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4,4'-(α,ω-聚亚甲基二硫)双(1-烷基碘化吡啶鎓)的合成及抗菌特性

Synthesis and antimicrobial characteristics of 4,4'-(alpha,omega-polymethylenedithio)bis(1-alkylpyridinium iodide)s.

作者信息

Okazaki K, Maeda T, Nagamune H, Manabe Y, Kourai H

机构信息

Faculty of Human Life Science, Shikoku University, Tokushima, Japan.

出版信息

Chem Pharm Bull (Tokyo). 1997 Dec;45(12):1970-4. doi: 10.1248/cpb.45.1970.

Abstract

Bis-quaternary ammonium compounds (bis-QACs), 4,4'-(alpha,omega-polymethylenedithio)bis(1-alkylpyridinium iodide)s (4DTBP-m,n), which have 3 to 10 carbon atoms in the connecting methylene chain (m) and 8 to 18 carbon atoms of the N-alkyl chain (n), were synthesized. 4DTBP-6,12 exhibited a wide antimicrobial spectrum against gram-positive and gram-negative bacteria and fungi. The activity was stronger than those of N-dodecylpyridinium iodide (P-12), benzyldodecyldimethylammonium chloride and 2-(4-thiazolyl)benzimidazole. The bactericidal activities of 4DTBP-m,n were scarcely affected by the lengths of the alkyl chain and methylene chain. The bis-QAC that showed the highest activity was 4DTBP-6,8 (minimum inhibitory concentration (MIC) = 1.6 microM, minimum bactericidal concentration (MBC) = 2.6 microM), and its activity was about 10 times that of N-hexadecylpyridinium iodide (P-16), which was the most active in the P-n series. In addition, 4DTBP-6,12 showed a high bactericidal activity in the ranges of pH 5 to 8.5 and 10 to 40 degrees C, in contrast to mono-QACs. The bis-QACs synthesized in this study have excellent bactericidal properties.

摘要

合成了双季铵化合物(双季铵盐),即4,4'-(α,ω-聚亚甲基二硫)双(1-烷基碘化吡啶)(4DTBP-m,n),其连接亚甲基链(m)中含有3至10个碳原子,N-烷基链(n)中含有8至18个碳原子。4DTBP-6,12对革兰氏阳性菌、革兰氏阴性菌和真菌具有广泛的抗菌谱。其活性强于碘化N-十二烷基吡啶(P-12)、苄基十二烷基二甲基氯化铵和2-(4-噻唑基)苯并咪唑。4DTBP-m,n的杀菌活性几乎不受烷基链和亚甲基链长度的影响。活性最高的双季铵盐是4DTBP-6,8(最小抑菌浓度(MIC)=1.6 microM,最小杀菌浓度(MBC)=2.6 microM),其活性约为P-n系列中活性最高的碘化N-十六烷基吡啶(P-16)的10倍。此外,与单季铵盐相比,4DTBP-6,12在pH 5至8.5和10至40℃范围内表现出高杀菌活性。本研究中合成的双季铵盐具有优异的杀菌性能。

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