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Frugoside

group of stereoisomers with the chemical formula C₂₉H₄₄O₉
ChemicalSubstance group_of_stereoisomers Q82006646
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Frugoside

Summary

Frugoside is a group of stereoisomers[1].

Key Facts

  • Frugoside's instance of is recorded as group of stereoisomers[2].
  • Frugoside's CAS Registry Number is recorded as 56324-39-1[3].
  • Frugoside's canonical SMILES is recorded as O=C1OCC(=C1)C2CCC3(O)C4CCC5CC(OC6OC(C)C(O)C(O)C6O)CCC5(CO)C4CCC23C[4].
  • Frugoside's InChI is recorded as InChI=1S/C29H44O9/c1-15-23(32)24(33)25(34)26(37-15)38-18-5-9-28(14-30)17(12-18)3-4-21-20(28)6-8-27(2)19(7-10-29(21,27)35)16-11-22(31)36-13-16/h11,15,17-21,23-26,30,32-35H,3-10,12-14H2,1-2H3/t15-,17-,18+,19-,20+,21-,23-,24-,25-,26?,27-,28-,29+/m1/s1[5].
  • Frugoside's InChIKey is recorded as WPVGSIBYLZQSIK-VEZJFPMXSA-N[6].
  • Frugoside's chemical formula is recorded as C₂₉H₄₄O₉[7].
  • Frugoside's subclass of is recorded as cardanolides[8].
  • Frugoside's PubChem CID is recorded as 120728[9].
  • Frugoside's found in taxon is recorded as Calotropis gigantea[10].
  • Frugoside's found in taxon is recorded as Asclepias curassavica[11].
  • Frugoside's found in taxon is recorded as Gomphocarpus sinaicus[12].
  • Frugoside's found in taxon is recorded as Asclepias tuberosa[13].
  • Frugoside's found in taxon is recorded as Danaus plexippus[14].
  • Frugoside's isomeric SMILES is recorded as C[C@H]1OC(O[C@H]2CC[C@]3(CO)[C@H]4CC[C@]5(C)C@@HCC[C@]5(O)[C@@H]4CC[C@@H]3C2)C@HC@H[C@@H]1OC@@HCC[C@]5(O)[C@@H]4CC[C@@H]3C2)C@HC@H[C@@H]1O">[15].
  • Frugoside's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+536.298532988'}[16].
  • Frugoside's NSC number is recorded as 115676[17].
  • Frugoside's SureChEMBL ID is recorded as 29813240[18].
  • Frugoside's DSSTox substance ID is recorded as DTXSID70276235[19].
  • Frugoside's DSSTOX compound identifier is recorded as DTXCID50227563[20].
  • Frugoside's UniChem compound ID is recorded as 58933000[21].

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] ↑ . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . Indonesian medicinal plants. I. Chemical structures of calotroposides A and B, two new oxypregnane-oligoglycosides from the root of Calotropis gigantea (Asclepiadaceae). wikidata.org.
  10. [11] ↑ . Cardenolide Glycosides from the Seeds of Asclepias curassavica.. wikidata.org.
  11. [12] ↑ . Re-investigation of the cardenolide glycosides from Gomphocarpus sinaicus. wikidata.org.
  12. [13] ↑ . An androstane bioside and 3'-thiazolidinone derivatives of doubly-linked cardenolide glycosides from the roots of Asclepias tuberosa. wikidata.org.
  13. [14] ↑ . New glucoside conjugates and other cardenolide glycosides from the monarch butterfly reared on Asclepias fruticosa L.. wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . wikidata.org.
  16. [17] ↑ . wikidata.org.
  17. [18] ↑ . wikidata.org.
  18. [19] ↑ . wikidata.org.
  19. [20] ↑ . wikidata.org.
  20. [21] ↑ . UniChem. wikidata.org.

Class ancestry

  1. [1] ↑ . Wikidata. wikidata.org.

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BibTeX @misc{4ortxyz_frugoside_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Frugoside}}, year = {2026}, url = {https://4ort.xyz/entity/frugoside}, note = {Accessed: 2026-05-03}}
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