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festuclavine

chemical compound
ChemicalSubstance type_of_chemical_entity Q15113508
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festuclavine

Summary

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

Key Facts

  • festuclavine's instance of is recorded as type of chemical entity[3].
  • festuclavine's chemical structure is recorded as Festuclavine.svg[4].
  • festuclavine's CAS Registry Number is recorded as 569-26-6[5].
  • festuclavine's canonical SMILES is recorded as CC1CC2C(CC3=CNC4=CC=CC2=C34)N(C1)C[6].
  • festuclavine's InChI is recorded as InChI=1S/C16H20N2/c1-10-6-13-12-4-3-5-14-16(12)11(8-17-14)7-15(13)18(2)9-10/h3-5,8,10,13,15,17H,6-7,9H2,1-2H3/t10-,13-,15-/m1/s1[7].
  • festuclavine's InChIKey is recorded as VLMZMRDOMOGGFA-WDBKCZKBSA-N[8].
  • festuclavine's chemical formula is recorded as C₁₆H₂₀N₂[9].
  • festuclavine's subclass of is recorded as ergoline alkaloid[10].
  • festuclavine's Commons category is recorded as Festuclavine[11].
  • festuclavine's ChEMBL ID is recorded as CHEMBL13866[12].
  • festuclavine's Freebase ID is recorded as /m/0wy3829[13].
  • festuclavine's UNII is recorded as 88ZK48D2QG[14].
  • festuclavine's ChemSpider ID is recorded as 294963[15].
  • festuclavine's PubChem CID is recorded as 332915[16].
  • festuclavine's ChEBI ID is recorded as 65035[17].
  • festuclavine's found in taxon is recorded as Epichloe typhina[18].
  • festuclavine's found in taxon is recorded as Aspergillus japonicus[19].
  • festuclavine's found in taxon is recorded as Aspergillus fumigatus[20].
  • festuclavine's Reaxys registry number is recorded as 87764[21].
  • festuclavine's isomeric SMILES is recorded as C[C@@H]1C[C@H]2C@@HN(C1)CC@@HN(C1)C">[22].
  • festuclavine's mass is recorded as {'unit': 'Q483261', 'amount': '+240.163'}[23].
  • festuclavine's NSC number is recorded as 332446[24].
  • festuclavine's SureChEMBL ID is recorded as 4506789[25].
  • festuclavine's DSSTox substance ID is recorded as DTXSID00205432[26].
  • festuclavine's stereoisomer of is recorded as costaclavin[27].

Why It Matters

festuclavine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (2 views/month).[2] festuclavine is known by 4 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] ↑ . wikidata.org.
  3. [5] ↑ . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: 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] ↑ . wikidata.org.
  10. [12] ↑ . ChEMBL. Retrieved . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . Q2311683. Retrieved . wikidata.org.
  14. [16] ↑ . PubChem. Retrieved . wikidata.org.
  15. [17] ↑ . ChEBI. Retrieved . wikidata.org.
  16. [18] ↑ . Ergot alkaloid identification in clavicipitaceae systemic fungi of pasture grasses. wikidata.org.
  17. [19] ↑ . Isolation of cycloclavine from the culture broth of Aspergillus japonicus SAITO.. wikidata.org.
  18. [20] ↑ . 398. The isolation of festuclavine and two new clavine alkaloids from Aspergillus fumigatus Fres. wikidata.org.
  19. [21] ↑ . ChEBI. Retrieved . wikidata.org.
  20. [22] ↑ . PubChem. Retrieved . wikidata.org.
  21. [23] ↑ . PubChem. Retrieved . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard. 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). festuclavine. Retrieved May 3, 2026, from https://4ort.xyz/entity/festuclavine
MLA “festuclavine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/festuclavine.
BibTeX @misc{4ortxyz_festuclavine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{festuclavine}}, year = {2026}, url = {https://4ort.xyz/entity/festuclavine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): festuclavine — https://4ort.xyz/entity/festuclavine (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. 27d ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Stereoisomer of → costaclavin, Ergoline, 6,8-dimethyl-, (8alpha)-
    Instance of → type of chemical entity
    Subclass of → ergoline alkaloid
    Aliases → —
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.