Park Hwangseo, Hwang Kyo Yeol, Kim Young Hoon, Oh Kyung Hwan, Lee Jae Yeon, Kim Keun
Department of Bioscience and Biotechnology, Sejong University, 98 Kunja-Dong, Kwangjin-Ku, Seoul 143-747, Republic of Korea.
Bioorg Med Chem Lett. 2008 Jul 1;18(13):3711-5. doi: 10.1016/j.bmcl.2008.05.056. Epub 2008 May 20.
Discovery of alpha-glucosidase inhibitors has been actively pursued with the aim to develop therapeutics for the treatment of diabetes and the other carbohydrate-mediated diseases. We have identified four novel alpha-glucosidase inhibitors by means of a drug design protocol involving the structure-based virtual screening under consideration of the effects of ligand solvation in the scoring function and in vitro enzyme assay. Because the newly identified inhibitors reveal in vivo antidiabetic activity as well as a significant potency with more than 70% inhibition of the catalytic activity of alpha-glucosidase at 50 microM, all of them seem to deserve further development to discover new drugs for diabetes. Structural features relevant to the interactions of the newly identified inhibitors with the active site residues of alpha-glucosidase are discussed in detail.
为了开发治疗糖尿病及其他碳水化合物介导疾病的疗法,人们一直在积极探索α-葡萄糖苷酶抑制剂。我们通过一种药物设计方案鉴定出了四种新型α-葡萄糖苷酶抑制剂,该方案涉及基于结构的虚拟筛选,并在评分函数中考虑了配体溶剂化的影响以及体外酶测定。由于新鉴定出的抑制剂显示出体内抗糖尿病活性,并且在50微摩尔浓度下对α-葡萄糖苷酶催化活性的抑制率超过70%,具有显著效力,因此它们似乎都值得进一步开发,以发现治疗糖尿病的新药。本文详细讨论了新鉴定出的抑制剂与α-葡萄糖苷酶活性位点残基相互作用的相关结构特征。