Details Top

Internal ID UUID64400a079343d507848172
Scientific name Arbutus menziesii
Authority Pursh
First published in Fl. Amer. Sept. 1: 282 (1813)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

In the Pacific Northwest, the evergreen leaves of Pacific madrone have long been made into infusions for urinary complaints. Among the Nlaka’pamux of the British Columbia interior, infusions of madrone leaf were taken to promote urination and treat “painful urine” (Turner et al., 1990). Coast Salish peoples of Washington and British Columbia also used a weak leaf infusion as a diuretic, while the Nootka of Vancouver Island made it a gargle for sore throat, steam inhalation for colds and coughs, and poultice of boiled leaves for sore muscles (Pojar and MacKinnon, 2004). Okanagan-Colville people in the interior likewise drank a leaf infusion for urinary difficulties (Moerman, 1998). These records match the pharmacognosy of the species, whose leaves contain the urinary antiseptic hydroquinone glycoside arbutin along with ursolic and oleanolic acids and significant tannins (O’Kennedy and Kremer, 1996).

For a simple soothing infusion, measure 1–2 teaspoons (about 1–2 g) of dried madrone leaf into a teapot or cup, pour over 8–10 fl oz (240–300 mL) of just‑boiled water, and steep covered for 10–15 minutes. Strain and sip up to 1–2 cups daily as needed. A more astringent gargle for a sore throat uses 3–4 teaspoons (≈3–4 g) of leaf in the same volume of water, steeped 10–15 minutes and used 2–3 times a day. Safety: madrone contains arbutin, which releases hydroquinone in the gut; use caution with kidney disease, liver disease, and during pregnancy or breastfeeding. Discontinue if stomach upset or dark urine develops and consult a qualified clinician.

Well‑documented constituents in Arbutus menziesii leaves explain these uses. Arbutin converts to hydroquinone, an antibacterial agent active against common urinary pathogens; ursolic and oleanolic acids have documented diuretic and anti‑inflammatory activity, while condensed tannins contribute an astringent effect helpful for sore throat and skin poultices (O’Kennedy and Kremer, 1996; O’Leary and Altland, 1957). These compounds align with the traditional practice of taking leaf infusions for genitourinary relief and using them topically for inflammatory or microbial irritation.

Commercial herbal suppliers still carry madrone leaf for teas and astringent gargles, and researchers continue to explore its antimicrobial and diuretic potential (O’Kennedy and Kremer, 1996). At the same time, Indigenous knowledge remains strong, with coastal communities of the Kwakwaka’wakw region retaining the practice of madrone leaf steam inhalation for colds and as a poultice for sore muscles (Turner et al., 1990; Pojar and MacKinnon, 2004).

General Uses Top

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Common products:
Arbutus menziesii is occasionally harvested for fuelwood, especially in the Pacific Northwest. Coarse, split firewood and low-temperature charcoal are the most consistent products from this species.

Industrial and craft applications:
The tree is seldom sawn into lumber. When used, its wood is made into small specialty items (e.g., small turned objects, novelties), tool handles, and furniture parts where durability and workability allow; it is not a major timber commodity. Bark has historical use in crafts and as a rough fiber for ties and lashings, with limited commercial relevance today.

Food and beverages (non-medicinal):
Fruits are occasionally used as flavoring and incorporated into beverages (e.g., syrups, infusions) as a culinary ingredient, without health claims. Processing is typically simple reduction and/or dilution as a flavoring element.

Colorants and tanning:
Bark has been used as a source of brown dyes for wool and protein fibers, and historically as a source of tannins for leather tanning; these are historically notable but not widely used today.

Wood and fiber:
The wood is described as hard, dense, and close-grained, with light reddish-brown to orange heartwood and pale sapwood, suitable for turning and specialty applications. Bark fibers are coarse.

Properties relevant to use:
High density (approaching or exceeding 0.70 g/cm³) and a dense, fine grain support burning performance and certain turned-wood uses. Bark contains hydrolyzable tannins relevant to historical dyeing and tanning. Fruit is used as a flavoring ingredient.

Standards and regulation:
No species-specific standards or regulatory frameworks are documented for this taxon.

Sustainability and sourcing:
Arbutus menziesii is a minor component in forest ecosystems of the Pacific Northwest. Although locally abundant, selective removal for fuelwood or small specialty items generally yields low volumes and has limited ecological impact at the stand scale; any harvesting should follow local forest management guidelines.

References: Tucker (1979, Flora of California); USDA Forest Service, Pacific Southwest Research Station; Calflora.

Synonyms Top

Scientific name Authority First published in
Arbutus menziesii var. elliptica DC. Prodr. 7: 582 (1839)
Arbutus menziesii var. oblongifolia DC. Prodr. 7: 582 (1839)
Arbutus procera Douglas ex Lindl. Edwards's Bot. Reg. 21: t. 1753 (1835)

Common names Top

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Language Common/alternative name
English bearberry
English madrone
English madrona
English pacific madrone
Arabic قطلب منزي
Catalan arboç del pacífic
Czech planika menziesova
German madrone
German amerikanischer erdbeerbaum
Esperanto menzies-arbuto
Finnish kalifornianmansikkapuu
Hebrew קטלב קליפורני
Hungarian kaliforniai szamócafa
Japanese マドローネ
Norwegian Bokmål madrona
Russian Земляничное дерево Менциса
Russian Земляничник Менциса
Slovenian jagodičnica
Slovenian pacifiška madrona
Chinese 草莓樹
Chinese 太平洋熊莓

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Northwest
    • Northwestern U.S.A.
      • Oregon
      • Washington
    • Southwestern U.S.A.
      • California
    • Western Canada
      • British Columbia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000543147
UNII 3178O591CY
Canadensys 5490
USDA Plants ARME
Tropicos 12302436
KEW urn:lsid:ipni.org:names:326479-1
The Plant List kew-2646696
Missouri Botanical Garden 280006
Open Tree Of Life 214287
NCBI Taxonomy 82758
Nature Serve 2.133817
IUCN Red List 61220272
IPNI 326479-1
iNaturalist 51046
GBIF 2882802
Freebase /m/02n5_s
FEIS plants/tree/arbmen
EPPO ARDME
EOL 582128
Calflora (Californian flora) 506
USDA GRIN 316002
Wikipedia Arbutus_menziesii
CMAUP NPO17602
PFAF Arbutus menziesii

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_046127765.1 ddArbMenz1_p1.1 Contig Canada's national platform for genome sequencing and analysis 2024-12-17 49.85 411.12 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Commodity risk assessment of Cornus alba and Cornus sanguinea plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Manda RR, Schulz OM, Kariampa P, Akrivou A, Antonatos S, Beris D, Debode J, Kritikos C, Kormpi M, Manceau C, Papachristos D, Reppa C, Gardi C, Potting R EFSA J 12-Mar-2024
PMCID:PMC10928767
doi:10.2903/j.efsa.2024.8657
PMID:38476319
The genus Fomitopsis (Polyporales, Basidiomycota) reconsidered Spirin V, Runnel K, Vlasák J, Viner I, Barrett MD, Ryvarden L, Bernicchia A, Rivoire B, Ainsworth AM, Grebenc T, Cartabia M, Niemelä T, Larsson KH, Miettinen O Stud Mycol 22-Feb-2024
PMCID:PMC11003443
doi:10.3114/sim.2024.107.03
PMID:38600960
The role of arbuscular mycorrhizal symbiosis in plant abiotic stress Wang Q, Liu M, Wang Z, Li J, Liu K, Huang D Front Microbiol 18-Jan-2024
PMCID:PMC10835807
doi:10.3389/fmicb.2023.1323881
PMID:38312502
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Metal toxin threat in wildland fires determined by geology and fire severity Lopez AM, Pacheco JL, Fendorf S Nat Commun 12-Dec-2023
PMCID:PMC10716285
doi:10.1038/s41467-023-43101-9
PMID:38086795
Broadening the Knowledge of Mexican Boletes: Addition of a New Genus, Seven New Species, and Three New Combinations Ayala-Vásquez O, Pérez-Moreno J, Pinzón JP, Garibay-Orijel R, García-Jiménez J, de la Fuente JI, Venegas-Barrera CS, Martínez-Reyes M, Montoya L, Bandala V, Aguirre-Acosta CE, Martínez-González CR, Hernández-Del Valle JF J Fungi (Basel) 21-Nov-2023
PMCID:PMC10744551
doi:10.3390/jof9121126
PMID:38132727
Commodity risk assessment of Quercus petraea plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613939
doi:10.2903/j.efsa.2023.8313
PMID:37908445
Commodity risk assessment of Quercus robur plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 30-Oct-2023
PMCID:PMC10613938
doi:10.2903/j.efsa.2023.8314
PMID:37908449
Plant-Associated Neoscytalidium dimidiatum—Taxonomy, Host Range, Epidemiology, Virulence, and Management Strategies: A Comprehensive Review Derviş S, Özer G J Fungi (Basel) 26-Oct-2023
PMCID:PMC10672476
doi:10.3390/jof9111048
PMID:37998855
Commodity risk assessment of Fagus sylvatica plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 28-Jul-2023
PMCID:PMC10375364
doi:10.2903/j.efsa.2023.8118
PMID:37522095
Commodity risk assessment of Acer pseudoplatanus plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323731
doi:10.2903/j.efsa.2023.8074
PMID:37427019
Commodity risk assessment of Acer platanoides plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323725
doi:10.2903/j.efsa.2023.8073
PMID:37427021
Commodity risk assessment of Acer campestre plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323733
doi:10.2903/j.efsa.2023.8071
PMID:37427018
Commodity risk assessment of Acer palmatum plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323724
doi:10.2903/j.efsa.2023.8075
PMID:37427020
Measurements of Atmosphere–Biosphere Exchange of Oxidized Nitrogen and Implications for the Chemistry of Atmospheric NOx Delaria ER, Cohen RC Acc Chem Res 22-Jun-2023
PMCID:PMC10324316
doi:10.1021/acs.accounts.3c00090
PMID:37347962

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
2-Hydroxy-6-[2-hydroxy-6-(hydroxymethyl)-4-methyl-phenoxy]-3-(3-methylbut-2-enyl)benzoic acid 23843930 Click to see 358.40 unknown via CMAUP database
6-[2-hydroxy-6-(hydroxymethyl)-4-methylphenoxy]-2-methoxy-3-[(1S)-1-methoxy-3-methylbutyl]benzoic acid 38351229 Click to see 404.50 unknown via CMAUP database
6-[2-hydroxy-6-(hydroxymethyl)-4-methylphenoxy]-3-[(1S)-1-hydroxy-3-methylbutyl]-2-methoxybenzoic acid 71608329 Click to see CC1=CC(=C(C(=C1)O)OC2=C(C(=C(C=C2)C(CC(C)C)O)OC)C(=O)O)CO 390.40 unknown via CMAUP database
7-O-Acetylsecopenicillide C 71460590 Click to see 400.40 unknown via CMAUP database
> Benzenoids / Tetralins
(1R,2S,3S)-2-chlorospiro[2,3-dihydro-1H-naphthalene-4,3'-2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene]-1,3,8-triol 51354127 Click to see 370.80 unknown via CMAUP database
(1R,3R)-spiro[2,3-dihydro-1H-naphthalene-4,3'-2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene]-1,3,8-triol 51354124 Click to see 336.30 unknown via CMAUP database
(1S,2R,3S)-2-chlorospiro[2,3-dihydro-1H-naphthalene-4,3'-2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene]-1,3,8-triol 51354126 Click to see 370.80 unknown via CMAUP database
(1S,3R)-spiro[2,3-dihydro-1H-naphthalene-4,3'-2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene]-1,3,8-triol 51354123 Click to see 336.30 unknown via CMAUP database
(3R)-3,8-dihydroxyspiro[2,3-dihydronaphthalene-4,3'-2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene]-1-one 51354122 Click to see 334.30 unknown via CMAUP database
[(6'R,8'R)-6',8'-dihydroxyspiro[2,4-dioxatricyclo[7.3.1.05,13]trideca-1(12),5,7,9(13),10-pentaene-3,5'-7,8-dihydro-6H-naphthalene]-1'-yl] hydrogen sulfate 51354125 Click to see C1C(C2=C(C=CC=C2OS(=O)(=O)O)C3(C1O)OC4=CC=CC5=C4C(=CC=C5)O3)O 416.40 unknown via CMAUP database
Sulfuric acid (2S)-1,1-[naphthalene-1,8-diylbis(oxy)]-2alpha,4beta-dihydroxy-3alpha-chlorotetralin-5-yl ester 51354407 Click to see C1=CC2=C3C(=C1)OC4(C(C(C(C5=C4C=CC=C5OS(=O)(=O)O)O)Cl)O)OC3=CC=C2 450.80 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dotriacontane 11008 Click to see 450.90 unknown via CMAUP database
Hentriacontane 12410 Click to see 436.80 unknown via CMAUP database
Heptacosane 11636 Click to see 380.70 unknown via CMAUP database
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown via CMAUP database
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown via CMAUP database
Pentacosane 12406 Click to see 352.70 unknown via CMAUP database
Pentatriacontane 12413 Click to see 492.90 unknown via CMAUP database
Triacontane 12535 Click to see 422.80 unknown via CMAUP database
Tritriacontane 12411 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 464.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ustusolate A 23843911 Click to see CC=CC=CC=CC(=O)OC1C=C(C(C2(C1C(CCC2)(C)C)C)(CO)O)CO 390.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
11-Octadecaenoic acid 122325 Click to see CCCCCCC=CCCCCCCCCCC(=O)O 282.50 unknown via CMAUP database
7-Hexadecenoic acid 543268 Click to see CCCCCCCCC=CCCCCCC(=O)O 254.41 unknown via CMAUP database
9-Heptadecenoic acid 3014063 Click to see 268.40 unknown via CMAUP database
9-Hexadecenoic acid 4668 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
Heptadecanoic Acid 10465 Click to see 270.50 unknown via CMAUP database
Myristic Acid 11005 Click to see 228.37 unknown via CMAUP database
Nonadecanoic Acid 12591 Click to see 298.50 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Pentadecanoic Acid 13849 Click to see 242.40 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
trans-3-Hexadecenoic acid 5312418 Click to see 254.41 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid 3893 Click to see 200.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4S,5R,9S,10R,13S)-13-(hydroxymethyl)-5,9-dimethyl-14-oxotetracyclo[11.2.1.01,10.04,9]hexadecane-5-carbaldehyde 11392987 Click to see 318.40 unknown via CMAUP database
(1S)-1-[(2S,4aR,4bR,5R,8aR)-5-hydroxy-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]ethane-1,2-diol 11602232 Click to see 322.50 unknown via CMAUP database
(1S)-1-[(2S,4aR,4bR,8aR)-2,4b,8,8-tetramethyl-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]ethane-1,2-diol 11551288 Click to see 306.50 unknown via CMAUP database
(1S)-1-[(2S,4aS,4bS,5R,8aS)-5-hydroxy-2,4b,8,8-tetramethyl-3,4,4a,5,6,7,8a,9-octahydro-1H-phenanthren-2-yl]ethane-1,2-diol 101202346 Click to see CC1(CCC(C2(C1CC=C3C2CCC(C3)(C)C(CO)O)C)O)C 322.50 unknown via CMAUP database
(4aR,4bR,7S,10aR)-7-[(1S)-1,2-dihydroxyethyl]-1,1,4a,7-tetramethyl-2,3,4b,5,6,9,10,10a-octahydrophenanthren-4-one 11702511 Click to see CC1(CCC(=O)C2(C1CCC3=CC(CCC32)(C)C(CO)O)C)C 320.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4S,5R,9S,10R,13S)-5-(hydroxymethyl)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecan-13-ol 100967711 Click to see 304.50 unknown via CMAUP database
(1S,4S,5R,9R,13R,14R)-14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-10-ene-5-carbaldehyde 11324617 Click to see 318.40 unknown via CMAUP database
(1S,4S,5R,9R,13S,14S)-13,14-dihydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadec-10-ene-5-carboxylic acid 11428064 Click to see 350.40 unknown via CMAUP database
(1S,4S,5R,9S,10R,13R,14R)-14-hydroxy-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carbaldehyde 44575992 Click to see 320.50 unknown via CMAUP database
(1S,4S,5R,9S,10R,13R,14S)-14-(hydroxymethyl)-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 46210307 Click to see 320.50 unknown via CMAUP database
(1S,4S,5R,9S,10R,13S,14S)-14-(chloromethyl)-13,14-dihydroxy-5,9-dimethyltetracyclo[11.2.1.01,10.04,9]hexadecane-5-carbaldehyde 21589750 Click to see 354.90 unknown via CMAUP database
[(1S,4S,5R,9S,10R,13R,14S)-5-(hydroxymethyl)-5,9-dimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methanol 102594837 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)CO)C)CO 306.50 unknown via CMAUP database
13-Hydroxykaur-16-en-18-al 100967712 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)(C(=C)C4)O)C)C=O 302.50 unknown via CMAUP database
ent-16beta,17-Dihydroxy-9(11)-kauren-19-oic acid 23249404 Click to see CC12CCCC(C1CCC34C2=CCC(C3)C(C4)(CO)O)(C)C(=O)O 334.40 unknown via CMAUP database
Kaurenol 443465 Click to see 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 11876093 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97404-1
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)85205-X
Bruguierin A 11513260 Click to see 727.20 unknown via CMAUP database
Bruguierin B 11657758 Click to see 727.20 unknown via CMAUP database
Bruguierin C 11629176 Click to see 759.20 unknown via CMAUP database
Lup-20(29)-en-28-oic acid, 3beta-hydroxy- 2371 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(00)85205-X
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97404-1
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)97404-1
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see 386.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
(3R,8R,9R,10S,13R,14R,17S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 162965363 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97404-1
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97404-1
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)97404-1
Isofucosterol 5281326 Click to see 412.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Ustusol C 44557563 Click to see 284.39 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Ustusol A 44480213 Click to see 268.35 unknown via CMAUP database
