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Dimethyltryptamine (DMT), also known as N,N-dimethyltryptamine (N,N-DMT), is a serotonergic hallucinogen and investigational drug of the tryptamine family that occurs naturally in many plants and animals. DMT is used as a psychedelic drug and prepared by various cultures for ritual purposes as an entheogen.
The analysis highlights History, Community, Culture and Applications as prominent areas in the source structure around Dimethyltryptamine.
Source areas are shown by the number of related topics found in each part of the analysis. Use smaller areas too: they can reveal specialized angles and content gaps.
Smaller areas are not necessarily less important. They contain fewer connections in this analysis and can be useful for finding specialized angles or coverage gaps.
High-confidence facts extracted from structured source data. Use them as anchors for further research.
Browse the complete topic structure, not only the most central items. Less prominent entities and concepts can reveal missing angles, specialized context and useful research gaps. 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.
The extracted context around Dimethyltryptamine shows recurring relationship patterns in the source. For example, Dimethyltryptamine → AADC, CH3, DMT, In, INMT, Its, L-tryptophan, N-dimethyltryptamine, N-methyltransferase, N-methyltryptamine, NMT, No, S-adenosylhomocysteine, S-adenosylmethionine, SAH, SAM, The, This, Tryptamine Another extracted example is Dimethyltryptamine → AU: S9 (Prohibited substance), BR: Class F2 (Prohibited psychotropics), CA: Schedule III, DE: Anlage I (Authorized scientific use only), EU: Illegal, SE: Illegal, UK: Class A, UN: Psychotropic Schedule I, US: Schedule I. Use these groups to spot repeated connection types before inspecting the individual relationships.
Use these terms to understand the vocabulary surrounding the topic, not as a checklist for keyword stuffing.
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TTTA extracted 135 structured relationships around Dimethyltryptamine. Examples in this analysis include Dimethyltryptamine → 3D model (JSmol) → Interactive image and Dimethyltryptamine → Addiction liability → None or very low. The table shows each extracted connection, where it came from and its confidence.
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Dimethyltryptamine | 3D model (JSmol) | Interactive image | 1.00 | infobox |
| Dimethyltryptamine | Addiction liability | None or very low | 1.00 | infobox |
| Dimethyltryptamine | ATC code | None | 1.00 | infobox |
| Dimethyltryptamine | Bioavailability | Very low and inactive (except with MAOITooltip monoamine oxidase inhibitor) | 1.00 | infobox |
| Dimethyltryptamine | Boiling point | 160 °C (320 °F) at 0.6 Torr (80 Pa) also reported as 80–135 °C (176–275 °F) at 0.03 Torr (4.0 Pa) | 1.00 | infobox |
| Dimethyltryptamine | CAS Number | 61-50-7 Y | 1.00 | infobox |
| Dimethyltryptamine | ChEBI | CHEBI:28969 Y | 1.00 | infobox |
| Dimethyltryptamine | ChEMBL | ChEMBL12420 Y | 1.00 | infobox |
| Dimethyltryptamine | ChemSpider | 5864 Y | 1.00 | infobox |
| Dimethyltryptamine | CompTox Dashboard (EPA) | DTXSID60110053 | 1.00 | infobox |
| Dimethyltryptamine | Density | 1.099 g/cm3 | 1.00 | infobox |
| Dimethyltryptamine | Dependence liability | None or very low | 1.00 | infobox |
| Dimethyltryptamine | Drug class | Serotonin receptor agonist; Serotonin 5-HT2A receptor agonist; Serotonergic psychedelic; Hallucinogen | 1.00 | infobox |
| Dimethyltryptamine | DrugBank | DB01488 Y | 1.00 | infobox |
| Dimethyltryptamine | Duration of action | Inhalation: ≤15 min | 1.00 | infobox |
| Dimethyltryptamine | Duration of action | Intravenous: ≤30 min | 1.00 | infobox |
| Dimethyltryptamine | Duration of action | Intramuscular: 30–60 min | 1.00 | infobox |
| Dimethyltryptamine | Duration of action | Oral with MAOITooltip monoamine oxidase inhibitor: 4–6 hours | 1.00 | infobox |
| Dimethyltryptamine | ECHA InfoCard | 100.000.463 | 1.00 | infobox |
| Dimethyltryptamine | Elimination half-life | Alone: 5–19 min | 1.00 | infobox |
| Dimethyltryptamine | Elimination half-life | With MAOITooltip monoamine oxidase inhibitor: 1–4 hours | 1.00 | infobox |
| Dimethyltryptamine | Excretion | Urine | 1.00 | infobox |
| Dimethyltryptamine | Formula | C12H16N2 | 1.00 | infobox |
| Dimethyltryptamine | IUPHAR/BPS | 141 | 1.00 | infobox |
| Dimethyltryptamine | KEGG | C08302 Y | 1.00 | infobox |
| Dimethyltryptamine | Legal status | AU: S9 (Prohibited substance) | 1.00 | infobox |
| Dimethyltryptamine | Legal status | BR: Class F2 (Prohibited psychotropics) | 1.00 | infobox |
| Dimethyltryptamine | Legal status | CA: Schedule III | 1.00 | infobox |
| Dimethyltryptamine | Legal status | DE: Anlage I (Authorized scientific use only) | 1.00 | infobox |
| Dimethyltryptamine | Legal status | UK: Class A | 1.00 | infobox |
The concept neighborhoods around Dimethyltryptamine bring nearby vocabulary together. In this analysis, examples include Intravenous, Injection and Administration. Use the clusters to find adjacent concepts and terminology that may deserve separate research.
For Dimethyltryptamine, one of the stronger structural bridges in this analysis connects Dimethyltryptamine with Overview. Bridges highlight paths between different parts of the map and can reveal research angles that are easy to miss in a flat list.
TTTA analyzes the structure around Dimethyltryptamine to surface related topics, entities, relationships, concept neighborhoods and bridge connections. Use the map to explore areas such as History, Community, Culture & Applications, including less central topics that may reveal useful research gaps. Automatically extracted connections are research leads rather than rewritten encyclopedia content.
Source: Wikipedia — Dimethyltryptamine · EN edition · Analysis: TopicsToTalkAbout