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Phencyclidine or phenylcyclohexyl piperidine (PCP), also known in its use as a street drug as angel dust among other names, is a dissociative anesthetic mainly used recreationally for its significant mind-altering effects. PCP may cause hallucinations, distorted perceptions of sounds, and psychotic behavior. As a recreational drug, it is typically…
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Explore the main themes, entities and connections around Phencyclidine. 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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| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Phencyclidine | 3D model (JSmol) | Interactive image | 1.00 | infobox |
| Phencyclidine | Addiction liability | Variable, reported from low to high | 1.00 | infobox |
| Phencyclidine | AHFS/Drugs.com | phencyclidine | 1.00 | infobox |
| Phencyclidine | ATC code | None | 1.00 | infobox |
| Phencyclidine | Boiling point | 136 °C (277 °F) | 1.00 | infobox |
| Phencyclidine | CAS Number | 77-10-1 Y | 1.00 | infobox |
| Phencyclidine | ChEBI | CHEBI:8058 N | 1.00 | infobox |
| Phencyclidine | ChEMBL | ChEMBL275528 Y | 1.00 | infobox |
| Phencyclidine | ChemSpider | 6224 Y | 1.00 | infobox |
| Phencyclidine | CompTox Dashboard (EPA) | DTXSID6023446 | 1.00 | infobox |
| Phencyclidine | Dependence liability | Physical: Low Psychological: Moderate | 1.00 | infobox |
| Phencyclidine | Drug class | NMDA receptor antagonists; General anesthetics; Dissociative hallucinogens | 1.00 | infobox |
| Phencyclidine | DrugBank | DB03575 Y | 1.00 | infobox |
| Phencyclidine | Duration of action | 6–48 hours | 1.00 | infobox |
| Phencyclidine | ECHA InfoCard | 100.150.427 | 1.00 | infobox |
| Phencyclidine | Elimination half-life | 7–46 hours | 1.00 | infobox |
| Phencyclidine | Excretion | Urine | 1.00 | infobox |
| Phencyclidine | Formula | C17H25N | 1.00 | infobox |
| Phencyclidine | IUPHAR/BPS | 4282 | 1.00 | infobox |
| Phencyclidine | KEGG | C07575 Y | 1.00 | infobox |
| Phencyclidine | Legal status | AU: S8 (Controlled drug) | 1.00 | infobox |
| Phencyclidine | Legal status | BR: Class A3 (Psychoactive drugs) | 1.00 | infobox |
| Phencyclidine | Legal status | CA: Schedule I | 1.00 | infobox |
| Phencyclidine | Legal status | DE: Anlage I (Authorized scientific use only) | 1.00 | infobox |
| Phencyclidine | Legal status | NZ: Class A | 1.00 | infobox |
| Phencyclidine | Legal status | UK: Class A | 1.00 | infobox |
| Phencyclidine | Legal status | US: Schedule II | 1.00 | infobox |
| Phencyclidine | Legal status | UN: Psychotropic Schedule II | 1.00 | infobox |
| Phencyclidine | Legal status | Tabella I in Italy | 1.00 | infobox |
| Phencyclidine | Melting point | 46.5 °C (115.7 °F) | 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.