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Racemic and optically active 2-methoxy-4-oxatetradecanoic acids: novel synthetic fatty acids with selective antifungal properties

机译:外消旋和旋光的2-甲氧基-4-草酸酯二磺酸:具有选择性抗真菌特性的新型合成脂肪酸

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摘要

The unprecedented (+/-)-2-methoxy-4-oxatetradecanoic acid and the optically pure (S)-2-methoxy-4-oxatetradecanoic acid were synthesized in six steps and in 11-14% overall yields starting with either 1,2-O-isopropylidene-rac-glyceroI or 1,2-O-isopropylidene-(S)-glycerol. The key step in the synthesis was the selective monosilylation of a dibutylstannylene intermediate. The title compounds displayed selective fungitoxicity in the range of 0.08-0.22 mM against Cryptococcus neoformans ATCC 66031 and Aspergillus niger ATCC 16404, but no significant activity against C. albicans ATCC 14053 and ATCC 60193 (> 2.6 mM). Albeit being good substrates for N-myristoyltransferases (NMTs), the racemic and the S-enantiomer of the oxygenated 2-methoxylated compounds showed no significant difference in antifungal activity. This finding suggests an alternative mechanism of fungitoxicity other than NMT inhibition. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
机译:前所未有的(+/-)-2-甲氧基-4-草酸酯双磺酸和光学纯的(S)-2-甲氧基-4-草酸酯双硬酸通过六个步骤合成,总收率从11或1开始, 2-O-异亚丙基-rac-甘油或1,2-O-异亚丙基-(S)-甘油。合成中的关键步骤是二丁基亚锡中间体的选择性单硅烷化。标题化合物对新型隐球菌ATCC 66031和黑曲霉ATCC 16404表现出0.08-0.22 mM的选择性真菌毒性,但对白色念珠菌ATCC 14053和ATCC 60193没有显着活性(> 2.6 mM)。尽管是N-肉豆蔻酰基转移酶(NMT)的良好底物,但氧化的2-甲氧基化化合物的外消旋和S-对映异构体在抗真菌活性方面没有显着差异。这一发现提示了除NMT抑制外的另一种真菌毒性机制。 (c)2005 Elsevier Ireland Ltd.保留所有权利。

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