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3,4-Methylenedioxymethamphetamine (MDMA), commonly known as ecstasy in tablet form, and molly in crystal form, is an entactogen with stimulant and minor psychedelic properties.
History, Community, Culture & Applications
Explore the main themes, entities and connections around MDMA. Start with the topic map, then use the sections below for research and deeper semantic analysis.
Start with a few of the strongest sections from the source topic. These are research directions, not a list of keywords you must use.
High-confidence facts extracted from structured source data. Use them as anchors for further research.
Browse the full topic structure. Each item opens a new analysis centered on that subject.
Deeper signals for content research, entity SEO and topical coverage. The plain-language headings explain what each technical view is useful for.
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Use these terms to understand the vocabulary surrounding the topic, not as a checklist for keyword stuffing.
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| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| MDMA | 3D model (JSmol) | Interactive image | 1.00 | infobox |
| MDMA | Addiction liability | Low–moderate | 1.00 | infobox |
| MDMA | AHFS/Drugs.com | MDMA | 1.00 | infobox |
| MDMA | ATC code | None | 1.00 | infobox |
| MDMA | Bioavailability | Oral: Unknown | 1.00 | infobox |
| MDMA | Boiling point | 105 °C (221 °F) at 0.4 mmHg (experimental) | 1.00 | infobox |
| MDMA | CAS Number | 42542-10-9 Y[TOXNET] 64057-70-1 (HCl) | 1.00 | infobox |
| MDMA | ChEBI | CHEBI:1391 Y | 1.00 | infobox |
| MDMA | ChEMBL | ChEMBL43048 Y | 1.00 | infobox |
| MDMA | ChemSpider | 1556 Y | 1.00 | infobox |
| MDMA | Chirality | Racemic mixture | 1.00 | infobox |
| MDMA | CompTox Dashboard (EPA) | DTXSID90860791 | 1.00 | infobox |
| MDMA | Density | 1.1 g/cm3 | 1.00 | infobox |
| MDMA | Dependence liability | Physical: Not typical Psychological: Moderate | 1.00 | infobox |
| MDMA | Drug class | Entactogen; Stimulant; Psychedelic; Serotonin–norepinephrine–dopamine releasing agent; 5-HT2 receptor agonist | 1.00 | infobox |
| MDMA | DrugBank | DB01454 Y | 1.00 | infobox |
| MDMA | Duration of action | 3–6 hours | 1.00 | infobox |
| MDMA | Elimination half-life | MDMA: 8.7 (range 4.6–16) hours | 1.00 | infobox |
| MDMA | Elimination half-life | (S)-MDMA: 5.1 (range 3.5–7.4) hours | 1.00 | infobox |
| MDMA | Elimination half-life | (R)-MDMA: 11 (range 5.1–24) hours | 1.00 | infobox |
| MDMA | Excretion | Kidney | 1.00 | infobox |
| MDMA | Formula | C11H15NO2 | 1.00 | infobox |
| MDMA | IUPHAR/BPS | 4574 | 1.00 | infobox |
| MDMA | KEGG | D11172 Y | 1.00 | infobox |
| MDMA | Legal status | AU: S8 (PTSD)S9 (all other uses) | 1.00 | infobox |
| MDMA | Legal status | S8 (PTSD) | 1.00 | infobox |
| MDMA | Legal status | S9 (all other uses) | 1.00 | infobox |
| MDMA | Legal status | BR: Class F2 (Prohibited psychotropics) | 1.00 | infobox |
| MDMA | Legal status | CA: Schedule I | 1.00 | infobox |
| MDMA | Legal status | DE: Anlage I (Authorized scientific use only) | 1.00 | infobox |
These clusters group vocabulary that occurs around closely connected concepts in the source material.
Bridges can reveal useful research angles that are easy to miss in a flat list of related terms.