血清白蛋白与降血糖药物相互作用的关键位点分析

用生物信息学的方法分析不同物种的血清白蛋白的亲缘关系,分析降血糖药物米格列醇和伏格列波糖与人血清白蛋白相互作用位点在其他亲缘关系较近的物种中相应的氨基酸变化特点。结果表明米格列醇、伏格列波糖与人血清白蛋白的结合位点都位于人血清白蛋白亚区IB的疏水腔中,其间的主要作用力是氢键和疏水作用力。米格列醇和伏格列波糖与血清白蛋白结合位点处的氨基酸在其他物种中大部分都是保守的,只有少数的氨基酸不同,且极性也不相同。血清白蛋白疏水性分析发现米格列醇和伏格列波糖与血清白蛋白结合位点处的氨基酸中亲水性的较多,疏水性的少,在其他4个亲缘关系较近的物种也具有同样的现象。这些分析结果为进一步研究降血糖药物在其他物种中的表现及相互作用等提供了重要的科学依据。     

Determination of the structures of four new isomeric cyclitols

A series of impurities, which were all of the same molecular formula, C17H33NO7, were obtained in the process of voglibose synthesis. After isolation and purification, four isomeric cyclitols were completely assigned by 2D NMR experiments. One of the compounds was established by single-crystal X-ray diffraction analysis as 5,6-dideoxy-5-{[2-hydroxy-1-(hydroxymethyl)ethyl]amino}-1-C-(methoxycyclohexylmethyl)-D-epi-inositol.