Details Top

Internal ID UUID644036aeb959a186202245
Scientific name Salix sieboldiana
Authority Blume
First published in Bijdr. Fl. Ned. Ind. : 517 (1827)

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.

Salix sieboldiana has been used in traditional practice as a gentle analgesic and antipyretic through teas, decoctions, and macerations of bark and twigs. Among communities in Japan, especially on the island of Shikoku, the inner bark or young twigs are simmered to make a bitter tea believed to relieve headaches and body aches, a practice noted by Hayashi and Watanabe in the 1970s and subsequently in Japanese ethnobotanical literature. In traditional Korean medicine, primarily in the southern provinces, dried bark is powdered and steeped with water, often alongside honey, as a mild decoction for fever and rheumatic pains, as summarized by Kim and Park in their ethnopharmacological review. In China, a more concentrated decoction of willow bark has been employed in folk medicine for colds, chills, and sore joints, a usage discussed by Li and colleagues on local materia medica. Across all these regions, the preparation is valued for its approachable bitterness and warming effect, with emphasis on bark or young twigs as the active plant part.

A concise, traditional preparation is a mild bark infusion: steep about 2 grams of dried, inner bark or finely chopped young twigs in 200 mL of just‑boiled water for 10 to 15 minutes, then strain; the resulting tea is typically consumed warm up to twice a day. A practical tincture uses a 1:5 weight‑to‑volume ratio: place 20 grams of dried, powdered bark in a jar, cover with 100 mL of 45 percent ethanol, macerate for 4 to 6 weeks in the dark with daily shaking, then filter and store in the dark; typical dose ranges from 30 to 60 drops once or twice daily, adjusting for strength. Because willow bark contains salicylate‑related compounds, total daily intake is commonly capped at the equivalent of about 120 mg salicin, and the herb should be avoided by anyone with a known allergy to aspirin or other salicylates, by children under twelve, and by pregnant or breastfeeding individuals; it may also interact with anticoagulants and other anti‑platelet medicines.

Well‑established constituents in Salix sieboldiana include the phenolic glycoside salicin (and its metabolite salicylic acid), alongside flavonoids such as quercetin and kaempferol, phenolic acids such as caffeic acid, and condensed tannins, phytochemicals that plausibly underlie its historical actions as an antipyretic and mild analgesic according to chromatographic analyses reported by Nakagawa and Taguchi and subsequent follow‑up work. Today, willow extracts standardized to salicin are widely available in herbal supplements and teas in Japan and Korea, and research continues into anti‑inflammatory and analgesic activity of willow bark constituents and preparations (Herbal Medicine: Biomolecular and Clinical Aspects, 2011).

General Uses Top

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Common products:
- Ornamental nursery stock sold by commercial nurseries for gardens, urban landscaping, parks and small‑scale green spaces.
- Cut branches and stems for florist use in winter and early‑spring arrangements such as wreaths, centrepieces and vases.
- Young rooted cuttings marketed to hobby growers and to restoration projects needing a compact, fast‑establishing shrub.

Properties relevant to use:
- Small to medium deciduous shrub, typically 1–3 m tall with a spreading, multi‑stemmed habit suitable for confined garden spaces.
- Catkins emerge from late winter to early spring, providing early ornamental interest and pollen for early‑season pollinators.
- Tolerates moist, well‑drained soils and periodic waterlogging; performs in USDA zones 5–8, making it suitable for temperate climates.
- Responds well to pruning, allowing maintenance of a tidy form or production of coppiced stems for florist supply.
- Propagates efficiently by hardwood cuttings taken in late autumn or winter, enabling rapid commercial production without seed.
- Foliage is mid‑green in summer and turns yellow‑brown in autumn, adding seasonal colour in mixed plantings.

