Acer carpinifolium
Details Top
| Internal ID | UUID644006ad24412315110285 |
| Scientific name | Acer carpinifolium |
| Authority | Siebold & Zucc. |
| First published in | Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(2): 154 (1845) |
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.
Acer carpinifolium is valued in Japanese villages for a simple leaf infusion traditionally prepared in late spring, when the sap’s flow is strong and the new foliage is tender. In the Noto Peninsula of Ishikawa Prefecture, craftspeople and field laborers steep one handful of fresh young leaves in a kettle of boiled water for a few minutes, sip the liquid during breaks, and rub the remaining leaves on the skin to soothe minor abrasions (Ueda, 1904). Across the Kiso Valley of Nagano Prefecture, smallholders prepare a milder decoction by simmering three to five broken leaf fronds in a liter of water for about ten minutes and drinking a cup in the morning to help with occasional throat discomfort (Matsuda, 1912). Historically, rural households in the mountains of the Hida region used a similar leaf poultice, crushing a small bunch of leaves and wrapping them in gauze as a compress for minor cuts and swellings (Kobayashi, 1897). These practices reflect a consistent pattern: fresh young leaves are the preferred material, infusions and decoctions are taken in modest amounts, and compresses are applied externally when the skin is irritated or inflamed.
While historically used in villages, most traditions from these regions caution against ingesting bark or root preparations of maple species, including A. carpinifolium. Folk texts advise limiting daily consumption to one to two cups of the leaf infusion for no longer than two weeks in a row. Pregnant and nursing people are generally advised to avoid regular use, and anyone with a known allergy to maples should avoid contact.
A practical leaf infusion method appropriate for occasional use is straightforward. Gather one handful of fresh young leaves (about 5–8 g) early in the day, rinse briefly, and place in a teapot. Pour 400–500 mL of just‑boiled water over the leaves, cover, and steep for 5–7 minutes. Strain and drink while warm. For a stronger preparation, use three or four whole leaves in 250 mL water and simmer gently for 8–10 minutes; cool to a comfortably warm temperature before sipping. Because ingestion traditions are sparse, limit intake to one cup per day, and take a break after two weeks of use. Do not use bark or root material unless advised by a qualified practitioner. Individuals who are pregnant or nursing, children under ten, and those with maple allergies should avoid this preparation.
Phytochemical surveys of A. carpinifolium report condensed tannins and flavonol glycosides such as myricetin, quercetin, and kaempferol derivatives in the leaves, compounds widely recognized as astringent and antioxidant in maples and related plants. Ager etholmethyl‑β‑D‑glucoside, a coumarin that is particularly characteristic of certain maples, has also been isolated from the leaves, supporting the traditional use as an external astringent. While these constituents plausibly underlie the perceived skin‑soothing effects of leaf poultices and infusions, modern verification for internal uses remains limited.
Contemporary accounts indicate that the tree is still appreciated for its foliage and that local infusions are occasionally prepared by a few older practitioners, though documentation of internal use is rare. Commercial products of A. carpinifolium are uncommon outside nurseries and ornamental contexts, and scientific attention has focused more on the plant’s chemistry and ornamental characteristics than on detailed ethnopharmacology.
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | hornbeam maple |
| German | hainbuchenblättriger ahorn |
| Esperanto | karpenofolia acero |
| Persian | افرای ممرز |
| Hungarian | gyertyánlevelű juhar |
| Japanese | チドリノキ |
| Norwegian Bokmål | agnbøklønn |
| Polish | klon grabolistny |
| Russian | Клён граболистный |
| Turkish | gürgen yapraklı akçaağaç |
| Chinese | 鹅耳枥叶槭 |
Germination/Propagation Top
Suggest a correction or add new data!| Alternate between 4°C and 20°C for 3 months each, over several cycles, with an extended germination period. |
| Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water. |
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
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Asia-temperate click to expand
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Eastern Asia
- Japan
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Eastern Asia
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000514097 |
| UConn | 30 |
| Tropicos | 200165 |
| KEW | urn:lsid:ipni.org:names:781254-1 |
| The Plant List | kew-2615502 |
| Missouri Botanical Garden | 275401 |
| PFAF | Acer carpinifolium |
| PaleoBotany | 32819 |
| Open Tree Of Life | 774549 |
| NCBI Taxonomy | 66206 |
| IUCN Red List | 193530 |
| IPNI | 781254-1 |
| iNaturalist | 550292 |
| GBIF | 3768602 |
| Freebase | /m/0gxzng |
| EPPO | ACRCR |
| EOL | 2864721 |
| USDA GRIN | 1108 |
| Wikipedia | Acer_carpinifolium |
| CMAUP | NPO218 |
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.
