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Phenethylamine (PEA) is an organic compound, natural monoamine alkaloid, and trace amine, which acts as a central nervous system stimulant in humans. In the brain, phenethylamine regulates monoamine neurotransmission by binding to trace amine-associated receptor 1 (TAAR1) and inhibiting vesicular monoamine transporter 2 (VMAT2) in monoamine neurons. To a…
The analysis highlights History, Chemistry and Pharmacology as prominent areas in the source structure around Phenethylamine. 1 topic appears in more than one source area, which can help identify connections that are less obvious in a linear reading.
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 Phenethylamine shows recurring relationship patterns in the source. For example, Phenethylamine → AANAT, AOC2, AOC3, By, FMO3, In, MAO-A, MAO-B, MAOI, N-acetyltransferase, N-Methylphenethylamine, N-methyltransferase, PEA, Phenylacetaldehyde, Phenylacetic, PNMT, SSAOs, When Another extracted example is Phenethylamine → ADHD, An ADHD, Because, Brain, Endogenous, In, L-phenylalanine, MAO-B, Monoamine, PEA, Reviews, Similarly, These, Thirty, Two. 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.
monoamine also dopamine acid amphetamine oxidase substituted trace many produced phenethylamines taar1 mg kg metabolism mao-b humans brain pea class
TTTA extracted 109 structured relationships around Phenethylamine. Examples in this analysis include Phenethylamine → 3D model (JSmol) → Interactive image and Phenethylamine → Addiction liability → None–low (w/o an MAO-B inhibitor) Moderate (with an MAO-B inhibitor). The table shows each extracted connection, where it came from and its confidence.
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Phenethylamine | 3D model (JSmol) | Interactive image | 1.00 | infobox |
| Phenethylamine | Addiction liability | None–low (w/o an MAO-B inhibitor) Moderate (with an MAO-B inhibitor) | 1.00 | infobox |
| Phenethylamine | ATC code | None | 1.00 | infobox |
| Phenethylamine | Biosynthesis | Aromatic L-amino acid decarboxylase (AADC) | 1.00 | infobox |
| Phenethylamine | Boiling point | 195 °C (383 °F) | 1.00 | infobox |
| Phenethylamine | CAS Number | 64-04-0 Y | 1.00 | infobox |
| Phenethylamine | ChEBI | CHEBI:18397 Y | 1.00 | infobox |
| Phenethylamine | ChEMBL | ChEMBL610 Y | 1.00 | infobox |
| Phenethylamine | ChemSpider | 13856352 Y | 1.00 | infobox |
| Phenethylamine | CompTox Dashboard (EPA) | DTXSID5058773 | 1.00 | infobox |
| Phenethylamine | Density | 0.9640 g/cm3 | 1.00 | infobox |
| Phenethylamine | Dependence liability | Psychological: Low–moderate[citation needed] Physical: None | 1.00 | infobox |
| Phenethylamine | Drug class | Norepinephrine–dopamine releasing agent; Trace amine-associated receptor 1 (TAAR1) agonist; Stimulant | 1.00 | infobox |
| Phenethylamine | DrugBank | DB04325 Y | 1.00 | infobox |
| Phenethylamine | ECHA InfoCard | 100.000.523 | 1.00 | infobox |
| Phenethylamine | Elimination half-life | Exogenous: 5–10 minutes | 1.00 | infobox |
| Phenethylamine | Elimination half-life | Endogenous: ~30 seconds | 1.00 | infobox |
| Phenethylamine | Excretion | Renal (kidneys) | 1.00 | infobox |
| Phenethylamine | Formula | C8H11N | 1.00 | infobox |
| Phenethylamine | IUPHAR/BPS | 2144 | 1.00 | infobox |
| Phenethylamine | KEGG | C05332 Y | 1.00 | infobox |
| Phenethylamine | Legal status | AU: Unscheduled | 1.00 | infobox |
| Phenethylamine | Legal status | CA: Unscheduled | 1.00 | infobox |
| Phenethylamine | Legal status | NZ: Unscheduled | 1.00 | infobox |
| Phenethylamine | Legal status | UK: Unscheduled | 1.00 | infobox |
| Phenethylamine | Legal status | US: Unscheduled | 1.00 | infobox |
| Phenethylamine | Legal status | UN: Unscheduled | 1.00 | infobox |
| Phenethylamine | Melting point | −60 °C (−76 °F) | 1.00 | infobox |
| Phenethylamine | Metabolism | Primarily: MAO-B Other enzymes: MAO-A, SSAOs (AOC2 & AOC3), PNMT, AANAT, FMO3, and others | 1.00 | infobox |
| Phenethylamine | Molar mass | 121.183 g·mol−1 | 1.00 | infobox |
The concept neighborhoods around Phenethylamine bring nearby vocabulary together. In this analysis, examples include Urinary, Acid and Also. Use the clusters to find adjacent concepts and terminology that may deserve separate research.
For Phenethylamine, one of the stronger structural bridges in this analysis connects Phenethylamine 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 Phenethylamine to surface related topics, entities, relationships, concept neighborhoods and bridge connections. Use the map to explore areas such as History, Chemistry & Pharmacology, including less central topics that may reveal useful research gaps. Automatically extracted connections are research leads rather than rewritten encyclopedia content.
Source: Wikipedia — Phenethylamine · EN edition · Analysis: TopicsToTalkAbout