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mangiferin

chemical compound
ChemicalSubstance type_of_chemical_entity Q1074417
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mangiferin

Summary

mangiferin is a type of chemical entity[1]. mangiferin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (29 views/month).[2]

Key Facts

  • mangiferin's instance of is recorded as type of chemical entity[3].
  • mangiferin's chemical structure is recorded as Mangiferin.PNG[4].
  • mangiferin's CAS Registry Number is recorded as 4773-96-0[5].
  • mangiferin's EC number is recorded as 624-757-7[6].
  • mangiferin's canonical SMILES is recorded as C1=C2C(=CC(=C1O)O)OC3=CC(=C(C(=C3C2=O)O)C4C(C(C(C(O4)CO)O)O)O)O[7].
  • mangiferin's InChI is recorded as InChI=1S/C19H18O11/c20-4-11-15(25)17(27)18(28)19(30-11)12-8(23)3-10-13(16(12)26)14(24)5-1-6(21)7(22)2-9(5)29-10/h1-3,11,15,17-23,25-28H,4H2/t11-,15-,17+,18-,19+/m1/s1[8].
  • mangiferin's InChIKey is recorded as AEDDIBAIWPIIBD-ZJKJAXBQSA-N[9].
  • mangiferin's chemical formula is recorded as C₁₉H₁₈O₁₁[10].
  • mangiferin's subclass of is recorded as 1,3,6,7-Tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one[11].
  • mangiferin's Commons category is recorded as Mangiferin[12].
  • mangiferin's ChEMBL ID is recorded as CHEMBL455364[13].
  • mangiferin's Freebase ID is recorded as /m/0c41lg1[14].
  • mangiferin's UNII is recorded as 1M84LD0UMD[15].
  • mangiferin's ChemSpider ID is recorded as 4444966[16].
  • mangiferin's PubChem CID is recorded as 5281647[17].
  • mangiferin's KEGG ID is recorded as C10077[18].
  • mangiferin's ChEBI ID is recorded as 6682[19].
  • mangiferin's found in taxon is recorded as Iris ensata[20].
  • mangiferin's found in taxon is recorded as Heptaptera triquetra[21].
  • mangiferin's found in taxon is recorded as Moraea australis[22].
  • mangiferin's found in taxon is recorded as Moraea setifolia[23].
  • mangiferin's found in taxon is recorded as Iris cengialti[24].
  • mangiferin's found in taxon is recorded as Iris suaveolens[25].
  • mangiferin's found in taxon is recorded as Iris pumila[26].
  • mangiferin's found in taxon is recorded as Iris unguicularis[27].

Why It Matters

mangiferin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (29 views/month).[2] mangiferin has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[28] mangiferin is known by 7 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] ↑ . ECHA Substance Infocard database. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. wikidata.org.
  6. [8] ↑ . PubChem. wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . PubChem. wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . wikidata.org.
  13. [15] ↑ . Global Substance Registration System. Retrieved . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . wikidata.org.
  16. [18] ↑ . wikidata.org.
  17. [19] ↑ . ChEBI release 2021-03-01. wikidata.org.
  18. [20] ↑ . Xanthone glycosides of Iris ensata. wikidata.org.
  19. [21] ↑ . Determination of phenolic compounds in Colladonia triquetra L.. wikidata.org.
  20. [22] ↑ . Biflavonoids, Quinones and Xanthones as Rare Chemical Markers in the Family Iridaceae. wikidata.org.
  21. [23] ↑ . Biflavonoids, Quinones and Xanthones as Rare Chemical Markers in the Family Iridaceae. wikidata.org.
  22. [24] ↑ . Biflavonoids, Quinones and Xanthones as Rare Chemical Markers in the Family Iridaceae. wikidata.org.
  23. [25] ↑ . Biflavonoids, Quinones and Xanthones as Rare Chemical Markers in the Family Iridaceae. wikidata.org.
  24. [26] ↑ . Biflavonoids, Quinones and Xanthones as Rare Chemical Markers in the Family Iridaceae. wikidata.org.
  25. [27] ↑ . Biflavonoids, Quinones and Xanthones as Rare Chemical Markers in the Family Iridaceae. 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). mangiferin. Retrieved May 3, 2026, from https://4ort.xyz/entity/mangiferin
MLA “mangiferin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/mangiferin.
BibTeX @misc{4ortxyz_mangiferin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{mangiferin}}, year = {2026}, url = {https://4ort.xyz/entity/mangiferin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): mangiferin — https://4ort.xyz/entity/mangiferin (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. 23d ago · Shuaib-bot bot · 2026-05-02 view diff on Wikidata ↗
    Found in taxon → Iris ensata, Heptaptera triquetra, Moraea australis +173
    Instance of → type of chemical entity
    Subclass of → 1,3,6,7-Tetrahydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]xanthen-9-one
    Mass → {'unit': 'Q483261', 'amount': '+422.084911396'}
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||ur */"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.