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Ledol

chemical compound
Class type of: viridiflorol (incomplete stereochemistry) Q19291552

Facts

8 properties
Instance of
type of chemical entity
Subclass of
viridiflorol (incomplete stereochemistry)
Canonical SMILES
CC1CCC2C1C3C(C3(C)C)CCC2(C)O[3]
Chemical formula
C₁₅H₂₆O[4]
Found in taxon
Cyperus rotundus, Teucrium leucocladum, Aristolochia indica, Baccharis genistelloides, Baccharis sagittalis, Bazzania tridens, Duguetia glabriuscula, Guarea macrophylla, Melaleuca leucadendra, Salvia tchihatcheffii, potato, Thymus camphoratus, Teucrium pseudoscorodonia, Hyssopus officinalis, Chrysanthemum indicum, Artemisia lagocephala, Artemisia rubripes, Aloysia gratissima, Vitex agnus-castus, Zanthoxylum zanthoxyloides, Humulus lupulus, Bazzania trilobata, Myrcia tricona, Baccharis dracunculifolia, Hamamelis virginiana, Santolina chamaecyparissus, Hyptis spicigera, Cantinoa americana, Melaleuca quinquenervia, Eucalyptus exserta, Helichrysum bracteiferum, Aristolochia asclepiadifolia, Lepechinia floribunda, Psiadia altissima, Rhododendron mucronulatum, Artemisia ammaniana, Artemisia sericea, Entandrophragma cylindricum, Tetradenia riparia, Ajuga chamaepitys, Salvia iodantha, Salvia absconditiflora, Callicarpa japonica, Psidium salutare, Salvia vermifolia, Micromeria sinaica, Conyza incana, Waitzia acuminata, Pittosporum tobira, Helichrysum petiolare, Lepicolea ochroleuca, Renealmia chrysotricha, Cassinia longifolia, Cyanthillium cinereum, Pegolettia retrofracta, Satureja cuneifolia, Eucalyptus nova-anglica, Eucalyptus camaldulensis, Baccharis venosa, Isotrema asclepiadifolium, Cannabis sativa, Artemisia herba-alba, Dendranthema indicum, Rhododendron groenlandicum, Eucalyptus oviformis, Eucalyptus globulus, Eucalyptus bosistoana, Eucalyptus paniculata, Eucalyptus tereticornis, Eucalyptus astringens, Eucalyptus dealbata[5][6][7][8][9][10][11][12][13][14][15][16][17][18]
Isomeric SMILES
C[C@@H]1CC[C@H]2[C@@H]1[C@H]3[C@H](C3(C)C)CC[C@@]2(C)O
Mass
+222.198365
Stereoisomer of
viridiflorol, (1aS,4S,4aR,7R,7aR,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol, epi-globulol, (1aR,4R,4aR,7S,7aS,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol, (+)-Globulol, (1aR,4R,4aS,7R,7aR,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol, Epiglobulol, (1aR,4R,4aS,7R,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol, (+)-Ledol, (1aR,4R,4aS,7S,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol, globulol, (1aR,4S,4aS,7S,7aS,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol, (3abeta,8aalpha)-1beta,4,9,9-Tetramethyl-7alpha,8alpha-methanodecahydroazulene-4alpha-ol, (1aR,4S,4aS,7S,7aS,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol, (1aR,4S,4aS,7R,7aR,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol, (1aR,4R,4aR,7R,7aR,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol
🏷️ Also known as
en Ledol fi ledoli ja レドル zh 喇叭茶醇 zh 杜香醇 zh-hans 喇叭茶醇
🔖 Identifiers · 16
CAS Registry Number
577-27-5
Cannabis Database ID
000316
ChEBI ID
6401
ChemSpider ID
83783
DSSTOX compound identifier
DTXCID401015979
DSSTox substance ID
DTXSID40877915
Freebase ID
/m/010vq0x_
InChI
InChI=1S/C15H26O/c1-9-5-6-10-12(9)13-11(14(13,2)3)7-8-15(10,4)16/h9-13,16H,5-8H2,1-4H3/t9-,10+,11-,12-,13-,15-/m1/s1
InChIKey
AYXPYQRXGNDJFU-AOWZIMASSA-N
KEGG ID
C09698
KNApSAcK ID
C00003161
Microsoft Academic ID (discontinued)
2777605015
Show all 16 identifiers +4
PubChem CID
92812
Römpp online ID
RD-12-00699
SureChEMBL ID
2196676
UniChem compound ID
1074187

Report an error or request removal Lineage (PROV-JSON)

🔗 Connections
Found in taxon 54
potato, Cannabis sativa, Humulus lupulus, Cyperus rotundus, Hyssopus officinalis, Eucalyptus globulus, Vitex agnus-castus, Eucalyptus camaldulensis +46 more
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Summary

Ledol is a type of chemical entity[1]. Ledol is a type of viridiflorol (incomplete stereochemistry)[2].

