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Selected Compounds Structurally Related to Acyclic Sesquiterpenoids and Their Antibacterial and Cytotoxic Activity

机译:结构上与无环倍半萜类化合物及其抗菌和细胞毒活性相关的选定化合物

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摘要

By implementing a common and industrially used method, 30 compounds which are structurally related to geranyl acetone, nerolidol, farnesal, farnesol and farnesyl acetate were obtained. Their antimicrobial activity against Staphylococcus aureus, Enterococcus faecalis, Enterococcus faecium, Escherichia coli, Klebsiella pneumoniae and Acinetobacter baumannii bacteria was investigated. Pharmacophore models were proposed based on the obtained results and 3D QSAR modelling. Cytotoxic effects against mainly human immortalised and normal cell lines of different origin (malignant melanoma MeWo, colorectal adenocarcinoma HT29, promyelocytic leukemia HL60, gingival fibroblasts HFIG, skin keratinocytes HaCaT and rat small intestine epithelium IEC6) were examined. The odour descriptions of newly synthesised compounds are given.
机译:通过实施工业上常用的方法,获得了30种在结构上与香叶基丙酮,橙花醇,法呢醛,法呢醇和乙酸法呢酯相关的化合物。研究了它们对金黄色葡萄球菌,粪肠球菌,粪便肠球菌,大肠杆菌,肺炎克雷伯菌和鲍曼不动杆菌的抗菌活性。基于获得的结果和3D QSAR建模,提出了药效学模型。研究了对不同来源的主要人类永生和正常细胞系(恶性黑色素瘤MeWo,结肠直肠腺癌HT29,早幼粒细胞白血病HL60,牙龈成纤维细胞HFIG,皮肤角质形成细胞HaCaT和大鼠小肠上皮细胞IEC6)的细胞毒性作用。给出了新合成化合物的气味描述。

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