The discovery of potent small molecule activators of human STING

被引:30
|
作者
Pryde, David C. [1 ]
Middya, Sandip [2 ]
Banerjee, Monali [2 ]
Shrivastava, Ritesh [2 ]
Basu, Sourav [2 ]
Ghosh, Rajib [2 ]
Yadav, Dharmendra B. [2 ]
Surya, Arjun [2 ]
机构
[1] Curadev Pharma Ltd, Innovat House,Discovery Pk,Ramsgate Rd, Sandwich CT13 9ND, Kent, England
[2] Curadev Pharma Pvt Ltd, B-87,Sect 83, Noida 201305, Uttar Pradesh, India
关键词
STING; Interferon genes; Immunotherapy; Cytokines; ANTIVIRAL RESPONSES; RECOGNITION; AGENT; SENSOR; MOUSE;
D O I
10.1016/j.ejmech.2020.112869
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The adaptor protein STING plays a major role in innate immune sensing of cytosolic nucleic acids, by triggering a robust interferon response. Despite the importance of this protein as a potential therapeutic target for serious unmet medical conditions including cancer and infectious disease there remains a paucity of STING ligands. Starting with a benzothiazinone series of weak STING activators (human EC50 similar to 10 mu M) we identified several chemotypes with sub-micromolar STING activity across all the major protein polymorphs. An example compound 53 based on an oxindole core structure demonstrated robust on-target functional activation of STING (human EC50 185 nM) in immortalised and primary cells and a cytokine induction fingerprint consistent with STING activation. Our study has identified several related series of potent small molecule human STING activators with potential to be developed as immunomodulatory therapeutics. (c) 2020 Elsevier Masson SAS. All rights reserved.
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收藏
页数:17
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