Chemicals and Drugs

F2-Isoprostanes

Isoprostanes derived from the free radical oxidation of ARACHIDONIC ACID. Although similar in structure to enzymatically synthesized prostaglandin F2alpha (DINOPROST), they occur through non-enzymatic oxidation of cell membrane lipids.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

Isoprostanes derived from the free radical oxidation of ARACHIDONIC ACID. Although similar in structure to enzymatically synthesized prostaglandin F2alpha (DINOPROST), they occur through non-enzymatic oxidation of cell membrane lipids.

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Classification

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Synonyms

3 entry terms
  • F2-Isoprostane
  • F2 Isoprostane
  • F2 Isoprostanes

MeSH Record

Aspects Covered

28 allowable subheadings

Indexed with the subheadings administration & dosage, adverse effects, agonists, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, urine.

MeSH Record

History Note

2002; use F2-ISOPROSTANES (NM) 1994-2001

MeSH Record

Previous Indexing

  • Arachidonic Acids (1994-1996)
  • Dinoprost (1994-2001)

MeSH Hierarchy

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AMA Style

References

  1. National Library of Medicine. F2-Isoprostanes. Medical Subject Headings (MeSH). 2026. Unique ID D028441. http://id.nlm.nih.gov/mesh/2026/D028441
  2. F2-Isoprostanes. In: Wikidata. https://www.wikidata.org/wiki/Q33659470