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α-Ethyltryptamine (αET, AET), also known as etryptamine, is an entactogen and stimulant drug of the tryptamine family. It was originally developed and marketed as an antidepressant under the brand name Monase by Upjohn in the 1960s before being withdrawn due to toxicity.
The analysis highlights History, Community, Culture and Applications as prominent areas in the source structure around Α-Ethyltryptamine.
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 Α-Ethyltryptamine shows recurring relationship patterns in the source. For example, Α-Ethyltryptamine → AET, BANTooltip British Approved Name, ET, Etryptamine, In, INNTooltip International Nonproprietary Name, Monase, Name, NSC-63963, NSC-88061, Other, PAL-125, Ro, U-17312E, USANTooltip United States Adopted Another extracted example is Α-Ethyltryptamine → BR: Class F2 (Prohibited psychotropics), CA: Schedule III, DE: Anlage I (Authorized scientific use only), 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.
αet serotonin effects drug antidepressant doses receptor agonist described used mg etryptamine name monoamine united releasing states also side monase
TTTA extracted 51 structured relationships around Α-Ethyltryptamine. Examples in this analysis include Α-Ethyltryptamine → 3D model (JSmol) → Interactive image and Α-Ethyltryptamine → ATC code → None. The table shows each extracted connection, where it came from and its confidence.
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Α-Ethyltryptamine | 3D model (JSmol) | Interactive image | 1.00 | infobox |
| Α-Ethyltryptamine | ATC code | None | 1.00 | infobox |
| Α-Ethyltryptamine | CAS Number | 2235-90-7 Y 118-68-3 (acetate) 26330-11-0 (hydrochloride) | 1.00 | infobox |
| Α-Ethyltryptamine | ChEBI | CHEBI:134838 | 1.00 | infobox |
| Α-Ethyltryptamine | ChEMBL | ChEMBL1619758 | 1.00 | infobox |
| Α-Ethyltryptamine | ChemSpider | 8064 Y | 1.00 | infobox |
| Α-Ethyltryptamine | CompTox Dashboard (EPA) | DTXSID1046764 | 1.00 | infobox |
| Α-Ethyltryptamine | Drug class | Entactogen; Stimulant; Serotonin-norepinephrine-dopamine releasing agent; Serotonin receptor agonist; Monoamine oxidase inhibitor; Serotonergic neurotoxin | 1.00 | infobox |
| Α-Ethyltryptamine | DrugBank | DB01546 Y | 1.00 | infobox |
| Α-Ethyltryptamine | Duration of action | 6–8 hours (100–150 mg) | 1.00 | infobox |
| Α-Ethyltryptamine | Elimination half-life | ~8 hours | 1.00 | infobox |
| Α-Ethyltryptamine | Excretion | Urine (majority) | 1.00 | infobox |
| Α-Ethyltryptamine | Formula | C12H16N2 | 1.00 | infobox |
| Α-Ethyltryptamine | KEGG | D04092 | 1.00 | infobox |
| Α-Ethyltryptamine | Legal status | BR: Class F2 (Prohibited psychotropics) | 1.00 | infobox |
| Α-Ethyltryptamine | Legal status | CA: Schedule III | 1.00 | infobox |
| Α-Ethyltryptamine | Legal status | DE: Anlage I (Authorized scientific use only) | 1.00 | infobox |
| Α-Ethyltryptamine | Legal status | UK: Class A | 1.00 | infobox |
| Α-Ethyltryptamine | Legal status | US: Schedule I | 1.00 | infobox |
| Α-Ethyltryptamine | Legal status | UN: Psychotropic Schedule I | 1.00 | infobox |
| Α-Ethyltryptamine | Melting point | 222 to 223 °C (432 to 433 °F) | 1.00 | infobox |
| Α-Ethyltryptamine | Metabolism | Hydroxylation | 1.00 | infobox |
| Α-Ethyltryptamine | Metabolites | • 6-Hydroxy-αET (inactive) | 1.00 | infobox |
| Α-Ethyltryptamine | Molar mass | 188.274 g·mol−1 | 1.00 | infobox |
| Α-Ethyltryptamine | Onset of action | 0.5–1.5 hours | 1.00 | infobox |
| Α-Ethyltryptamine | Other names | alpha-Ethyltryptamine; αET; AET; α-ET; Etryptamine; PAL-125; 3-(2-Aminobutyl)indole; 3-Indolylbutylamine; U-17312E; U17312E; Ro 3-1932; NSC-63963; NSC-88061, Etryptamine (USAN US) | 1.00 | infobox |
| Α-Ethyltryptamine | PubChem CID | 8367 | 1.00 | infobox |
| Α-Ethyltryptamine | PubChem SID | 46507084 | 1.00 | infobox |
| Α-Ethyltryptamine | Routes of administration | Oral | 1.00 | infobox |
| Α-Ethyltryptamine | Trade names | Monase | 1.00 | infobox |
The concept neighborhoods around Α-Ethyltryptamine bring nearby vocabulary together. In this analysis, examples include Aet, 3- and Also. Use the clusters to find adjacent concepts and terminology that may deserve separate research.
For Α-Ethyltryptamine, one of the stronger structural bridges in this analysis connects Α-Ethyltryptamine with Pharmacology. 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 Α-Ethyltryptamine 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 — Α-Ethyltryptamine · EN edition · Analysis: TopicsToTalkAbout