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 ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (21 views/month).[2]

Key Facts

  • indole-3-carbinol's instance of is recorded as type of chemical entity[3].
  • indole-3-carbinol's chemical structure is recorded as Indol-3-carbinol.svg[4].
  • indole-3-carbinol's CAS Registry Number is recorded as 700-06-1[5].
  • indole-3-carbinol's EC number is recorded as 211-836-2[6].
  • indole-3-carbinol's canonical SMILES is recorded as C1=CC=C2C(=C1)C(=CN2)CO[7].
  • indole-3-carbinol's InChI is recorded as InChI=1S/C9H9NO/c11-6-7-5-10-9-4-2-1-3-8(7)9/h1-5,10-11H,6H2[8].
  • indole-3-carbinol's InChIKey is recorded as IVYPNXXAYMYVSP-UHFFFAOYSA-N[9].
  • indole-3-carbinol's chemical formula is recorded as C₉H₉NO[10].
  • indole-3-carbinol's subclass of is recorded as indole alkaloid[11].
  • indole-3-carbinol's part of is recorded as response to indole-3-methanol[12].
  • indole-3-carbinol's part of is recorded as cellular response to indole-3-methanol[13].
  • indole-3-carbinol's Commons category is recorded as Indole-3-carbinol[14].
  • indole-3-carbinol's MeSH descriptor ID is recorded as C016517[15].
  • indole-3-carbinol's ChEMBL ID is recorded as CHEMBL155625[16].
  • indole-3-carbinol's Guide to Pharmacology Ligand ID is recorded as 10047[17].
  • indole-3-carbinol's Freebase ID is recorded as /m/0dpyhn[18].
  • indole-3-carbinol's UNII is recorded as C11E72455F[19].
  • indole-3-carbinol's RTECS number is recorded as NL9483000[20].
  • indole-3-carbinol's ChemSpider ID is recorded as 3581[21].
  • indole-3-carbinol's PubChem CID is recorded as 3712[22].
  • indole-3-carbinol's ChEBI ID is recorded as 24814[23].
  • indole-3-carbinol's found in taxon is recorded as Pinus sylvestris[24].
  • indole-3-carbinol's found in taxon is recorded as Brassicaceae[25].
  • indole-3-carbinol's found in taxon is recorded as Haliclona oculata[26].
  • indole-3-carbinol's found in taxon is recorded as Brassica oleracea[27].

Why It Matters

indole-3-carbinol ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (21 views/month).[2] indole-3-carbinol has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[28] indole-3-carbinol is known by 6 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . Gene Ontology release 2019-11-16. wikidata.org.
  11. [13] . Gene Ontology release 2019-11-16. wikidata.org.
  12. [14] . wikidata.org.
  13. [15] . Medical Subject Headings. Retrieved . wikidata.org.
  14. [16] . ChEMBL. Retrieved . wikidata.org.
  15. [17] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  16. [18] . Freebase Data Dumps. wikidata.org.
  17. [19] . Global Substance Registration System. Retrieved . wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . Q2311683. Retrieved . wikidata.org.
  20. [22] . PubChem. Retrieved . wikidata.org.
  21. [23] . ChEMBL. Retrieved . wikidata.org.
  22. [24] . Identification and Quantification of Indole-3-methanol in Etiolated Seedlings of Scots Pine (Pinus sylvestris L.).. wikidata.org.
  23. [25] . Indole-3-carbinol inhibits LPS-induced inflammatory response by blocking TRIF-dependent signaling pathway in macrophages. wikidata.org.
  24. [26] . Oculatol, oculatolide, and A-nor sterols from the sponge Haliclona oculata. wikidata.org.
  25. [27] . High-performance liquid chromatographic analysis of anticarcinogenic indoles in Brassica oleracea. wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . 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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