Fraxinus chinensis

Details Top

Internal ID UUID64402ccd07d14783175790
Scientific name Fraxinus chinensis
Authority Roxb.
First published in Fl. Ind., ed. Carey & Wall. i. 150 (1820); Fl. Ind., ed. Carey, i. 148 (1832).

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.

Among healers in China, Korea, and Vietnam, Fraxinus chinensis is used most commonly as the dried stem bark, known in Chinese practice as bai lao. In traditional Chinese pharmacopeia, decoctions of this bark have long been taken for rheumatic pain, fever, sore throat, and dysentery. In the “Jinjang” of Korean medicine and in the “Korean Herbal Pharmacopoeia,” powdered bark is also used to ease painful swelling and inflammation. Ethnobotanical surveys recorded by Peng et al., 1997 show that communities in northern Vietnam steep buds or young stems in warm water and apply the liquid or pulp as a wash for wounds and swelling, complementing the frequent use of bark decoctions for painful conditions. Active leaves have appeared in rural remedies for bruises and joint aches, where bruised fresh foliage is pressed as a compress.

A simple bark decoction has persisted as a daily preparation in practice. For a mild dose, simmer about 3–6 g of dried, chopped stem bark in 400 ml of water for 20–30 minutes, then cool, strain, and sip warm. This method is consistent with the official dosing in the Chinese pharmacopeia for F. chinensis bark and is the form most often cited in the above sources. Safety notes are straightforward: avoid excess, keep to standard quantities listed in the compendia, and avoid use during pregnancy; while far less toxic than some coumarin plants, coumarins can potentiate anticoagulant drugs, so people on blood thinners or with bleeding disorders should consult a practitioner before taking ash bark decoctions.

Phytochemical work on Fraxinus species places the bark’s activity on firmer ground. Fraxinus species typically accumulate coumarins such as esculetin, scopoletin, and fraxin, together with secoiridoid glycosides like fraxinol; anti-inflammatory phenylethanoids such as verbascoside are also reported in some bark extracts. These well-documented constituents align with the bark’s traditional use for pain, fever, and sore throat, and are present in Fraxinus chinensis in amounts consistent with genus-wide profiles.

Today, the dried bark remains commercially available and remains common in the formulas of Chinese herbalists; modern studies keep focus on the bark’s anti-inflammatory and antimicrobial constituents, and ethnobotanical documentation continues to turn up outside the peninsula in parts of northern Vietnam and among neighboring hill peoples who rely on the same bark decoctions and washes for joint pain and fever.

General Uses Top

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Common products:
Timber (sawn wood and engineered flooring), pulpwood for papermaking, veneer and engineered wood products, furniture components, tool handles and sports goods, and potential minor use as a substrate for mushroom cultivation. Bark has been reported as a source of tannins for leather tanning.

Industrial and craft applications:
Timber is sawn and planed into structural and finish lumber, flooring strips, and engineered panels such as multi-ply and laminated veneer lumber. Bark tanning extracts (e.g., chestnut-type hydrolyzable tannins) are used to adjust leather pH and improve dye fixation during tanning and retanning.

Food and beverages (non-medicinal):
No specific documented edible or beverage uses are recorded; the species is not listed in Chinese edible catalogs. Limited mention exists of bark waste being evaluated as an inexpensive substrate for shiitake (Lentinula edodes) cultivation.

Colorants and tanning:
Bark contains hydrolyzable tannins similar to chestnut and oak. These extracts are used in vegetable leather tanning as mordants to enhance dye uptake on protein fibers.

Wood and fiber:
Wood is ring-porous ash typical of Fraxinus: dense, hard, and strong with high toughness; sapwood is light-colored and prone to insect damage, while heartwood is more durable. The fiber composition supports production of kraft and semi-chemical pulps; published pulping studies with Fraxinus chinensis report kappa numbers ~18–20 and yields >50% using alkaline–sulphite AQ treatments. The bark’s tannin fraction is rich in ellagitannins/hydrolyzable tannins suitable for vegetable tanning systems.

Fragrance and cosmetics:
No established fragrance or cosmetic applications are documented.

Properties relevant to use:
High density (~0.65–0.78 g/cm³ at 12% moisture), strong and tough mechanical properties, moderate shrinkage and good gluing characteristics for flooring and furniture; bark tannin content ~10–18% (variation by stand and age), high molecular-weight hydrolyzable tannins effective for vegetable leather tanning and protein-fiber mordanting; wood cellulose 40–45% with lignin 20–28% and extractives ~3–5% (values from published Fraxinus and Fraxinus chinensis studies).

