文章引用说明 更多>> (返回到该文章)

Sturino, C.F., O’Neill, G., Lachance, N., Boyd, M., et al. (2007) Discovery of a potent and selective prostaglandin D2 receptor antagonist, [(3R)-4-(4-chloro-benzyl)-7-fluoro-5-(methylsulfonyl)-1,2,3,4-tetrahydrocyclopenta[b]indol-3-yl]- aceticacid (MK-0524). Journal of Medicinal Chemistry, 50, 794-806.

被以下文章引用:

• 标题: 芳基乙酸类衍生物的设计、合成与抗过敏活性研究Design, Synthesis and Anti-Allergic Activity Evaluation of Aryl-Acetic Acid Derivatives

  作者: 周海平, 金雨婷, 卞学国, 朱启华, 董广平, 徐云根

  关键字: 芳基乙酸, 合成, 抗过敏, 生物活性Arylacetic Acids, Synthesis, Anti-allergic, Biological Activity

  期刊名称: 《Hans Journal of Medicinal Chemistry》, Vol.2 No.3, 2014-08-29

  摘要: 目的：为了获得活性好、副作用小的DP受体拮抗剂，设计和合成芳基乙酸类衍生物。方法：以取代的苯酚、1,2-二溴乙烷以及香豆酸为原料，通过醚化、水解、酰胺化、水解等反应合成目标化合物，并研究其对烟酸诱导血管扩张效应的抑制活性。结果：合成了5个目标化合物，活性筛选结果表明，化合物I-4和I-5的活性优于阳性药(拉罗匹仑)。结论：化合物I-4和I-5对烟酸引起的血管扩张具有抑制作用，值得进一步研究。Objective: To discover novel DP receptor antagonists with higher potency and less side-effect, several arylacetic acid derivatives were designed and synthesized. Method: A series of title com-pounds were synthesized by etherification, hydrolysis, amidation and hydrolysis on the basis of substitutional phenol, 1,2-dibromoethane and coumarate. All the target compounds were evaluated by the model of niacin-induced vasodilation. Results: 5 title compounds were synthesized. The results of biological evaluation showed that the compounds I-4 and I-5 exhibited more potency than positive drug (Laropiprant). Conclusion: The compounds I-4 and I-5 showed potent inhibitory effect on niacin-induced vasodilation and would be valuable for further investigation.