Department of Pharmaceutical Sciences, College of Pharmacy and Health Sciences, St. John's University, Queens, New York 11439, United States.
J Med Chem. 2020 Jun 11;63(11):5625-5663. doi: 10.1021/acs.jmedchem.9b01617. Epub 2020 Feb 19.
The use of an acetylene (ethynyl) group in medicinal chemistry coincides with the launch of the in 1959. Since then, the acetylene group has been broadly exploited in drug discovery and development. As a result, it has become recognized as a privileged structural feature for targeting a wide range of therapeutic target proteins, including MAO, tyrosine kinases, BACE1, steroid receptors, mGlu5 receptors, FFA1/GPR40, and HIV-1 RT. Furthermore, a terminal alkyne functionality is frequently introduced in chemical biology probes as a click handle to identify molecular targets and to assess target engagement. This Perspective is divided into three parts encompassing: (1) the physicochemical properties of the ethynyl group, (2) the advantages and disadvantages of the ethynyl group in medicinal chemistry, and (3) the impact of the ethynyl group on chemical biology approaches.
乙炔基(乙炔基)在药物化学中的应用恰逢 1959 年的推出。从那时起,乙炔基已广泛应用于药物发现和开发中。结果,它已被公认为针对包括 MAO、酪氨酸激酶、BACE1、甾体受体、mGlu5 受体、FFA1/GPR40 和 HIV-1 RT 在内的多种治疗靶蛋白的特权结构特征。此外,末端炔基官能团通常作为点击手柄引入化学生物学探针中,以鉴定分子靶标并评估靶标结合。本观点分为三部分:(1)乙炔基的物理化学性质,(2)乙炔基在药物化学中的优缺点,以及(3)乙炔基对化学生物学方法的影响。