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1D-和1L-1,2-脱水肌醇的新合成方法及其糖苷酶抑制活性评估。

New syntheses of 1D- and 1L-1,2-anhydro-myo-inositol and assessment of their glycosidase inhibitory activities.

作者信息

Falshaw A, Hart J B, Tyler P C

机构信息

Industrial Research Ltd., Lower Hutt, New Zealand.

出版信息

Carbohydr Res. 2000 Nov 3;329(2):301-8. doi: 10.1016/s0008-6215(00)00192-0.

Abstract

The 1D and 1L enantiomers of 1,2-anhydro-myo-inositol (conduritol B epoxide) were synthesised from 1D-pinitol and 1L-quebrachitol, respectively, and their activities were compared in selected glycosidase inhibition assays. The 1D enantiomer was found to be the active isomer, functioning as an irreversible inhibitor of sweet almond beta-D-glucosidase. Neither isomer was active against the alpha-D-glucosidase from Bacillus stearothermophilus or the beta-D-galactosidase from Aspergillus oryzae.

摘要

分别从1D-松醇和1L-克氏假吐叶醇合成了1,2-脱水肌醇(壳二孢醇环氧化物)的1D和1L对映体,并在选定的糖苷酶抑制试验中比较了它们的活性。发现1D对映体是活性异构体,可作为甜杏仁β-D-葡萄糖苷酶的不可逆抑制剂。两种异构体对嗜热脂肪芽孢杆菌的α-D-葡萄糖苷酶或米曲霉的β-D-半乳糖苷酶均无活性。

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