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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 ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (3 views/month).[2]

Key Facts

  • rescinnamine's instance of is recorded as type of chemical entity[3].
  • rescinnamine's chemical structure is recorded as Rescinnamine.svg[4].
  • rescinnamine's CAS Registry Number is recorded as 24815-24-5[5].
  • rescinnamine's EC number is recorded as 246-471-8[6].
  • 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[7].
  • rescinnamine's InChI is recorded as InChI=1S/C35H42N2O9/c1-40-21-8-9-22-23-11-12-37-18-20-15-29(46-30(38)10-7-19-13-27(41-2)33(43-4)28(14-19)42-3)34(44-5)31(35(39)45-6)24(20)17-26(37)32(23)36-25(22)16-21/h7-10,13-14,16,20,24,26,29,31,34,36H,11-12,15,17-18H2,1-6H3/b10-7+/t20-,24+,26-,29-,31+,34+/m1/s1[8].
  • rescinnamine's InChIKey is recorded as SZLZWPPUNLXJEA-QEGASFHISA-N[9].
  • rescinnamine's ATC code is recorded as C02AA01[10].
  • rescinnamine's chemical formula is recorded as C₃₅H₄₂N₂O₉[11].
  • rescinnamine's subclass of is recorded as yohimbinoid alkaloid[12].
  • rescinnamine's has use is recorded as medication[13].
  • rescinnamine's ChEMBL ID is recorded as CHEMBL1668[14].
  • rescinnamine's Guide to Pharmacology Ligand ID is recorded as 7098[15].
  • rescinnamine's Freebase ID is recorded as /m/0cx49w[16].
  • rescinnamine's UNII is recorded as Q6W1F7DJ2D[17].
  • rescinnamine's ChemSpider ID is recorded as 4444446[18].
  • rescinnamine's PubChem CID is recorded as 5280954[19].
  • rescinnamine's KEGG ID is recorded as D00198[20].
  • rescinnamine's ChEBI ID is recorded as 28572[21].
  • rescinnamine's found in taxon is recorded as Rauvolfia volkensii[22].
  • rescinnamine's found in taxon is recorded as Rauvolfia[23].
  • rescinnamine's found in taxon is recorded as Rauvolfia mannii[24].
  • rescinnamine's found in taxon is recorded as Rauvolfia serpentina[25].
  • rescinnamine's found in taxon is recorded as Vinca erecta[26].
  • rescinnamine's found in taxon is recorded as Vinca herbacea[27].

Why It Matters

rescinnamine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (3 views/month).[2] rescinnamine has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[28] rescinnamine is known by 5 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . wikidata.org.
  3. [5] ↑ . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . DrugBank. wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . ChEMBL. Retrieved . wikidata.org.
  13. [15] ↑ . IUPHAR/BPS Guide to PHARMACOLOGY. Retrieved . wikidata.org.
  14. [16] ↑ . Freebase Data Dumps. wikidata.org.
  15. [17] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  16. [18] ↑ . Q2311683. Retrieved . wikidata.org.
  17. [19] ↑ . PubChem. Retrieved . wikidata.org.
  18. [20] ↑ . ChEBI. Retrieved . wikidata.org.
  19. [21] ↑ . ChEMBL. Retrieved . wikidata.org.
  20. [22] ↑ . Alkaloid distribution in some african rauvolfia species. wikidata.org.
  21. [23] ↑ . Centrifugal thin-layer chromatography of alkaloids from vegetable sources using an aluminium oxide layer. wikidata.org.
  22. [24] ↑ . The Alkaloids of Rauwolfia cumminsii.. wikidata.org.
  23. [25] ↑ . Development of an efficient system for the separation of indole alkaloids by high performance liquid chromatography and its applications.. wikidata.org.
  24. [26] ↑ . Vinca Alkaloids. wikidata.org.
  25. [27] ↑ . Vinca Alkaloids. 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). 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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