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Conolidine’s analgesic outcomes stem from its interaction with non-opioid pain pathways. Contrary to opioids, which bind to µ-opioid receptors inside the central nervous procedure, conolidine modulates alternate molecular targets. A Science Advancements study observed that conolidine interacts With all the atypical chemokine receptor ACKR3/CXCR7
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Elucidating the specific pharmacological mechanism of motion (MOA) of naturally occurring compounds is often difficult. Even though Tarselli et al. (60) designed the first de novo artificial pathway to conolidine and showcased that this naturally developing compound successfully suppresses responses to each chemically induced and inflammation-deriv
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