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leukotriene c4

chemical compound
ChemicalSubstance type_of_chemical_entity Q2704310
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leukotriene c4

Summary

leukotriene c4 is a type of chemical entity[1]. It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • leukotriene c4's instance of is recorded as type of chemical entity[3].
  • leukotriene c4's canonical SMILES is recorded as CCCCCC=CCC=CC=CC=CC(C(CCCC(=O)O)O)SCC(C(=O)NCC(=O)O)NC(=O)CCC(C(=O)O)N[4].
  • leukotriene c4's chemical formula is recorded as C₃₀H₄₇N₃O₉S[5].
  • leukotriene c4 is a type of leukotriene[6].
  • leukotriene c4's found in taxon is recorded as Homo sapiens[7].
  • leukotriene c4's isomeric SMILES is recorded as CCCCC/C=C\C/C=C\C=C\C=C[C@H](C@HO)SCC@@HNC(=O)CCC@@HNC@HO)SCC@@HNC(=O)CCC@@HN">[8].
  • leukotriene c4's mass is recorded as {'unit': 'Q483261', 'amount': '+625.303'}[9].
  • leukotriene c4's subject has role is recorded as primary metabolite[10].
  • leukotriene c4's stereoisomer of is recorded as (5S,6R)-6-{[(2R)-2-{[(4S)-4-amino-4-carboxy-1-hydroxybutylidene]amino}-2-(carboxymethyl-C-hydroxycarbonimidoyl)ethyl]sulfanyl}-5-hydroxyicosa-7,9,11,14-tetraenoic acid[11].
  • leukotriene c4's stereoisomer of is recorded as 11-trans-Leukotriene C4[12].

Why It Matters

leukotriene c4 has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] It is known by 24 alternative names across languages and contexts.[13]

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [5] ↑ . PubChem. Retrieved . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . Recon 2.2: from reconstruction to model of human metabolism. wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . Reactome. reactome.org. Provenance: wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata sitelinks. wikidata.org.
  2. [13] ↑ . Wikidata aliases. wikidata.org.

📑 Cite this page

Use these citations when quoting this entity in research, articles, AI prompts, or wherever provenance matters. We aggregate Wikidata + Wikipedia + authoritative open-data sources; the stitched, scored, cross-referenced view is what 4ort.xyz contributes.

APA 4ort.xyz Knowledge Graph. (2026). leukotriene c4. Retrieved May 3, 2026, from https://4ort.xyz/entity/leukotriene-c4
MLA “leukotriene c4.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/leukotriene-c4.
BibTeX @misc{4ortxyz_leukotriene-c4_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{leukotriene c4}}, year = {2026}, url = {https://4ort.xyz/entity/leukotriene-c4}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): leukotriene c4 — https://4ort.xyz/entity/leukotriene-c4 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/leukotriene-c4 · Last refreshed:

Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 5w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of → (5S,6R)-6-{[(2R)-2-{[(4S)-4-amino-4-carboxy-1-hydroxybutylidene]amino}-2-(carboxymethyl-C-hydroxycarbonimidoyl)ethyl]sulfanyl}-5-hydroxyicosa-7,9,11,14-tetraenoic acid, 11-trans-Leukotriene C4
    Instance of → type of chemical entity
    Subclass of → —
    Aliases → —
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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