artemisinin

chemical compound
ChemicalSubstance type_of_chemical_entity Q426921
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artemisinin

Summary

artemisinin is a type of chemical entity[1]. artemisinin ranks in the top 3% of type_of_chemical_entity entities by monthly Wikipedia readership (343 views/month).[2]

Key Facts

  • artemisinin's instance of is recorded as type of chemical entity[3].
  • artemisinin's chemical structure is recorded as Artemisinin.svg[4].
  • artemisinin's physically interacts with is recorded as taste receptor type 2[5].
  • artemisinin's CAS Registry Number is recorded as 63968-64-9[6].
  • artemisinin's EC number is recorded as 700-290-5[7].
  • artemisinin's canonical SMILES is recorded as O=C1OC2OC3(OOC24C(CCC(C)C4CC3)C1C)C[8].
  • artemisinin's InChI is recorded as InChI=1S/C15H22O5/c1-8-4-5-11-9(2)12(16)17-13-15(11)10(8)6-7-14(3,18-13)19-20-15/h8-11,13H,4-7H2,1-3H3/t8-,9-,10+,11+,13-,14-,15-/m1/s1[9].
  • artemisinin's InChIKey is recorded as BLUAFEHZUWYNDE-NNWCWBAJSA-N[10].
  • artemisinin's Library of Congress authority ID is recorded as sh2007003203[11].
  • artemisinin's ATC code is recorded as P01BE01[12].
  • artemisinin's chemical formula is recorded as C₁₅H₂₂O₅[13].
  • artemisinin's subclass of is recorded as antimalarial[14].
  • artemisinin's subclass of is recorded as carboxylate ester[15].
  • artemisinin's subclass of is recorded as cyclic compound[16].
  • artemisinin's subclass of is recorded as ethers[17].
  • artemisinin's subclass of is recorded as organic peroxide[18].
  • artemisinin's subclass of is recorded as artemisinin (unspec.)[19].
  • artemisinin's subclass of is recorded as (1R,13R)-1,5,9-trimethyl-11,14,15,16-tetraoxatetracyclo[10.3.1.04,13.08,13]hexadecan-10-one[20].
  • artemisinin's has use is recorded as medication[21].
  • artemisinin's Commons category is recorded as Artemisinin[22].
  • artemisinin's MeSH descriptor ID is recorded as C031327[23].
  • artemisinin's ChEMBL ID is recorded as CHEMBL77[24].
  • artemisinin's ChEMBL ID is recorded as CHEMBL269671[25].
  • artemisinin's Guide to Pharmacology Ligand ID is recorded as 9954[26].
  • artemisinin's Freebase ID is recorded as /m/0361st[27].

Why It Matters

artemisinin ranks in the top 3% of type_of_chemical_entity entities by monthly Wikipedia readership (343 views/month).[2] artemisinin has Wikipedia articles in 25 language editions, a strong signal of global cultural recognition.[28] artemisinin is known by 13 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] . Broad tuning of the human bitter taste receptor hTAS2R46 to various sesquiterpene lactones, clerodane and labdane diterpenoids, strychnine, and denatonium. wikidata.org.
  4. [6] . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  5. [7] . wikidata.org.
  6. [8] . wikidata.org.
  7. [9] . PubChem. wikidata.org.
  8. [10] . PubChem. wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . PubChem. wikidata.org.
  12. [14] . ChEBI. wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . wikidata.org.
  15. [17] . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . wikidata.org.
  18. [20] . wikidata.org.
  19. [21] . wikidata.org.
  20. [22] . wikidata.org.
  21. [23] . Medical Subject Headings. Retrieved . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  24. [26] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  25. [27] . Freebase Data Dumps. 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). artemisinin. Retrieved May 3, 2026, from https://4ort.xyz/entity/artemisinin
MLA “artemisinin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/artemisinin.
BibTeX @misc{4ortxyz_artemisinin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{artemisinin}}, year = {2026}, url = {https://4ort.xyz/entity/artemisinin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): artemisinin — https://4ort.xyz/entity/artemisinin (retrieved 2026-05-03)

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