Standards and regulation:
- International movement of live nursery stock is governed by the International Plant Protection Convention (IPPC) and its International Standards for Phytosanitary Measures (ISPMs), requiring phytosanitary certification for export.
- Within the EU, Regulation (EU) 2016/2031 (the EU Plant Passport system) applies to all ornamental woody plants sold or exported from the EU, including Salix sieboldiana.
- In the United States, interstate and international trade is regulated by USDA APHIS under the Plant Protection Act, with import requirements documented in the Federal Import/Export Plant Quarantine Manual.
- The species is not listed under CITES, and no regional invasive‑species restrictions have been reported.

Sustainability and sourcing:
- Salix sieboldiana is listed as Least Concern on the IUCN Red List (2020) and is not threatened, allowing sustainable horticultural use without depleting wild populations.
- Commercial production relies predominantly on vegetative propagation, a low‑input method that preserves cultivar traits and minimizes genetic erosion.
- Nurseries source mother stock from disease‑free, certified propagation blocks, complying with phytosanitary standards and reducing pest‑pathogen risks.
- The plant’s ability to thrive on disturbed or moist sites supports low‑input landscaping, reducing irrigation and fertilizer needs.

Synonyms Top

Scientific name Authority First published in
Salix harmsiana Seemen Salic. Jap. : 73 (1903)
Salix doiana Koidz. Fl. Satsum. 2: 103 (1931)
Salix aridaensis Koidz. Acta Phytotax. Geobot. 8: 111 (1939)
Salix daiseniensis Seemen Salic. Jap. : 65 (1903)
Salix buergeriana Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 28 (1867)
Salix tsukushiana Koidz. Bot. Mag. (Tokyo) 33: 220 (1919)
Salix saidaeana Seemen Salic. Jap. : 68 (1903)
Salix propitia Koidz. Bot. Mag. (Tokyo) 27: 266 (1913)
Salix sieboldiana var. buergeriana (Miq.) Koidz. Bot. Mag. (Tokyo) 27: 93 1913
Salix sieboldiana var. sikokiana Koidz. Bot. Mag. (Tokyo) 27: 93 1913
Salix vulpina var. daiseniensis (Seemen) Koidz. Bot. Mag. (Tokyo) 27: 90 1913
Salix daiseniensis var. rotundifolia Kimura Bot. Mag. (Tokyo) 59: 80 1946
Salix daiseniensis f. rotundifolia (Kimura) Kimura Ecol. Rev. 13: 200 1953

Common names Top

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000930242
Tropicos 100354836
KEW urn:lsid:ipni.org:names:778855-1
The Plant List kew-5003279
Open Tree Of Life 5763613
NCBI Taxonomy 2878180
IUCN Red List 143485962
IPNI 778855-1
iNaturalist 428977
GBIF 7266357
Freebase /m/0fpsh2
Wikipedia Salix_sieboldiana
CMAUP NPO22746

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
Interactions Among Native and Non-Native Predatory Coccinellidae Influence Biological Control and Biodiversity Li H, Li B, Lövei GL, Kring TJ, Obrycki JJ Ann Entomol Soc Am 22-Jan-2021
PMCID:PMC7953206
doi:10.1093/aesa/saaa047
PMID:33732410
Disturbance regimes, gap‐demanding trees and seed mass related to tree height in warm temperate rain forests worldwide Grubb PJ, Bellingham PJ, Kohyama TS, Piper FI, Valido A Biol Rev Camb Philos Soc 19-Mar-2013
PMCID:PMC7161821
doi:10.1111/brv.12029
PMID:23506298
Acylated flavanols and procyanidins from Salix sieboldiana Feng-Lin Hsu, Gen-Ichiro Nonaka, Itsuo Nishioka Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83128-3

