Literature DB >> 6125597

2-Amino-4,7-dimethoxyindan derivatives: synthesis and assessment of dopaminergic and cardiovascular actions.

R D Sindelar, J Mott, C F Barfknecht, S P Arneric, J R Flynn, J P Long, R K Bhatnagar.   

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.

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Year:  1982        PMID: 6125597     DOI: 10.1021/jm00349a019

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  2 in total

1.  Synthesis and in silico ADME/Tox profiling studies of heterocyclic hybrids based on chloroquine scaffolds with potential antimalarial activity.

Authors:  Hegira Ramírez; Esteban Fernandez-Moreira; Juan R Rodrigues; Michael R Mijares; Jorge E Ángel; Jaime E Charris
Journal:  Parasitol Res       Date:  2021-11-15       Impact factor: 2.289

2.  Derivatives of 4-(2-N,N-di-n-propylaminoethyl)-5-hydroxyindole: synthesis and pharmacological effects.

Authors:  J G Cannon; I Roufos; S X Ma; J P Long
Journal:  Pharm Res       Date:  1992-06       Impact factor: 4.200

  2 in total

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