Antiinflammatory imidazothiazoles and thiazolopyrimidines
摘要:
某些咪唑噻唑和噻唑并嘧啶被发现可以预防和抑制动物中肉芽肿组织的形成。这一结果是通过向动物主体给药具有以下公式化合物的治疗有效量来实现的:其中 R 是氢或甲基,R' 是氢、低级烷基或硫代烷基、羧甲基或苯基;R" 是低级烷基、2-苯并呋喃基、萘基、苯基或单或二取代苯基。这些化合物的一些水合前体以及这些化合物及其水合前体的酸加成盐和季铵盐均可使用。
Effect of structural change on acute toxicity and antiinflammatory activity in a series of imidazothiazoles and thiazolobenzimidazoles
作者:Larry J. Powers、S. W. Fogt、Z. S. Ariyan、D. J. Rippin、R. D. Heilman、Richard J. Matthews
DOI:10.1021/jm00137a022
日期:1981.5
The effect of structural change on the biological activity of a series of imidazothiazoles and thiazolobenzimidazoles is described. It was found that compounds with polar substituents at the 2 or 3 position of the ring system are less acutely toxic while maintaining antiinflammatoryactivity. Other structural changes, such as the incorporation of a gem-dimethyl substituent in the 6 position, increase