Omega-3-fatty acids in senescence (Homo sapiens)
From WikiPathways
Description
No description
Quality Tags
Ontology Terms
Bibliography
View all... |
- Nourooz-Zadeh J, Halliwell B, Anggård EE; ''Evidence for the formation of F3-isoprostanes during peroxidation of eicosapentaenoic acid.''; Biochem Biophys Res Commun, 1997 PubMed Europe PMC Scholia
- Galano JM, Lee YY, Oger C, Vigor C, Vercauteren J, Durand T, Giera M, Lee JC; ''Isoprostanes, neuroprostanes and phytoprostanes: An overview of 25years of researchin chemistry and biology.''; Prog Lipid Res, 2017 PubMed Europe PMC Scholia
- Petrie JR, Shrestha P, Liu Q, Mansour MP, Wood CC, Zhou XR, Nichols PD, Green AG, Singh SP; ''Rapid expression of transgenes driven by seed-specific constructs in leaf tissue: DHA production.''; Plant Methods, 2010 PubMed Europe PMC Scholia
- Serhan CN, Levy BD; ''Resolvins in inflammation: emergence of the pro-resolving superfamily of mediators.''; J Clin Invest, 2018 PubMed Europe PMC Scholia
- Mainka M, George S, Angioni C, Ebert R, Goebel T, Kampschulte N, Krommes A, Weigert A, Thomas D, Schebb NH, Steinhilber D, Kahnt AS; ''On the biosynthesis of specialized pro-resolving mediators in human neutrophils and the influence of cell integrity.''; Biochim Biophys Acta Mol Cell Biol Lipids, 2022 PubMed Europe PMC Scholia
- Koletzko B, Reischl E, Tanjung C, Gonzalez-Casanova I, Ramakrishnan U, Meldrum S, Simmer K, Heinrich J, Demmelmair H; ''FADS1 and FADS2 Polymorphisms Modulate Fatty Acid Metabolism and Dietary Impact on Health.''; Annu Rev Nutr, 2019 PubMed Europe PMC Scholia
- Gabbs M, Leng S, Devassy JG, Monirujjaman M, Aukema HM; ''Advances in Our Understanding of Oxylipins Derived from Dietary PUFAs.''; Adv Nutr, 2015 PubMed Europe PMC Scholia
- Lefils-Lacourtablaise J, Socorro M, Géloën A, Daira P, Debard C, Loizon E, Guichardant M, Dominguez Z, Vidal H, Lagarde M, Bernoud-Hubac N; ''The eicosapentaenoic acid metabolite 15-deoxy-δ(12,14)-prostaglandin J3 increases adiponectin secretion by adipocytes partly via a PPARγ-dependent mechanism.''; PLoS One, 2013 PubMed Europe PMC Scholia
- Deng B, Wang CW, Arnardottir HH, Li Y, Cheng CY, Dalli J, Serhan CN; ''Maresin biosynthesis and identification of maresin 2, a new anti-inflammatory and pro-resolving mediator from human macrophages.''; PLoS One, 2014 PubMed Europe PMC Scholia
- Reich EE, Zackert WE, Brame CJ, Chen Y, Roberts LJ 2nd, Hachey DL, Montine TJ, Morrow JD; ''Formation of novel D-ring and E-ring isoprostane-like compounds (D4/E4-neuroprostanes) in vivo from docosahexaenoic acid.''; Biochemistry, 2000 PubMed Europe PMC Scholia
- Liu M, He H, Chen L; ''Protective Potential of Maresins in Cardiovascular Diseases.''; Front Cardiovasc Med, 2022 PubMed Europe PMC Scholia
- Yang M, Song XQ, Han M, Liu H; ''The role of Resolvin D1 in liver diseases.''; Prostaglandins Other Lipid Mediat, 2022 PubMed Europe PMC Scholia
- Li QF, Hao H, Tu WS, Guo N, Zhou XY; ''Maresins: anti-inflammatory pro-resolving mediators with therapeutic potential.''; Eur Rev Med Pharmacol Sci, 2020 PubMed Europe PMC Scholia
