yohimbine

chemical compound
ChemicalSubstance type_of_chemical_entity Q412226
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yohimbine

Summary

yohimbine is a type of chemical entity[1]. yohimbine ranks in the top 3% of type_of_chemical_entity entities by monthly Wikipedia readership (445 views/month).[2]

Key Facts

  • yohimbine is credited with the discovery of Leopold Julius Spiegel[3].
  • yohimbine's instance of is recorded as type of chemical entity[4].
  • yohimbine's chemical structure is recorded as Yohimbin.svg[5].
  • yohimbine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1A[6].
  • yohimbine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1B[7].
  • yohimbine's physically interacts with is recorded as 5-hydroxytryptamine (serotonin) receptor 1B[8].
  • yohimbine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1D[9].
  • yohimbine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1E[10].
  • yohimbine's physically interacts with is recorded as 5-hydroxytryptamine receptor 1F[11].
  • yohimbine's physically interacts with is recorded as 5-hydroxytryptamine receptor 2B[12].
  • yohimbine's physically interacts with is recorded as 5-hydroxytryptamine (serotonin) receptor 5A[13].
  • yohimbine's physically interacts with is recorded as 5-hydroxytryptamine receptor 5A[14].
  • yohimbine's physically interacts with is recorded as 5-hydroxytryptamine receptor 7[15].
  • yohimbine's physically interacts with is recorded as Adrenoceptor alpha 2A[16].
  • yohimbine's physically interacts with is recorded as Adrenoceptor alpha 2B[17].
  • yohimbine's physically interacts with is recorded as Adrenoceptor alpha 2C[18].
  • yohimbine's physically interacts with is recorded as taste receptor type 2[19].
  • yohimbine's CAS Registry Number is recorded as 146-48-5[20].
  • yohimbine's EC number is recorded as 205-672-0[21].
  • yohimbine's canonical SMILES is recorded as COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O[22].
  • yohimbine's InChI is recorded as InChI=1S/C21H26N2O3/c1-26-21(25)19-15-10-17-20-14(13-4-2-3-5-16(13)22-20)8-9-23(17)11-12(15)6-7-18(19)24/h2-5,12,15,17-19,22,24H,6-11H2,1H3/t12-,15-,17-,18-,19+/m0/s1[23].
  • yohimbine's InChIKey is recorded as BLGXFZZNTVWLAY-SCYLSFHTSA-N[24].
  • yohimbine's ATC code is recorded as G04BE04[25].
  • yohimbine's chemical formula is recorded as C₂₁H₂₆N₂O₃[26].
  • yohimbine's subclass of is recorded as yohimbinoid alkaloid[27].

Body

Works and Contributions

yohimbine is credited with the discovery of Leopold Julius Spiegel[3].

Why It Matters

yohimbine ranks in the top 3% of type_of_chemical_entity entities by monthly Wikipedia readership (445 views/month).[2] yohimbine has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[28] yohimbine is known by 27 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [4] . wikidata.org.
  2. [3] . Kauperts Straßenführer durch Berlin. berlin.kauperts.de. Provenance: wikidata.org.
  3. [5] . wikidata.org.
  4. [6] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  5. [7] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  6. [8] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  7. [9] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  8. [10] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  9. [11] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  10. [12] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  11. [13] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  12. [14] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  13. [15] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  14. [16] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  15. [17] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  16. [18] . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  17. [19] . The Molecular Receptive Ranges of Human TAS2R Bitter Taste Receptors. wikidata.org.
  18. [20] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  19. [21] . Global Substance Registration System. Retrieved . wikidata.org.
  20. [22] . PubChem. Retrieved . wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . PubChem. Retrieved . wikidata.org.
  23. [25] . DrugBank. wikidata.org.
  24. [26] . PubChem. Retrieved . wikidata.org.
  25. [27] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . 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). yohimbine. Retrieved May 3, 2026, from https://4ort.xyz/entity/yohimbine
MLA “yohimbine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/yohimbine.
BibTeX @misc{4ortxyz_yohimbine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{yohimbine}}, year = {2026}, url = {https://4ort.xyz/entity/yohimbine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): yohimbine — https://4ort.xyz/entity/yohimbine (retrieved 2026-05-03)

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