ergine

chemical compound
ChemicalSubstance type_of_chemical_entity Q2041643
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ergine

Summary

ergine is a type of chemical entity[1]. ergine ranks in the top 4% of type_of_chemical_entity entities by monthly Wikipedia readership (302 views/month).[2]

Key Facts

  • ergine's instance of is recorded as type of chemical entity[3].
  • ergine's chemical structure is recorded as Struktur Ergin.svg[4].
  • ergine's chemical structure is recorded as Ergine.png[5].
  • ergine's CAS Registry Number is recorded as 478-94-4[6].
  • ergine's EC number is recorded as 207-524-0[7].
  • ergine's canonical SMILES is recorded as CN1CC(C=C2C1CC3=CNC4=CC=CC2=C34)C(=O)N[8].
  • ergine's InChI is recorded as InChI=1S/C16H17N3O/c1-19-8-10(16(17)20)5-12-11-3-2-4-13-15(11)9(7-18-13)6-14(12)19/h2-5,7,10,14,18H,6,8H2,1H3,(H2,17,20)/t10-,14-/m1/s1[9].
  • ergine's InChIKey is recorded as GENAHGKEFJLNJB-QMTHXVAHSA-N[10].
  • ergine's chemical formula is recorded as C₁₆H₁₇N₃O[11].
  • ergine's subclass of is recorded as ergoline alkaloid[12].
  • ergine's Commons category is recorded as Ergines[13].
  • ergine's ChEMBL ID is recorded as CHEMBL227213[14].
  • ergine's Freebase ID is recorded as /m/020t10[15].
  • ergine's UNII is recorded as 073830XH10[16].
  • ergine's ChemSpider ID is recorded as 390611[17].
  • ergine's PubChem CID is recorded as 442072[18].
  • ergine's KEGG ID is recorded as C09160[19].
  • ergine's ChEBI ID is recorded as 4819[20].
  • ergine's found in taxon is recorded as Ipomoea asarifolia[21].
  • ergine's found in taxon is recorded as Ipomoea corymbosa[22].
  • ergine's found in taxon is recorded as Turbina corymbosa[23].
  • ergine's found in taxon is recorded as Acremonium[24].
  • ergine's found in taxon is recorded as Argyreia nervosa[25].
  • ergine's found in taxon is recorded as Claviceps fusiformis[26].
  • ergine's found in taxon is recorded as Claviceps purpurea[27].

Why It Matters

ergine ranks in the top 4% of type_of_chemical_entity entities by monthly Wikipedia readership (302 views/month).[2] ergine has Wikipedia articles in 17 language editions, a strong signal of global cultural recognition.[28] ergine is known by 5 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] . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] . 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] . Freebase Data Dumps. wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . Q2311683. Retrieved . wikidata.org.
  16. [18] . PubChem. Retrieved . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . ChEMBL. Retrieved . wikidata.org.
  19. [21] . Resin glycosides from Ipomoea pes-caprae. wikidata.org.
  20. [22] . Resin glycosides from Ipomoea pes-caprae. wikidata.org.
  21. [23] . Resin glycosides from Ipomoea pes-caprae. wikidata.org.
  22. [24] . High Levels of Ergonovine and Lysergic Acid Amide in ToxicAchnatherum inebriansAccompany Infection by anAcremonium-like Endophytic Fungus. wikidata.org.
  23. [25] . Isolation and Identification of Lysergic Acid Amide and Isolysergic Acid Amide as the Principal Ergoline Alkaloids in Argyreia nervosa, a Tropical Wood Rose. wikidata.org.
  24. [26] . Microbiological C-17-Oxidation of Clavine Alkaloids, I. Substrate Specificity of Agroclavine Hydroxylase of Claviceps fusiformis. wikidata.org.
  25. [27] . Role of the δ 8 double bond of agroclavine in lysergic acid amide biosynthesis byClaviceps purpurea. 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). ergine. Retrieved May 3, 2026, from https://4ort.xyz/entity/ergine
MLA “ergine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/ergine.
BibTeX @misc{4ortxyz_ergine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{ergine}}, year = {2026}, url = {https://4ort.xyz/entity/ergine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): ergine — https://4ort.xyz/entity/ergine (retrieved 2026-05-03)

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