- Perry SC, Kalyanaraman C, Tourdot BE, Conrad WS, Akinkugbe O, Freedman JC, Holinstat M, Jacobson MP, Holman TR; ''15-Lipoxygenase-1 biosynthesis of 7S,14S-diHDHA implicates 15-lipoxygenase-2 in biosynthesis of resolvin D5.''; J Lipid Res, 2020 PubMed Europe PMC Scholia
- William L Smith; ''Cyclooxygenases, peroxide tone and the allure of fish oil''; Curr Opin Cell Biol, 2005 PubMed Europe PMC Scholia
- Saini RK, Keum YS; ''Omega-3 and omega-6 polyunsaturated fatty acids: Dietary sources, metabolism, and significance - A review.''; Life Sci, 2018 PubMed Europe PMC Scholia
- Hansen TV, Dalli J, Serhan CN; ''The novel lipid mediator PD1(n-3 DPA): An overview of the structural elucidation, synthesis, biosynthesis and bioactions.''; Prostaglandins Other Lipid Mediat, 2017 PubMed Europe PMC Scholia
- Dasilva G, Muñoz S, Lois S, Medina I; ''Non-Targeted LC-MS/MS Assay for Screening Over 100 Lipid Mediators from ARA, EPA, and DHA in Biological Samples Based on Mass Spectral Fragmentations.''; Molecules, 2019 PubMed Europe PMC Scholia
- Stenvik Haatveit Å, Hansen TV; ''The biosynthetic pathways of the protectins.''; Prostaglandins Other Lipid Mediat, 2023 PubMed Europe PMC Scholia
- Wallis JG, Watts JL, Browse J; ''Polyunsaturated fatty acid synthesis: what will they think of next?''; Trends Biochem Sci, 2002 PubMed Europe PMC Scholia
- Tjonahen E, Oh SF, Siegelman J, Elangovan S, Percarpio KB, Hong S, Arita M, Serhan CN; ''Resolvin E2: identification and anti-inflammatory actions: pivotal role of human 5-lipoxygenase in resolvin E series biosynthesis.''; Chem Biol, 2006 PubMed Europe PMC Scholia
- Reinertsen AF, Primdahl KG, Shay AE, Serhan CN, Hansen TV, Aursnes M; ''Stereoselective Synthesis and Structural Confirmation of the Specialized Pro-Resolving Mediator Resolvin E4.''; J Org Chem, 2021 PubMed Europe PMC Scholia
- Kohli P, Levy BD; ''Resolvins and protectins: mediating solutions to inflammation.''; Br J Pharmacol, 2009 PubMed Europe PMC Scholia
- Gao L, Yin H, Milne GL, Porter NA, Morrow JD; ''Formation of F-ring isoprostane-like compounds (F3-isoprostanes) in vivo from eicosapentaenoic acid.''; J Biol Chem, 2006 PubMed Europe PMC Scholia
- Steffen Braune, Jan-Heiner Küpper, Friedrich Jung; ''Effect of Prostanoids on Human Platelet Function: An Overview''; , 2020 PubMed Europe PMC Scholia
- Jordan PM, Werz O; ''Specialized pro-resolving mediators: biosynthesis and biological role in bacterial infections.''; FEBS J, 2022 PubMed Europe PMC Scholia
- Dyall SC, Balas L, Bazan NG, Brenna JT, Chiang N, da Costa Souza F, Dalli J, Durand T, Galano JM, Lein PJ, Serhan CN, Taha AY; ''Polyunsaturated fatty acids and fatty acid-derived lipid mediators: Recent advances in the understanding of their biosynthesis, structures, and functions.''; Prog Lipid Res, 2022 PubMed Europe PMC Scholia
- Yang P, Jiang Y, Fischer SM; ''Prostaglandin E3 metabolism and cancer.''; Cancer Lett, 2014 PubMed Europe PMC Scholia
- Oh SF, Pillai PS, Recchiuti A, Yang R, Serhan CN; ''Pro-resolving actions and stereoselective biosynthesis of 18S E-series resolvins in human leukocytes and murine inflammation.''; J Clin Invest, 2011 PubMed Europe PMC Scholia
