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Sabia japonica

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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 UUID64404d983b83b430179322
Scientific name Sabia japonica
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 11: 430 (1867)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sabia bullockii Hance J. Bot. 16: 9 (1878)
Sabia japonica var. spinosa Lecomte Bull. Soc. Bot. France 54: 673, in text 1907

Common names Top

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Language Common/alternative name
Japanese セイフウトウ
Chinese 清风藤
Chinese 寻风藤
Chinese 清風藤

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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 South-central
      • China Southeast
    • Eastern Asia
      • Japan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001133457
Tropicos 28200221
KEW urn:lsid:ipni.org:names:776427-1
The Plant List tro-28200221
Open Tree Of Life 8373
NCBI Taxonomy 400538
IPNI 776427-1
GBIF 7842442
EOL 2889131
CMAUP NPO28422

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
Combining Traditional Chinese Herbs and csDMARDs for the Treatment of Rheumatoid Arthritis Involves Tapering and Discontinuing Glucocorticoids: Protocol for a Two-Stage Non-Randomized Controlled Trial Wang X, Yang X, Wang S, Tian X, Yin J, Liu N, Di P, Qi J, Li Y, Chen J, Wu Y, Wu J, Zhao W, Peng J, Zhang L, Gu L Int J Gen Med 05-Mar-2024
PMCID:PMC10933510
doi:10.2147/IJGM.S444056
PMID:38481616
Complete chloroplast genomes of 11 Sabia samples: Genomic features, comparative analysis, and phylogenetic relationship Chen Q, Chen C, Wang B, Wang Z, Xu W, Huang Y, Sun Q Front Plant Sci 16-Dec-2022
PMCID:PMC9800934
doi:10.3389/fpls.2022.1052920
PMID:36589084
Emerging pharmaceutical therapeutics and delivery technologies for osteoarthritis therapy Shentu CY, Yan G, Xu DC, Chen Y, Peng LH Front Pharmacol 17-Nov-2022
PMCID:PMC9712996
doi:10.3389/fphar.2022.945876
PMID:36467045
Post-infectious cough of different syndromes treated by traditional Chinese medicines: A review Jiang W, Qi J, Li X, Chen G, Zhou D, Xiao W, Li N Chin Herb Med 28-Sep-2022
PMCID:PMC9669398
doi:10.1016/j.chmed.2022.09.002
PMID:36405059
Ethnobotanical study of Hakka traditional medicine in Ganzhou, China and their antibacterial, antifungal, and cytotoxic assessments Hu H, Yang Y, Aissa A, Tekin V, Li J, Panda SK, Huang H, Luyten W BMC Complement Med Ther 19-Sep-2022
PMCID:PMC9484230
doi:10.1186/s12906-022-03712-z
PMID:36123737
Potential roles of gut microbiota and microbial metabolites in chronic inflammatory pain and the mechanisms of therapy drugs Li JS, Su SL, Xu Z, Zhao LH, Fan RY, Guo JM, Qian DW, Duan JA Ther Adv Chronic Dis 28-Jul-2022
PMCID:PMC9340317
doi:10.1177/20406223221091177
PMID:35924009
Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China Lu Z, Chen H, Lin C, Ou G, Li J, Xu W J Ethnobiol Ethnomed 21-Jun-2022
PMCID:PMC9210605
doi:10.1186/s13002-022-00544-6
PMID:35729593
Recycling of Chinese herb residues by endophytic and probiotic fungus Aspergillus cristatus CB10002 for the production of medicinal valuable anthraquinones Kong W, Huang C, Shi J, Li Y, Jiang X, Duan Q, Huang Y, Duan Y, Zhu X Microb Cell Fact 04-Jun-2019
PMCID:PMC6547571
doi:10.1186/s12934-019-1150-9
PMID:31164126
Combined treatment with sinomenine and acupuncture on collagen-induced arthritis through the NF-κB and MAPK signaling pathway Xu M, Liu S, Wan R, Chen Y Oncol Lett 30-Mar-2018
PMCID:PMC5950530
doi:10.3892/ol.2018.8394
PMID:29805616
Floral morphology and anatomy of Ophiocaryon, a paedomorphic genus of Sabiaceae Thaowetsuwan P, Honorio Coronado EN, Ronse De Craene LP Ann Bot 25-Oct-2017
PMCID:PMC5691798
doi:10.1093/aob/mcx115
PMID:29077782
<i>ω</i>-Methylsulfinylalkyl Isothiocyanates in Wasabi,<i>Wasabia japonica</i>Matsum Hideo Etoh, Akiyoshi Nishimura, Reiko Takasawa, Akihito Yagi, Kazuhide Saito, Kanzo Sakata, Isao Kishima, Kazuo Ina Oxford University Press (OUP) 13-Apr-2016
doi:10.1080/00021369.1990.10870168
The efficacy of QingfengGanke granule in treating postinfectious cough in pathogenic wind invading lungs syndrome: a multicenter, randomized, double-blind, placebo-controlled trial Jiang H, Mao B, Wang L, Zhang R, She B, Jin F, Xu Y, Ma J, Liu Q Chin Med 09-Aug-2015
PMCID:PMC4529711
doi:10.1186/s13020-015-0049-6
PMID:26257822
Antioxidant phenylpropanoid glycosides from the leaves of Wasabia japonica. Hosoya T, Yun YS, Kunugi A Phytochemistry 01-Feb-2008
doi:10.1016/J.PHYTOCHEM.2007.08.021
PMID:17920090
Five novel flavonoids from Wasabia japonica Takahiro Hosoya, Young Sook Yun, Akira Kunugi Elsevier BV 10-Jun-2005
doi:10.1016/J.TET.2005.04.061

