(Q43868947)

English

Studies toward the discovery of the next generation of antidepressants. Part 2: incorporating a 5-HT(1A) antagonist component into a class of serotonin reuptake inhibitors

scientific article published in February 2002

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Europe PubMed Central

PubMed publication ID

27 November 2017

Studies toward the discovery of the next generation of antidepressants. Part 2: incorporating a 5-HT(1A) antagonist component into a class of serotonin reuptake inhibitors (English)

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

author name string

Richard E Mewshaw

1

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

Kristin L Meagher

2

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

Ping Zhou

3

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

Dahui Zhou

4

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

Xiaojie Shi

5

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

Rosemary Scerni

6

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

Deborah Smith

7

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

Lee E Schechter

8

1 reference

Europe PubMed Central

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27 November 2017

Terrance H Andree

9

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Europe PubMed Central

PubMed publication ID

27 November 2017

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publication date

1 February 2002

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PubMed publication ID

27 November 2017

Bioorganic & Medicinal Chemistry Letters

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Europe PubMed Central

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27 November 2017

12

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27 November 2017

3

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27 November 2017

307-310

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27 November 2017

5-HT and antidepressants: new views from microdialysis studies

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Acceleration of the effect of selected antidepressant drugs in major depression by 5-HT1A antagonists.

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Effectiveness of Pindolol With Selected Antidepressant Drugs in the Treatment of Major Depression

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The 5-HT1A antagonist WAY-100635 selectively potentiates the presynaptic effects of serotonergic antidepressants in rat brain

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N-[2-[(substituted chroman-8-yl)oxy]ethyl]-4-(4-methoxyphenyl)butylamines: synthesis and wide range of antagonism at the human 5-HT1A receptor

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S14063: a new potent 5-HT1A receptor antagonist devoid of beta-adrenoceptor blocking properties

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New generation dopaminergic agents. 1. Discovery of a novel scaffold which embraces the D2 agonist pharmacophore. Structure-activity relationships of a series of 2-(aminomethyl)chromans

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The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products

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[3H]paroxetine binding in rat frontal cortex strongly correlates with [3H]5-HT uptake: effect of administration of various antidepressant treatments

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[3H]8-hydroxy-2-(di-n-propylamino)tetralin binding to pre- and postsynaptic 5-hydroxytryptamine sites in various regions of the rat brain

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Pharmacological characterization of acetylcholine-stimulated [35S]-GTP gamma S binding mediated by human muscarinic m1-m4 receptors: antagonist studies

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Characterization of 5-HT1A receptor functional coupling in cells expressing the human 5-HT1A receptor as assessed with the cytosensor microphysiometer

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Identifiers

10.1016/S0960-894X(01)00746-6

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

27 November 2017

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