Suppr超能文献

基于吡咯并哌嗪酮生物碱隆酰胺B发现一种新型支架作为吲哚胺2,3-双加氧酶1(IDO1)抑制剂

Discovery of a Novel Scaffold as an Indoleamine 2,3-Dioxygenase 1 (IDO1) Inhibitor Based on the Pyrrolopiperazinone Alkaloid, Longamide B.

作者信息

Shiokawa Zenyu, Kashiwabara Emi, Yoshidome Daisuke, Fukase Koichi, Inuki Shinsuke, Fujimoto Yukari

机构信息

Department of Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama, Kanagawa, 223-8522, Japan.

Department of Chemistry, Graduate School of Science, Osaka University, 1-1 Machikaneyama-cho, Toyonaka-shi, Osaka, 560-0043, Japan.

出版信息

ChemMedChem. 2016 Dec 16;11(24):2682-2689. doi: 10.1002/cmdc.201600446. Epub 2016 Dec 5.

Abstract

Indoleamine 2,3-dioxygenase 1 (IDO1) has emerged as a key target for cancer therapy, as IDO1 plays a critical role in the capacity of tumor cells to evade the immune system. The pyrrolopiperazinone alkaloid longamide B and its derivatives were identified as novel IDO1 inhibitors based on docking studies and small library synthesis. The thioamide derivative showed higher IDO1 inhibitory activity than longamide B, and displayed an activity similar to that of a representative IDO1 inhibitor, 1-methyl-tryptophan. These results suggest that the pyrrolopiperazinone scaffold of longamide B could be used in the development of IDO1 inhibitors.

摘要

吲哚胺2,3-双加氧酶1(IDO1)已成为癌症治疗的关键靶点,因为IDO1在肿瘤细胞逃避免疫系统的能力中起着关键作用。基于对接研究和小型文库合成,吡咯并哌嗪酮生物碱隆加胺B及其衍生物被鉴定为新型IDO1抑制剂。硫代酰胺衍生物显示出比隆加胺B更高的IDO1抑制活性,并且表现出与代表性IDO1抑制剂1-甲基色氨酸相似的活性。这些结果表明,隆加胺B的吡咯并哌嗪酮支架可用于开发IDO1抑制剂。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验