- Primdahl KG, Aursnes M, Walker ME, Colas RA, Serhan CN, Dalli J, Hansen TV, Vik A; ''Synthesis of 13(R)-Hydroxy-7Z,10Z,13R,14E,16Z,19Z Docosapentaenoic Acid (13R-HDPA) and Its Biosynthetic Conversion to the 13-Series Resolvins.''; J Nat Prod, 2016 PubMed Europe PMC Scholia
- Ferreira I, Falcato F, Bandarra N, Rauter AP; ''Resolvins, Protectins, and Maresins: DHA-Derived Specialized Pro-Resolving Mediators, Biosynthetic Pathways, Synthetic Approaches, and Their Role in Inflammation.''; Molecules, 2022 PubMed Europe PMC Scholia
- Dalli J, Colas RA, Serhan CN; ''Novel n-3 immunoresolvents: structures and actions.''; Sci Rep, 2013 PubMed Europe PMC Scholia
- Tang S, Wan M, Huang W, Stanton RC, Xu Y; ''Maresins: Specialized Proresolving Lipid Mediators and Their Potential Role in Inflammatory-Related Diseases.''; Mediators Inflamm, 2018 PubMed Europe PMC Scholia
- Zhuang XY, Zhang YH, Xiao AF, Zhang AH, Fang BS; ''Key Enzymes in Fatty Acid Synthesis Pathway for Bioactive Lipids Biosynthesis.''; Front Nutr, 2022 PubMed Europe PMC Scholia
- Hernandez-Segura A, Nehme J, Demaria M; ''Hallmarks of Cellular Senescence.''; Trends Cell Biol, 2018 PubMed Europe PMC Scholia
- Serhan CN, Dalli J, Colas RA, Winkler JW, Chiang N; ''Protectins and maresins: New pro-resolving families of mediators in acute inflammation and resolution bioactive metabolome.''; Biochim Biophys Acta, 2015 PubMed Europe PMC Scholia
- Wiktorowska-Owczarek A, Berezińska M, Nowak JZ; ''PUFAs: Structures, Metabolism and Functions.''; Adv Clin Exp Med, 2015 PubMed Europe PMC Scholia
- Libreros S, Shay AE, Nshimiyimana R, Fichtner D, Martin MJ, Wourms N, Serhan CN; ''A New E-Series Resolvin: RvE4 Stereochemistry and Function in Efferocytosis of Inflammation-Resolution.''; Front Immunol, 2020 PubMed Europe PMC Scholia
- Dalli J, Ramon S, Norris PC, Colas RA, Serhan CN; ''Novel proresolving and tissue-regenerative resolvin and protectin sulfido-conjugated pathways.''; FASEB J, 2015 PubMed Europe PMC Scholia
- Kahnt AS, Schebb NH, Steinhilber D; ''Formation of lipoxins and resolvins in human leukocytes.''; Prostaglandins Other Lipid Mediat, 2023 PubMed Europe PMC Scholia
- Vidar Hansen T, Serhan CN; ''Protectins: Their biosynthesis, metabolism and structure-functions.''; Biochem Pharmacol, 2022 PubMed Europe PMC Scholia
- Dalli J, Vlasakov I, Riley IR, Rodriguez AR, Spur BW, Petasis NA, Chiang N, Serhan CN; ''Maresin conjugates in tissue regeneration biosynthesis enzymes in human macrophages.''; Proc Natl Acad Sci U S A, 2016 PubMed Europe PMC Scholia
- Hong S, Lu Y, Tian H, Alapure BV, Wang Q, Bunnell BA, Laborde JM; ''Maresin-like lipid mediators are produced by leukocytes and platelets and rescue reparative function of diabetes-impaired macrophages.''; Chem Biol, 2014 PubMed Europe PMC Scholia
- Yin H, Musiek ES, Gao L, Porter NA, Morrow JD; ''Regiochemistry of neuroprostanes generated from the peroxidation of docosahexaenoic acid in vitro and in vivo.''; J Biol Chem, 2005 PubMed Europe PMC Scholia
- Smith W; ''Eicosanoid nomenclature.''; Prostaglandins, 1989 PubMed Europe PMC Scholia
- Serhan CN, Petasis NA; ''Resolvins and protectins in inflammation resolution.''; Chem Rev, 2011 PubMed Europe PMC Scholia
