Home › Entities › type_of_chemical_entity › corynanthine

corynanthine

chemical compound
ChemicalSubstance type_of_chemical_entity Q5173746
Press Enter · cited answer in seconds

corynanthine

Summary

corynanthine is a type of chemical entity[1]. corynanthine has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]

Key Facts

  • corynanthine's instance of is recorded as type of chemical entity[3].
  • corynanthine's canonical SMILES is recorded as COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O[4].
  • corynanthine's chemical formula is recorded as C₂₁H₂₆N₂O₃[5].
  • corynanthine is a type of yohimbinoid alkaloid[6].
  • corynanthine's Commons category is recorded as Corynanthine[7].
  • corynanthine's found in taxon is recorded as Rauvolfia serpentina[8].
  • corynanthine's found in taxon is recorded as Corynanthe johimbe[9].
  • corynanthine's found in taxon is recorded as Corynanthe pachyceras[10].
  • corynanthine's found in taxon is recorded as Rauvolfia biauriculata[11].
  • corynanthine's found in taxon is recorded as Rauvolfia tetraphylla[12].
  • corynanthine's found in taxon is recorded as Rauvolfia mannii[13].
  • corynanthine's found in taxon is recorded as Uncaria callophylla[14].
  • corynanthine's found in taxon is recorded as Corynanthe macroceras[15].
  • corynanthine's found in taxon is recorded as Alstonia mollis[16].
  • corynanthine's found in taxon is recorded as Alstonia constricta[17].
  • corynanthine's isomeric SMILES is recorded as COC(=O)[C@@H]1C@HOC@HO">[18].
  • corynanthine's mass is recorded as {'unit': 'Q483261', 'amount': '+354.194343'}[19].
  • corynanthine's stereoisomer of is recorded as α-yohimbine[20].
  • corynanthine's stereoisomer of is recorded as yohimbine[21].
  • corynanthine's stereoisomer of is recorded as methyl (1S,15R,18R,19R,20S)-18-hydroxy-3,13-diazapentacyclo[11.8.0.0²,¹⁰.0⁴,⁹.0¹⁵,²⁰]henicosa-2(10),4,6,8-tetraene-19-carboxylate[22].
  • corynanthine's stereoisomer of is recorded as (1R,15R,18S,19R,20R)-18-hydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylic acid methyl ester[23].
  • corynanthine's stereoisomer of is recorded as pseudoyohimbine[24].
  • corynanthine's stereoisomer of is recorded as 3-epi-beta-Yohimbine[25].
  • corynanthine's stereoisomer of is recorded as methyl (1S,15R,18R,19R,20R)-18-hydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate[26].
  • corynanthine's stereoisomer of is recorded as methyl (1R,15S,18S,19S,20R)-18-hydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate[27].

Why It Matters

corynanthine has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[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] ↑ . wikidata.org.
  6. [8] ↑ . Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968. wikidata.org.
  7. [9] ↑ . Alkaloid-Bearing Plants and Their Contained Alkaloids. 1957-1968. wikidata.org.
  8. [10] ↑ . Leishmanicidal, antiplasmodial and cytotoxic activity of indole alkaloids from Corynanthe pachyceras. wikidata.org.
  9. [11] ↑ . Indole alkaloids from Rauvolfia media. wikidata.org.
  10. [12] ↑ . Alkaloids from Rauvolfia canescens. wikidata.org.
  11. [13] ↑ . Root alkaloids of Rauwolfia cumminsii Stapf. wikidata.org.
  12. [14] ↑ . Recent research progress of Uncaria spp. based on alkaloids: phytochemistry, pharmacology and structural chemistry. wikidata.org.
  13. [15] ↑ . Alkaloids of Pausinystalia macroceras. wikidata.org.
  14. [16] ↑ . New alkaloids of Alstonia constricta. wikidata.org.
  15. [17] ↑ . New alkaloids of Alstonia constricta. wikidata.org.
  16. [18] ↑ . PubChem. Retrieved . wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . wikidata.org.
  19. [21] ↑ . wikidata.org.
  20. [22] ↑ . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikidata sitelinks. 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). corynanthine. Retrieved October 8, 2026, from https://4ort.xyz/entity/corynanthine
MLA “corynanthine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 8 Oct. 2026, https://4ort.xyz/entity/corynanthine.
BibTeX @misc{4ortxyz_corynanthine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{corynanthine}}, year = {2026}, url = {https://4ort.xyz/entity/corynanthine}, note = {Accessed: 2026-10-08}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): corynanthine — https://4ort.xyz/entity/corynanthine (retrieved 2026-10-08)

Canonical URL: https://4ort.xyz/entity/corynanthine · Last refreshed:

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. 15w ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Stereoisomer of → α-yohimbine, yohimbine, methyl (1S,15R,18R,19R,20S)-18-hydroxy-3,13-diazapentacyclo[11.8.0.0²,¹⁰.0⁴,⁹.0¹⁵,²⁰]henicosa-2(10),4,6,8-tetraene-19-carboxylate +8
    Instance of → type of chemical entity
    Subclass of → —
    Aliases → —
    + 4 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]]"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.