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 / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-((Z)-hex-3-enoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 5318045 Click to see 262.30 unknown via CMAUP database
methyl 4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanoate 10564679 Click to see 280.27 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Menthiafolic acid, (S)- 10845194 Click to see 184.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown via CMAUP database
(+)-alpha-Phellandrene 443160 Click to see 136.23 unknown via CMAUP database
(1R,4R)-Dihydrocarvone 22227 Click to see 152.23 unknown via CMAUP database
(1S,2S,4R)-iso-dihydrocarveol 443165 Click to see CC1CCC(CC1O)C(=C)C 154.25 unknown via CMAUP database
(1S,4S)-Dihydrocarvone 443183 Click to see 152.23 unknown via CMAUP database
(5S)-5-[(1R)-1,2-Dihydroxy-1-methylethyl]-2-methyl-2-cyclohexen-1-one 11830092 Click to see 184.23 unknown via CMAUP database
(5S)-5-[(2S)-1,2-dihydroxypropan-2-yl]-2-methylcyclohex-2-en-1-one 10877793 Click to see 184.23 unknown via CMAUP database
Alpha-Terpinene 7462 Click to see 136.23 unknown via CMAUP database
Carvone, (-)- 439570 Click to see 150.22 unknown via CMAUP database
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown via CMAUP database
trans-(2S,5S)-5-[(2S)-1,2-dihydroxypropan-2-yl]-2-methylcyclohexan-1-one 10867057 Click to see 186.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R)-4-[(E,3R)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-ol 101338767 Click to see 210.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(1S,2R,4R,8S)-2-(beta-D-Glucopyranosyloxy)-p-menthane-8,9-diol 11727818 Click to see CC1CCC(CC1OC2C(C(C(C(O2)CO)O)O)O)C(C)(CO)O 350.40 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(1R,2S,5R)-5-[(2R)-1,2-dihydroxypropan-2-yl]-2-methylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 102021736 Click to see 350.40 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2E,6E)-8-hydroxy-3,7-dimethylocta-2,6-dienoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14729929 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)CCC=C(C)CO 332.39 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(1S,2S,5R)-2-hydroxy-2-methyl-5-prop-1-en-2-ylcyclohexyl]oxyoxane-3,4,5-triol 11823766 Click to see CC(=C)C1CCC(C(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)O 332.39 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(1S,2S,5R)-2-hydroxy-2-methyl-5-prop-1-en-2-ylcyclohexyl]oxyoxane-3,4,5-triol 10885097 Click to see 464.50 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(1S,2S,5R)-2-hydroxy-5-(2-hydroxypropan-2-yl)-2-methylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 11810246 Click to see 350.40 unknown via CMAUP database
(2S,5S)-5-[(2S)-2-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2-methylcyclohexan-1-one 11089348 Click to see CC1CCC(CC1=O)C(C)(COC2C(C(C(C(O2)CO)O)O)O)O 348.39 unknown via CMAUP database
(5S)-5-[(2S)-2-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2-methylcyclohex-2-en-1-one 11024434 Click to see 346.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Umbelliprenin 1781413 Click to see CC(=CCCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C)C 366.50 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
5-Methyluridine 445408 Click to see 258.23 unknown via CMAUP database
Uridine 6029 Click to see 244.20 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides / Pyrimidine 2-deoxyribonucleosides
Thymidine 5789 Click to see CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O 242.23 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Polyols / 1,2-diols
(2R,3R,4S)-pentane-1,2,3,4-tetrol 10796790 Click to see 136.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
5-Deoxy-D-ribitol 166761 Click to see 136.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(1S,2S,4R)-2-hydroxy-1-methyl-4-prop-1-en-2-ylcyclohexyl]oxyoxane-3,4,5-triol 11099619 Click to see 332.39 unknown via CMAUP database
4-Hydroxybenzyl beta-d-glucopyranoside 49871127 Click to see C1=CC(=CC=C1COC2C(C(C(C(O2)CO)O)O)O)O 286.28 unknown via CMAUP database
Benzyl beta-d-glucopyranoside 188977 Click to see 270.28 unknown via CMAUP database
ethyl beta-D-glucopyranoside 121667 Click to see CCOC1C(C(C(C(O1)CO)O)O)O 208.21 unknown via CMAUP database
glycerol 2-O-alpha-l-fucopyranoside 101159096 Click to see 238.23 unknown via CMAUP database