- Marhuenda J, Medina S, Martínez-Hernández P, Arina S, Zafrilla P, Mulero J, Oger C, Galano JM, Durand T, Solana A, Ferreres F, López-García JJ, Gil-Izquierdo A; ''Effect of the dietary intake of melatonin- and hydroxytyrosol-rich wines by healthy female volunteers on the systemic lipidomic-related oxylipins.''; Food Funct, 2017 PubMed Europe PMC Scholia
- Serhan CN, Libreros S, Nshimiyimana R; ''E-series resolvin metabolome, biosynthesis and critical role of stereochemistry of specialized pro-resolving mediators (SPMs) in inflammation-resolution: Preparing SPMs for long COVID-19, human clinical trials, and targeted precision nutrition.''; Semin Immunol, 2022 PubMed Europe PMC Scholia
- Musiek ES, Cha JK, Yin H, Zackert WE, Terry ES, Porter NA, Montine TJ, Morrow JD; ''Quantification of F-ring isoprostane-like compounds (F4-neuroprostanes) derived from docosahexaenoic acid in vivo in humans by a stable isotope dilution mass spectrometric assay.''; J Chromatogr B Analyt Technol Biomed Life Sci, 2004 PubMed Europe PMC Scholia
- Reich EE, Markesbery WR, Roberts LJ 2nd, Swift LL, Morrow JD, Montine TJ; ''Brain regional quantification of F-ring and D-/E-ring isoprostanes and neuroprostanes in Alzheimer's disease.''; Am J Pathol, 2001 PubMed Europe PMC Scholia
- Wiley CD, Brumwell AN, Davis SS, Jackson JR, Valdovinos A, Calhoun C, Alimirah F, Castellanos CA, Ruan R, Wei Y, Chapman HA, Ramanathan A, Campisi J, Jourdan Le Saux C; ''Secretion of leukotrienes by senescent lung fibroblasts promotes pulmonary fibrosis.''; JCI Insight, 2019 PubMed Europe PMC Scholia
- Liening S, Romp E, Werz O, Scriba GKE, Garscha U; ''Liquid chromatography-coupled mass spectrometry analysis of glutathione conjugates of oxygenated polyunsaturated fatty acids.''; Prostaglandins Other Lipid Mediat, 2019 PubMed Europe PMC Scholia
- Chiang N, Serhan CN; ''Specialized pro-resolving mediator network: an update on production and actions.''; Essays Biochem, 2020 PubMed Europe PMC Scholia
- Wiley CD, Sharma R, Davis SS, Lopez-Dominguez JA, Mitchell KP, Wiley S, Alimirah F, Kim DE, Payne T, Rosko A, Aimontche E, Deshpande SM, Neri F, Kuehnemann C, Demaria M, Ramanathan A, Campisi J; ''Oxylipin biosynthesis reinforces cellular senescence and allows detection of senolysis.''; Cell Metab, 2021 PubMed Europe PMC Scholia
- Rodriguez AR, Spur BW; ''First total syntheses of the pro-resolving lipid mediators 7(S),13(R),20(S)-Resolvin T1 and 7(S),13(R)-Resolvin T4.''; Tetrahedron Lett, 2020 PubMed Europe PMC Scholia
- Brenna JT, Kothapalli KSD; ''New understandings of the pathway of long-chain polyunsaturated fatty acid biosynthesis.''; Curr Opin Clin Nutr Metab Care, 2022 PubMed Europe PMC Scholia
- ''Protectins, Resolvins and Maresins - Specialized Pro-Resolving Mediators''; ,
- Djuricic I, Calder PC; ''Beneficial Outcomes of Omega-6 and Omega-3 Polyunsaturated Fatty Acids on Human Health: An Update for 2021.''; Nutrients, 2021 PubMed Europe PMC Scholia
History
View all... |
External references
DataNodes
View all... |
Name | Type | Database reference | Comment |
---|---|---|---|
10,11,dihydro-12-oxo-RvE1 | Metabolite | CHEBI:165276 (ChEBI) | |
