bromocriptine

medication which has significant effects on dopamine levels in the brain
ChemicalSubstance type_of_chemical_entity Q413581
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bromocriptine

Summary

bromocriptine is a type of chemical entity[1]. bromocriptine ranks in the top 4% of type_of_chemical_entity entities by monthly Wikipedia readership (227 views/month).[2]

Key Facts

  • bromocriptine's instance of is recorded as type of chemical entity[3].
  • bromocriptine's chemical structure is recorded as Bromocriptine.svg[4].
  • bromocriptine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1A[5].
  • bromocriptine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1B[6].
  • bromocriptine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1D[7].
  • bromocriptine's physically interacts with is recorded as 5-hydroxytryptamine receptor 2A[8].
  • bromocriptine's physically interacts with is recorded as 5-hydroxytryptamine receptor 2B[9].
  • bromocriptine's physically interacts with is recorded as 5-hydroxytryptamine receptor 2C[10].
  • bromocriptine's physically interacts with is recorded as 5-hydroxytryptamine receptor 6[11].
  • bromocriptine's physically interacts with is recorded as Adrenoceptor alpha 2A[12].
  • bromocriptine's physically interacts with is recorded as Adrenoceptor alpha 2B[13].
  • bromocriptine's physically interacts with is recorded as Adrenoceptor alpha 2C[14].
  • bromocriptine's physically interacts with is recorded as Dopamine receptor D1[15].
  • bromocriptine's physically interacts with is recorded as Dopamine receptor D2[16].
  • bromocriptine's physically interacts with is recorded as Dopamine receptor D3[17].
  • bromocriptine's physically interacts with is recorded as Dopamine receptor D4[18].
  • bromocriptine's physically interacts with is recorded as Dopamine receptor D5[19].
  • bromocriptine's CAS Registry Number is recorded as 25614-03-3[20].
  • bromocriptine's EC number is recorded as 247-128-5[21].
  • bromocriptine's canonical SMILES is recorded as CC(C)CC1C(=O)N2CCCC2C3(N1C(=O)C(O3)(C(C)C)NC(=O)C4CN(C5CC6=C(NC7=CC=CC(=C67)C5=C4)Br)C)O[22].
  • bromocriptine's InChI is recorded as InChI=1S/C32H40BrN5O5/c1-16(2)12-24-29(40)37-11-7-10-25(37)32(42)38(24)30(41)31(43-32,17(3)4)35-28(39)18-13-20-19-8-6-9-22-26(19)21(27(33)34-22)14-23(20)36(5)15-18/h6,8-9,13,16-18,23-25,34,42H,7,10-12,14-15H2,1-5H3,(H,35,39)/t18-,23-,24+,25+,31-,32+/m1/s1[23].
  • bromocriptine's InChIKey is recorded as OZVBMTJYIDMWIL-AYFBDAFISA-N[24].
  • bromocriptine's ATC code is recorded as N04BC01[25].
  • bromocriptine's ATC code is recorded as G02CB01[26].
  • bromocriptine's chemical formula is recorded as C₃₂H₄₀BrN₅O₅[27].

Why It Matters

bromocriptine ranks in the top 4% of type_of_chemical_entity entities by monthly Wikipedia readership (227 views/month).[2] bromocriptine has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[28] bromocriptine is known by 36 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] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . 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] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  19. [21] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  20. [22] ↑ . PubChem. Retrieved . wikidata.org.
  21. [23] ↑ . PubChem. Retrieved . wikidata.org.
  22. [24] ↑ . PubChem. Retrieved . wikidata.org.
  23. [25] ↑ . DrugBank. wikidata.org.
  24. [26] ↑ . DrugBank. wikidata.org.
  25. [27] ↑ . PubChem. Retrieved . 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). bromocriptine. Retrieved October 1, 2026, from https://4ort.xyz/entity/bromocriptine
MLA “bromocriptine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 1 Oct. 2026, https://4ort.xyz/entity/bromocriptine.
BibTeX @misc{4ortxyz_bromocriptine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{bromocriptine}}, year = {2026}, url = {https://4ort.xyz/entity/bromocriptine}, note = {Accessed: 2026-10-01}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): bromocriptine — https://4ort.xyz/entity/bromocriptine (retrieved 2026-10-01)

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