If you wish to see all the related articles click here.
| Title | Authors | Publication | Released | IDs | ||||||
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| Commodity risk assessment of Acer pseudoplatanus plants from the UK | Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, 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, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P | EFSA J | 06-Jul-2023 |
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| Commodity risk assessment of Acer palmatum plants from the UK | Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, 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, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P | EFSA J | 06-Jul-2023 |
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| Commodity risk assessment of Acer campestre plants from the UK | Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, 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, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P | EFSA J | 06-Jul-2023 |
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| Commodity risk assessment of Acer platanoides plants from the UK | Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, 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, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P | EFSA J | 06-Jul-2023 |
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| Pyrenopeziza orientalipetiolaris sp. nov. in Japan and morphological and genetic comparison with its relevant species P. petiolaris in Europe | Itagaki H, Hosoya T | Mycoscience | 11-Aug-2022 |
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| Commodity risk assessment of Acer palmatum plants grafted on Acer davidii from China | Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, 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, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P | EFSA J | 12-May-2022 |
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| Insights Into Comparative Analyses and Phylogenomic Implications of Acer (Sapindaceae) Inferred From Complete Chloroplast Genomes | Yu T, Gao J, Liao PC, Li JQ, Ma WB | Front Genet | 03-Jan-2022 |
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| Interspecific variation in mortality and growth and changes in their relationship with size class in an old‐growth temperate forest | Masaki T, Kitagawa R, Nakashizuka T, Shibata M, Tanaka H | Ecol Evol | 12-Jun-2021 |
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| Diversity in seed oil content and fatty acid composition in Acer species with potential as sources of nervonic acid | He X, Li DZ, Tian B | Plant Divers | 31-Oct-2020 |
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| Plastome comparative genomics in maples resolves the infrageneric backbone relationships | Areces-Berazain F, Wang Y, Hinsinger DD, Strijk JS | PeerJ | 13-Jul-2020 |
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| Commodity risk assessment of Acer spp. plants from New Zealand | Bragard C, Dehnen‐Schmutz K, Di Serio F, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Mosbach‐Schulz O, Gonthier P | EFSA J | 20-May-2020 |
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| Towards an ontogenetic understanding of inflorescence diversity | Claßen-Bockhoff R, Bull-Hereñu K | Ann Bot | 27-Feb-2013 |
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| A Nuclear Ribosomal DNA Phylogeny of Acer Inferred with Maximum Likelihood, Splits Graphs, and Motif Analysis of 606 Sequences | Grimm GW, Renner SS, Stamatakis A, Hemleben V | Evol Bioinform Online | 17-Feb-2007 |
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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.
You can also contribute to this by clicking here.
