Schalli Michael, Tysoe Christina, Fischer Roland, Pabst Bettina M, Thonhofer Martin, Paschke Eduard, Rappitsch Tanja, Stütz Arnold E, Tschernutter Marion, Windischhofer Werner, Withers Stephen G
Glycogroup, Institute of Organic Chemistry, Graz University of Technology, Stremayrgasse 9, A-8010, Graz, Austria.
Chemistry Department, University of British Columbia, 2036 Main Mall, Vancouver, BC, V6T 1Z1, Canada.
Carbohydr Res. 2017 Apr 18;443-444:15-22. doi: 10.1016/j.carres.2017.03.009. Epub 2017 Mar 11.
From 1,2;3,4-di-O-isopropylidene-α-D-galactopyranose, a series of highly functionalized (hydroxymethyl)cyclopentanes was easily available. In line with reports by Reymond and Jäger on similar structures, these amine containing basic carbasugars are potent inhibitors of β-D-galactosidases and, for the first time, could be shown to act as pharmacological chaperones for G-gangliosidosis-associated lysosomal acid β-galactosidase mutant R201C, thus representing a new structural type of pharmacological chaperones for this lysosomal storage disease.
从1,2;3,4-二-O-异亚丙基-α-D-吡喃半乳糖可以很容易地得到一系列高度官能化的(羟甲基)环戊烷。与雷蒙德和耶格尔关于类似结构的报道一致,这些含胺的碱性碳环糖是β-D-半乳糖苷酶的有效抑制剂,并且首次被证明可作为与G-神经节苷脂病相关的溶酶体酸性β-半乳糖苷酶突变体R201C的药理伴侣,因此代表了这种溶酶体贮积病的一种新型药理伴侣结构类型。