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chebulagic acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q5089009
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chebulagic acid

Summary

chebulagic acid is a type of chemical entity[1]. It ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (8 views/month).[2]

Key Facts

  • chebulagic acid's instance of is recorded as type of chemical entity[3].
  • chebulagic acid's chemical structure is recorded as Chebulagic acid.svg[4].
  • chebulagic acid's canonical SMILES is recorded as C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C(C(C(=O)O3)CC(=O)O)C(C(=O)O6)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O[5].
  • chebulagic acid's InChI is recorded as InChI=1S/C41H30O27/c42-13-1-8(2-14(43)24(13)49)35(56)68-41-34-33-31(64-39(60)12(6-19(47)48)22-23-11(38(59)67-34)5-17(46)27(52)32(23)65-40(61)30(22)55)18(63-41)7-62-36(57)9-3-15(44)25(50)28(53)20(9)21-10(37(58)66-33)4-16(45)26(51)29(21)54/h1-5,12,18,22,30-31,33-34,41-46,49-55H,6-7H2,(H,47,48)/t12-,18+,22-,30-,31+,33-,34+,41-/m0/s1[6].
  • chebulagic acid's InChIKey is recorded as HGJXAVROWQLCTP-YABCKIEDSA-N[7].
  • chebulagic acid's chemical formula is recorded as C₄₁H₃₀O₂₇[8].
  • chebulagic acid's subclass of is recorded as macrolides[9].
  • chebulagic acid's MeSH descriptor ID is recorded as C076178[10].
  • chebulagic acid's ChEMBL ID is recorded as CHEMBL525240[11].
  • chebulagic acid's Freebase ID is recorded as /m/04yh0r2[12].
  • chebulagic acid's ChemSpider ID is recorded as 391031[13].
  • chebulagic acid's PubChem CID is recorded as 442674[14].
  • chebulagic acid's KEGG ID is recorded as C10214[15].
  • chebulagic acid's ChEBI ID is recorded as 3583[16].
  • chebulagic acid's found in taxon is recorded as Cunonia macrophylla[17].
  • chebulagic acid's found in taxon is recorded as Excoecaria agallocha[18].
  • chebulagic acid's found in taxon is recorded as Vernicia fordii[19].
  • chebulagic acid's found in taxon is recorded as Euphorbia humifusa[20].
  • chebulagic acid's found in taxon is recorded as Euphorbia maculata[21].
  • chebulagic acid's found in taxon is recorded as Excoecaria kawakamii[22].
  • chebulagic acid's found in taxon is recorded as Macaranga sinensis[23].
  • chebulagic acid's found in taxon is recorded as Terminalia chebula[24].
  • chebulagic acid's found in taxon is recorded as Terminalia catappa[25].
  • chebulagic acid's found in taxon is recorded as Phyllanthus flexuosus[26].
  • chebulagic acid's found in taxon is recorded as Caryocar villosum[27].

Why It Matters

chebulagic acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (8 views/month).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[28]

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] ↑ . PubChem. Retrieved . wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . wikidata.org.
  8. [10] ↑ . Medical Subject Headings. Retrieved . wikidata.org.
  9. [11] ↑ . ChEMBL. Retrieved . wikidata.org.
  10. [12] ↑ . wikidata.org.
  11. [13] ↑ . Q2311683. Retrieved . wikidata.org.
  12. [14] ↑ . PubChem. Retrieved . wikidata.org.
  13. [15] ↑ . ChEBI. Retrieved . wikidata.org.
  14. [16] ↑ . ChEBI. Retrieved . wikidata.org.
  15. [17] ↑ . Bioactive ellagitannins from Cunonia macrophylla, an endemic Cunoniaceae from New Caledonia. wikidata.org.
  16. [18] ↑ . Inhibitory effects of polyphenols toward HCV from the mangrove plant Excoecaria agallocha L.. wikidata.org.
  17. [19] ↑ . Tannins and related compounds. XCII. Isolation and characterization of cyanogenic ellagitannins, aleurinins A and B, and a related O-glycosidic ellagitannin, aleurinin C, from Aleurites fordii Hemsley.. wikidata.org.
  18. [20] ↑ . Tannins and related polyphenols of euphorbiaceous plants. XI. Three new hydrolyzable tannins and a polyphenol glucoside from Euphorbia humifusa. wikidata.org.
  19. [21] ↑ . Four new hydrolyzable tannins and an acylated flavonol glycoside from Euphorbiamaculata. wikidata.org.
  20. [22] ↑ . Tannins and related compounds. XCVIII. Structures of three new dimeric ellagitannins, excoecarianin and excoecarinins A and B, isolated from the leaves of Excoecaria kawakamii Hayata.. wikidata.org.
  21. [23] ↑ . Tannins and related compounds. XCVI. Structures of macaranins and macarinins, new hydrolyzable tannins possessing macaranoyl and tergalloyl ester groups, from the leaves of Macaranga sinensis (Baill.) Muell.-Arg.. wikidata.org.
  22. [24] ↑ . Polyphenolic compounds in the fruits of Egyptian medicinal plants (Terminalia bellerica, Terminalia chebula and Terminalia horrida): characterization, quantitation and determination of antioxidant capacities. wikidata.org.
  23. [25] ↑ . Antioxidant and hepatoprotective actions of medicinal herb, Terminalia catappa L. from Okinawa Island and its tannin corilagin. wikidata.org.
  24. [26] ↑ . Tannins and Related Polyphenols of Euphorbiaceous Plants. IX. Hydrolyzable Tannins with 1C4 Glucose Core from Phyllanthus flexuosus MUELL. ARG.. wikidata.org.
  25. [27] ↑ . Phenolic glycosides from the stem bark of Caryocar villosum and C. glabrum. 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.

📑 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). chebulagic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/chebulagic-acid
MLA “chebulagic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/chebulagic-acid.
BibTeX @misc{4ortxyz_chebulagic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{chebulagic acid}}, year = {2026}, url = {https://4ort.xyz/entity/chebulagic-acid}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): chebulagic acid — https://4ort.xyz/entity/chebulagic-acid (retrieved 2026-05-03)

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