Abstract
Janus tyrosine kinase (JAK) inhibitors have been on the market for several years, but their use is limited by drug resistance and intolerable side effects. Herein, we propose a novel strategy of JAK tyrosine kinase (TK) and pseudokinase (PK) domain co-inhibition system to consolidate robust JAK inhibition and on-demand activation. A photoexcited prodrug PAT-SIL-TG-1&AT exhibits the synergy effects of TK-PK co-inhibition and enable the spatiotemporal control of JAK2 signaling. The hypoxia-activated prodrug HAT-SIL-TG-1&AT significantly inhibited HEL cells proliferation and downregulated phosphorylated STAT3/5 under hypoxic conditions. Importantly, HAT-SIL-TG-1&AT showed synergistic antitumor effects and selectively inhibited the JAK-STAT signaling in tumor tissues in vivo. This work demonstrates a viable solution to achieve superior JAK2 inhibition, and provides an inspiration for other kinases containing PK domain.
Original language | English (US) |
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Article number | 115198 |
Journal | European journal of medicinal chemistry |
Volume | 250 |
DOIs | |
State | Published - Mar 15 2023 |
Externally published | Yes |
Keywords
- Co-inhibition
- JAK
- Produrg
- Pseudokinase
- Tyrosine kinase
ASJC Scopus subject areas
- Pharmacology
- Drug Discovery
- Organic Chemistry