Icariside F2 14079045 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O 402.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[3-methoxy-5-prop-2-enyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]oxane-3,4,5-triol 15714546 Click to see COC1=C(C(=CC(=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O)OC3C(C(C(C(O3)CO)O)O)O 504.50 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(2S)-2,3-dihydroxypropyl]-3-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 102021738 Click to see 360.36 unknown via CMAUP database
Gastrodin 115067 Click to see 286.28 unknown via CMAUP database
Syringin 5316860 Click to see 372.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
1-Deoxy-D-glucitol 10678630 Click to see 166.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
2-C-methyl-D-erythritol 11400799 Click to see CC(CO)(C(CO)O)O 136.15 unknown via CMAUP database
D-Threitol 169019 Click to see C(C(C(CO)O)O)O 122.12 unknown via CMAUP database
Erythritol 222285 Click to see 122.12 unknown via CMAUP database
Glycerin 753 Click to see C(C(CO)O)O 92.09 unknown via CMAUP database
L-Apiitol 10820745 Click to see C(C(C(CO)(CO)O)O)O 152.15 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Apiole 10659 Click to see 222.24 unknown via CMAUP database
Dillapiol 10231 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC 222.24 unknown via CMAUP database
Safrole 5144 Click to see 162.18 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Anethofuran 126537 Click to see 152.23 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(4S,5R)-4-hydroxy-5-(hydroxymethyl)dihydrofuran-2(3H)-one 161815 Click to see C1C(C(OC1=O)CO)O 132.11 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Graveolone 177751 Click to see CC1(CC(=O)C2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 244.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
[(2R,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] (1S)-1-hydroxy-6-oxocyclohex-2-ene-1-carboxylate 163071351 Click to see 716.60 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
[(2R,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] (1S)-1-hydroxy-6-oxocyclohex-2-ene-1-carboxylate 162892751 Click to see 1004.90 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
[(2R,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] (1S)-1-hydroxy-6-oxocyclohex-2-ene-1-carboxylate 163071352 Click to see 716.60 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
[2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 1-hydroxy-6-oxocyclohex-2-ene-1-carboxylate 73822586 Click to see 716.60 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
[2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 1-hydroxy-6-oxocyclohex-2-ene-1-carboxylate 162892750 Click to see 1004.90 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
Arecatannin A1 13752000 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
Arecatannin C1 9876038 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
ent-Epicatechin-(4alpha->6)-ent-epicatechin 13990892 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
Procyanidin B 130556 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
Procyanidin B3 146798 Click to see 578.50 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
Procyanidin B6 474540 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
Procyanidin B7 13990893 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
Procyanidin trimer T2 13751990 Click to see 866.80 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
[(2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] (1R)-1-hydroxy-6-oxocyclohex-2-ene-1-carboxylate 162941986 Click to see 428.40 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
[(2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] (1S,6S)-1,6-dihydroxycyclohex-2-ene-1-carboxylate 162999489 Click to see C1CC(C(C=C1)(C(=O)OC2CC3=C(C=C(C=C3OC2C4=CC(=C(C=C4)O)O)O)O)O)O 430.40 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 1-hydroxy-6-oxocyclohex-2-ene-1-carboxylate 73822582 Click to see C1CC(=O)C(C=C1)(C(=O)OC2CC3=C(C=C(C=C3OC2C4=CC(=C(C=C4)O)O)O)O)O 428.40 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 1,6-dihydroxycyclohex-2-ene-1-carboxylate 74977176 Click to see C1CC(C(C=C1)(C(=O)OC2CC3=C(C=C(C=C3OC2C4=CC(=C(C=C4)O)O)O)O)O)O 430.40 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1016/S0031-9422(00)83128-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown via CMAUP database

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