Literature DB >> 19726184

Discovery of the imidazo[1,5-a][1,2,4]-triazolo[1,5-d][1,4]benzodiazepine scaffold as a novel, potent and selective GABA(A) alpha5 inverse agonist series.

Guido Achermann1, Theresa M Ballard, Francesca Blasco, Pierre-Emmanuel Broutin, Bernd Büttelmann, Holger Fischer, Martin Graf, Maria-Clemencia Hernandez, Peter Hilty, Frédéric Knoflach, Andreas Koblet, Henner Knust, Anke Kurt, James R Martin, Raffaello Masciadri, Richard H P Porter, Heinz Stadler, Andrew W Thomas, Gerhard Trube, Jürgen Wichmann.   

Abstract

Through iterative design cycles we have discovered a number of novel new classes where the imidazo[1,5-a][1,2,4]-triazolo[1,5-d][1,4]benzodiazepine was deemed the most promising GABA(A) alpha5 inverse agonist class with potential for cognitive enhancement. This class combines a modest subtype binding selectivity with inverse agonism and has the most favourable molecular properties for further lead optimisation towards a central nervous system (CNS) acting medicine.

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Year:  2009        PMID: 19726184     DOI: 10.1016/j.bmcl.2009.07.153

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


  2 in total

Review 1.  A novel GABA(A) receptor pharmacology: drugs interacting with the α(+) β(-) interface.

Authors:  Werner Sieghart; Joachim Ramerstorfer; Isabella Sarto-Jackson; Zdravko Varagic; Margot Ernst
Journal:  Br J Pharmacol       Date:  2012-05       Impact factor: 8.739

2.  Synthesis of new tricyclic 5,6-dihydro-4H-benzo[b][1,2,4]triazolo[1,5-d][1,4]diazepine derivatives by [3+ + 2]-cycloaddition/rearrangement reactions.

Authors:  Lin-Bo Luan; Zi-Jie Song; Zhi-Ming Li; Quan-Rui Wang
Journal:  Beilstein J Org Chem       Date:  2018-07-18       Impact factor: 2.883

  2 in total

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