[Biological effects of substances similar to salicylanilides. 3-aryl-2H, 4H-benz(e)(1,3)oxazine-2, 4-diones and thiosalicylanilides].

Ceskoslovenska farmacie Pub Date : 1993-10-01
K Waisser, L Kubicová
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Abstract

The review paper is the first collected communication about the biological activity of 3-aryl-2H,4H-benz(e)(1,3)oxazine-2,4-diones and thiosalicylanilides. The substances of the above mentioned structures show a number of biological activities (antibacterial, antituberculous, antimycotic, anthelmintic, molluscocidal, neuroleptic, analgesic and anti-inflammatory) which can be modelled by structural changes. Only very few of them have been hitherto introduced into practice as anthelmintic agents, or agents with a special purpose (destroying the sea lamprey in Canadian lakes). In the group of 3-aryl-2H,3H-benz(e)(1,3)-oxazine-2,4-diones, i.e. substances developed from salicylanilides by the action of alkyl-chloroformiates, antibacterial activity is reported in refs. 3-12, antituberculous activity in refs. 13, 14, antimycotic activity in refs. 5, 6, 9, 12, 15, 16, anthelmintic activity in refs. 6,917-20, molluscocidal activity in refs. 6, 21, analgesic and anti-inflammatory activity in refs. 22-24, herbicidal activity in refs. 25, 26, allergenic activity in ref. 27. In the group of salicylanilides, antibacterial activity is reported in refs. 28-37, antimycotic activity in refs. 28-36, antiprotozoal activity in ref. 35, anthelmintic activity in refs. 28-40, 49, molluscocidal activity in refs. 7, 28-36. The present paper furthermore sums up the papers concerned with the toxicities of the above-mentioned agents. Though the peak of research of the groups of the above-mentioned structure was in the 1960s and 1970s, papers investigating their biological activity can be encountered also at present.

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[类似水杨酸苯胺类物质的生物效应。]3-芳基- 2h, 4h -苯并(e)(1,3)恶嗪- 2,4 -二酮和硫代水杨酰苯胺]。
本文是首次收集到的有关3-芳基- 2h, 4h -苯并(e)(1,3)恶嗪-2,4-二酮类化合物和硫代水杨酰苯胺类化合物生物活性的文献报道。上述结构的物质显示出许多生物活性(抗菌、抗结核、抗真菌、驱虫药、杀软体、抗神经、镇痛和抗炎),这些活性可以通过结构变化来模拟。迄今为止,它们中只有极少数被用作驱虫剂或有特殊目的的剂(摧毁加拿大湖泊中的海七鳃鳗)。在3-芳基- 2h, 3h -苯并(e)(1,3)-恶嗪-2,4-二酮基团中,即由水杨酸酰苯胺通过烷基氯甲酸酯的作用而产生的物质,其抗菌活性在文献中有报道。3-12,植物的抗结核活性。13,14,植物的抗真菌活性。5、6、9、12、15、16,珊瑚礁的驱虫活性。6,917-20,珊瑚礁的杀软体活性。6, 21,参的镇痛和抗炎活性。22-24,珊瑚礁除草活性。25,26,参考文献27中的致敏活性。在水杨酸苯胺类中,抑菌活性有文献报道。28-37,细菌的抗真菌活性。28-36,参考文献35中的抗原虫活性,参考文献中的驱虫活性。28- 40,49,珊瑚礁的杀软体活性。7,几个。本文进一步总结了有关上述药剂毒性的文献。虽然上述结构基团的研究高峰是在20世纪60年代和70年代,但目前也可以遇到研究其生物活性的论文。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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