Compound
all-cis-5,8,11,14,17-icosapentaenoic acid
EPA, the all-cis-5,8,11,14,17 isomer present in fish oil; ChEBI labels it by its systematic name. THREE BOUNDARIES, because this subject is rarely given alone. (1) EPA CO-ADMINISTERED WITH DHA IS NOT AN EPA TRIAL. Fish oil and nearly every omega-3 supplement deliver both, and a pooled result cannot separate their contributions, so it belongs to neither compound alone. That is a combination exposure. WHAT MAKES IT ONE IS DHA BEING PRESENT ONLY WHERE THE EPA IS. A trial giving the SAME DHA in both arms has DHA as balanced background and its randomised contrast isolates EPA — extract it, and record the background in population. So does an EPA-only arm against placebo, and an EPA arm where DHA is the comparator. Icosapent ethyl (Vascepa) is purified EPA with no DHA and belongs here. A trial that doses DHA rather than EPA is not homeless: DHA is CHEBI:28125, so decline subject_species_mismatch and name it in dosed_subject. (2) THE ESTER FORM IS RECORDED, NOT EXCLUDED. Ethyl ester, re-esterified triglyceride and free fatty acid differ several-fold in bioavailability and the field disputes it; all three are this node, with the form written into dose_regimen as the paper words it. Splitting them would divide one literature across nodes that tie on every paper; discarding the form would hide the dispute inside the graph rather than let it be read off it. (3) THE OTHER OMEGA-3S ARE NOT THIS NODE. Alpha-linolenic acid and docosapentaenoic acid are different compounds, and a trial dosing them is a subject mismatch rather than a preparation of this one.
Studied for
4 endpoints, 4 findings, from 1 paper.
- HOMA-IRlowersGrade A, Well established. Replicated human trial evidence, consistent direction.
- Serum albuminraisesGrade A, Well established. Replicated human trial evidence, consistent direction.
- C-reactive protein concentrationlowersGrade B, Likely. Human evidence, limited replication or design limits.
- Erythrocyte sedimentation ratelowersGrade B, Likely. Human evidence, limited replication or design limits.
Structure
- Class
- Organic compound
- Formula
- C20H30O2
- Mass
- 302.458 g/mol
- Charge
- 0
- InChIKey
- JAZBEHYOTPTENJ-JLNKQSITSA-N
- SMILES
- CC/C=CC/C=CC/C=CC/C=CC/C=CCCCC(=O)O
- Look it up
- ChEBIBy InChIKey
Identity from ChEBI. Not evidence — none of it carries a grade.
What the evidence says
How to read these marks4 findings across 4 endpoints, from 1 paper, strongest first.
What moved
4 findings
Decreases HOMA-IR
Well establishedGrade A, Well established. Replicated human trial evidence, consistent direction.Finding“Insulin resistance (HOMA-IR) significantly decreased in the EPA-rich fish oil than the controls (p = 0.001).”
Quoted verbatim from Eicosapentaenoic acid decreases inflammation and improves glucose homeostasis in patients with burns: a randomized clinical trial.. - Study
- RCT
- Participants
- 24
- Duration
- 3 weeks
- Dose
- 1.5 g/day EPA as EPA-rich fish oil capsules (500 mg EPA per capsule, three times daily with meals)
- Population
- Hospitalised adults aged 18-65 with non-severe burns covering less than 20% of total body surface area, able to take more than 90% of their daily calorie requirement by mouth, without diabetes, organ failure, cancer or immune disorder; both the EPA arm and the control arm also received 600 mg/day DHA.
Eicosapentaenoic acid decreases inflammation and improves glucose homeostasis in patients with burns: a randomized clinical trial.2025PMID:41254027
Increases serum albumin
Well establishedGrade A, Well established. Replicated human trial evidence, consistent direction.Finding“Serum albumin was significantly higher in the EPA-rich fish oil group than the controls (p = 0.03), however this difference was not clinically significant.”
Quoted verbatim from Eicosapentaenoic acid decreases inflammation and improves glucose homeostasis in patients with burns: a randomized clinical trial.. - Study
- RCT
- Participants
- 24
- Duration
- 3 weeks
- Dose
- 1.5 g/day EPA as EPA-rich fish oil capsules (500 mg EPA per capsule, three times daily with meals)
- Population
- Hospitalised adults aged 18-65 with non-severe burns covering less than 20% of total body surface area, able to take more than 90% of their daily calorie requirement by mouth, without diabetes, organ failure, cancer or immune disorder; both the EPA arm and the control arm also received 600 mg/day DHA.
