4-methoxymethylfentanyl has been researched along with fentanyl in 5 studies
*Fentanyl: A potent narcotic analgesic, abuse of which leads to habituation or addiction. It is primarily a mu-opioid agonist. Fentanyl is also used as an adjunct to general anesthetics, and as an anesthetic for induction and maintenance. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1078) [MeSH]
*Fentanyl: A potent narcotic analgesic, abuse of which leads to habituation or addiction. It is primarily a mu-opioid agonist. Fentanyl is also used as an adjunct to general anesthetics, and as an anesthetic for induction and maintenance. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1078) [MeSH]
Studies (4-methoxymethylfentanyl) | Trials (4-methoxymethylfentanyl) | Recent Studies (post-2010) (4-methoxymethylfentanyl) | Studies (fentanyl) | Trials (fentanyl) | Recent Studies (post-2010) (fentanyl) |
---|---|---|---|---|---|
5 | 0 | 0 | 15,288 | 4,310 | 4,483 |
Protein | Taxonomy | 4-methoxymethylfentanyl (IC50) | fentanyl (IC50) |
---|---|---|---|
ATP-dependent translocase ABCB1 | Homo sapiens (human) | 6.5 | |
Delta-type opioid receptor | Mus musculus (house mouse) | 0.6342 | |
Delta-type opioid receptor | Rattus norvegicus (Norway rat) | 0.0122 | |
Mu-type opioid receptor | Rattus norvegicus (Norway rat) | 0.1888 | |
Kappa-type opioid receptor | Rattus norvegicus (Norway rat) | 0.0122 | |
Mu-type opioid receptor | Homo sapiens (human) | 0.0058 | |
Delta-type opioid receptor | Homo sapiens (human) | 0.3092 | |
Kappa-type opioid receptor | Cavia porcellus (domestic guinea pig) | 5.893 | |
Kappa-type opioid receptor | Homo sapiens (human) | 1.58 | |
Mu-type opioid receptor | Cavia porcellus (domestic guinea pig) | 0.0031 | |
Potassium voltage-gated channel subfamily H member 2 | Homo sapiens (human) | 1.8197 | |
Sigma non-opioid intracellular receptor 1 | Cavia porcellus (domestic guinea pig) | 4.973 | |
Sigma non-opioid intracellular receptor 1 | Homo sapiens (human) | 0.354 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (20.00) | 18.7374 |
1990's | 3 (60.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ferguson, DM; Paterlini, MG; Portoghese, PS; Subramanian, G | 1 |
Costa, EM; Hoffmann, BB; Loew, GH | 1 |
Cometta-Morini, C; Kamal, J; Loew, G; Maguire, P; Tsai, N; Upton, C | 1 |
He, K; Qiu, ZY; Quan, YZ | 1 |
Andrews, P; Martin, J | 1 |
5 other study(ies) available for 4-methoxymethylfentanyl and fentanyl
Article | Year |
---|---|
Molecular docking reveals a novel binding site model for fentanyl at the mu-opioid receptor.
Topics: Amino Acid Sequence; Binding Sites; Fentanyl; Humans; Ligands; Models, Molecular; Molecular Conformation; Molecular Sequence Data; Receptors, Opioid, delta; Receptors, Opioid, kappa; Receptors, Opioid, mu; Stereoisomerism; Structure-Activity Relationship | 2000 |
Opioid agonists binding and responses in SH-SY5Y cells.
Topics: Alprostadil; Analgesics; Cyclic AMP; Endorphins; Enkephalin, Ala(2)-MePhe(4)-Gly(5)-; Enkephalins; Fentanyl; GTP Phosphohydrolases; Humans; Meperidine; Morphinans; Naloxone; Narcotics; Oxymorphone; Receptors, Opioid; Receptors, Opioid, mu; Tumor Cells, Cultured | 1992 |
Pharmacological profiles of fentanyl analogs at mu, delta and kappa opiate receptors.
Topics: Analgesics, Opioid; Animals; Benzeneacetamides; Brain; Enkephalin, Ala(2)-MePhe(4)-Gly(5)-; Enkephalin, D-Penicillamine (2,5)-; Enkephalins; Fentanyl; Guinea Pigs; Ileum; Male; Mice; Naltrexone; Pyrrolidines; Receptors, Opioid; Receptors, Opioid, delta; Receptors, Opioid, kappa; Receptors, Opioid, mu; Vas Deferens | 1992 |
[The stereoselective binding of praziquantel enantiomers to plasma proteins].
Topics: Albumins; Animals; Blood Proteins; Cattle; Fentanyl; Humans; Praziquantel; Protein Binding; Rabbits; Species Specificity; Stereoisomerism | 1991 |
Conformation-activity relationships of opiate analgesics.
Topics: Analgesics, Opioid; Benzimidazoles; Computer Graphics; Etorphine; Fentanyl; Models, Molecular; Molecular Conformation; Molecular Structure; Receptors, Opioid; Structure-Activity Relationship | 1987 |