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α-ergocryptine

chemical compound
ChemicalSubstance type_of_chemical_entity Q5385811
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α-ergocryptine

Summary

α-ergocryptine is a type of chemical entity[1]. α-ergocryptine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (9 views/month).[2]

Key Facts

  • α-ergocryptine's instance of is recorded as type of chemical entity[3].
  • α-ergocryptine's chemical structure is recorded as Ergocryptine.svg[4].
  • α-ergocryptine's CAS Registry Number is recorded as 511-09-1[5].
  • α-ergocryptine's EC number is recorded as 208-121-2[6].
  • α-ergocryptine's canonical SMILES is recorded as CC(C)CC1C(=O)N2CCCC2C3(N1C(=O)C(O3)(C(C)C)NC(=O)C4CN(C5CC6=CNC7=CC=CC(=C67)C5=C4)C)O[7].
  • α-ergocryptine's InChI is recorded as InChI=1S/C32H41N5O5/c1-17(2)12-25-29(39)36-11-7-10-26(36)32(41)37(25)30(40)31(42-32,18(3)4)34-28(38)20-13-22-21-8-6-9-23-27(21)19(15-33-23)14-24(22)35(5)16-20/h6,8-9,13,15,17-18,20,24-26,33,41H,7,10-12,14,16H2,1-5H3,(H,34,38)/t20-,24-,25+,26+,31-,32+/m1/s1[8].
  • α-ergocryptine's InChIKey is recorded as YDOTUXAWKBPQJW-NSLWYYNWSA-N[9].
  • α-ergocryptine's chemical formula is recorded as C₃₂H₄₁N₅O₅[10].
  • α-ergocryptine's subclass of is recorded as (4R,7R)-N-[(1S)-2-hydroxy-4-isopropyl-7-(2-methylpropyl)-5,8-dioxo-3-oxa-6,9-diazatricyclo[7.3.0.0²,⁶]dodecan-4-yl]-6-methyl-6,11-diazatetracyclo[7.6.1.0²,⁷.0¹²,¹⁶]hexadeca-1(16),2,9,12,14-pentaene-4-carboximidic acid[11].
  • α-ergocryptine's Commons category is recorded as Ergocryptine[12].
  • α-ergocryptine's MeSH descriptor ID is recorded as C100269[13].
  • α-ergocryptine's ChEMBL ID is recorded as CHEMBL1403281[14].
  • α-ergocryptine's Guide to Pharmacology Ligand ID is recorded as 271[15].
  • α-ergocryptine's Freebase ID is recorded as /m/05760ms[16].
  • α-ergocryptine's UNII is recorded as 6WFB60157B[17].
  • α-ergocryptine's ChemSpider ID is recorded as 118591[18].
  • α-ergocryptine's PubChem CID is recorded as 134551[19].
  • α-ergocryptine's KEGG ID is recorded as C07545[20].
  • α-ergocryptine's ChEBI ID is recorded as 10276[21].
  • α-ergocryptine's found in taxon is recorded as Claviceps purpurea[22].
  • α-ergocryptine's found in taxon is recorded as Claviceps grohii[23].
  • α-ergocryptine's found in taxon is recorded as Festuca arundinacea[24].
  • α-ergocryptine's found in taxon is recorded as Claviceps zizaniae[25].
  • α-ergocryptine's found in taxon is recorded as Festuca rubra[26].
  • α-ergocryptine's Reaxys registry number is recorded as 78810[27].

Why It Matters

α-ergocryptine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (9 views/month).[2]

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] ↑ . 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] ↑ . wikidata.org.
  11. [13] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  12. [14] ↑ . ChEMBL. Retrieved . wikidata.org.
  13. [15] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] ↑ . Q2311683. Retrieved . wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . ChEBI. Retrieved . wikidata.org.
  19. [21] ↑ . ChEBI. Retrieved . wikidata.org.
  20. [22] ↑ . Isolation of ergovaline, ergoptine, and ergonine, new alkaloids of the peptide type, from ergot sclerotia. wikidata.org.
  21. [23] ↑ . Claviceps nigricans and Claviceps grohii: their alkaloids and phylogenetic placement. wikidata.org.
  22. [24] ↑ . Detection of ergopeptine alkaloids in endophyte-infected, toxic Ky-31 tall fescue by mass spectrometry/mass spectrometry. wikidata.org.
  23. [25] ↑ . Ergot alkaloids produced by submerged cultures of Claviceps zizaniae.. wikidata.org.
  24. [26] ↑ . Detection of ergopeptine alkaloids in endophyte-infected, toxic Ky-31 tall fescue by mass spectrometry/mass spectrometry. wikidata.org.
  25. [27] ↑ . ChEBI. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.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). α-ergocryptine. Retrieved May 3, 2026, from https://4ort.xyz/entity/ergocryptine
MLA “α-ergocryptine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/ergocryptine.
BibTeX @misc{4ortxyz_ergocryptine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{α-ergocryptine}}, year = {2026}, url = {https://4ort.xyz/entity/ergocryptine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): α-ergocryptine — https://4ort.xyz/entity/ergocryptine (retrieved 2026-05-03)

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