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rescinnamine

chemical compound
ChemicalSubstance type_of_chemical_entity Q409978
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rescinnamine

Summary

rescinnamine is a type of chemical entity[1]. rescinnamine has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • rescinnamine's instance of is recorded as type of chemical entity[3].
  • rescinnamine's canonical SMILES is recorded as COC1C(CC2CN3CCC4=C(C3CC2C1C(=O)OC)NC5=C4C=CC(=C5)OC)OC(=O)C=CC6=CC(=C(C(=C6)OC)OC)OC[4].
  • rescinnamine's chemical formula is recorded as C₃₅H₄₂N₂O₉[5].
  • rescinnamine is a type of yohimbinoid alkaloid[6].
  • rescinnamine is used for medication[7].
  • rescinnamine's found in taxon is recorded as Rauvolfia volkensii[8].
  • rescinnamine's found in taxon is recorded as Rauvolfia[9].
  • rescinnamine's found in taxon is recorded as Rauvolfia mannii[10].
  • rescinnamine's found in taxon is recorded as Rauvolfia serpentina[11].
  • rescinnamine's found in taxon is recorded as Vinca erecta[12].
  • rescinnamine's found in taxon is recorded as Vinca herbacea[13].
  • rescinnamine's found in taxon is recorded as Vinca major[14].
  • rescinnamine's found in taxon is recorded as Aspidosperma excelsum[15].
  • rescinnamine's found in taxon is recorded as Aspidosperma marcgravianum[16].
  • rescinnamine's found in taxon is recorded as Ochrosia alyxioides[17].
  • rescinnamine's found in taxon is recorded as Rauvolfia mombasiana[18].
  • rescinnamine's found in taxon is recorded as Rauvolfia afra[19].
  • rescinnamine's isomeric SMILES is recorded as CO[C@H]1C@@HOC(=O)/C=C/C6=CC(=C(C(=C6)OC)OC)OCC@@HOC(=O)/C=C/C6=CC(=C(C(=C6)OC)OC)OC">[20].
  • rescinnamine's mass is recorded as {'unit': 'Q483261', 'amount': '+634.289031'}[21].
  • rescinnamine's stereoisomer of is recorded as Methyl (15beta,16beta,17alpha,18beta,20alpha)-11,17-dimethoxy-18-{[(2E)-3-(3,4,5-trimethoxyphenyl)-2-propenoyl]oxy}yohimban-16-carboxylate[22].
  • rescinnamine's stereoisomer of is recorded as (1R,15S,17R,18R,19S,20S)-6,18-dimethoxy-17-[1-oxo-3-(3,4,5-trimethoxyphenyl)prop-2-enoxy]-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylic acid methyl ester[23].

Why It Matters

rescinnamine has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2] rescinnamine is known by 5 alternative names across languages and contexts.[24]

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] ↑ . wikidata.org.
  6. [8] ↑ . Alkaloid distribution in some african rauvolfia species. wikidata.org.
  7. [9] ↑ . Centrifugal thin-layer chromatography of alkaloids from vegetable sources using an aluminium oxide layer. wikidata.org.
  8. [10] ↑ . The Alkaloids of Rauwolfia cumminsii.. wikidata.org.
  9. [11] ↑ . Development of an efficient system for the separation of indole alkaloids by high performance liquid chromatography and its applications.. wikidata.org.
  10. [12] ↑ . Vinca Alkaloids. wikidata.org.
  11. [13] ↑ . Vinca Alkaloids. wikidata.org.
  12. [14] ↑ . Vinca Alkaloids. wikidata.org.
  13. [15] ↑ . Aspidosperma de Guyane: Alcaloïdes de Aspidosperma marcgravianum. wikidata.org.
  14. [16] ↑ . Aspidosperma de Guyane: Alcaloïdes de Aspidosperma marcgravianum. wikidata.org.
  15. [17] ↑ . Alcaoëdes d'Ochrosia alyxioides. wikidata.org.
  16. [18] ↑ . The Alkaloids of Rauwolfia mombasiana Roots. wikidata.org.
  17. [19] ↑ . Estimation of the alkaloids of Rauwolfia caffra by quantitative thin-layer chromatography. African Rauwolfia species. XIV. wikidata.org.
  18. [20] ↑ . PubChem. Retrieved . wikidata.org.
  19. [21] ↑ . PubChem. Retrieved . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata sitelinks. wikidata.org.
  2. [24] ↑ . Wikidata aliases. 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). rescinnamine. Retrieved May 3, 2026, from https://4ort.xyz/entity/rescinnamine
MLA “rescinnamine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/rescinnamine.
BibTeX @misc{4ortxyz_rescinnamine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{rescinnamine}}, year = {2026}, url = {https://4ort.xyz/entity/rescinnamine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): rescinnamine — https://4ort.xyz/entity/rescinnamine (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. 20d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of → Methyl (15beta,16beta,17alpha,18beta,20alpha)-11,17-dimethoxy-18-{[(2E)-3-(3,4,5-trimethoxyphenyl)-2-propenoyl]oxy}yohimban-16-carboxylate, (1R,15S,17R,18R,19S,20S)-6,18-dimethoxy-17-[1-oxo-3-(3,4,5-trimethoxyphenyl)prop-2-enoxy]-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylic acid methyl ester
    Instance of → type of chemical entity
    Has use → medication
    Subclass of → —
    + 5 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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