Iboxygaine

group of stereoisomers with the chemical formula C₂₀H₂₆N₂O₂
ChemicalSubstance group_of_stereoisomers Q83112450
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Iboxygaine

Summary

Iboxygaine is a group of stereoisomers[1].

Key Facts

  • Iboxygaine's instance of is recorded as group of stereoisomers[2].
  • Iboxygaine's CAS Registry Number is recorded as 82-55-3[3].
  • Iboxygaine's canonical SMILES is recorded as OC(C)C1CC2CN3CCC=4C=5C=C(OC)C=CC5NC4C(C2)C31[4].
  • Iboxygaine's InChI is recorded as InChI=1S/C20H26N2O2/c1-11(23)15-7-12-8-17-19-14(5-6-22(10-12)20(15)17)16-9-13(24-2)3-4-18(16)21-19/h3-4,9,11-12,15,17,20-21,23H,5-8,10H2,1-2H3/t11-,12+,15-,17-,20-/m0/s1[5].
  • Iboxygaine's InChIKey is recorded as QLSITYRYHBQHBY-BFRPBLBHSA-N[6].
  • Iboxygaine's chemical formula is recorded as C₂₀H₂₆N₂O₂[7].
  • Iboxygaine's subclass of is recorded as iboga alkaloid[8].
  • Iboxygaine's PubChem CID is recorded as 71656190[9].
  • Iboxygaine's found in taxon is recorded as Tabernanthe iboga[10].
  • Iboxygaine's found in taxon is recorded as Tabernaemontana catharinensis[11].
  • Iboxygaine's found in taxon is recorded as Tabernaemontana corymbosa[12].
  • Iboxygaine's found in taxon is recorded as Tabernaemontana orientalis[13].
  • Iboxygaine's found in taxon is recorded as Tabernaemontana lundii[14].
  • Iboxygaine's found in taxon is recorded as Tabernaemontana humblotii[15].
  • Iboxygaine's found in taxon is recorded as Tabernaemontana pandacaqui[16].
  • Iboxygaine's found in taxon is recorded as Tabernaemontana hystrix[17].
  • Iboxygaine's isomeric SMILES is recorded as COc1ccc2[nH]c3c(c2c1)CCN1C[C@H]2C[C@@H]3[C@@H]1C@HC2C@HC2">[18].
  • Iboxygaine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+326.19942807199993'}[19].
  • Iboxygaine's SureChEMBL ID is recorded as 30046153[20].
  • Iboxygaine's DSSTox substance ID is recorded as DTXSID90231508[21].
  • Iboxygaine's DSSTOX compound identifier is recorded as DTXCID50153999[22].
  • Iboxygaine's UniChem compound ID is recorded as 43702989[23].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . CAS Common Chemistry. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . PubChem. Retrieved . wikidata.org.
  9. [10] . Alcaloides de Tabernanthe pubescens. wikidata.org.
  10. [11] . Alcalóides de Peschiera affinis (Muell. Arg) Miers (Apocynaceae). wikidata.org.
  11. [12] . Alkaloids from leaves and root bark ofErvatamia hirta. wikidata.org.
  12. [13] . Tabernaemontana L. (Apocynaceae): A review of its taxonomy, phytochemistry, ethnobotany and pharmacology. wikidata.org.
  13. [14] . Tabernaemontana L. (Apocynaceae): A review of its taxonomy, phytochemistry, ethnobotany and pharmacology. wikidata.org.
  14. [15] . Tabernaemontana L. (Apocynaceae): A review of its taxonomy, phytochemistry, ethnobotany and pharmacology. wikidata.org.
  15. [16] . Tabernaemontana L. (Apocynaceae): A review of its taxonomy, phytochemistry, ethnobotany and pharmacology. wikidata.org.
  16. [17] . Tabernaemontana L. (Apocynaceae): A review of its taxonomy, phytochemistry, ethnobotany and pharmacology. wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . wikidata.org.
  19. [20] . wikidata.org.
  20. [21] . wikidata.org.
  21. [22] . wikidata.org.
  22. [23] . UniChem. wikidata.org.

Class ancestry

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

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APA 4ort.xyz Knowledge Graph. (2026). Iboxygaine. Retrieved May 3, 2026, from https://4ort.xyz/entity/iboxygaine
MLA “Iboxygaine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/iboxygaine.
BibTeX @misc{4ortxyz_iboxygaine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Iboxygaine}}, year = {2026}, url = {https://4ort.xyz/entity/iboxygaine}, note = {Accessed: 2026-05-03}}
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