Page last updated: 2024-09-03

way 100135 and corticosterone

way 100135 has been researched along with corticosterone in 2 studies

Compound Research Comparison

Studies (way 100135)	Trials (way 100135)	Recent Studies (post-2010) (way 100135)	Studies (corticosterone)	Trials (corticosterone)	Recent Studies (post-2010) (corticosterone)
143	0	34	27,121	124	6,622

Protein Interaction Comparison

Protein	Taxonomy	corticosterone (IC50)
Solute carrier family 22 member 3	Homo sapiens (human)	0.945
Solute carrier family 22 member 3	Rattus norvegicus (Norway rat)	4.9
Solute carrier family 22 member 2	Rattus norvegicus (Norway rat)	4.1

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Canton, H; Gobert, A; Lejeune, F; Millan, MJ; Rivet, JM	1
Chocyk, A; Czyrak, A; Fijał, K; Gadek-Michalska, A; Maćkowiak, M; Wedzony, K	1

Other Studies

2 other study(ies) available for way 100135 and corticosterone

Article	Year
WAY 100,135 and (-)-tertatolol act as antagonists at both 5-HT1A autoreceptors and postsynaptic 5-HT1A receptors in vivo. European journal of pharmacology, 1993, Aug-24, Volume: 240, Issue:2-3 Topics: Animals; Binding Sites; Corticosterone; Dose-Response Relationship, Drug; Male; Piperazines; Propanolamines; Raphe Nuclei; Rats; Rats, Wistar; Serotonin Antagonists; Serotonin Receptor Agonists; Stereoisomerism; Thiophenes	1993
8-OHDPAT-induced disruption of prepulse inhibition in rats is attenuated by prolonged corticosterone treatment. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2003, Volume: 28, Issue:7 Topics: 8-Hydroxy-2-(di-n-propylamino)tetralin; Adrenal Glands; Animals; Anti-Inflammatory Agents; Autoradiography; Binding Sites; Body Weight; Corticosterone; Dose-Response Relationship, Drug; Drug Interactions; Gene Expression Regulation; Hippocampus; Hydroxyindoleacetic Acid; In Situ Hybridization; Male; Neural Inhibition; Organ Size; Piperazines; Raphe Nuclei; Rats; Receptors, Serotonin; Receptors, Serotonin, 5-HT1; Reflex, Startle; RNA, Messenger; Serotonin; Serotonin Antagonists; Serotonin Receptor Agonists; Time Factors	2003

Article

Year

WAY 100,135 and (-)-tertatolol act as antagonists at both 5-HT1A autoreceptors and postsynaptic 5-HT1A receptors in vivo.

European journal of pharmacology, 1993, Aug-24, Volume: 240, Issue:2-3

Topics: Animals; Binding Sites; Corticosterone; Dose-Response Relationship, Drug; Male; Piperazines; Propanolamines; Raphe Nuclei; Rats; Rats, Wistar; Serotonin Antagonists; Serotonin Receptor Agonists; Stereoisomerism; Thiophenes

1993

8-OHDPAT-induced disruption of prepulse inhibition in rats is attenuated by prolonged corticosterone treatment.

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2003, Volume: 28, Issue:7

Topics: 8-Hydroxy-2-(di-n-propylamino)tetralin; Adrenal Glands; Animals; Anti-Inflammatory Agents; Autoradiography; Binding Sites; Body Weight; Corticosterone; Dose-Response Relationship, Drug; Drug Interactions; Gene Expression Regulation; Hippocampus; Hydroxyindoleacetic Acid; In Situ Hybridization; Male; Neural Inhibition; Organ Size; Piperazines; Raphe Nuclei; Rats; Receptors, Serotonin; Receptors, Serotonin, 5-HT1; Reflex, Startle; RNA, Messenger; Serotonin; Serotonin Antagonists; Serotonin Receptor Agonists; Time Factors

2003