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Research draft

icosanoid

vr.tr.icosanoid · PHY.MAT

Let an agent explain eicosanoids and their pathways, relay classes, functions and drug targets from biochemistry and pharmacology references, describe their roles in disease, and distinguish eicosanoids from other lipid mediators.

Thing Registry Physical world and living systems

Research draft, second pass

A second pass drafted this model: the structure a model of this thing needs, and what is known about it in the world. The line under this one says how the second half was obtained - researched against sources, or recalled without web access, in which case nothing here was read anywhere and every claim is a lead to verify. Unreviewed either way.

written by Claude from model knowledge without web access - no source was read, every claim is a lead to verify

Researched by: Claude

Purpose and description

Let an agent explain eicosanoids and their pathways, relay classes, functions and drug targets from biochemistry and pharmacology references, describe their roles in disease, and distinguish eicosanoids from other lipid mediators.

A class of signalling molecules derived from twenty-carbon polyunsaturated fatty acids, chiefly arachidonic acid, through cyclooxygenase, lipoxygenase and cytochrome P450 pathways, including prostaglandins, thromboxanes, leukotrienes, lipoxins, hydroxy and hydroperoxy eicosatetraenoic acids such as 20-HETE and 15-HPETE, and epoxy and dihydroxy derivatives; eicosanoids act locally to regulate inflammation, immunity, blood flow, blood clotting and many other processes, and are targets of aspirin, NSAIDs and asthma drugs.

What it is for: Not applicable; a class of signalling lipids.

It can be explain pathways and classes; relay functions; describe drug targets and disease; distinguish from other lipid mediators.

Distinguishing features

Arachidonic acid origin

Three enzyme pathways

Local hormone action

Drug targets

What it looks like

Not a visible object; lipid molecules acting locally.

Physical character

carbon skeleton: 20 carbons

main precursor: arachidonic acid compound

Nobel Prize: 1982 year - Bergstrom, Samuelsson, Vane

How it is recognised

Twenty-carbon fatty acid derived mediators

Prostaglandins, thromboxanes, leukotrienes, lipoxins, HETEs, HPETEs, EETs and DHETs

Endocannabinoids and resolvins are related lipid mediators; steroids are different lipids

Related models

is a kind of - in registry terms, as derivatives

unsaturated fatty acid

is a kind of - in registry terms

olefinic compound

includes - as a major class

prostaglandins

is inhibited by - through cyclooxygenase

nonsteroidal anti-inflammatory drug

In practice

Families and kinds

prostaglandins and prostacyclin

thromboxanes

leukotrienes

lipoxins

hydroxyeicosatetraenoic and hydroperoxyeicosatetraenoic acids such as 20-HETE and 15-HPETE

epoxyeicosatrienoic and dihydroxyeicosatrienoic acids

isoprostanes formed non-enzymatically

Identifiers

MeSH D015786 eicosanoids

ChEBI CHEBI:23899 icosanoid

Standards and regulation

IUPAC lipid nomenclature

Drug regulation of NSAIDs, leukotriene antagonists and prostaglandin analogues

Failure modes and hazards

Agents giving personal medication advice

Confusing eicosanoid classes

Registry aliases with unwieldy systematic names

Also called

(5Z,9E,12S,14Z)-8,11,12-trihydroxyicosa-5,9,14-trienoic acid14,15-Dihydroxyicosa-5,8,11-trienoic acidhydroxy and hydroperoxyeicosatetraenoic acids15-hydroperoxyicosa-5,8,11,13-tetraenoic acidArachidonic acid omega-9 hydroperoxide20-Hydroxyicosa-5,8,11,14-tetraenoic acideoxin12-hydroxyheptadecatrienoic acid20-HETE5-oxo-eicosatetraenoic acid12R-HETE(R)-12-hpete(S)-12-HpETE(S)-15-hpete16-HETE18-HETE5-HETE11,12-DHET8,9-DHET5,6-DHET11(R)-HPETE11,12,15-THETA11,14,15-THETA12-oxo-ETE8(S)-HPETE9(S)-HPETE(5S,6S)-di-HETE14,15-DHET17-HETE19-HETE(5Z,8Z,11Z,13E)-15-HETE5,6-Ep-15S-HETE11-HETE15-HEPE8-HETE15-hydroxy-8,11,13-eicosatrienoic acid12-hydroxyeicosapentaenoic acid9-hydroxy-5E,7Z,11Z,14Z-eicosatetraenoic acid9-hydroxy-5Z,7E,11Z,14Z-eicosatetraenoic acid5-HEPE

+129

Where this came from

wikidata · CC0 1.0

Drafted structure

Bundle to layer to finding to question, as the second pass will find it: 4 bundles · 8 layers · 8 findings · 16 questions.

Understand What eicosanoids are.

Science.

Definition

Definition and pathways.

Definition

Definition.

  1. What are eicosanoids, and how do the cyclooxygenase, lipoxygenase and cytochrome P450 pathways produce them? definition
  2. Is the question about eicosanoids in general, a class such as prostaglandins, or a specific compound? boundary

Classes

Classes.

Classes

Classes.

  1. How do prostaglandins, thromboxanes, leukotrienes, lipoxins, HETEs and EETs differ? definition
  2. Which entry fits the specific class? action
Biology Functions.

Science.

Roles

Physiological roles.

Roles

Roles.

  1. How do eicosanoids regulate inflammation, immunity, blood flow, clotting and kidney function? provenance
  2. Which references are standard? provenance

Disease

Disease.

Disease

Disease.

  1. What roles do eicosanoids play in asthma, cardiovascular disease, pain and cancer, in general terms? provenance
  2. Which entry fits the specific disease? action
Medicine Drugs.

Clinical.

Drugs

Drug targets.

Drugs

Drugs.

  1. How do aspirin, NSAIDs, leukotriene antagonists and prostaglandin analogues act on eicosanoid pathways? provenance
  2. Is the user asking about their own medication, which needs a clinician or pharmacist? boundary

Research

Research.

Research

Research.

  1. What research explores resolvins, 20-HETE and new eicosanoid targets, with findings attributed? provenance
  2. Which sources are cited? provenance
Context History and methods.

Context.

History

History.

History

History.

  1. How were eicosanoids discovered and characterised, with Nobel recognition? provenance
  2. Which entry fits the history of pharmacology? action

Methods

Analysis.

Methods

Methods.

  1. How are eicosanoids measured by mass spectrometry and immunoassay? provenance
  2. Which entry fits lipidomics? action

What the second pass must settle

  • Should leukotriene and thromboxane be separate primary entries?
  • How should pharmacology references be linked?
  • The registry entry has merged aliases with systematic names; should they be split off?