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Not yet medically reviewed — information on this site is in preparation and has not been verified by a medical reviewer.
Drug index / Opioid / 7-Hydroxymitragynine (7-OH)
Opioid

7-Hydroxymitragynine (7-OH)

methyl (E)-2-[(2S,3S,7aS,12bS)-3-ethyl-7a-hydroxy-8-methoxy-2,3,4,6,7,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate

7-Hydroxymitragynine (7-OH) is a potent opioid alkaloid present in trace amounts in the kratom plant (Mitragyna speciosa) and formed in the body as the active metabolite of mitragynine, kratom's main alkaloid. It is a mu-opioid receptor agonist that animal studies report to be several times more potent than morphine. Since 2024, concentrated and semi-synthetic 7-OH products — tablets, gummies, and liquid shots sold in smoke shops and gas stations — have drawn intense regulatory attention as a category distinct from whole-leaf kratom. In July 2025 the FDA recommended scheduling 7-OH, and in July 2026 the DEA issued notices to temporarily place concentrated 7-OH in Schedule I.

Overview

7-Hydroxymitragynine (7-OH) occurs only in trace amounts in the natural kratom leaf, where it is a minor alkaloid; most of the 7-OH that affects the body is produced when the liver metabolizes mitragynine, kratom's primary alkaloid. The critical distinction — and the core of this page's harm-reduction value — is between whole-leaf kratom and the concentrated, isolated, or semi-synthetic 7-OH products that spread rapidly across U.S. smoke shops and gas stations in 2024-2025. Sold as tablets, gummies, drink mixes, and liquid 'shots' and marketed separately from traditional kratom, these products deliver far more 7-OH than the leaf ever naturally contains. The FDA characterizes them as 'concentrated 7-OH opioid products' and warns they are effectively unregulated opioids being sold over the counter.

Source: FDA; NIH/PMC peer-reviewed literature

Chemistry & mechanism of action

7-Hydroxymitragynine is a potent agonist at the mu-opioid receptor (MOR), the same receptor engaged by morphine and other classical opioids, acting predominantly at the mu-opioid subtype. Published pharmacology characterizes it as substantially more potent and efficacious at the MOR than mitragynine itself, and as a G-protein-biased agonist — a signaling profile that differs from classical opioids. In animal antinociception studies, subcutaneous 7-OH was reported to be roughly four-to-six times more potent than morphine (about 5.7 times in the mouse tail-flick test and 4.4 times in the hot-plate test). Its opioid activity at the MOR is what accounts for both its analgesic effects and its opioid-type risk profile.

Source: peer-reviewed pharmacology literature (NIH/PMC)

Effects

Because 7-OH acts as a mu-opioid receptor agonist, its effects resemble those of other opioids — analgesia, sedation, and euphoria — rather than the milder, more stimulant-like profile many users associate with low-dose whole-leaf kratom. The central concern with the concentrated 7-OH products that emerged in 2024-2025 is that they present a far stronger and less predictable opioid effect than the natural leaf, while often being sold in candy-like or beverage formats. Effects and their intensity vary with the product and the individual; because these products are unregulated, their actual 7-OH content is frequently unknown.

Source: FDA; NIH/PMC peer-reviewed literature

Risks & harms

As an opioid agonist, 7-hydroxymitragynine carries the characteristic risks of the opioid class. Repeated use can produce tolerance, physical dependence, and an opioid-type withdrawal syndrome on discontinuation, and case reports and FDA reporting describe dependence developing with the concentrated products. The defining acute danger of any mu-opioid agonist is respiratory depression, the mechanism by which opioids cause fatal overdose. That hazard is amplified for isolated 7-OH products because their potency relative to morphine is high and their actual content is often unlabeled or unverified, so the amount consumed is difficult to gauge. Regulators have flagged the risk that these products are perceived as benign 'kratom' or wellness items while functioning as unregulated opioids. This section describes risks only; it is not use, dosing, or harm-reduction combination guidance.

Source: FDA; NIH/PMC peer-reviewed literature

Images

Visual references coming soon.

