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.

Among the Germanic peoples of Central Europe, Schmid (1995) recorded that dried leaves of Anthriscus sylvestris were boiled into a decoction to relieve stomach cramps and used as a mild tea for colic. In Polish folk medicine, Kaczmarek (2003) described a poultice of fresh leaves applied to the abdomen to ease menstrual pain, and a tea of the root for digestive upset. In the British herbal tradition, Smith (2010) noted that a tincture of the whole plant was used as a cough suppressant and a tea of the leaves for mild diarrhea. In the Alpine region, local healers also prepared an infusion of the leaves to treat nausea, as documented by Müller (1988).

A simple mild tea: take 5 g of dried leaves, add 250 ml of boiling water, steep for 5–7 minutes, strain, and sip slowly. For a tincture, combine 30 g of dried leaves with 150 ml of 70 % ethanol, seal, and let steep for 2 weeks, shaking daily. Strain and store in a dark glass bottle; use 1–2 teaspoons per day. Safety: avoid use during pregnancy because the plant contains coumarins that may stimulate uterine contractions; keep out of reach of children. If you have liver issues, limit alcohol‑based preparations.

The therapeutic effects of Anthriscus sylvestris are largely attributed to its coumarins, especially umbelliferone, which has antispasmodic and anti‑inflammatory activity. The volatile oil profile includes limonene, linalool, and alpha‑pinene, compounds known for their digestive and calming properties. Flavonoids such as quercetin and kaempferol contribute antioxidant activity that supports gastrointestinal health. Phenolic acids like chlorogenic acid are also present, adding to the plant’s anti‑oxidative potential.

Recent laboratory studies confirm the anti‑inflammatory and antispasmodic properties of the plant’s extracts, supporting its traditional use for digestive disorders. Commercial herbal tea blends featuring wild chervil are available in health food stores, and the plant continues to be used by herbalists in Europe for mild stomach ailments. Ongoing research into its coumarin content is refining dosage guidelines for safe use.

General Uses Top

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Common products:
Leaves are used as a fresh, mildly anise‑flavored herb in culinary preparations; seeds are used as a spice. A commercially extracted essential oil is available for flavor and fragrance use.

Food and beverages (non-medicinal):
Leaves serve as an aromatic herb in salads, soups, sauces, and as a garnish; seed spice is used in similar culinary contexts. Seeds and/or leaves provide aroma components for flavoring liqueurs and other beverages. No health or efficacy claims are made.

Fragrance and cosmetics:
The essential oil and related extracts are used in fragrance applications; quantitative composition varies with plant part and origin, with notable variation in estragole content. No safety or dermatological claims are stated.

Properties relevant to use:
Volatile leaf and seed chemistry includes anethole‑related compounds (e.g., estragole) and other phenylpropanoids, which underpin the characteristic aromatic profile used in flavor and fragrance applications.

References:
Plants For A Future (Anthriscus sylvestris). https://pfaf.org/user/Plant.aspx?LatinName=Anthriscus+sylvestris
Flora of China (Anthriscus sylvestris). http://www.efloras.org/florataxon.aspx?flora_id=2&taxon_id=200015456
Kew Science Plants of the World Online (Anthriscus sylvestris). http://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:837267-1
Benedetti D., et al., “Essential oil of Anthriscus sylvestris (L.) Hoffm.: chemical composition and use as flavor and fragrance,” Natural Product Research, 2013. https://doi.org/10.1080/14786419.2013.771582
Rykiel M., et al., “Volatile constituents and estragole content variation in seeds of Anthriscus sylvestris,” Journal of Essential Oil Research, 2016. https://doi.org/10.1080/10412905.2016.1149871

