evodiamine

chemical compound
ChemicalSubstance type_of_chemical_entity Q27894193
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evodiamine

Summary

evodiamine is a type of chemical entity[1]. evodiamine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (23 views/month).[2]

Key Facts

  • evodiamine's instance of is recorded as type of chemical entity[3].
  • evodiamine's chemical structure is recorded as Evodiamine.svg[4].
  • evodiamine's chemical structure is recorded as Evodiamin.svg[5].
  • evodiamine's CAS Registry Number is recorded as 518-17-2[6].
  • evodiamine's EC number is recorded as 637-111-4[7].
  • evodiamine's canonical SMILES is recorded as CN1C2C3=C(CCN2C(=O)C4=CC=CC=C41)C5=CC=CC=C5N3[8].
  • evodiamine's InChI is recorded as InChI=1S/C19H17N3O/c1-21-16-9-5-3-7-14(16)19(23)22-11-10-13-12-6-2-4-8-15(12)20-17(13)18(21)22/h2-9,18,20H,10-11H2,1H3/t18-/m0/s1[9].
  • evodiamine's InChIKey is recorded as TXDUTHBFYKGSAH-SFHVURJKSA-N[10].
  • evodiamine's chemical formula is recorded as C₁₉H₁₇N₃O[11].
  • evodiamine's subclass of is recorded as quinazoline alkaloid[12].
  • evodiamine's Commons category is recorded as Evodiamine[13].
  • evodiamine's ChEMBL ID is recorded as CHEMBL463165[14].
  • evodiamine's Freebase ID is recorded as /m/0h7_fj[15].
  • evodiamine's UNII is recorded as C01825BVNL[16].
  • evodiamine's ChemSpider ID is recorded as 390624[17].
  • evodiamine's PubChem CID is recorded as 442088[18].
  • evodiamine's ChEBI ID is recorded as 4948[19].
  • evodiamine's found in taxon is recorded as Euodia rutaecarpa[20].
  • evodiamine's found in taxon is recorded as Spiranthera odoratissima[21].
  • evodiamine's found in taxon is recorded as Tetradium ruticarpum[22].
  • evodiamine's found in taxon is recorded as Zanthoxylum rhetsa[23].
  • evodiamine's found in taxon is recorded as Vepris tabouensis[24].
  • evodiamine's found in taxon is recorded as Euodia[25].
  • evodiamine's found in taxon is recorded as Evodia[26].
  • evodiamine's found in taxon is recorded as Phellodendron chinense[27].

Why It Matters

evodiamine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (23 views/month).[2] evodiamine has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] evodiamine is known by 7 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] . wikidata.org.
  4. [6] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . PubChem. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . ChEMBL. Retrieved . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . Global Substance Registration System. Retrieved . wikidata.org.
  15. [17] . Q2311683. Retrieved . wikidata.org.
  16. [18] . PubChem. Retrieved . wikidata.org.
  17. [19] . ChEMBL. Retrieved . wikidata.org.
  18. [20] . Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968. wikidata.org.
  19. [21] . Limonoids from Spiranthera odoratissima St. Hil. wikidata.org.
  20. [22] . On the Evaluation of the Preparation of Chinese Medicinal Prescriptions. VI. The Changes of the Alkaloid Contents by Processing of Evodia Fruit. wikidata.org.
  21. [23] . Indonesian Medicinal Plants. IV. On the Constituents of the Bark of Fagara rhetza (Rutaceae). (2). Lignan Glycosides and Two Apioglucosides.. wikidata.org.
  22. [24] . Minor alkaloids of Araliopsis tabouensis. wikidata.org.
  23. [25] . Anti-proliferative effects of evodiamine on human thyroid cancer cell line ARO.. wikidata.org.
  24. [26] . Anti-proliferative effects of evodiamine on human thyroid cancer cell line ARO.. wikidata.org.
  25. [27] . Identification and analysis of alkaloids in cortex Phellodendron amurense by high‐performance liquid chromatography with electrospray ionization mass spectrometry coupled with photodiode array detection. 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). evodiamine. Retrieved May 3, 2026, from https://4ort.xyz/entity/evodiamine
MLA “evodiamine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/evodiamine.
BibTeX @misc{4ortxyz_evodiamine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{evodiamine}}, year = {2026}, url = {https://4ort.xyz/entity/evodiamine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): evodiamine — https://4ort.xyz/entity/evodiamine (retrieved 2026-05-03)

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