Panx1 and drug discovery: from non-specific inhibitors to tailored drug compounds

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Authors: Michael Kohr, Carola Meier
Cited by: 1
References: 117

Abstract

Pannexin (Panx)-1-mediated ATP release has been associated with a broad range of pathological conditions. Conversely, the use of Panx1-inhibitors has shown promising results in the medication of diseases, such as neuroinflammation, melanoma and epilepsy. In addition, Panx1-inhibitors are an indispensable tool for the elucidation of both structure and physiology of Panx1. Over the past years, numerous applications of Panx1-inhibitors have led to new insights into Panx1 influences in health and disease. The major drawback of conventional Panx1-inhibitors, however, is the lack of selectivity resulting in undesired side effects. Nevertheless, these inhibitors are useful resources for drug discovery and lead optimisation approaches have therefore found their way into Panx1 research. Newly developed inhibitors show both high efficacy and selectivity. The combination of drug development and molecular dynamics simulations is a powerful tool to further elucidate both structure and gating mechanisms of Panx1.

Fields of Study & Subjects

Connexins and lens biology S100 Proteins and Annexins Adenosine and Purinergic Signaling

Publication details

Journal / source
Cell and Tissue Research
Publisher
Springer Science and Business Media LLC
Volume
403
Issue
1
Pages
6–6
Publication date
1 January 2026
Language
EN