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Gleditsia japonica

Gleditsia japonica - Unknown
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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 UUID643fd98780f17589997223
Scientific name Gleditsia japonica
Authority Miq.
First published in Ann. Mus. Bot. Lugduno-Batavi3: 54 (1867)

Description Top

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Gleditsia japonica, also known as the Japanese locust, is a flowering plant in the Fabaceae family. It is native to various regions in Asia, including the eastern Himalayas, central and southern China, Manchuria, Korea, and Japan. This tree is commonly used as a street tree in cities in China and Europe. There are four accepted varieties of Gleditsia japonica, each found in different regions of Asia. This plant is known for its distinctive thorns and produces pods that are used in traditional medicine.

Synonyms Top

Scientific name Authority First published in
Caesalpiniodes japonica (Miq.) Kuntze Revis. Gen. Pl.1: 167 (1891)
Gleditsia melanacantha Tang & F.T.Wang ? 80, f. 80 1955

Common names Top

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Language Common/alternative name
Arabic غلاديشية يابانية
German japanische gleditschie
Japanese 梍
Japanese さいかち
Japanese カワラフジノキ
Japanese ソウキョウ
Japanese 皀莢
Japanese 皁莢
Japanese サイカチ
Korean 주엽나무
Chinese 皂角刺
Chinese 山皂荚
Chinese 山皂角
Chinese 山皂莢

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Gleditsia japonica var. delavayi (Franch.) L.C.Li Acta Phytotax. Sin.20: 228 (1982)
Gleditsia japonica var. japonica Miq. Unknown
Gleditsia japonica var. stenocarpa Nakai J. Jap. Bot.27: 130 (1952)
Gleditsia japonica var. velutina L.C.Li Acta Phytotax. Sin.20: 228 (1982)

Subvarieties (abbr. subvar.) Top

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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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000185997
UNII NHH89EE756
USDA Plants GLJA4
Tropicos 13019637
KEW urn:lsid:ipni.org:names:496595-1
The Plant List ild-32334
Open Tree Of Life 787616
Observations.org 129668
NCBI Taxonomy 66093
IUCN Red List 144259089
IPNI 496596-1
iNaturalist 340545
GBIF 2959514
EPPO GLIJA
EOL 643677
Elurikkus 341753
USDA GRIN 17636
Wikipedia Gleditsia_japonica
CMAUP NPO7631

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
Metabolite components and nutritional composition of the endosperm in seven species from Gleditsia Xiao F, Zhao Y, Wang X, Jian X, Liu F Food Chem X 04-Apr-2024
PMCID:PMC11063355
doi:10.1016/j.fochx.2024.101340
PMID:38699588
Characterization of the chloroplast genome of Gleditsia species and comparative analysis Xiao F, Zhao Y, Wang X, Jian X Sci Rep 21-Feb-2024
PMCID:PMC10881578
doi:10.1038/s41598-024-54608-6
PMID:38383559
Chemical component of differences in the endosperm of Gleditsia species seeds revealed based on comparative metabolomics Lu G, Ren T, Zhao Z, Li B, Tan S Food Chem X 12-Dec-2023
PMCID:PMC10767367
doi:10.1016/j.fochx.2023.101060
PMID:38187947
Full-length transcriptome characterization and comparative analysis of Gleditsia sinensis Xiao F, Zhao Y, Wang X, Jian X BMC Genomics 08-Dec-2023
PMCID:PMC10709882
doi:10.1186/s12864-023-09843-y
PMID:38066414
An ethnobotanical study on medicinal plants of Shexian Dryland Stone Terraced System in northern China Bai Y, Zhang Q, He X, Wang H, Li W, Zhu J, Meng Y, Long C J Ethnobiol Ethnomed 14-Oct-2022
PMCID:PMC9569107
doi:10.1186/s13002-022-00560-6
PMID:36242037
Anti-Obesity Effects of Aqueous Extracts of Sunbanghwalmyung-Eum in High-Fat- and High-Cholesterol-Diet-Induced Obese C57BL/6J Mice Kim HL, Ahn YM, Lee SM, Seo CS, Park SH, Bang OS, Jung J Nutrients 17-Jul-2022
PMCID:PMC9318667
doi:10.3390/nu14142929
PMID:35889886
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
Anthropogenic legacies shaping the present composition of demarcation trees in a temperate upland field landscape in Japan Yoshinori T, Kenichiro K, Mitsunori O J Ethnobiol Ethnomed 16-Jun-2022
PMCID:PMC9202135
doi:10.1186/s13002-022-00543-7
PMID:35706010
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
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
How the seed coat affects the mother’s oviposition preference and larval performance in the bean beetle (Acanthoscelides obtectus, Coleoptera: Chrysomelidae, Bruchinae) in leguminous species Szentesi Á BMC Ecol Evol 08-Sep-2021
PMCID:PMC8425149
doi:10.1186/s12862-021-01892-9
PMID:34496762
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
Natural Products with Inhibitory Activity against Human Immunodeficiency Virus Type 1 Serna-Arbeláez MS, Florez-Sampedro L, Orozco LP, Ramírez K, Galeano E, Zapata W Adv Virol 29-May-2021
PMCID:PMC8181102
doi:10.1155/2021/5552088
PMID:34194504

