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tertatolol

Known as: 1-((3,4-Dihydro-2H-1-benzothiopyran-8-yl)oxy)-3-((1,1-dimethylethyl)amino)-2-propanol, 2-propanol, 1-((3,40dihydro-2H-1-benzothiopyran-8-yl)oxy)-3-((1,1-dimethylethyl)amino)-, Racemic Teraterol 
National Institutes of Health

Related topics

Related topics

6 relations

Broader (4)

Adrenergic beta-AntagonistsAnti-Arrhythmia AgentsPropanolaminesThiophenes

Narrower (2)

ArtexS 2395

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2004
2004
Stereoselectivity for interactions of agonists and antagonists at mouse, rat and human beta3-adrenoceptors.
2001
2001
Mechanism of action of flibanserin in the learned helplessness paradigm in rats.
Highly Cited
2000
Highly Cited
2000
TR146 cells grown on filters as a model of human buccal epithelium: IV. Permeability of water, mannitol, testosterone and beta-adrenoceptor antagonists. Comparison to human, monkey and porcine buccal…
1999
1999
Prevention by 5-HT1A receptor agonists of restraint stress- and yohimbine-induced release of cholecystokinin in the frontal cortex of the freely moving rat
Highly Cited
1994
Highly Cited
1994
Contrasting behavioural effects of 8-OH DPAT in the dorsal raphénucleus and ventral hippocampus
1991
1991
Localization and characterization of two propranolol resistant (-) [125I]cyanopindolol binding sites in rat skeletal muscle.
1991
1991
5-Hydroxytryptamine-induced vasodilatation in the isolated perfused rat kidney: are endothelial 5-HT1A receptors involved?
1988
1988
Certain beta-blockers can decrease beta-adrenergic receptor number: I. Acute reduction in receptor number by tertatolol and bopindolol.
We have previously reported that a potent new beta-blocker, tertatolol, when given at therapeutic doses to healthy volunteers… 
1986
1986
Reduction of beta‐adrenergic receptors by tertatolol: An additional mechanism for beta‐adrenergic blockade
Tertatolol is a potent new β‐blocker with no intrinsic sympathomimetic activity or β1/β2‐receptor subtype selectivity. When given… 
1985
1985
Central and peripheral sites for cardiovascular actions of dynorphin-(1-13) in rats.
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