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(1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene

group of stereoisomers with the chemical formula C₂₀H₂₆N₂O
ChemicalSubstance group_of_stereoisomers Q104375568
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(1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene

Summary

(1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene is a group of stereoisomers[1].

Key Facts

  • (1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene's instance of is recorded as group of stereoisomers[2].
  • (1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene's canonical SMILES is recorded as O(C=1C=CC2=C(C1)NC3=C2CCN4CC5CC3C4C(CC)C5)C[3].
  • (1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene's InChI is recorded as InChI=1S/C20H26N2O/c1-3-13-8-12-9-17-19-16(6-7-22(11-12)20(13)17)15-5-4-14(23-2)10-18(15)21-19/h4-5,10,12-13,17,20-21H,3,6-9,11H2,1-2H3/t12-,13-,17-,20?/m0/s1[4].
  • (1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene's InChIKey is recorded as UCIDWKVIQZIKEK-CICBKQEESA-N[5].
  • (1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene's chemical formula is recorded as C₂₀H₂₆N₂O[6].
  • (1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene's subclass of is recorded as iboga alkaloid[7].
  • (1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene's PubChem CID is recorded as 137628544[8].
  • (1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene's found in taxon is recorded as Voacanga africana[9].
  • (1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene's found in taxon is recorded as Tabernaemontana laurifolia[10].
  • (1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene's isomeric SMILES is recorded as CC[C@H]1C[C@H]2C[C@H]3c4[nH]c5cc(OC)ccc5c4CCN(C2)C13[11].
  • (1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+310.204513452'}[12].
  • (1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene's UniChem compound ID is recorded as 169090186[13].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . Alkaloids with Anti-Onchocercal Activity from Voacanga africana Stapf (Apocynaceae): Identification and Molecular Modeling. wikidata.org.
  9. [10] ↑ . Chemotaxonomic study of the genusTabernaemontana (Apocynaceae) based on their indole alkaloid content. wikidata.org.
  10. [11] ↑ . wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.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). (1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene. Retrieved May 3, 2026, from https://4ort.xyz/entity/-1r-15s-17s-17-ethyl-6-methoxy-3-13-diazapentacyclo-13-3-1-02-10-04-9-013-18-nonadeca-2-10-4-9-5-7-tetraene
MLA “(1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-1r-15s-17s-17-ethyl-6-methoxy-3-13-diazapentacyclo-13-3-1-02-10-04-9-013-18-nonadeca-2-10-4-9-5-7-tetraene.
BibTeX @misc{4ortxyz_-1r-15s-17s-17-ethyl-6-methoxy-3-13-diazapentacyclo-13-3-1-02-10-04-9-013-18-nonadeca-2-10-4-9-5-7-tetraene_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene}}, year = {2026}, url = {https://4ort.xyz/entity/-1r-15s-17s-17-ethyl-6-methoxy-3-13-diazapentacyclo-13-3-1-02-10-04-9-013-18-nonadeca-2-10-4-9-5-7-tetraene}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): (1R,15S,17S)-17-ethyl-6-methoxy-3,13-diazapentacyclo[13.3.1.02,10.04,9.013,18]nonadeca-2(10),4(9),5,7-tetraene — https://4ort.xyz/entity/-1r-15s-17s-17-ethyl-6-methoxy-3-13-diazapentacyclo-13-3-1-02-10-04-9-013-18-nonadeca-2-10-4-9-5-7-tetraene (retrieved 2026-05-03)

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