coronaridine

chemical compound
ChemicalSubstance group_of_stereoisomers Q5172181
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coronaridine

Summary

coronaridine is a group of stereoisomers[1]. coronaridine draws 40 Wikipedia views per month (group_of_stereoisomers category, ranking #180 of 1,063).[2]

Key Facts

  • coronaridine's instance of is recorded as group of stereoisomers[3].
  • coronaridine's chemical structure is recorded as Coronaridine.svg[4].
  • coronaridine's CAS Registry Number is recorded as 467-77-6[5].
  • coronaridine's EC number is recorded as 207-398-7[6].
  • coronaridine's canonical SMILES is recorded as CCC1CC2CC3(C1N(C2)CCC4=C3NC5=CC=CC=C45)C(=O)OC[7].
  • coronaridine's InChI is recorded as InChI=1S/C21H26N2O2/c1-3-14-10-13-11-21(20(24)25-2)18-16(8-9-23(12-13)19(14)21)15-6-4-5-7-17(15)22-18/h4-7,13-14,19,22H,3,8-12H2,1-2H3/t13-,14-,19-,21+/m0/s1[8].
  • coronaridine's InChIKey is recorded as NVVDQMVGALBDGE-KSWFMABOSA-N[9].
  • coronaridine's InChIKey is recorded as NVVDQMVGALBDGE-PZXGUROGSA-N[10].
  • coronaridine's chemical formula is recorded as C₂₁H₂₆N₂O₂[11].
  • coronaridine's subclass of is recorded as methyl (15S,17S)-17-ethyl-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4,6,8-tetraene-1-carboxylate[12].
  • coronaridine's Commons category is recorded as Coronaridine[13].
  • coronaridine's ChEMBL ID is recorded as CHEMBL364613[14].
  • coronaridine's Freebase ID is recorded as /m/0b6f__0[15].
  • coronaridine's ChemSpider ID is recorded as 66179[16].
  • coronaridine's PubChem CID is recorded as 73489[17].
  • coronaridine's PubChem CID is recorded as 6426909[18].
  • coronaridine's KEGG ID is recorded as C09139[19].
  • coronaridine's found in taxon is recorded as Tabernanthe iboga[20].
  • coronaridine's found in taxon is recorded as Tabernaemontana divaricata[21].
  • coronaridine's found in taxon is recorded as Tabernaemontana catharinensis[22].
  • coronaridine's found in taxon is recorded as Tabernaemontana oppositifolia[23].
  • coronaridine's found in taxon is recorded as Tabernaemontana laeta[24].
  • coronaridine's found in taxon is recorded as Tabernaemontana calcarea[25].
  • coronaridine's found in taxon is recorded as Tabernaemontana bufalina[26].
  • coronaridine's found in taxon is recorded as Tabernaemontana vanheurckii[27].

Why It Matters

coronaridine draws 40 Wikipedia views per month (group_of_stereoisomers category, ranking #180 of 1,063).[2]

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] . ChEBI. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . ECHA Substance Infocard database. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . ChEBI release 2020-09-01. wikidata.org.
  9. [11] . PubChem. Retrieved . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . wikidata.org.
  12. [14] . ChEMBL. Retrieved . wikidata.org.
  13. [15] . wikidata.org.
  14. [16] . Q2311683. Retrieved . wikidata.org.
  15. [17] . PubChem. Retrieved . wikidata.org.
  16. [18] . wikidata.org.
  17. [19] . ChEBI. Retrieved . wikidata.org.
  18. [20] . Alcaloides de Tabernanthe pubescens. wikidata.org.
  19. [21] . Indole alkaloids from three species of the Ervatamia genus: E. officinalis, E. divaricata, and E. divaricata Gouyahua. wikidata.org.
  20. [22] . Catharinensine, an oxindole alkaloid from Peschiera catharinensis. wikidata.org.
  21. [23] . Alkaloids from Apocynaceae. III.1Alkaloids of Tabernaemontana and Ervatamia. The Structure of Coronaridine, A New Alkaloid Related to Ibogamine2. wikidata.org.
  22. [24] . Indole alkaloids from Peschiera laeta that enhance vinblastine-mediated cytotoxicity with multidrug-resistant cells. wikidata.org.
  23. [25] . New Cytotoxic Indole Alkaloids from Tabernaemontana calcarea from the Madagascar Rainforest. wikidata.org.
  24. [26] . Indole alkaloids from Ervatamia hainanensis with potent acetylcholinesterase inhibition activities. wikidata.org.
  25. [27] . Systematically Significant Indole Alkaloids from Peschiera van heurckii. wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.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). coronaridine. Retrieved May 3, 2026, from https://4ort.xyz/entity/coronaridine
MLA “coronaridine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/coronaridine.
BibTeX @misc{4ortxyz_coronaridine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{coronaridine}}, year = {2026}, url = {https://4ort.xyz/entity/coronaridine}, note = {Accessed: 2026-05-03}}
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