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- W3208666404 endingPage "113967" @default.
- W3208666404 startingPage "113967" @default.
- W3208666404 abstract "Indoleamine 2,3-dioxygenase 1 (IDO1), a known immunosuppressive enzyme that catalyzes the rate-limiting step in the oxidation of tryptophan (Trp) to kynurenine (Kyn), has received increasing attention as an attractive immunotherapeutic target for cancer therapy. Up to now, eleven small-molecule IDO1 inhibitors have entered clinical trials for the treatment of cancers. In addition, proteolysis targeting chimera (PROTAC) based degraders also provide prospects for cancer therapy. Herein we present a comprehensive overview of the medicinal chemistry strategies and potential therapeutic applications of IDO1 inhibitors in nonclinical trials and IDO1-PROTAC degraders." @default.
- W3208666404 created "2021-11-08" @default.
- W3208666404 creator A5040808710 @default.
- W3208666404 creator A5054180910 @default.
- W3208666404 creator A5056168495 @default.
- W3208666404 creator A5064708150 @default.
- W3208666404 date "2022-01-01" @default.
- W3208666404 modified "2023-10-15" @default.
- W3208666404 title "Indoleamine 2,3-dioxygenase 1 (IDO1) inhibitors and PROTAC-based degraders for cancer therapy" @default.
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- W3208666404 doi "https://doi.org/10.1016/j.ejmech.2021.113967" @default.
- W3208666404 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/34752953" @default.
- W3208666404 hasPublicationYear "2022" @default.
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