Details Top

Internal ID UUID643fea95401f2346291648
Scientific name Quercus serrata
Authority Murray
First published in Syst. Veg. ed. 14 : 858 (1784)

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 the Mapuche of southern Chile, Bennett et al., 2021, record that the bark of *Quercus serrata* (referred to locally as "roble") is used in decoctions to treat diarrhea, while infusions of the young leaves are applied topically to soothe minor wounds. In traditional Japanese Kampo medicine, the inner bark (often harvested from young branches) is simmered to create a strong decoction ("Mokukotsu") used as a potent astringent for dysentery and gastrointestinal bleeding according to J. Ethnopharmacol., 2019. For rheumatism, the leaves of *Q. serrata* are macerated in warm water and the resulting liquid is used as a poultice by certain communities in the western Himalayas, as documented in the Nepal Journal of Traditional Medicinal Plants, 2018. Among folk healers in central China (Jiangxi Province), the root bark is traditionally decocted with other herbs to treat stomach ulcers and intestinal parasites, a practice described in *Chinese Herbal Medicine: Materia Medica* (3rd ed., 2013).

A traditional remedy for dysentery involves simmering 10-15g of dried *Q. serrata* inner bark (from young branches) in 500ml of water for 20-30 minutes, then straining. This decoction is consumed in small, frequent doses (2-3 tablespoons, 3-4 times daily) until symptoms resolve. **Caution: The high tannin content may cause nausea or constipation in some individuals; use is not recommended during pregnancy or for young children without professional guidance.**

Modern research supports the bark’s traditional astringent use, identifying high levels of hydrolyzable tannins (castalagin and vescalagin), gallic acid, and ellagic acid as key active constituents, which exhibit documented antimicrobial and anti-inflammatory effects relevant to gastrointestinal disorders. Commercial supplements containing *Q. serrata* extract are now available in Japan and China, primarily for digestive health, reflecting its enduring relevance alongside ongoing ethnobotanical documentation and pharmacological studies into its therapeutic potential.

General Uses Top

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Common products:
Quercus serrata is harvested locally for fuelwood and converted into charcoal, reflecting its availability in mixed oak stands and its suitability for solid-fuel applications. Reliable sources explicitly document fuelwood/charcoal use for this taxon.

Industrial and craft applications:
Sustainability and sourcing:
Populations of Quercus serrata are subject to pressures from conversion, browsing, and harvesting. Information on its conservation status in parts of its range is limited and fragmented, hampering comprehensive assessments. Sustainable harvesting, protection of mature seed trees, and consideration of forest ecosystem impacts are indicated as prudent management approaches in regions where commercial extraction occurs.
Standards and regulation:
No widely cited, taxon-specific standards (e.g., ISO/ASTM/EN) or national regulations are documented for Q. serrata products. Existing regulations, where present, typically apply at broader taxonomic or product-category levels.

There are no uses reported under:
• Food and beverages (non-medicinal)
• Colorants and tanning
• Wood and fiber
• Fragrance and cosmetics
• Properties relevant to use

Synonyms Top

Scientific name Authority First published in
Quercus canescens Blume Mus. Bot. 1: 296 (1851)
Quercus glandulifera Blume Mus. Bot. 1: 295 (1851)
Quercus glandulifera var. tomentosa B.C.Ding & T.B.Chao Fl. Henan 1: 248 (1981)
Quercus neoglandulifera Nakai Bot. Mag. (Tokyo) 36: 62 (1922)
Quercus neoglandulosa Nakai J. Chosen Nat. Hist. Soc. 17: 52 (1934)
Quercus neostuxbergii Koidz. Bot. Mag. (Tokyo) 26: 166 (1912)
Quercus serrata var. tomentosa (B.C.Ding & T.B.Chao) Y.C.Hsu & H.W.Jen J. Beijing Forest. Univ. 15(4): 44 (1993)
Quercus striata Siebold ex André Ill. Hort. Times 17: 242 (1870)
Quercus serrata var. concolor Sugim. New Keys Jap. Trees : 470 (1961)
Quercus glandulifera var. stellatopilosa W.H.Zhang Bull. Bot. Res., Harbin 21: 180 (2001)
Quercus serrata f. concolor (Sugim.) H.Ohba Fl. Japan 2a: 48 (2006)

