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narirutin

chemical compound
ChemicalSubstance type_of_chemical_entity Q13569061
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narirutin

Summary

narirutin is a type of chemical entity[1]. narirutin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (16 views/month).[2]

Key Facts

  • narirutin's instance of is recorded as type of chemical entity[3].
  • narirutin's chemical structure is recorded as Narirutin.png[4].
  • narirutin's CAS Registry Number is recorded as 14259-46-2[5].
  • narirutin's EC number is recorded as 238-138-0[6].
  • narirutin's canonical SMILES is recorded as CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)O)O)O)O)O)O[7].
  • narirutin's InChI is recorded as InChI=1S/C27H32O14/c1-10-20(31)22(33)24(35)26(38-10)37-9-18-21(32)23(34)25(36)27(41-18)39-13-6-14(29)19-15(30)8-16(40-17(19)7-13)11-2-4-12(28)5-3-11/h2-7,10,16,18,20-29,31-36H,8-9H2,1H3/t10-,16-,18+,20-,21+,22+,23-,24+,25+,26+,27+/m0/s1[8].
  • narirutin's InChIKey is recorded as HXTFHSYLYXVTHC-AJHDJQPGSA-N[9].
  • narirutin's chemical formula is recorded as C₂₇H₃₂O₁₄[10].
  • narirutin's subclass of is recorded as 5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one[11].
  • narirutin's Commons category is recorded as Narirutin[12].
  • narirutin's ChEMBL ID is recorded as CHEMBL446246[13].
  • narirutin's UNII is recorded as 06M5EAT0YC[14].
  • narirutin's ChemSpider ID is recorded as 390871[15].
  • narirutin's PubChem CID is recorded as 442431[16].
  • narirutin's KEGG ID is recorded as C09793[17].
  • narirutin's ChEBI ID is recorded as 28705[18].
  • narirutin's found in taxon is recorded as Citrus excelsa[19].
  • narirutin's found in taxon is recorded as Citrus grandis[20].
  • narirutin's found in taxon is recorded as Citrus hystrix[21].
  • narirutin's found in taxon is recorded as Citrus latipes[22].
  • narirutin's found in taxon is recorded as Citrus longispina[23].
  • narirutin's found in taxon is recorded as Citrus shunkokan[24].
  • narirutin's found in taxon is recorded as Citrus sulcata[25].
  • narirutin's found in taxon is recorded as Citrus tengu[26].
  • narirutin's found in taxon is recorded as Citrus ujukitsu[27].

Why It Matters

narirutin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (16 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] ↑ . wikidata.org.
  3. [5] ↑ . ChEBI. 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] ↑ . ChEMBL. Retrieved . wikidata.org.
  12. [14] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  13. [15] ↑ . Q2311683. Retrieved . wikidata.org.
  14. [16] ↑ . PubChem. Retrieved . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . ChEBI. Retrieved . wikidata.org.
  17. [19] ↑ . Phenolic composition of various tissues of rutaceae species. wikidata.org.
  18. [20] ↑ . High-performance liquid chromatographic determination of naturally occurring flavonoids in Citrus with a photodiode-array detector. wikidata.org.
  19. [21] ↑ . Limonoid and flavonoid composition in varieties of Papeda and Papedocitrus. wikidata.org.
  20. [22] ↑ . Limonoid and flavonoid composition in varieties of Papeda and Papedocitrus. wikidata.org.
  21. [23] ↑ . Phenolic composition of various tissues of rutaceae species. wikidata.org.
  22. [24] ↑ . Phenolic composition of various tissues of rutaceae species. wikidata.org.
  23. [25] ↑ . Phenolic composition of various tissues of rutaceae species. wikidata.org.
  24. [26] ↑ . Phenolic composition of various tissues of rutaceae species. wikidata.org.
  25. [27] ↑ . Phenolic composition of various tissues of rutaceae species. 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). narirutin. Retrieved May 3, 2026, from https://4ort.xyz/entity/narirutin
MLA “narirutin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/narirutin.
BibTeX @misc{4ortxyz_narirutin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{narirutin}}, year = {2026}, url = {https://4ort.xyz/entity/narirutin}, note = {Accessed: 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. 22d ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Stereoisomer of → (2S)-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one
    Instance of → type of chemical entity
    Subclass of → —
    Subclass of → 5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update:0| */"
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