Shah S K, Brause K A, Chandler G O, Finke P E, Ashe B M, Weston H, Knight W B, Maycock A L, Doherty J B
Department of Medicinal Chemical Research, Merck Sharp and Dohme Research Laboratories, Rahway, New Jersey 07065.
J Med Chem. 1990 Sep;33(9):2529-35. doi: 10.1021/jm00171a030.
Several 3'-substituted cephalosporin sulfones were synthesized from 3-(hydroxymethyl)cephalosporin, which was prepared by Ti(OiPr)4 hydrolysis of the corresponding acetate. A method was also developed to prepare a 3-vinylcephalosporin. Some of these compound were found to be potent time-dependent inhibitors of human leukocyte elastase (HLE). The HLE inhibitory activity was correlated with sigma 1 and it was concluded that the potency was determined by the electron-withdrawing ability as well as the size of the substituent. A mechanism for inhibition of HLE by cephalosporin sulfones is proposed.
以相应乙酸酯经Ti(OiPr)4水解制备的3-(羟甲基)头孢菌素为原料,合成了几种3'-取代的头孢菌素砜。还开发了一种制备3-乙烯基头孢菌素的方法。发现其中一些化合物是人类白细胞弹性蛋白酶(HLE)的强效时间依赖性抑制剂。HLE抑制活性与σ1相关,得出其效力由取代基的吸电子能力和大小决定的结论。提出了头孢菌素砜抑制HLE的机制。