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Staphylea bumalda

Staphylea bumalda - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

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

Description Top

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No description added yet. Help us by writing one.

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

Common names Top

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Language Common/alternative name
English japanese bladdernut
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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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

Suggest others/fix!
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 CCC(CCOC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O)C(C)C 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 CCC(CCOC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O)C(C)C 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 CC(C=CC1(C(CC(CC1(C)O)O)(C)C)OC)OC2C(C(C(C(O2)CO)O)O)O 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 CC(C=CC12C(CC(C(C1(O2)C)O)O)(C)C)OC3C(C(C(C(O3)CO)O)O)O 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 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
(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 CC(C=CC12C(CC(CC1(O2)C)O)(C)C)OC3C(C(C(C(O3)CO)O)O)O 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 CC(C=CC1C(CC(C(C1(C)O)O)O)(C)C)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,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 CC1=C(C(CC(C1=O)O)(C)C)C=CC(C)OC2C(C(C(C(O2)CO)O)O)O 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 CCC(CCOC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O)C(C)C 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 CC(C=CC1C(CC(C(C1(C)O)O)O)(C)C)OC2C(C(C(C(O2)CO)O)O)O 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 CC(C=CC12C(CC(CC1(O2)C)O)(C)C)OC3C(C(C(C(O3)CO)O)O)O 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 CC(C=CC1(C(CC(CC1(C)O)O)(C)C)OC)OC2C(C(C(C(O2)CO)O)O)O 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 CC(C=CC12C(CC(C(C1(O2)C)O)O)(C)C)OC3C(C(C(C(O3)CO)O)O)O 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 CC1=C(C(CC(C1=O)O)(C)C)C=CC(C)OC2C(C(C(C(O2)CO)O)O)O 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 CC1C2CCC3C(C2CC4=C1C=CO4)(CCCC3(CO)C(=O)O)C 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 CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)C=CC(C)OC3C(C(C(C(O3)CO)O)O)O 534.60 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 CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)CCC(C)OC3C(C(C(C(O3)CO)O)O)O 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 CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)C=CC(C)OC3C(C(C(C(O3)CO)O)O)O 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 CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)C=CC(C)OC3C(C(C(C(O3)CO)O)O)O 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 CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)CCC(C)OC3C(C(C(C(O3)CO)O)O)O 536.60 unknown https://doi.org/10.1248/CPB.53.800
CID 15628135 15628135 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C 386.40 unknown https://doi.org/10.1248/CPB.53.800
Icariside B1 15628136 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C 386.40 unknown https://doi.org/10.1248/CPB.53.800
Staphylionoside E 11211418 Click to see CC1=C(C(CC(C1O)OC2C(C(C(C(O2)CO)O)O)O)(C)C)C=CC(C)O 388.50 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-[(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 C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 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 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
Benzyl beta-d-glucopyranoside 188977 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.3987/COM-09-S(S)22
Glc(b1-6)Glc(b)-O-EtPh 11539591 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
Icariside B2 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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-[4-(3-Hydroxybutyl)-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163020369 Click to see CC(CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC)O 358.40 unknown https://doi.org/10.3987/COM-09-S(S)22
Bumaldoside C 102283324 Click to see CC(CCC1=CC(=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC)O 358.40 unknown https://doi.org/10.3987/COM-09-S(S)22
Zingerone beta-D-glucopyranoside 90743708 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
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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