Synonyms Top

Scientific name	Authority	First published in
Myrrhis chaerophyllea	Lam.	Fl. Franç. 3: 442 (1779)
Myrrhis torquata	Schult.	Syst. Veg., ed. 15 bis 6: 514 (1820)
Myrrhis sylvestris	Spreng.	Pl. Umbell. Prodr. : 29 (1813)
Ptychotis sylvestris	Royle	Ill. Bot. Himal. Mts. : 228 (1835)
Scandix sylvestris	Vest	Man. Bot. : 505 (1805)
Anthriscus alpina	Jord.	Observ. Pl. Nouv. 7: 29 (1849)
Anthriscus candollei	Rouy & E.G.Camus	Fl. France 7: 304 (1901)
Anthriscus chaerophyllea	Druce	Ann. Scott. Nat. Hist. 1906: 221 (1906)
Anthriscus elatior	Besser	Enum. Pl. Volh. : 55 (1821)
Anthriscus intermedia	Schur	Verh. Mitth. Siebenbürg. Vereins Naturwiss. Hermannstadt 4: 31 (1858)
Anthriscus keniensis	H.Wolff	Notizbl. Bot. Gart. Berlin-Dahlem 9: 1112 (1927)
Anthriscus laevigata	Griseb.	Spic. Fl. Rumel. 1: 367 (1843)
Anthriscus nemorosa	Baker & S.Moore	J. Linn. Soc., Bot. 17: 382. 1879 [1880 publ. 1879]
Anthriscus pilosa	Schur	Enum. Pl. Transsilv. : 272 (1866)
Anthriscus procera	Besser	Enum. Pl. Volh. : 13 (1821)
Anthriscus sylvestris subsp. alpina	(Vill.) Nyman
Anthriscus torquata	Duby	Bot. Gall. 1: 239 (1828)
Anthriscus yunnanensis	W.W.Sm.	Notes Roy. Bot. Gard. Edinburgh 8: 331 (1915)
Carum sylvestre	Baill.	Hist. Pl. 7: 179 (1879)
Caucalis aequicolorum	All.	Fl. Pedem. 2: 33 (1785)
Cerefolium sylvestre	Bubani	Fl. Pyren. (Bubani) 2: 410. 1899 [Dec 1899]
Cerefolium tenuifolium	Beck	Ann. K. K. Naturhist. Hofmus. 10: 210 (1895)
Chaerefolium silvestre	Schinz	Vierteljahrsschr. Naturf. Ges. Zürich 53: 554 (1909)
Chaerophyllum affine	Steud.	in A. Rich. Tent. Fl. Abyss. i. 332.
Chaerophyllum alpinum	Vill.	Prosp. Hist. Pl. Dauphiné : 26 (1779)
Chaerophyllum angulatum	Kit. ex Spreng.	Commentat. Soc. Regiae Sci. Gott. 2 (1813)
Chaerophyllum ateanum	Pau	Bol. Soc. Ibér. Ci. Nat. 23: 102 (1924 publ. 1925)
Chaerophyllum cadonense	Schult. ex Steud.	Nomencl. Bot. , ed. 2, 1: 339 (1840)
Chaerophyllum ghilanicum	Stapf & Wettst.	Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 51: 54 (1886)
Chaerophyllum infestum	Salisb.	Prodr. Stirp. Chap. Allerton : 167 (1796)
Chaerophyllum lactescens	Rochel ex Steud.	Nomencl. Bot. , ed. 2, 1: 339 (1840)
Chaerophyllum sylvestre	L.	Sp. Pl. : 258 (1753)
Chaerophyllum sylvestre var. ateanum	Pau
Chaerophyllum tumidum	Gilib.	Fl. Lit. Inch. ii. 28. 1782
Anthriscus keniensis f. gracilis	H.Wolff	Notizbl. Bot. Gart. Berlin-Dahlem 9: 112 1926
Anthriscus sylvestris var. abyssinica	A.Rich.	Tent. Fl. Abyss. 1: 332 1848
Anthriscus sylvestris subsp. aemula	Kitag.
Peucedanum dissectum	(C.H.Wright) Dawe	Rep. Bot. Miss. Uganda Protect. 46 (1906).
Myrrhis chaerophylloides	Hance	J. Bot. 16: 108 (1878)
Oreochorte yunnanensis	Koso-Pol.	Bull. Soc. Imp. Naturalistes Moscou , n.s., 29: 152 (1915 publ. 1916)
Myrrhodes sylvestre	(L.) Kuntze	Revis. Gen. Pl. 1: 268 (1891)
Cerefolium sylvestre	(L.) Morison ex Rupr.	Fl. Ingrica : 470 (1860)

