Falshaw A, Hart J B, Tyler P C
Industrial Research Ltd., Lower Hutt, New Zealand.
Carbohydr Res. 2000 Nov 3;329(2):301-8. doi: 10.1016/s0008-6215(00)00192-0.
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.
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。