Scientific name	Authority	First published in
Frasera pseudochinensis	(H.Hara) Toyok.	Symb. Asahikaw. 1: 156 (1965)
Ophelia pseudochinensis	(H.Hara) Czerep.	Vasc. Pl. Russia & Adj. States (former USSR) 271 (1995), isonym;.
Swertia chinensis f. grandiflora	Franch.	Bull. Soc. Bot. France 46: 322 (1899)

Common names Top

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Filter by language:

Language	Common/alternative name
Japanese	ムラサキセンブリ
Chinese	当药
Chinese	瘤毛獐牙菜
Chinese	瘤毛獐牙菜（紫花当药）
Chinese	紫花当药

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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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 click to expand
- China
  - China North-central
  - Inner Mongolia
- Eastern Asia
  - Japan
  - Korea
- Russian Far East
  - Primorye

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000498064
UNII	N6UGT4Q998
Tropicos	13800992
KEW	urn:lsid:ipni.org:names:371045-1
The Plant List	kew-2590275
Open Tree Of Life	416290
NCBI Taxonomy	676131
IPNI	371045-1
GBIF	7270188
EPPO	SWEPS
EOL	2892751
CMAUP	NPO14381

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

Sweroside plays a role in mitigating high glucose-induced damage in human renal tubular epithelial HK-2 cells by regulating the SIRT1/NF-κB signaling pathway

Ma X, Guo Z, Zhao W, Chen L

Korean J Physiol Pharmacol

01-Nov-2023

PMCID:	PMC10613573
doi:	10.4196/kjpp.2023.27.6.533
PMID:	37884285

Activation of Nrf2 signaling: A key molecular mechanism of protection against cardiovascular diseases by natural products

Wu X, Wei J, Yi Y, Gong Q, Gao J

Front Pharmacol

08-Dec-2022

PMCID:	PMC9772885
doi:	10.3389/fphar.2022.1057918
PMID:	36569290

Biological Mechanisms and Related Natural Inhibitors of CD36 in Nonalcoholic Fatty Liver

Feng Y, Sun W, Sun F, Yin G, Liang P, Chen S, Liu X, Jiang T, Zhang F

Drug Des Devel Ther

04-Nov-2022

PMCID:	PMC9642071
doi:	10.2147/DDDT.S386982
PMID:	36388082

Application of herbs and active ingredients ameliorate non-alcoholic fatty liver disease under the guidance of traditional Chinese medicine

Zhou Z, Zhang J, You L, Wang T, Wang K, Wang L, Kong X, Gao Y, Sun X

Front Endocrinol (Lausanne)

20-Sep-2022

PMCID:	PMC9530134
doi:	10.3389/fendo.2022.1000727
PMID:	36204095

Advances on Natural Abietane, Labdane and Clerodane Diterpenes as Anti-Cancer Agents: Sources and Mechanisms of Action

Acquaviva R, Malfa GA, Loizzo MR, Xiao J, Bianchi S, Tundis R

Molecules

26-Jul-2022

PMCID:	PMC9330018
doi:	10.3390/molecules27154791
PMID:	35897965

The NLRP3 Inflammasome in Non-Alcoholic Fatty Liver Disease and Steatohepatitis: Therapeutic Targets and Treatment

Yu L, Hong W, Lu S, Li Y, Guan Y, Weng X, Feng Z

Front Pharmacol

08-Mar-2022

PMCID:	PMC8957978
doi:	10.3389/fphar.2022.780496
PMID:	35350750

РАСТИТЕЛЬНЫЕ ПРЕПАРАТЫ КАК ПОТЕНЦИАЛЬНЫЕ ПРОТИВОВИРУСНЫЕ СРЕДСТВА ДЛЯ ЛЕЧЕНИЯ SARS-COV-2 ИНФЕКЦИИ

Душенков B, Душенкова A

Paemi Sino

01-Jan-2022

PMCID:	PMC9553026
doi:	10.25005/2074-0581-2022-24-1-113-122
PMID:	36225268

Mitochondrial Targeting Therapeutics: Promising Role of Natural Products in Non-alcoholic Fatty Liver Disease

Xu J, Shen J, Yuan R, Jia B, Zhang Y, Wang S, Zhang Y, Liu M, Wang T

Front Pharmacol

23-Dec-2021

PMCID:	PMC8733608
doi:	10.3389/fphar.2021.796207
PMID:	35002729

Antibacterial Activity Prediction Model of Traditional Chinese Medicine Based on Combined Data-Driven Approach and Machine Learning Algorithm: Constructed and Validated

