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What Is Mitragynine Pseudoindoxyl?

Mitragynine pseudoindoxyl, often abbreviated as MP and sometimes casually called “pseudo,” is a kratom-related compound connected to mitragynine and 7-hydroxymitragynine, also known as 7-OH. These compounds come from or are derived from Mitragyna speciosa, the plant commonly known as kratom. Mitragynine pseudoindoxyl is not the same as ordinary kratom leaf. It is a potent opioid …

What Is Mitragynine Pseudoindoxyl? Portland Treatment Blog

Mitragynine pseudoindoxyl, often abbreviated as MP and sometimes casually called “pseudo,” is a kratom-related compound connected to mitragynine and 7-hydroxymitragynine, also known as 7-OH. These compounds come from or are derived from Mitragyna speciosa, the plant commonly known as kratom.

Mitragynine pseudoindoxyl is not the same as ordinary kratom leaf. It is a potent opioid receptor-active compound that may appear in newer kratom-related products, including some products marketed as kratom alternatives, 7-OH products, or semi-synthetic kratom derivatives.

Researchers have described mitragynine pseudoindoxyl as a highly selective mu-opioid receptor agonist. The mu-opioid receptor is the same broad receptor system involved in the effects of traditional opioids, including pain relief, euphoria, tolerance, dependence, withdrawal, and overdose risk.

Why Is Mitragynine Pseudoindoxyl Being Discussed?

Mitragynine pseudoindoxyl has become more concerning because it is now being identified in commercial products. A 2025 study reported that products containing semi-synthetic kratom-derived compounds, including 7-OH and mitragynine pseudoindoxyl, had emerged in online sales. Researchers noted that both compounds are highly selective mu-opioid receptor agonists and may pose public health risks.

This matters because many people still think of kratom products as natural, mild, or less risky than opioids. That assumption becomes even more dangerous when products are no longer simple kratom leaf and instead contain concentrated or semi-synthetic opioid-active compounds.

Mitragynine, 7-OH, and Mitragynine Pseudoindoxyl

Mitragynine pseudoindoxyl is part of a larger kratom chemistry pathway. Mitragynine is the major alkaloid in kratom. The body can metabolize mitragynine into 7-hydroxymitragynine, and 7-OH can be further converted into mitragynine pseudoindoxyl.

CompoundWhat It IsWhy It Matters
MitragynineMain alkaloid found in kratom leafHas opioid receptor activity but is generally less potent than 7-OH or MP
7-hydroxymitragynine / 7-OHPotent kratom-related opioid-active compoundMore potent at the mu-opioid receptor than mitragynine
Mitragynine pseudoindoxyl / MP7-OH-related metabolite and semi-synthetic product compoundHighly potent opioid receptor-active compound with growing public health concern

Mitragynine pseudoindoxyl can occur as a metabolite, but the main concern is not what the body may produce in tiny amounts. The bigger issue is concentrated or semi-synthetic products that may deliver much larger amounts than someone would encounter from traditional kratom leaf.

Is Mitragynine Pseudoindoxyl an Opioid?

Mitragynine pseudoindoxyl is best understood as an opioid-active kratom-derived compound. It is not identical to heroin, fentanyl, oxycodone, or morphine, but it interacts with opioid receptor systems involved in opioid-like effects.

Possible opioid-like effects may include:

Possible EffectWhy It Matters
Euphoria or emotional reliefMay reinforce repeated use
SedationCan impair driving, work, and decision-making
Pain reliefMay increase repeated use or self-medication
Nausea or dizzinessCommon with opioid-active substances
ConstipationCommon opioid-related side effect
ToleranceMore may be needed over time
DependenceWithdrawal symptoms may appear when stopping
Overdose riskRisk may rise when mixed with other depressants

Some early research suggested mitragynine pseudoindoxyl might have unusual opioid receptor activity, such as mu-opioid agonism and delta-opioid antagonism. However, that does not mean it is safe for human use outside controlled research or clinical settings.

Is Mitragynine Pseudoindoxyl FDA-Approved?

No. Mitragynine pseudoindoxyl is not FDA-approved for pain, opioid withdrawal, anxiety, sleep, opioid use disorder, or any other medical condition.

