Altmann Eva, Cowan-Jacob Sandra W, Missbach Martin
Novartis Institutes for BioMedical Research, CH-4002 Basel, Switzerland.
J Med Chem. 2004 Nov 18;47(24):5833-6. doi: 10.1021/jm0493111.
Starting from the high-throughput screening hit 1a, novel cathepsin K inhibitors have been developed based on a purine scaffold. High-resolution X-ray structures of several derivatives have revealed the binding mode of these unique cysteine protease inhibitors.
从高通量筛选命中物1a开始,基于嘌呤骨架开发了新型组织蛋白酶K抑制剂。几种衍生物的高分辨率X射线结构揭示了这些独特的半胱氨酸蛋白酶抑制剂的结合模式。