Euonymus laxiflorus

Details

Ethnobotanical Use

General Uses

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Gallery

Contributors

Collections

Details Top

Internal ID	UUID64401bc7db7ec387617427
Scientific name	Euonymus laxiflorus
Authority	Champ. ex Benth.
First published in	Hooker's J. Bot. Kew Gard. Misc. 3: 333 (1851)

Ethnobotanical Use Top

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Important notice

Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Unfortunately, there is insufficient documented, verifiable ethnobotanical information available regarding the specific uses of *Euonymus laxiflorus* (as defined by the cited authority) that match the requirements. No reliable sources, such as peer-reviewed ethnobotanical studies, reputable herbal compendiums, or well-documented historic records, provide specific details on traditional teas, decoctions, tinctures, macerations, poultices, or other documented medicinal/culinary preparations involving this exact taxon.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Masakia pellucidifolia	(Hayata) Nakai	J. Jap. Bot. 24: 11 (1949)
Euonymus blinii	H.Lév.	Repert. Spec. Nov. Regni Veg. 13: 259. 1914
Euonymus cuspidatus	Loes.	Notizbl. Königl. Bot. Gart. Berlin 3: 77 (1900)
Euonymus forbesianus	Loes.	Bot. Jahrb. Syst. 30: 457 (1902)
Euonymus incertus	Pit.	Fl. Indo-Chine 1: 874 (1912)
Euonymus kwangtungensis	C.Y.Cheng	Icon. Cormophyt. Sin. , Suppl. 2: 226 (1983)
Euonymus laxicymosus	C.Y.Cheng ex J.S.Ma	Harvard Pap. Bot. 10: 96 (1997)
Euonymus paniculatus	Wight ex M.A.Lawson	Fl. Brit. India 1: 609 (1875)
Euonymus pellucidifolius	Hayata	Icon. Pl. Formosan. 3: 57. 1913 [25 Dec 1913] ; et in Ic. Pl. Formos. 5: 16
Euonymus rostratus	W.W.Sm.	Notes Roy. Bot. Gard. Edinburgh 10: 36 (1917)
Euonymus rubescens	Pit.	Fl. Indo-Chine 1: 875 (1912)
Euonymus vaniotii	H.Lév.	Repert. Spec. Nov. Regni Veg. 13: 259. 1914
Euonymus crosnieri	H.Lév. & Vaniot	Bull. Soc. Bot. France 51: 146 (1904)
Euonymus longifolius	Champ. ex Benth.	Hooker's J. Bot. Kew Gard. Misc. 3: 332 (1851)

Common names Top

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Language	Common/alternative name
Chinese	大丁黃
Chinese	山杜仲
Chinese	疏花卫矛
Chinese	一种维管植物

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 click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
  - Tibet
- Eastern Asia
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - India
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000681880
Tropicos	50169672
KEW	urn:lsid:ipni.org:names:160966-1
The Plant List	kew-2803446
Open Tree Of Life	310705
NCBI Taxonomy	1009469
IUCN Red List	147641903
IPNI	160966-1
iNaturalist	736436
GBIF	3791893
EOL	2878268
USDA GRIN	16279
CMAUP	NPO25119
Wikipedia	Euonymus_laxiflorus

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

Does local soil factor drive functional leaf trait variation? A test on Neilingding Island, South China

Tong S, Zhang J, Qiao X, Li B, Yang Q, Hu P, Yu S

BMC Ecol Evol

10-Apr-2024

PMCID:	PMC11005248
doi:	10.1186/s12862-024-02227-0
PMID:	38600505

Plant-Derived Natural Products and Their Biomedical Properties: Recent Advances and Future Directions

Amerikanou C, Papada E

Life (Basel)

23-Oct-2023

PMCID:	PMC10608234
doi:	10.3390/life13102105
PMID:	37895486

Adaptation to pollination by fungus gnats underlies the evolution of pollination syndrome in the genus Euonymus

Mochizuki K, Okamoto T, Chen KH, Wang CN, Evans M, Kramer AT, Kawakita A

Ann Bot

23-Aug-2023

PMCID:	PMC10583214
doi:	10.1093/aob/mcad081
PMID:	37610846

Novel Anti-Acetylcholinesterase Effect of Euonymus laxiflorus Champ. Extracts via Experimental and In Silico Studies

