Suppr超能文献

色氨酸衍生物作为刚地弓形虫抑制剂——6 位的结构-活性关系。

Tryptanthrin derivatives as Toxoplasma gondii inhibitors--structure-activity-relationship of the 6-position.

机构信息

Department of Chemistry & Biochemistry, University of Minnesota Duluth, 1039 University Drive, Duluth, MN 55812, USA.

出版信息

Bioorg Med Chem Lett. 2013 Feb 15;23(4):1032-5. doi: 10.1016/j.bmcl.2012.12.024. Epub 2012 Dec 20.

Abstract

A panel of derivatives of the natural product tryptanthrin was synthesized and screened for its in vitro activity against the intracellular parasite Toxoplasma gondii. We concentrated on the modification of the 6-keto group of tryptanthrin and prepared a series of oximes, hydrazones and alcohols based on tryptanthrin. We evaluated parasite growth inhibition and host cell cytotoxicity. Our results indicate that in particular alcohol analogs are promising candidates for further investigation.

摘要

合成了天然产物色胺酮的一组衍生物,并对其进行了体外抗弓形虫的活性筛选。我们专注于色胺酮 6-酮基的修饰,基于色胺酮制备了一系列肟、腙和醇。我们评估了寄生虫生长抑制和宿主细胞毒性。结果表明,特别是醇类似物是进一步研究的有希望的候选物。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验