Literature DB >> 21420861

Design and synthesis of 1-(2-alkanamidoethyl)-6-methoxy-7-azaindole derivatives as potent melatonin agonists.

Matthieu Jeanty1, Franck Suzenet, Philippe Delagrange, Olivier Nosjean, Jean A Boutin, Daniel H Caignard, Gérald Guillaumet.   

Abstract

A series of 7-azaindolic ligands bearing a methoxy group and a N-acetyl chain as melatoninergic pharmacophores were synthesized and their binding affinities towards MT(1) and MT(2) receptors were evaluated. Compounds 7a-c and 12 (cyclohexyl ring connected at C-2 and C-3 position) appears as important melatonin MT(2) and MT(1) receptors agonists. On the other hand, the presence of basic groups (amines) at position C-3 was detrimental to the melatoninergic affinities.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21420861     DOI: 10.1016/j.bmcl.2011.02.097

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Original Design of Fluorescent Ligands by Fusing BODIPY and Melatonin Neurohormone.

Authors:  Jérémy Thireau; Justine Marteaux; Philippe Delagrange; Francois Lefoulon; Laurence Dufourny; Gérald Guillaumet; Franck Suzenet
Journal:  ACS Med Chem Lett       Date:  2013-11-20       Impact factor: 4.345

2.  Exploring 6-Azaindole and 7-Azaindole Rings for Developing Cannabinoid Receptor 1 Allosteric Modulators.

Authors:  Sri Sujana Immadi; Rachel Dopart; Zhixing Wu; Boqiao Fu; Debra A Kendall; Dai Lu
Journal:  Cannabis Cannabinoid Res       Date:  2018-12-10
  2 in total

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