laudanosine

chemical compound
ChemicalSubstance type_of_chemical_entity Q408074
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laudanosine

Summary

laudanosine is a type of chemical entity[1]. laudanosine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (22 views/month).[2]

Key Facts

  • laudanosine's instance of is recorded as type of chemical entity[3].
  • laudanosine's chemical structure is recorded as Laudanosine.svg[4].
  • laudanosine's CAS Registry Number is recorded as 2688-77-9[5].
  • laudanosine's EC number is recorded as 220-253-2[6].
  • laudanosine's canonical SMILES is recorded as CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)OC[7].
  • laudanosine's InChI is recorded as InChI=1S/C21H27NO4/c1-22-9-8-15-12-20(25-4)21(26-5)13-16(15)17(22)10-14-6-7-18(23-2)19(11-14)24-3/h6-7,11-13,17H,8-10H2,1-5H3/t17-/m0/s1[8].
  • laudanosine's InChIKey is recorded as KGPAYJZAMGEDIQ-KRWDZBQOSA-N[9].
  • laudanosine's chemical formula is recorded as C₂₁H₂₇NO₄[10].
  • laudanosine's subclass of is recorded as isoquinoline alkaloid[11].
  • laudanosine's Commons category is recorded as Laudanosine[12].
  • laudanosine's MeSH descriptor ID is recorded as C001522[13].
  • laudanosine's ChEMBL ID is recorded as CHEMBL519894[14].
  • laudanosine's Freebase ID is recorded as /m/03g_k_5[15].
  • laudanosine's UNII is recorded as DA7R5WVN48[16].
  • laudanosine's ChemSpider ID is recorded as 66114[17].
  • laudanosine's PubChem CID is recorded as 73397[18].
  • laudanosine's KEGG ID is recorded as C09558[19].
  • laudanosine's ChEBI ID is recorded as 6389[20].
  • laudanosine's found in taxon is recorded as Hubera cerasoides[21].
  • laudanosine's found in taxon is recorded as Berberis heteropoda[22].
  • laudanosine's found in taxon is recorded as Berberis nummularia[23].
  • laudanosine's found in taxon is recorded as Cissampelos pareira[24].
  • laudanosine's found in taxon is recorded as Guatteria amplifolia[25].
  • laudanosine's found in taxon is recorded as Papaver macrostomum[26].
  • laudanosine's found in taxon is recorded as Papaver setigerum[27].

Why It Matters

laudanosine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (22 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] . Global Substance Registration System. 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] . Freebase Data Dumps. wikidata.org.
  14. [16] . Global Substance Registration System. Retrieved . wikidata.org.
  15. [17] . Q2311683. Retrieved . wikidata.org.
  16. [18] . PubChem. Retrieved . wikidata.org.
  17. [19] . ChEBI. Retrieved . wikidata.org.
  18. [20] . ChEMBL. Retrieved . wikidata.org.
  19. [21] . Bioactive constituents of the roots of Polyalthia cerasoides. wikidata.org.
  20. [22] . Berberis alkaloids. XVII. Investigation of the alkaloids of Berberis heteropoda. wikidata.org.
  21. [23] . Berberis alkaloids. XXIV. Structure of bernumine. wikidata.org.
  22. [24] . Alkaloids of Cissampelos pareira. wikidata.org.
  23. [25] . Aporphine alkaloids from Guatteria spp. with leishmanicidal activity. wikidata.org.
  24. [26] . Antimicrobial Activity and Phytochemical Studies on Turkish Samples ofPapaver macrostomum.. wikidata.org.
  25. [27] . Alkaloids from Papaver setigerum DC.. 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). laudanosine. Retrieved May 3, 2026, from https://4ort.xyz/entity/laudanosine
MLA “laudanosine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/laudanosine.
BibTeX @misc{4ortxyz_laudanosine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{laudanosine}}, year = {2026}, url = {https://4ort.xyz/entity/laudanosine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): laudanosine — https://4ort.xyz/entity/laudanosine (retrieved 2026-05-03)

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