Structure–Stability Relationship of NLRP3 Inflammasome-Inhibiting Sulfonylureas
Author:
Affiliation:
1. Pharmaceutical Institute, University of Bonn, 53121 Bonn, Germany
2. Institute of Structural Biology, University of Bonn, 53127 Bonn, Germany
Funder
Deutsche Forschungsgemeinschaft
Studienstiftung des Deutschen Volkes
J?rgen Manchot Stiftung
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acsomega.2c00125
Reference32 articles.
1. Mechanisms and Characteristics of Sulfonylureas and Glinides
2. Glutathione S-Transferase Omega 1-1 Is a Target of Cytokine Release Inhibitory Drugs and May Be Responsible for Their Effect on Interleukin-1औ Posttranslational Processing
3. Novel Synthesis of 1-(1,2,3,5,6,7-Hexahydro-s-indacen-4-yl)-3-[4-(1-hydroxy-1-methyl-ethyl)-furan-2-sulfonyl]urea, an Anti-inflammatory Agent
4. Sulfonylureas as Concomitant Insulin Secretagogues and NLRP3 Inflammasome Inhibitors
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