10,11-dihydro-RvE1 | Metabolite | CHEBI:165277 (ChEBI) | |
10-D4-NeuroP | Metabolite | LMFA04010186 (LIPID MAPS) | |
10-E4-NeuroP | Metabolite | LMFA04010314 (LIPID MAPS) | |
10-F4-NeuroP | Metabolite | LMFA04010005 (LIPID MAPS) | |
10-G4-NeuroP* | Metabolite | ||
10-H4-NeuroP | Metabolite | CHEBI:185511 (ChEBI) | |
10R/S,17S-dihydroxy-DHA | Metabolite | ||
10S,17S-11E,13Z,15E-diHpDHA | Metabolite | ||
10S,17S-dihydroxy-DHA | Metabolite | CHEBI:138653 (ChEBI) | |
10epi-S15Δ-trans PD1 | Metabolite | ||
11-D4-NeuroP | Metabolite | LMFA04010202 (LIPID MAPS) | |
11-E4-NeuroP | Metabolite | LMFA04010330 (LIPID MAPS) | |
11-F3-IsoP* | Metabolite | ||
11-F4-NeuroP | Metabolite | LMFA04010006 (LIPID MAPS) | |
11-G3-IsoP* | Metabolite | ||
11-G4-NeuroP* | Metabolite | ||
11-H3-IsoP* | Metabolite | ||
11-H4-NeuroP | Metabolite | CHEBI:187424 (ChEBI) | |
12-F3-IsoP* | Metabolite | ||
12-G3-IsoP* | Metabolite | ||
12-H3-IsoP* | Metabolite | ||
12-oxo-RvE1 | Metabolite | CHEBI:165264 (ChEBI) | |
13,14-epoxy-DPA* | Metabolite | ||
13-D4-NeuroP | Metabolite | LMFA04010218 (LIPID MAPS) | |
13-E4-NeuroP | Metabolite | LMFA04010346 (LIPID MAPS) | |
13-F4-NeuroP | Metabolite | LMFA04010003 (LIPID MAPS) | |
13-G4-NeuroP* | Metabolite | ||
13-H4-NeuroP* | Metabolite | ||
13R-HpDPA* | Metabolite | ||
13S,14S-epoxy-maresin | Metabolite | CHEBI:131958 (ChEBI) | (13R)-S-glutathionyl-(14S)-hydroxy-(4Z,7Z,9E,11E,16Z,19Z)-docosahexaenoic acid |
14-D4-NeuroP | Metabolite | LMFA04010234 (LIPID MAPS) | |
14-E4-NeuroP | Metabolite | LMFA04010362 (LIPID MAPS) | |
14-F4-NeuroP | Metabolite | LMFA04010004 (LIPID MAPS) | |
14-G4-NeuroP* | Metabolite | ||
14-H4-NeuroP | Metabolite | HMDB0062292 (HMDB) | |
14-HpDPA | Metabolite | CHEBI:136353 (ChEBI) | |
14R-HDHA | Metabolite | CHEBI:137346 (ChEBI) | |
14S-HDHA | Metabolite | CHEBI:137347 (ChEBI) | |
14S-HpDHA | Metabolite | CHEBI:136526 (ChEBI) | |
15-F3-IsoP | Metabolite | CHEBI:157746 (ChEBI) | = 8-epi PGF3 |
15-G3-IsoP* | Metabolite | = 8-epi PGF3 | |
15-H3-IsoP* | Metabolite | = 8-epi PGF3 | |
15S-HpEPE | Metabolite | CHEBI:165266 (ChEBI) | |
15S-hydroxy-5S-HpEPE* | Metabolite | ||
15d-PGD3* | Metabolite | ||
15d-PGJ3 | Metabolite | CHEBI:140223 (ChEBI) | |
15Δ-trans PD1 | Metabolite | ||
16-oxo-RvD2 | Metabolite | CHEBI:138281 (ChEBI) | |
16R/S,17S-dihydroxy-DHA | Metabolite | ||
16S,17S-epoxy-DPA | Metabolite | CHEBI:140224 (ChEBI) | |
16S,17S-epoxyprotectin | Metabolite | CHEBI:140225 (ChEBI) | |
17-D4-NeuroP | Metabolite | LMFA04010250 (LIPID MAPS) | = 17-F4c-NP |
17-E4-NeuroP | Metabolite | LMFA04010378 (LIPID MAPS) | = 17-F4c-NP |
17-F4-NeuroP | Metabolite | LMFA04010002 (LIPID MAPS) | = 17-F4c-NP |
17-G4-NeuroP* | Metabolite | = 17-F4c-NP | |
17-H4-NeuroP* | Metabolite | = 17-F4c-NP | |
17-oxo-RvD1 | Metabolite | CHEBI:132800 (ChEBI) | |
17R-HDHA | Metabolite | CHEBI:91137 (ChEBI) | |
17R-HpDHA | Metabolite | CHEBI:138590 (ChEBI) | |
17S-HDHA | Metabolite | CHEBI:138640 (ChEBI) | |
17S-HpDHA | Metabolite | CHEBI:136113 (ChEBI) | |
17S-HpDPA | Metabolite | CHEBI:136118 (ChEBI) | |
18-F3-IsoP* | Metabolite | ||
18-G3-IsoP* | Metabolite | ||
18-H3-IsoP* | Metabolite | ||
