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 (71 views/month).[2]

Key Facts

  • N6-benzyladenine's instance of is recorded as type of chemical entity[3].
  • N6-benzyladenine's chemical structure is recorded as Benzylaminopurine.svg[4].
  • N6-benzyladenine's CAS Registry Number is recorded as 1214-39-7[5].
  • N6-benzyladenine's EC number is recorded as 214-927-5[6].
  • N6-benzyladenine's canonical SMILES is recorded as C1=CC=C(C=C1)CNC2=NC=NC3=C2NC=N3[7].
  • N6-benzyladenine's InChI is recorded as InChI=1S/C12H11N5/c1-2-4-9(5-3-1)6-13-11-10-12(15-7-14-10)17-8-16-11/h1-5,7-8H,6H2,(H2,13,14,15,16,17)[8].
  • N6-benzyladenine's InChIKey is recorded as NWBJYWHLCVSVIJ-UHFFFAOYSA-N[9].
  • N6-benzyladenine's chemical formula is recorded as C₁₂H₁₁N₅[10].
  • N6-benzyladenine's subclass of is recorded as purine alkaloid[11].
  • N6-benzyladenine's Commons category is recorded as 6-Benzylaminopurine[12].
  • N6-benzyladenine's MeSH descriptor ID is recorded as C480551[13].
  • N6-benzyladenine's ChEMBL ID is recorded as CHEMBL228862[14].
  • N6-benzyladenine's PDB structure ID is recorded as 4YXS[15].
  • N6-benzyladenine's PDB structure ID is recorded as 1W1S[16].
  • N6-benzyladenine's PDB structure ID is recorded as 4QP1[17].
  • N6-benzyladenine's PDB structure ID is recorded as 4JHI[18].
  • N6-benzyladenine's PDB structure ID is recorded as 3T4K[19].
  • N6-benzyladenine's Freebase ID is recorded as /m/0dyb_m[20].
  • N6-benzyladenine's UNII is recorded as KXG6A989PS[21].
  • N6-benzyladenine's ChemSpider ID is recorded as 56177[22].
  • N6-benzyladenine's PubChem CID is recorded as 62389[23].
  • N6-benzyladenine's KEGG ID is recorded as C11263[24].
  • N6-benzyladenine's ChEBI ID is recorded as 29022[25].
  • N6-benzyladenine's found in taxon is recorded as Mangifera indica[26].
  • N6-benzyladenine's found in taxon is recorded as Panax ginseng[27].

Why It Matters

N6-benzyladenine ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (71 views/month).[2] N6-benzyladenine has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[28] N6-benzyladenine is known by 28 alternative names across languages and contexts.[29]

References

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

Direct Wikidata claims

  1. [3] . wikidata.org.
  2. [4] . wikidata.org.
  3. [5] . Global Substance Registration System. Retrieved . commonchemistry.cas.org. Provenance: wikidata.org.
  4. [6] . Global Substance Registration System. Retrieved . wikidata.org.
  5. [7] . PubChem. Retrieved . wikidata.org.
  6. [8] . PubChem. Retrieved . wikidata.org.
  7. [9] . PubChem. Retrieved . wikidata.org.
  8. [10] . PubChem. Retrieved . wikidata.org.
  9. [11] . wikidata.org.
  10. [12] . wikidata.org.
  11. [13] . Medical Subject Headings. Retrieved . wikidata.org.
  12. [14] . ChEMBL. Retrieved . wikidata.org.
  13. [15] . Protein Data Bank. Retrieved . wikidata.org.
  14. [16] . Protein Data Bank. Retrieved . wikidata.org.
  15. [17] . Protein Data Bank. Retrieved . wikidata.org.
  16. [18] . Protein Data Bank. Retrieved . wikidata.org.
  17. [19] . Protein Data Bank. Retrieved . wikidata.org.
  18. [20] . Freebase Data Dumps. wikidata.org.
  19. [21] . Global Substance Registration System. Retrieved . wikidata.org.
  20. [22] . Q2311683. Retrieved . wikidata.org.
  21. [23] . PubChem. Retrieved . wikidata.org.
  22. [24] . wikidata.org.
  23. [25] . ChEMBL. Retrieved . wikidata.org.
  24. [26] . Cytokinins of the Developing Mango Fruit : Isolation, Identification, and Changes in Levels during Maturation. wikidata.org.
  25. [27] . High-frequency plant regeneration via somatic embryogenesis and organogenesis and in vitro flowering of regenerated plantlets in Panax ginseng. wikidata.org.

Class ancestry

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

Aggregate / graph-position facts

  1. [2] . Wikimedia Foundation. dumps.wikimedia.org.
  2. [28] . Wikidata sitelinks. wikidata.org.
  3. [29] . 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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