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chebulinic acid

chemical compound
ChemicalSubstance type_of_chemical_entity Q5089010
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chebulinic acid

Summary

chebulinic 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

  • chebulinic acid's instance of is recorded as type of chemical entity[3].
  • chebulinic acid's chemical structure is recorded as Chebulinic acid.svg[4].
  • chebulinic acid's CAS Registry Number is recorded as 18942-26-2[5].
  • chebulinic acid's canonical SMILES is recorded as C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C3C(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(=C7)O)O)O[6].
  • chebulinic acid's InChI is recorded as InChI=1S/C41H32O27/c42-15-1-10(2-16(43)26(15)51)35(56)62-9-22-31-33(66-36(57)11-3-17(44)27(52)18(45)4-11)34(41(63-22)68-37(58)12-5-19(46)28(53)20(47)6-12)67-38(59)13-7-21(48)29(54)32-25(13)24(30(55)40(61)65-32)14(8-23(49)50)39(60)64-31/h1-7,14,22,24,30-31,33-34,41-48,51-55H,8-9H2,(H,49,50)/t14-,22-,24+,30+,31-,33+,34-,41+/m1/s1[7].
  • chebulinic acid's InChIKey is recorded as YGVHOSGNOYKRIH-JHSYUSIXSA-N[8].
  • chebulinic acid's InChIKey is recorded as YGVHOSGNOYKRIH-FJPMMHPYSA-N[9].
  • chebulinic acid's chemical formula is recorded as C₄₁H₃₂O₂₇[10].
  • chebulinic acid's subclass of is recorded as chebulinic acid[11].
  • chebulinic acid's ChEMBL ID is recorded as CHEMBL501154[12].
  • chebulinic acid's Freebase ID is recorded as /m/09v6k33[13].
  • chebulinic acid's ChemSpider ID is recorded as 398347[14].
  • chebulinic acid's PubChem CID is recorded as 452240[15].
  • chebulinic acid's PubChem CID is recorded as 72284[16].
  • chebulinic acid's ChEBI ID is recorded as 3584[17].
  • chebulinic acid's found in taxon is recorded as Terminalia chebula[18].
  • chebulinic acid's found in taxon is recorded as Terminalia[19].
  • chebulinic acid's found in taxon is recorded as Lumnitzera racemosa[20].
  • chebulinic acid's isomeric SMILES is recorded as C1=C(C=C(C(=C1O)O)O)C(=O)OC[C@@H]2[C@@H]3C@@HOC(=O)C7=CC(=C(C(=C7)O)O)OC@HOC(=O)C5=CC(=C(C6=C5C@HC@@HO)O">[21].
  • chebulinic acid's mass is recorded as {'unit': 'Q483261', 'amount': '+956.113096'}[22].
  • chebulinic acid's NSC number is recorded as 69862[23].
  • chebulinic acid's SureChEMBL ID is recorded as 30192061[24].
  • chebulinic acid's SureChEMBL ID is recorded as 29399095[25].
  • chebulinic acid's DSSTox substance ID is recorded as DTXSID30940460[26].
  • chebulinic acid's stereoisomer of is recorded as 2-[(4R,5S,7R,8R,11S,12S,13R,21S)-13,17,18-trihydroxy-2,10,14-trioxo-5,21-bis[(3,4,5-trihydroxybenzoyl)oxy]-7-[(3,4,5-trihydroxybenzoyl)oxymethyl]-3,6,9,15-tetraoxatetracyclo[10.7.1.14,8.016,20]henicosa-1(19),16(20),17-trien-11-yl]acetic acid[27].

Why It Matters

chebulinic acid ranks in the top 6% of type_of_chemical_entity entities by monthly Wikipedia readership (8 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] ↑ . wikidata.org.
  4. [6] ↑ . PubChem. Retrieved . wikidata.org.
  5. [7] ↑ . PubChem. Retrieved . wikidata.org.
  6. [8] ↑ . PubChem. Retrieved . wikidata.org.
  7. [9] ↑ . ChEBI release 2020-09-01. wikidata.org.
  8. [10] ↑ . PubChem. Retrieved . wikidata.org.
  9. [11] ↑ . wikidata.org.
  10. [12] ↑ . ChEMBL. Retrieved . wikidata.org.
  11. [13] ↑ . wikidata.org.
  12. [14] ↑ . Q2311683. Retrieved . wikidata.org.
  13. [15] ↑ . PubChem. Retrieved . wikidata.org.
  14. [16] ↑ . wikidata.org.
  15. [17] ↑ . ChEBI release 2019-10-02. wikidata.org.
  16. [18] ↑ . Inhibition of cancer cell growth by crude extract and the phenolics of Terminalia chebula retz. fruit. wikidata.org.
  17. [19] ↑ . 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.
  18. [20] ↑ . Antihypertensive Activity of Corilagin and Chebulinic Acid, Tannins from Lumnitzera, racemosa. wikidata.org.
  19. [21] ↑ . PubChem. Retrieved . wikidata.org.
  20. [22] ↑ . PubChem. Retrieved . wikidata.org.
  21. [23] ↑ . wikidata.org.
  22. [24] ↑ . wikidata.org.
  23. [25] ↑ . wikidata.org.
  24. [26] ↑ . wikidata.org.
  25. [27] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

Aggregate / graph-position facts

  1. [2] ↑ . Wikimedia Foundation. dumps.wikimedia.org.

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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). chebulinic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/chebulinic-acid
MLA “chebulinic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/chebulinic-acid.
BibTeX @misc{4ortxyz_chebulinic-acid_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{chebulinic acid}}, year = {2026}, url = {https://4ort.xyz/entity/chebulinic-acid}, 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. 27d ago · Shuaib-bot bot · 2026-05-02 view diff on Wikidata ↗
    Instance of → —
    Stereoisomer of → 2-[(4R,5S,7R,8R,11S,12S,13R,21S)-13,17,18-trihydroxy-2,10,14-trioxo-5,21-bis[(3,4,5-trihydroxybenzoyl)oxy]-7-[(3,4,5-trihydroxybenzoyl)oxymethyl]-3,6,9,15-tetraoxatetracyclo[10.7.1.14,8.016,20]henicosa-1(19),16(20),17-trien-11-yl]acetic acid
    Found in taxon → Terminalia chebula, Terminalia, Lumnitzera racemosa
    Subclass of → chebulinic acid
    + 4 other properties edited (see Wikidata diff for full list)
    "/* wbeditentity-update-languages-and-other-short:0||ur */"
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