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7-OH-mitragynine

kratom metabolite

7-OH-mitragynine ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: 7-OH-mitragynine ballicule

What it isCYP3A4 oxidation metabolite of mitragynine; kratom’s principal mu-opioid full agonist, with roughly 5x the parent alkaloid’s mu-receptor affinity.

Why it mattersDrives most of kratom's analgesic, euphoric, and dependence-producing opioid effect. Concentrated synthetic 7-OH products prompted FDA warnings and a 2026 DEA move to Schedule I.

What it changesBecause it is generated by CYP3A4, strong 3A4 inhibitors or inducers shift its exposure, and its mu agonism carries real respiratory-depression and dependence risk, compounded by other opioids or sedatives.

7-OH-mitragynine molecular structure (skeletal formula)
Molecular structure: 7-OH-mitragynine

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