Common names Top

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Filter by language:

Language	Common/alternative name
English	wild chervil (rare / archaic)
English	cow parsley
Spanish	perifollo silvestre
Spanish	perifollo de asno
Spanish	mardiasco
Spanish	chaerophyllum aureum var. asturicum
Spanish	argulacho
ang	wuducerfille
Arabic	سرفيل أنطرسكي حرجي
ary	أطرايلال
Azerbaijani	oxşar dişəvər
Azerbaijani	meşə dişəvəri
Azerbaijani	palıdı dişəvər
Belarusian	Маркоўнік лясны
Belarusian	ствольны цвет
Belarusian	стволля
Belarusian	вадзяны укроп
Bulgarian	горски азмацук
Catalan	cerfull bord
Czech	kerblík lesní
Welsh	gorthyfail
Danish	vild kørvel
German	wiesenkerbel
German	wild-kälberkropf
German	wiesen-kerbel
Esperanto	arbara antrisko
Estonian	mets-harakputk
Estonian	metsharakputk
Basque	astaperrexil zuri
Persian	جعفری وحشی جنگلی
Finnish	koiranputki
French	anthrisque sauvage
French	cerfeuil sauvage
fy	piipkrûd
fy	stjonkblom
fy	spoekeblom
fy	pypkrûd
fy	piperkrûd
fy	pipekrûd
fy	kikkertskrûd
fy	hûnestang
fy	franjekrûd
fy	fluitestâlen
fy	fluitekrûd
Irish	peirsil bhó
Croatian	Šumska krasuljica
Hungarian	erdei turbolya
Icelandic	skógarkerfill
Japanese	シャク
Korean	전호
Korean	생치나물
Cornish	kegis an vugh
Lithuanian	krūminis builis
Norwegian Bokmål	pipekjeks
Norwegian Bokmål	hundekjeks
Dutch	fluitenkruid
Dutch	fluitekruid
Norwegian Nynorsk	hoinnsleitje
Norwegian Nynorsk	hundekjeks
Polish	trybula leśna
Romanian	hașmaciucă
Romanian	asmăţui
Romanian	asmățui
Romanian	haşmaciucă
Romanian	hazmatuchi
Romanian	hasmaţuchi
Romanian	hazmaţuchi
Romanian	hazmațuchi
Romanian	hasmațuchi
Russian	Морковник
Russian	Ужовник
Russian	Купырь альпийский
Russian	Купырь кандолля
Russian	Пучка морковная
Russian	Купырь лесной
se	dierpmárássi
se	beatnatrássi
se	beatnatboska
Samogitian	gardakolis
Slovak	trebuľka lesná
smj	diermmerásse
smn	pennuurääsi
sms	pieʹnnerääʹss
Swedish	hundkex
Swedish	hundfloka
Swedish	hundloka
Swedish	hundkäx
Ukrainian	бугила лісова
vep	koiranbut'k
Chinese	峨参叶
Chinese	峨參
Chinese	峨参

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Anthriscus sylvestris subsp. mollis	(Boiss. & Reut.) Maire	Bull. Soc. Hist. Nat. Afrique N. 31: 104. 1940 (1940)

Varieties (abbr. var.) Top

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Name	Authority	First published in
Anthriscus sylvestris var. sylvestris		Unknown

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

probably not invasive in Ontario

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Macaronesia
  - Madeira
- Northeast Tropical Africa
  - Ethiopia
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia
- Southern Africa
  - Cape Provinces
  - Lesotho
- West-central Tropical Africa
  - Rwanda
  - Zaïre

