lisuride

chemical compound
ChemicalSubstance type_of_chemical_entity Q424446
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lisuride

Summary

lisuride is a type of chemical entity[1]. lisuride ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (86 views/month).[2]

Key Facts

  • lisuride's instance of is recorded as type of chemical entity[3].
  • lisuride's chemical structure is recorded as Lisuride.png[4].
  • lisuride's physically interacts with is recorded as 5-hydroxytryptamine receptor 1A[5].
  • lisuride's physically interacts with is recorded as 5-hydroxytryptamine receptor 1B[6].
  • lisuride's physically interacts with is recorded as 5-hydroxytryptamine receptor 1D[7].
  • lisuride's physically interacts with is recorded as 5-hydroxytryptamine receptor 2A[8].
  • lisuride's physically interacts with is recorded as 5-hydroxytryptamine receptor 2B[9].
  • lisuride's physically interacts with is recorded as 5-hydroxytryptamine receptor 2C[10].
  • lisuride's physically interacts with is recorded as 5-hydroxytryptamine receptor 6[11].
  • lisuride's physically interacts with is recorded as Adrenoceptor alpha 1A[12].
  • lisuride's physically interacts with is recorded as Adrenoceptor alpha 2A[13].
  • lisuride's physically interacts with is recorded as Adrenoceptor alpha 2B[14].
  • lisuride's physically interacts with is recorded as Adrenoceptor alpha 2C[15].
  • lisuride's physically interacts with is recorded as Dopamine receptor D1[16].
  • lisuride's physically interacts with is recorded as Dopamine receptor D2[17].
  • lisuride's physically interacts with is recorded as Dopamine receptor D3[18].
  • lisuride's physically interacts with is recorded as Dopamine receptor D4[19].
  • lisuride's physically interacts with is recorded as Dopamine receptor D5[20].
  • lisuride's CAS Registry Number is recorded as 18016-80-3[21].
  • lisuride's EC number is recorded as 241-925-1[22].
  • lisuride's canonical SMILES is recorded as CCN(CC)C(=O)NC1CN(C2CC3=CNC4=CC=CC(=C34)C2=C1)C[23].
  • lisuride's InChI is recorded as InChI=1S/C20H26N4O/c1-4-24(5-2)20(25)22-14-10-16-15-7-6-8-17-19(15)13(11-21-17)9-18(16)23(3)12-14/h6-8,10-11,14,18,21H,4-5,9,12H2,1-3H3,(H,22,25)/t14-,18+/m0/s1[24].
  • lisuride's InChIKey is recorded as BKRGVLQUQGGVSM-KBXCAEBGSA-N[25].
  • lisuride's ATC code is recorded as N02CA07[26].
  • lisuride's ATC code is recorded as G02CB02[27].

Why It Matters

lisuride ranks in the top 5% of type_of_chemical_entity entities by monthly Wikipedia readership (86 views/month).[2] lisuride has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[28] lisuride is known by 11 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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  19. [21] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  20. [22] . Global Substance Registration System. 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). lisuride. Retrieved May 3, 2026, from https://4ort.xyz/entity/lisuride
MLA “lisuride.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/lisuride.
BibTeX @misc{4ortxyz_lisuride_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{lisuride}}, year = {2026}, url = {https://4ort.xyz/entity/lisuride}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): lisuride — https://4ort.xyz/entity/lisuride (retrieved 2026-05-03)

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