Heterophylliin A

group of stereoisomers with the chemical formula C₃₄H₂₆O₂₂
ChemicalSubstance group_of_stereoisomers Q105181290
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Heterophylliin A

Summary

Heterophylliin An is a group of stereoisomers[1].

Key Facts

  • Heterophylliin A's instance of is recorded as group of stereoisomers[2].
  • Heterophylliin A's CAS Registry Number is recorded as 87687-52-3[3].
  • Heterophylliin A's canonical SMILES is recorded as O=C(OC1OC2COC(=O)C=3C=C(O)C(O)=C(O)C3C4=C(O)C(O)=C(O)C=C4C(=O)OC2C(OC(=O)C5=CC(O)=C(O)C(O)=C5)C1O)C6=CC(O)=C(O)C(O)=C6[4].
  • Heterophylliin A's InChI is recorded as InChI=1S/C34H26O22/c35-12-1-8(2-13(36)21(12)41)30(48)55-29-27(47)34(56-31(49)9-3-14(37)22(42)15(38)4-9)53-18-7-52-32(50)10-5-16(39)23(43)25(45)19(10)20-11(33(51)54-28(18)29)6-17(40)24(44)26(20)46/h1-6,18,27-29,34-47H,7H2[5].
  • Heterophylliin A's InChIKey is recorded as NLDMNSXOCDLTTB-UHFFFAOYSA-N[6].
  • Heterophylliin A's chemical formula is recorded as C₃₄H₂₆O₂₂[7].
  • Heterophylliin A's subclass of is recorded as chemical compound[8].
  • Heterophylliin A's PubChem CID is recorded as 471120[9].
  • Heterophylliin A's ChEBI ID is recorded as 167703[10].
  • Heterophylliin A's found in taxon is recorded as clove[11].
  • Heterophylliin A's found in taxon is recorded as Fordia fruticosa[12].
  • Heterophylliin A's Human Metabolome Database ID is recorded as HMDB0039264[13].
  • Heterophylliin A's KNApSAcK ID is recorded as C00054313[14].
  • Heterophylliin A's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+786.091572472'}[15].
  • Heterophylliin A's SureChEMBL ID is recorded as 12824705[16].
  • Heterophylliin A's SureChEMBL ID is recorded as 30385544[17].
  • Heterophylliin A's DSSTox substance ID is recorded as DTXSID201102546[18].
  • Heterophylliin A's UniChem compound ID is recorded as 32015597[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] . ChEBI release 2022-06-13. wikidata.org.
  10. [11] . Isolation of virus-cell fusion inhibitory components from Eugenia caryophyllata. wikidata.org.
  11. [12] . Woodfordin C, a macro-ring hydrolyzable tannin dimer with antitumor activity, and accompanying dimers from Woodfordia fruticosa flowers. wikidata.org.
  12. [13] . wikidata.org.
  13. [14] . wikidata.org.
  14. [15] . wikidata.org.
  15. [16] . wikidata.org.
  16. [17] . wikidata.org.
  17. [18] . wikidata.org.
  18. [19] . UniChem. wikidata.org.

Class ancestry

  1. [1] . Wikidata. wikidata.org.

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APA 4ort.xyz Knowledge Graph. (2026). Heterophylliin A. Retrieved May 3, 2026, from https://4ort.xyz/entity/heterophylliin-a
MLA “Heterophylliin A.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/heterophylliin-a.
BibTeX @misc{4ortxyz_heterophylliin-a_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Heterophylliin A}}, year = {2026}, url = {https://4ort.xyz/entity/heterophylliin-a}, note = {Accessed: 2026-05-03}}
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