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)
- 1 January 1983
- journal article
- research article
- Published by Wiley in Drug Development Research
- Vol. 3 (3) , 221-231
- https://doi.org/10.1002/ddr.430030304
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Potent anorexic-like effects of RDS-127 (2-di-n-propylamino-4,7-dimethoxyindane) in the rat: A comparison with other dopamine-receptor agonistsNeuropharmacology, 1982
- An orally effective, long-acting dopaminergic prodrug: (−)-10,11-methylenedioxy-N-propylnoraporphineEuropean Journal of Pharmacology, 1982
- Neurochemical and Behavioral Evidence for a Selective Presynaptic Dopamine Receptor AgonistScience, 1980
- Oral bioavailability of apomorphine in the rat with a portacaval venous anastomosisEuropean Journal of Pharmacology, 1980
- Ergot Alkaloids and Related CompoundsPublished by Springer Nature ,1978
- Dopamine ?Autoreceptors?: Pharmacological characterization by microiontophoretic single cell recording studiesNaunyn-Schmiedebergs Archiv für experimentelle Pathologie und Pharmakologie, 1977
- Evidence for dopamine receptors mediating sedation in the mouse brainNature, 1976
- Prolonged apomorphine-like behavioural effects of apomorphine estersNeuropharmacology, 1976
- Drug‐Induced Changes in the Release of 3H‐Monoamines from Field Stimulated Rat Brain SlicesActa Physiologica Scandinavica, 1971
- A NOTE ON APOMORPHINE AS A SEDATIVEAmerican Journal of Psychiatry, 1945