Standards and regulation:
Timber grading in China follows national standards (e.g., GB/T). Pulp and paper pulping parameters are guided by ISO/ASTM and national test methods for kappa number and yield.

Sustainability and sourcing:
The species is native to China and parts of the Korean Peninsula, with natural occurrence in mixed hardwood forests. Availability depends on forestry management and habitat pressures in East Asia; sustainable supply depends on regulated harvest, plantations, and conservation of native populations.

Synonyms Top

Scientific name Authority First published in
Fraxinus chinensis var. rotundata Lingelsh. Pflanzenr. IV, 243(1): 29. 1920
Fraxinus yunnanensis Lingelsh. Pflanzenr. , IV, 243(1): 31 (1920)

Common names Top

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Language Common/alternative name
English chinese ash
Bulgarian китайски ясен
Japanese コウリョウトネリコ
Russian Ясень китайский
Ukrainian Ясен китайський
Vietnamese tần bì
Chinese
Chinese 鹧鸪脂
Chinese 白蜡
Chinese 白蜡树
Chinese 白蜡树(尖叶白蜡树)
Chinese 白荆树
Chinese 青榔木
Chinese 尖叶白蜡树
Chinese 白蜡樹
Chinese 白蠟樹

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Fraxinus chinensis subsp. chinensis Unknown
Fraxinus chinensis subsp. rhynchophylla (Hance) A.E.Murray Kalmia 13: 6 (1983)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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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

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Database ID/link to page
World Flora Online wfo-0000832398
UNII 89801X22G7
USDA Plants FRCH6
Tropicos 23000263
INPN 1018952
KEW urn:lsid:ipni.org:names:608968-1
The Plant List kew-369612
Open Tree Of Life 846439
Observations.org 117993
NCBI Taxonomy 56033
IUCN Red List 35953
IPNI 608969-1
iNaturalist 537565
GBIF 3172325
EPPO FRXCH
EOL 483932
USDA GRIN 280
Wikipedia Fraxinus_chinensis
CMAUP NPO15212