It should not be treated like a regulated medication. Products sold online, in gas stations, in vape shops, or through supplement-style retailers may have unclear ingredients, inaccurate labeling, inconsistent dosing, or contamination. A product being available for purchase does not mean it has been proven safe.

Why Mitragynine Pseudoindoxyl Products Are Risky

Mitragynine pseudoindoxyl products are concerning because they sit in a dangerous gray zone between kratom, research chemicals, and opioid-like drugs.

Risk FactorWhy It Matters
Limited human dataThere is no reliable safety profile for regular human use
Opioid receptor activityMP acts on systems tied to tolerance, dependence, and withdrawal
Potency concernsMP may be more potent than mitragynine and 7-OH in some receptor studies
Product labeling issuesConsumers may not know what dose or compound they are taking
Marketing confusionProducts may be presented as kratom, nootropics, or “legal” alternatives
Polysubstance dangerMixing with alcohol, benzos, opioids, or sedatives may increase overdose risk
Lack of medical oversightThere is no approved dose, detox protocol, or prescribing standard

For people with a history of opioid addiction, these products may also trigger cravings, relapse patterns, or a return to compulsive opioid-like use.

Can Mitragynine Pseudoindoxyl Cause Withdrawal?

Human data is still limited, but withdrawal is a major concern. A 2026 case report described severe early-onset withdrawal after intentional mitragynine pseudoindoxyl use. The authors noted that semisynthetic derivatives such as MP may produce rapid-onset, full-spectrum opioid-like withdrawal.

Possible withdrawal symptoms may include:

Symptom CategoryPossible Symptoms
Physical symptomsSweating, chills, body aches, nausea, vomiting, diarrhea
Sleep symptomsInsomnia, restless sleep, vivid dreams
Mood symptomsAnxiety, depression, irritability, panic, agitation
Nervous system symptomsRestlessness, tremors, racing heart, blood pressure changes
Opioid-like symptomsRunny nose, watery eyes, goosebumps, muscle aches
CravingsStrong urges to use MP, 7-OH, kratom, or other opioids
Severe symptomsConfusion, severe agitation, dehydration, relapse risk

Because MP products are new and inconsistent, there is no single withdrawal timeline that applies to everyone. Symptoms may depend on the dose, frequency of use, duration of use, other substances, and the actual contents of the product.

Mitragynine Pseudoindoxyl Withdrawal Timeline

There is no standardized withdrawal timeline for mitragynine pseudoindoxyl. However, based on emerging case reports and its opioid-like activity, withdrawal may appear quickly after stopping, especially if the person has been using concentrated products.

StagePossible Symptoms
First 12–24 hoursAnxiety, cravings, restlessness, sweating, insomnia
Days 1–3Worsening withdrawal, stomach upset, body aches, chills, agitation
Days 3–7Sleep disruption, mood swings, cravings, fatigue, diarrhea, dehydration risk
1–2 weeksLingering anxiety, low mood, sleep problems, reduced energy
Several weeks or longerCravings, emotional instability, post-acute symptoms in some people

This timeline is only a general guide. People using MP with 7-OH, kratom extracts, fentanyl, oxycodone, benzodiazepines, alcohol, phenibut, or other substances may have a more complex and dangerous withdrawal experience.

Can Mitragynine Pseudoindoxyl Cause Overdose?

There is not enough public human data to define a clear mitragynine pseudoindoxyl overdose profile. However, because MP is opioid receptor-active, overdose risk is a serious concern, especially when it is combined with other depressants.

Risk may increase when MP is taken with:

SubstanceWhy the Combination Is Risky
AlcoholCan worsen sedation and poor coordination
BenzodiazepinesMay increase dangerous central nervous system depression
OpioidsCan compound opioid-like effects
FentanylGreatly increases overdose risk
Sleep medicationsCan worsen impairment and sedation
PhenibutMay increase sedation and withdrawal complexity
Gabapentin or pregabalinMay worsen dizziness, sedation, and impairment

Possible opioid-related overdose signs include extreme sleepiness, slow or stopped breathing, blue or gray lips, gurgling sounds, limp body, vomiting while unconscious, or inability to wake the person.

