absinthin

group of stereoisomers with the chemical formula C₃₀H₄₀O₆
ChemicalSubstance group_of_stereoisomers Q105216980
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absinthin

Summary

absinthin is a group of stereoisomers[1].

Key Facts

  • absinthin's instance of is recorded as group of stereoisomers[2].
  • absinthin's canonical SMILES is recorded as O=C1OC2C3=C(C)C4C(C5C=C(C)C64C7OC(=O)C(C)C7CCC(O)(C)C56)C3C(O)(C)CCC2C1C[3].
  • absinthin's InChI is recorded as InChI=1S/C30H40O6/c1-12-11-18-20-21(30(12)24(18)29(6,34)10-8-17-14(3)27(32)36-25(17)30)15(4)19-22(20)28(5,33)9-7-16-13(2)26(31)35-23(16)19/h11,13-14,16-18,20-25,33-34H,7-10H2,1-6H3[4].
  • absinthin's InChIKey is recorded as PZHWYURJZAPXAN-UHFFFAOYSA-N[5].
  • absinthin's chemical formula is recorded as C₃₀H₄₀O₆[6].
  • absinthin's subclass of is recorded as chemical compound[7].
  • absinthin's PubChem CID is recorded as 348165[8].
  • absinthin's found in taxon is recorded as Artemisia rutifolia[9].
  • absinthin's found in taxon is recorded as Artemisia carvifolia[10].
  • absinthin's found in taxon is recorded as Artemisia caruifolia[11].
  • absinthin's found in taxon is recorded as Artemisia absinthium[12].
  • absinthin's found in taxon is recorded as Artemisia sieversiana[13].
  • absinthin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+496.282489'}[14].
  • absinthin's UniChem compound ID is recorded as 31998944[15].
  • absinthin's Probes And Drugs ID is recorded as PD087711[16].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . PubChem. Retrieved . wikidata.org.
  8. [9] . Guaiane dimers and germacranolide from Artemisia caruifolia. wikidata.org.
  9. [10] . Dimeric guaianolides from Artemisia sieversiana. wikidata.org.
  10. [11] . Dimeric guaianolides from Artemisia sieversiana. wikidata.org.
  11. [12] . Dimeric guaianolides from Artemisia sieversiana. wikidata.org.
  12. [13] . Guaiane dimers and germacranolide from Artemisia caruifolia. wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . UniChem. wikidata.org.
  15. [16] . wikidata.org.

Class ancestry

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

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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). absinthin. Retrieved May 3, 2026, from https://4ort.xyz/entity/absinthin-q105216980
MLA “absinthin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/absinthin-q105216980.
BibTeX @misc{4ortxyz_absinthin-q105216980_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{absinthin}}, year = {2026}, url = {https://4ort.xyz/entity/absinthin-q105216980}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): absinthin — https://4ort.xyz/entity/absinthin-q105216980 (retrieved 2026-05-03)

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