Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
XB-ART-11277
Bioorg Med Chem Lett 2000 Mar 20;106:591-6. doi: 10.1016/s0960-894x(00)00054-8.
Show Gene links Show Anatomy links

8-Methylureido-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazines: highly potent in vivo AMPA antagonists.

Mignani S , Bohme GA , Boireau A , Cheve M , Damour D , Debono MW , Genevois-Borella A , Imperato A , Jimonet P , Pratt J , Randle JC , Ribeill Y , Vuilhorgne M , Stutzmann JM .


???displayArticle.abstract???
A novel series of readily water soluble 8-methylureido-4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]++ +pyrazines were synthesized. The -10-yl acetic acid ((+)-3) and -10-carboxylidene (4) derivatives exhibit potent affinities (IC50=4 and 19 nM, respectively) and antagonist properties (IC50 = 2 and 3 nM, respectively) at the ionotropic AMPA receptor. These compounds also display anticonvulsant properties against both electrically and sound-induced convulsions in mice after ip, sc and iv administration with ED50 values between 0.9 and 11 mg/kg, thus suggesting adequate brain penetration.

???displayArticle.pubmedLink??? 10741560
???displayArticle.link??? Bioorg Med Chem Lett