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Conolidine’s analgesic consequences stem from its conversation with non-opioid pain pathways. In contrast to opioids, which bind to µ-opioid receptors within the central anxious technique, conolidine modulates alternate molecular targets. A Science Innovations review located that conolidine interacts Using the atypical chemokine receptor ACKR3/C

Even though the opiate receptor depends on G protein coupling for sign transduction, this receptor was identified to benefit from arrestin activation for internalization from the receptor. Normally, the receptor promoted no other signaling cascades (fifty nine) Modifications of conolidine have resulted in variable advancement in binding efficacy. T