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1-O-Galloylpedunculagin

group of stereoisomers with the chemical formula C₄₁H₂₈O₂₆
ChemicalSubstance group_of_stereoisomers Q104390224
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Summary

1-O-Galloylpedunculagin is a group of stereoisomers[1].

Key Facts

  • 1-O-Galloylpedunculagin's instance of is recorded as group of stereoisomers[2].
  • 1-O-Galloylpedunculagin's CAS Registry Number is recorded as 82262-94-0[3].
  • 1-O-Galloylpedunculagin's CAS Registry Number is recorded as 79786-00-8[4].
  • 1-O-Galloylpedunculagin's canonical SMILES is recorded as O=C1OCC2OC(OC(=O)C3=CC(O)=C(O)C(O)=C3)C4OC(=O)C5=CC(O)=C(O)C(O)=C5C6=C(O)C(O)=C(O)C=C6C(=O)OC4C2OC(=O)C7=CC(O)=C(O)C(O)=C7C8=C(O)C(O)=C(O)C=C18[5].
  • 1-O-Galloylpedunculagin's InChI is recorded as InChI=1S/C41H28O26/c42-13-1-8(2-14(43)24(13)48)36(57)67-41-35-34(65-39(60)11-5-17(46)27(51)31(55)22(11)23-12(40(61)66-35)6-18(47)28(52)32(23)56)33-19(63-41)7-62-37(58)9-3-15(44)25(49)29(53)20(9)21-10(38(59)64-33)4-16(45)26(50)30(21)54/h1-6,19,33-35,41-56H,7H2[6].
  • 1-O-Galloylpedunculagin's InChIKey is recorded as SWRFKGRMQVLMKA-UHFFFAOYSA-N[7].
  • 1-O-Galloylpedunculagin's chemical formula is recorded as C₄₁H₂₈O₂₆[8].
  • 1-O-Galloylpedunculagin's subclass of is recorded as chemical compound[9].
  • 1-O-Galloylpedunculagin's PubChem CID is recorded as 452242[10].
  • 1-O-Galloylpedunculagin's found in taxon is recorded as Quercus acutissima[11].
  • 1-O-Galloylpedunculagin's found in taxon is recorded as Terminalia calamansanai[12].
  • 1-O-Galloylpedunculagin's found in taxon is recorded as clove[13].
  • 1-O-Galloylpedunculagin's found in taxon is recorded as Rosa rugosa[14].
  • 1-O-Galloylpedunculagin's found in taxon is recorded as Fragaria[15].
  • 1-O-Galloylpedunculagin's found in taxon is recorded as Castanopsis sieboldii[16].
  • 1-O-Galloylpedunculagin's found in taxon is recorded as Lotus japonicus[17].
  • 1-O-Galloylpedunculagin's found in taxon is recorded as Rubus idaeus[18].
  • 1-O-Galloylpedunculagin's found in taxon is recorded as Juglans[19].
  • 1-O-Galloylpedunculagin's found in taxon is recorded as Rhoiptelea chiliantha[20].
  • 1-O-Galloylpedunculagin's found in taxon is recorded as Ovatus malisuctus[21].
  • 1-O-Galloylpedunculagin's Human Metabolome Database ID is recorded as HMDB0039244[22].
  • 1-O-Galloylpedunculagin's KNApSAcK ID is recorded as C00057574[23].
  • 1-O-Galloylpedunculagin's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+936.086881016'}[24].
  • 1-O-Galloylpedunculagin's SureChEMBL ID is recorded as 1430141[25].
  • 1-O-Galloylpedunculagin's DSSTox substance ID is recorded as DTXSID501318192[26].

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] ↑ . Chemical Abstracts Service. Retrieved . wikidata.org.
  4. [5] ↑ . wikidata.org.
  5. [6] ↑ . wikidata.org.
  6. [7] ↑ . wikidata.org.
  7. [8] ↑ . wikidata.org.
  8. [9] ↑ . wikidata.org.
  9. [10] ↑ . PubChem. Retrieved . wikidata.org.
  10. [11] ↑ . Tannin production in callus cultures of Quercus acutissima. wikidata.org.
  11. [12] ↑ . Tannins and related compounds. CIII. Isolation and characterization of new monomeric, dimeric and trimeric ellagitannins, calamansanin and calamanins A, B and C, from Terminalia calamansanai (Blanco) Rolfe.. wikidata.org.
  12. [13] ↑ . Hydrolysable Tannins Isolated from Syzygium aromaticum: Structure of a New C-Glucosidic Ellagitannin and Spectral Features of Tannins with a Tergalloyl Group. wikidata.org.
  13. [14] ↑ . Simultaneous determination of hydrolysable tannins in the petals of Rosa rugosa and allied plants. wikidata.org.
  14. [15] ↑ . Overall dietary polyphenol intake in a bowl of strawberries: The influence of Fragaria spp. in nutritional studies. wikidata.org.
  15. [16] ↑ . Tannins and related compounds. LXXVI. Isolation and characterization of cercidinins A and B and cuspinin, unusual 2,3-(R)-hexahydroxydiphenoyl glucoses from Cercidiphyllum japonicum and Castanopsis cuspidata var. sieboldii.. wikidata.org.
  16. [17] ↑ . Tannins and related compounds. LXXXIV. Isolation and characterization of five new hydrolyzable tannins from the bark of Mallotus japonicus. wikidata.org.
  17. [18] ↑ . Food ellagitannins-occurrence, effects of processing and storage. wikidata.org.
  18. [19] ↑ . Food ellagitannins-occurrence, effects of processing and storage. wikidata.org.
  19. [20] ↑ . Euphane-Type Triterpene Tridesmosides from the Leaves of Rhoiptelea chiliantha.. wikidata.org.
  20. [21] ↑ . Euscaphinin, a new ellagitannin dimer from Euscaphis japonica (THUNB.) KANITZ. wikidata.org.
  21. [22] ↑ . wikidata.org.
  22. [23] ↑ . wikidata.org.
  23. [24] ↑ . wikidata.org.
  24. [25] ↑ . wikidata.org.
  25. [26] ↑ . wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.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). 1-O-Galloylpedunculagin. Retrieved May 3, 2026, from https://4ort.xyz/entity/1-o-galloylpedunculagin
MLA “1-O-Galloylpedunculagin.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/1-o-galloylpedunculagin.
BibTeX @misc{4ortxyz_1-o-galloylpedunculagin_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{1-O-Galloylpedunculagin}}, year = {2026}, url = {https://4ort.xyz/entity/1-o-galloylpedunculagin}, note = {Accessed: 2026-05-03}}
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