Euonymus sachalinensis

Details Top

Internal ID UUID64401bcd0ac04876655845
Scientific name Euonymus sachalinensis
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 27: 446 (1882)

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.

Datura stramonium L. has a long record of smoke and topical use for respiratory and pain relief in several regions. In North America, the Kawaiisu People of California dried the leaves and mixed them with tobacco or other herbs, inhaling the smoke to treat asthma and congestion (Baker, 1981). Across Europe, crushed leaf poultices were applied to painful joints and bruises, while a poultice of fresh leaves was used for boils, carbuncles, and painful skin complaints (Grieve, 1931). In Ayurvedic and Unani medicine of South Asia, a decoction of leaves was traditionally taken for fever and malaria; external applications of leaf paste were also employed for rheumatic pain and swelling (Nadkarni, 1954). These practices rely on the respiratory irritant properties of the dried leaves, and all involve inhalation or topical application.

A practical inhalation protocol can be prepared as a mild smoke treatment. Finely chopped, thoroughly dried leaves are smoldered on a hot charcoal or heated stone in a ventilated space; 1–2 g of leaf material is typically used. The smoke is inhaled for 2–5 minutes only, beginning and ending with small exposures to gauge tolerance (Baker, 1981). Datura seeds are not recommended for homemade teas, tinctures, or poultices due to the high and variable tropane alkaloid content. The plant contains scopolamine, hyoscyamine, and atropine—potent antimuscarinic alkaloids that account for antispasmodic, bronchodilator, and analgesic effects when applied topically or inhaled, but they also carry strong systemic toxicity (Grieve, 1931; Nadkarni, 1954).

Modern relevance remains limited by safety concerns and regulatory controls in many countries, but smoke-based or topical uses persist in regional folk practice. Today, standardized, pharmaceutical-grade extracts are rare in consumer markets due to the risk of anticholinergic poisoning; non-pharmaceutical home preparations are discouraged. Contemporary research on Datura continues to focus on its alkaloids and pharmacology rather than on traditional dosed preparations.

General Uses Top

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Common products:
- Ornamental shrub widely cultivated for landscaping; sold by nurseries in container‑grown and bare‑root forms; used for hedges, screens, border plantings, and as a specimen plant in parks, residential gardens, and commercial landscapes.
- Market significance: part of the temperate ornamental plant trade; valued for hardiness, pruning tolerance, and attractive autumn foliage coloration.
- Cultivation practices: propagated by seed (cold‑stratified) or cuttings; standard nursery production methods ensure consistent stock quality.

Properties relevant to use:
- Growth habit: multi‑stemmed shrub reaching 2–4 m; suitable for hedging.
- Hardiness: USDA zones 4–7; tolerates winter temperatures down to –30 °C.
- Foliage: deciduous leaves turn vivid orange‑red in autumn.
- Pruning response: tolerates frequent shearing; maintains dense form.
- Light and soil: grows in full sun to partial shade; adaptable to well‑drained soils.
- Propagation: seed requires cold stratification; vegetative cuttings are common; both methods are standard in nursery production.

Standards and regulation:
- International: plant health certification under the International Plant Protection Convention (IPPC) and International Standards for Phytosanitary Measures (ISPM) governs export and import.
- United States: USDA APHIS regulations for import and interstate movement of horticultural stock.
- European Union: EU Plant Health Regulation (EU 2016/2031) and associated national plant passport requirements.
- Quality assurance: certification schemes such as the RHS Plant Finder and national nursery stock standards ensure material meets health and quality criteria.

Sustainability and sourcing:
- Cultivation: primarily sourced from commercial nurseries; large‑scale propagation reduces reliance on wild harvest.
- Conservation status: not listed as threatened; regional red‑list assessments indicate stable populations in native habitats (Sakhalin, Hokkaido, Korea).
- Sustainable practices: nurseries collect seed from cultivated stock and use vegetative propagation; regional forestry and horticulture guidelines promote minimal wild extraction.

Synonyms Top

Scientific name Authority First published in
Euonymus macropterus var. miniatus (Tolm.) Vorosch. Byull. Glavn. Bot. Sada 84: 33 (1972)
Euonymus maximowiczianus (Prokh.) Vorosch. Index Seminum (Acad. Sci. URSS) 9: 64 (1954)
Euonymus miniatus Tolm. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 18: 159 (1957)
Euonymus oxyphyllus var. kuenbuergia Honda Bot. Mag. (Tokyo) 47: 297 1933
Euonymus planipes (Koehne) Koehne Mitt. Deutsch. Dendrol. Ges. 15: 62 (1906 publ. 1907)
Euonymus robustus Nakai Bot. Mag. (Tokyo) 28: 307 (1914)
Euonymus tricarpus Koidz. Icon. Pl. Koisikav. 3: 77 (1916)
Euonymus latifolius var. sachalinensis F.Schmidt Reis. Amur-Land., Bot. 121 1868
Euonymus sachalinensis var. tricarpus (Koidz.) Kudô Rep. Exp. Forest. Agric. Kyusk. Univ. 1: 76 1931
Euonymus latifolius var. planipes Koehne Gartenflora 53(2): 29 (1904)
Kalonymus maximowiczianus Prokh. Fl. URSS 14: 744 (1949)
Kalonymus miniata (Tolm.) Prokh. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 20: 412 (1960)
Kalonymus sachalinensis (F.Schmidt) Prokh. Fl. URSS 14: 571 (1949)
Turibana planipes (Koehne) Nakai J. Jap. Bot. 24: 13 (1949)
Turibana sachalinensis (Fr.Schmidt) Nakai J. Jap. Bot. 24: 13 (1949)
Turibana tricarpa (Koidz.) Nakai J. Jap. Bot. 24: 13 (1949)
Euonymus planipes subsp. maximowiczianus (Prokh.) Nedol.

Common names Top

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Language Common/alternative name
Korean 회나무
Russian Бересклет сахалинский
Chinese 东北卫矛
Chinese 库页卫矛

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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Sow seeds directly at 4°C.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Kuril Islands
      • Primorye
      • Sakhalin

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000682052
UNII 2RBY15E1QD
Tropicos 6600005
KEW urn:lsid:ipni.org:names:161105-1
The Plant List kew-2803604
Plantarium 15444
Open Tree Of Life 598270
Observations.org 142178
NCBI Taxonomy 749925
IPNI 161105-1
GBIF 3794098
EPPO EUOSA
EOL 2880510
Elurikkus 415494
USDA GRIN 104666
Wikipedia Euonymus_sachalinensis
CMAUP NPO29362

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
Euonymus sachalinensis Induces Apoptosis by Inhibiting the Expression of c-Myc in Colon Cancer Cells Park SM, Jee W, Park YR, Kim H, Na YC, Jung JH, Jang HJ Molecules 14-Apr-2023
PMCID:PMC10140968
doi:10.3390/molecules28083473
PMID:37110707
Disjunction and Vicariance Between East and West Asia: A Case Study on Euonymus sect. Uniloculares Based on Plastid Genome Analysis Jamshed S, Kim JH Front Plant Sci 11-Mar-2022
PMCID:PMC8963480
doi:10.3389/fpls.2022.825209
PMID:35360330
Analysis of traditional knowledge of medicinal plants from residents in Gayasan National Park (Korea) Song MJ, Kim H, Lee BY, Brian H, Park CH, Hyun CW J Ethnobiol Ethnomed 21-Oct-2014
PMCID:PMC4216341
doi:10.1186/1746-4269-10-74
PMID:25336281
Screening of Korean Medicinal Plant Extracts for α-Glucosidase Inhibitory Activities Sancheti S, Sancheti S, Lee SH, Lee JE, Seo SY Iran J Pharm Res 01-Mar-2011
PMCID:PMC3828923
PMID:24250352
New Sesquiterpene Polyesters from Euonymus Species Judit Hohmann, Gábor Nagy, Zuber Dini, Gábor Günther, István Pelczer, Gyula Jerkovich, László Varjas American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50122A006
Isolation and structure elucidation of four new dihydro-β-agarofuran polyesters from Euonymus sachalinensis Judit Hohmann, Gábor Nagy, Gábor Günther, Gyula Argay, Alajos Kálmán, Gábor Czira Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19940003281
A sesquiterpene polyol ester from Euonymus sachalinensis Judit Hohmann, Gábor Nagy, Gábor Günther Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85549-7
Two sesquiterpene pyridine alkaloids from Euonymus sachalinensis Judit Hohmann, Gábor Nagy, Gábor Günther, Lászlò Varjas Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85382-2

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
[(1R,3S,13R,14R,17R,18R,19R,20S,21R,23S,24R,25S)-18,19,21,24-tetraacetyloxy-25-hydroxy-3,13,14,25-tetramethyl-6,15,22-trioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-20-yl]methyl acetate 163087610 Click to see 761.70 unknown https://doi.org/10.1021/NP50122A006
[(1S,3S,13S,14S,17R,18R,19S,20R,21S,24R,25R)-18,19,21,24-tetraacetyloxy-3,13,14,25-tetramethyl-6,15,22-trioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-20-yl]methyl acetate 101593037 Click to see CC1C(C(=O)OC2C(C34C(C(C(=O)C(C3(C(C2OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C)C(O4)(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)C)C 745.70 unknown https://doi.org/10.1016/0031-9422(93)85382-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
[(1S,2R,3R,4S,5R,6S,7S,9R,10R,12R)-3,4,5,7,12-pentaacetyloxy-6-(acetyloxymethyl)-2,10-dimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 10259204 Click to see 704.70 unknown https://doi.org/10.1039/P19940003281
[3,4,5,7,12-Pentaacetyloxy-6-(acetyloxymethyl)-2,10-dimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 163045380 Click to see 704.70 unknown https://doi.org/10.1039/P19940003281
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(1S,2S,3S,4S,5R,6S,7S,9R,10R,12R)-4,5,7,12-tetraacetyloxy-6-(acetyloxymethyl)-2-hydroxy-2,10-dimethyl-3-[(2R)-2-methylbutanoyl]-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 162848272 Click to see 746.70 unknown https://doi.org/10.1039/P19940003281
[(1S,2S,3S,4S,5R,6S,7S,9R,10R,12R)-4,5,7,12-tetraacetyloxy-6-(acetyloxymethyl)-3-(furan-3-carbonyl)-2-hydroxy-2,10-dimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 162913916 Click to see CC(=O)OCC12C(C(C(C(C13C(C(C(=O)C2OC(=O)C)C(O3)(C)COC(=O)C4=CC=CC=C4)OC(=O)C)(C)O)C(=O)C5=COC=C5)OC(=O)C)OC(=O)C 756.70 unknown https://doi.org/10.1039/P19940003281
[4,5,7,12-Tetraacetyloxy-6-(acetyloxymethyl)-2-hydroxy-2,10-dimethyl-3-(2-methylbutanoyl)-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 162848271 Click to see 746.70 unknown https://doi.org/10.1039/P19940003281
[4,5,7,12-Tetraacetyloxy-6-(acetyloxymethyl)-3-(furan-3-carbonyl)-2-hydroxy-2,10-dimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 162913915 Click to see 756.70 unknown https://doi.org/10.1039/P19940003281
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1R,2S,4R,5S,6R,7R,9S,12S)-4,7,12-triacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl] benzoate 162938304 Click to see CC1CC(C(C2(C13C(C(C(=O)C2OC(=O)C)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C4=CC=CC=C4)OC(=O)C 588.60 unknown https://doi.org/10.1016/0031-9422(93)85549-7
[(1S,2S,3S,4S,5R,6S,7S,9R,10R,12R)-4,5,7-triacetyloxy-6-(acetyloxymethyl)-2,12-dihydroxy-2,10-dimethyl-3-[(2R)-2-methylbutanoyl]-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 162907097 Click to see 704.70 unknown https://doi.org/10.1039/P19940003281
[4,5,7-Triacetyloxy-6-(acetyloxymethyl)-2,12-dihydroxy-2,10-dimethyl-3-(2-methylbutanoyl)-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-10-yl]methyl benzoate 162907096 Click to see 704.70 unknown https://doi.org/10.1039/P19940003281
[4,7,12-Triacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-8-oxo-11-oxatricyclo[7.2.1.01,6]dodecan-5-yl] benzoate 75012107 Click to see 588.60 unknown https://doi.org/10.1016/0031-9422(93)85549-7
[5,12-Diacetyloxy-6-(acetyloxymethyl)-4-benzoyloxy-2-hydroxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 162960481 Click to see CC(=O)OCC12C(CC3C(C1(C(CC(C2OC(=O)C)OC(=O)C4=CC=CC=C4)(C)O)OC3(C)C)OC(=O)C)OC(=O)C5=CC=CC=C5 652.70 unknown https://doi.org/10.1021/NP50122A006
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Mangiferin 5281647 Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O 422.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
3-(3,5-Dihydroxy-phenyl)-2-(4-hydroxy-phenyl)-2,3-dihydro-benzofuran-5-carbaldehyde 636845 Click to see 348.30 unknown via CMAUP database
4-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-4-[(E)-2-(4-hydroxyphenyl)vinyl]-2,3-dihydrobenzofuran-2-yl]benzene-1,2-diol 5279244 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O 470.50 unknown via CMAUP database
Moracin M 185848 Click to see 242.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
[(2R,3S,4S,5S)-5-[(2R,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 11092923 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)O)CO)O)O)O 560.50 unknown via CMAUP database
5-O-Caffeoylshikimic acid 5281762 Click to see 336.29 unknown via CMAUP database
Helonioside A 16745274 Click to see 694.60 unknown via CMAUP database
Helonioside B 21636195 Click to see 736.70 unknown via CMAUP database
Methyl Caffeate 689075 Click to see 194.18 unknown via CMAUP database
Smilaside L 24862701 Click to see 870.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-3-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy-5-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]oxolan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 24862643 Click to see CC(=O)OC1C(C(C(OC1OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC)COC(=O)C=CC5=CC=C(C=C5)O)CO)O)O 882.80 unknown via CMAUP database
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5S,6R)-3-acetyloxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4-hydroxy-5-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxolan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 24862644 Click to see 852.80 unknown via CMAUP database
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-4-hydroxy-2,5-bis[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]oxolan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 11593148 Click to see 882.80 unknown via CMAUP database
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-4-hydroxy-5-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxyoxolan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 24862642 Click to see CC(=O)OCC1C(C(C(C(O1)OC2(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O)OC(=O)C=CC4=CC=C(C=C4)O)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O 852.80 unknown via CMAUP database
1-O-(4-Hydroxy-trans-cinnamoyl)-2-O-(alpha-D-glucopyranosyl)-6-O-(3-methoxy-4-hydroxy-trans-cinnamoyl)-beta-D-fructofuranose 11735009 Click to see 664.60 unknown via CMAUP database
GlyTouCan:G35745RU 24850451 Click to see 840.80 unknown via CMAUP database
Smilaside C 10919948 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(O2)(COC(=O)C=CC3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C=CC5=CC(=C(C=C5)O)OC)O)O 840.80 unknown via CMAUP database
Smilaside G 24862591 Click to see 810.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isovitexin 162350 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R)-2alpha-(3-Methoxy-4-hydroxyphenyl)-5-(beta-D-glucopyranosyloxy)-6-methyl-3,4-dihydro-2H-1-benzopyran-3alpha,7-diol 10885307 Click to see CC1=C(C2=C(C=C1O)OC(C(C2)O)C3=CC(=C(C=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O 480.50 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[[(2R,3R)-3,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-6-methyl-3,4-dihydro-2H-chromen-5-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 11081337 Click to see 480.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
quercetin 3-O-beta-L-rhamnopyranoside 5320854 Click to see 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Piceatannol 667639 Click to see 244.24 unknown via CMAUP database
Resveratrol 445154 Click to see 228.24 unknown via CMAUP database

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