lisuride

chemical compound
ChemicalSubstance type_of_chemical_entity Q424446
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lisuride

Summary

lisuride is a type of chemical entity[1]. lisuride has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • lisuride's instance of is recorded as type of chemical entity[3].
  • lisuride's physically interacts with is recorded as 5-hydroxytryptamine receptor 1A[4].
  • lisuride's physically interacts with is recorded as 5-hydroxytryptamine receptor 1B[5].
  • lisuride's physically interacts with is recorded as 5-hydroxytryptamine receptor 1D[6].
  • lisuride's physically interacts with is recorded as 5-hydroxytryptamine receptor 2A[7].
  • lisuride's physically interacts with is recorded as 5-hydroxytryptamine receptor 2B[8].
  • lisuride's physically interacts with is recorded as 5-hydroxytryptamine receptor 2C[9].
  • lisuride's physically interacts with is recorded as 5-hydroxytryptamine receptor 6[10].
  • lisuride's physically interacts with is recorded as Adrenoceptor alpha 1A[11].
  • lisuride's physically interacts with is recorded as Adrenoceptor alpha 2A[12].
  • lisuride's physically interacts with is recorded as Adrenoceptor alpha 2B[13].
  • lisuride's physically interacts with is recorded as Adrenoceptor alpha 2C[14].
  • lisuride's physically interacts with is recorded as Dopamine receptor D1[15].
  • lisuride's physically interacts with is recorded as Dopamine receptor D2[16].
  • lisuride's physically interacts with is recorded as Dopamine receptor D3[17].
  • lisuride's physically interacts with is recorded as Dopamine receptor D4[18].
  • lisuride's physically interacts with is recorded as Dopamine receptor D5[19].
  • lisuride's canonical SMILES is recorded as CCN(CC)C(=O)NC1CN(C2CC3=CNC4=CC=CC(=C34)C2=C1)C[20].
  • lisuride's chemical formula is recorded as C₂₀H₂₆N₄O[21].
  • lisuride is a type of chemical compound[22].
  • lisuride is used for medication[23].
  • lisuride's Commons category is recorded as Lisuride[24].
  • lisuride's isomeric SMILES is recorded as CCN(CC)C(=O)N[C@@H]1CN([C@@H]2CC3=CNC4=CC=CC(=C34)C2=C1)C[25].
  • lisuride's mass is recorded as {'unit': 'Q483261', 'amount': '+338.210661'}[26].
  • lisuride's World Health Organisation international non-proprietary name is recorded as {'lang': 'en', 'text': 'lisuride'}[27].

Why It Matters

lisuride has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[2] lisuride is known by 11 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] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . 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] . PubChem. Retrieved . wikidata.org.
  19. [21] . PubChem. Retrieved . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . PubChem. Retrieved . wikidata.org.
  24. [26] . PubChem. Retrieved . wikidata.org.
  25. [27] . ChEBI. Retrieved . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikidata sitelinks. wikidata.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). 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)

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

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. 16d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Defined daily dose {'unit': 'Q3241121', 'amount': '+0.6'}
    Stereoisomer of (-)-(5S,8R)-Lisuride, 3-[(6aR,9R)-7-methyl-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-yl]-1,1-diethylurea
    Instance of type of chemical entity
    Has use medication
    + 7 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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