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Synthesis and biological evaluation of nojirimycin- and pyrrolidine-based trehalase inhibitors

机译:诺奇霉素和吡咯烷类海藻糖酶抑制剂的合成和生物学评估

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摘要

A small set of nojirimycin- and pyrrolidine-based iminosugar derivatives has been synthesized and evaluated as potential inhibitors of porcine and insect trehalases. Compounds 12, 13 and 20 proved to be active against both insect and porcine trehalases with selectivity towards the insect glycosidase, while compounds 10, 14 and 16 behaved as inhibitors only of insect trehalase. Despite the fact that the activity was found in the micromolar range, these findings may help in elucidating the structural features of this class of enzymes of different origin, which are still scarcely characterised.
机译:已经合成了少量的基于诺奇霉素和吡咯烷的亚氨基糖衍生物,并评估了它们是猪和昆虫海藻糖酶的潜在抑制剂。化合物12、13和20证明对昆虫和猪海藻糖酶均具有活性,并且对昆虫糖苷酶具有选择性,而化合物10、14和16仅充当昆虫海藻糖酶的抑制剂。尽管发现了在微摩尔范围内的活性,但这些发现可能有助于阐明这一类来源不同的酶的结构特征,这些特征仍很少被表征。

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