18-oxo-RvE1 | Metabolite | CHEBI:131617 (ChEBI) | |
18R-HpEPE | Metabolite | CHEBI:138565 (ChEBI) | |
18S-HpEPE* | Metabolite | ||
18S-RvE1 | Metabolite | CHEBI:137038 (ChEBI) | |
18S-RvE2 | Metabolite | CHEBI:137034 (ChEBI) | |
19-hydroxy-RvE1 | Metabolite | CHEBI:165268 (ChEBI) | |
20-D4-NeuroP | Metabolite | LMFA04010266 (LIPID MAPS) | |
20-E4-NeuroP | Metabolite | LMFA04010394 (LIPID MAPS) | |
20-F4-NeuroP | Metabolite | LMFA04010001 (LIPID MAPS) | |
20-G4-NeuroP* | Metabolite | ||
20-H4-NeuroP* | Metabolite | ||
20-carboxy-RvE1* | Metabolite | ||
20-hydroxy-RvE1 | Metabolite | CHEBI:165269 (ChEBI) | |
4-D4-NeuroP | Metabolite | LMFA04010154 (LIPID MAPS) | |
4-E4-NeuroP | Metabolite | LMFA04010282 (LIPID MAPS) | |
4-F4-NeuroP | Metabolite | LMFA04010008 (LIPID MAPS) | |
4-G4-NeuroP* | Metabolite | ||
4-H4-NeuroP* | Metabolite | ||
4S,5-epoxy-17R-HDHA | Metabolite | CHEBI:187528 (ChEBI) | |
4S,5-epoxy-17S-HDHA | Metabolite | CHEBI:138647 (ChEBI) | |
4S-HpDHA | Metabolite | ||
4S-hydroperoxy-17S-HDHA | Metabolite | CHEBI:138641 (ChEBI) | |
5(S)-HpEPE | Metabolite | CHEBI:165271 (ChEBI) | |
5,6-epoxy-15(S)-HEPE* | Metabolite | ||
5-F3-IsoP* | Metabolite | ||
5-G3-IsoP* | Metabolite | ||
5-H3-IsoP* | Metabolite | ||
5S,12R,18R-TriHEPE* | Metabolite | ||
5S,12S,18R-TriHEPE | Metabolite | CHEBI:133822 (ChEBI) | |
5S,6R,18R-TriHEPE* | Metabolite | ||
5S,6S,18R-TriHEPE* | Metabolite | ||
5S,6S-epoxy-18R-HEPE | Metabolite | CHEBI:132219 (ChEBI) | |
5S,6S-epoxy-18S-HEPE | Metabolite | CHEBI:138490 (ChEBI) | |
5S-hydroxyperoxy-18R-HEPE | Metabolite | CHEBI:81562 (ChEBI) | |
5S-hydroxyperoxy-18S-HEPE | Metabolite | CHEBI:91287 (ChEBI) | |
6-keto-PGF2α* | Metabolite | ||
7,8-epoxy-13R-HDPA* | Metabolite | ||
7-D4-NeuroP | Metabolite | LMFA04010170 (LIPID MAPS) | |
7-E4-NeuroP | Metabolite | LMFA04010298 (LIPID MAPS) | |
7-F4-NeuroP | Metabolite | LMFA04010007 (LIPID MAPS) | |
7-G4-NeuroP* | Metabolite | ||
7-H4-NeuroP* | Metabolite | ||
7-hydroperoxy-13R-HpDPA* | Metabolite | ||
7-oxo-RvD2 | Metabolite | CHEBI:138279 (ChEBI) | |
7S,17S-diHpDHA | Metabolite | CHEBI:140245 (ChEBI) | |
7S,17S-diHpDPA | Metabolite | CHEBI:140248 (ChEBI) | |
7S,8-epoxy-17R-HDHA | Metabolite | CHEBI:138613 (ChEBI) | |
7S,8-epoxy-17S-HDHA | Metabolite | 53477500 (PubChem-compound) | |
7S,8R-epoxy-17S-HDPA* | Metabolite | ||
7S-HpDHA | Metabolite | InChIKey=IYPGULUSNSBANC-VPNHEHDPSA-M (InChIKey) | |
7S-hydroperoxy-17S-HDHA | Metabolite | CHEBI:138642 (ChEBI) | |
8-F3-IsoP* | Metabolite | ||
8-G3-IsoP* | Metabolite | ||
8-H3-IsoP* | Metabolite | ||
8-oxo-RvD1 | Metabolite | CHEBI:132797 (ChEBI) | |
ALOX12 | GeneProduct | ENSG00000108839 (Ensembl) | Enzyme 12LOX |
ALOX15B | GeneProduct | ENSG00000179593 (Ensembl) | |
ALOX15 | GeneProduct | ENSG00000161905 (Ensembl) | |
ALOX5 | GeneProduct | ENSG00000012779 (Ensembl) | |
AT-RvD1 | Metabolite | CHEBI:138179 (ChEBI) | |
AT-RvD2 | Metabolite | CHEBI:138614 (ChEBI) | |
AT-RvD3 | Metabolite | CHEBI:138615 (ChEBI) | |
AT-RvD4 | Metabolite | CHEBI:138616 (ChEBI) | |
CMKLR1 | Complex | ENSG00000174600 (Ensembl) | =ChemR23 |
CYP1A2 | GeneProduct | ENSG00000140505 (Ensembl) | |
CYP2C8 | GeneProduct | ENSG00000138115 (Ensembl) | |
