Research Center, Green Cross Corporation, Yongin, Gyeonggi-Do, Republic of Korea.
Bioorg Med Chem Lett. 2011 Jun 15;21(12):3759-63. doi: 10.1016/j.bmcl.2011.04.063. Epub 2011 Apr 28.
Novel C-aryl glucoside SGLT2 inhibitors containing cyclic diarylpolynoid motif were designed and synthesized for biological evaluation. Alkylzinc bromides have been efficiently prepared by the direct insertion of zinc metal into alkyl bromides. The organozinc reagents underwent smooth Pd-catalyzed cross-coupling reactions. Subsequent ring closing metathesis using 2nd generation Grubbs catalyst successfully generated novel class of ansa-compounds. These glucosides with cyclic diarylpolynoids demonstrated moderate in vitro inhibitory activity against SGLT2 in this series to date (IC(50)=59.5-103 nM).
为了进行生物评估,设计并合成了含有环状二芳基多环骨架的新型 C-芳基葡萄糖苷 SGLT2 抑制剂。通过直接将锌金属插入烷基溴化物中,高效地制备了烷基锌溴化物。有机锌试剂经历了顺利的 Pd 催化交叉偶联反应。随后使用第二代 Grubbs 催化剂进行闭环复分解反应,成功地生成了新型的ansa-化合物。到目前为止,这些具有环状二芳基多环骨架的葡萄糖苷在体外对 SGLT2 表现出适度的抑制活性(IC50=59.5-103 nM)。