Literature DB >> 573798

N-Alkyl derivatives of (+/-)-alpha-methyldopamine.

J G Cannon, Z Perez, J P Long, D B Rusterholz, J R Flynn, B Costall, D H Fortune, R J Naylor.   

Abstract

A series of N-alkylated alpha-methyldopamine derivatives has been prepared for comparison of their biological effects with those of semirigid dopamine congeners derived from 2-aminotetralin systems. All of the alpha-methyldopamine derivatives were inert as dopaminergic agonists in a variety of animal assays, both centrally and peripherally, although certain compounds produced powerful and prolonged locomotor hyperactivity on intra-accumbens injection in mice, by indirect mechanism(s). A rationalization, based upon conformational analysis, is presented for the lack of direct dopaminergic agonist activity of alpha-methyldopamine derivatives.

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Year:  1979        PMID: 573798     DOI: 10.1021/jm00194a003

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


  2 in total

1.  Synthesis and neurotoxicity profile of 2,4,5-trihydroxymethamphetamine and its 6-(N-acetylcystein-S-yl) conjugate.

Authors:  Anne Neudörffer; Melanie Mueller; Claire-Marie Martinez; Annis Mechan; Una McCann; George A Ricaurte; Martine Largeron
Journal:  Chem Res Toxicol       Date:  2011-05-18       Impact factor: 3.739

2.  Structure-activity relationships for apomorphine congeners. Conformational energies vs. biological activities.

Authors:  I Pettersson; T Liljefors
Journal:  J Comput Aided Mol Des       Date:  1987-07       Impact factor: 3.686

  2 in total

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