Brazilin is a natural product inhibitor of the NLRP3 inflammasome
iScience, ISSN: 2589-0042, Vol: 27, Issue: 2, Page: 108968
2024
- 8Citations
- 8Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations8
- Citation Indexes8
- CrossRef8
- Captures8
- Readers8
Article Description
Excessive or aberrant NLRP3 inflammasome activation has been implicated in the progression and initiation of many inflammatory conditions; however, currently no NLRP3 inflammasome inhibitors have been approved for therapeutic use in the clinic. Here we have identified that the natural product brazilin effectively inhibits both priming and activation of the NLRP3 inflammasome in cultured murine macrophages, a human iPSC microglial cell line and in a mouse model of acute peritoneal inflammation. Through computational modeling, we predict that brazilin can adopt a favorable binding pose within a site of the NLRP3 protein which is essential for its conformational activation. Our results not only encourage further evaluation of brazilin as a therapeutic agent for NLRP3-related inflammatory diseases, but also introduce this small-molecule as a promising scaffold structure for the development of derivative NLRP3 inhibitor compounds.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S2589004224001895; http://dx.doi.org/10.1016/j.isci.2024.108968; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85184070433&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/38327788; https://linkinghub.elsevier.com/retrieve/pii/S2589004224001895; https://dx.doi.org/10.1016/j.isci.2024.108968
Elsevier BV
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