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社论:未来嘌呤能治疗学的小分子和生物制剂。

Editorial: Small molecules and biologics for future purinergic therapeutics.

机构信息

Molecular Recognition Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, 20892, USA.

Department of Pharmacology and Physiology and the Henry and Amelia Nasrallah Center for Neuroscience, Saint Louis University School of Medicine, 1402 South Grand Blvd, St. Louis, MO, 63104, USA.

出版信息

Purinergic Signal. 2023 Sep;19(3):465-466. doi: 10.1007/s11302-023-09964-9.

DOI:10.1007/s11302-023-09964-9
PMID:37676356
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10539233/
Abstract

Receptor agonists and antagonists and other modulators of purinergic signalling have potential as novel therapeutics for a broad range of diseases and conditions. This special issue focuses on compounds or approaches that are either in clinical trials or headed in that direction. It is intended to serve as an up-to-date description of selected efforts to discover and develop new small molecular purinergic drugs.

摘要

激动剂和拮抗剂以及其他嘌呤能信号转导的调节剂有可能成为广泛疾病和病症的新型治疗药物。本期特刊重点介绍了处于临床试验或朝这一方向发展的化合物或方法。它旨在作为发现和开发新型小分子嘌呤能药物的精选努力的最新描述。

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引用本文的文献

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Editorial-Translation of purinergic drugs into therapeutic use.社论——嘌呤能药物转化为治疗用途
Purinergic Signal. 2025 Apr;21(2):193. doi: 10.1007/s11302-025-10077-8.

本文引用的文献

1
International Union of Basic and Clinical Pharmacology. CXII: Adenosine Receptors: A Further Update.国际基础和临床药理学联合会。CXII:腺苷受体:进一步更新。
Pharmacol Rev. 2022 Apr;74(2):340-372. doi: 10.1124/pharmrev.121.000445.
2
Update of P2X receptor properties and their pharmacology: IUPHAR Review 30.P2X 受体特性及其药理学更新:国际药理学联合会评论 30.
Br J Pharmacol. 2021 Feb;178(3):489-514. doi: 10.1111/bph.15299. Epub 2020 Dec 21.
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Update of P2Y receptor pharmacology: IUPHAR Review 27.P2Y受体药理学更新:IUPHAR综述27
Br J Pharmacol. 2020 Jun;177(11):2413-2433. doi: 10.1111/bph.15005. Epub 2020 Apr 6.
4
Action of MK-7264 (gefapixant) at human P2X3 and P2X2/3 receptors and in vivo efficacy in models of sensitisation.MK-7264(gefapixant)在人 P2X3 和 P2X2/3 受体上的作用及其在致敏模型中的体内疗效。
Br J Pharmacol. 2019 Jul;176(13):2279-2291. doi: 10.1111/bph.14677. Epub 2019 May 11.
5
Blockade of P2X4 Receptors Inhibits Neuropathic Pain-Related Behavior by Preventing MMP-9 Activation and, Consequently, Pronociceptive Interleukin Release in a Rat Model.在大鼠模型中,P2X4受体阻断通过防止MMP-9激活以及由此防止伤害性白细胞介素释放来抑制神经性疼痛相关行为。
Front Pharmacol. 2017 Feb 16;8:48. doi: 10.3389/fphar.2017.00048. eCollection 2017.
6
A novel P2X4 receptor-selective antagonist produces anti-allodynic effect in a mouse model of herpetic pain.一种新型 P2X4 受体选择性拮抗剂在疱疹疼痛小鼠模型中产生抗痛觉过敏作用。
Sci Rep. 2016 Aug 31;6:32461. doi: 10.1038/srep32461.