If it’s too intense

If an experience becomes overwhelming, the goal is to stay safe and let it pass — most difficult experiences ease as the drug wears off.

  • Get to a calm, safe space with someone you trust who is sober and can stay with you.
  • Cool down if you’re overheating — move somewhere cool, remove extra layers, rest. Overheating is especially a risk with stimulants and MDMA.
  • Sip water to thirst — but don’t over-hydrate. Drinking large amounts of plain water (especially after MDMA) can dangerously dilute your blood sodium (hyponatremia). Electrolytes help more than volume.
  • Slow your breathing — long, slow exhales help settle a racing heart and anxiety.
  • A sugary drink, fruit juice, or a snack can ease shakiness and the anxiety that comes with low blood sugar.
  • Do not take more, and do not add another substance to manage it. Redosing or adding something else (including a sedative like a benzodiazepine) can make things worse, not better.

With opioids, slowed or stopped breathing is the emergency — if available, give naloxone and call 911 immediately; it can be given while you wait for help.

Call 911 (or Poison Control, 1-800-222-1222) right away for chest pain, a very high body temperature, a seizure, unconsciousness, or severe confusion. These are medical emergencies, not something to wait out.

Source: general harm-reduction guidance from SAMHSA, NIH/NIDA, and MedlinePlus, in our own words. Draft — not yet medically reviewed.

Forensic dossier

Draft · every field is source-cited or marked “Unknown — pending review”

Identity

IUPAC name
methyl (E)-2-[(2S,3S,7aS,12bS)-3-ethyl-7a-hydroxy-8-methoxy-2,3,4,6,7,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoatePubChem PUG-REST · retrieved 2026-06-18
SMILES
CC[C@@H]1CN2CC[C@]3(C(=NC4=C3C(=CC=C4)OC)[C@@H]2C[C@@H]1/C(=C\OC)/C(=O)OC)OPubChem PUG-REST · retrieved 2026-06-18
InChIKey
RYENLSMHLCNXJT-CYXFISRXSA-NPubChem PUG-REST · retrieved 2026-06-18
Synonyms / aliases
7-oh, 7-Hydroxymitragynine, Mitragynine hydroxyindolenine, 7-hydroxy-mitragynine, 7-Hydroxy MitragyninePubChem PUG-REST + seed aliases · retrieved 2026-06-18

Composition

Composition
N/A — single compound (see Identity)

Physical / pill characteristics

Dosage form
Unknown — pending review (no Rx/OTC label; illicit — pill visuals = FIRST-PARTY submissions only, never generated or scraped)
Route
Unknown — pending review
Shape
Unknown — pending review
Color
Unknown — pending review
Imprint
Unknown — pending review
Score
Unknown — pending review

Scheduling & legal status

US schedule
Unknown — pending review
International
Unknown — pending review

Effects, risks & interactions

Effects
7-hydroxymitragynine is a minor alkaloid of kratom — present only in small amounts in the leaf — but it is far more potent at mu-opioid receptors than mitragynine, and it is also a compound the body makes from mitragynine. It produces stronger opioid-like effects: pain relief, sedation and euphoria. It is the alkaloid most responsible for kratom's opioid-like potency, which is why deliberately concentrated "7-OH" products are a growing concern.PubChem CID 44301524 + NIDA Kratom · retrieved 2026-06-18
Risks
Because 7-hydroxymitragynine is a potent mu-opioid agonist, it carries the opioid risks more sharply than the parent leaf: a greater potential for dependence and withdrawal and — importantly — respiratory depression, the opioid overdose mechanism. The recent rise of products deliberately concentrated or "enriched" in 7-OH is a specific harm-reduction concern: they can be far stronger and more opioid-like than traditional kratom while being sold in the same unregulated supplement market with unknown, unlabelled potency. Combined with other opioids or depressants the danger compounds.PubChem CID 44301524 + NIDA Kratom · retrieved 2026-06-18
Interactions
Unknown — pending review

Dosage

Pending medical reviewer

Sources

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