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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Fluorine-substituted tetracationic ABAB-phthalocyanines for efficient photodynamic inactivation of Gram-positive and Gram-negative bacteria
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Fluorine-substituted tetracationic ABAB-phthalocyanines for efficient photodynamic inactivation of Gram-positive and Gram-negative bacteria

机译:氟取代的曲邻酞菁,用于高效的光动力灭活革兰氏阳性和革兰氏阴性细菌

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Herein, we report the synthesis and characterization of new amphiphilic phthalocyanines (Pcs), the study of their singlet oxygen generation capabilities, and biological assays to determine their potential as photosensitizers for photodynamic inactivation of bacteria. In particular, Pcs with an ARAB geometry (where A and B refer to differently substituted isoindole constituents) have been synthesized. These molecules are endowed with bulky bis(trifiuoromethylphenyl) groups in two facing isoindoles, which hinder aggregation and favour singlet oxygen generation, and pyridinium or alkylammonium moieties in the other two isoindoles. In particular, two water-soluble Pc derivatives (PS-1 and PS-2) have proved to be efficient in the photoinactivation of S. aureus and E. coli, selected as models of Gram-positive and Gram-negative bacteria. (C) 2019 Published by Elsevier Masson SAS.
机译:在此,我们报告了新的两亲性酞菁(PC)的合成和表征,它们的单线磷生成能力的研究以及生物学测定,以确定其作为光敏性灭活细菌的光敏剂的潜力。 特别地,已经合成了具有阿拉伯几何形状的PC(其中A和B参考不同取代的异吲哚成分)。 这些分子在两种面对的异吲哚中赋予庞大的双(三氟甲基苯基)基团,其在其他两种异吲哚中妨碍聚集并致力于吡啶鎓或烷基铵部分。 特别地,已经证明,两种水溶性的PC衍生物(PS-1和PS-2)在S. aureus和大肠杆菌的光灭绝中有效,被选为革兰氏阳性和革兰氏阴性细菌的模型。 (c)2019年由Elsevier Masson SA发布。

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