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
> Alkaloids and derivatives / Cytochalasans
(16-Benzyl-5,12-dihydroxy-5,7,14-trimethyl-13-methylidene-18-oxo-17-azatricyclo[9.7.0.01,15]octadeca-3,9-dien-2-yl) acetate 2921 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(C=CC(C1)(C)O)OC(=O)C)C(=O)NC3CC4=CC=CC=C4)C)O 493.60 unknown via CMAUP database
[(3E,9Z)-16-benzyl-5,12-dihydroxy-5,7,14-trimethyl-13-methylidene-18-oxo-17-azatricyclo[9.7.0.01,15]octadeca-3,9-dien-2-yl] acetate 17751001 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(C=CC(C1)(C)O)OC(=O)C)C(=O)NC3CC4=CC=CC=C4)C)O 493.60 unknown via CMAUP database
CID 101706637 101706637 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(C=CC(C1)(C)O)OC(=O)C)C(=O)NC3CC4=CC=CC=C4)C)O 493.60 unknown via CMAUP database
Cytochalasin H (>90%) 13892272 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(C=CC(C1)(C)O)OC(=O)C)C(=O)NC3CC4=CC=CC=C4)C)O 493.60 unknown via CMAUP database
Cytochalasin-H 6434468 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(C=CC(C1)(C)O)OC(=O)C)C(=O)NC3CC4=CC=CC=C4)C)O 493.60 unknown via CMAUP database
Kodocytochalasin 1 5351303 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(C=CC(C1)(C)O)OC(=O)C)C(=O)NC3CC4=CC=CC=C4)C)O 493.60 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3R,4S,5R,6S)-2-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-6-methyloxane-3,4,5-triol;[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5S,6S)-5-hydroxy-3,4-bis[[(2E,6S)-6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoyl]oxy]-6-methyloxan-2-yl]oxymethyl]oxan-2-yl] (5R,6aR,6aS,6bR,8aR,10S,12aR)-10-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4R,5R)-3,4-dihydroxy-5-[(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-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 6475456 Click to see CC1C(C(C(C(O1)OC2C(C(C(CO2)O)OC3C(C(C(CO3)O)O)O)O)O)O)O.CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4O)C)C)(C)C)OC8C(C(C(C(O8)COC9C(C(C(CO9)OC1C(C(C(CO1)O)O)O)O)O)O)O)O)C)(C)C)O)O)O)OC(=O)C(=CCCC(C)(C=C)O)CO)OC(=O)C(=CCCC(C)(C=C)O)CO)O 2000.20 unknown https://doi.org/10.1021/NP50123A006
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5R,6S)-5-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5S,6S)-5-hydroxy-3-[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dienoyl]oxy-4-[(2E,6S)-6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoyl]oxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl] (5R,6aS,6bR,10S,12aR)-10-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-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 6475388 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4O)C)C)(C)C)OC8C(C(C(C(O8)COC9C(C(C(CO9)O)O)OC1C(C(C(CO1)O)O)O)O)O)O)C)(C)C)OC1C(C(C(C(O1)C)OC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)O)O)O)O)OC(=O)C(=CCCC(C)(C=C)O)C)OC(=O)C(=CCCC(C)(C=C)O)CO)O 1966.20 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5R,6S)-5-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5S,6S)-5-hydroxy-3-[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dienoyl]oxy-4-[(2E)-6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoyl]oxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl] (4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-6-[[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-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 100987820 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4O)C)C)(C)C)OC8C(C(C(C(O8)COC9C(C(C(CO9)O)O)OC1C(C(C(CO1)O)O)O)O)O)O)C)(C)C)OC1C(C(C(C(O1)C)OC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)O)O)O)O)OC(=O)C(=CCCC(C)(C=C)O)C)OC(=O)C(=CCCC(C)(C=C)O)CO)O 1966.20 unknown https://doi.org/10.1021/NP50123A006
