Small Targeted Cytotoxics: Current State and Promises from DNA-Encoded Chemical Libraries

被引:125
|
作者
Krall, Nikolaus [1 ]
Scheuermann, Joerg [1 ]
Neri, Dario [1 ]
机构
[1] Swiss Fed Inst Technol, Swiss Fed Inst Technol Zurich, Inst Pharmaceut Sci, Dept Chem & Appl Biosci, CH-8093 Zurich, Switzerland
基金
中国国家自然科学基金;
关键词
cancer; DNA-encoded libraries; drug conjugates; drug delivery; prodrugs; HORMONE-RELEASING HORMONE; IN-VITRO SELECTION; RECEPTOR-MEDIATED ENDOCYTOSIS; ANTIBODY-DRUG CONJUGATE; BOMBESIN ANALOG AN-215; ED-B DOMAIN; FOLATE-RECEPTOR; MEMBRANE ANTIGEN; ANTITUMOR-ACTIVITY; PROSTATE-CANCER;
D O I
10.1002/anie.201204631
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The targeted delivery of potent cytotoxic agents has emerged as a promising strategy for the treatment of cancer and other serious conditions. Traditionally, antibodies against markers of disease have been used as drug-delivery vehicles. More recently, lower molecular weight ligands have been proposed for the generation of a novel class of targeted cytotoxics with improved properties. Advances in this field crucially rely on efficient methods for the identification and optimization of organic molecules capable of high-affinity binding and selective recognition of target proteins. The advent of DNA-encoded chemical libraries allows the construction and screening of compound collections of unprecedented size. In this Review, we survey developments in the field of small ligand-based targeted cytotoxics and show how innovative library technologies will help develop the drugs of the future.
引用
收藏
页码:1384 / 1402
页数:19
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