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corilagin

chemical compound
ChemicalSubstance type_of_chemical_entity Q909822
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corilagin

Summary

corilagin is a type of chemical entity[1]. corilagin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (3 views/month).[2]

Key Facts

  • corilagin's instance of is recorded as type of chemical entity[3].
  • corilagin's chemical structure is recorded as Corilagin.svg[4].
  • corilagin's CAS Registry Number is recorded as 23094-69-1[5].
  • corilagin's canonical SMILES is recorded as C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O[6].
  • corilagin's InChI is recorded as InChI=1S/C27H22O18/c28-9-1-6(2-10(29)16(9)32)24(39)45-27-22(38)23-19(35)13(43-27)5-42-25(40)7-3-11(30)17(33)20(36)14(7)15-8(26(41)44-23)4-12(31)18(34)21(15)37/h1-4,13,19,22-23,27-38H,5H2/t13-,19-,22-,23+,27+/m1/s1[7].
  • corilagin's InChIKey is recorded as TUSDEZXZIZRFGC-XIGLUPEJSA-N[8].
  • corilagin's chemical formula is recorded as C₂₇H₂₂O₁₈[9].
  • corilagin's subclass of is recorded as macrolides[10].
  • corilagin's ChEMBL ID is recorded as CHEMBL449392[11].
  • corilagin's Freebase ID is recorded as /m/0b6nqnd[12].
  • corilagin's UNII is recorded as 62LOS9TW6D[13].
  • corilagin's ChemSpider ID is recorded as 66248[14].
  • corilagin's PubChem CID is recorded as 73568[15].
  • corilagin's KEGG ID is recorded as C10219[16].
  • corilagin's ChEBI ID is recorded as 3884[17].
  • corilagin's found in taxon is recorded as Phyllanthus niruri[18].
  • corilagin's found in taxon is recorded as Euphorbia hyssopifolia[19].
  • corilagin's found in taxon is recorded as Acalypha hispida[20].
  • corilagin's found in taxon is recorded as Terminalia catappa[21].
  • corilagin's found in taxon is recorded as Terminalia chebula[22].
  • corilagin's found in taxon is recorded as Cunonia macrophylla[23].
  • corilagin's found in taxon is recorded as Geranium thunbergii[24].
  • corilagin's found in taxon is recorded as Pelargonium reniforme[25].
  • corilagin's found in taxon is recorded as pomegranate[26].
  • corilagin's found in taxon is recorded as Acalypha australis[27].

Why It Matters

corilagin ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (3 views/month).[2] corilagin has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28] corilagin is known by 4 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] ↑ . ChEBI. Retrieved . wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . PubChem. Retrieved . wikidata.org.
  8. [10] ↑ . wikidata.org.
  9. [11] ↑ . ChEMBL. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . Q2311683. Retrieved . wikidata.org.
  13. [15] ↑ . PubChem. Retrieved . wikidata.org.
  14. [16] ↑ . ChEBI. Retrieved . wikidata.org.
  15. [17] ↑ . ChEBI. Retrieved . wikidata.org.
  16. [18] ↑ . Validated HPLC method for the standardization of Phyllanthus niruri (herb and commercial extracts) using corilagin as a phytochemical marker. wikidata.org.
  17. [19] ↑ . HIV-1 reverse transcriptase inhibitory principles from Chamaesyce hyssopifolia. wikidata.org.
  18. [20] ↑ . Antimicrobial constituents of the leaves of Acalypha wilkesiana and Aacalypha hispida. wikidata.org.
  19. [21] ↑ . Tannins and related compounds. XLII. Isolation and characterization of four new hydrolyzable tannins, terflavins A and B, tergallagin and tercatain from the leaves of Terminalia catappa L.. wikidata.org.
  20. [22] ↑ . Tannins and related compounds. CII. Structures of terchebulin, an ellagitannin having a novel tetraphenylcarboxylic acid (terchebulic acid) moiety, and biogenetically related tannins from Terminalia chebula Retz.. wikidata.org.
  21. [23] ↑ . Bioactive ellagitannins from Cunonia macrophylla, an endemic Cunoniaceae from New Caledonia. wikidata.org.
  22. [24] ↑ . Elaeocarpusin, a proto-type of geraniin from Geranium thunbergii.. wikidata.org.
  23. [25] ↑ . Pelargoniins, new ellagitannins from Pelargonium reniforme. wikidata.org.
  24. [26] ↑ . Two ellagitannins from Punica granatum heartwood. wikidata.org.
  25. [27] ↑ . Phenolic compounds from Acalypha australis. 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). corilagin. Retrieved May 3, 2026, from https://4ort.xyz/entity/corilagin
MLA “corilagin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/corilagin.
BibTeX @misc{4ortxyz_corilagin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{corilagin}}, year = {2026}, url = {https://4ort.xyz/entity/corilagin}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): corilagin — https://4ort.xyz/entity/corilagin (retrieved 2026-05-03)

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