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Castaneiolide

group of stereoisomers with the chemical formula C₂₂H₂₈O₈
ChemicalSubstance group_of_stereoisomers Q105238439
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Castaneiolide

Summary

Castaneiolide is a group of stereoisomers[1].

Key Facts

  • Castaneiolide's instance of is recorded as group of stereoisomers[2].
  • Castaneiolide's CAS Registry Number is recorded as 125300-50-7[3].
  • Castaneiolide's canonical SMILES is recorded as O=C1OC(=O)C2=C1CC(C=3C(=O)OC(=O)C3CC(O)(CCCC)C2O)CCCCC[4].
  • Castaneiolide's InChI is recorded as InChI=1S/C22H28O8/c1-3-5-7-8-12-10-13-16(21(27)29-18(13)24)17(23)22(28,9-6-4-2)11-14-15(12)20(26)30-19(14)25/h12,17,23,28H,3-11H2,1-2H3[5].
  • Castaneiolide's InChIKey is recorded as RKHYCZRKSYBVGA-UHFFFAOYSA-N[6].
  • Castaneiolide's chemical formula is recorded as C₂₂H₂₈O₈[7].
  • Castaneiolide's subclass of is recorded as chemical compound[8].
  • Castaneiolide's PubChem CID is recorded as 366241[9].
  • Castaneiolide's ChEBI ID is recorded as 175360[10].
  • Castaneiolide's found in taxon is recorded as Macrophoma castaneicola[11].
  • Castaneiolide's Human Metabolome Database ID is recorded as HMDB0034876[12].
  • Castaneiolide's KNApSAcK ID is recorded as C00054136[13].
  • Castaneiolide's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+420.178417856'}[14].
  • Castaneiolide's DSSTox substance ID is recorded as DTXSID501108874[15].
  • Castaneiolide's UniChem compound ID is recorded as 32005539[16].

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] ↑ . "Castaneiolide, abscisic acid and monorden, phytotoxic compounds isolated from fungi (Macrophoma castaneicola and Didymosporium radicicola) cause \"black root rot disease\" in chestnut trees.". wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . wikidata.org.
  15. [16] ↑ . UniChem. 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). Castaneiolide. Retrieved May 3, 2026, from https://4ort.xyz/entity/castaneiolide
MLA “Castaneiolide.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/castaneiolide.
BibTeX @misc{4ortxyz_castaneiolide_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Castaneiolide}}, year = {2026}, url = {https://4ort.xyz/entity/castaneiolide}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Castaneiolide — https://4ort.xyz/entity/castaneiolide (retrieved 2026-05-03)

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