Call 911 immediately if overdose is possible. Naloxone may help if opioid receptor activity is involved, but emergency medical care is still necessary.

Mitragynine Pseudoindoxyl vs. 7-OH

Mitragynine pseudoindoxyl is often discussed alongside 7-OH because they are chemically related and may appear in similar products.

Category7-OHMitragynine Pseudoindoxyl
Full name7-hydroxymitragynineMitragynine pseudoindoxyl
Common shorthand7-OHMP or “pseudo”
Relationship to kratomMinor kratom alkaloid and mitragynine metabolite7-OH-related metabolite and semi-synthetic product compound
Opioid activityPotent mu-opioid receptor activityHighly selective mu-opioid receptor activity
Product concernConcentrated 7-OH tablets, shots, gummies, and extractsNewer products marketed as kratom or kratom alternatives
Main riskDependence, withdrawal, opioid-like effects, overdose concernsLimited human data, severe withdrawal concern, opioid-like effects

Neither 7-OH nor MP should be treated like ordinary kratom leaf. These compounds may create stronger opioid-like effects and a higher risk of dependence than traditional kratom products.

What To Do If You Have Been Using Mitragynine Pseudoindoxyl

If you have been using mitragynine pseudoindoxyl, do not assume that it is safe simply because it may be marketed as kratom-related. It may be more opioid-like than expected, and stopping suddenly may be difficult.

Consider getting professional support if you:

SituationWhy Support May Help
Use MP daily or near-dailyMay indicate physical dependence
Feel sick when you stopWithdrawal may need clinical support
Use 7-OH or kratom extracts tooWithdrawal may be stronger or more confusing
Mix with alcohol, benzos, or opioidsOverdose risk may increase
Have opioid addiction historyMP may trigger relapse pathways
Cannot cut downMay indicate addiction or loss of control
Feel severe anxiety or depressionMental health support may reduce relapse risk

If you are experiencing confusion, severe dehydration, chest pain, hallucinations, suicidal thoughts, or overdose symptoms, seek emergency medical help immediately.

Treatment for MP, 7-OH, Kratom, and Opioid Use in Maine

At Portland Treatment, we support people struggling with kratom-related products, 7-OH, mitragynine pseudoindoxyl, opioid use, withdrawal symptoms, and co-occurring mental health concerns. Many people do not realize they are using an opioid-active substance until they try to stop and feel withdrawal symptoms.

Treatment may include clinical assessment, medical referral when needed, therapy, relapse prevention planning, coping skills, medication-assisted treatment coordination when appropriate, and support for anxiety, depression, trauma, or polysubstance use.

Recovery starts with getting clear about what is happening and building a safer plan forward.

Frequently Asked Questions About Mitragynine Pseudoindoxyl

What is mitragynine pseudoindoxyl?

Mitragynine pseudoindoxyl is a kratom-related compound connected to mitragynine and 7-hydroxymitragynine. It is opioid receptor-active and has appeared in newer kratom-related products.

Is mitragynine pseudoindoxyl the same as 7-OH?

No. Mitragynine pseudoindoxyl and 7-OH are related, but they are not the same compound. MP may form from 7-OH and is also appearing in semi-synthetic product formulations.

Is mitragynine pseudoindoxyl FDA-approved?

No. Mitragynine pseudoindoxyl is not FDA-approved for any medical use.

Can mitragynine pseudoindoxyl cause withdrawal?

Yes, withdrawal is a serious concern. Emerging reports describe opioid-like withdrawal after use of mitragynine pseudoindoxyl products.

Is mitragynine pseudoindoxyl stronger than kratom?

It should not be viewed like ordinary kratom leaf. MP is a more potent opioid receptor-active compound and may carry stronger opioid-like risks.

Can naloxone reverse mitragynine pseudoindoxyl overdose?

There is limited human data, but because MP is opioid receptor-active, naloxone may help if opioid-related overdose is occurring. Call 911 immediately and use naloxone when opioid overdose is suspected.

Can Portland Treatment help with MP or 7-OH use?

