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salvinorin a and guanosine 5'-o-(3-thiotriphosphate)

salvinorin a has been researched along with guanosine 5'-o-(3-thiotriphosphate) in 5 studies

Compound Research Comparison

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))
24771285,5428368

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (80.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cowan, A; Holzgrabe, U; Huang, P; Inan, S; Lee, DY; Li, JG; Liu-Chen, LY; Siebert, D; Tang, K; Wang, Y1
Beguin, C; Carlezon, WA; Chen, Y; Cohen, B; He, M; Kondaveti, L; Lee, DY; Li, JG; Liu-Chen, LY; Ma, Z; Wang, Y1
Dersch, CM; Godin, JA; Murphy, DL; Partilla, JS; Prisinzano, TE; Rothman, RB; Schmidt, M; Tidgewell, K; Xu, H1
Guan, HC; Hirbec, H; Seeman, P1
Carroll, FI; Gilliam, AF; Gilmour, BP; King, LS; Navarro, HA; Seltzman, HH; Thomas, BF; Twine, CE; Vann, RE; Walentiny, DM; Warner, JA; Wiley, JL1

Other Studies

5 other study(ies) available for salvinorin a and guanosine 5'-o-(3-thiotriphosphate)

ArticleYear
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.
    The Journal of pharmacology and experimental therapeutics, 2005, Volume: 312, Issue:1

    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.
    Bioorganic & medicinal chemistry letters, 2005, Oct-01, Volume: 15, Issue:19

    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.
    The Journal of pharmacology and experimental therapeutics, 2007, Volume: 320, Issue:2

    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.
    Synapse (New York, N.Y.), 2009, Volume: 63, Issue:8

    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.
    Psychopharmacology, 2010, Volume: 210, Issue:2

    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