Echinatine

group of stereoisomers with the chemical formula C₁₅H₂₅NO₅
ChemicalSubstance group_of_stereoisomers Q105252083
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Echinatine

Summary

Echinatine is a group of stereoisomers[1].

Key Facts

  • Echinatine's instance of is recorded as group of stereoisomers[2].
  • Echinatine's canonical SMILES is recorded as O=C(OCC1=CCN2CCC(O)C12)C(O)(C(O)C)C(C)C[3].
  • Echinatine's InChI is recorded as InChI=1S/C15H25NO5/c1-9(2)15(20,10(3)17)14(19)21-8-11-4-6-16-7-5-12(18)13(11)16/h4,9-10,12-13,17-18,20H,5-8H2,1-3H3[4].
  • Echinatine's InChIKey is recorded as SFVVQRJOGUKCEG-UHFFFAOYSA-N[5].
  • Echinatine's chemical formula is recorded as C₁₅H₂₅NO₅[6].
  • Echinatine's subclass of is recorded as pyrrolizidine alkaloid[7].
  • Echinatine's PubChem CID is recorded as 22384[8].
  • Echinatine's ChEBI ID is recorded as 182293[9].
  • Echinatine's found in taxon is recorded as Eupatorium compositifolium[10].
  • Echinatine's found in taxon is recorded as Eupatorium altissimum[11].
  • Echinatine's found in taxon is recorded as Eupatorium fortunei[12].
  • Echinatine's found in taxon is recorded as Critonia portoricensis[13].
  • Echinatine's found in taxon is recorded as Amsinckia menziesii var. intermedia[14].
  • Echinatine's Human Metabolome Database ID is recorded as HMDB0253457[15].
  • Echinatine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+299.1732729'}[16].
  • Echinatine's SureChEMBL ID is recorded as 16058911[17].
  • Echinatine's DSSTox substance ID is recorded as DTXSID60864145[18].
  • Echinatine's MassBank accession ID is recorded as MSBNK-RIKEN-PR310570[19].
  • Echinatine's UniChem compound ID is recorded as 32059268[20].
  • Echinatine's Probes And Drugs ID is recorded as PD093743[21].

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 2022-06-13. wikidata.org.
  9. [10] . THE ALKALOIDS OF EUPATORIUM MACULATUM L.. wikidata.org.
  10. [11] . THE ALKALOIDS OF EUPATORIUM MACULATUM L.. wikidata.org.
  11. [12] . Dammaradienyl acetate and taraxasterol from Eupatorium cannabinum: Mass spectrometric study of dammaradienyl acetate and its derivatives. wikidata.org.
  12. [13] . Dammaradienyl acetate and taraxasterol from Eupatorium cannabinum: Mass spectrometric study of dammaradienyl acetate and its derivatives. wikidata.org.
  13. [14] . The alkaloids of Amsinckia species: A. intermedia Fisch. & Mey., A. hispida (Ruiz. & Pav.) Johnst. and A. lycopsoides Lehm. wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  19. [20] . UniChem. wikidata.org.
  20. [21] . wikidata.org.

Class ancestry

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

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APA 4ort.xyz Knowledge Graph. (2026). Echinatine. Retrieved May 3, 2026, from https://4ort.xyz/entity/echinatine
MLA “Echinatine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/echinatine.
BibTeX @misc{4ortxyz_echinatine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Echinatine}}, year = {2026}, url = {https://4ort.xyz/entity/echinatine}, note = {Accessed: 2026-05-03}}
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