Synthesis of 3,4-dihydro-4-oxoquinazoline derivatives as potential anticonvulsants.
In: Journal of medicinal chemistry, Jg. 26 (1983-10-01), Heft 10, S. 1422-5
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Zugriff:
Twenty-three substituted 3,4-dihydro-4-oxoquinazolines or 3,4-dihydro-4-oxoazaquinazolines have been synthesized utilizing 2-amino-3-cyano-4,5-dimethylfuran and methyl acrylate as precursors for synthesis of the required substituted anthranilates. Six additional azaquinazolones were synthesized from 2-aminonicotinic or 3-aminopicolinic acid for comparison studies. All compounds were evaluated in mice with the maximal electroshock (MES) seizure and pentylenetetrazol (sc Met) seizure threshold tests for potential anticonvulsant activity and in the rotorod test to evaluate neurotoxicity. Nine of the twenty-nine compounds in the series demonstrated anticonvulsant action. The azaquinazolones were found to possess the most significant activity.
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Synthesis of 3,4-dihydro-4-oxoquinazoline derivatives as potential anticonvulsants.
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Autor/in / Beteiligte Person: | Vaidya, NA ; Panos, CH ; Kite, A ; Iturrian, WB ; Blanton CD Jr |
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Zeitschrift: | Journal of medicinal chemistry, Jg. 26 (1983-10-01), Heft 10, S. 1422-5 |
Veröffentlichung: | Washington Dc : American Chemical Society ; <i>Original Publication</i>: [Easton, Pa.] : American Chemical Society, [c1963-, 1983 |
Medientyp: | academicJournal |
ISSN: | 0022-2623 (print) |
DOI: | 10.1021/jm00364a012 |
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