Li JT, Wei YW, Wang MY, Yan CX, Ren X, Fu XJ

Front Microbiol

22-Nov-2021

PMCID:	PMC8645695
doi:	10.3389/fmicb.2021.763498
PMID:	34880839

Sweroside Protects Against Myocardial Ischemia–Reperfusion Injury by Inhibiting Oxidative Stress and Pyroptosis Partially via Modulation of the Keap1/Nrf2 Axis

Li J, Zhao C, Zhu Q, Wang Y, Li G, Li X, Li Y, Wu N, Ma C

Front Cardiovasc Med

19-Mar-2021

PMCID:	PMC8017130
doi:	10.3389/fcvm.2021.650368
PMID:	33816579

Potential compounds from several Indonesian plants to prevent SARS-CoV-2 infection: A mini-review of SARS-CoV-2 therapeutic targets

Illian DN, Siregar ES, Sumaiyah S, Utomo AR, Nuryawan A, Basyuni M

Heliyon

16-Jan-2021

PMCID:	PMC7833933
doi:	10.1016/j.heliyon.2021.e06001
PMID:	33532640

Analysis of therapeutic targets for SARS-CoV-2 and discovery of potential drugs by computational methods

Wu C, Liu Y, Yang Y, Zhang P, Zhong W, Wang Y, Wang Q, Xu Y, Li M, Li X, Zheng M, Chen L, Li H

Acta Pharm Sin B

27-Feb-2020

PMCID:	PMC7102550
doi:	10.1016/j.apsb.2020.02.008
PMID:	32292689

Somatic Embryogenesis in the Family Gentianaceae and Its Biotechnological Application

Tomiczak K, Mikuła A, Niedziela A, Wójcik-Lewandowska A, Domżalska L, Rybczyński JJ

Front Plant Sci

11-Jun-2019

PMCID:	PMC6579898
doi:	10.3389/fpls.2019.00762
PMID:	31244878

Therapeutic Potential of Plants and Plant Derived Phytochemicals against Acetaminophen-Induced Liver Injury

Subramanya SB, Venkataraman B, Meeran MF, Goyal SN, Patil CR, Ojha S

Int J Mol Sci

28-Nov-2018

PMCID:	PMC6321362
doi:	10.3390/ijms19123776
PMID:	30486484

Preclinical Models for Investigation of Herbal Medicines in Liver Diseases: Update and Perspective

Tan HY, San-Marina S, Wang N, Hong M, Li S, Li L, Cheung F, Wen XY, Feng Y

Evid Based Complement Alternat Med

28-Jan-2016

PMCID:	PMC4749812
doi:	10.1155/2016/4750163
PMID:	26941826

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid	10742	Click to see COC1=CC(=CC(=C1O)OC)C(=O)O	198.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
[2-[(4-Ethenyl-4a-hydroxy-8-oxo-3,4,5,6-tetrahydropyrano[3,4-c]pyran-3-yl)oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 2,4-dihydroxy-6-(3-hydroxyphenyl)benzoate	12305846	Click to see C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=C(C=C(C=C4O)O)C5=CC(=CC=C5)O	602.50	unknown	https://doi.org/10.1248/BPB.28.534
Amaroswerin	45359883	Click to see C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=C(C=C(C=C4O)O)C5=CC(=CC=C5)O	602.50	unknown	https://doi.org/10.1248/BPB.28.534
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3R,4S,4aR)-4-ethenyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one	9906781	Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O	358.34	unknown	via CMAUP database
(4R,4aR)-4-ethenyl-4a-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,5,6-tetrahydropyrano[3,4-c]pyran-8-one	12443156	Click to see C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)CO)O)O)O	374.34	unknown	via CMAUP database
4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one	581257	Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O	358.34	unknown	https://doi.org/10.1248/BPB.28.534
4-Ethenyl-4a-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4,5,6-tetrahydropyrano[3,4-c]pyran-8-one	3515878	Click to see C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)CO)O)O)O	374.34	unknown	https://doi.org/10.1248/BPB.28.534 https://doi.org/10.1248/CPB.56.485
Gentiopicrin	88708	Click to see C=CC1C(OC=C2C1=CCOC2=O)OC3C(C(C(C(O3)CO)O)O)O	356.32	unknown	via CMAUP database
Sucrose	5988	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
Sweroside	161036	Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O	358.34	unknown	https://doi.org/10.1248/CPB.56.485 https://doi.org/10.1248/BPB.28.534
Swertiamarin	442435	Click to see C=CC1C(OC=C2C1(CCOC2=O)O)OC3C(C(C(C(O3)CO)O)O)O	374.34	unknown	https://doi.org/10.1248/BPB.28.534 https://doi.org/10.1248/CPB.36.1575
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Di-O-Methylcrenatin	10736338	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CO	346.33	unknown	via CMAUP database
Isotachioside	15098566	Click to see COC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O	302.28	unknown	via CMAUP database
Multifidol glucoside	14412552	Click to see CCC(C)C(=O)C1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)O)O	372.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1-Hydroxy-3,7-dimethoxyxanthone	5488808	Click to see COC1=CC2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)OC	272.25	unknown	https://doi.org/10.1248/BPB.28.534
1-hydroxy-4,5-dimethoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one	5316768	Click to see COC1=CC=CC2=C1OC3=C(C2=O)C(=CC(=C3OC)OC4C(C(C(C(O4)CO)O)O)O)O	450.40	unknown	via CMAUP database
1,3-Dihydroxy-4,5-dimethoxyxanthone	5316765	Click to see COC1=CC=CC2=C1OC3=C(C2=O)C(=CC(=C3OC)O)O	288.25	unknown	via CMAUP database
1,3,5,8-Tetrahydroxyxanthone	5281626	Click to see C1=CC(=C2C(=C1O)C(=O)C3=C(C=C(C=C3O2)O)O)O	260.20	unknown	https://doi.org/10.1248/BPB.28.534
1,5-Dihydroxy-3-methoxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one	5858086	Click to see COC1=CC(=C2C(=C1)OC3=C(C=CC(=C3C2=O)OC4C(C(C(C(O4)CO)O)O)O)O)O	436.40	unknown	https://doi.org/10.1248/BPB.28.534
3-hydroxy-4,5-dimethoxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one	5316767	Click to see COC1=CC=CC2=C1OC3=C(C(=CC(=C3C2=O)OC4C(C(C(C(O4)CO)O)O)O)O)OC	450.40	unknown	via CMAUP database
3-hydroxy-6,7-dimethyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyxanthen-9-one	5316774	Click to see CC1=CC2=C(C=C1C)OC3=C(C2=O)C(=CC(=C3)O)OC4C(C(C(C(O4)CO)O)O)O	418.40	unknown	via CMAUP database
4,8-Dihydroxy-6-methoxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4-tetrahydroxanthen-9-one	163037619	Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C(CCC3O)OC4C(C(C(C(O4)CO)O)O)O)O	440.40	unknown	https://doi.org/10.1248/BPB.28.534
8-[(2S,3R,4S,5R)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-1,5-dihydroxy-3-methoxyxanthen-9-one	11330321	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3=C4C(=C(C=C3)O)OC5=CC(=CC(=C5C4=O)O)OC)O)O)O)O)O	552.50	unknown	https://doi.org/10.1248/BPB.28.534
8-[4,5-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-1,5-dihydroxy-3-methoxyxanthen-9-one	72803945	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3=C4C(=C(C=C3)O)OC5=CC(=CC(=C5C4=O)O)OC)O)O)O)O)O	552.50	unknown	https://doi.org/10.1248/BPB.28.534
Bellidifolin	5281623	Click to see COC1=CC(=C2C(=C1)OC3=C(C=CC(=C3C2=O)O)O)O	274.22	unknown	https://doi.org/10.1248/CPB.56.485 https://doi.org/10.1248/BPB.28.534
Gentisin	5281636	Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O	258.23	unknown	via CMAUP database
Mangiferin	5281647	Click to see C1=C2C(=CC(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C4C(C(C(C(O4)CO)O)O)O)O	422.30	unknown	via CMAUP database
Methylswertianin	5281653	Click to see COC1=C(C2=C(C=C1)OC3=CC(=CC(=C3C2=O)O)OC)O	288.25	unknown	https://doi.org/10.1248/BPB.28.534
Swerchirin	5281660	Click to see COC1=C2C(=C(C=C1)O)C(=O)C3=C(C=C(C=C3O2)OC)O	288.25	unknown	https://doi.org/10.1248/BPB.28.534
Swertianin	5281661	Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C(=C(C=C3)O)O)O	274.22	unknown	via CMAUP database
Swertianolin	5281662	Click to see COC1=CC(=C2C(=C1)OC3=C(C=CC(=C3C2=O)OC4C(C(C(C(O4)CO)O)O)O)O)O	436.40	unknown	https://doi.org/10.1248/BPB.28.534
Tetrahydroswertianolin	10343169	Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C(CCC3O)OC4C(C(C(C(O4)CO)O)O)O)O	440.40	unknown	https://doi.org/10.1248/BPB.28.534
> Phenylpropanoids and polyketides / Coumarins and derivatives
Urolithin C	60198001	Click to see C1=CC2=C(C=C1O)OC(=O)C3=CC(=C(C=C23)O)O	244.20	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Isooxypeucedanin	625383	Click to see CC(C)C(=O)COC1=C2C=CC(=O)OC2=CC3=C1C=CO3	286.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol	102115501	Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)C4=CC5=C(C=C4O)OC(C(C5O)O)C6=CC(=C(C=C6)O)O)O)O)O	562.50	unknown	via CMAUP database
(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,4,7-triol	102115500	Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)C4=CC5=C(C=C4O)OC(C(C5O)O)C6=CC(=C(C=C6)O)O)O)O)O	562.50	unknown	via CMAUP database
(2R,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4R)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	102400061	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	via CMAUP database
(2R,3S)-8-[(2R,3S,4R)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol	102400062	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O	594.50	unknown	via CMAUP database
Bileucofisetinidin	101297694	Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)C4=CC5=C(C=C4O)OC(C(C5O)O)C6=CC(=C(C=C6)O)O)O)O)O	562.50	unknown	via CMAUP database
Epirobinetinidol-(4beta,8)-catechin	51042196	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	via CMAUP database
Fisetinidol-(4A8)-catechin	14332862	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	562.50	unknown	via CMAUP database
Fisetinidol-(4alpha,6)-gallocatechin	51041987	Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O	578.50	unknown	via CMAUP database
Fisetinidol-(4alpha,8)-catechin	11731408	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	562.50	unknown	via CMAUP database
Robinetinidol-(4alpha->8)-catechin-(6->4alpha)-robinetinidol	442689	Click to see C1C(C(OC2=C(C(=C(C(=C21)O)C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)C6C(C(OC7=C6C=CC(=C7)O)C8=CC(=C(C(=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O	866.80	unknown	via CMAUP database
Robinetinidol-(4alpha,8)-catechin	70697937	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O	578.50	unknown	via CMAUP database
Robinetinidol-(4alpha,8)-gallocatechin	70697956	Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O	594.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
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 / Catechins / Epigallocatechins
Gallocatechin	65084	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
5-[(2R,3R)-3,7-dihydroxy-3,4-dihydro-2H-chromen-2-yl]benzene-1,2,3-triol	101846310	Click to see C1C(C(OC2=C1C=CC(=C2)O)C3=CC(=C(C(=C3)O)O)O)O	290.27	unknown	via CMAUP database
Robinetinidol	12314983	Click to see C1C(C(OC2=C1C=CC(=C2)O)C3=CC(=C(C(=C3)O)O)O)O	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Butin	92775	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O	272.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Garbanzol	442410	Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O	272.25	unknown	via CMAUP database
Taxifolin	439533	Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	304.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Leucoanthocyanidins
ent-Epifisetinidol-4beta-ol	44257142	Click to see C1=CC(=C(C=C1C2C(C(C3=C(O2)C=C(C=C3)O)O)O)O)O	290.27	unknown	via CMAUP database
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	via CMAUP database
> 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	via CMAUP database
Robinetin	5281692	Click to see C1=CC2=C(C=C1O)OC(=C(C2=O)O)C3=CC(=C(C(=C3)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	44257906	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	via CMAUP database
6-beta-D-glucopyranosyl-3',4',5-trihydroxy-7-methoxyflavone	44258368	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)C4C(C(C(C(O4)CO)O)O)O	462.40	unknown	via CMAUP database
6-beta-D-Glucopyranosyl-4',5-dihydroxy-7-methoxyflavone	369636	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O	446.40	unknown	via CMAUP database
6-beta-D-Glucopyranosyl-4',5,7-trihydroxyflavone	44257794	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
7-O-Methylapigenin 6-C-beta-D-glucopyranoside	44258316	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O	446.40	unknown	via CMAUP database
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	via CMAUP database
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
Leucanthoside	3556303	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)C4C(C(C(C(O4)CO)O)O)O	462.40	unknown	https://doi.org/10.1248/CPB.56.485
Swertiajaponin	442659	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)C4C(C(C(C(O4)CO)O)O)O	462.40	unknown	https://doi.org/10.1248/CPB.56.485
Swertisin	124034	Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4C(C(C(C(O4)CO)O)O)O	446.40	unknown	https://doi.org/10.1248/CPB.56.485
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
4'-O-methylrobinetinidol 3'-O-beta-D-glucopyranoside	51041986	Click to see COC1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)C3C(CC4=C(O3)C=C(C=C4)O)O)O	466.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Fisetin 3-methyl ether	9839293	Click to see COC1=C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O	300.26	unknown	via CMAUP database
Geraldone	5281618	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C=C3)O)O	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Fisetin tetramethyl ether	631171	Click to see COC1=CC2=C(C=C1)C(=O)C(=C(O2)C3=CC(=C(C=C3)OC)OC)OC	342.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,6-bis-O-galloyl-beta-D-glucose	440221	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	484.40	unknown	via CMAUP database

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Swertia pseudochinensis

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