An efficient synthesis of optically active metabolites of platelet adhesion inhibitor OPC-29030 by lipase-catalyzed enantioselective transesterification
作者:Kazuyoshi Kitano、Jun Matsubara、Tadaaki Ohtani、Kenji Otsubo、Yoshikazu Kawano、Seiji Morita、Minoru Uchida
DOI:10.1016/s0040-4039(99)00946-6
日期:1999.7
The optically active metabolites of (S)-3,4-dihydro-6-[3-(1-o-tolyl-2-imidazolyl)sulfinyl-propoxy]-2(1H)-quinolinone (OPC-29030, 1), which is a new anti-platelet agent (platelet adhesion inhibitor), were effectively synthesized by the enzyme-catalyzed enantioselective transesterification of the racemic sulfinyl metabolites. The enzymes can recognize a stereogenic sulfur atom remote from the reaction
的光学活性的代谢物(小号)-3,4-二氢-6- [3-(1- ö甲苯基- 2-咪唑基)亚磺酰基丙氧基] -2(1 H ^) -喹啉酮(OPC-29030,1) ,是一种新型的抗血小板药物(血小板粘附抑制剂),是通过酶催化的外消旋亚磺酰基代谢物的对映选择性酯交换反应而有效合成的。这些酶可以识别远离反应位点的立体硫原子。