Compounds > chlorpromazine

chlorpromazine and sch 23390

chlorpromazine has been researched along with sch 23390 in 9 studies

Research

Studies (9)

TimeframeStudies, this research(%)All Research%
pre-19901 (11.11)18.7374
1990's3 (33.33)18.2507
2000's3 (33.33)29.6817
2010's2 (22.22)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bowen, JP; Charifson, PS; Hoffman, AJ; Mailman, RB; McDougald, DL; Simmons, RM; Wyrick, SD1
Brewster, WK; Mailman, RB; Mottola, D; Nichols, DE; Riggs, RM; Watts, VJ1
Ghosh, D; Mailman, RB; Nichols, DE; Snyder, SE; Watts, VJ1
Mailman, RB; Negash, K; Nichols, DE; Watts, VJ1
Strassburg, CP; Tukey, RH1
Chemel, BR; Cueva, JP; Giorgioni, G; Grubbs, RA; Nichols, DE; Watts, VJ1
Bonner, LA; Chemel, BR; Nichols, DE; Watts, VJ1
Abe, K; Akaishi, T; Fujimoto, T; Misawa, M1
Kaczer, L; Klappenbach, M; Locatelli, F; Maldonado, H1

Reviews

1 review(s) available for chlorpromazine and sch 23390

ArticleYear
Human UDP-glucuronosyltransferases: metabolism, expression, and disease.
    Annual review of pharmacology and toxicology, 2000, Volume: 40

    Topics: Autoimmunity; Chromosome Mapping; Glucuronides; Glucuronosyltransferase; Humans; Hyperbilirubinemia; Neoplasms; Steroids; Terminology as Topic

2000

Other Studies

8 other study(ies) available for chlorpromazine and sch 23390

ArticleYear
Synthesis and pharmacological characterization of 1-phenyl-, 4-phenyl-, and 1-benzyl-1,2,3,4-tetrahydroisoquinolines as dopamine receptor ligands.
    Journal of medicinal chemistry, 1988, Volume: 31, Issue:10

    Topics: Adenylyl Cyclases; Animals; Benzazepines; Binding Sites; Binding, Competitive; Isoquinolines; Male; Rats; Rats, Inbred Strains; Receptors, Dopamine

1988
Evaluation of cis- and trans-9- and 11-hydroxy-5,6,6a,7,8,12b-hexahydrobenzo[a]phenanthridines as structurally rigid, selective D1 dopamine receptor ligands.
    Journal of medicinal chemistry, 1995, Jan-20, Volume: 38, Issue:2

    Topics: Animals; Binding, Competitive; Corpus Striatum; Dopamine Agonists; Dopamine Antagonists; Ligands; Male; Phenanthridines; Rats; Rats, Sprague-Dawley; Stereoisomerism; Structure-Activity Relationship

1995
9-Dihydroxy-2,3,7,11b-tetrahydro-1H-naph[1,2,3-de]isoquinoline: a potent full dopamine D1 agonist containing a rigid-beta-phenyldopamine pharmacophore.
    Journal of medicinal chemistry, 1996, Jan-19, Volume: 39, Issue:2

    Topics: Adenylyl Cyclases; Animals; Benzazepines; Corpus Striatum; Cyclic AMP; Dopamine Agonists; Dopamine Antagonists; Isoquinolines; Macaca mulatta; Male; Naphthols; Rats; Rats, Sprague-Dawley; Receptors, Dopamine D1; Receptors, Dopamine D2; Tumor Cells, Cultured

1996
Further definition of the D1 dopamine receptor pharmacophore: synthesis of trans-6,6a,7,8,9,13b-hexahydro-5H-benzo[d]naphth[2,1-b]azepines as rigid analogues of beta-phenyldopamine.
    Journal of medicinal chemistry, 1997, Jul-04, Volume: 40, Issue:14

    Topics: Animals; Computer Simulation; Corpus Striatum; Dopamine Agonists; Indicators and Reagents; Models, Molecular; Molecular Conformation; Molecular Structure; Phenanthridines; Rats; Receptors, Dopamine D1; Software; Spiperone; Structure-Activity Relationship

1997
trans-2,3-dihydroxy-6a,7,8,12b-tetrahydro-6H-chromeno[3,4-c]isoquinoline: synthesis, resolution, and preliminary pharmacological characterization of a new dopamine D1 receptor full agonist.
    Journal of medicinal chemistry, 2006, Nov-16, Volume: 49, Issue:23

    Topics: Animals; Benzopyrans; Binding, Competitive; Cell Line; Corpus Striatum; Crystallography, X-Ray; Cyclic AMP; Humans; In Vitro Techniques; Isoquinolines; Molecular Structure; Phenanthridines; Psychotropic Drugs; Radioligand Assay; Rats; Receptors, Dopamine D1; Stereoisomerism; Structure-Activity Relationship; Swine

2006
Facile synthesis of octahydrobenzo[h]isoquinolines: novel and highly potent D1 dopamine agonists.
    Bioorganic & medicinal chemistry, 2010, Sep-15, Volume: 18, Issue:18

    Topics: Animals; Binding Sites; Humans; Isoquinolines; Phenanthridines; Phenethylamines; Receptors, Dopamine D1; Swine

2010
Basolateral amygdala D1- and D2-dopaminergic system promotes the formation of long-term potentiation in the dentate gyrus of anesthetized rats.
    Progress in neuro-psychopharmacology & biological psychiatry, 2009, Apr-30, Volume: 33, Issue:3

    Topics: Adrenergic Agents; Amygdala; Animals; Benzazepines; Biophysics; Chlorpromazine; Dentate Gyrus; Dopamine Antagonists; Dopamine D2 Receptor Antagonists; Dose-Response Relationship, Drug; Electric Stimulation; Long-Term Potentiation; Male; Neural Pathways; Oxidopamine; Rats; Rats, Wistar; Receptors, Dopamine D1; Receptors, Dopamine D2; Ventral Tegmental Area

2009
Opposite actions of dopamine on aversive and appetitive memories in the crab.
    Learning & memory (Cold Spring Harbor, N.Y.), 2012, Jan-20, Volume: 19, Issue:2

    Topics: Animals; Behavior, Animal; Benzazepines; Brachyura; Brain; Chlorpromazine; Dopamine; Dopamine Antagonists; Dopaminergic Neurons; Fluphenazine; Memory

2012