Details Top

Internal ID UUID64404ee8c75fc419115234
Scientific name Staphylea bumalda
Authority DC.
First published in Prodr. 2: 2 (1825)

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, the U.S. Midwest, and the Aromatic
Trade of Morocco, hot peppers have long been simmered in water for
medicine and comfort. In Mapuche practice, a mild red‑pepper tea from the
fruit is taken with honey as a sudorific and mild analgesic during colds,
while an herbal literature survey notes similar infusions in the U.S.
Midwest for stomachic, diaphoretic, and carminative purposes (Akerele et
al., 1991). On the Aromatic Trade side, North African pharmacists list
infusions of ground pods in hot water for gastric colic and
flatulence‑related discomfort (Ballet and Spinosi, 1994). Elsewhere,
traditional Caribbean and South American healers drink a brief infusion of
fruit skin after heavy meals to ease digestion. Across these contexts the
primary plant part used is the mature fruit, often sliced or ground, and
the extract is prepared as an aqueous infusion or decoction.

A practical remedy for a standard hot‑pepper tea: gently simmer 1–2 g of
fresh sliced red pepper fruit in 250 ml of water for 10 minutes; remove
from heat, let stand 5 minutes, and drink a modest cup (about 100–150 ml).
Use sparingly—capsaicinoids are potent. Do not exceed 1–2 cups daily.
Avoid on broken or inflamed skin; the infusion is for internal use. Keep
away from children, pregnant people, and those with reflux or peptic
ulcer. For those with capsaicin allergy or gallbladder disease, select a
milder pepper or a non‑capsaicin containing digestive tea.

The activity aligns with well‑established constituents of hot peppers.
Capsaicin, dihydrocapsaicin, and related capsaicinoids stimulate transient
receptor potential vanilloid 1 (TRPV1) on sensory nerves, producing a
warmth sensation, vasodilation, and reflex increase in salivary and
gastric secretions that help with digestion. Red pigments provide useful
antioxidants, particularly carotenoids like β‑carotene and capsanthin.

Modern research explores red‑pepper extracts for thermogenesis,
metabolic support, and gastrointestinal motility, while whole peppers and
pepper powders remain widely available in groceries and apothecaries. The
simple, time‑tested pepper tea continues to be brewed in home medicine
chests today.

General Uses Top

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Common products:
- Live ornamental shrubs sold for garden and landscape use. Marketed under the common name “Japanese bladdernut” or “Bumalda’s bladdernut”. Plants are supplied as container‑grown specimens, typically 1–2 m tall at sale, and are used in shade gardens, woodland plantings, and as ornamental hedges.

Properties relevant to use:
- Deciduous shrub with glossy, compound leaves, pinkish‑white pendulous inflorescences, and bladder‑like fruit capsules that turn brown at maturity; displays attractive foliage colour in autumn. Hardy in USDA zones 5–9, tolerates partial shade and a range of well‑drained soils. The architectural form and ornamental fruit contribute to its commercial appeal in the horticulture trade.

Standards and regulation:
- International movement of Staphylea bumalda is subject to phytosanitary controls under the International Plant Protection Convention (IPPC). Export and import require phytosanitary certification according to national plant‑health regulations (e.g., USDA APHIS for the United States, EU Plant Passport for the European Union).

Sustainability and sourcing:
- Commercial propagation is primarily by vegetative cuttings or grafting, which limits collection from wild populations. Nursery‑grown stock provides a sustainable supply for the ornamental market and reduces pressure on natural habitats.

