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3,3'-diindolylmethane

chemical compound
ChemicalSubstance type_of_chemical_entity Q4634053
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3,3'-diindolylmethane

Summary

3,3'-diindolylmethane is a type of chemical entity[1]. 3,3'-diindolylmethane ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (102 views/month).[2]

Key Facts

  • 3,3'-diindolylmethane's instance of is recorded as type of chemical entity[3].
  • 3,3'-diindolylmethane's CAS Registry Number is recorded as 1968-05-4[4].
  • 3,3'-diindolylmethane's EC number is recorded as 606-355-3[5].
  • 3,3'-diindolylmethane's canonical SMILES is recorded as C1=CC=C2C(=C1)C(=CN2)CC3=CNC4=CC=CC=C43[6].
  • 3,3'-diindolylmethane's InChI is recorded as InChI=1S/C17H14N2/c1-3-7-16-14(5-1)12(10-18-16)9-13-11-19-17-8-4-2-6-15(13)17/h1-8,10-11,18-19H,9H2[7].
  • 3,3'-diindolylmethane's InChIKey is recorded as VFTRKSBEFQDZKX-UHFFFAOYSA-N[8].
  • 3,3'-diindolylmethane's chemical formula is recorded as C₁₇H₁₄N₂[9].
  • 3,3'-diindolylmethane's subclass of is recorded as indole alkaloid[10].
  • 3,3'-diindolylmethane's MeSH descriptor ID is recorded as C016392[11].
  • 3,3'-diindolylmethane's ChEMBL ID is recorded as CHEMBL446452[12].
  • 3,3'-diindolylmethane's Guide to Pharmacology Ligand ID is recorded as 11208[13].
  • 3,3'-diindolylmethane's Freebase ID is recorded as /m/052m55[14].
  • 3,3'-diindolylmethane's UNII is recorded as SSZ9HQT61Z[15].
  • 3,3'-diindolylmethane's ChemSpider ID is recorded as 2963[16].
  • 3,3'-diindolylmethane's PubChem CID is recorded as 3071[17].
  • 3,3'-diindolylmethane's ChEBI ID is recorded as 50182[18].
  • 3,3'-diindolylmethane's found in taxon is recorded as Arundina graminifolia[19].
  • 3,3'-diindolylmethane's found in taxon is recorded as Arundo donax[20].
  • 3,3'-diindolylmethane's found in taxon is recorded as Brassica[21].
  • 3,3'-diindolylmethane's found in taxon is recorded as Vibrio parahaemolyticus[22].
  • 3,3'-diindolylmethane's found in taxon is recorded as Brassica oleracea[23].
  • 3,3'-diindolylmethane's found in taxon is recorded as Gastrodia elata[24].
  • 3,3'-diindolylmethane's DrugBank ID is recorded as DB11875[25].
  • 3,3'-diindolylmethane's Reaxys registry number is recorded as 223072[26].
  • 3,3'-diindolylmethane's Human Metabolome Database ID is recorded as HMDB0246001[27].

Why It Matters

3,3'-diindolylmethane ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (102 views/month).[2] 3,3'-diindolylmethane is known by 8 alternative names across languages and contexts.[28]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [5] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  10. [12] ↑ . ChEMBL. Retrieved . wikidata.org.
  11. [13] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  12. [14] ↑ . Freebase Data Dumps. wikidata.org.
  13. [15] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  14. [16] ↑ . Q2311683. Retrieved . wikidata.org.
  15. [17] ↑ . PubChem. Retrieved . wikidata.org.
  16. [18] ↑ . ChEMBL. Retrieved . wikidata.org.
  17. [19] ↑ . Two stilbenoids from the orchid arundina bambusifolia. wikidata.org.
  18. [20] ↑ . Alkaloids of Arundo donax L.. wikidata.org.
  19. [21] ↑ . Indole-3-carbinol inhibits 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone plus benzo(a)pyrene-induced lung tumorigenesis in A/J mice and modulates carcinogen-induced alterations in protein levels. wikidata.org.
  20. [22] ↑ . New indole alkaloids from the North Sea bacterium Vibrio parahaemolyticus Bio249.. wikidata.org.
  21. [23] ↑ . High-performance liquid chromatographic analysis of anticarcinogenic indoles in Brassica oleracea. wikidata.org.
  22. [24] ↑ . Two new compounds isolated from the aerial parts of gastrodia elata blume. wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . ChEBI. Retrieved . wikidata.org.
  25. [27] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] ↑ . 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). 3,3'-diindolylmethane. Retrieved May 3, 2026, from https://4ort.xyz/entity/3-3-diindolylmethane
MLA “3,3'-diindolylmethane.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/3-3-diindolylmethane.
BibTeX @misc{4ortxyz_3-3-diindolylmethane_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{3,3'-diindolylmethane}}, year = {2026}, url = {https://4ort.xyz/entity/3-3-diindolylmethane}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 3,3'-diindolylmethane — https://4ort.xyz/entity/3-3-diindolylmethane (retrieved 2026-05-03)

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