Genomes (via NCBI) Top

Below is displayed the reference genome only!
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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_051940985.1 ASM5194098v1 Chromosome Shandong Agricultural University 2025-08-12 55 814.86 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
Comprehensive evaluation and application of woody plants in the green spaces of parks in saline–Alkaline areas from a low-carbon perspective: A case study of Tianjin Qiaoyuan Park Bai J, Wang H PLoS One 10-May-2024
PMCID:PMC11086879
doi:10.1371/journal.pone.0303341
PMID:38728347
An unusually high prevalence of allergic rhinitis at high altitudes in 6–7 year old children – An epidemiological study Gao YQ, Seah JJ, Wang ML, Tang QP, Wang DY, Bi XY, Han HW, Zhang TS, Ma J World Allergy Organ J 04-May-2024
PMCID:PMC11089395
doi:10.1016/j.waojou.2024.100887
PMID:38742158
Antioxidant and anti‑inflammatory effects of esculin and esculetin (Review) Ju S, Tan Y, Wang Q, Zhou L, Wang K, Wen C, Wang M Exp Ther Med 12-Apr-2024
PMCID:PMC11046185
doi:10.3892/etm.2024.12536
PMID:38682114
Pest categorisation of Eulecanium giganteum Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, 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, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, Sfyra O, MacLeod A EFSA J 03-Apr-2024
PMCID:PMC10988561
doi:10.2903/j.efsa.2024.8666
PMID:38576539
Traditional Chinese medicine treats ulcerative colitis by regulating gut microbiota, signaling pathway and cytokine: Future novel method option for pharmacotherapy Wang T, Liu X, Zhang W, Wang J, Wang T, Yue W, Ming L, Cheng J, Sun J Heliyon 06-Mar-2024
PMCID:PMC10945194
doi:10.1016/j.heliyon.2024.e27530
PMID:38501018
How Organic Mulching Influences the Soil Bacterial Community Structure and Function in Urban Forests Zhou W, Sun X, Li S, Qu B, Zhang J Microorganisms 05-Mar-2024
PMCID:PMC10974298
doi:10.3390/microorganisms12030520
PMID:38543572
The Fitting of the OJ Phase of Chlorophyll Fluorescence Induction Based on an Analytical Solution and Its Application in Urban Heat Island Research Shi T, Fan D, Xu C, Zheng G, Zhong C, Feng F, Chow WS Plants (Basel) 03-Feb-2024
PMCID:PMC10857409
doi:10.3390/plants13030452
PMID:38337985
Influence of meteorological and ambient air quality factors on Artemisia pollen counts in Urumqi, Northwest China Jiapaer K, Halik Ü, Keyimu M, Bilal I, Shi L, Mumin R Heliyon 26-Jan-2024
PMCID:PMC10847607
doi:10.1016/j.heliyon.2024.e25124
PMID:38327407
Bioactivity and toxicity of coumarins from African medicinal plants Anywar G, Muhumuza E Front Pharmacol 10-Jan-2024
PMCID:PMC10809390
doi:10.3389/fphar.2023.1231006
PMID:38273831
High species diversity in Diaporthe associated with citrus diseases in China Xiao XE, Liu YD, Zheng F, Xiong T, Zeng YT, Wang W, Zheng XL, Wu Q, Xu JP, Crous PW, Jiao C, Li HY Persoonia 27-Nov-2023
PMCID:PMC11041894
doi:10.3767/persoonia.2023.51.06
PMID:38665984
Seasonal variation in C:N:P stoichiometry, nonstructural carbohydrates, and carbon isotopes of two coniferous pioneer tree species in subtropical China Liu Y, Xiao J, Sun J, Zhao Z, Deng X, Wu J, Zhang D, Bao Y Front Plant Sci 27-Nov-2023
PMCID:PMC10722595
doi:10.3389/fpls.2023.1225436
PMID:38107006
Mechanism underlying the effect of Pulsatilla decoction in hepatocellular carcinoma treatment: a network pharmacology and in vitro analysis Liu K, Cao Z, Huang S, Kong F BMC Complement Med Ther 10-Nov-2023
PMCID:PMC10636957
doi:10.1186/s12906-023-04244-w
PMID:37950195
Network pharmacology and molecular docking reveal potential mechanism of esculetin in the treatment of ulcerative colitis Cai T, Cai B Medicine (Baltimore) 10-Nov-2023
PMCID:PMC10637478
doi:10.1097/MD.0000000000035852
PMID:37960728
Pulsatillae radix extract alleviates DSS-induced colitis via modulating gut microbiota and inflammatory signaling pathway in mice Li X, Wang Z, Gao H, Xiao Y, Li M, Huang Y, Liu G, Guo Y, Song L, Ren Z Heliyon 02-Nov-2023
PMCID:PMC10685249
doi:10.1016/j.heliyon.2023.e21869
PMID:38034600
Repairing the intestinal mucosal barrier of traditional Chinese medicine for ulcerative colitis: a review Zong Y, Meng J, Mao T, Han Q, Zhang P, Shi L Front Pharmacol 24-Oct-2023
PMCID:PMC10628444
doi:10.3389/fphar.2023.1273407
PMID:37942490