CYP2C9 | GeneProduct | ENSG00000138109 (Ensembl) | |
CYP2D6 | GeneProduct | ENSG00000100197 (Ensembl) | |
CYP2E1 | GeneProduct | ENSG00000130649 (Ensembl) | |
CYP3A4 | GeneProduct | ENSG00000160868 (Ensembl) | |
DPEP1 | GeneProduct | ENSG00000015413 (Ensembl) | dipeptidase 1 |
Dehydration | |||
Dehydration* | |||
Docosahexaenoic acid (22:6,w3) | Metabolite | CHEBI:36005 (ChEBI) | |
Docosapentaenoic acid (22:5,w3) | Metabolite | CHEBI:53488 (ChEBI) | |
ELOVL2 | GeneProduct | ENSG00000197977 (Ensembl) | |
ELOVL5 | GeneProduct | ENSG00000012660 (Ensembl) | fatty acid elongase 5 |
EPHX2 | GeneProduct | ENSG00000120915 (Ensembl) | |
Eicosapentaenoic acid (20:5,w3) | Metabolite | CHEBI:28364 (ChEBI) | |
Eicosatetraenoic acid (20:4,w3) | Metabolite | CHEBI:166893 (ChEBI) | |
Eicosatrienoic acid (20:3,w3) | Metabolite | 5312529 (PubChem-compound) | |
Enzymatic Epoxidation | |||
Enzymatic Hydrolysis | Protein | ||
Enzymatic dehydrogenation | GeneProduct | ||
FADS1 | GeneProduct | ENSG00000149485 (Ensembl) | gene=FADS1 Δ5-Desaturase |
FADS2 | GeneProduct | ENSG00000134824 (Ensembl) | |
FPR2 | GeneProduct | ENSG00000171049 (Ensembl) | =formyl peptide receptor 2 =ALX |
GGT1 | GeneProduct | ENSG00000100031 (Ensembl) | gamma-glutamyltransferase 1 |
GPR32 | GeneProduct | ENSG00000142511 (Ensembl) | =G protein-coupled receptor 32 =RVDR1 |
GPx-4 | Protein | ENSG00000167468 (Ensembl) | Glutathione Peroxidase 4 |
GSTM4 | GeneProduct | ENSG00000168765 (Ensembl) | glutathione S-transferase mu 4 |
HPGD | GeneProduct | ENSG00000164120 (Ensembl) | |
Hydrolase | |||
Hydrolase* | GeneProduct | ||
Hydrolysis (Unknown Hydrolase) | Protein | ||
Hydrolysis* | GeneProduct | ||
Irradiation-induced Senescence | |||
Irradiation-induced senescence | |||
LGR6 receptor | Metabolite | ||
LTA4H | GeneProduct | ENSG00000111144 (Ensembl) | |
LTA5* | Metabolite | ||
LTB5 | Metabolite | 5283125 (PubChem-compound) | |
LTC4S | GeneProduct | ENSG00000213316 (Ensembl) | |
LTC5 | Metabolite | CHEBI:172777 (ChEBI) | |
LTD5 | Metabolite | CHEBI:175815 (ChEBI) | |
LXA5 | Metabolite | 110657-98-2 (CAS) | |
MCTR1 | Metabolite | CHEBI:138202 (ChEBI) | (13R)-S-glutathionyl-(14S)-hydroxy-(4Z,7Z,9E,11E,16Z,19Z)-docosahexaenoic acid |
MCTR2 | Metabolite | CHEBI:138206 (ChEBI) | (13R)-S-cysteinylglycinyl-(14S)-hydroxy-(4Z,7Z,9E,11E,16Z,19Z)-docosahexaenoic acid |
MCTR3 | Metabolite | CHEBI:138209 (ChEBI) | (13R)-S-cysteinyl-(14S)-hydroxy-(4Z,7Z,9E,11E,16Z,19Z)-docosahexaenoic acid |
MaR-L1 | Metabolite | CHEBI:137349 (ChEBI) | |
MaR-L2 | Metabolite | CHEBI:137350 (ChEBI) | |
Mar1(n-3 DPA) | Metabolite | CHEBI:140256 (ChEBI) | |
Mar2(n-3 DPA)* | Metabolite | ||
Mar3(n-3 DPA) | Metabolite | CHEBI:140258 (ChEBI) | |
Maresin 1 | Metabolite | CHEBI:138249 (ChEBI) | 7R,14S-dihydroxy-4Z,8E,10E,12Z,16Z,19Z-docosahexaenoic acid |
Maresin 2 | Metabolite | CHEBI:138248 (ChEBI) | (13R,14S)-dihydroxy-(4Z,7Z,9E,11E,16Z,19Z)-docosahexaenoic acid |
Mitochondrial dysfunction-associated senescence Oncogene-induced senescence(RAS) | |||
Mitochondrial dysfunction-associated senescence
Oncogene-induced senescence(RAS) Irradiation-induced senescence | |||