Gleditsia saponin C 44584163 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC(=O)C34CCC(CC3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4O)C)C)(C)C)OC8C(C(C(C(O8)COC9C(C(C(CO9)O)O)OC1C(C(C(CO1)O)O)O)O)O)O)C)(C)C)OC1C(C(C(C(O1)C)OC1C(C(C(CO1)O)OC1C(C(C(CO1)O)O)O)O)O)O)O)O)OC(=O)C(=CCCC(C)(C=C)O)C)OC(=O)C(=CCCC(C)(C=C)O)CO)O 1966.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 45483610 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Echinocystic Acid 73309 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C(=O)O)C 472.70 unknown https://doi.org/10.2478/ACPH-2013-0036
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Glycosylamines
6-amino-3-(3-methylbut-2-enyl)-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]purin-2-one 102261380 Click to see CC(=CCN1C2=C(C(=NC1=O)N)N(C=N2)C3C(C(C(C(O3)CO)O)O)O)C 381.38 unknown https://doi.org/10.1016/J.PHYTOL.2010.07.006
6-Amino-3-(4-hydroxy-3-methylbut-2-enyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]purin-2-one 75149030 Click to see CC(=CCN1C2=C(C(=NC1=O)N)N(C=N2)C3C(C(C(C(O3)CO)O)O)O)CO 397.38 unknown https://doi.org/10.1016/J.TETLET.2010.01.090
6-amino-3-[(Z)-4-hydroxy-3-methylbut-2-enyl]-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]purin-2-one 46209725 Click to see CC(=CCN1C2=C(C(=NC1=O)N)N(C=N2)C3C(C(C(C(O3)CO)O)O)O)CO 397.38 unknown https://doi.org/10.1016/J.TETLET.2010.01.090
> Organoheterocyclic compounds / Isoindoles and derivatives / Isoindoles
Cytochalasin H from Phomopsis sp. 16211932 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(C=CC(C1)(C)O)OC(=O)C)C(=O)NC3CC4=CC=CC=C4)C)O 493.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 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 / Flavonoids / Flavans / Catechins
(+)-Epicatechin 182232 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2S,3S)-3,4',5,7-Tetrahydroxyflavanone 9838882 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown via CMAUP database
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown via CMAUP database
Fustin 5317435 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 288.25 unknown https://doi.org/10.1248/YAKUSHI1947.77.11_1208
Tetrahydroxyflavanone 246330 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 288.25 unknown https://doi.org/10.1248/YAKUSHI1947.77.11_1208
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Leucoanthocyanidins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,4,7-triol 3508976 Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)O)O)O)O 290.27 unknown https://doi.org/10.1248/YAKUSHI1947.77.11_1208
Fisetinidol-4alpha-ol 164762 Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)O)O)O)O 290.27 unknown https://doi.org/10.1248/YAKUSHI1947.77.11_1208
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Fisetin 5281614 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C=C(C=C3)O)O)O)O 286.24 unknown https://doi.org/10.1248/YAKUSHI1947.77.11_1208
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.25.3408
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1248/CPB.25.3408
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 154497677 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1248/CPB.25.3408

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