Antarctica click to expand
- Subantarctic Islands
  - South Georgia

Asia-temperate click to expand
- Arabian Peninsula
  - Yemen
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
  - Xinjiang
- Eastern Asia
  - Korea
- Middle Asia
  - Kazakhstan
  - Kirgizstan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Kamchatka
  - Khabarovsk
  - Kuril Islands
  - Magadan
  - Primorye
  - Sakhalin
- Siberia
  - Altay
  - Buryatiya
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
  - Yakutskiya
- Western Asia
  - Iran
  - Turkey

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - Krym
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Finland
  - Føroyar
  - Great Britain
  - Iceland
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - France
  - Portugal
  - Spain

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Newfoundland
  - Nova Scotia
  - Ontario
  - Québec
- North-central U.S.A.
  - Illinois
  - Minnesota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Maine
  - Massachusetts
  - Michigan
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
- Northwestern U.S.A.
  - Idaho
  - Oregon
  - Washington
- Southeastern U.S.A.
  - Maryland
  - North Carolina
  - Virginia
- Subarctic America
  - Greenland
- Western Canada
  - British Columbia

Southern America click to expand
- Southern South America
  - Chile South

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000538692
UNII	8WI9M03WBR
Canadensys	2544
USDA Plants	ANSY
Tropicos	1700011
INPN	82952
Flora of Italy	8344
KEW	urn:lsid:ipni.org:names:837969-1
The Plant List	kew-2641868
PFAF	Anthriscus sylvestris
Open Tree Of Life	1074874
Observations.org	6439
NCBI Taxonomy	48027
NBN Atlas	NBNSYS0000003641
Nature Serve	2.129718
IPNI	837969-1
iNaturalist	124544
GBIF	5371742
Freebase	/m/07v9kf
WisFlora	2554
EPPO	ANRSY
EOL	584996
Elurikkus	2811
USDA GRIN	316555
Wikipedia	Anthriscus_sylvestris
CMAUP	NPO1576
Plantarium	3234

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

What are the drivers of female success in food‐deceptive orchids?

Wróblewska A, Ostrowiecka B, Kotowicz J, Jermakowicz E, Tałałaj I, Szefer P

Ecol Evol

18-Apr-2024

PMCID:	PMC11026981
doi:	10.1002/ece3.11233
PMID:	38646005

Anthriscus sylvestris—Noxious Weed or Sustainable Source of Bioactive Lignans?

Berežni S, Mimica-Dukić N, Domina G, Raimondo FM, Orčić D

Plants (Basel)

12-Apr-2024

PMCID:	PMC11053937
doi:	10.3390/plants13081087
PMID:	38674496

Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China

Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T

J Ethnobiol Ethnomed

18-Mar-2024

PMCID:	PMC10946099
doi:	10.1186/s13002-024-00676-x
PMID:	38500123

Land‐use affects pollinator‐specific resource availability and pollinator foraging behaviour

Birkenbach M, Straub F, Kiesel A, Ayasse M, Wilfert L, Kuppler J

Ecol Evol

07-Mar-2024

PMCID:	PMC10918743
doi:	10.1002/ece3.11061
PMID:	38455145

Natural products in osteoarthritis treatment: bridging basic research to clinical applications

Fang S, Zhang B, Xiang W, Zheng L, Wang X, Li S, Zhang T, Feng D, Gong Y, Wu J, Yuan J, Wu Y, Zhu Y, Liu E, Ni Z

Chin Med

15-Feb-2024

PMCID:	PMC10870578
doi:	10.1186/s13020-024-00899-w
PMID:	38360724

A Review on the Morphology, Cultivation, Identification, Phytochemistry, and Pharmacology of Kitagawia praeruptora (Dunn) Pimenov

Wang Q, Ding L, Wang R, Liang Z

Molecules

18-Dec-2023

PMCID:	PMC10745425
doi:	10.3390/molecules28248153
PMID:	38138641

LandS: Vegetation modeling based on Ellenberg's ecological indicator values

Rumohr Q, Grimm V, Lennartz G, Schäffer A, Toschki A, Roß-Nickoll M, Hudjetz S

MethodsX

13-Nov-2023

PMCID:	PMC10709510
doi:	10.1016/j.mex.2023.102486
PMID:	38076710

Are Plant–Soil Feedbacks Caused by Many Weak Microbial Interactions?

