Abstract
The growing use of nitazene synthetic opioids heralds a new phase of the opioid crisis. However, limited information exists on the toxic effects of these drugs, aside from a propensity for respiratory depression. With restricted research availability of nitazenes, we used machine-learning-based tools to evaluate five nitazene compounds' interaction potential with the hERG potassium channel, a key drug antitarget in the heart. All nitazenes were predicted to inhibit hERG with low μM IC50 values. These findings indicate a potential for proarrhythmic hERG block by nitazene opioids, warranting detailed cardiac safety evaluations of these drugs.
| Original language | English |
|---|---|
| Article number | 100118 |
| Number of pages | 5 |
| Journal | Journal of Molecular and Cellular Cardiology Plus |
| Volume | 10 |
| Early online date | 22 Oct 2024 |
| DOIs | |
| Publication status | Published - 1 Dec 2024 |
Bibliographical note
Publisher Copyright:© 2024 The Author(s).
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