Yes. Portland Treatment supports people struggling with kratom-related products, 7-OH, MP, opioids, withdrawal, and co-occurring mental health symptoms.

Sources

Center for Forensic Science Research and Education. (2025). Mitragynine pseudoindoxyl. NPS Discovery.
https://www.cfsre.org/nps-discovery/monographs/mitragynine-pseudoindoxyl

Hill, K., Behnke, M., Cotten, S., Huestis, M. A., & McCurdy, C. R. (2025). Characterization of novel 7-hydroxymitragynine and mitragynine pseudoindoxyl product marketing. Drug and Alcohol Dependence.
https://pubmed.ncbi.nlm.nih.gov/40373645/

Kamble, S. H., Sharma, A., León, F., Chear, N. J. Y., King, T. I., Berthold, E. C., Ramanathan, S., McMahon, L. R., Avery, B. A., & McCurdy, C. R. (2020). Metabolism of a kratom alkaloid metabolite in human plasma increases its opioid potency and efficacy. ACS Pharmacology & Translational Science, 3(6), 1063–1068.
https://pmc.ncbi.nlm.nih.gov/articles/PMC7737207/

Kruegel, A. C., Gassaway, M. M., Kapoor, A., Váradi, A., Majumdar, S., Filizola, M., Javitch, J. A., & Sames, D. (2016). Synthetic and receptor signaling explorations of the mitragyna alkaloids: Mitragynine as an atypical molecular framework for opioid receptor modulators. Journal of the American Chemical Society, 138(21), 6754–6764.
https://pmc.ncbi.nlm.nih.gov/articles/PMC5189718/

Stanciu, C. N., Penders, T. M., Gnanasegaram, S. A., & Penders, A. S. (2026). Severe early-onset withdrawal following intentional use of mitragynine pseudoindoxyl. Journal of Addiction Medicine.
https://pubmed.ncbi.nlm.nih.gov/41982589/

United Nations Office on Drugs and Crime. (2025, August 29). Emergence of potent kratom-related products containing 7-hydroxymitragynine and mitragynine pseudoindoxyl.
https://www.unodc.org/LSS/Announcement/Details/d0c66623-b200-4537-9f25-7df89fbdbf8b

Váradi, A., Marrone, G. F., Palmer, T. C., Narayan, A., Szabó, M. R., Le Rouzic, V., Grinnell, S. G., Subrath, J. J., Warner, E., Kalra, S., Hunkele, A., Pagirsky, J., Eans, S. O., Medina, J. M., Xu, J., Pan, Y. X., Borics, A., Pasternak, G. W., McLaughlin, J. P., & Majumdar, S. (2016). Mitragynine/corynantheidine pseudoindoxyls as opioid analgesics with μ agonism and δ antagonism, which do not recruit β-arrestin-2. Journal of Medicinal Chemistry, 59(18), 8381–8397.
https://pmc.ncbi.nlm.nih.gov/articles/PMC5344672/

Wilson, L. L., Harris, H. M., Eans, S. O., Brice-Tutt, A. C., Cirino, T. J., Stacy, H. M., Simons, C. A., Simpson, G. G., Grinnell, S. G., Lindsley, C. W., McCurdy, C. R., McLaughlin, J. P., & Prisinzano, T. E. (2021). Kratom alkaloids, natural and semi-synthetic, show less physical dependence and ameliorate precipitated withdrawal in morphine-dependent mice. British Journal of Pharmacology, 178(9), 1888–1903.
https://pmc.ncbi.nlm.nih.gov/articles/PMC8164968/

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John Ingham

John Ingham

John Ingham is a respected leader and medical content writer specializing in behavioral health, addiction treatment, and other mental health. With more than a decade of experience in the recovery and treatment field, his work has been featured across leading treatment networks and educational platforms, and has contributed as a lecturer in graduate level seminars within the Steve Hicks School of Social Work at University of Texas at Austin, and undergraduate seminars at Vanderbilt University. John's work has also been recognized in public service announcements, documentaries and more, including a feature that won an Emmy Award. John has collaborated with presidential appointees in the White House, clinicians, program directors, and other leaders throughout the behavioral health space, further establishing his role as a trusted voice in the field.

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