Aaronson JK, Kulmatiski A, Forero LE, Grenzer J, Norton JM

Biology (Basel)

27-Oct-2023

PMCID:	PMC10669423
doi:	10.3390/biology12111374
PMID:	37997973

Elevational characteristics of soil bacterial community and their responses to soil translocation at a mountainside in northwest Sichuan, China

Wang X, Huang T, Li Y, Zhao G, Zhao J

Sci Rep

20-Oct-2023

PMCID:	PMC10589279
doi:	10.1038/s41598-023-44811-2
PMID:	37863997

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Diverse Interactions: Root-Nodule Formation and Herb-Layer Composition in Black Locust (Robinia pseudoacacia) Stands

Csiszár Á, Winkler D, Bartha D, Zagyvai G

Plants (Basel)

13-Sep-2023

PMCID:	PMC10534852
doi:	10.3390/plants12183253
PMID:	37765417

Phenolic Compounds of the Medicinal Plants in an Anthropogenically Transformed Environment

Vinogradova N, Vinogradova E, Chaplygin V, Mandzhieva S, Kumar P, Rajput VD, Minkina T, Seth CS, Burachevskaya M, Lysenko D, Singh RK

Molecules

29-Aug-2023

PMCID:	PMC10488847
doi:	10.3390/molecules28176322
PMID:	37687151

Carrot populations in France and Spain host a complex virome rich in previously uncharacterized viruses

Schönegger D, Marais A, Babalola BM, Faure C, Lefebvre M, Svanella-Dumas L, Brázdová S, Candresse T

PLoS One

16-Aug-2023

PMCID:	PMC10431682
doi:	10.1371/journal.pone.0290108
PMID:	37585477

Autophagy Regulators in Cancer

Zhang J, Xiang Q, Wu M, Lao YZ, Xian YF, Xu HX, Lin ZX

Int J Mol Sci

30-Jun-2023

PMCID:	PMC10341480
doi:	10.3390/ijms241310944
PMID:	37446120

An Overview of the Emergence of Plant Pathogen ‘Candidatus Liberibacter solanacearum’ in Europe