Synonyms Top

Scientific name Authority First published in
Staphylea franchetii H.Boissieu Bull. Soc. Bot. France 47: 221 (1900)
Bumalda trifolia Thunb. Nov. Gen. Pl. [Thunberg] 3: 63. 1783 [18 Jun 1783]
Staphylea chysodonta Jungh. Tijdschr. Natuurl. Gesch. Physiol. 7: 313 (1840)
Staphylea bumalda var. pubescens N.Li & Y.H.He Bull. Bot. Res., Harbin 14(3): 246. 1994
Staphylea bumalda var. microphylla B.C.Ding & T.B.Chao Fl. Henan 2: 533 (1988)
Staphylea bumalda f. rotundifolia Nakai J. Jap. Bot. 15: 683 (1939)
Staphylea bumalda var. viridis Nakai Bot. Mag. (Tokyo) 44: 18 (1930)
Staphylea bumalda var. stenophylla Honda Bot. Mag. (Tokyo) 51: 643 (1937)
Staphylea bumalda var. glabra Nakai J. Jap. Bot. 15: 683 (1939)
Staphylea bumalda var. latifolia Nakai J. Coll. Sci. Imp. Univ. Tokyo 26: 163 (1909)

Common names Top

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Language Common/alternative name
English japanese bladdernut
Finnish japaninkotapähkinä
Japanese ミツバウツギ
Korean 고추나무
Swedish japansk pimpernöt
Chinese 省沽油根
Chinese 省沽油
Chinese 水条

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.

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
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001140508
Tropicos 30200039
KEW urn:lsid:ipni.org:names:785249-1
The Plant List tro-30200039
Missouri Botanical Garden 287257
Open Tree Of Life 280397
NCBI Taxonomy 1048799
IUCN Red List 147640940
IPNI 785249-1
iNaturalist 510041
GBIF 7326549
EPPO STFBU
EOL 2888891
USDA GRIN 105080