References

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

Direct Wikidata claims

  1. [3] ↑ . PubChem. Retrieved . wikidata.org.
  2. [4] ↑ . PubChem. Retrieved . wikidata.org.
  3. [2] ↑ . wikidata.org.
  4. [5] ↑ . Chemical composition, antiproliferative, antioxidant and antibacterial activities of essential oils from aromatic plants growing in Sudan. wikidata.org.
  5. [6] ↑ . Chemical analysis and biological activities of the essential oil of Teucrium leucocladum Boiss. (Lamiaceae). wikidata.org.
  6. [7] ↑ . (12S)-7,12-Secoishwaran-12-ol, a new type of sesquiterpene from Aristolochia indica Linn. wikidata.org.
  7. [8] ↑ . On terpenes. CXX. Sesquiterpenic compounds of Baccharis genistelloides PERS.; Structure of palustrol. wikidata.org.
  8. [9] ↑ . On terpenes. CXX. Sesquiterpenic compounds of Baccharis genistelloides PERS.; Structure of palustrol. wikidata.org.
  9. [10] ↑ . Isocalamenenes from the LiverwortBazzania tridens. wikidata.org.
  10. [11] ↑ . Antineoplastic activity of selected constituents of Duguetia glabriuscula. wikidata.org.
  11. [12] ↑ . Terpenes from leaves of Guarea macrophylla (Meliaceae).. wikidata.org.
  12. [13] ↑ . A New Norlupene from the Leaves ofMelaleucaleucadendron. wikidata.org.
  13. [14] ↑ . Diterpenoids from the roots of Salvia sclarea. wikidata.org.
  14. [15] ↑ . Leaf surface sesquiterpene alcohols of the potato (Solanum tuberosum) and their influence on colorado beetle (Leptinotarsa decemlineata Say) feeding. wikidata.org.
  15. [16] ↑ . Composition and infraspecific variability of essential oil from Thymus camphoratus. wikidata.org.
  16. [17] ↑ . Chemical and genetic differentiation of two Mediterranean subspecies of Teucrium scorodonia L. wikidata.org.
  17. [18] ↑ . Volatile Components and Odor Intensity of Four Phenotypes of Hyssop (Hyssopus officinalis L.). 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). Ledol. Retrieved November 7, 2026, from https://4ort.xyz/entity/ledol
MLA “Ledol.” 4ort.xyz Knowledge Graph, 4ort.xyz, 7 Nov. 2026, https://4ort.xyz/entity/ledol.
BibTeX @misc{4ortxyz_ledol_2026, author = {{4ort.xyz Knowledge Graph}}, title = {{Ledol}}, year = {2026}, url = {https://4ort.xyz/entity/ledol}, note = {Accessed: 2026-11-07}}
LLM prompt According to 4ort.xyz Knowledge Graph (aggregator of Wikidata, Wikipedia, and authoritative open-data sources): Ledol — https://4ort.xyz/entity/ledol (retrieved 2026-11-07)

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Edit History

Rolling log of changes to this entity's Wikidata record. Values shown reflect the current state of each edited property — follow the history link to see the precise diff for any edit.

  1. 26w ago · Shuaib-bot bot · 2026-05-06 view diff on Wikidata ↗
    Found in taxon → Cyperus rotundus, Teucrium leucocladum, Aristolochia indica +1
    Stereoisomer of → viridiflorol, (1aS,4S,4aR,7R,7aR,7bR)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,, epi-globulol +1
    Mass → 222.198365 dalton
    Instance of → type of chemical entity
    + 1 other property edited (see Wikidata diff for full list)
    "Changed the item"
Live feed via Wikidata EventStreams. New edits appear within minutes of being made on Wikidata.