Sabia japonica

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Common Names

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Scientific Literature

Phytochemical Profile

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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)

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan

Links to other databases Top

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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

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
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
Sabphenol B	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
> 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-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
5-Hydroxyferulic acid methyl	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
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-Dihydroxy-5-methoxycinnamoyl 6-O-[2-O-[(E)-3-methoxy-4-hydroxycinnamoyl]-beta-D-glucopyranosyl]-beta-D-glucopyranoside	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
(E)-3,4-Dihydroxy-5-methoxycinnamoyl 6-O-[2-O-[(E)-3,4-dihydroxy-5-methoxycinnamoyl]-beta-D-glucopyranosyl]-beta-D-glucopyranoside	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
(E)-3,4-Dihydroxy-5-methoxycinnamoyl 6-O-[2-O-[(E)-3,5-dimethoxy-4-hydroxycinnamoyl]-beta-D-glucopyranosyl]-beta-D-glucopyranoside	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
(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)-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
[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-[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-(beta-D-glucopyranosyl)-7-(3,5-dimethoxy-4-hydroxycinnamoyloxy)-4H-1-benzopyran-4-one	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
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
[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
2-[4-(beta-D-Glucopyranosyloxy)phenyl]-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	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
2-[4-[6-O-(3,5-Dimethoxy-4-hydroxycinnamoyl)-beta-D-glucopyranosyloxy]phenyl]-5-hydroxy-6-(beta-D-glucopyranosyl)-7-(3,5-dimethoxy-4-hydroxycinnamoyloxy)-4H-1-benzopyran-4-one	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
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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Sabia japonica

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