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咖啡因的药物化学。

The Medicinal Chemistry of Caffeine.

机构信息

Institute of Pharmaceutical Chemistry, Goethe University Frankfurt, Max-von-Laue-Str. 9, 60438 Frankfurt, Germany.

出版信息

J Med Chem. 2021 Jun 10;64(11):7156-7178. doi: 10.1021/acs.jmedchem.1c00261. Epub 2021 May 21.

Abstract

The purine alkaloid caffeine is the most widely consumed psychostimulant drug in the world and has multiple beneficial pharmacological activities, for example, in neurodegenerative diseases. However, despite being an extensively studied bioactive natural product, the mechanistic understanding of caffeine's pharmacological effects is incomplete. While several molecular targets of caffeine such as adenosine receptors and phosphodiesterases have been known for decades and inspired numerous medicinal chemistry programs, new protein interactions of the xanthine are continuously discovered providing potentially improved pharmacological understanding and a molecular basis for future medicinal chemistry. In this Perspective, we gather knowledge on the confirmed protein interactions, structure activity relationship, and chemical biology of caffeine on well-known and upcoming targets. The diversity of caffeine's molecular activities on receptors and enzymes, many of which are abundant in the CNS, indicates a complex interplay of several mechanisms contributing to neuroprotective effects and highlights new targets as attractive subjects for drug discovery.

摘要

嘌呤生物碱咖啡因是世界上使用最广泛的精神兴奋剂药物,具有多种有益的药理活性,例如在神经退行性疾病中。然而,尽管咖啡因是一种经过广泛研究的生物活性天然产物,但对其药理作用的机制理解尚不完全。虽然几十年来已经知道咖啡因的几个分子靶点,如腺苷受体和磷酸二酯酶,并激发了许多药物化学计划,但黄嘌呤的新蛋白质相互作用不断被发现,为未来的药物化学提供了潜在的改善的药理学理解和分子基础。在本观点中,我们汇集了关于咖啡因在知名和新兴靶标上的已确认蛋白质相互作用、构效关系和化学生物学的知识。咖啡因在受体和酶上的分子活性的多样性,其中许多在中枢神经系统中丰富,表明几种机制的复杂相互作用有助于神经保护作用,并突出了新的靶标作为药物发现的有吸引力的主题。

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