221164-30-3Relevant academic research and scientific papers
Design, synthesis, and AMPA receptor antagonistic activity of a novel 6-nitro-3-oxoquinoxaline-2-carboxylic acid with a substituted phenyl group at the 7 position
Takano, Yasuo,Shiga, Futoshi,Asano, Jun,Ando, Naoki,Uchiki, Hideharu,Fukuchi, Kazunori,Anraku, Tsuyosi
, p. 5841 - 5863 (2007/10/03)
We describe the design, synthesis, and biological properties of a novel series of 7-substituted 6-nitro-3-oxoquinoxaline-2-carboxylic acids. After designing, studying the structure-activity relationships, and evaluating the properties of various compounds
Synthesis and AMPA receptor antagonistic activity of a novel class of quinoxalinecarboxylic acid with a substituted phenyl group at the C-7 position
Takano, Yasuo,Shiga, Futoshi,Asano, Jun,Ando, Naoki,Uchiki, Hideharu,Anraku, Tsuyosi
, p. 3521 - 3525 (2007/10/03)
The synthesis and biological properties of a novel class of 7-heterocycle-substituted quinoxalinecarboxylic acids, which bear a substituted phenyl group through a urethane linkage at the C-7 position, are described. One of the synthesized compounds, 15l,
6,7-asymmetrically disubstituted quinoxalinecarboxylic acid derivatives, addition salts thereof, and processes for the preparation of both
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Page column 125, (2010/11/30)
The present invention provides 6,7-asymmetrically disubstituted quinoxalinecarboxylic acid compounds and their addition salts, and processes for preparing them, which have antagonism against excitatory amino acid receptors, in particular, an AMPA receptor
