salvinorin a has been researched along with guanosine 5'-o-(3-thiotriphosphate) in 5 studies
Studies (salvinorin a) | Trials (salvinorin a) | Recent Studies (post-2010) (salvinorin a) | Studies (guanosine 5'-o-(3-thiotriphosphate)) | Trials (guanosine 5'-o-(3-thiotriphosphate)) | Recent Studies (post-2010) (guanosine 5'-o-(3-thiotriphosphate)) |
---|---|---|---|---|---|
247 | 7 | 128 | 5,542 | 8 | 368 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (80.00) | 29.6817 |
2010's | 1 (20.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Cowan, A; Holzgrabe, U; Huang, P; Inan, S; Lee, DY; Li, JG; Liu-Chen, LY; Siebert, D; Tang, K; Wang, Y | 1 |
Beguin, C; Carlezon, WA; Chen, Y; Cohen, B; He, M; Kondaveti, L; Lee, DY; Li, JG; Liu-Chen, LY; Ma, Z; Wang, Y | 1 |
Dersch, CM; Godin, JA; Murphy, DL; Partilla, JS; Prisinzano, TE; Rothman, RB; Schmidt, M; Tidgewell, K; Xu, H | 1 |
Guan, HC; Hirbec, H; Seeman, P | 1 |
Carroll, FI; Gilliam, AF; Gilmour, BP; King, LS; Navarro, HA; Seltzman, HH; Thomas, BF; Twine, CE; Vann, RE; Walentiny, DM; Warner, JA; Wiley, JL | 1 |
5 other study(ies) available for salvinorin a and guanosine 5'-o-(3-thiotriphosphate)
Article | Year |
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Comparison of pharmacological activities of three distinct kappa ligands (Salvinorin A, TRK-820 and 3FLB) on kappa opioid receptors in vitro and their antipruritic and antinociceptive activities in vivo.
Topics: 3,4-Dichloro-N-methyl-N-(2-(1-pyrrolidinyl)-cyclohexyl)-benzeneacetamide, (trans)-Isomer; Analgesics; Animals; Antipruritics; Aza Compounds; Binding, Competitive; Diterpenes; Diterpenes, Clerodane; Down-Regulation; Endocytosis; Female; Guanosine 5'-O-(3-Thiotriphosphate); Humans; Hydrocarbons, Fluorinated; Male; Mice; Morphinans; Nociceptin Receptor; Receptors, Opioid; Receptors, Opioid, delta; Receptors, Opioid, kappa; Receptors, Opioid, mu; Spiro Compounds; Sulfur Radioisotopes | 2005 |
Synthesis and in vitro pharmacological studies of C(4) modified salvinorin A analogues.
Topics: Analgesics, Opioid; Diterpenes; Diterpenes, Clerodane; Drug Evaluation, Preclinical; Guanosine 5'-O-(3-Thiotriphosphate); Humans; Inhibitory Concentration 50; Receptors, Opioid, kappa; Structure-Activity Relationship | 2005 |
Salvinorin A: allosteric interactions at the mu-opioid receptor.
Topics: Allosteric Regulation; Animals; CHO Cells; Cricetinae; Cricetulus; Cyclic AMP; Diprenorphine; Diterpenes; Diterpenes, Clerodane; Enkephalin, Ala(2)-MePhe(4)-Gly(5)-; Guanosine 5'-O-(3-Thiotriphosphate); Humans; Kinetics; Morphinans; Receptors, Opioid, kappa; Receptors, Opioid, mu | 2007 |
Dopamine D2High receptors stimulated by phencyclidines, lysergic acid diethylamide, salvinorin A, and modafinil.
Topics: Animals; Benzhydryl Compounds; Binding, Competitive; Central Nervous System Stimulants; Corpus Striatum; Diterpenes, Clerodane; Domperidone; Dopamine; Dopamine Antagonists; Dose-Response Relationship, Drug; Guanosine 5'-O-(3-Thiotriphosphate); Hallucinogens; Lysergic Acid Diethylamide; Modafinil; Models, Chemical; Phencyclidine; Protein Binding; Rats; Rats, Sprague-Dawley; Receptors, Dopamine D2; Sodium Chloride | 2009 |
Kappa opioid mediation of cannabinoid effects of the potent hallucinogen, salvinorin A, in rodents.
Topics: Animals; Calcium; Cannabinoid Receptor Modulators; Discrimination Learning; Diterpenes, Clerodane; Dronabinol; Guanosine 5'-O-(3-Thiotriphosphate); Hypothermia; Locomotion; Male; Mice; Mice, Inbred C57BL; Mice, Inbred ICR; Pain Measurement; Piperidines; Pyrazoles; Radioligand Assay; Receptor, Cannabinoid, CB1; Receptors, Opioid, kappa; Rimonabant; Salvia; Tetrahydroisoquinolines | 2010 |