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Lochnerinine

chemical compound
ChemicalSubstance group_of_stereoisomers Q27107224
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Lochnerinine

Summary

Lochnerinine is a group of stereoisomers[1].

Key Facts

  • Lochnerinine's instance of is recorded as group of stereoisomers[2].
  • Lochnerinine's canonical SMILES is recorded as CCC12CC(=C3C4(C1N(CC4)CC5C2O5)C6=C(N3)C=C(C=C6)OC)C(=O)OC[3].
  • Lochnerinine's chemical formula is recorded as C₂₂H₂₆N₂O₄[4].
  • Lochnerinine is a type of aspidospermine / aspidofractine / kopsane alkaloid[5].
  • Lochnerinine's found in taxon is recorded as Vinca herbacea[6].
  • Lochnerinine's found in taxon is recorded as Catharanthus roseus[7].
  • Lochnerinine's found in taxon is recorded as Alstonia yunnanensis[8].
  • Lochnerinine's found in taxon is recorded as Catharanthus lanceus[9].
  • Lochnerinine's found in taxon is recorded as Catharanthus pusillus[10].
  • Lochnerinine's isomeric SMILES is recorded as CC[C@]12CC(=C3[C@@]4([C@H]1N(CC4)CC5C2O5)C6=C(N3)C=C(C=C6)OC)C(=O)OC[11].
  • Lochnerinine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+382.189257'}[12].

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] ↑ . Vinca Alkaloids. wikidata.org.
  6. [7] ↑ . Analysis of Indole Alkaloids from Leaves of Catharanthus roseus by Means of Supercritical Fluid Chromatography/ Mass Spectrometry. wikidata.org.
  7. [8] ↑ . Cytotoxic monoterpenoid indole alkaloids from Alstonia yunnanensis Diels. wikidata.org.
  8. [9] ↑ . Structure Elucidation and Chemistry of Catharanthus Alkaloids II. Isolation and Partial Structure of Catharine, a Dimeric Indole Alkaloid From C. Zanceus and C. Roseus. wikidata.org.
  9. [10] ↑ . Catharanthus alkaloids. XXI. Isolation of lochnerinine, one of the cytotoxic principles of C. pusillus. wikidata.org.
  10. [11] ↑ . PubChem. Retrieved . wikidata.org.
  11. [12] ↑ . 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). Lochnerinine. Retrieved May 3, 2026, from https://4ort.xyz/entity/lochnerinine
MLA “Lochnerinine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/lochnerinine.
BibTeX @misc{4ortxyz_lochnerinine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Lochnerinine}}, year = {2026}, url = {https://4ort.xyz/entity/lochnerinine}, note = {Accessed: 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. 11w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Isomeric smiles → CC[C@]12CC(=C3[C@@]4([C@H]1N(CC4)CC5C2O5)C6=C(N3)C=C(C=C6)OC
    Found in taxon → Vinca herbacea, Catharanthus roseus, Alstonia yunnanensis +2
    Subclass of → aspidospermine / aspidofractine / kopsane alkaloid
    Chemical formula → C₂₂H₂₆N₂O₄
    + 13 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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