N6-benzyladenine

chemical compound
ChemicalSubstance type_of_chemical_entity Q419946
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N6-benzyladenine

Summary

N6-benzyladenine is a type of chemical entity[1]. N6-benzyladenine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (130 views/month).[2]

Key Facts

  • N6-benzyladenine's instance of is recorded as type of chemical entity[3].
  • N6-benzyladenine's canonical SMILES is recorded as C1=CC=C(C=C1)CNC2=NC=NC3=C2NC=N3[4].
  • N6-benzyladenine's chemical formula is recorded as C₁₂H₁₁N₅[5].
  • N6-benzyladenine is a type of purine alkaloid[6].
  • N6-benzyladenine's Commons category is recorded as 6-Benzylaminopurine[7].
  • N6-benzyladenine's found in taxon is recorded as Mangifera indica[8].
  • N6-benzyladenine's found in taxon is recorded as Panax ginseng[9].
  • N6-benzyladenine's found in taxon is recorded as Humulus lupulus[10].
  • N6-benzyladenine's found in taxon is recorded as Nymphaea alba[11].
  • N6-benzyladenine's found in taxon is recorded as Cocos nucifera[12].
  • N6-benzyladenine's found in taxon is recorded as Oryza sativa[13].
  • N6-benzyladenine's found in taxon is recorded as Rehmannia glutinosa[14].
  • N6-benzyladenine's found in taxon is recorded as Trifolium pratense[15].
  • N6-benzyladenine's mass is recorded as {'unit': 'Q483261', 'amount': '+225.101'}[16].
  • N6-benzyladenine's melting point is recorded as {'unit': 'Q25267', 'amount': '+231'}[17].
  • N6-benzyladenine's subject has role is recorded as plant growth regulator[18].
  • N6-benzyladenine's subject has role is recorded as primary metabolite[19].

Why It Matters

N6-benzyladenine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (130 views/month).[2] N6-benzyladenine has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[20] N6-benzyladenine is known by 28 alternative names across languages and contexts.[21]

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] . Cytokinins of the Developing Mango Fruit : Isolation, Identification, and Changes in Levels during Maturation. wikidata.org.
  7. [9] . High-frequency plant regeneration via somatic embryogenesis and organogenesis and in vitro flowering of regenerated plantlets in Panax ginseng. wikidata.org.
  8. [10] . In vitro tetraploid induction and generation of tetraploids from mixoploids in hop (Humulus lupulus L.). wikidata.org.
  9. [11] . Breaking Seed Dormancy of Water Lily (Nymphaea AlbaL.) UnderIn VitroConditons. wikidata.org.
  10. [12] . Simultaneous analysis of different classes of phytohormones in coconut (Cocos nucifera L.) water using high-performance liquid chromatography and liquid chromatography-tandem mass spectrometry after solid-phase extraction. wikidata.org.
  11. [13] . The interaction between nitrogen availability and auxin, cytokinin, and strigolactone in the control of shoot branching in rice (Oryza sativa L.). wikidata.org.
  12. [14] . Shoot organogenesis, molecular analysis and secondary metabolite production of micropropagated Rehmannia glutinosa Libosch. wikidata.org.
  13. [15] . LC-ESI-MS study of the flavonoid glycoside malonates of red clover (Trifolium pratense). wikidata.org.
  14. [16] . PubChem. Retrieved . wikidata.org.
  15. [17] . Jean-Claude Bradley Open Melting Point Dataset. wikidata.org.
  16. [18] . Medical Subject Headings. Retrieved . wikidata.org.
  17. [19] . Reactome. plantreactome.gramene.org. Provenance: wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [20] . Wikidata sitelinks. wikidata.org.
  3. [21] . Wikidata aliases. wikidata.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). N6-benzyladenine. Retrieved May 3, 2026, from https://4ort.xyz/entity/n6-benzyladenine
MLA “N6-benzyladenine.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/n6-benzyladenine.
BibTeX @misc{4ortxyz_n6-benzyladenine_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{N6-benzyladenine}}, year = {2026}, url = {https://4ort.xyz/entity/n6-benzyladenine}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): N6-benzyladenine — https://4ort.xyz/entity/n6-benzyladenine (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. 8d ago · Nabbegat · 2026-06-19 view diff on Wikidata ↗
    Instance of type of chemical entity
    Subclass of
    Aliases
    Found in taxon Mangifera indica, Panax ginseng, Humulus lupulus +5
    + 5 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-short:0||tr */ QuickStatements 3.0 [[:toollabs:qs-dev/batch/37300|batch #37300]]"
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