Eicosapentaenoic acid decreases inflammation and improves glucose homeostasis in patients with burns: a randomized clinical trial.2025PMID:41254027
Decreases erythrocyte sedimentation rate
LikelyGrade B, Likely. Human evidence, limited replication or design limits.Finding“Serum ESR and CRP levels significantly decreased in the EPA-rich fish oil (p < 0.001).”
Quoted verbatim from Eicosapentaenoic acid decreases inflammation and improves glucose homeostasis in patients with burns: a randomized clinical trial.. - Study
- RCT
- Participants
- 24
- Duration
- 3 weeks
- Dose
- 1.5 g/day EPA as EPA-rich fish oil capsules (500 mg EPA per capsule, three times daily with meals)
- Population
- Hospitalised adults aged 18-65 with non-severe burns covering less than 20% of total body surface area, able to take more than 90% of their daily calorie requirement by mouth, without diabetes, organ failure, cancer or immune disorder; both the EPA arm and the control arm also received 600 mg/day DHA.
Eicosapentaenoic acid decreases inflammation and improves glucose homeostasis in patients with burns: a randomized clinical trial.2025PMID:41254027
Decreases C-reactive protein concentration
LikelyGrade B, Likely. Human evidence, limited replication or design limits.Finding“Serum ESR and CRP levels significantly decreased in the EPA-rich fish oil (p < 0.001).”
Quoted verbatim from Eicosapentaenoic acid decreases inflammation and improves glucose homeostasis in patients with burns: a randomized clinical trial.. - Study
- RCT
- Participants
- 24
- Duration
- 3 weeks
- Dose
- 1.5 g/day EPA as EPA-rich fish oil capsules (500 mg EPA per capsule, three times daily with meals)
- Population
- Hospitalised adults aged 18-65 with non-severe burns covering less than 20% of total body surface area, able to take more than 90% of their daily calorie requirement by mouth, without diabetes, organ failure, cancer or immune disorder; both the EPA arm and the control arm also received 600 mg/day DHA.
Eicosapentaenoic acid decreases inflammation and improves glucose homeostasis in patients with burns: a randomized clinical trial.2025PMID:41254027
What it touches on the way
A finding says all-cis-5,8,11,14,17-icosapentaenoic acid moved an endpoint. This is the biology in between: the proteins and reactions it runs through to get there. It is where to look for the two things a list of findings cannot answer — why a result might happen, and what else acts on the same machinery.
19 of these are proteins with a page of their own, and that is the door: a protein page says what else it carries, which is how one compound leads to the next.
Mechanistic reach
19 entities
19 entities reached, most connected first. Hub metabolites are excluded, so this is not a claim that the compound touches everything.
0 reported hop19 assembled from the scaffold
- PTGS2ProteinUNIPROT:P35354substrate ofInferred only102 paths17 endpoints
- CYP2C8ProteinUNIPROT:P10632metabolized byInferred only68 paths17 endpoints
- CYP2C9ProteinUNIPROT:P11712metabolized byInferred only68 paths17 endpoints
- ABCD3ProteinUNIPROT:P28288substrate of, transported byInferred only62 paths62 endpoints
- CYP1A1ProteinUNIPROT:P04798metabolized byInferred only30 paths15 endpoints
- ALOX5ProteinUNIPROT:P09917substrate ofInferred only29 paths29 endpoints
- CYP2C19ProteinUNIPROT:P33261metabolized byInferred only26 paths13 endpoints
- CYP4F3ProteinUNIPROT:Q08477metabolized byInferred only22 paths11 endpoints
- CYP2J2ProteinUNIPROT:P51589metabolized byInferred only20 paths10 endpoints
- CYP1A2ProteinUNIPROT:P05177metabolized byInferred only19 paths19 endpoints
- CYP3A4ProteinUNIPROT:P08684metabolized byInferred only15 paths15 endpoints
- CYP2D6ProteinUNIPROT:P10635metabolized byInferred only15 paths15 endpoints
Show the remaining 7
- CYP2E1ProteinUNIPROT:P05181metabolized byInferred only14 paths14 endpoints
- ALOX12ProteinUNIPROT:P18054substrate ofInferred only13 paths13 endpoints
- CYP4F2ProteinUNIPROT:P78329metabolized byInferred only12 paths12 endpoints
- ACSL4ProteinUNIPROT:O60488substrate ofInferred only9 paths9 endpoints
- ACSL3ProteinUNIPROT:O95573substrate ofInferred only9 paths9 endpoints
- CYP4V2ProteinUNIPROT:Q6ZWL3metabolized byInferred only8 paths8 endpoints
- ALOX12BProteinUNIPROT:O75342substrate ofInferred only5 paths5 endpoints
Where it reaches
9 systems, 17 regions, 44 tissues, 44 transporter routes.
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