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Anthecotulide

group of stereoisomers with the chemical formula C₁₅H₂₀O₃
ChemicalSubstance group_of_stereoisomers Q104399461
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Anthecotulide

Summary

Anthecotulide is a group of stereoisomers[1].

Key Facts

  • Anthecotulide's instance of is recorded as group of stereoisomers[2].
  • Anthecotulide's canonical SMILES is recorded as O=C1OCC(C1=C)CC=C(C)CC(=O)C=C(C)C[3].
  • Anthecotulide's InChI is recorded as InChI=1S/C15H20O3/c1-10(2)7-14(16)8-11(3)5-6-13-9-18-15(17)12(13)4/h5,7,13H,4,6,8-9H2,1-3H3/b11-5+[4].
  • Anthecotulide's InChIKey is recorded as WSKLYRKBPFVGEJ-VZUCSPMQSA-N[5].
  • Anthecotulide's chemical formula is recorded as C₁₅H₂₀O₃[6].
  • Anthecotulide's subclass of is recorded as chemical compound[7].
  • Anthecotulide's PubChem CID is recorded as 11962174[8].
  • Anthecotulide's ChEBI ID is recorded as 141397[9].
  • Anthecotulide's found in taxon is recorded as Anthemis cotula[10].
  • Anthecotulide's found in taxon is recorded as Anthemis auriculata[11].
  • Anthecotulide's isomeric SMILES is recorded as C=C1C(=O)OCC1C/C=C(\C)CC(=O)C=C(C)C[12].
  • Anthecotulide's Human Metabolome Database ID is recorded as HMDB0302733[13].
  • Anthecotulide's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+248.1412445'}[14].
  • Anthecotulide's SureChEMBL ID is recorded as 3206793[15].
  • Anthecotulide's NMRShiftDB structure ID is recorded as 20182291[16].
  • Anthecotulide's UniChem compound ID is recorded as 211535[17].

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] ↑ . ChEBI release 2021-03-01. wikidata.org.
  9. [10] ↑ . Anthecotulide: purification, analytical data, absence from chamomile preparations, stability and reactivity, and anti-infective testing. wikidata.org.
  10. [11] ↑ . Inhibiting enoyl-ACP reductase (FabI) across pathogenic microorganisms by linear sesquiterpene lactones from Anthemis auriculata. wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . UniChem. 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). Anthecotulide. Retrieved May 3, 2026, from https://4ort.xyz/entity/anthecotulide
MLA “Anthecotulide.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/anthecotulide.
BibTeX @misc{4ortxyz_anthecotulide_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Anthecotulide}}, year = {2026}, url = {https://4ort.xyz/entity/anthecotulide}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Anthecotulide — https://4ort.xyz/entity/anthecotulide (retrieved 2026-05-03)

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