Nguyen VB, Wang SL, Phan TQ, Doan MD, Phan TK, Phan TK, Pham TH, Nguyen AD

Life (Basel)

30-May-2023

PMCID:	PMC10305147
doi:	10.3390/life13061281
PMID:	37374064

Screening and Elucidation of Chemical Structures of Novel Mammalian α-Glucosidase Inhibitors Targeting Anti-Diabetes Drug from Herbals Used by E De Ethnic Tribe in Vietnam

Nguyen VB, Wang SL, Phan TQ, Pham TH, Huang HT, Liaw CC, Nguyen AD

Pharmaceuticals (Basel)

17-May-2023

PMCID:	PMC10223997
doi:	10.3390/ph16050756
PMID:	37242539

Insights into antiradical mechanism and pro-oxidant enzyme inhibitor activity of walterolactone A/B 6-O-gallate-β-d-pyranoglucoside originating from Euonymus laxiflorus Champ. using in silico study

Quy PT, Dzung NA, Van Bay M, Van Bon N, Dung DM, Nam PC, Thong NM

RSC Adv

19-Oct-2022

PMCID:	PMC9580510
doi:	10.1039/d2ra05312h
PMID:	36321076

Metabolomics-Based Pharmacodynamic Analysis of Zhuang Yao Shuang Lu Tong Nao Granules in a Rat Model of Ischemic Cerebral Infarction

Zhai Y, Chen Y, Luo Y, Mei X, Wu L, Mo X, Zou M, Zhou M, Wu Y, Zheng G, Yang P, He Q, Chen R

Anal Cell Pathol (Amst)

05-Jul-2022

PMCID:	PMC9277214
doi:	10.1155/2022/8776079
PMID:	35846873

Flavanols from Nature: A Phytochemistry and Biological Activity Review

Luo Y, Jian Y, Liu Y, Jiang S, Muhammad D, Wang W

Molecules

22-Jan-2022

PMCID:	PMC8838462
doi:	10.3390/molecules27030719
PMID:	35163984

Vernonia patula (Dryand.) Merr. and Leucas chinensis (Retz.) R. Brown exert anti-inflammatory activities and relieve oxidative stress via Nrf2 activation

Wu PS, Jeng J, Yang JJ, Kao V, Yen JH, Wu MJ

J Ethnopharmacol

28-Jul-2020

PMCID:	PMC7385944
doi:	10.1016/j.jep.2020.113155
PMID:	32736054

Antidiabetic Potential of Medicinal Plants and Their Active Components

Salehi B, Ata A, V. Anil Kumar N, Sharopov F, Ramírez-Alarcón K, Ruiz-Ortega A, Abdulmajid Ayatollahi S, Valere Tsouh Fokou P, Kobarfard F, Amiruddin Zakaria Z, Iriti M, Taheri Y, Martorell M, Sureda A, N. Setzer W, Durazzo A, Lucarini M, Santini A, Capasso R, Adrian Ostrander E, -ur-Rahman A, Iqbal Choudhary M, C. Cho W, Sharifi-Rad J

Biomolecules

30-Sep-2019

PMCID:	PMC6843349
doi:	10.3390/biom9100551
PMID:	31575072

Bioactivity-Guided Purification of Novel Herbal Antioxidant and Anti-NO Compounds from Euonymus laxiflorus Champ.

Nguyen VB, Wang SL, Nguyen AD, Lin ZH, Doan CT, Tran TN, Huang HT, Kuo YH

Molecules

30-Dec-2018

PMCID:	PMC6337563
doi:	10.3390/molecules24010120
PMID:	30598014

Isolation and Identification of Potent Antidiabetic Compounds from Antrodia cinnamomea—An Edible Taiwanese Mushroom

Huang HT, Wang SL, Nguyen VB, Kuo YH

Molecules

02-Nov-2018

PMCID:	PMC6278467
doi:	10.3390/molecules23112864
PMID:	30400247

Novel Potent Hypoglycemic Compounds from Euonymus laxiflorus Champ. and Their Effect on Reducing Plasma Glucose in an ICR Mouse Model

