Department of Pharmaceutical/Medicinal Chemistry, Eberhard Karls University Tübingen, Auf der Morgenstelle 8, 72076 Tübingen, Germany.
Cluster of Excellence iFIT (EXC 2180) "Image-Guided & Functionally Instructed Tumor Therapies", University of Tübingen, 72076 Tübingen, Germany.
J Med Chem. 2024 May 23;67(10):7668-7758. doi: 10.1021/acs.jmedchem.3c01825. Epub 2024 May 6.
Covalent inhibitors and other types of covalent modalities have seen a revival in the past two decades, with a variety of new targeted covalent drugs having been approved in recent years. A key feature of such molecules is an intrinsically reactive group, typically a weak electrophile, which enables the irreversible or reversible formation of a covalent bond with a specific amino acid of the target protein. This reactive group, often called the "warhead", is a critical determinant of the ligand's activity, selectivity, and general biological properties. In 2019, we summarized emerging and re-emerging warhead chemistries to target cysteine and other amino acids (Gehringer, M.; Laufer, S. A. 2019, 62, 5673-5724; DOI: 10.1021/acs.jmedchem.8b01153). Since then, the field has rapidly evolved. Here we discuss the progress on covalent warheads made since our last Perspective and their application in medicinal chemistry and chemical biology.
在过去的二十年中,共价抑制剂和其他类型的共价模式重新受到关注,近年来已经批准了多种新型靶向共价药物。此类分子的一个关键特征是内在反应性基团,通常是弱亲电体,能够与靶蛋白的特定氨基酸不可逆或可逆地形成共价键。这种反应性基团通常称为“弹头”,是配体活性、选择性和一般生物学性质的关键决定因素。2019 年,我们总结了新兴和重新出现的弹头化学,以针对半胱氨酸和其他氨基酸(Gehringer,M.;Laufer,S. A. 2019,62,5673-5724;DOI:10.1021/acs.jmedchem.8b01153)。自那时以来,该领域发展迅速。在这里,我们讨论了自我们上次观点以来在共价弹头方面取得的进展及其在药物化学和化学生物学中的应用。