Novel Substituted Tetrahydropyrrolooxazolones as RIPK1 Inhibitors

This patent discloses tetrahydropyrrolooxazolones as novel receptor-interacting protein kinase 1 (RIPK1) inhibitors as potential treatments for RIPK1-related diseases. It provides details in the synthesis of the tetrahydropyrrolooxazolones, pharmaceutical compositions, and therapeutic applications for RIPK1-related diseases.

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Publication Details

Journal
ACS Medicinal Chemistry Letters
Published
2026-04-21
DOI
https://doi.org/10.1021/acsmedchemlett.6c00188
Primary Topic
Ubiquitin and proteasome pathways
Type
article
Field-Weighted Citation Impact
0.00
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article

Novel Substituted Tetrahydropyrrolooxazolones as RIPK1 Inhibitors

Steven H. Liang, Jian Rong
ACS Medicinal Chemistry Letters
Ubiquitin and proteasome pathways
article

Novel Substituted Tetrahydropyrrolooxazolones as RIPK1 Inhibitors

Steven H. Liang, Jian Rong
article en

Abstract

This patent discloses tetrahydropyrrolooxazolones as novel receptor-interacting protein kinase 1 (RIPK1) inhibitors as potential treatments for RIPK1-related diseases. It provides details in the synthesis of the tetrahydropyrrolooxazolones, pharmaceutical compositions, and therapeutic applications for RIPK1-related diseases.

ACS Medicinal Chemistry Letters
Emory University (US), Union Hospital (CN)
Openalex Percentile: Top 9%
Ubiquitin and proteasome pathways
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