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首页> 外文期刊>Journal of Medicinal Chemistry >Acetylene Group, Friend or Foe in Medicinal Chemistry
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Acetylene Group, Friend or Foe in Medicinal Chemistry

机译:药用化学的乙炔基,朋友或敌人

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摘要

The use of an acetylene (ethynyl) group in medicinal chemistry coincides with the launch of the Journal of Medicinal Chemistry 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.
机译:在1959年,使用药物化学中的乙炔(乙炔基)基团的使用恰逢药物化学杂志的推出。从那时起,乙炔基被广泛利用药物发现和发育。 结果,它已经被认为是用于靶向各种治疗靶蛋白的特权结构特征,包括MAO,酪氨酸激酶,BACE1,类固醇受体,MGLU5受体,FFA1 / GPR40和HIV-1 RT。 此外,在化学生物学探针中经常引入终端炔烃功能,作为点击手柄以识别分子目标并评估目标接合。 这种观点分为三个部分,包括:(1)乙炔基的物理化学性质,(2)药物化学中的乙炔基的优点和缺点,(3)乙炔基对化学生物学方法的影响。

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