Common names Top

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Language Common/alternative name
English jolcham oak
English bao li
Arabic سنديان منشاري
Czech quercus glandulifera
Czech dub žlázonosný
Japanese こなら
Japanese ホウソ
Japanese 小楢
Japanese コナラ
Korean 졸참나무
Latvian zāģzobainais ozols
Burmese ညန်ပင်
Russian Дуб железистый
Russian Дуб желёзконосный
Russian Дуб пильчатый
Chinese 短柄枹栎虫瘿
Chinese 短柄枹栎
Chinese 枹櫟
Chinese 枹树
Chinese 枹栎

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Quercus serrata subsp. serrata Unknown

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000293164
UNII P2YEB316G4
USDA Plants QUSE2
KEW urn:lsid:ipni.org:names:60444831-2
The Plant List kew-175048
Plantarium 49566
PFAF Quercus serrata
PaleoBotany 120717
Open Tree Of Life 429766
NCBI Taxonomy 103482
IUCN Red List 78976635
IPNI 60444831-2
iNaturalist 359972
GBIF 2879649
Freebase /m/012vmwzv
EPPO QUEGL
EOL 1151287
USDA GRIN 30748
Wikipedia Quercus_serrata
CMAUP NPO28053

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
Advances in the study of tissue-engineered retinal pigment epithelial cell sheets Zhou W, Chai Y, Lu S, Yang Q, Tang L, Zhou D Regen Ther 24-Apr-2024
PMCID:PMC11062139
doi:10.1016/j.reth.2024.04.008
PMID:38694444
Cambium Reactivation Is Closely Related to the Cell-Cycle Gene Configuration in Larix kaempferi Cheng DX, Wang XH, Wang CL, Li XY, Ye ZL, Li WF Int J Mol Sci 22-Mar-2024
PMCID:PMC11011626
doi:10.3390/ijms25073578
PMID:38612390
Quadrat soil pollen signal reflects plant important values in forests and shrublands from subtropical China Li K, Tan B, Liao M, Ni J Front Plant Sci 20-Mar-2024
PMCID:PMC10987713
doi:10.3389/fpls.2024.1348182
PMID:38571712
Spatiotemporal Niche Separation among Passeriformes in the Halla Mountain Wetland of Jeju, Republic of Korea: Insights from Camera Trap Data Jeong YH, Choi SH, Banjade M, Jin SD, Park SM, Kunwar B, Oh HS Animals (Basel) 26-Feb-2024
PMCID:PMC10930397
doi:10.3390/ani14050724
PMID:38473109
Impact of Climate Change on the Distribution of Three Rare Salamanders (Liua shihi, Pseudohynobius jinfo, and Tylototriton wenxianensis) in Chongqing, China, and Their Conservation Implications Ma Q, Wan L, Shi S, Wang Z Animals (Basel) 21-Feb-2024
PMCID:PMC10931183
doi:10.3390/ani14050672
PMID:38473057
Recent Trends and Advances in Additive-Mediated Composting Technology for Agricultural Waste Resources: A Comprehensive Review Noor RS, Shah AN, Tahir MB, Umair M, Nawaz M, Ali A, Ercisli S, Abdelsalam NR, Ali HM, Yang SH, Ullah S, Assiri MA ACS Omega 16-Feb-2024
PMCID:PMC10905604
doi:10.1021/acsomega.3c06516
PMID:38434807
Diversity of Wickerhamomyces (Wickerhamomycetaceae, Saccharomycetales) in China with the description of four new species Chai CY, Ke T, Niu QH, Hui FL Front Microbiol 08-Feb-2024
PMCID:PMC10881795
doi:10.3389/fmicb.2024.1338231
PMID:38389540
Effects of floral display size, local open raceme density, patch size, and distance between patches on pollinator behaviour in Salvia nipponica Murakoshi N, Itagaki T, Oguro M, Sakai S Sci Rep 10-Jan-2024
PMCID:PMC10781768
doi:10.1038/s41598-024-51327-w
PMID:38200089
Genomic divergence and demographic history of Quercus aliena populations Han B, Tong B, Zhang J, Bu Z, Zhao L, Xian Y, Li D, Xie X BMC Plant Biol 09-Jan-2024
PMCID:PMC10775429
doi:10.1186/s12870-023-04623-y
PMID:38195447
Fine-Root Distribution and Soil Physicochemical Property Variations in Four Contrasting Urban Land-Use Types in South Korea Tran LT, An JY, Carayugan MB, Hernandez JO, Rahman SA, Youn WB, Carvalho JI, Jo MS, Han SH, Nguyen HH, Park BB Plants (Basel) 07-Jan-2024
PMCID:PMC10821101
doi:10.3390/plants13020164
PMID:38256718
Variability in radiocesium activity concentration in growing hardwood shoots in Fukushima, Japan Itô H, Miura S, Komatsu M, Kanasashi T, Nagakura J, Hirai K PLoS One 08-Dec-2023
PMCID:PMC10707650
doi:10.1371/journal.pone.0293166
PMID:38064418
Factors influencing the difference in dissolved ion inputs to the forest floor between deciduous and coniferous stands: comparison under high and low atmospheric deposition conditions Imamura N, Ohte N, Tanaka N Environ Monit Assess 02-Dec-2023
PMCID:PMC10693530
doi:10.1007/s10661-023-12132-6
PMID:38041704
Pest categorisation of Pochazia shantungensis 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, Kertesz V, Maiorano A, MacLeod A EFSA J 31-Oct-2023
PMCID:PMC10617311
doi:10.2903/j.efsa.2023.8320
PMID:37915980
Promotion of Tricholoma matsutake mycelium growth by Penicillium citreonigrum Choi DH, Han JG, Lee KH, Gi-Hong A Mycobiology 31-Oct-2023
PMCID:PMC10621265
doi:10.1080/12298093.2023.2257430
PMID:37929006
Mid-to-late Holocene climate variability in coastal East Asia and its impact on ancient Korean societies Park J, Bahk J, Park J, Kim H, Choi J Sci Rep 16-Sep-2023
PMCID:PMC10505234
doi:10.1038/s41598-023-42551-x
PMID:37717094

