| Literature DB >> 27863031 |
Zenyu Shiokawa1,2, Emi Kashiwabara1, Daisuke Yoshidome3, Koichi Fukase2, Shinsuke Inuki1, Yukari Fujimoto1.
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.Entities:
Keywords: docking models; hanishin; indoleamine 2,3-dioxygenase 1; longamide B; piperazinones
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Year: 2016 PMID: 27863031 DOI: 10.1002/cmdc.201600446
Source DB: PubMed Journal: ChemMedChem ISSN: 1860-7179 Impact factor: 3.466