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(±)-nuciferine

pair of enantiomers
ChemicalSubstance group_of_stereoisomers Q105197609
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(±)-nuciferine

Summary

(±)-nuciferine is a group of stereoisomers[1].

Key Facts

  • (±)-nuciferine's instance of is recorded as group of stereoisomers[2].
  • (±)-nuciferine's CAS Registry Number is recorded as 5868-18-8[3].
  • (±)-nuciferine's canonical SMILES is recorded as O(C=1C=C2C3=C(C1OC)C4=CC=CC=C4CC3N(C)CC2)C[4].
  • (±)-nuciferine's InChI is recorded as InChI=1S/C19H21NO2/c1-20-9-8-13-11-16(21-2)19(22-3)18-14-7-5-4-6-12(14)10-15(20)17(13)18/h4-7,11,15H,8-10H2,1-3H3[5].
  • (±)-nuciferine's InChIKey is recorded as ORJVQPIHKOARKV-UHFFFAOYSA-N[6].
  • (±)-nuciferine's chemical formula is recorded as C₁₉H₂₁NO₂[7].
  • (±)-nuciferine's subclass of is recorded as aporphine alkaloids[8].
  • (±)-nuciferine's Commons category is recorded as Nuciferine[9].
  • (±)-nuciferine's PubChem CID is recorded as 3108374[10].
  • (±)-nuciferine's found in taxon is recorded as Nelumbo nucifera[11].
  • (±)-nuciferine's found in taxon is recorded as Q158783[12].
  • (±)-nuciferine's Human Metabolome Database ID is recorded as HMDB0243520[13].
  • (±)-nuciferine's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+295.157228912'}[14].
  • (±)-nuciferine's SureChEMBL ID is recorded as 634777[15].
  • (±)-nuciferine's NMRShiftDB structure ID is recorded as 10017671[16].
  • (±)-nuciferine's UniChem compound ID is recorded as 26854025[17].
  • (±)-nuciferine's Probes And Drugs ID is recorded as PD056568[18].

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] ↑ . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . An aporphine alkaloid fromNelumbo nuciferaas an acetylcholinesterase inhibitor and the primary investigation for structure–activity correlations. wikidata.org.
  11. [12] ↑ . Alkaloids of Liriodendron tulipifera. wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . UniChem. wikidata.org.
  17. [18] ↑ . 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). (±)-nuciferine. Retrieved May 3, 2026, from https://4ort.xyz/entity/-nuciferine
MLA “(±)-nuciferine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/-nuciferine.
BibTeX @misc{4ortxyz_-nuciferine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{(±)-nuciferine}}, year = {2026}, url = {https://4ort.xyz/entity/-nuciferine}, note = {Accessed: 2026-05-03}}
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