Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic v.v.i., Flemingovo nám. 2, 166 10 Prague 6, Czech Republic.
J Med Chem. 2011 Nov 24;54(22):7884-98. doi: 10.1021/jm2009343. Epub 2011 Nov 1.
Novel compounds termed lipophosphonoxins were prepared using a simple and efficient synthetic approach. The general structure of lipophosphonoxins consists of four modules: (i) a nucleoside module, (ii) an iminosugar module, (iii) a hydrophobic module (lipophilic alkyl chain), and (iv) a phosphonate linker module that holds together modules i-iii. Lipophosphonoxins displayed significant antibacterial properties against a panel of Gram-positive species, including multiresistant strains. The minimum inhibitory concentration (MIC) values of the best inhibitors were in the 1-12 μg/mL range, while their cytotoxic concentrations against human cell lines were significantly above this range. The modular nature of this artificial scaffold offers a large number of possibilities for further modifications/exploitation of these compounds.
新型化合物被称为脂磷酰胺,采用简单有效的合成方法制备。脂磷酰胺的一般结构由四个模块组成:(i)核苷模块,(ii)亚氨基糖模块,(iii)疏水模块(亲脂性烷基链)和(iv)将模块 i-iii 连接在一起的膦酸酯连接模块。脂磷酰胺对一系列革兰氏阳性物种表现出显著的抗菌特性,包括多耐药菌株。最佳抑制剂的最小抑菌浓度(MIC)值在 1-12μg/mL 范围内,而它们对人细胞系的细胞毒性浓度明显高于该范围。这种人工支架的模块性质为进一步修饰/利用这些化合物提供了大量可能性。