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
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Hydroxytyrosol 82755 Click to see C1=CC(=C(C=C1CCO)O)O 154.16 unknown via CMAUP database
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-dihydroxy-5-[(E)-4-hydroxy-3-methylbut-2-enyl]-2-(3-methylbut-2-enyl)benzaldehyde 44477997 Click to see CC(=CCC1=C(C=C(C(=C1O)O)CC=C(C)CO)C=O)C 290.40 unknown via CMAUP database
Sabphenol A 15229438 Click to see CC(=CCC1=CC(=C(C(=C1O)O)CC=C(C)C)C=O)C 274.35 unknown via CMAUP database
> Organosulfur compounds / Allyl sulfur compounds
Diallyl sulfide 11617 Click to see C=CCSCC=C 114.21 unknown via CMAUP database
> Organosulfur compounds / Isothiocyanates
1-Isothiocyanato-6-(methylthio)hexane 165224 Click to see CSCCCCCCN=C=S 189.30 unknown via CMAUP database
1-Isothiocyanato-7-(methylthio)heptane 10125146 Click to see CSCCCCCCCN=C=S 203.40 unknown via CMAUP database
1-Isothiocyanato-8-(methylthio)octane 10171359 Click to see CSCCCCCCCCN=C=S 217.40 unknown via CMAUP database
Allyl isothiocyanate 5971 Click to see C=CCN=C=S 99.16 unknown via CMAUP database
> Organosulfur compounds / Sulfoxides
1-Isothiocyanato-6-(methylsulfinyl)hexane 9815648 Click to see CS(=O)CCCCCCN=C=S 205.30 unknown https://doi.org/10.1080/00021369.1990.10870168
1-isothiocyanato-6-[(S)-methylsulfinyl]hexane 94046233 Click to see CS(=O)CCCCCCN=C=S 205.30 unknown https://doi.org/10.1080/00021369.1990.10870168
Alyssin, (S)- 51548324 Click to see CS(=O)CCCCCN=C=S 191.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(R)-N-Trans-Feruloyloctopamine 11151622 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCC(C2=CC=C(C=C2)O)O)O 329.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3,4-Dihydroxy-5-methoxy-trans-cinnamic acid methyl ester 14843288 Click to see COC1=CC(=CC(=C1O)O)C=CC(=O)OC 224.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
3,4-Dimethoxycinnamic acid 717531 Click to see COC1=C(C=C(C=C1)C=CC(=O)O)OC 208.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
Methyl 3-(3,4-dihydroxy-5-methoxyphenyl)prop-2-enoate 70007640 Click to see COC1=CC(=CC(=C1O)O)C=CC(=O)OC 224.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
Methyl 4-hydroxy-3-methoxy-cinnamate 16830 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O 208.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
Methyl ferulate 5357283 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC)O 208.21 unknown via CMAUP database
Methyl sinapate 5321318 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC 238.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
(E)-3-Methoxy-4-hydroxycinnamoyl 6-O-[2-O-[(E)-3,5-dimethoxy-4-hydroxycinnamoyl]-beta-D-glucopyranosyl]-beta-D-glucopyranoside 24827806 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(OC2OCC3C(C(C(C(O3)OC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O)O)CO)O)O 724.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
(E)-3,4-Dihydroxy-5-methoxycinnamoyl 6-O-(beta-D-glucopyranosyl)-beta-D-glucopyranoside 24827938 Click to see COC1=CC(=CC(=C1O)O)C=CC(=O)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O 534.50 unknown via CMAUP database
(E)-3,4-Dihydroxycinnamoyl 6-O-[2-O-[(E)-3,5-dimethoxy-4-hydroxycinnamoyl]-beta-D-glucopyranosyl]-beta-D-glucopyranoside 24827807 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(OC2OCC3C(C(C(C(O3)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)CO)O)O 710.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
