hebeclinolide

chemical compound
ChemicalSubstance group_of_stereoisomers Q27251373
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hebeclinolide

Summary

hebeclinolide is a group of stereoisomers[1].

Key Facts

  • hebeclinolide's instance of is recorded as group of stereoisomers[2].
  • hebeclinolide's CAS Registry Number is recorded as 63147-18-2[3].
  • hebeclinolide's canonical SMILES is recorded as CC1=CC(=O)CC(C1CCC2=CCC(OC2=O)C3=COC=C3)(C)C[4].
  • hebeclinolide's InChI is recorded as InChI=1S/C20H24O4/c1-13-10-16(21)11-20(2,3)17(13)6-4-14-5-7-18(24-19(14)22)15-8-9-23-12-15/h5,8-10,12,17-18H,4,6-7,11H2,1-3H3/t17?,18-/m1/s1[5].
  • hebeclinolide's InChIKey is recorded as JVCOVRPXVQTCSZ-QRWMCTBCSA-N[6].
  • hebeclinolide's chemical formula is recorded as C₂₀H₂₄O₄[7].
  • hebeclinolide's subclass of is recorded as 10,15-cyclophytane diterpenoid[8].
  • hebeclinolide's UNII is recorded as 125AT37EON[9].
  • hebeclinolide's ChemSpider ID is recorded as 32698858[10].
  • hebeclinolide's PubChem CID is recorded as 13858018[11].
  • hebeclinolide's isomeric SMILES is recorded as CC1=CC(=O)CC(C1CCC2=CCC@@HC3=COC=C3)(C)CC@@HC3=COC=C3)(C)C">[12].
  • hebeclinolide's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+328.167'}[13].
  • hebeclinolide's DSSTox substance ID is recorded as DTXSID30212492[14].
  • hebeclinolide's DSSTOX compound identifier is recorded as DTXCID30134983[15].
  • hebeclinolide's UniChem compound ID is recorded as 62587006[16].

References

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

Direct Wikidata claims

  1. [2] . wikidata.org.
  2. [3] . Global Substance Registration System. Retrieved . wikidata.org.
  3. [4] . PubChem. Retrieved . wikidata.org.
  4. [5] . PubChem. Retrieved . wikidata.org.
  5. [6] . PubChem. Retrieved . wikidata.org.
  6. [7] . PubChem. Retrieved . wikidata.org.
  7. [8] . wikidata.org.
  8. [9] . Global Substance Registration System. Retrieved . wikidata.org.
  9. [10] . Q2311683. Retrieved . wikidata.org.
  10. [11] . PubChem. Retrieved . wikidata.org.
  11. [12] . PubChem. Retrieved . wikidata.org.
  12. [13] . PubChem. Retrieved . wikidata.org.
  13. [14] . Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard. 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). hebeclinolide. Retrieved May 3, 2026, from https://4ort.xyz/entity/hebeclinolide
MLA “hebeclinolide.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/hebeclinolide.
BibTeX @misc{4ortxyz_hebeclinolide_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{hebeclinolide}}, year = {2026}, url = {https://4ort.xyz/entity/hebeclinolide}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): hebeclinolide — https://4ort.xyz/entity/hebeclinolide (retrieved 2026-05-03)

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