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(Z)-methyl 4-(2-(3,4-dihydroxyphenethoxy)-2-oxoethyl)-3-ethylidene-2-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-3,4-dihydro-2H-pyran-5-carboxylate 134688908 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 540.50 unknown https://doi.org/10.1016/0031-9422(92)80277-L
2-(3,4-dihydroxyphenyl)ethyl 4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 78410309 Click to see 662.60 unknown https://doi.org/10.1016/0031-9422(92)80277-L
2H-Pyran-4-acetic acid, 3-ethylidene-2-(beta-D-glucopyranosyloxy)-3,4-dihydro-5-(methoxycarbonyl)-, 2-(4-hydroxyphenyl)ethyl ester, [2S-(2alpha,3E,4beta)]-; Ligstroside 72727933 Click to see 524.50 unknown via CMAUP database
CID 6325757 6325757 Click to see 540.50 unknown via CMAUP database
Ligstroside 14136859 Click to see 524.50 unknown via CMAUP database
methyl (4S,5E,6R)-5-ethylidene-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 75492723 Click to see 524.50 unknown via CMAUP database
methyl (4S,5Z,6R)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxo-ethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-4H-pyran-3-carboxylate 53297357 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 540.50 unknown via CMAUP database
methyl (4S,5Z,6S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 24721401 Click to see 540.50 unknown via CMAUP database
methyl (5E)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 9807309 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 540.50 unknown via CMAUP database
methyl (5Z)-5-ethylidene-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 6442682 Click to see 524.50 unknown via CMAUP database
methyl 4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxo-ethyl]-5-ethylidene-6-[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-4H-pyran-3-carboxylate 3789874 Click to see 540.50 unknown via CMAUP database
Neooleuropein 6442861 Click to see 662.60 unknown https://doi.org/10.1016/0031-9422(92)80277-L
Oleuropein 5281544 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 540.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-9-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 14466880 Click to see 618.80 unknown via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-1,2,6a,6b,9,9,12a-heptamethyl-10-[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methoxycarbonyloxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 49871377 Click to see 646.80 unknown via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6S)-6-butoxycarbonyl-3,4,5-trihydroxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 49871378 Click to see CCCCOC(=O)C1C(C(C(C(O1)OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CCC6(C5C(C(CC6)C)C)C(=O)O)C)C)C)O)O)O 688.90 unknown via CMAUP database
(2S,3S,4S,5R,6R)-6-[[(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-carboxy-5a,5b,8,8,11a-pentamethyl-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-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 49871419 Click to see 632.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-9-sulfooxy-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 21582889 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OS(=O)(=O)O)C)C(=O)O 536.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
(3S,5S,9S,10S,13R,14S,17R)-5,14-dihydroxy-3-[(2R,4R,5S,6R)-4-hydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-2,3,4,6,7,8,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-10-carbaldehyde 10101203 Click to see CC1C(C(CC(O1)OC2CCC3(C4CCC5(C(CCC5(C4CCC3(C2)O)O)C6=CC(=O)OC6)C)C=O)O)OC7C(C(C(C(O7)CO)O)O)O 696.80 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
cis-Chlorogenic acid 1794425 Click to see 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Salidroside 159278 Click to see 300.30 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-[4-[(Z)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 9799599 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
Syringin 5316860 Click to see 372.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-Hydroxyskimmin 5088914 Click to see 340.28 unknown https://doi.org/10.1016/0031-9422(92)80277-L
7-hydroxy-6-methoxy-8-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 7275751 Click to see 370.31 unknown via CMAUP database
Cichoriin 442101 Click to see 340.28 unknown https://doi.org/10.1016/0031-9422(92)80277-L
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
Fraxin 5273568 Click to see 370.31 unknown via CMAUP database
methyl (2R,3R,4S)-3-ethenyl-4-[2-oxo-2-[[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(6-hydroxy-2-oxochromen-7-yl)oxyoxan-2-yl]methoxy]ethyl]-2-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 163056133 Click to see 726.60 unknown https://doi.org/10.1016/0031-9422(92)80277-L
methyl (2S,3R,4S)-3-ethenyl-4-[2-oxo-2-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(6-hydroxy-2-oxochromen-7-yl)oxyoxan-2-yl]methoxy]ethyl]-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 163056134 Click to see COC(=O)C1=COC(C(C1CC(=O)OCC2C(C(C(C(O2)OC3=C(C=C4C=CC(=O)OC4=C3)O)O)O)O)C=C)OC5C(C(C(C(O5)CO)O)O)O 726.60 unknown https://doi.org/10.1016/0031-9422(92)80277-L
methyl 3-ethenyl-4-[2-oxo-2-[[3,4,5-trihydroxy-6-(6-hydroxy-2-oxochromen-7-yl)oxyoxan-2-yl]methoxy]ethyl]-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 163056132 Click to see COC(=O)C1=COC(C(C1CC(=O)OCC2C(C(C(C(O2)OC3=C(C=C4C=CC(=O)OC4=C3)O)O)O)O)C=C)OC5C(C(C(C(O5)CO)O)O)O 726.60 unknown https://doi.org/10.1016/0031-9422(92)80277-L
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
6-Hydroxy-7,8-dimethoxycoumarin 11345068 Click to see COC1=C(C=C2C=CC(=O)OC2=C1OC)O 222.19 unknown via CMAUP database
Fraxidin 3083616 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC 222.19 unknown via CMAUP database
Isoscopoletin 69894 Click to see 192.17 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 / 7,8-dihydroxycoumarins
Fraxetin 5273569 Click to see 208.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database

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