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Serotonin N-acetyltransferase: Mechanism and Inhibition

机译:5-羟色胺N-乙酰基转移酶的作用机理与抑制作用

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Serotonin N-acetyltransferase (arylalkylamine N-acetyltransferase, AANAT) catalyzes the rate-limiting step in the biosynthesis of the circadian hormone melatonin from serotonin. Although melatonin was identified 40 years ago, relatively little is known about its (patho)physiological roles, and a solid scientific foundation is still lacking for most therapeutic applications currently claimed for melatonin. The development of potent, specific, and cell permeable inhibitors for AANAT should constitute an important strategy to address these issues. These inhibitors are also potential therapeutics for various sleep / mood disorders. This review will focus on the efforts toward developing in vitro and in vivo AANAT inhibitors, including basic mechanistic studies on AANAT, which have played an important role in design.
机译:5-羟色胺N-乙酰基转移酶(芳基烷基胺N-乙酰基转移酶,AANAT)催化从五羟色胺生物合成昼夜节律激素褪黑素的限速步骤。尽管褪黑激素是40年前发现的,但对其(病理)生理作用的了解相对较少,对于目前声称褪黑激素的大多数治疗应用仍缺乏坚实的科学基础。开发有效,特异性和可渗透细胞的AANAT抑制剂应该构成解决这些问题的重要策略。这些抑制剂也是各种睡眠/情绪障碍的潜在疗法。这篇综述将集中在开发体外和体内AANAT抑制剂的努力上,包括在设计中发挥了重要作用的AANAT的基础机理研究。

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