2-MMC
2-methylmethcathinone
Standing risks
| Risk | Recorded values | Confidence | Article section |
|---|---|---|---|
| Compulsive use risk, monitor frequency |
| low | View in article: Compulsive use risk, monitor frequency |
| High dependence, taper carefully |
| low | View in article: High dependence, taper carefully |
Lethal interactions
| Combination | Type | Severity | Mechanisms | Confidence |
|---|---|---|---|---|
| MAOIs | Drug class | lethal | 3 | high |
Dangerous interactions
25 dangerous interactions recorded for this substance.
See the full interactions tableContraindications
| Condition | Severity | Note |
|---|---|---|
| Cardiovascular | ||
| Cardiovascular disease | absolute | coronary artery disease, heart failure, uncontrolled hypertension, structural heart defects, history of arrhythmia Cathinone-induced norepinephrine release produces dose-dependent increases in heart rate and blood pressure. Serious cardiac events including myocardial infarction, cardiac arrest, and ventricular tachycardia are documented in the synthetic cathinone class. No 2-MMC-specific cardiac data exist; classification based on shared sympathomimetic mechanism with 3-MMC and mephedrone. |
| Neurological | ||
| Seizure disorders | relative | epilepsy, history of seizures, conditions lowering seizure threshold Seizures are documented in approximately 8% of 3-MMC intoxication presentations (Swedish STRIDA project data). Monoamine releasing agents lower seizure threshold through excessive catecholamine release. No 2-MMC-specific seizure data exist; risk inferred from cathinone class. |
| Psychiatric | ||
| Active psychosis, bipolar disorder, severe anxiety | relative | active psychosis, bipolar disorder, severe anxiety disorders, schizophrenia spectrum disorders Dopaminergic stimulation from monoamine releasing agents can precipitate or exacerbate psychotic symptoms, manic episodes, and panic attacks. Cathinone-class literature documents hallucinations in 20% and agitation in 42% of intoxication presentations. Individuals with pre-existing psychiatric vulnerability are at elevated risk. |
| Hepatic | ||
| Hepatic impairment | relative | liver disease, hepatic insufficiency, CYP2D6 poor metabolizer status If CYP2D6 and CYP2E1 mediate 2-MMC metabolism as predicted from 3-MMC hepatocyte data (Dias da Silva 2019), impaired hepatic function would alter drug clearance and potentially increase exposure to toxic metabolites. 3-MMC induces oxidative stress, apoptosis, and autophagy in rat hepatocytes at human-relevant concentrations. |
| Pregnancy & Breastfeeding | ||
| Pregnancy and lactation | absolute | pregnancy, lactation No reproductive toxicity data exist for 2-MMC. Sympathomimetic stimulants as a class carry risks of placental vasoconstriction, fetal tachycardia, preterm labor, and developmental effects. The contraindication is mechanism-based and applies to all monoamine releasing agents. |
| Other | ||
| Concurrent MAOI therapy | absolute | phenelzine use, tranylcypromine use, moclobemide use, selegiline use, harmine/harmaline use Combination of any monoamine oxidase inhibitor with a monoamine releasing agent like 2-MMC produces catastrophic monoamine accumulation. This can result in hypertensive crisis, serotonin syndrome, hyperthermia, and death. The contraindication is absolute and mechanism-based — no substance-specific data are needed to classify this interaction as life-threatening. |
| Vigorous activity in hot environments | relative | vigorous physical exertion, hot environmental conditions, dehydration Physical exertion in hot environments compounds the cathinone-class risk of hyperthermia, which is documented in 6% of 3-MMC intoxication presentations. Cathinones impair thermoregulation through sympathomimetic mechanisms. Dance venues and festivals represent particular risk settings. |