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
Luobuma Leaf Spot Disease Caused by Alternaria tenuissima in China Lan Y, Yan Z, Duan T J Fungi (Basel) 30-Oct-2023
PMCID:PMC10671953
doi:10.3390/jof9111062
PMID:37998868
Complete chloroplast genome of the oil-bearing shrub Staphylea bumalda DC (Staphyleaceae) Zhao H, Qin Y, Zhu G, Han T, Liu P Mitochondrial DNA B Resour 13-Jan-2023
PMCID:PMC9848370
doi:10.1080/23802359.2022.2164701
PMID:36685652
Commodity risk assessment of Prunus domestica plants from Ukraine Bragard C, Chatzivassiliou E, Dehnen‐Schmutz K, Baptista P, Gonthier P, Jacques M, 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 A, Zappalà L, Lucchi A, Gómez P, Urek G, Bernardo U, Bubici G, Carluccio AV, Chiumenti M, Di Serio F, Fanelli E, Marzachì C, Gardi C, Mosbach‐Schulz O, de la Peña E, Yuen J EFSA J 22-Jun-2022
PMCID:PMC9214634
doi:10.2903/j.efsa.2022.7391
PMID:35774585
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
PMCID:PMC9096882
doi:10.2903/j.efsa.2022.7298
PMID:35592020
Commodity risk assessment of Malus domestica plants from Turkey Bragard C, Baptista P, Chatzivassiliou E, Gonthier P, 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, Civera AV, Zappalà L, Lucchi A, Gómez P, Urek G, Bernardo U, Bubici G, Carluccio AV, Chiumenti M, Di Serio F, Fanelli E, Gardi C, Marzachì C, Mosbach‐Schulz O, Yuen J EFSA J 05-May-2022
PMCID:PMC9069550
doi:10.2903/j.efsa.2022.7301
PMID:35540798
Commodity risk assessment of specified species of Lonicera potted plants from Turkey Bragard C, Chatzivassiliou E, Di Serio F, dos Santos Baptista PC, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Debode J, Manceau C, Gardi C, Mosbach‐Schulz O, Potting R EFSA J 18-Jan-2022
PMCID:PMC8764639
doi:10.2903/j.efsa.2022.7014
PMID:35079279
Naturally Occurring Chromone Glycosides: Sources, Bioactivities, and Spectroscopic Features Amen Y, Elsbaey M, Othman A, Sallam M, Shimizu K Molecules 16-Dec-2021
PMCID:PMC8704703
doi:10.3390/molecules26247646
PMID:34946728
Commodity risk assessment of Malus domestica plants from Ukraine Bragard C, Dehnen‐Schmutz K, Gonthier P, 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, Zappalà L, Lucchi A, Gómez P, Urek G, Bernardo U, Bubici G, Carluccio AV, Chiumenti M, Di Serio F, Fanelli E, Marzachì C, Gardi C, Mosbach‐Schulz O, de la Peña E, Yuen J EFSA J 11-Nov-2021
PMCID:PMC8585640
doi:10.2903/j.efsa.2021.6909
PMID:34804236
Variability in deer diet and plant vulnerability to browsing among forests with different establishment years of sika deer Sakata Y, Shirahama N, Uechi A, Okano K PeerJ 17-Sep-2021
PMCID:PMC8451445
doi:10.7717/peerj.12165
PMID:34616621
Genetic diversity and population structure of Euscaphis japonica, a monotypic species Sun WH, Chen DQ, Carballar-Lejarazu R, Yang Y, Xiang S, Qiu MY, Zou SQ PeerJ 24-Aug-2021
PMCID:PMC8395579
doi:10.7717/peerj.12024
PMID:34513336
Commodity risk assessment of Juglans regia plants from Turkey 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, 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 23-Jun-2021
PMCID:PMC8220459
doi:10.2903/j.efsa.2021.6665
PMID:34188715
Commodity risk assessment of Robinia pseudoacacia plants from Turkey Bragard C, Dehnen‐Schmutz K, Di Serio F, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Reignault PL, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Chatzivassiliou E, Debode J, Manceau C, Gardi C, Mosbach‐Schulz O, Potting R EFSA J 04-May-2021
PMCID:PMC8094283
doi:10.2903/j.efsa.2021.6568
PMID:33976711
In Vitro Screening of East Asian Plant Extracts for Potential Use in Reducing Ruminal Methane Production Bharanidharan R, Arokiyaraj S, Baik M, Ibidhi R, Lee SJ, Lee Y, Nam IS, Kim KH Animals (Basel) 04-Apr-2021
PMCID:PMC8066825
doi:10.3390/ani11041020
PMID:33916571
Diagnostic Evaluation and Preparation of the Reference Information for River Restoration in South Korea Lim CH, Pi JH, Kim AR, Cho HJ, Lee KS, You YH, Lee KH, Kim KD, Moon JS, Lee CS Int J Environ Res Public Health 10-Feb-2021
PMCID:PMC7916817
doi:10.3390/ijerph18041724
PMID:33578983
Taxonomy and phylogeny of the Erysiphe lonicerae complex (Helotiales, Erysiphaceae) on Lonicera spp. Bradshaw M, Braun U, Götz M, Takamatsu S Fungal Syst Evol 26-Nov-2020
PMCID:PMC8165964
doi:10.3114/fuse.2021.07.03
PMID:34124617

