Hypaconitine

chemical compound
ChemicalSubstance group_of_stereoisomers Q27106904
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Hypaconitine

Summary

Hypaconitine is a group of stereoisomers[1].

Key Facts

  • Hypaconitine's instance of is recorded as group of stereoisomers[2].
  • Hypaconitine's canonical SMILES is recorded as CC(=O)OC12C3C(CC(C3OC(=O)C4=CC=CC=C4)(C(C1O)OC)O)C56C(CCC7(C5C(C2C6N(C7)C)OC)COC)OC[3].
  • Hypaconitine's chemical formula is recorded as C₃₃H₄₅NO₁₀[4].
  • Hypaconitine is a type of aconitane alkaloid[5].
  • Hypaconitine's found in taxon is recorded as Aconitum carmichaelii[6].
  • Hypaconitine's found in taxon is recorded as Aconitum firmum[7].
  • Hypaconitine's found in taxon is recorded as Aconitum kusnezoffii[8].
  • Hypaconitine's found in taxon is recorded as Aconitum napiforme[9].
  • Hypaconitine's found in taxon is recorded as Aconitum[10].
  • Hypaconitine's found in taxon is recorded as Q158783[11].
  • Hypaconitine's found in taxon is recorded as Aconitum japonicum[12].
  • Hypaconitine's isomeric SMILES is recorded as CC(=O)O[C@@]12[C@@H]3C@@H[C@]56C@HOCC@@H[C@]56C@HOC">[13].
  • Hypaconitine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+615.304347'}[14].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . PubChem. Retrieved . wikidata.org.
  3. [4] . PubChem. Retrieved . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . A study ofaconitum alkaloids from aconite roots in Aconitum carmichaeli Debx using matrix-assisted laser desorption/ionization mass spectrometry. wikidata.org.
  6. [7] . Alkaloids of Aconitum firmum and A. tokii. wikidata.org.
  7. [8] . Beiwudine, a norditerpenoid alkaloid from aconitum kusnezoffii. wikidata.org.
  8. [9] . Diterpene alkaloids from Aconitum kirinense. wikidata.org.
  9. [10] . Hypaconitine, the dominant constituent responsible for the neuromuscular blocking action of the Japanese-sino medicine "bushi" (aconite root). wikidata.org.
  10. [11] . Quaternary Isoquinoline Alkaloids and Some Diterpenoid Alkaloids in Plants of the Czech Republic. wikidata.org.
  11. [12] . Determination of Aconitum alkaloids in the tubers of Aconitum japonicum using gas chromatography/selected ion monitoring. wikidata.org.
  12. [13] . PubChem. Retrieved . wikidata.org.
  13. [14] . PubChem. Retrieved . 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). Hypaconitine. Retrieved May 3, 2026, from https://4ort.xyz/entity/hypaconitine
MLA “Hypaconitine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hypaconitine.
BibTeX @misc{4ortxyz_hypaconitine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Hypaconitine}}, year = {2026}, url = {https://4ort.xyz/entity/hypaconitine}, note = {Accessed: 2026-05-03}}
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Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 12w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Dsstox substance id DTXSID50988763
    Echa substance infocard id 100.208.656
    Imported from
    Kegg id C08688
    + 20 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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