chebulinic acid

group of stereoisomers with the chemical formula C₄₁H₃₂O₂₇
ChemicalSubstance group_of_stereoisomers Q105348274
Press Enter · cited answer in seconds

chebulinic acid

Summary

chebulinic acid is a group of stereoisomers[1].

Key Facts

  • chebulinic acid's instance of is recorded as group of stereoisomers[2].
  • chebulinic acid's canonical SMILES is recorded as O=C(O)CC1C(=O)OC2C(OC(OC(=O)C3=CC(O)=C(O)C(O)=C3)C(OC(=O)C4=CC(O)=C(O)C=5OC(=O)C(O)C1C54)C2OC(=O)C6=CC(O)=C(O)C(O)=C6)COC(=O)C7=CC(O)=C(O)C(O)=C7[3].
  • 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)[4].
  • chebulinic acid's InChIKey is recorded as YGVHOSGNOYKRIH-UHFFFAOYSA-N[5].
  • chebulinic acid's chemical formula is recorded as C₄₁H₃₂O₂₇[6].
  • chebulinic acid's subclass of is recorded as chemical compound[7].
  • chebulinic acid's PubChem CID is recorded as 250396[8].
  • chebulinic acid's found in taxon is recorded as Terminalia chebula[9].
  • chebulinic acid's Human Metabolome Database ID is recorded as HMDB0249898[10].
  • chebulinic acid's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+956.1130957640007'}[11].
  • chebulinic acid's SureChEMBL ID is recorded as 992969[12].
  • chebulinic acid's DSSTox substance ID is recorded as DTXSID30940460[13].
  • chebulinic acid's UniChem compound ID is recorded as 27155054[14].
  • chebulinic acid's Probes And Drugs ID is recorded as PD118039[15].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . wikidata.org.
  3. [4] . wikidata.org.
  4. [5] . wikidata.org.
  5. [6] . wikidata.org.
  6. [7] . wikidata.org.
  7. [8] . PubChem. Retrieved . wikidata.org.
  8. [9] . 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.
  9. [10] . wikidata.org.
  10. [11] . wikidata.org.
  11. [12] . wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . UniChem. wikidata.org.
  14. [15] . wikidata.org.

Class ancestry

  1. [1] . Wikidata. 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). chebulinic acid. Retrieved May 3, 2026, from https://4ort.xyz/entity/chebulinic-acid-q105348274
MLA “chebulinic acid.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/chebulinic-acid-q105348274.
BibTeX @misc{4ortxyz_chebulinic-acid-q105348274_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{chebulinic acid}}, year = {2026}, url = {https://4ort.xyz/entity/chebulinic-acid-q105348274}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): chebulinic acid — https://4ort.xyz/entity/chebulinic-acid-q105348274 (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/chebulinic-acid-q105348274 · Last refreshed: