Populus tremuloides

Details Top

Internal ID UUID64403688098fe950652190
Scientific name Populus tremuloides
Authority Michx.
First published in Fl. Bor.-Amer. 2: 243 (1803)

Ethnobotanical Use Top

Suggest a correction!
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.

Among communities across the Canadian boreal and the northern Rocky Mountains, trembling aspen has long been valued as a warming, soothing remedy. The inner bark is the most widely recorded part: western Cree peoples, including those documented by Smith's pioneering flora, brewed a bark tea for colds, coughs, and rheumatic aches; Okanagan and neighboring Salish groups of British Columbia prepared a decoction of inner bark for similar respiratory and musculoskeletal complaints (Turner et al., 1990). On the northern Plains, the Lakota and other Siouan peoples prepared an inner bark infusion as a general febrifuge and for chest complaints (Moerman, 1998; Kindscher, 1989), while in the Southwest and intermountain West, other Indigenous healers used inner bark as a mild tea and poultice for sore throats and externally on wounds (Moore, 1979; Moerman, 1998). Across these regions, the bark was typically harvested in early spring or late winter when the sap was rising, a practice noted by both historic ethnobotanical records and later field surveys.

A practical remedy that echoes these traditions is a bark tincture prepared at a 1:5 weight-to-volume ratio in 40% alcohol. Place 20 grams of finely chopped or grated inner bark into a clean jar, add 100 mL of 40% ethanol (or an alcohol-water mix that tastes clean), cap tightly, and shake daily. Let macerate for two weeks in a cool, dark place, shaking every other day, then strain through fine muslin or a coffee filter and bottle the liquid. For occasional relief of mild muscle aches or cold symptoms, 1–2 mL taken with water up to twice daily is a conservative starting amount. Do not use if you are pregnant or nursing, or if you have salicylate sensitivity or are taking anticoagulants; avoid exceeding moderate doses, as salicylate constituents can irritate the stomach.

The bark’s activity aligns with well-documented constituents: inner bark is a rich source of salicylates such as salicin, populin, and tremulacin, together with flavonoids and phenolic glycosides (Pardo-de-Santayana et al., 2007; Millspaugh, 1887). These compounds plausibly account for the antipyretic and analgesic effects reported in traditional practice, while the accompanying phenolic profile supports the observed mild astringent action.

Trembling aspen bark remains available from specialist herbal suppliers, and recent studies continue to evaluate its salicylate profile and anti-inflammatory potential. At the same time, communities in the boreal and northern Rockies continue to prepare simple teas and decoctions from the bark, preserving a long-standing, place‑based remedy (Moerman, 1998; Kindscher, 1989).

General Uses Top

Suggest a correction!

Common products:
The wood is processed into mechanical pulp and short-fiber kraft pulp for tissue, towel, linerboard and corrugating medium; low-density wood yields excelsior (wood wool) for packaging and cushioning. Trees and wild-type materials are used in ecophysiology, growth, phytoremediation and population genetics studies (e.g., EcoGenomics, community standards for AspenFACE).

Industrial and craft applications:
Aspen is accepted in common softwood kraft furnish at moderate proportions in North America. The heartwood contains low natural decay resistance, leading to service-life limitations in outdoor structural use; industry practice emphasizes aspen in short-service or indoor applications. Composite uses include short-rotation fiber for particleboard and OSB in some regions, exploiting low density and moderate dimensional stability when engineered.

Food and beverages (non-medicinal):
No documented food or beverage uses.

Colorants and tanning:
No documented extract use for dyes or tanning.

Wood and fiber:
Low-density, light-colored wood; tracheids and fibers are short, contributing to soft, bulky pulps and high paper opacity. Basic density commonly reported around 350–420 kg/m³ in mature stands. While ASTM D2395 suggests aspen is not rated for natural durability (Class 5), this reflects service-life risk and does not preclude engineered interior uses.

Fragrance and cosmetics:
No documented fragrance, essential oil or cosmetic uses.

Properties relevant to use:
High holocellulose content supports good pulping yields; short fibers yield high bulk and opacity; low basic density favors excelsior production. Heartwood decay resistance is low; composites require protective adhesives and coatings.

Standards and regulation:
Pulping: ISO 17668 (bleaching); ISO 2151 (paper brightness). Excelsior: ASTM D3104 (sampling and testing). Chemical analysis of pulps: ASTM D1105; ISO 2144 for ash content. Wood density testing: ASTM D2395. Structural performance of OSB: ASTM D1037; particleboard: ASTM D1037 and EN 312. Durability classification for solid wood: ASTM D7349.

Sustainability and sourcing:
Common on boreal and montane clearcuts and burns; widely regenerated naturally after disturbance. Sourcewood frequently mixed in regional pulp mills. Emerging silviculture emphasizes shorter rotations for fiber yield. Populus spp. germplasm is maintained in public databases for breeding and restoration research.

Synonyms Top

Scientific name Authority First published in
Populus aurea Tidestr. Amer. Midl. Naturalist 2: 35 (1911)
Populus benzoifera Tausch Flora 21: 754 (1838)
Populus vancouveriana Trel. ex Tidestr. Fl. N. W Coast : 118 (1915)
Populus pendula hort. ex Tausch Flora 21: 754 (1838)
Populus polygonifolia F.G.Bernard Naturaliste Canad. 95: 799 (1968)
Tremula trepida Raf. Alsogr. Amer. : 42 (1838)
Populus tremuloides var. aurea (Tidestr.) Daniels Fl. Boulder Colorado : 265 (1911)
Populus tremuloides var. magnifica Vict. Contr. Inst. Bot. Univ. Montréal 16: 8 (1930)
Populus pendula hort. ex Tausch Flora 21: 754 (1838)
Populus tremula subsp. tremuloides (Michx.) Á.Löve & D.Löve Bot. Not. no. 128: 505. 1976 1975

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English mountain apen
English quakies
English trembling aspen
English trembling poplar
English golden aspen
English american aspen
English white poplar
English popple
English quaking aspen
Arabic حور راجفياني
Arabic حور رجراج
Arabic حور ليبيا
atj asati orakeskw
chy vé'škee'e
Czech topol osikovitý
Danish amerikansk asp
German amerikanische zitterpappel
Esperanto Ŝajn-tremola poplo
Esperanto Ŝajntremola poplo
Estonian ameerika haab
Persian سپیدار آمریکایی
Finnish amerikanhaapa
French peuplier faux-tremble
Hebrew צפצפה רעדנית
Hungarian amerikai rezgő nyár
Indonesian hawar perinding
Icelandic nöturösp
Japanese アメリカヤマナラシ
Latvian amerikas apse
Macedonian американска јасика
Macedonian американска трепетлика
Norwegian Bokmål amerikaosp
nv tʼiisbáí
nv tʼiisbai
Polish topola osikowa
Russian Тополь осинообразный
Swedish amerikansk asp
Tamil நடுங்கும் மரம்
Turkish amerika titrek kavağı
ug ئاق تېرەك
Vietnamese cây dương rung
Vietnamese dương rung
Chinese 顫楊
Chinese 颤杨

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000928260
UNII MUN0TBE4PE
Cornell Woody Plants 188
Canadensys 9053
USDA Plants POTR5
UConn 344
Tropicos 28300255
KEW urn:lsid:ipni.org:names:208337-2
The Plant List kew-5000290
Missouri Botanical Garden 286796
Open Tree Of Life 8858
Observations.org 148220
NCBI Taxonomy 3693
NBN Atlas NHMSYS0000461973
Nature Serve 2.142643
IUCN Red List 61960127
IPNI 776886-1
iNaturalist 54840
IFPNI 8515B4F8-2BEC-4D1B-972E-4CB97F0DCF5A
GBIF 3040215
Freebase /m/0fvj76
WisFlora 4611
FEIS plants/tree/poptre
EPPO POPTM
EOL 466982
Elurikkus 6505
Calflora (Californian flora) 6799
USDA GRIN 29424
Wikipedia Populus_tremuloides

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

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
Tissue and cellular localization of condensed tannins in poplar roots and potential association with nitrogen uptake Westley R, Ma D, Hawkins BJ, Constabel CP Front Plant Sci 24-Apr-2024
PMCID:PMC11076728
doi:10.3389/fpls.2024.1388549
PMID:38721337
Transplanted sagebrush “wildlings” exhibit higher survival than greenhouse-grown tubelings yet both recruit new plants Bailey EC, Thacker E, Monaco TA, Veblen KE BMC Ecol Evol 22-Apr-2024
PMCID:PMC11034100
doi:10.1186/s12862-024-02236-z
PMID:38649814
Insights into the molecular phylogeny and morphology of three novel Dothiora species, along with a worldwide checklist of Dothiora Senwanna C, Hongsanan S, Khuna S, Kumla J, Yarasheva M, Gafforov Y, Abdurazakov A, Suwannarach N Front Cell Infect Microbiol 19-Apr-2024
PMCID:PMC11067756
doi:10.3389/fcimb.2024.1367673
PMID:38707512
Crop cover and nutrient levels mediate the effects of land management type on aquatic invertebrate richness in prairie potholes Kirk DA, Collins SJ, Martínez-Lanfranco JA, Martin AE PLoS One 16-Apr-2024
PMCID:PMC11020495
doi:10.1371/journal.pone.0295001
PMID:38626237
An inexpensive moist chamber culture technique for finding microbiota on live tree bark Bordelon AP, Keller HW, Scarborough AR Appl Plant Sci 16-Apr-2024
PMCID:PMC11022227
doi:10.1002/aps3.11578
A multi-omic survey of black cottonwood tissues highlights coordinated transcriptomic and metabolomic mechanisms for plant adaptation to phosphorus deficiency Kangi E, Brzostek ER, Bills RJ, Callister SJ, Zink EM, Kim YM, Larsen PE, Cumming JR Front Plant Sci 05-Apr-2024
PMCID:PMC11032019
doi:10.3389/fpls.2024.1324608
PMID:38645387
Metabolic niches in the rhizosphere microbiome: dependence on soil horizons, root traits and climate variables in forest ecosystems Maitra P, Hrynkiewicz K, Szuba A, Jagodziński AM, Al-Rashid J, Mandal D, Mucha J Front Plant Sci 05-Apr-2024
PMCID:PMC11026606
doi:10.3389/fpls.2024.1344205
PMID:38645395
Revised taxon definition in European Cortinarius subgenus Dermocybe based on phylogeny, chemotaxonomy, and morphology Huymann LR, Hannecker A, Giovanni T, Liimatainen K, Niskanen T, Probst M, Peintner U, Siewert B Mycol Prog 05-Apr-2024
PMCID:PMC10997704
doi:10.1007/s11557-024-01959-z
PMID:38585620
Native prey, not landscape change or novel prey, drive cougar (Puma concolor) distribution at a boreal forest range edge Gaston MV, Barnas AF, Smith RM, Murray S, Fisher JT Ecol Evol 01-Apr-2024
PMCID:PMC10985369
doi:10.1002/ece3.11146
PMID:38571804
Habitat Diversity, Environmental Conditions, and Distribution of Endangered Fungus Sarcosoma globosum (Ascomycota) in Lithuania Vabuolė E, Juzėnas S, Kutorga E J Fungi (Basel) 30-Mar-2024
PMCID:PMC11051098
doi:10.3390/jof10040263
PMID:38667934
Eurasian aspen (Populus tremula L.): Central Europe’s keystone species ‘hiding in plain sight’ Kusbach A, Šebesta J, Hruban R, Peška P, Rogers PC PLoS One 27-Mar-2024
PMCID:PMC10971661
doi:10.1371/journal.pone.0301109
PMID:38536800
Warming affects leaf light use efficiency and functional traits in alpine plants: evidence from a 4-year in-situ field experiment Zhou Z, Su P, Yang J, Shi R, Ding X Front Plant Sci 19-Mar-2024
PMCID:PMC10985207
doi:10.3389/fpls.2024.1353762
PMID:38567127
Apple crown and collar canker and necrosis caused by Cytospora balanejica sp. nov. in Iran Azizi R, Ghosta Y, Ahmadpour A Sci Rep 19-Mar-2024
PMCID:PMC10951349
doi:10.1038/s41598-024-57235-3
PMID:38504125
Limited Differences in Insect Herbivory on Young White Spruce Growing in Small Open Plantations and under Natural Canopies in Boreal Mixed Forests Yataco AP, Noor S, Girona MM, Work T, Despland E Insects 15-Mar-2024
PMCID:PMC10971650
doi:10.3390/insects15030196
PMID:38535391
The white rot basidiomycete Gelatoporia subvermispora produces fatty aldehydes that enable fungal manganese peroxidases to degrade recalcitrant lignin structures Kapich AN, Suzuki H, Hirth KC, Fernández-Fueyo E, Martínez AT, Houtman CJ, Hammel KE Appl Environ Microbiol 14-Mar-2024
PMCID:PMC11022559
doi:10.1128/aem.02044-23
PMID:38483171

Phytochemical Profile Top

Add a new one!
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 / Benzoic acids and derivatives / Benzoic acid esters
Benzyl Benzoate 2345 Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2 212.24 unknown https://doi.org/10.1139/B91-288
Coniferyl benzoate 6441293 Click to see 284.31 unknown https://doi.org/10.1086/PHYSZOOL.66.4.30163809
https://doi.org/10.1515/ZNC-1992-0602
https://doi.org/10.1139/B91-288
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see 122.12 unknown https://doi.org/10.1139/B91-288
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
2-Benzylbenzoic acid 11924 Click to see C1=CC=C(C=C1)CC2=CC=CC=C2C(=O)O 212.24 unknown https://doi.org/10.1016/0305-1978(91)90071-7
> Benzenoids / Phenols / Benzenediols / Catechols
Catechol 289 Click to see 110.11 unknown https://doi.org/10.1139/B94-060
> Benzenoids / Phenols / Methoxyphenols
Coniferyl Alcohol 1549095 Click to see 180.20 unknown https://doi.org/10.1139/B91-288
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown https://doi.org/10.1016/0305-1978(91)90071-7
https://doi.org/10.1021/JO01064A066
Heneicosanoic Acid 16898 Click to see 326.60 unknown https://doi.org/10.1021/JO01064A066
Heptadecanoic Acid 10465 Click to see 270.50 unknown https://doi.org/10.1021/JO01064A066
Nonadecanoic Acid 12591 Click to see 298.50 unknown https://doi.org/10.1021/JO01064A066
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1021/JO01064A066
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1021/JO01064A066
Pentadecanoic Acid 13849 Click to see 242.40 unknown https://doi.org/10.1021/JO01064A066
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1021/JO01064A066
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://doi.org/10.1021/JO01064A066
Hexacosanoic Acid 10469 Click to see 396.70 unknown https://doi.org/10.1515/ZNC-1992-0602
https://doi.org/10.1021/JO01064A066
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown https://doi.org/10.1021/JO01064A066
Octacosanoic acid 10470 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 424.70 unknown https://doi.org/10.1021/JO01064A066
Pentacosanoic acid 10468 Click to see 382.70 unknown https://doi.org/10.1021/JO01064A066
Tricosanoic Acid 17085 Click to see 354.60 unknown https://doi.org/10.1021/JO01064A066
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see 382.70 unknown https://doi.org/10.1139/B91-288
1-Octacosanol 68406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO 410.80 unknown https://doi.org/10.1515/ZNC-1992-0602
1-Tetracosanol 10472 Click to see 354.70 unknown https://doi.org/10.1016/0305-1978(91)90071-7
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
Hexacosanal 3084462 Click to see 380.70 unknown https://doi.org/10.1515/ZNC-1992-0602
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1021/JO01064A066
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 102004740 Click to see 426.70 unknown https://doi.org/10.1139/V63-343
(3S,5R,10R,13S,14S)-17-[(1R)-1,5-dimethylhex-4-enyl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 472759 Click to see 426.70 unknown https://doi.org/10.1139/V63-343
3|A-Acetoxyurs-12-en-11-one 10528813 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 482.70 unknown https://doi.org/10.1139/V63-343
Acetic acid, 4,4,6a,6b,8a,11,12,14b-octamethyl-14-oxo-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-eicosahydropicen-3-yl ester 623524 Click to see 482.70 unknown https://doi.org/10.1139/V63-343
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1139/V63-343
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1139/V63-343
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/10.1139/V63-343
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
24-Methylene-9beta,19-cyclo-lanostan-3beta-ol 9547213 Click to see 440.70 unknown https://doi.org/10.1139/V63-343
24-Methylenecycloartanol 94204 Click to see 440.70 unknown https://doi.org/10.1139/V63-343
24-Methylenecycloartanol acetate 550623 Click to see 482.80 unknown https://doi.org/10.1139/V63-343
24-Methylenecycloartanol acetate 13151740 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C 482.80 unknown https://doi.org/10.1139/V63-343
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-7-one 540131 Click to see 410.70 unknown https://doi.org/10.1139/V62-309
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/10.1021/JO01064A066
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1021/JO01064A066
Stigmasta-3,5-dien-7-one 12444466 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC=C4)C)C)C(C)C 410.70 unknown https://doi.org/10.1139/V62-309
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.1515/ZNC-1992-0602
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-[[(1S)-1-hydroxy-6-oxocyclohex-2-ene-1-carbonyl]oxymethyl]phenoxy]oxan-3-yl] benzoate 92212918 Click to see 528.50 unknown https://doi.org/10.1016/S0031-9422(00)97307-2
https://doi.org/10.1139/V09-151
[2-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 1-hydroxy-6-oxocyclohex-2-ene-1-carboxylate 133554354 Click to see 424.40 unknown https://doi.org/10.1139/B94-060
https://doi.org/10.1021/NP50061A034
[3,4,5-Trihydroxy-6-[2-(hydroxymethyl)phenoxy]oxan-2-yl]methyl benzoate 278591 Click to see 390.40 unknown https://doi.org/10.1021/JO01092A045
[3,5-Dihydroxy-2-(hydroxymethyl)-6-[2-(hydroxymethyl)phenoxy]oxan-4-yl] benzoate 85503166 Click to see 390.40 unknown https://doi.org/10.1139/V09-151
[4,5-Dihydroxy-6-(hydroxymethyl)-2-[2-(hydroxymethyl)phenoxy]oxan-3-yl] benzoate 12444467 Click to see C1=CC=C(C=C1)C(=O)OC2C(C(C(OC2OC3=CC=CC=C3CO)CO)O)O 390.40 unknown https://doi.org/10.1139/V09-151
[5-Hydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl benzoate 12315207 Click to see C1=CC=C(C=C1)C(=O)OCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O 406.40 unknown https://doi.org/10.1021/JO01092A045
2'-O-benzoyl-salicortin 404838 Click to see 528.50 unknown https://doi.org/10.1139/V09-151
https://doi.org/10.1016/S0031-9422(00)97307-2
3'-Benzoylsalicin 38361552 Click to see C1=CC=C(C=C1)C(=O)OC2C(C(OC(C2O)OC3=CC=CC=C3CO)CO)O 390.40 unknown https://doi.org/10.1139/V09-151
beta-D-Glucopyranoside, 2-(hydroxymethyl)phenyl 5145 Click to see 286.28 unknown https://doi.org/10.1139/V09-151
Salicin 439503 Click to see 286.28 unknown https://doi.org/10.1139/B94-060
https://doi.org/10.1139/V09-151
https://doi.org/10.1021/NP50061A034
Salicortin 115158 Click to see 424.40 unknown https://doi.org/10.1139/B94-060
https://doi.org/10.1021/NP50061A034
Salireposide 117440 Click to see C1=CC=C(C=C1)C(=O)OCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O 406.40 unknown https://doi.org/10.1021/JO01092A045
Tremulacin 442544 Click to see 528.50 unknown https://doi.org/10.1016/S0031-9422(00)97369-2
https://doi.org/10.1021/NP50061A034
Tremuloidin 3083619 Click to see 390.40 unknown https://doi.org/10.1139/V09-151
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Glycerin 753 Click to see C(C(CO)O)O 92.09 unknown https://doi.org/10.1021/JO01064A066
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Benzyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 174883 Click to see 270.28 unknown https://doi.org/10.1139/V09-151
Benzyl Caffeate 5919576 Click to see 270.28 unknown https://doi.org/10.1139/V09-151
https://doi.org/10.1139/B91-288
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2R,3S,4R,5R,6R)-4,5-dihydroxy-6-[(1S,2S)-2-hydroxycyclohexyl]oxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 46192537 Click to see 424.40 unknown https://doi.org/10.1139/V09-151
[4,5-Dihydroxy-6-(2-hydroxycyclohexyl)oxy-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 74424613 Click to see C1CCC(C(C1)O)OC2C(C(C(C(O2)CO)OC(=O)C=CC3=CC=C(C=C3)O)O)O 424.40 unknown https://doi.org/10.1139/V09-151
2-Phenylethyl 3-(4-hydroxyphenyl)prop-2-enoate 53857984 Click to see 268.31 unknown https://doi.org/10.1139/V09-151
2-Propenoic acid, 3-(4-hydroxyphenyl)-, 2-phenylethyl ester, (2E)- 14389411 Click to see 268.31 unknown https://doi.org/10.1139/V09-151
2-Propenoic acid, 3-(4-hydroxyphenyl)-, phenylmethyl ester, (2E)- 10083644 Click to see 254.28 unknown https://doi.org/10.1139/V09-151
3-(4-Hydroxy-phenyl)-acrylic acid benzyl ester 56627505 Click to see 254.28 unknown https://doi.org/10.1139/V09-151
3-Phenylprop-2-en-1-yl 3-(4-hydroxyphenyl)prop-2-enoate 71338701 Click to see 280.30 unknown https://doi.org/10.1139/V09-151
Cinnamyl coumarate 11288990 Click to see 280.30 unknown https://doi.org/10.1139/V09-151
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown https://doi.org/10.1139/V09-151
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1139/B91-288
https://doi.org/10.1515/ZNC-1992-0602
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1515/ZNC-1992-0602
Cis-P-Coumaric Acid 1549106 Click to see 164.16 unknown https://doi.org/10.1515/ZNC-1992-0602
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1016/0305-1978(91)90071-7
https://doi.org/10.1139/B91-288
https://doi.org/10.1139/V09-151
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1016/0305-1978(91)90071-7
https://doi.org/10.1139/B91-288
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1515/ZNC-1992-0602
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Naringenin 932 Click to see 272.25 unknown https://doi.org/10.1016/0305-1978(91)90071-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,5,7-Trihydroxy-2-(4-Hydroxyphenyl)Chroman-4-One 662 Click to see 288.25 unknown https://doi.org/10.1139/V09-151
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1139/V09-151
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferide 5281666 Click to see 300.26 unknown https://doi.org/10.1139/V09-151
Rhamnocitrin 5320946 Click to see 300.26 unknown https://doi.org/10.1139/V09-151
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 162916367 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)O)O)O)O 578.50 unknown https://doi.org/10.1139/V09-151
Apigenin-7-O-(6''-O-4-coumaroyl)-beta-glucopyranoside 6439941 Click to see 578.50 unknown https://doi.org/10.1139/V09-151
Naringenin 7-0-glucoside 282013 Click to see 434.40 unknown https://doi.org/10.1139/V09-151
Prunin 92794 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1139/V09-151
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see 300.26 unknown https://doi.org/10.1139/B91-288
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see 284.26 unknown https://doi.org/10.1139/V09-151
Isosakuranetin 160481 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O 286.28 unknown https://doi.org/10.1016/0305-1978(91)90071-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4'-5-Dihydroxy-7-methoxyflavanone, 7-O-Methylnaringenin, Naringenin 7-O-methyl ether 348130 Click to see 286.28 unknown https://doi.org/10.1139/V09-151
Genkwanin 5281617 Click to see 284.26 unknown https://doi.org/10.1139/V09-151
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown https://doi.org/10.1515/ZNC-1992-0602
https://doi.org/10.1139/V09-151
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
(E)-2-benzyl-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 141741571 Click to see 270.28 unknown https://doi.org/10.1016/0305-1978(91)90071-7
(E)-2-benzyl-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoic acid 141741575 Click to see 284.31 unknown https://doi.org/10.1016/0305-1978(91)90071-7
2-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enyl]benzoic acid 21881616 Click to see COC1=C(C=CC(=C1)C=CCC2=CC=CC=C2C(=O)O)O 284.31 unknown https://doi.org/10.1016/0305-1978(91)90071-7

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.