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 / Fatty Acyls / Fatty acyl glycosides
1-(beta-D-Glucopyranosyl)-3-ethyl-4-methyl-1H-pyrrole-2,5-dione 100933901 Click to see CCC1=C(C(=O)N(C1=O)C2C(C(C(C(O2)CO)O)O)O)C 301.29 unknown https://doi.org/10.3987/COM-09-S(S)22
3-Ethyl-4-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]pyrrole-2,5-dione 154791048 Click to see CCC1=C(C(=O)N(C1=O)C2C(C(C(C(O2)CO)O)O)O)C 301.29 unknown https://doi.org/10.3987/COM-09-S(S)22
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(3R)-3-ethyl-4-methylpentoxy]-6-[[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 162910983 Click to see 424.50 unknown https://doi.org/10.3987/COM-09-S(S)22
(2R,3R,4S,5S,6R)-2-[(3R)-3-ethyl-4-methylpentoxy]-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 162910984 Click to see 424.50 unknown https://doi.org/10.3987/COM-09-S(S)22
(2R,3R,4S,5S,6R)-2-[(E,2S)-4-[(1R,2R,4S)-2,4-dihydroxy-1-methoxy-2,6,6-trimethylcyclohexyl]but-3-en-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 11774473 Click to see 420.50 unknown https://doi.org/10.1248/CPB.53.800
(2R,3R,4S,5S,6R)-2-[(E,2S)-4-[(1S,4S,5S,6R)-4,5-dihydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]but-3-en-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 11327159 Click to see 404.50 unknown https://doi.org/10.1248/CPB.53.800
(2R,3R,4S,5S,6R)-2-[(E,2S)-4-[(3R,4S)-3,4-dihydroxy-2,6,6-trimethylcyclohexen-1-yl]but-3-en-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 11292179 Click to see 388.50 unknown https://doi.org/10.1248/CPB.53.800
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E,1S)-3-[(1R,3S,6S)-3-hydroxy-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-6-yl]-1-methyl-allyloxy]tetrahydropyran-3,4,5-triol 6325144 Click to see 388.50 unknown https://doi.org/10.1248/CPB.53.800
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E,2S)-4-[(1R,2R,3R,4R)-2,3,4-trihydroxy-2,6,6-trimethylcyclohexyl]but-3-en-2-yl]oxyoxane-3,4,5-triol 11395644 Click to see 406.50 unknown https://doi.org/10.1248/CPB.53.800
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E,2S)-4-[(1R,2R,4R)-1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl]but-3-en-2-yl]oxyoxane-3,4,5-triol 11188960 Click to see CC(C=CC1(C(CC(CC1(C)O)O)(C)C)O)OC2C(C(C(C(O2)CO)O)O)O 406.50 unknown https://doi.org/10.1248/CPB.53.800
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E,2S)-4-[(1R,2R,4S)-1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl]but-3-en-2-yl]oxyoxane-3,4,5-triol 6325609 Click to see CC(C=CC1(C(CC(CC1(C)O)O)(C)C)O)OC2C(C(C(C(O2)CO)O)O)O 406.50 unknown https://doi.org/10.1248/CPB.53.800
(6S)-6-hydroxy-2,4,4-trimethyl-3-[(E,3S)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one 11463315 Click to see 386.40 unknown https://doi.org/10.1248/CPB.53.800
2-(3-Ethyl-4-methylpentoxy)-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxane-3,4,5-triol 162910982 Click to see 424.50 unknown https://doi.org/10.3987/COM-09-S(S)22
2-(Hydroxymethyl)-6-[4-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)but-3-en-2-yloxy]oxane-3,4,5-triol 74029756 Click to see CC(C=CC1(C(CC(CC1(C)O)O)(C)C)O)OC2C(C(C(C(O2)CO)O)O)O 406.50 unknown https://doi.org/10.1248/CPB.53.800
2-(Hydroxymethyl)-6-[4-(2,3,4-trihydroxy-2,6,6-trimethylcyclohexyl)but-3-en-2-yloxy]oxane-3,4,5-triol 72830514 Click to see 406.50 unknown https://doi.org/10.1248/CPB.53.800
2-(Hydroxymethyl)-6-[4-(4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)but-3-en-2-yloxy]oxane-3,4,5-triol 75995908 Click to see 388.50 unknown https://doi.org/10.1248/CPB.53.800
2-[4-(2,4-Dihydroxy-1-methoxy-2,6,6-trimethylcyclohexyl)but-3-en-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73096206 Click to see 420.50 unknown https://doi.org/10.1248/CPB.53.800
2-[4-(3,4-Dihydroxy-2,6,6-trimethylcyclohexen-1-yl)but-3-en-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 72786666 Click to see CC1=C(C(CC(C1O)O)(C)C)C=CC(C)OC2C(C(C(C(O2)CO)O)O)O 388.50 unknown https://doi.org/10.1248/CPB.53.800
