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• W2483163315 abstract "Indoleamine 2,3-dioxygenase 2 (IDO2) is a potential therapeutic target for the treatment of diseases that involve immune escape such as cancer. In contrast to IDO1, only a very limited number of inhibitors have been described for IDO2 due to inherent difficulties in expressing and purifying a functionally active, soluble form of the enzyme. Starting from our previously discovered highly efficient 4-aryl-1,2,3-triazole IDO1 inhibitor scaffold, we used computational structure-based methods to design inhibitors of IDO2 which we then tested in cellular assays. Our approach yielded low molecular weight inhibitors of IDO2, the most active displaying an IC50 value of 51μM for mIDO2, and twofold selectivity over hIDO1. These compounds could be useful as molecular probes to investigate the biological role of IDO2, and could inspire the design of new IDO2 inhibitors." @default.
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• W2483163315 date "2016-09-01" @default.
• W2483163315 modified "2023-10-02" @default.
• W2483163315 title "1,2,3-Triazoles as inhibitors of indoleamine 2,3-dioxygenase 2 (IDO2)" @default.
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• W2483163315 doi "https://doi.org/10.1016/j.bmcl.2016.07.031" @default.
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