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Nupharamine

chemical compound
ChemicalSubstance type_of_chemical_entity Q15425305
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Nupharamine

Summary

Nupharamine is a type of chemical entity[1]. Nupharamine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (6 views/month).[2]

Key Facts

  • Nupharamine's instance of is recorded as type of chemical entity[3].
  • Nupharamine's canonical SMILES is recorded as CC1CCC(NC1CCC(C)(C)O)C2=COC=C2[4].
  • Nupharamine's chemical formula is recorded as C₁₅H₂₅NO₂[5].
  • Nupharamine is a type of farnesane sesquiterpenoid[6].
  • Nupharamine is a type of piperidine alkaloids[7].
  • Nupharamine's found in taxon is recorded as Nuphar japonicum[8].
  • Nupharamine's found in taxon is recorded as Nuphar japonica[9].
  • Nupharamine's isomeric SMILES is recorded as C[C@@H]1CCC@HC2=COC=C2C@HC2=COC=C2">[10].
  • Nupharamine's mass is recorded as {'unit': 'Q483261', 'amount': '+251.189'}[11].
  • Nupharamine's stereoisomer of is recorded as 3-Epinupharamine[12].

Why It Matters

Nupharamine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (6 views/month).[2]

References

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

Direct Wikidata claims

  1. [3] ↑ . wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [5] ↑ . PubChem. Retrieved . wikidata.org.
  4. [6] ↑ . wikidata.org.
  5. [7] ↑ . wikidata.org.
  6. [8] ↑ . A concise enantiospecific synthesis of nuphar piperidine alkaloids: total synthesis of (–)-anhydronupharamine, (–)-nupharamine, (–)-nuphenine and (+)-3-epinupharamine. wikidata.org.
  7. [9] ↑ . A concise enantiospecific synthesis of nuphar piperidine alkaloids: total synthesis of (–)-anhydronupharamine, (–)-nupharamine, (–)-nuphenine and (+)-3-epinupharamine. wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . PubChem. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.

📑 Cite this page

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). Nupharamine. Retrieved May 3, 2026, from https://4ort.xyz/entity/nupharamine
MLA “Nupharamine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/nupharamine.
BibTeX @misc{4ortxyz_nupharamine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Nupharamine}}, year = {2026}, url = {https://4ort.xyz/entity/nupharamine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Nupharamine — https://4ort.xyz/entity/nupharamine (retrieved 2026-05-03)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 4w ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Instance of → —
    Found in taxon → Nuphar japonicum, Nuphar japonica
    Stereoisomer of → 3-Epinupharamine
    Subclass of → —
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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