Literature DB >> 497

N-Isopropyl derivatives of dopamine and 5,6-dihydroxy-2-aminotetralin.

J G Cannon, J P O'Donnell, T Lee, C R Hoppin, J P Long, M Ilhan, B Costall, R J Naylor.   

Abstract

Secondary and tertiary amino homologs of the title compounds have been prepared, bearing an N-isopropyl group. In peripheral evaluation, certain members of the series exhibited beta-adrenergic agonist effects of lower activity than isoproterenol. N-Methyl-N-isopropyl-5,6-dihydroxytetralin exhibited marked properties consistent with its being an alpha agonist, and it is concluded that introduction of considerable bulk about the nitrogen of a catecholamine does not a priori destroy alpha-agonist effects. The compounds qualitatively paralleled the effects of dopamine in assays based upon direct intrastriatal administration in rats, although they were less potent than dopamine.

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Year:  1975        PMID: 497     DOI: 10.1021/jm00246a008

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


  1 in total

1.  Conformational requirements for dopamine-induced vasodilation.

Authors:  P H Volkman; J D Kohli; L I Goldberg; J G Cannon; T Lee
Journal:  Proc Natl Acad Sci U S A       Date:  1977-08       Impact factor: 11.205

  1 in total

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