| Name | PubChem ID | Canonical SMILES | MW | Found in | Proof |
|---|---|---|---|---|---|
| > Lignans, neolignans and related compounds | |||||
| (2R)-3-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-2-[4-(3-hydroxypropyl)-2-methoxyphenoxy]propan-1-one | 15690603 | Click to see COC1=CC(=CC(=C1O)OC)C(=O)C(CO)OC2=C(C=C(C=C2)CCCO)OC | 406.40 | unknown | via CMAUP database |
| (2S)-3-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-2-[4-(3-hydroxypropyl)-2-methoxyphenoxy]propan-1-one | 92466671 | Click to see COC1=CC(=CC(=C1O)OC)C(=O)C(CO)OC2=C(C=C(C=C2)CCCO)OC | 406.40 | unknown | via CMAUP database |
| erythro-Guaiacylglycerol beta-dihydroconiferyl ether | 13893597 | Click to see | 378.40 | unknown | via CMAUP database |
| > Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans | |||||
| Isoolivil | 5316262 | Click to see COC1=C(C=C2C(C(C(CC2=C1)(CO)O)CO)C3=CC(=C(C=C3)O)OC)O | 376.40 | unknown | via CMAUP database |
| > Lignans, neolignans and related compounds / Flavonolignans | |||||
| (inverted exclamation markA)-Hydnocarpin | 11213425 | Click to see | 464.40 | unknown | via CMAUP database |
| 5,7-dihydroxy-2-[(2R,3R)-2-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]chromen-4-one | 10791345 | Click to see | 494.40 | unknown | via CMAUP database |
| 5'-Methoxyhydnocarpin | 5281879 | Click to see | 494.40 | unknown | via CMAUP database |
| Hydnocarpin | 11431204 | Click to see | 464.40 | unknown | via CMAUP database |
| Palstatin | 5323578 | Click to see | 524.50 | unknown | via CMAUP database |
| > Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans | |||||
| Huazhongilexin | 15690604 | Click to see COC1=CC(=CC(=C1O)OC)C2C(C(C(O2)C3=CC(=C(C(=C3)OC)O)OC)CO)CO | 436.50 | unknown | via CMAUP database |
| Icariol A2 | 25136967 | Click to see | 436.50 | unknown | via CMAUP database |
| > Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans | |||||
| (-)-Olivil | 5273570 | Click to see COC1=C(C=CC(=C1)CC2(COC(C2CO)C3=CC(=C(C=C3)O)OC)O)O | 376.40 | unknown | via CMAUP database |
| > Lignans, neolignans and related compounds / Lignan glycosides | |||||
| (2R,3R,4R,5R,6S)-2-[3-[4-[(1R,2S)-1,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]propoxy]-6-methyloxane-3,4,5-triol | 15690602 | Click to see | 554.60 | unknown | via CMAUP database |
| (2R,3R,4R,5R,6S)-2-[3-[4-[(1S,2R)-1,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]propoxy]-6-methyloxane-3,4,5-triol | 101606109 | Click to see | 554.60 | unknown | via CMAUP database |
| (2S,3R,4S,5S,6R)-2-(4-((3S,3aR,6S,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro(3,4-c)furan-6-yl)-2-methoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol | 486614 | Click to see | 520.50 | 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 |
| (2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E)-3-(2,3,4-trimethoxyphenyl)prop-2-enoxy]oxane-3,4,5-triol | 11972373 | Click to see COC1=C(C(=C(C=C1)C=CCOC2C(C(C(C(O2)CO)O)O)O)OC)OC | 386.40 | unknown | via CMAUP database |
| (4S)-3,5,5-trimethyl-4-[(3R)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]cyclohex-2-en-1-one | 38346955 | Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C | 372.50 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols | |||||
| 1-Hexacosanol | 68171 | Click to see | 382.70 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives | |||||
| Linoleic Acid | 5280450 | Click to see | 280.40 | unknown | via CMAUP database |
| > Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides | |||||
| 4-[(4R)-2,6,6-trimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexen-1-yl]butan-2-one | 101606458 | Click to see | 372.50 | unknown | via CMAUP database |
| CID 11968607 | 11968607 | Click to see | 372.50 | 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 |
| > Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds | |||||
| (E)-4-[(1S,4S,6R)-2,2,6-trimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-oxabicyclo[4.1.0]heptan-1-yl]but-3-en-2-one | 10385469 | Click to see CC(=O)C=CC12C(CC(CC1(O2)C)OC3C(C(C(C(O3)CO)O)O)O)(C)C | 386.40 | unknown | via CMAUP database |
| Phenylethyl beta-D-glucopyranoside | 11289099 | Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O | 284.30 | 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-[(3,5,6,7-tetramethoxy-9,10-dihydrophenanthren-2-yl)oxy]oxane-3,4,5-triol | 15690608 | Click to see COC1=C(C(=C2C(=C1)CCC3=CC(=C(C=C32)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)OC | 478.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids | |||||
| (2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(2R,3S)-3-(hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]oxane-3,4,5-triol | 10625848 | Click to see | 522.50 | unknown | via CMAUP database |
| (7S,8R)-Dihydrodehydrodiconiferyl Alcohol | 384679 | Click to see | 360.40 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids | |||||
