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2-Amino-4,7-dimethoxyindan derivatives: synthesis and assessment of dopaminergic and cardiovascular actions
- Source :
- Journal of Medicinal Chemistry. 25:858-864
- Publication Year :
- 1982
- Publisher :
- American Chemical Society (ACS), 1982.
-
Abstract
- N-Alkylated derivatives of 2-amino-4,7-dimethoxyindan were prepared for evaluation of central and peripheral dopaminergic activity using biochemical and behavioral tests in the rat and cardiovascular responses in the cat. 2-(Di-n-propylamino)-4,7-dimethoxyindan (4e) demonstrated equal activity with apomorphine to activate peripheral presynaptic dopamine receptors. Central pre- and postsynaptic dopamine receptors were also activated with 4e. In contrast to the intense long-acting sympathomimetic actions previously reported for the 2-amino-5,8-dimethoxytetralins, these compounds produced weak, transient effects in heart rate and blood pressure. The majority of 2-amino-4,7-dimethoxyindan derivatives tested are weak or inactive pre- and postsynaptic dopamine receptor agonists.
- Subjects :
- Central Nervous System
Male
Chemical Phenomena
Dopamine
In Vitro Techniques
Motor Activity
Pharmacology
Binding, Competitive
Mice
Postsynaptic potential
Drug Discovery
Heart rate
medicine
Animals
Humans
Neurotransmitter Agents
Chemistry
Dopaminergic
Hemodynamics
Rats, Inbred Strains
Electric Stimulation
Rats
Peripheral
Apomorphine
Blood pressure
Behavioral test
Indenes
Spiperone
Dopamine receptor
Indans
Cats
Molecular Medicine
Cattle
Stereotyped Behavior
medicine.drug
Subjects
Details
- ISSN :
- 15204804 and 00222623
- Volume :
- 25
- Database :
- OpenAIRE
- Journal :
- Journal of Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....f2a1f93a30ef4f448cc55ff5dcfc3634
- Full Text :
- https://doi.org/10.1021/jm00349a019