Non-enzymatic Hydrolysis | Protein | ||
Non-enzymatic hydrolysis | |||
P450 | GeneProduct | ||
PCTR1 | Metabolite | LMFA04040004 (LIPID MAPS) | |
PCTR2 | Metabolite | LMFA04040005 (LIPID MAPS) | |
PCTR3 | Metabolite | LMFA04040006 (LIPID MAPS) | |
PD1(n-3 DPA) | Metabolite | CHEBI:140265 (ChEBI) | |
PD1 | Metabolite | 195348 (ChEBI) | |
PD2(n-3 DPA)* | Metabolite | ||
PD2* | Metabolite | ||
PDX | Metabolite | 138653 (ChEBI) | (4Z,7Z,10S,11E,13Z,15E,17S,19Z)-10,17-dihydroxydocosahexaenoic acid |
PGD3 | Metabolite | CHEBI:34939 (ChEBI) | |
PGDS | GeneProduct | 5.3.99.2 (Enzyme Nomenclature) | |
PGE3 | Metabolite | CHEBI:28031 (ChEBI) | |
PGES | GeneProduct | 5.3.99.3 (Enzyme Nomenclature) | |
PGF3α | Metabolite | CHEBI:36075 (ChEBI) | |
PGG3 | Metabolite | CHEBI:134406 (ChEBI) | |
PGH3 | Metabolite | CHEBI:134407 (ChEBI) | |
PGI3 | Metabolite | ||
PGIS | GeneProduct | 5.3.99.4 (Enzyme Nomenclature) | |
PGJ3 | Metabolite | CHEBI:140267 (ChEBI) | |
PTGS1 | GeneProduct | ENSG00000095303 (Ensembl) | =Prostaglandin-endoperoxide synthase 1 =cyclooxygenase (COX) |
PTGS2 | GeneProduct | ||
PTGS2 | GeneProduct | ENSG00000073756 (Ensembl) | |
Peroxidase | |||
Peroxidase* | GeneProduct | ||
Peroxisomal beta-oxidation | Pathway | / (WikiPathways) | |
Phospholipase A2 | GeneProduct | P47712 (Uniprot-TrEMBL) | |
Prostaglandin F synthase | |||
RCTR1 | Metabolite | LMFA04030014 (LIPID MAPS) | |
RCTR2 | Metabolite | LMFA04030015 (LIPID MAPS) | |
RCTR3 | Metabolite | LMFA04030016 (LIPID MAPS) | |
RORalpha | Metabolite | ||
Reduction | |||
Reduction* | |||
RvD1(n-3 DPA)* | Metabolite | ||
RvD1 | Metabolite | CHEBI:81564 (ChEBI) | |
RvD2(n-3 DPA)* | Metabolite | ||
RvD2 | Metabolite | CHEBI:81565 (ChEBI) | |
RvD3 | Metabolite | CHEBI:138648 (ChEBI) | |
RvD4 | Metabolite | CHEBI:138649 (ChEBI) | |
RvD5 | Metabolite | ||
RvD5(n-3 DPA)* | Metabolite | ||
RvD6 | Metabolite | CHEBI:138643 (ChEBI) | |
RvE1 | Metabolite | CHEBI:81559 (ChEBI) | |
RvE2 | Metabolite | CHEBI:81560 (ChEBI) | |
RvE3 | Metabolite | CHEBI:138542 (ChEBI) | |
RvE4 | Metabolite | 1025684-60-9 (CAS) | |
RvT1 | Metabolite | CHEBI:137011 (ChEBI) | |
RvT2 | Metabolite | CHEBI:137018 (ChEBI) | |
RvT3 | Metabolite | CHEBI:137019 (ChEBI) | |
RvT4 | Metabolite | CHEBI:137020 (ChEBI) | |
Stearidonic acid (18:4,w3) | Metabolite | CHEBI:32389 (ChEBI) | |
TXAS | GeneProduct | 5.3.99.5 (Enzyme Nomenclature) | |
Tetracosahexanoic acid (22:6,n-3) | Metabolite | 11792612 (PubChem-compound) | |
Tetracosapentanoic acid (24:5,n-3) | Metabolite | HMDB0006323 (HMDB) | |
TxA3 | Metabolite | CHEBI:165349 (ChEBI) | |
TxB3 | Metabolite | CHEBI:84444 (ChEBI) | |
Unknown | |||
h15-LOX1 | Protein | ||
Δ12-PGJ3 | Metabolite | CHEBI:140274 (ChEBI) | |
Δ9-Elongase* | |||
α-Linolenic acid (18:3,w3) | Metabolite | CHEBI:27432 (ChEBI) | IUPAC Name: (9Z,12Z,15Z)-octadeca-9,12,15-trienoic acid |
Annotated Interactions
Source | Target | Type | Database reference | Comment |
---|---|---|---|---|
5S,6S-epoxy-18R-HEPE | 5S,12S,18R-TriHEPE | mim-conversion | 50868 (Rhea) | |
5S-hydroxyperoxy-18R-HEPE | RvE2 | mim-conversion | 52020 (Rhea) | |
5S-hydroxyperoxy-18S-HEPE | 18S-RvE2 | mim-conversion | 52024 (Rhea) |