Discovery of Icotinib-1,2,3-Triazole Derivatives as IDO1 Inhibitors.

ABSTRACT: Tumor immunotherapy is considered to be a highlight in cancer treatment in recent years. Indoleamine 2,3-dioxygenase 1 (IDO1) is closely related to the over expression of many cancers, and is therefore a promising target for tumor immunotherapy. To search for novel IDO1-targeting therapeutic agents, 22 icotinib-linked 1,2,3-triazole derivatives were prepared and evaluated for their inhibitory activity against IDO1. The structures of the prepared compounds were confirmed with¹H NMR, ¹³C NMR and HR MS. IDO1 inhibitory activity assay results indicated that 10 of those compounds showed remarkable inhibitory activity against IDO1, among which compound a17 was the most potent with IC₅₀value of 0.37 μM. The binding model between the prepared compounds and I

SUBMITTER: Mao LF 

PROVIDER: S-EPMC7555427 | biostudies-literature | 2020

REPOSITORIES: biostudies-literature