[(2R,3R,4S,5S,6R)-2-[[(2R,3S,4S,5R,6S)-6-[(E)-3-(3,4-dihydroxy-5-methoxyphenyl)prop-2-enoyl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(3,4-dihydroxy-5-methoxyphenyl)prop-2-enoate 24827808 Click to see COC1=CC(=CC(=C1O)O)C=CC(=O)OC2C(C(C(OC2OCC3C(C(C(C(O3)OC(=O)C=CC4=CC(=C(C(=C4)OC)O)O)O)O)O)CO)O)O 726.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
[(2R,3R,4S,5S,6R)-2-[[(2R,3S,4S,5R,6S)-6-[(E)-3-(3,4-dihydroxy-5-methoxyphenyl)prop-2-enoyl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 24827937 Click to see COC1=CC(=CC(=C1O)O)C=CC(=O)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O)O 710.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[[(2R,3S,4S,5S,6S)-3,4,5-trihydroxy-6-[(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxyoxan-2-yl]methoxy]oxan-3-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 163188975 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(OC2OCC3C(C(C(C(O3)OC(=O)C=CC4=CC(=C(C(=C4)OC)O)OC)O)O)O)CO)O)O 754.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-3-[(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (E)-3-(3,4-dihydroxy-5-methoxyphenyl)prop-2-enoate 24827679 Click to see COC1=CC(=CC(=C1O)O)C=CC(=O)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC(=C(C(=C4)OC)O)OC)O)O)O 740.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
[2-[[6-[3-(3,4-Dihydroxy-5-methoxyphenyl)prop-2-enoyloxy]-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3-(3,4-dihydroxy-5-methoxyphenyl)prop-2-enoate 74327020 Click to see COC1=CC(=CC(=C1O)O)C=CC(=O)OC2C(C(C(OC2OCC3C(C(C(C(O3)OC(=O)C=CC4=CC(=C(C(=C4)OC)O)O)O)O)O)CO)O)O 726.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
[2-[[6-[3-(3,4-Dihydroxy-5-methoxyphenyl)prop-2-enoyloxy]-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 74327079 Click to see COC1=CC(=CC(=C1O)O)C=CC(=O)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC)O)O)O 710.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
[4,5-Dihydroxy-6-(hydroxymethyl)-2-[[3,4,5-trihydroxy-6-[3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyloxy]oxan-2-yl]methoxy]oxan-3-yl] 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 74327017 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(OC2OCC3C(C(C(C(O3)OC(=O)C=CC4=CC(=C(C(=C4)OC)O)OC)O)O)O)CO)O)O 754.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
[6-[[4,5-Dihydroxy-3-[3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyloxy]-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 74327019 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(OC2OCC3C(C(C(C(O3)OC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)CO)O)O 710.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid 709 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
5-Hydroxyferulic acid 446834 Click to see COC1=CC(=CC(=C1O)O)C=CC(=O)O 210.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
CID 160594 160594 Click to see COC1=CC(=CC(=C1O)O)C=CC(=O)O 210.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
Sinapic acid 10743 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.08.021
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
[5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-7-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 11239109 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)C5C(C(C(C(O5)CO)O)O)O 638.60 unknown https://doi.org/10.1016/J.TET.2005.04.061
[5-Hydroxy-2-(4-hydroxyphenyl)-4-oxo-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-7-yl] 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 72764433 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)C5C(C(C(C(O5)CO)O)O)O 638.60 unknown https://doi.org/10.1016/J.TET.2005.04.061
2-(4-Hydroxyphenyl)-5-hydroxy-6-[6-O-[2-O-(3,5-dimethoxy-4-hydroxycinnamoyl)-beta-D-glucopyranosyl]-beta-D-glucopyranosyl]-7-(3,5-dimethoxy-4-hydroxycinnamoyloxy)-4H-1-benzopyran-4-one 11787982 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(OC2OCC3C(C(C(C(O3)C4=C(C=C5C(=C4O)C(=O)C=C(O5)C6=CC=C(C=C6)O)OC(=O)C=CC7=CC(=C(C(=C7)OC)O)OC)O)O)O)CO)O)O 1006.90 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 4475102 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/10.1016/J.TET.2005.04.061
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-7-[(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy-4-oxo-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-6-yl]oxan-2-yl]methoxy]oxan-3-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 11228635 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(C(OC2OCC3C(C(C(C(O3)C4=C(C=C5C(=C4O)C(=O)C=C(O5)C6=CC=C(C=C6)OC7C(C(C(C(O7)CO)O)O)O)OC(=O)C=CC8=CC(=C(C(=C8)OC)O)OC)O)O)O)CO)O)O 1169.00 unknown https://doi.org/10.1016/J.TET.2005.04.061
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[4-[5-hydroxy-7-[(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxy-4-oxo-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-2-yl]phenoxy]oxan-2-yl]methyl (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 102352342 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)C4=CC(=O)C5=C(C(=C(C=C5O4)OC(=O)C=CC6=CC(=C(C(=C6)OC)O)OC)C7C(C(C(C(O7)CO)O)O)O)O)O)O)O 1006.90 unknown via CMAUP database
[3,4,5-Trihydroxy-6-[4-[5-hydroxy-7-[3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyloxy]-4-oxo-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-2-yl]phenoxy]oxan-2-yl]methyl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate 163080199 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)C4=CC(=O)C5=C(C(=C(C=C5O4)OC(=O)C=CC6=CC(=C(C(=C6)OC)O)OC)C7C(C(C(C(O7)CO)O)O)O)O)O)O)O 1006.90 unknown https://doi.org/10.1016/J.TET.2005.04.061
2-[4-(beta-D-Glucopyranosyloxy)phenyl]-5-hydroxy-6-(beta-D-glucopyranosyl)-7-(3,5-dimethoxy-4-hydroxycinnamoyloxy)-4H-1-benzopyran-4-one 11764267 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2=C(C(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O)C6C(C(C(C(O6)CO)O)O)O 800.70 unknown https://doi.org/10.1016/J.TET.2005.04.061
Flavonoid LP 73981632 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)OC5C(C(C(C(O5)CO)O)O)O 594.50 unknown https://doi.org/10.1016/J.TET.2005.04.061
Isosaponarin 154105 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)OC5C(C(C(C(O5)CO)O)O)O 594.50 unknown https://doi.org/10.1016/J.TET.2005.04.061
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Helicianeoide B 91758417 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC5C(C(C(C(O5)COC6C(C(C(CO6)O)O)O)O)O)O)O)O 742.60 unknown via CMAUP database
quercetin 3-O-beta-D-glucopyranosyl-(1->2)-rhamnopyranoside 10167806 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 610.50 unknown via CMAUP database

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