Chebulagic acid

group of stereoisomers with the chemical formula C₄₁H₃₀O₂₇
ChemicalSubstance group_of_stereoisomers Q103785778
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Summary

Chebulagic acid is a group of stereoisomers[1].

Key Facts

  • Chebulagic acid's instance of is recorded as group of stereoisomers[2].
  • Chebulagic acid's CAS Registry Number is recorded as 23094-71-5[3].
  • Chebulagic acid's canonical SMILES is recorded as O=C(O)CC1C(=O)OC2C3OC(OC(=O)C4=CC(O)=C(O)C(O)=C4)C(OC(=O)C5=CC(O)=C(O)C=6OC(=O)C(O)C1C65)C2OC(=O)C7=CC(O)=C(O)C(O)=C7C=8C(O)=C(O)C(O)=CC8C(=O)OC3[4].
  • 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)[5].
  • Chebulagic acid's InChIKey is recorded as HGJXAVROWQLCTP-UHFFFAOYSA-N[6].
  • Chebulagic acid's chemical formula is recorded as C₄₁H₃₀O₂₇[7].
  • Chebulagic acid's subclass of is recorded as macrolides[8].
  • Chebulagic acid's PubChem CID is recorded as 250397[9].
  • Chebulagic acid's found in taxon is recorded as Phyllanthus[10].
  • Chebulagic acid's found in taxon is recorded as Terminalia chebula[11].
  • Chebulagic acid's found in taxon is recorded as Phyllanthus emblica[12].
  • Chebulagic acid's found in taxon is recorded as Acalypha indica[13].
  • Chebulagic acid's Human Metabolome Database ID is recorded as HMDB0249897[14].
  • Chebulagic acid's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+954.0974457'}[15].
  • Chebulagic acid's SureChEMBL ID is recorded as 1877153[16].
  • Chebulagic acid's DSSTox substance ID is recorded as DTXSID401026980[17].
  • Chebulagic acid's UniChem compound ID is recorded as 27155055[18].
  • Chebulagic acid's Probes And Drugs ID is recorded as PD100424[19].

References

Programmatic citations — every numbered marker resolves to a verifiable graph row below.

Direct Wikidata claims

  1. [2] ↑ . wikidata.org.
  2. [3] ↑ . Chemical Abstracts Service. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . Phyllanemblinins A−F, New Ellagitannins from Phyllanthus emblica. wikidata.org.
  10. [11] ↑ . Inhibition of HIV-1 integrase by galloyl glucoses from Terminalia chebula and flavonol glycoside gallates from Euphorbia pekinensis. wikidata.org.
  11. [12] ↑ . Novel norsesquiterpenoids from the roots of Phyllanthus emblica. wikidata.org.
  12. [13] ↑ . Phenolics fromAcalypha indica. wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . UniChem. wikidata.org.
  18. [19] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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BibTeX @misc{4ortxyz_chebulagic-acid-q103785778_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Chebulagic acid}}, year = {2026}, url = {https://4ort.xyz/entity/chebulagic-acid-q103785778}, note = {Accessed: 2026-05-03}}
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