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Juvabione

chemical compound
Class type of: bisabolanes Q10861158

Facts

8 properties
Instance of
type of chemical entity
Subclass of
bisabolanes
Canonical SMILES
CC(C)CC(=O)CC(C)C1CCC(=CC1)C(=O)OC
Chemical formula
C₁₆H₂₆O₃
Found in taxon
Abies sachalinensis, Abies lasiocarpa, Abies veitchii
Isomeric SMILES
C[C@H](CC(=O)CC(C)C)[C@@H]1CCC(=CC1)C(=O)OC
Mass
+266.188195
Stereoisomer of
(-)-Juvabione, (+)-Epijuvabione
🏷️ Also known as
en Juvabione de Juvabion es Juvabiona fa ژووابیون zh 保幼酮
🔖 Identifiers · 16
CAS Registry Number
17904-27-7
ChEBI ID
6095
ChemSpider ID
390830
DSSTOX compound identifier
DTXCID30809548
DSSTox substance ID
DTXSID30858798
Freebase ID
/m/065_t0l
InChI
InChI=1S/C16H26O3/c1-11(2)9-15(17)10-12(3)13-5-7-14(8-6-13)16(18)19-4/h7,11-13H,5-6,8-10H2,1-4H3/t12-,13+/m1/s1
InChIKey
IIWNDLDEVPJIBT-OLZOCXBDSA-N
KEGG ID
C09693
KNApSAcK ID
C00003156
Microsoft Academic ID (discontinued)
2781352329
PubChem CID
442381
Show all 16 identifiers +4
Römpp online ID
RD-10-00201
SureChEMBL ID
2199849
UNII
NG8LD2D5B4
UniChem compound ID
1068260

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🔗 Connections
Found in taxon 3
Abies lasiocarpa, Abies sachalinensis, Abies veitchii
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Summary

Juvabione is a type of chemical entity[1].

Key Facts

  • Canonical SMILES: CC(C)CC(=O)CC(C)C1CCC(=CC1)C(=O)OC[2]
  • Chemical formula: C₁₆H₂₆O₃[3]
  • Subclass of: bisabolanes[4]
  • Found in taxon: Abies sachalinensis[5], Abies lasiocarpa[6], Abies veitchii[7]
  • Isomeric SMILES: CC@H[C@@H]1CCC(=CC1)C(=O)OCC@H[C@@H]1CCC(=CC1)C(=O)OC">[8]
  • Mass: 266.188195 dalton[9]
  • Stereoisomer of: (-)-Juvabione[10], (+)-Epijuvabione[11]

References

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

Direct Wikidata claims

  1. [2] ↑ . PubChem. Retrieved . wikidata.org.
  2. [3] ↑ . PubChem. Retrieved . wikidata.org.
  3. [4] ↑ . wikidata.org.
  4. [5] ↑ . Chemical differences between two populations of Abies sachalinensis. wikidata.org.
  5. [6] ↑ . Juvabione and its analogues.: IV. Isolation, identification, and occurrence of juvabione, juvabiol, and epijuvabiol from the whole wood of Abies lasiocarpa. wikidata.org.
  6. [7] ↑ . Juvabione analogues from two Abies sachalinensis trees. wikidata.org.
  7. [8] ↑ . PubChem. Retrieved . wikidata.org.
  8. [9] ↑ . PubChem. Retrieved . wikidata.org.
  9. [10] ↑ . wikidata.org.
  10. [11] ↑ . 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). Juvabione. Retrieved November 10, 2026, from https://4ort.xyz/entity/juvabione
MLA “Juvabione.” 4ort.xyz Knowledge Graph, 4ort.xyz, 10 Nov. 2026, https://4ort.xyz/entity/juvabione.
BibTeX @misc{4ortxyz_juvabione_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Juvabione}}, year = {2026}, url = {https://4ort.xyz/entity/juvabione}, note = {Accessed: 2026-11-10}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Juvabione — https://4ort.xyz/entity/juvabione (retrieved 2026-11-10)

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