A convenient diastereoselective total synthesis of andrimid
作者:AV Rama Rao、A.K. Singh、Ch.V.N.S. Varaprasad
DOI:10.1016/s0040-4039(00)92179-8
日期:1991.1
A convenientdiastereoselectivesynthesis of andrimid was accomplished in a straightforward approach and also several β-substituted cyclic imides were prepared in a facile manner.
Non-natural ribonuclease conjugates as cytotoxic agents
申请人:Strong E. Laura
公开号:US20050261232A1
公开(公告)日:2005-11-24
The present invention is directed toward the delivery of a toxic protein to pathogenic cells, particularly cancer cells. In preferred embodiments, the toxic protein is a ribonuclease that has been modified to make it toxic to target cells and that can be conjugated to a target cell-specific delivery vector, such as an antibody, for delivery to pathogenic cells.