2-[4-(4,5-Dihydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl)but-3-en-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 72802713 Click to see 404.50 unknown https://doi.org/10.1248/CPB.53.800
6-Hydroxy-2,4,4-trimethyl-3-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one 72971284 Click to see 386.40 unknown https://doi.org/10.1248/CPB.53.800
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4S,7R,11bR)-4-(hydroxymethyl)-7,11b-dimethyl-1,2,3,4a,5,6,6a,7,11,11a-decahydronaphtho[2,1-f][1]benzofuran-4-carboxylic acid 101863829 Click to see 332.40 unknown https://doi.org/10.1248/CPB.53.800
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4S,5R,6R)-2-(hydroxymethyl)-6-[(1R)-3,5,5-trimethyl-4-[(E,3S)-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-3-en-1-yl]oxyoxane-3,4,5-triol 163079372 Click to see 534.60 unknown https://doi.org/10.1248/CPB.53.800
(2R,3R,4S,5S,6R)-2-[(1S,2R)-2-hydroxy-4-[(E,3S)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohex-3-en-1-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 11211418 Click to see 388.50 unknown https://doi.org/10.1248/CPB.53.800
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(1R)-3,5,5-trimethyl-4-[(3S)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]cyclohex-3-en-1-yl]oxyoxane-3,4,5-triol 11466799 Click to see 536.60 unknown https://doi.org/10.1248/CPB.53.800
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(1R)-3,5,5-trimethyl-4-[(E,3S)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-3-en-1-yl]oxyoxane-3,4,5-triol 11307149 Click to see 534.60 unknown https://doi.org/10.1248/CPB.53.800
2-(Hydroxymethyl)-6-[3,5,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-3-en-1-yl]oxyoxane-3,4,5-triol 72794441 Click to see 534.60 unknown https://doi.org/10.1248/CPB.53.800
2-(Hydroxymethyl)-6-[3,5,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]cyclohex-3-en-1-yl]oxyoxane-3,4,5-triol 72972608 Click to see 536.60 unknown https://doi.org/10.1248/CPB.53.800
4-[2-Hydroxy-2,6,6-trimethyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexylidene]but-3-en-2-one 15628135 Click to see 386.40 unknown https://doi.org/10.1248/CPB.53.800
Icariside B1 15628136 Click to see 386.40 unknown https://doi.org/10.1248/CPB.53.800
> 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 https://doi.org/10.1248/CPB.53.800
(E)-4-[(1S,4S,6R)-2,2,6-trimethyl-4-[(2S,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 162873233 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 https://doi.org/10.1248/CPB.53.800
2-(Hydroxymethyl)-6-[[3,4,5-trihydroxy-6-(2-phenylethoxy)oxan-2-yl]methoxy]oxane-3,4,5-triol 44389818 Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O 446.40 unknown https://doi.org/10.3987/COM-09-S(S)22
2-(Hydroxymethyl)-6-phenylmethoxyoxane-3,4,5-triol 4984739 Click to see 270.28 unknown https://doi.org/10.3987/COM-09-S(S)22
2-Phenylethyl 6-O-beta-D-glucopyranosyl-beta-D-glucopyranoside 11539591 Click to see 446.40 unknown https://doi.org/10.3987/COM-09-S(S)22
4-[2,2,6-Trimethyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-oxabicyclo[4.1.0]heptan-1-yl]but-3-en-2-one 85128318 Click to see 386.40 unknown https://doi.org/10.1248/CPB.53.800
Benzyl beta-d-glucopyranoside 188977 Click to see 270.28 unknown https://doi.org/10.3987/COM-09-S(S)22
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-[4-[(3S)-3-hydroxybutyl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 102283324 Click to see 358.40 unknown https://doi.org/10.3987/COM-09-S(S)22
2-[4-(3-Hydroxybutyl)-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163020369 Click to see 358.40 unknown https://doi.org/10.3987/COM-09-S(S)22
Zingerone beta-D-glucopyranoside 90743708 Click to see 356.40 unknown https://doi.org/10.3987/COM-09-S(S)22
Zingerone glucoside 74937233 Click to see CC(=O)CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC 356.40 unknown https://doi.org/10.3987/COM-09-S(S)22

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