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aconifine

chemical compound
ChemicalSubstance group_of_stereoisomers Q27105662
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aconifine

Summary

aconifine is a group of stereoisomers[1]. aconifine is known by 4 alternative names across languages and contexts.[2]

Key Facts

  • aconifine's instance of is recorded as group of stereoisomers[3].
  • aconifine's canonical SMILES is recorded as CCN1CC2(C(CC(C34C2C(C(C31)C5(C6C4(CC(C6OC(=O)C7=CC=CC=C7)(C(C5O)OC)O)O)OC(=O)C)OC)OC)O)COC[4].
  • aconifine's chemical formula is recorded as C₃₄H₄₇NO₁₂[5].
  • aconifine is a type of aconitane alkaloid[6].
  • aconifine's found in taxon is recorded as Aconitum karakolicum[7].
  • aconifine's found in taxon is recorded as Aconitum nagarum[8].
  • aconifine's found in taxon is recorded as Aconitum soongaricum[9].
  • aconifine's found in taxon is recorded as Aconitum carmichaelii[10].
  • aconifine's isomeric SMILES is recorded as CCN1C[C@@]2(C@@HO)COCC@@HO)COC">[11].
  • aconifine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+661.309826'}[12].

Why It Matters

aconifine is known by 4 alternative names across languages and contexts.[2]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [5] ↑ . PubChem. Retrieved . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . A QSAR analysis of toxicity of Aconitum alkaloids. wikidata.org.
  6. [8] ↑ . A QSAR analysis of toxicity of Aconitum alkaloids. wikidata.org.
  7. [9] ↑ . Extraction of the total alkaloids fromAconitum soongoricum tubers. wikidata.org.
  8. [10] ↑ . Neutral Fragment Filtering for Rapid Identification of New Diester-Diterpenoid Alkaloids in Roots of Aconitum carmichaeli by Ultra-High-Pressure Liquid Chromatography Coupled with Linear Ion Trap-Orbitrap Mass Spectrometry. wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . PubChem. Retrieved . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . 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). aconifine. Retrieved May 3, 2026, from https://4ort.xyz/entity/aconifine
MLA “aconifine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/aconifine.
BibTeX @misc{4ortxyz_aconifine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{aconifine}}, year = {2026}, url = {https://4ort.xyz/entity/aconifine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): aconifine — https://4ort.xyz/entity/aconifine (retrieved 2026-05-03)

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Edit History

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 ↗
    Chembl id → CHEMBL2062833
    Dsstox substance id → DTXSID80962016
    Imported from → —
    Kegg id → C08655
    + 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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