Ivković Ivana, Novaković Miroslav, Veljić Milan, Mojsin Marija, Stevanović Milena, Marin Petar D, Bukvički Danka
Institute of Botany and Botanical Garden "Jevremovac", Faculty of Biology, University of Belgrade, 11000 Begrade, Serbia.
Department of Chemistry, Institute of Chemistry, Technology and Metallurgy, University of Belgrade, 11000 Belgrade, Serbia.
Plants (Basel). 2021 May 26;10(6):1063. doi: 10.3390/plants10061063.
Based on previous investigations where bis-bibenzyls isolated from liverworts showed various biological activities (cytotoxic, antimicrobial, and antiviral), we investigated their cytotoxic activity in several human cancer cell lines. From the methylene-chloride/methanol extract of the liverwort , three bis-bibenzyls of the perrottetin type were isolated, namely perrottetin E, 10'-hydroxyperrottetin E, and 10,10'-dihydroxyperrottetin E. The last two were found for the first time in this species. Their structures were resolved using 1D and 2D NMR, as well as by comparison with data in the literature. Cytotoxic activity of the isolated compounds was tested on three human leukemia cell lines, HL-60 (acute promyelocytic leukemia cells), U-937 (acute monocytic leukemia cells), and K-562 (human chronic myelogenous leukemia cells), as well as on human embryonal teratocarcinoma cell line (NT2/D1) and human glioblastoma cell lines A-172 and U-251, and compared to the previously isolated bis-bibenzyls (perrottetins) of similar structure. The isolated compounds exhibited modest activity against leukemia cells and significant activity against NT2/D1 and A-172. Overall, the most active cytotoxic compounds in this investigation were perrottetin E (1), isolated in this work from , and perrottetin F phenanthrene derivative (7), previously isolated from and added for a comparison of their cytotoxic activity.
基于之前的研究,从地钱中分离出的双苄基化合物显示出多种生物活性(细胞毒性、抗菌和抗病毒活性),我们研究了它们在几种人类癌细胞系中的细胞毒性活性。从该种植物的二氯甲烷/甲醇提取物中,分离出了三种佩罗特汀型双苄基化合物,即佩罗特汀E、10'-羟基佩罗特汀E和10,10'-二羟基佩罗特汀E。后两种是首次在该物种中发现。它们的结构通过一维和二维核磁共振以及与文献数据比较得以解析。对分离得到的化合物在三种人类白血病细胞系HL-60(急性早幼粒细胞白血病细胞)、U-937(急性单核细胞白血病细胞)和K-562(人类慢性粒细胞白血病细胞),以及人类胚胎性癌细胞系(NT2/D1)和人类胶质母细胞瘤细胞系A-172和U-251上测试了细胞毒性活性,并与之前分离得到的结构相似的双苄基化合物(佩罗特汀)进行了比较。分离得到的化合物对白血病细胞表现出适度活性,对NT2/D1和A-172表现出显著活性。总体而言,本研究中细胞毒性活性最强的化合物是本工作中从[具体来源未明确]分离得到的佩罗特汀E(1),以及之前从[具体来源未明确]分离得到并用于比较其细胞毒性活性的菲衍生物佩罗特汀F(7)。