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合成新型色胺酮衍生物作为吲哚胺 2,3-双加氧酶 1 和色氨酸 2,3-双加氧酶的双重抑制剂。

Synthesis of novel tryptanthrin derivatives as dual inhibitors of indoleamine 2,3-dioxygenase 1 and tryptophan 2,3-dioxygenase.

机构信息

Shanghai Key Lab of Chemical Assessment and Sustainability, School of Chemical Science and Engineering, Tongji University, 1239 Siping Road, 200092 Shanghai, China.

State Key Laboratory of Genetic Engineering, Department of Biochemistry, School of Life Sciences, Fudan University, 2005 Songhu Road, 200438 Shanghai, China.

出版信息

Bioorg Med Chem Lett. 2020 Jun 1;30(11):127159. doi: 10.1016/j.bmcl.2020.127159. Epub 2020 Mar 29.

Abstract

Indoleamine 2,3-dioxygenase 1 (IDO1) and tryptophan 2,3-dioxygenase (TDO) are promising drug development targets due to their implications in pathologies such as cancer and neurodegenerative diseases. The search for IDO1 inhibitor has been intensely pursued but there is a paucity of potent TDO and IDO1/TDO dual inhibitors. Natural product tryptanthrin has been confirmed to bear IDO1 and/or TDO inhibitory activities. Herein, twelve novel tryptanthrin derivatives were synthesized and evaluated for the IDO1 and TDO inhibitory potency. All of the compounds were found to be IDO1/TDO dual inhibitors, in particular, compound 9a and 9b bore IDO1 inhibitory activity similar to that of INCB024360, and compound 5a and 9b had remarkable TDO inhibitory activity superior to that of the well-known TDO inhibitor LM10. This work enriches the collection of IDO1/TDO dual inhibitors and provides chemical molecules for potential development into drugs.

摘要

吲哚胺 2,3-双加氧酶 1(IDO1)和色氨酸 2,3-双加氧酶(TDO)是很有前途的药物开发靶点,因为它们与癌症和神经退行性疾病等病理学有关。因此,人们一直在积极寻找 IDO1 抑制剂,但缺乏有效的 TDO 和 IDO1/TDO 双重抑制剂。天然产物色烯酮已被证实具有 IDO1 和/或 TDO 抑制活性。在此,合成了 12 种新型色烯酮衍生物,并对其 IDO1 和 TDO 抑制活性进行了评价。所有化合物均为 IDO1/TDO 双重抑制剂,特别是化合物 9a 和 9b 具有与 INCB024360 相似的 IDO1 抑制活性,化合物 5a 和 9b 具有显著的 TDO 抑制活性,优于著名的 TDO 抑制剂 LM10。这项工作丰富了 IDO1/TDO 双重抑制剂的库,并为潜在的药物开发提供了化学分子。

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