Page last updated: 2024-11-12
lipoxin a4 methyl ester
Description
Research Excerpts
Clinical Trials
Roles
Classes
Pathways
Study Profile
Bioassays
Related Drugs
Related Conditions
Protein Interactions
Research Growth
Market Indicators
Description
lipoxin A4 methyl ester: attenuates morphine antinociceptive tolerance [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]
Cross-References
ID Source | ID |
---|---|
PubMed CID | 9969174 |
CHEBI ID | 197104 |
SCHEMBL ID | 23347492 |
MeSH ID | M0575423 |
Synonyms (9)
Synonym |
---|
CHEBI:197104 |
methyl (5s,6r,7e,9e,11z,13e,15s)-5,6,15-trihydroxyicosa-7,9,11,13-tetraenoate |
5(s),6(r)-lipoxin a4 methyl ester |
97643-35-1 |
5(s),6(r),15(s)-trihete methyl ester |
SCHEMBL23347492 |
5(s),6(r)-lxa4 methyl ester |
lipoxin a4 methyl ester |
AKOS040755015 |
Research Excerpts
Overview
Lipoxin A4 methyl ester (LXA4 ME) is an inflammation inhibitor that exhibits potent protective effects in experimental stroke models.
Excerpt | Reference | Relevance |
---|---|---|
"Lipoxin A4 methyl ester (LXA4 ME), is a stable synthetic analog of lipoxin with anti-inflammatory properties." | ( Lipoxin A4 Methyl Ester Reduces Early Brain Injury by Inhibition of the Nuclear Factor Kappa B (NF-κB)-Dependent Matrix Metallopeptidase 9 (MMP-9) Pathway in a Rat Model of Intracerebral Hemorrhage. Cui, J; Cui, Y; Gao, J; Song, Y; Wang, K; Yang, Y, 2019) | 2.68 |
"Lipoxin A4 methyl ester (LXA4 ME) is an inflammation inhibitor that exhibits potent protective effects in experimental stroke models." | ( Lipoxin A4 methyl ester alleviates vascular cognition impairment by regulating the expression of proteins related to autophagy and ER stress in the rat hippocampus. Dong, Y; Fan, M; Jia, Y; Jin, W; Li, L; Lv, P; Meng, N; Wang, T; Xiao, Y; Xu, J, 2015) | 2.58 |
Toxicity
Excerpt | Reference | Relevance |
---|---|---|
" Treatment emergent adverse events (TEAEs) were assessed for safety, the primary outcome." | ( Safety and Preliminary Efficacy of a Novel Host-Modulatory Therapy for Reducing Gingival Inflammation. Chiu, CJ; Cugini, M; Floros, C; Hardt, M; Hasturk, H; Martins, M; Schulte, F; Sherzai, H; Van Dyke, T, 2021) | 0.62 |
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
Drug Classes (1)
Class | Description |
---|---|
lipoxin | A nonclassic icosanoid and signalling molecule that has four conjugated double bonds and is derived from arachidonic acid. |
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Research
Studies (7)
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 5 (71.43) | 24.3611 |
2020's | 2 (28.57) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Market Indicators
Research Demand Index: 12.44
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
| This Compound (12.44) All Compounds (24.57) |
Study Types
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 1 (14.29%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 6 (85.71%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |