An alternative approach to developing dopamine-receptor agonists with central presynaptic actions following oral administration: A comparison between apomorphine, bromocriptine, and the novel compound RDS-127 (2-di-n-propylamino-4,7-dimethoxyindane)-Reference-Cited by-同舟云学术

An alternative approach to developing dopamine-receptor agonists with central presynaptic actions following oral administration: A comparison between apomorphine, bromocriptine, and the novel compound RDS-127 (2-di-n-propylamino-4,7-dimethoxyindane)

Published:1983 Issue:3 Volume:3 Page:221-231
ISSN:0272-4391
Container-title:Drug Development Research
language:en
Short-container-title:Drug Dev. Res.

Author:

Arneri? Stephen P.,Long John P.

Publisher

Wiley

Subject

Drug Discovery

Reference40 articles.

1. Dopamine ?Autoreceptors?: Pharmacological characterization by microiontophoretic single cell recording studies

2. Potent anorexic-like effects of RDS-127 (2-di-n-propylamino-4,7-dimethoxyindane) in the rat: A comparison with other dopamine-receptor agonists

3. An orally effective, long-acting dopaminergic prodrug: (−)-10,11-methylenedioxy-N-propylnoraporphine

4. Prolonged apomorphine-like behavioural effects of apomorphine esters

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1. Dopamine receptor agonists, N, N-dipropyl-2-aminotetralin (TL-68) and 2-di-n-propylamino-4,7-dimethoxyindane (RDS-127) antagonize oxotremorine-induced tremors antimuscarinic action in mice;Archives Internationales de Physiologie et de Biochimie;1990-01

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