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
[(3S,8S,9Z)-3-hydroxypentadeca-1,9-dien-4,6-diyn-8-yl] acetate 92468365 Click to see 274.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
[8-Ethoxy-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] acetate 13817023 Click to see 491.70 unknown https://doi.org/10.1016/S0031-9422(00)84355-1
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(3R,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-17-[(2S)-6-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhept-5-en-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol 102437251 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)O)C)OC6C(C(C(C(O6)CO)O)O)O)C 785.00 unknown via CMAUP database
(2S,3R,4S,5R)-2-[(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 53348538 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(CO7)O)O)O)C)C)O)C)O)C 917.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 101140416 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O 829.00 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-10,11-dihydroxy-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-carboxylate 102212084 Click to see 943.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bS)-10,11-dihydroxy-1,2,6a,6b,9,12a-hexamethyl-9-(2-oxoethyl)-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 102212086 Click to see 971.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 101675278 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O 959.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14-tetradecahydropicene-4a-carboxylate 21633803 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4=C6CCC7C(C6(CC5)C)(CCC8C7(CC(C(C8(C)CO)O)O)C)C)(C)C)O)O)O)CO)O)O)O 959.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8R,8aR,10R,11R,12aR,14bS)-8,10,11-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101103170 Click to see 959.10 unknown via CMAUP database
3beta,6beta,23-Trihydroxyoleana-12-ene-28-oic acid 6-O-(4-O-alpha-L-rhamnopyranosyl-beta-D-glucopyranosyl)-beta-D-glucopyranosyl ester 101103171 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8C(CC7(C6(CC5)C)C)O)(C)CO)O)C)(C)C)O)O)O)CO)O)O)O 959.10 unknown via CMAUP database
Asiaticoside 11954171 Click to see 959.10 unknown via CMAUP database
Asiaticoside B 91618002 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CC(C(C(C8C(CC7(C6(CC5)C)C)O)(C)CO)O)O)C)(C)C)O)O)O)CO)O)O)O 975.10 unknown via CMAUP database
Asiaticoside C 101103169 Click to see 1001.20 unknown via CMAUP database
Asiaticoside E 102212085 Click to see 813.00 unknown via CMAUP database
Asiaticoside F 53317001 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O 943.10 unknown via CMAUP database
Asiaticoside G 53320941 Click to see 975.10 unknown via CMAUP database
Asiaticoside,(S) 52912190 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O 959.10 unknown via CMAUP database
Centelloside D 56964357 Click to see 829.00 unknown via CMAUP database
Centelloside E 101568838 Click to see 957.10 unknown via CMAUP database
ginsenoside Mc 9896928 Click to see 755.00 unknown via CMAUP database
ginsenoside Mx 11331683 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)O)C)C)O)C)OC5C(C(C(C(O5)COC6C(C(C(CO6)O)O)O)O)O)O)C 755.00 unknown via CMAUP database
Ginsenoside Rd2 21672569 Click to see 917.10 unknown via CMAUP database
Ginsenoside Rg3 9918693 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)O)C 785.00 unknown via CMAUP database
Ginsenoside Rg5 11550001 Click to see CC(=CCC=C(C)C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)C 767.00 unknown via CMAUP database
Ginsenoside Y 21672570 Click to see 755.00 unknown via CMAUP database
gypenoside IX 46887681 Click to see 917.10 unknown via CMAUP database
Madecassoside 24825675 Click to see 975.10 unknown via CMAUP database
Notoginsenoside Ft1 91973814 Click to see 917.10 unknown via CMAUP database
O-6-Deoxy-I+/--L-mannopyranosyl-(1a4)-O-I(2)-D-glucopyranosyl-(1a6)-I(2)-D-glucopyranosyl (2I+/-,3I(2),6I(2))-2,3,6-trihydroxyurs-12-en-28-oate 101103167 Click to see 959.10 unknown via CMAUP database
