Shiokawa Zenyu, Kashiwabara Emi, Yoshidome Daisuke, Fukase Koichi, Inuki Shinsuke, Fujimoto Yukari
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.
ChemMedChem. 2016 Dec 16;11(24):2682-2689. doi: 10.1002/cmdc.201600446. Epub 2016 Dec 5.
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.
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。