Page last updated: 2024-09-03

o-demethyltramadol and Ache

o-demethyltramadol has been researched along with Ache in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (50.00)29.6817
2010's3 (37.50)24.3611
2020's1 (12.50)2.80

Authors

AuthorsStudies
Court, MH; Greene, SA; Grubb, TL; Joo, H; Kukanich, B; Mealey, KL; Perez Jimenez, TE1
Brosen, K; Damkier, P; Larsen, F; Noehr-Jensen, L; Sindrup, SH; Zwisler, ST1
Akgül, O; Aypar, U; Dogrul, A; Kozak, O; Kurt, E; Sahin, A; Seyrek, M; Sizlan, A; Yanarates, O; Yildirim, V1
Leppert, W; Mikolajczak, P1
Balzarini, P; Baratelli, E; Bianchi, M; Broggini, M; Ferrario, P; Panerai, AE; Sacerdote, P1
Abolin, C; Hewitt, MC; Koch, P; Shao, L; Varney, M1
Bakale, R; Bhongle, N; Currie, M; Fang, K; Grover, P; Hewitt, M; Jerussi, TP; Koch, P; Malcolm, S; Ribe, S; Senanayake, C; Shao, L; Wu, F1
Fu, W; Huang, H; Li, W; Liu, J; Wang, W; Wang, Y; Xu, X; Zhu, C1

Trials

3 trial(s) available for o-demethyltramadol and Ache

ArticleYear
Oral Coadministration of Fluconazole with Tramadol Markedly Increases Plasma and Urine Concentrations of Tramadol and the
    Drug metabolism and disposition: the biological fate of chemicals, 2019, Volume: 47, Issue:1

    Topics: Administration, Oral; Analgesics, Opioid; Animals; Cross-Over Studies; Dogs; Drug Interactions; Female; Fluconazole; Male; Pain; Random Allocation; Tramadol

2019
Escitalopram is a weak inhibitor of the CYP2D6-catalyzed O-demethylation of (+)-tramadol but does not reduce the hypoalgesic effect in experimental pain.
    Clinical pharmacology and therapeutics, 2009, Volume: 86, Issue:6

    Topics: Adult; Analgesics, Opioid; Biotransformation; Citalopram; Cross-Over Studies; Cytochrome P-450 CYP2D6; Cytochrome P-450 CYP2D6 Inhibitors; Dealkylation; Double-Blind Method; Drug Interactions; Enzyme Inhibitors; Female; Humans; Male; Pain; Pain Measurement; Reflex, Pupillary; Selective Serotonin Reuptake Inhibitors; Tramadol; Young Adult

2009
Effects of tramadol on synovial fluid concentrations of substance P and interleukin-6 in patients with knee osteoarthritis: comparison with paracetamol.
    International immunopharmacology, 2003, Volume: 3, Issue:13-14

    Topics: Acetaminophen; Administration, Oral; Aged; Double-Blind Method; Female; Humans; Interleukin-6; Male; Middle Aged; Osteoarthritis, Knee; Pain; Pain Measurement; Prospective Studies; Substance P; Synovial Fluid; Time Factors; Tramadol

2003

Other Studies

5 other study(ies) available for o-demethyltramadol and Ache

ArticleYear
Spinal 5-HT7 receptors play an important role in the antinociceptive and antihyperalgesic effects of tramadol and its metabolite, O-Desmethyltramadol, via activation of descending serotonergic pathways.
    Anesthesiology, 2010, Volume: 112, Issue:3

    Topics: Analgesics; Analgesics, Opioid; Animals; Dose-Response Relationship, Drug; Hot Temperature; Hyperalgesia; Injections, Spinal; Male; Mice; Mice, Inbred BALB C; Neural Pathways; Pain; Pain Measurement; Pain, Postoperative; Reaction Time; Receptors, Serotonin; Serotonin; Serotonin Antagonists; Spinal Cord; Tramadol

2010
Analgesic effects and assays of controlled-release tramadol and o-desmethyltramadol in cancer patients with pain.
    Current pharmaceutical biotechnology, 2011, Feb-01, Volume: 12, Issue:2

    Topics: Aged; Aged, 80 and over; Analgesia; Analgesics, Opioid; Codeine; Delayed-Action Preparations; Dose-Response Relationship, Drug; Drug Interactions; Female; Humans; Male; Middle Aged; Neoplasms; Pain; Pain Measurement; Tramadol

2011
Derivatives of tramadol for increased duration of effect.
    Bioorganic & medicinal chemistry letters, 2006, Volume: 16, Issue:3

    Topics: Analgesics, Opioid; Animals; Binding Sites; Codeine; Models, Chemical; Morphine; Pain; Rats; Time Factors; Tramadol

2006
In vitro and in vivo evaluation of O-alkyl derivatives of tramadol.
    Bioorganic & medicinal chemistry letters, 2008, Mar-01, Volume: 18, Issue:5

    Topics: Analgesics, Opioid; Animals; Humans; Microsomes, Liver; Molecular Structure; Pain; Protein Binding; Rats; Structure-Activity Relationship; Tramadol

2008
Discovery of 3-((dimethylamino)methyl)-4-hydroxy-4-(3-methoxyphenyl)-N-phenylpiperidine-1-carboxamide as novel potent analgesic.
    European journal of medicinal chemistry, 2020, Mar-01, Volume: 189

    Topics: Analgesics; Animals; Female; Ligands; Mice; Models, Molecular; Pain; Piperidines; Receptors, Opioid, delta; Receptors, Opioid, kappa; Receptors, Opioid, mu; Structure-Activity Relationship

2020