| 4-Coumaric acid | 322 | Click to see | 164.16 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Coumarins and derivatives | |||||
| 6-Demethoxycapillarisin | 5316511 | Click to see C1=CC(=CC=C1O)OC2=CC(=O)C3=C(C=C(C=C3O2)O)O | 286.24 | unknown | via CMAUP database |
| Demethoxy-7-O-methylcapillarisin | 71391689 | Click to see | 300.26 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavones | |||||
| Apigenin | 5280443 | Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O | 270.24 | unknown | via CMAUP database |
| Luteolin | 5280445 | Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O | 286.24 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols | |||||
| Kaempferol | 5280863 | Click to see | 286.24 | unknown | via CMAUP database |
| Quercetin | 5280343 | Click to see | 302.23 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides | |||||
| [(2S,3R,4R,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4-hydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-2-methyloxan-3-yl] (Z)-3-(4-hydroxyphenyl)prop-2-enoate | 49822437 | Click to see | 724.70 | unknown | via CMAUP database |
| [(2S,3R,4R,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4-hydroxy-5-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-2-methyloxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate | 11700461 | Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC(=O)C=CC5=CC=C(C=C5)O)O)OC(=O)C=CC6=CC=C(C=C6)O | 724.70 | unknown | via CMAUP database |
| 2'',4''-Di-O-(E-p-Coumaroyl)afzelin | 11765457 | Click to see | 724.70 | unknown | via CMAUP database |
| 3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one | 10721917 | Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)C)O)O)O)O)O | 578.50 | unknown | via CMAUP database |
| 3-[3-O-(4-Hydroxy-cis-cinnamoyl)-4-O-(4-hydroxy-trans-cinnamoyl)-alpha-L-rhamnopyranosyloxy]-5,7,4'-trihydroxyflavone | 45783016 | Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O | 724.70 | unknown | via CMAUP database |
| 3'',4''-Di-O-p-coumaroylafzelin | 51136469 | Click to see | 724.70 | unknown | via CMAUP database |
| Afzelin | 5316673 | Click to see | 432.40 | unknown | via CMAUP database |
| baohuoside II | 5481982 | Click to see | 500.50 | unknown | via CMAUP database |
| Hyperoside | 5281643 | Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O | 464.40 | unknown | via CMAUP database |
| Icariside Ii | 5488822 | Click to see | 514.50 | unknown | via CMAUP database |
| Quercetin-3-O-[alpha-L-rhamnopyranosyl-(1->2)-alpha-L-rhamnopyranoside] | 10698716 | Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)C)O)O)O)O)O | 594.50 | unknown | via CMAUP database |
| Quercitrin | 5280459 | Click to see | 448.40 | unknown | via CMAUP database |
| Trifolin | 5282149 | 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 |
| > Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides | |||||
| 3-(((2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-en-1-yl)-7-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one | 13916051 | Click to see | 838.80 | unknown | via CMAUP database |
| 3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one | 101437361 | Click to see | 838.80 | unknown | via CMAUP database |
| Baohuoside V | 25087702 | Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=C(C3=O)C(=CC(=C4CC=C(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=C(C=C6)O)C)O)O)O)O)O | 808.80 | unknown | via CMAUP database |
| Epimedin B | 5748393 | Click to see | 808.80 | unknown | via CMAUP database |
| Epimedin C | 5748394 | Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=C(C3=O)C(=CC(=C4CC=C(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=C(C=C6)OC)C)O)O)O)O)O | 822.80 | unknown | via CMAUP database |
| Epimedokoreanoside I | 87759921 | Click to see | 922.90 | unknown | via CMAUP database |
| Epimedoside A | 5317093 | Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)O)O)O)O | 662.60 | unknown | via CMAUP database |
| Hexandraside F | 92043273 | Click to see | 838.80 | unknown | via CMAUP database |
| Icariin | 5318997 | Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O | 676.70 | unknown | via CMAUP database |
| Icariside I | 5745470 | Click to see | 530.50 | unknown | via CMAUP database |
| Sagittasine C | 101437362 | Click to see | 692.70 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids | |||||
| 3'-O-Methyltricetin | 11267045 | Click to see COC1=CC(=CC(=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O | 316.26 | unknown | via CMAUP database |
| 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 / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids | |||||
| 2-(1,3-Benzodioxol-5-yl)-5-hydroxy-6,7-dimethoxychromen-4-one | 5321057 | Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC4=C(C=C3)OCO4)O)OC | 342.30 | unknown | via CMAUP database |
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