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Syntheses and Biological Activity of Some Derivatives of C-9154 Antibiotic

机译:C-9154抗生素某些衍生物的合成及生物活性

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This research was undertaken to design several new antibiotics, by structurally modifying the C-9154 antibiotic, simultaneously improving its activity and lowering toxicity. This was achieved by synthesizing an analogue to the C-9154 antibiotic and seven derivatives of this analogue. The approach was to significantly reduce the polarity of the synthesized analogue in the derivatives to achieve increased permeability across cell membranes by conversion of the highly polar carboxylic group to an ester functional group. The compounds were fully characterized using infrared, GC-MS, and 1D and 2D NMR experiments. Thein vitrobiological activity of the compounds showed that the derivatives were more active than the analogue as was anticipated and both were more active than the standard drugs used for comparison. Work is ongoing to establish applications for the compounds as antiplasmodials, antivirals, anticancers/tumours, antitrypanosomiasis, anthelminthic, and as general antibiotics for human, veterinary, and even agricultural use as they had marked effect on both Gram-positive and Gram-negative bacteria and some fungi.
机译:通过结构上修饰C-9154抗生素,同时提高其活性和降低毒性,进行了几种新型抗生素的设计研究。这是通过合成C-9154抗生素的类似物和该类似物的七种衍生物来实现的。该方法是显着降低衍生物中合成类似物的极性,以通过将高极性羧基转化为酯官能团来提高细胞膜的通透性。使用红外,GC-MS以及1D和2D NMR实验对化合物进行了全面表征。该化合物的体外生物学活性表明,该衍生物比预期的类似物具有更高的活性,并且两者均比用于比较的标准药物更具活性。目前正在努力开发该化合物的应用,如抗疟原虫,抗病毒药,抗癌药/肿瘤,抗锥虫病,驱虫药,以及作为人类,兽医乃至农业用途的通用抗生素,因为它们对革兰氏阳性和革兰氏阴性细菌均具有显著作用和一些真菌。

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