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cephaeline

group of stereoisomers with the chemical formula C₂₈H₃₈N₂O₄
ChemicalSubstance group_of_stereoisomers Q104988715
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cephaeline

Summary

cephaeline is a group of stereoisomers[1].

Key Facts

  • cephaeline's instance of is recorded as group of stereoisomers[2].
  • cephaeline's CAS Registry Number is recorded as 10159-64-5[3].
  • cephaeline's canonical SMILES is recorded as OC=1C=C2C(=CC1OC)C(NCC2)CC3CC4C5=CC(OC)=C(OC)C=C5CCN4CC3CC[4].
  • cephaeline's InChI is recorded as InChI=1S/C28H38N2O4/c1-5-17-16-30-9-7-19-13-27(33-3)28(34-4)15-22(19)24(30)11-20(17)10-23-21-14-26(32-2)25(31)12-18(21)6-8-29-23/h12-15,17,20,23-24,29,31H,5-11,16H2,1-4H3[5].
  • cephaeline's InChIKey is recorded as DTGZHCFJNDAHEN-UHFFFAOYSA-N[6].
  • cephaeline's chemical formula is recorded as C₂₈H₃₈N₂O₄[7].
  • cephaeline's subclass of is recorded as isoquinoline alkaloid[8].
  • cephaeline's PubChem CID is recorded as 2665[9].
  • cephaeline's ChEBI ID is recorded as 181712[10].
  • cephaeline's found in taxon is recorded as Carapichea ipecacuanha[11].
  • cephaeline's found in taxon is recorded as Alangium longiflorum[12].
  • cephaeline's Human Metabolome Database ID is recorded as HMDB0249806[13].
  • cephaeline's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+466.283157696'}[14].
  • cephaeline's SureChEMBL ID is recorded as 13912580[15].
  • cephaeline's DSSTox substance ID is recorded as DTXSID00862004[16].
  • cephaeline's MassBank accession ID is recorded as MSBNK-RIKEN-PR310641[17].
  • cephaeline's UniChem compound ID is recorded as 30450055[18].

References

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

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Chemical Abstracts Service. Retrieved . 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] ↑ . ChEBI release 2022-06-13. wikidata.org.
  10. [11] ↑ . Chemical Constituents of Psychotria nemorosa Gardner and Antinociceptive Activity. wikidata.org.
  11. [12] ↑ . Two Alangium alkaloids from Alangium lamarckii. wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . MassBank/MassBank-data: release version 2022.06 to wikidata. Retrieved . wikidata.org.
  17. [18] ↑ . 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). cephaeline. Retrieved May 3, 2026, from https://4ort.xyz/entity/cephaeline-q104988715
MLA “cephaeline.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/cephaeline-q104988715.
BibTeX @misc{4ortxyz_cephaeline-q104988715_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{cephaeline}}, year = {2026}, url = {https://4ort.xyz/entity/cephaeline-q104988715}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): cephaeline — https://4ort.xyz/entity/cephaeline-q104988715 (retrieved 2026-05-03)

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