Author/Authors :
Klaus Urbahns، نويسنده , , Michael H?rter، نويسنده , , Andrea Vaupel، نويسنده , , Markus Albers، نويسنده , , Delf Schmidt، نويسنده , , Ulf Brüggemeier، نويسنده , , Beatrix Stelte-Ludwig، نويسنده , , Christoph Gerdes، نويسنده , , Hideki Tsujishita، نويسنده ,
Abstract :
Vitronectin receptor (αVβ3) antagonism has been implicated in a variety of disease states, like restenosis, osteoporosis and cancer. In this work, we present the development of a novel class of biphenyl vitronectin receptor antagonists. Identified from a focused combinatorial library based on para-bromo phenylalanine, these compounds show nanomolar affinity to the vitronectin receptor and display unprecedented SAR. Their binding mode can be rationalized by computational docking studies using the X-ray structure of αVβ3.