etoxadrol has been researched along with phencyclidine in 4 studies
*Phencyclidine: A hallucinogen formerly used as a veterinary anesthetic, and briefly as a general anesthetic for humans. Phencyclidine is similar to KETAMINE in structure and in many of its effects. Like ketamine, it can produce a dissociative state. It exerts its pharmacological action through inhibition of NMDA receptors (RECEPTORS, N-METHYL-D-ASPARTATE). As a drug of abuse, it is known as PCP and Angel Dust. [MeSH]
*Phencyclidine: A hallucinogen formerly used as a veterinary anesthetic, and briefly as a general anesthetic for humans. Phencyclidine is similar to KETAMINE in structure and in many of its effects. Like ketamine, it can produce a dissociative state. It exerts its pharmacological action through inhibition of NMDA receptors (RECEPTORS, N-METHYL-D-ASPARTATE). As a drug of abuse, it is known as PCP and Angel Dust. [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Harrison, EA; Jacobson, AE; Mattson, MV; Mirsadeghi, S; Monn, JA; Ornstein, PL; Rice, KC; Richardson, S; Thurkauf, A | 1 |
| Bigge, CF; Colbry, NL; Hays, SJ; Johnson, G; Lescosky, LJ; Malone, TC; Michael, A; Novak, PM; Ortwine, DF; Reily, MD | 1 |
| Köhler, J; Utech, T; Wünsch, B | 1 |
| Amantini, C; Barocelli, E; Bertoni, S; Bonifazi, A; Cimarelli, C; Del Bello, F; Flammini, L; Mammoli, V; Nabissi, M; Pellei, M; Petrelli, R; Piergentili, A; Quaglia, W; Santoni, G; Schepmann, D; Vistoli, G; Wünsch, B | 1 |
4 other study(ies) available for etoxadrol and phencyclidine
| Article | Year |
|---|---|
Analogues of the dioxolanes dexoxadrol and etoxadrol as potential phencyclidine-like agents. Synthesis and structure-activity relationships.
Topics: Analgesics; Animals; Binding Sites; Brain; Dioxolanes; Phencyclidine; Piperidines; Rats; Structure-Activity Relationship | 1992 |
Synthesis and pharmacological evaluation of hexahydrofluorenamines as noncompetitive antagonists at the N-methyl-D-aspartate receptor.
Topics: Animals; Binding Sites; Fluorenes; Magnetic Resonance Spectroscopy; Male; Mice; Models, Molecular; Phencyclidine; Rats; Receptors, N-Methyl-D-Aspartate; Seizures; Stereoisomerism; Structure-Activity Relationship | 1993 |
Synthesis of 4-(aminoalkyl) substituted 1,3-dioxanes as potent NMDA and σ receptor antagonists.
Topics: Animals; Brain; Dioxanes; Molecular Structure; Receptors, N-Methyl-D-Aspartate; Receptors, sigma; Stereoisomerism; Structure-Activity Relationship; Swine | 2011 |
Novel Potent N-Methyl-d-aspartate (NMDA) Receptor Antagonists or σ1 Receptor Ligands Based on Properly Substituted 1,4-Dioxane Ring.
Topics: Analgesics; Animals; Binding Sites; Dioxanes; Drug Design; Ligands; Mice; Models, Molecular; Pain; Phencyclidine; Rats; Receptors, N-Methyl-D-Aspartate; Receptors, sigma; Sigma-1 Receptor | 2015 |