 ± 1.4, 43 ± 0.8 and 50.1 ± 1.12 μg mL−1, respectively. The antiprofilerative activity of the tested compounds was evaluated. The cell cycle profile of cells treated with Sideroxylonal-B and Macrocarpal-A indicates possible S-phase specific effects.
机译:两种酰基间苯三酚化合物分别为:从桉树幼叶的富含Sideroxylonal的提取物(SRE)中分离出Sideroxylonal B(1)和Macrocarpal A(2)。 F.穆埃尔。前Benth在埃及种植。根据理化性质和光谱分析(1D和2D NMR)确定分离出的化合物。首次从该物种中分离出两种化合物。 SRE与分离的化合物一起针对三种人类癌细胞系进行了测试。 MCF7(乳腺癌细胞系),HEP2(喉癌),CaCo(结肠腺癌)和一种正常的人类细胞系; 10 FS(成纤维细胞)。 SRE,(1)和(2)显示出对HEP2的IC50分别为13.6±0.62、7.2±0.5、14.8±0.55μgmL-1、11.6±0.47、4±0.36、11.4±0.45μgmL-1的细胞毒性活性分别针对CaCo和MCF7分别为8.6±0.29、4.4±0.25和7.8±0.3μgmL-1。同时,(SRE)与(1)和(2)一起表现出对正常细胞系10 lowFS的低细胞毒性,IC50分别为55.4±1.4、43±0.8和50.1±1.12μgmL-1。评估了所测试化合物的抗轮廓活性。用Sideroxylonal-B和Macrocarpal-A处理的细胞的细胞周期概况表明可能存在S期特异性作用。

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