化学
烷基
抗菌剂
立体化学
糖苷水解酶
内酰胺
组合化学
有机化学
水解
作者
Óscar López,Emil Lindbäck,Monika Moreń,Ana Laura Pereira Lourenço,Marta Cerdà‐Cuéllar,Karl Kochanowski,Kåre B. Jørgensen,Magne O. Sydnes
出处
期刊:Synthesis
[Georg Thieme Verlag KG]
日期:2024-10-22
标识
DOI:10.1055/s-0043-1773494
摘要
Abstract A series of six N-alkyl isofagomine lactam derivatives is synthesized over ten steps from d-arabinose. The compounds are evaluated as glycosidase inhibitors. It was found that the N-alkyl groups have a detrimental effect on the glycosidase inhibition activities, as the prepared N-alkyl isofagomine lactam derivatives are much less potent glycosidase inhibitors than native isofagomine lactam.
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