Chemical and Pharmaceutical Bulletin p. 1452 - 1461 (1992)
Update date:2022-08-04
Topics:
Kuno
Sugiyama
Katsuta
Kamitani
Takasugi
Novel 4-arylpyrimidine derivatives were synthesized by the oxidation of 4-aryl-1,4-dihydropyrimidines, and their effects on anti-anoxic (AA) activity in mice and anti-lipid peroxidation (ALP) activity in rat brain mitochondria were investigated. Among these compounds, ethyl 6-methyl-2-phenyl-4-(4-pyridyl)-5-pyrimidinecarboxylate (4b) has AA activity (10mg/kg, i.p.) and ethyl 6-methyl-4-(3-nitrophenyl)-2-phenyl-5-pyrimidinecarboxylate (4f) has ALP activity (73% inhibition at 10-5 g/ml). The latter compound (100mg/kg, i.p.) was also effective on arachidonate-induced cerebral edema in rats with comparable potency to that of vitamin E.
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Doi:10.1139/V08-033
(2008)Doi:10.1016/S0040-4020(98)00360-3
(1998)Doi:10.1039/b802580k
(2008)Doi:10.1055/s-0031-1290458
(2012)Doi:10.1021/ol800920d
(2008)Doi:10.1055/s-2008-1032203
(2008)
