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gem-diamine 1-N-iminosugars of L-fucose-type, the extremely potent L-fucosidase inhibitors.

机译:L-岩藻糖型的宝石二胺1-N-亚氨基糖,一种非常有效的L-岩藻糖苷酶抑制剂。

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摘要

An efficient route from D-ribono-gamma-lactone to gem-diamine 1-N-iminosugars of L-fucose-type, a new family of glycosidase inhibitor, has been developed in a formation of a gem-diamine 1-N-iminopyranose ring by the Mitsunobu reaction of an aminal as a key step. The analogues were proved to be the extremely potent inhibitors against alpha-L-fucosidase (IC50 approximately 3 ng mL(-1), Ki approximately 5 x 10(-9) M). The present study has shown that a cyclic methanediamine generated in media affects glycosidases as a real active-form of the gem-diamine 1-N-iminosugars of L-fucose-type.
机译:从D-核糖体-γ-内酯到L-岩藻糖型的宝石二胺1-N-亚氨基糖的新途径,这是一种有效的途径,这是一种宝石二胺1-N-亚氨基吡喃糖的形成。作为关键步骤,通过氨基的Mitsunobu反应产生环。事实证明,这些类似物是针对α-L-岩藻糖苷酶的极强抑制剂(IC50约为3 ng mL(-1),Ki约为5 x 10(-9)M)。本研究表明,在培养基中产生的环状甲烷二胺会影响糖苷酶,这是L-岩藻糖型宝石二胺1-N-亚氨基糖的真正活性形式。

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