cabergoline

chemical compound
ChemicalSubstance type_of_chemical_entity Q423308
Press Enter · cited answer in seconds

cabergoline

Summary

cabergoline is a type of chemical entity[1]. cabergoline ranks in the top 4% of type_of_chemical_entity entities by monthly Wikipedia readership (289 views/month).[2]

Key Facts

  • cabergoline's instance of is recorded as type of chemical entity[3].
  • cabergoline's chemical structure is recorded as Cabergoline.svg[4].
  • cabergoline's chemical structure is recorded as Cabergolin.svg[5].
  • cabergoline's physically interacts with is recorded as 5-hydroxytryptamine receptor 1A[6].
  • cabergoline's physically interacts with is recorded as 5-hydroxytryptamine receptor 1B[7].
  • cabergoline's physically interacts with is recorded as 5-hydroxytryptamine receptor 1D[8].
  • cabergoline's physically interacts with is recorded as 5-hydroxytryptamine receptor 2A[9].
  • cabergoline's physically interacts with is recorded as 5-hydroxytryptamine receptor 2B[10].
  • cabergoline's physically interacts with is recorded as 5-hydroxytryptamine receptor 2C[11].
  • cabergoline's physically interacts with is recorded as Adrenoceptor alpha 1A[12].
  • cabergoline's physically interacts with is recorded as Adrenoceptor alpha 2A[13].
  • cabergoline's physically interacts with is recorded as Adrenoceptor alpha 2B[14].
  • cabergoline's physically interacts with is recorded as Adrenoceptor alpha 2C[15].
  • cabergoline's physically interacts with is recorded as Dopamine receptor D1[16].
  • cabergoline's physically interacts with is recorded as Dopamine receptor D2[17].
  • cabergoline's physically interacts with is recorded as Dopamine receptor D3[18].
  • cabergoline's physically interacts with is recorded as Dopamine receptor D4[19].
  • cabergoline's physically interacts with is recorded as Dopamine receptor D5[20].
  • cabergoline's CAS Registry Number is recorded as 81409-90-7[21].
  • cabergoline's EC number is recorded as 627-031-8[22].
  • cabergoline's canonical SMILES is recorded as CCNC(=O)N(CCCN(C)C)C(=O)C1CC2C(CC3=CNC4=CC=CC2=C34)N(C1)CC=C[23].
  • cabergoline's InChI is recorded as InChI=1S/C26H37N5O2/c1-5-11-30-17-19(25(32)31(26(33)27-6-2)13-8-12-29(3)4)14-21-20-9-7-10-22-24(20)18(16-28-22)15-23(21)30/h5,7,9-10,16,19,21,23,28H,1,6,8,11-15,17H2,2-4H3,(H,27,33)/t19-,21-,23-/m1/s1[24].
  • cabergoline's InChIKey is recorded as KORNTPPJEAJQIU-KJXAQDMKSA-N[25].
  • cabergoline's ATC code is recorded as N04BC06[26].
  • cabergoline's ATC code is recorded as G02CB03[27].

Why It Matters

cabergoline ranks in the top 4% of type_of_chemical_entity entities by monthly Wikipedia readership (289 views/month).[2] cabergoline has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[28] cabergoline is known by 20 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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  5. [7] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  6. [8] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  7. [9] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  8. [10] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  9. [11] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  10. [12] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  11. [13] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  12. [14] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  13. [15] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  14. [16] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  15. [17] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  16. [18] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  17. [19] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  18. [20] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  19. [21] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  20. [22] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . PubChem. Retrieved . wikidata.org.
  23. [25] . PubChem. Retrieved . wikidata.org.
  24. [26] . DrugBank. wikidata.org.
  25. [27] . DrugBank. 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). cabergoline. Retrieved May 3, 2026, from https://4ort.xyz/entity/cabergoline
MLA “cabergoline.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cabergoline.
BibTeX @misc{4ortxyz_cabergoline_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cabergoline}}, year = {2026}, url = {https://4ort.xyz/entity/cabergoline}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): cabergoline — https://4ort.xyz/entity/cabergoline (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/cabergoline · Last refreshed: