首页 | 本学科首页   官方微博 | 高级检索  
     


Structure-based design and synthesis of HIV-1 protease inhibitors employing beta-D-mannopyranoside scaffolds
Authors:Murphy Paul V  O'Brien Julie L  Gorey-Feret Lorraine J  Smith Amos B
Affiliation:Chemistry Department, Centre for Synthesis and Chemical Biology, Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Belfield, Dublin 4, Ireland. paul.v.murphey@ucd.ie
Abstract:A preliminary account on the structure-based design, synthesis and evaluation of peptidomimetic inhibitors of HIV-1 protease containing beta-D-mannopyranoside scaffolds is given. The compounds prepared had IC(50) values in the micromolar range. The results provide a platform for the development of more potent carbohydrate-based inhibitors of HIV-1 and other aspartic proteases.
Keywords:
本文献已被 PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号