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eritoran

Also Known As:
3-O-decyl-2-deoxy-6-O-(2-deoxy-3-O-(3-methoxydecyl)-6-O-methyl-2-((1-oxo-11-octadecenyl)amino)-4-O-phosphonoglucopyranosyl)-2-((1,3-dioxotetradecyl)amino)-1-(dihydroxy phosphate)glucopyranose
Networked: 45 relevant articles (10 outcomes, 13 trials/studies)

Relationship Network

Bio-Agent Context: Research Results

Experts

1. Rossignol, Daniel P: 6 articles (05/2013 - 09/2004)
2. Lynn, Melvyn: 6 articles (03/2013 - 09/2004)
3. LaRosa, Steven P: 4 articles (08/2016 - 05/2011)
4. Gusovsky, Fabian: 3 articles (01/2019 - 05/2013)
5. Opal, Steven M: 3 articles (03/2013 - 01/2010)
6. Tidswell, Mark: 3 articles (03/2013 - 01/2010)
7. Wong, Nancy: 3 articles (12/2008 - 09/2004)
8. Blanco, Jorge C G: 2 articles (01/2019 - 05/2013)
9. Lai, Wendy: 2 articles (01/2019 - 05/2013)
10. Shirey, Kari Ann: 2 articles (01/2019 - 05/2013)

Related Diseases

1. Sepsis (Septicemia)
2. Infections
01/01/2016 - "If treatment is initiated 3 h before PR8 infection and continued daily for 4 days, Eritoran failed to protect WT and TLR4(-/-) mice, implying that Eritoran must block a virus-induced, non-TLR4 signal that is required for protection. "
01/01/2017 - "Hence, these studies are the first to demonstrate the role of TLR4 in the pathogenesis of EBOV disease and indicate that eritoran is a prime candidate for further evaluation as a clinically viable therapeutic intervention strategy for EBOV and MARV infections.IMPORTANCE A hallmark of bacterial sepsis is the uncontrolled activation of the TLR4 pathway, which is the primary cause of the pathological features associated with this disease. "
01/01/2019 - "Our findings support the conclusion that selective suppression of CXCL1/CXCL2 represents an IFN-β-mediated "training" of the macrophage transcriptional response to TLR2 agonists and that blocking of TLR4 therapeutically with Eritoran after influenza virus infection reverses this suppression by blunting influenza-induced IFN-β."
01/01/2017 - "Here, we show that eritoran effectively promotes survival of mice of filovirus infection, as 70% and 90% of mice receiving daily eritoran treatment survived lethal EBOV and MARV infections, respectively. "
01/01/2017 - "Considering the importance of TLR4 signaling in bacterial sepsis and the remarkable pathological similarities associated with infections caused by filoviruses Ebola virus (EBOV) and Marburg virus (MARV), we assessed the ability of eritoran, a TLR4 antagonist, to protect mice against these viruses. "
3. Reperfusion Injury
4. Wounds and Injuries (Trauma)
5. Pneumonia (Pneumonitis)

Related Drugs and Biologics

1. E5564
2. Toll-Like Receptor 4
3. Anti-Inflammatory Agents (Anti-Inflammatories)
4. Lipid A
5. Antiviral Agents (Antivirals)
6. Oseltamivir (Tamiflu)
7. Lipopolysaccharides
8. Interleukin-1 Receptors (Interleukin 1 Receptor)
9. Therapeutic Uses
10. Antithrombins

Related Therapies and Procedures

1. Therapeutics
2. Catheters
3. Resuscitation
4. Subcutaneous Injections