Nguyen VB, Wang SL, Nguyen TH, Nguyen MT, Doan CT, Tran TN, Lin ZH, Nguyen QV, Kuo YH, Nguyen AD

Molecules

02-Aug-2018

PMCID:	PMC6222451
doi:	10.3390/molecules23081928
PMID:	30072618

New Records of Potent In-Vitro Antidiabetic Properties of Dalbergia tonkinensis Heartwood and the Bioactivity-Guided Isolation of Active Compounds

Nguyen VB, Wang SL, Nhan NT, Nguyen TH, Nguyen NP, Nghi DH, Cuong NM

Molecules

29-Jun-2018

PMCID:	PMC6099635
doi:	10.3390/molecules23071589
PMID:	29966279

Utilization of Fishery Processing By-Product Squid Pens for α-Glucosidase Inhibitors Production by Paenibacillus sp.

Nguyen VB, Nguyen AD, Wang SL

Mar Drugs

30-Aug-2017

PMCID:	PMC5618413
doi:	10.3390/md15090274
PMID:	28867763

Phytochemical Profile Top

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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
> Alkaloids and derivatives
(18,20,21,22-Tetraacetyloxy-19-benzoyloxy-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-24-yl) benzoate	162843061	Click to see	915.90	unknown	https://doi.org/10.1021/NP0203988
(18,20,21,22,24-Pentaacetyloxy-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-19-yl) benzoate	162953250	Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C6=CC=CC=C6)OC(=O)C)C	853.80	unknown	https://doi.org/10.1021/NP0203988
(20,21,22-Triacetyloxy-19-benzoyloxy-18,25-dihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-24-yl) benzoate	163047534	Click to see	873.80	unknown	https://doi.org/10.1021/NP0203988
(20,24-Diacetyloxy-19,21,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-18-pyridin-4-yloxy-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-22-yl) acetate	162883057	Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)O)OC(=O)C)O)OC6=CC=NC=C6)C	742.70	unknown	https://doi.org/10.1021/NP0203988
[(1R,3R,13R,14R,17S,18R,19R,20R,21R,22R,23S,24S,25S)-22,24-diacetyloxy-20-(acetyloxymethyl)-19,21,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-18-yl] 1-methyl-6-oxopyridine-3-carboxylate	162935876	Click to see	814.80	unknown	https://doi.org/10.1021/NP0203988
[(1R,3R,13R,14S,17R,18R,19R,20S,21S,22S,23S,24R,25S)-18,20,21,22,24-pentaacetyloxy-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-19-yl] benzoate	162953251	Click to see	853.80	unknown	https://doi.org/10.1021/NP0203988
[(1R,3R,13R,14S,17R,18S,19R,20S,21S,22S,23S,24R,25S)-20,24-diacetyloxy-19,21,25-trihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-18-pyridin-4-yloxy-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-22-yl] acetate	162883058	Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)O)OC(=O)C)O)OC6=CC=NC=C6)C	742.70	unknown	https://doi.org/10.1021/NP0203988
[(1R,3S,13R,14S,17R,18S,19S,20S,21R,22S,23S,24S,25R)-18,21,22,24-tetraacetyloxy-20-(acetyloxymethyl)-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-19-yl] benzoate	133562434	Click to see	867.80	unknown	https://doi.org/10.1021/NP0203988
[(1S,3R,13S,14S,17S,18S,19R,20S,21S,22S,23R,24S,25R)-21,22-diacetyloxy-20-(acetyloxymethyl)-19-benzoyloxy-18,25-dihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-24-yl] benzoate	162892973	Click to see	887.90	unknown	https://doi.org/10.1021/NP0203988
[(1S,3R,14S,17S,18R,19R,20R,21S,22R,24R,25S)-18,21,22-triacetyloxy-20-(acetyloxymethyl)-19-benzoyloxy-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-24-yl] benzoate	131675970	Click to see	929.90	unknown	https://doi.org/10.1021/NP0203988
[(1S,3S,13S,14R,17S,18S,19S,20R,21S,22R,24R,25S)-21,22-diacetyloxy-20-(acetyloxymethyl)-19-benzoyloxy-18,25-dihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-24-yl] benzoate	102056156	Click to see	887.90	unknown	https://doi.org/10.1021/NP0203988
[(1S,3S,13S,14S,17S,18S,19S,20R,21S,22R,23R,24R,25R)-20,21,22-triacetyloxy-19-benzoyloxy-18,25-dihydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-24-yl] benzoate	163047535	Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C6=CC=CC=C6)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C7=CC=CC=C7)O)C	873.80	unknown	https://doi.org/10.1021/NP0203988
[(1S,3S,13S,14S,17S,18S,19S,20S,21S,22R,23R,24R,25R)-18,20,21,22-tetraacetyloxy-19-benzoyloxy-25-hydroxy-3,13,14,25-tetramethyl-6,15-dioxo-2,5,16-trioxa-11-azapentacyclo[15.7.1.01,20.03,23.07,12]pentacosa-7(12),8,10-trien-24-yl] benzoate	162843062	Click to see	915.90	unknown	https://doi.org/10.1021/NP0203988
Emarginatine E	10033345	Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)O)COC(=O)C)O)OC(=O)C6=CN(C(=O)C=C6)C)C	814.80	unknown	via CMAUP database
Euojaponine C	44566781	Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C6=CC=CC=C6)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C7=CC=CC=C7)O)C	887.90	unknown	via CMAUP database
Mayteine	3086511	Click to see CC1C(C(=O)OC2C(C(C3(C(C(C4C(C3(C2(C)O)OC4(COC(=O)C5=C1N=CC=C5)C)OC(=O)C)OC(=O)C)OC(=O)C)COC(=O)C)OC(=O)C6=CC=CC=C6)OC(=O)C)C	867.80	unknown	https://doi.org/10.1021/NP0203988
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben	7456	Click to see	152.15	unknown	via CMAUP database
> Lignans, neolignans and related compounds
(1R,2S)-1-(3-Methoxy-4-hydroxyphenyl)-2-[2-methoxy-4-[(E)-3-hydroxy-1-propenyl]phenoxy]-1,3-propanediol	14274760	Click to see COC1=C(C=CC(=C1)C=CCO)OC(CO)C(C2=CC(=C(C=C2)O)OC)O	376.40	unknown	via CMAUP database
erythro-Guaiacylglycerol beta-dihydroconiferyl ether	13893597	Click to see	378.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid	10467	Click to see	312.50	unknown	via CMAUP database
Stearic Acid	5281	Click to see	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid	2266	Click to see C(CCCC(=O)O)CCCC(=O)O	188.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Tocopherol quinone	2734086	Click to see	446.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(2R,4aR,6aS,6aR,6bS,8aS,9R,12aS,14aS,14bS)-2-hydroxy-2,6a,6a,8a,9,14a-hexamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid	44566791	Click to see	458.70	unknown	https://doi.org/10.1021/NP0203988
(4R,4aS,6aS,6aS,6bR,8aR,11R,12aS,14aS,14bS)-8a,11-dihydroxy-4,4a,6a,6b,11,14a-hexamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	44566785	Click to see	430.70	unknown	https://doi.org/10.1021/NP0203988
2-hydroxy-2,6a,6a,8a,9,14a-hexamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-4a-carboxylic acid	75072169	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)O)C(=O)O)C)C)C)C	458.70	unknown	https://doi.org/10.1021/NP0203988
8a,11-dihydroxy-4,4a,6a,6b,11,14a-hexamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	75072167	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)O)O)C)C)C)C	430.70	unknown	https://doi.org/10.1021/NP0203988
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S)-4alpha-Ethenyl-2alpha-hydroxy-3beta-[1-(hydroxymethyl)ethenyl]-6alpha-[[2-(hydroxymethyl)-1-oxo-2-propenyl]oxy	13891365	Click to see CC1(CC(C(C(C1C(=C)CO)O)C(=C)C(=O)OC)OC(=O)C(=C)CO)C=C	380.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Sesterstatin 5	10362737	Click to see	386.60	unknown	https://doi.org/10.1021/NP0203988
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones
Hemistepsin	10043230	Click to see	346.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
5,8a,9',13'-Tetramethyl-4'-methylidenespiro[3a,4,9,9a-tetrahydrobenzo[f][1]benzofuran-3,15'-6-oxatetracyclo[9.2.2.01,9.03,7]pentadec-12-ene]-2,5',6,10'-tetrone	14021299	Click to see	488.60	unknown	https://doi.org/10.1021/NP0203988
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aS,4S,5E,9Z,11aR)-6-formyl-10-methyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate	53494931	Click to see	346.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3S,3aR,4S,6aR,8S,9aR,9bR)-4,8-dihydroxy-3-methyl-6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one	12047617	Click to see	264.32	unknown	via CMAUP database
[(3S,3aR,4S,6aR,8S,9aR,9bR)-8-hydroxy-3-methyl-6,9-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate	71503391	Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)OC(=O)C(=C)CO	348.40	unknown	via CMAUP database
Cynaropicrin	119093	Click to see	346.40	unknown	via CMAUP database
Desacylcynaropicrin	13943205	Click to see	262.30	unknown	via CMAUP database
Isolipidiol	14589530	Click to see CC1C(CC2C1C3C(C(C(=O)O3)C)C(CC2=C)O)O	266.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,4,5,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicene-3,6-dione	14466933	Click to see	440.70	unknown	https://doi.org/10.1021/NP0203988
10-methoxy-2,2,4a,6a,6b,9,9,12a-octamethyl-4,5,6,6a,7,8,8a,10,11,12,14,14a-dodecahydro-3H-picen-13-one	73814464	Click to see CC1(CCC2(CCC3(C(C2=C1)CC(=O)C4C3(CCC5C4(CCC(C5(C)C)OC)C)C)C)C)C	454.70	unknown	https://doi.org/10.1021/NP0203988
11-Hydroxy-2,5,6,10,10,14,21-heptamethyl-22-oxahexacyclo[19.5.1.02,19.05,18.06,15.09,14]heptacos-17-en-23-one	162980987	Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC6(CC5CCCC(=O)O6)C)C)C)C)C	496.80	unknown	https://doi.org/10.1021/NP0203988
3,22-Dihydroxyolean-12-en-29-oic acid	5257562	Click to see	472.70	unknown	https://doi.org/10.1021/NP0203988
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,4a,5,6,7,8,9,10,12,12a,14a-dodecahydropicene-3,14-dione	14287355	Click to see	438.70	unknown	https://doi.org/10.1021/NP0203988
7-Oxofriedelin	21596176	Click to see	440.70	unknown	https://doi.org/10.1021/NP0203988
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	via CMAUP database
Betulonic acid	122844	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O	454.70	unknown	via CMAUP database
D:A-Friedooleanane-3,7-dione	634915	Click to see	440.70	unknown	https://doi.org/10.1021/NP0203988
Laxifolone A	21629610	Click to see CC1(CCC2(CCC3(C(C2=C1)CC(=O)C4C3(CCC5C4(CCC(C5(C)C)OC)C)C)C)C)C	454.70	unknown	https://doi.org/10.1021/NP0203988
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
Maytenfolic Acid	21594203	Click to see	472.70	unknown	https://doi.org/10.1021/NP0203988
Olean-12-ene-3,11-dione	14287354	Click to see	438.70	unknown	https://doi.org/10.1021/NP0203988
Oleanolic Acid	10494	Click to see	456.70	unknown	via CMAUP database
Taraxasterol	115250	Click to see	426.70	unknown	via CMAUP database
Taraxasterol Acetate	13889352	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C	468.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde	8768	Click to see	138.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
Indole-3-carboxylic acid	69867	Click to see C1=CC=C2C(=C1)C(=CN2)C(=O)O	161.16	unknown	via CMAUP database
Methyl indole-3-carboxylate	589098	Click to see	175.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3,4-Dihydroxycinnamic acid methyl ester	92202	Click to see	194.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	Click to see	610.50	unknown	via CMAUP database

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Euonymus laxiflorus

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