indole-3-carbinol

chemical compound
ChemicalSubstance type_of_chemical_entity Q1770257
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indole-3-carbinol

Summary

indole-3-carbinol is a type of chemical entity[1]. indole-3-carbinol has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • indole-3-carbinol's instance of is recorded as type of chemical entity[3].
  • indole-3-carbinol's canonical SMILES is recorded as C1=CC=C2C(=C1)C(=CN2)CO[4].
  • indole-3-carbinol's chemical formula is recorded as C₉H₉NO[5].
  • indole-3-carbinol is a type of indole alkaloid[6].
  • indole-3-carbinol is part of response to indole-3-methanol[7].
  • indole-3-carbinol is part of cellular response to indole-3-methanol[8].
  • indole-3-carbinol's Commons category is recorded as Indole-3-carbinol[9].
  • indole-3-carbinol's found in taxon is recorded as Pinus sylvestris[10].
  • indole-3-carbinol's found in taxon is recorded as Brassicaceae[11].
  • indole-3-carbinol's found in taxon is recorded as Haliclona oculata[12].
  • indole-3-carbinol's found in taxon is recorded as Brassica oleracea[13].
  • indole-3-carbinol's found in taxon is recorded as Dalbergia[14].
  • indole-3-carbinol's found in taxon is recorded as Leptosphaeria maculans[15].
  • indole-3-carbinol's found in taxon is recorded as Brassica[16].
  • indole-3-carbinol's found in taxon is recorded as Raphanus sativus[17].
  • indole-3-carbinol's found in taxon is recorded as Picea abies[18].
  • indole-3-carbinol's mass is recorded as {'unit': 'Q483261', 'amount': '+147.068'}[19].
  • indole-3-carbinol's melting point is recorded as {'unit': 'Q25267', 'amount': '+98.0'}[20].
  • indole-3-carbinol's subject has role is recorded as anticarcinogens[21].
  • indole-3-carbinol's safety classification and labelling is recorded as NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response[22].

Why It Matters

indole-3-carbinol has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[2] indole-3-carbinol is known by 6 alternative names across languages and contexts.[23]

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] . Gene Ontology release 2019-11-16. wikidata.org.
  6. [8] . Gene Ontology release 2019-11-16. wikidata.org.
  7. [9] . wikidata.org.
  8. [10] . Identification and Quantification of Indole-3-methanol in Etiolated Seedlings of Scots Pine (Pinus sylvestris L.).. wikidata.org.
  9. [11] . Indole-3-carbinol inhibits LPS-induced inflammatory response by blocking TRIF-dependent signaling pathway in macrophages. wikidata.org.
  10. [12] . Oculatol, oculatolide, and A-nor sterols from the sponge Haliclona oculata. wikidata.org.
  11. [13] . High-performance liquid chromatographic analysis of anticarcinogenic indoles in Brassica oleracea. wikidata.org.
  12. [14] . Detection of abscisic acid, indole-3-acetic acid and indole-3-ethanol in seeds of Dalbergia dolichopetala. wikidata.org.
  13. [15] . The cruciferous phytoalexins rapalexin A, brussalexin A and erucalexin: Chemistry and metabolism in Leptosphaeria maculans. wikidata.org.
  14. [16] . N-Alkoxy derivatization of indole-3-carbinol increases the efficacy of the G1 cell cycle arrest and of I3C-specific regulation of cell cycle gene transcription and activity in human breast cancer cells. wikidata.org.
  15. [17] . Deciphering the Nutraceutical Potential of -A Comprehensive Overview. wikidata.org.
  16. [18] . Dynamics of indole-3-acetic acid during germination of Picea abies seeds. wikidata.org.
  17. [19] . PubChem. Retrieved . wikidata.org.
  18. [20] . Jean-Claude Bradley Open Melting Point Dataset. wikidata.org.
  19. [21] . Medical Subject Headings. Retrieved . wikidata.org.
  20. [22] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.org.
  2. [23] . 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). indole-3-carbinol. Retrieved May 3, 2026, from https://4ort.xyz/entity/indole-3-carbinol
MLA “indole-3-carbinol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/indole-3-carbinol.
BibTeX @misc{4ortxyz_indole-3-carbinol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{indole-3-carbinol}}, year = {2026}, url = {https://4ort.xyz/entity/indole-3-carbinol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): indole-3-carbinol — https://4ort.xyz/entity/indole-3-carbinol (retrieved 2026-05-03)

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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. 23d ago · FlocciNivis · 2026-06-25 view diff on Wikidata ↗
    Pdb ligand id FXK
    "/* wbcreateclaim-create:1| */ [[Property:P3636]]: FXK, [[:toollabs:quickstatements/#/batch/259826|batch #259826]]"
  2. 4w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Described at url
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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