Literature DB >> 11133083

Synthesis and potent anticonvulsant activities of 4-oxo-imidazo[1,2-a]inden.

J Pratt1, P Jimonet, G A Bohme, A Boireau, D Damour, M W Debono, A Genevois-Borella, J C Randle, Y Ribeill, J M Stutzmann, M Vuilhorgne, S Mignani.   

Abstract

The over-stimulation of excitatory amino acid receptors such as the glutamate AMPA receptor has been suggested to be associated with neurodegenerative disorders. Here we describe an original series of readily water soluble 4-oxo-imidazo[1,2-a] indeno[1,2-e]pyrazin-8- and -9-carboxylic (acetic) acid derivatives. One of these compounds, 4f, exhibited nanomolar binding affinity, potent competitive antagonism at the ionotropic AMPA receptor and a long duration of anticonvulsant activity after administration by parenteral route in vivo.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11133083     DOI: 10.1016/s0960-894x(00)00561-8

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


  1 in total

1.  2-(2-Bromo-phen-yl)acetic acid.

Authors:  Rajni Kant; Kamini Kapoor; B Narayana
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2012-05-12
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.