作者:Leifeng Cheng、Christopher A. Goodwin、Michael F. Scully、Vijay V. Kakkar、Göran Claeson
DOI:10.1016/0040-4039(91)80512-5
日期:1991.12
peptidomimetics, D-Aa-Pro-AaP(OPh)2, with lipophilic amino acids at the P3 positions1 and amino phosphonic acids with neutral side chains in the P1 position have been designed and synthesized as thrombin inhibitors.
新的含磷肽模拟物,d-AA-PRO-AA P(OPH)2,其中一个P亲脂性氨基酸3点的位置1和氨基膦酸与在P中性侧链1位置已经被设计并作为凝血酶抑制剂合成。