Department of Chemistry and Applied Biosciences, Institute of Pharmaceutical Sciences, Swiss Federal Institute of Technology Zurich, Wolfgang-Pauli-Strasse 10, CH-8093 Zürich, Switzerland.
Angew Chem Int Ed Engl. 2013 Jan 28;52(5):1384-402. doi: 10.1002/anie.201204631. Epub 2013 Jan 7.
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.
靶向递送有效细胞毒素已成为治疗癌症和其他严重疾病的一种有前途的策略。传统上,针对疾病标志物的抗体被用作药物递送载体。最近,小分子配体已被提议用于生成一类新型的靶向细胞毒素,具有改善的性质。该领域的进展关键依赖于高效的方法来鉴定和优化能够高亲和力结合和选择性识别靶蛋白的有机分子。DNA 编码化学文库的出现允许构建和筛选前所未有的化合物集合。在这篇综述中,我们调查了基于小分子配体的靶向细胞毒素领域的发展,并展示了创新的文库技术将如何帮助开发未来的药物。