Home › Entities › group_of_stereoisomers › 13-Episclareol

13-Episclareol

group of stereoisomers with the chemical formula C₂₀H₃₆O₂
ChemicalSubstance group_of_stereoisomers Q104251412
Press Enter · cited answer in seconds

13-Episclareol

Summary

13-Episclareol is a group of stereoisomers[1].

Key Facts

  • 13-Episclareol's instance of is recorded as group of stereoisomers[2].
  • 13-Episclareol's canonical SMILES is recorded as OC(C=C)(C)CCC1C(O)(C)CCC2C(C)(C)CCCC12C[3].
  • 13-Episclareol's InChI is recorded as InChI=1S/C20H36O2/c1-7-18(4,21)13-9-16-19(5)12-8-11-17(2,3)15(19)10-14-20(16,6)22/h7,15-16,21-22H,1,8-14H2,2-6H3/t15-,16+,18?,19-,20+/m0/s1[4].
  • 13-Episclareol's InChIKey is recorded as XVULBTBTFGYVRC-SVPXJYONSA-N[5].
  • 13-Episclareol's chemical formula is recorded as C₂₀H₃₆O₂[6].
  • 13-Episclareol's subclass of is recorded as labdanes[7].
  • 13-Episclareol's PubChem CID is recorded as 56842011[8].
  • 13-Episclareol's found in taxon is recorded as Jungermannia infusca[9].
  • 13-Episclareol's found in taxon is recorded as Cistus creticus[10].
  • 13-Episclareol's found in taxon is recorded as Nicotiana glutinosa[11].
  • 13-Episclareol's isomeric SMILES is recorded as C=CC(C)(O)CC[C@@H]1[C@@]2(C)CCCC(C)(C)[C@@H]2CC[C@@]1(C)O[12].
  • 13-Episclareol's mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+308.271530392'}[13].
  • 13-Episclareol's SureChEMBL ID is recorded as 15503382[14].
  • 13-Episclareol's UniChem compound ID is recorded as 68606503[15].
  • 13-Episclareol's Probes And Drugs ID is recorded as PD132214[16].

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] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . ChemInform Abstract: Diterpenoids from the Japanese Liverwort Jungermannia infusca.. wikidata.org.
  9. [10] ↑ . Chemical analysis and antimicrobial activity of the resin Ladano, of its essential oil and of the isolated compounds. wikidata.org.
  10. [11] ↑ . Biosynthesis of labdenediol and sclareol in cell-free extracts from trichomes of Nicotiana glutinosa. wikidata.org.
  11. [12] ↑ . wikidata.org.
  12. [13] ↑ . wikidata.org.
  13. [14] ↑ . wikidata.org.
  14. [15] ↑ . UniChem. wikidata.org.
  15. [16] ↑ . 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). 13-Episclareol. Retrieved May 3, 2026, from https://4ort.xyz/entity/13-episclareol
MLA “13-Episclareol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 3 May. 2026, https://4ort.xyz/entity/13-episclareol.
BibTeX @misc{4ortxyz_13-episclareol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{13-Episclareol}}, year = {2026}, url = {https://4ort.xyz/entity/13-episclareol}, note = {Accessed: 2026-05-03}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): 13-Episclareol — https://4ort.xyz/entity/13-episclareol (retrieved 2026-05-03)

Canonical URL: https://4ort.xyz/entity/13-episclareol · Last refreshed: