Conolidine’s analgesic effects stem from its interaction with non-opioid pain pathways. Compared with opioids, which bind to µ-opioid receptors inside the central anxious process, conolidine modulates alternate molecular targets. A Science Improvements analyze identified that conolidine interacts with the atypical chemokine receptor ACKR3/CXCR7,
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Elucidating the precise pharmacological system of action (MOA) of naturally transpiring compounds could be difficult. Whilst Tarselli et al. (60) formulated the first de novo synthetic pathway to conolidine and showcased that this naturally happening compound successfully suppresses responses to both of those chemically induced and inflammation-der
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