天然产物
化学
去肽
半胱氨酸蛋白酶
全合成
组织蛋白酶B
半胱氨酸
蛋白酶
酶
生物化学
组合化学
组织蛋白酶L
立体化学
作者
Arthur H. Tang,Richard J. Payne
出处
期刊:Tetrahedron
[Elsevier]
日期:2023-05-01
卷期号:139: 133445-133445
被引量:2
标识
DOI:10.1016/j.tet.2023.133445
摘要
Gallinamide A is a depsipeptide natural product produced by cyanobacteria that possesses potent anti-parasitic activity through the inhibition of essential cysteine protease enzymes. Recently, gallinamide A was also shown to possess potent antiviral activity against SARS-CoV-2 via the covalent inhibition of the host cysteine protease cathepsin L that plays a role in viral entry. In order to perform detailed pre-clinical studies on gallinamide A as a potential antiviral for COVID-19, access to significant quantities of the natural product was necessary and required the design of a more efficient synthetic route to the natural product. Herein, we describe a second generation total synthesis of gallinamide A that delivered the natural product on a 315 mg scale over 16 total steps (9 steps in the longest linear sequence) in an overall yield of 32%.
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