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首页> 外文期刊>Scientia pharmaceutica >SYNTHESIS AND ANTIINFLAMMATORY ACTIVITY OF CERTAIN NEW 1,2,3-TRIARYL-2,3-DIHYDRO-4(1H)- QUINAZOLINONES
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SYNTHESIS AND ANTIINFLAMMATORY ACTIVITY OF CERTAIN NEW 1,2,3-TRIARYL-2,3-DIHYDRO-4(1H)- QUINAZOLINONES

机译:某些新型1,2,3-三芳基-2,3-二氢-4(1H)-喹唑啉酮的合成及抗炎活性

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A series of 1,2,3-triaryl-2,3-dihydro-4(1H)-quinazolinones, 4a-e, Sa-e, 6a-e, 7a-e, 8a-d and 9a-d was prepared. The structures of the prepared compound were established from their analytical data, 1R spectra, ~1H-NMR and mass spectroscopy. Compounds 4a, 4b, 4c, 5b, 5c, 5d, 6a, 6b, 6d, 7a, 7b, 7c, 8a, 8b, 8c, 9a and 9b were tested for antiinflammatory activity in the rat paw edema test. The results revealed that compounds 9b, 9a, 7a and 7b produced significant antiiflammatory activity at a dose of 100 mg/kg, i.e, about 30-70% inhibition of edema. Whereas, flufenamic acid at a dose of 10 mg/kg caused 70% inhibition.
机译:制备一系列1,2,3-三芳基-2,3-二氢-4(1H)-喹唑啉酮,4a-e,Sa-e,6a-e,7a-e,8a-d和9a-d。制备的化合物的结构由其分析数据,1R光谱,〜1H-NMR和质谱确定。在大鼠爪水肿测试中测试了化合物4a,4b,4c,5b,5c,5d,6a,6b,6d,7a,7b,7c,8a,8b,8c,9a和9b的抗炎活性。结果表明,化合物9b,9a,7a和7b以100mg / kg的剂量产生显着的抗炎活性,即抑制水肿约30-70%。而氟苯那酸以10 mg / kg的剂量引起70%的抑制作用。

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