Abstract
Abstract: IFN-β is a cytokine that plays a significant role in the immune system. Inhibition of IFN-β might be used as a therapeutic approach to treat septic shock. A peptidomimetic previously developed by our research team, 1-benzyl-5-methyl-4-(n-octylamino)pyrimidin-2(1H)-one (LT87), was used as an cardioprotective agent in a myocardial ischemia (MI) mouse model. We have developed new LT87 derivatives by synthetizing its dimers in an attempt to extend its structural variety and enhance its biological activity. A dimeric derivative, LT127, exhibited a dose-dependent inhibition of LPS-mediated IFN-β and subsequent CXCL10 mRNA transcription. The effect was selective and transduced through TLR4- and TRAM/TRIF-mediated signaling, with no significant effect on MyD88-dependent signaling. However, this effect was not specific to TLR4, since a similar effect was observed both on TLR8- and MDA5/RIG-I-stimulated IFN-β expression. Nevertheless, LT127 might serve as a drug candidate, specifically as an inhibitor for IFN-β production in order to develop a novel therapeutic approach to prevent septic shock. Graphic abstract: [Figure not available: see fulltext.]
| Original language | English |
|---|---|
| Pages (from-to) | 2175-2188 |
| Number of pages | 14 |
| Journal | Molecular Diversity |
| Volume | 26 |
| Issue number | 4 |
| DOIs | |
| State | Published - Aug 2022 |
Keywords
- CXCL10
- Interferon-β
- Pyrimidine derivatives
- TLR
- TNF
All Science Journal Classification (ASJC) codes
- Catalysis
- Information Systems
- Molecular Biology
- Drug Discovery
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry
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