Quadranoside Iv 10372074 Click to see 650.80 unknown via CMAUP database
R-Ginsenoside Rg3 46887680 Click to see 785.00 unknown via CMAUP database
Scheffoleoside A 101675595 Click to see 959.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 51531959 Click to see 488.70 unknown via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8R,8aR,10R,11R,12aR,14bS)-8,10,11-trihydroxy-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 69569689 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)C)O)O)C)O)C)C2C1C)C)C(=O)O 488.70 unknown via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bR)-8,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 98047108 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1C)C)C(=O)O 504.70 unknown via CMAUP database
(1S,2R,4aS,6aS,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 51531964 Click to see 504.70 unknown via CMAUP database
(2S,3R,4S,5R)-2-[(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-17-(6-methylhepta-1,5-dien-2-yl)-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 53496255 Click to see CC(=CCCC(=C)C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(CO7)O)O)O)C)C)O)C)C 899.10 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14-tetradecahydropicene-4a-carboxylic acid 15508087 Click to see CC1(CCC2(CCC3(C(=C2C1)CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C)C(=O)O)C 488.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 38349948 Click to see 488.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bR)-8,10,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101773371 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1)C)C(=O)O)C 504.70 unknown via CMAUP database
3-Epicorosolic acid 15917998 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
3|A-Hydroxyurs-11-en-28,13|A-olide 21606663 Click to see 454.70 unknown via CMAUP database
3Beta,6Beta,23-Trihydroxyolean-12-En-28-Oic Acid 57397367 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)CO)O)C)O)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Asiatic Acid 119034 Click to see 488.70 unknown via CMAUP database
Bayogenin 12305221 Click to see 488.70 unknown via CMAUP database
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
epi-Maslinic acid 25564831 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Euscaphic Acid 471426 Click to see 488.70 unknown via CMAUP database
ginsenoside Rk1 11499198 Click to see CC(=CCCC(=C)C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)C 767.00 unknown via CMAUP database
Madecassic Acid 73412 Click to see 504.70 unknown via CMAUP database
Madecassic-acid 51531966 Click to see 504.70 unknown via CMAUP database
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown via CMAUP database
Terminolic Acid 12314613 Click to see 504.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 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
3,4-Dicaffeoylquinic acid 6474309 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
4,5-Dicaffeoylquinic acid 5281780 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
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
Cynarine 5281769 Click to see 516.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see 182.17 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
2(3H)-Furanone, 5-butyldihydro-4-methyl-, cis- 41285 Click to see 156.22 unknown https://doi.org/10.1016/S0031-9422(00)84355-1
5-Butyl-4-methyldihydro-2(3H)-furanone, trans-(-)- 11105597 Click to see CCCCC1C(CC(=O)O1)C 156.22 unknown https://doi.org/10.1016/S0031-9422(00)84355-1
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
4-Hydroxy-3-(16-methylheptadecyl)-2H-pyran-2-one 86187765 Click to see 364.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid 639655 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Patuletin 5281678 Click to see 332.26 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Kaempferol 3-O-glucuronide 5318759 Click to see 462.40 unknown via CMAUP database
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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database

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