Ustusol B 44557562 Click to see 268.35 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
1',2'-Dehydropenicillide 9896819 Click to see CC1=CC2=C(C(=C1)O)OC3=C(C(=C(C=C3)C=CC(C)(C)O)OC)C(=O)OC2 370.40 unknown via CMAUP database
3-[(R)-1-Hydroxy-3-methylbutyl]-4-methoxy-9-methyl-11-hydroxy-5H,7H-dibenzo[b,g][1,5]dioxocin-5-one 25273618 Click to see CC1=CC2=C(C(=C1)O)OC3=C(C(=C(C=C3)C(CC(C)C)O)OC)C(=O)OC2 372.40 unknown via CMAUP database
3'-O-Methyldehydroisopenicillide 9864866 Click to see CC1=CC2=C(C(=C1)O)OC3=C(C(=C(C=C3)C=CC(C)(C)OC)OC)C(=O)OC2 384.40 unknown via CMAUP database
Neosarphenol B 71451577 Click to see CC1=CC2=C(C(=C1)O)OC3=C(C(=C(C=C3)C=CC(=C)C)OC)C(=O)OC2 352.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(1S,9R)-1-methyl-12-oxatricyclo[7.2.1.02,7]dodeca-2,4,6-triene-4,5-diol 11367742 Click to see 206.24 unknown via CMAUP database
(1S,9R)-1-methyl-12-oxatricyclo[7.2.1.02,7]dodeca-2(7),3,5-trien-5-ol 11148193 Click to see 190.24 unknown via CMAUP database
(2S,7R,9S)-9-methoxy-7-methyl-2-propan-2-yl-7,9-dihydro-6H-furo[3,2-h]isochromen-3-one 73356791 Click to see 276.33 unknown via CMAUP database
7H-Furo(3,2-h)(2)benzopyran-3(2H)-one, 6,9-dihydro-7-hydroxy-7-methyl-2-(1-methylethylidene)-, (7R)- 156523 Click to see CC(=C1C(=O)C2=C(O1)C3=C(CC(OC3)(C)O)C=C2)C 260.28 unknown via CMAUP database
Aspergillumarin A 38346998 Click to see 248.27 unknown via CMAUP database
Aspergillumarin B 38347996 Click to see 250.29 unknown via CMAUP database
Bruguierol C 17752611 Click to see 206.24 unknown via CMAUP database
Ustusorane B 44557645 Click to see 242.27 unknown via CMAUP database
Ustusorane C 44557646 Click to see 274.31 unknown via CMAUP database
> Organoheterocyclic compounds / Dithiolanes / 1,2-dithiolanes
Bruguiesulfurol 11513780 Click to see 154.21 unknown via CMAUP database
> Organoheterocyclic compounds / Furopyrans
4,25-Dehydro-22-deoxyminiolutelide B 71608261 Click to see CC1C2(C3(C4C(O1)OC(=O)C4(CC5C3(C(O2)C=C6C(=CC(=O)OC6(C)C)C5=C)C)C)C(=O)OC)O 486.50 unknown via CMAUP database
4,25-Dehydrominiolutelide B 71608260 Click to see CC1C2(C3(C4(C(CC5(C3(C(O1)OC5=O)O)C)C(=C)C6=CC(=O)OC(C6=CC4O2)(C)C)C)C(=O)OC)O 502.50 unknown via CMAUP database
Berkeleyacetal A 24179625 Click to see 472.50 unknown via CMAUP database
Berkeleyacetal B 24179626 Click to see 486.50 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
[(5R,5As,9aS,9bS)-9b-hydroxy-6,6,9a-trimethyl-1-oxo-3,5,5a,7,8,9-hexahydrobenzo[e][2]benzofuran-5-yl] (2E,4E,6E)-octa-2,4,6-trienoate 10407821 Click to see CC=CC=CC=CC(=O)OC1C=C2COC(=O)C2(C3(C1C(CCC3)(C)C)C)O 386.50 unknown via CMAUP database
[(5R,5aS,9aS,9bS)-9b-hydroxy-6,6,9a-trimethyl-1-oxo-3,5,5a,7,8,9-hexahydrobenzo[e][2]benzofuran-5-yl] (2E,4E,7S)-7-hydroxyocta-2,4-dienoate 51693297 Click to see CC(CC=CC=CC(=O)OC1C=C2COC(=O)C2(C3(C1C(CCC3)(C)C)C)O)O 404.50 unknown via CMAUP database
Ustusolate D 44557643 Click to see CC1(CCCC2(C1C(C=C3C2(C(=O)OC3)O)OC(=O)C=CC=CC(OC)OC)C)C 420.50 unknown via CMAUP database
Ustusolate E 44480472 Click to see 374.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
octadecyl (2R,3S)-2-(3-hydroxy-5-methoxyphenyl)-7-methoxy-5-[(E)-3-octadecoxy-3-oxoprop-1-enyl]-2,3-dihydro-1-benzofuran-3-carboxylate 25105546 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC2=C(C(=C1)OC)OC(C2C(=O)OCCCCCCCCCCCCCCCCCC)C3=CC(=CC(=C3)OC)O 891.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolactams
CID 53235715 53235715 Click to see 553.60 unknown via CMAUP database
CID 53235716 53235716 Click to see CCC1CCC(=O)C=C2C(=CC3=C(O2)C(=CC(=C3)O)NC(=O)CC=C(C(=O)OC(C(C=C1)O)C=C(C)C)C)C 535.60 unknown via CMAUP database
CID 72715428 72715428 Click to see CCC1CCC(=O)C2=C(C(=CC3=C2C(=O)C=C4C3(C(C=C(C(=O)OC(C=C1)C(C=C(C)C)O)C)C(=O)N4)O)C)O 549.60 unknown via CMAUP database

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