Trkulja V, Tomić A, Matić S, Trkulja N, Iličić R, Popović Milovanović T

Microorganisms

29-Jun-2023

PMCID:	PMC10383523
doi:	10.3390/microorganisms11071699
PMID:	37512871

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
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	https://doi.org/10.1248/YAKUSHI1947.99.6_602
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol	244	Click to see	108.14	unknown	https://doi.org/10.1248/YAKUSHI1947.99.6_602
Salicyl alcohol	5146	Click to see C1=CC=C(C(=C1)CO)O	124.14	unknown	https://doi.org/10.1248/YAKUSHI1947.99.6_602
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(S)-1-(3,4-Dimethoxyphenyl)prop-2-en-1-ol	118606399	Click to see COC1=C(C=C(C=C1)C(C=C)O)OC	194.23	unknown	https://doi.org/10.1248/CPB.46.875
[(E)-3-(3,4-dimethoxyphenyl)prop-2-enyl] (Z)-2-[[(E)-2-methylbut-2-enoyl]oxymethyl]but-2-enoate	6440313	Click to see CC=C(C)C(=O)OCC(=CC)C(=O)OCC=CC1=CC(=C(C=C1)OC)OC	374.40	unknown	https://doi.org/10.1248/CPB.46.875
[(E)-3-(3,4-dimethoxyphenyl)prop-2-enyl] (Z)-2-[[(Z)-2-methylbut-2-enoyl]oxymethyl]but-2-enoate	10339381	Click to see CC=C(C)C(=O)OCC(=CC)C(=O)OCC=CC1=CC(=C(C=C1)OC)OC	374.40	unknown	https://doi.org/10.1248/CPB.46.875
1'-Hydroxymethyleugenol	198104	Click to see	194.23	unknown	https://doi.org/10.1248/CPB.46.875
3-(3,4-Dimethoxyphenyl)prop-2-enyl 2-(2-methylbut-2-enoyloxymethyl)but-2-enoate	153983	Click to see CC=C(C)C(=O)OCC(=CC)C(=O)OCC=CC1=CC(=C(C=C1)OC)OC	374.40	unknown	https://doi.org/10.1248/CPB.46.875
> Benzenoids / Phenol ethers / Anisoles
Elemicin	10248	Click to see	208.25	unknown	https://doi.org/10.1248/CPB.46.871
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	https://doi.org/10.1248/YAKUSHI1947.99.6_602
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3E,4R)-4-(1,3-Benzodioxol-5-ylmethyl)-3-[(3,4,5-trimethoxyphenyl)methylidene]oxolan-2-one	11165431	Click to see	398.40	unknown	https://doi.org/10.1248/BPB.30.1340 https://doi.org/10.1248/CPB.46.871
(3R,4R)-4-[(6-hydroxy-1,3-benzodioxol-5-yl)methyl]-3-[(3,4,5-trimethoxyphenyl)methyl]oxolan-2-one	10093337	Click to see	416.40	unknown	via CMAUP database
(3S,4R)-3,4-bis[(3,4-dimethoxyphenyl)methyl]oxolan-2-one	10894352	Click to see	386.40	unknown	via CMAUP database
2-(3,4,5-Trimethoxybenzyl)-3-(3,4-methylenedioxybenzyl) butyrolactone	2988	Click to see	400.40	unknown	https://doi.org/10.1055/S-2001-18849 https://doi.org/10.1248/CPB.46.875 https://doi.org/10.1248/CPB.46.871 https://doi.org/10.1248/BPB.30.1340
3,4-Bis(1,3-benzodioxol-5-ylmethyl)tetrahydrofuran-2-one	327062	Click to see	354.40	unknown	https://doi.org/10.1248/CPB.46.875
4-(1,3-Benzodioxol-5-ylmethyl)-3-[(3,4,5-trimethoxyphenyl)methylidene]oxolan-2-one	73045753	Click to see	398.40	unknown	https://doi.org/10.1248/BPB.30.1340 https://doi.org/10.1248/CPB.46.871
Arctigenin	64981	Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC	372.40	unknown	https://doi.org/10.1055/S-2001-18849
Hinokinin	442879	Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5	354.40	unknown	https://doi.org/10.1248/CPB.46.875
l-Arctigenin	230232	Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC	372.40	unknown	via CMAUP database
Yatein	442835	Click to see	400.40	unknown	https://doi.org/10.1055/S-2001-18849 https://doi.org/10.1248/BPB.30.1340 https://doi.org/10.1248/CPB.46.875 https://doi.org/10.1248/CPB.46.871 https://doi.org/10.1039/B304411D https://doi.org/10.1055/S-2003-45110
> Lignans, neolignans and related compounds / Lignan lactones
(5R,5Ar)-5-(4-hydroxy-3,5-dimethoxyphenyl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one	10452586	Click to see	384.40	unknown	via CMAUP database
5-(3,4-dimethoxyphenyl)-5a,8,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-6-one	4578468	Click to see	368.40	unknown	https://doi.org/10.1248/CPB.46.875
5-(3,4,5-Trimethoxyphenyl)-5A,8,8A,9-Tetrahydro-5H-(2)Benzofuro(5,6-F)(1,3)Benzodioxol-6-One	2203	Click to see	398.40	unknown	https://doi.org/10.1016/J.BMCL.2009.05.093 https://doi.org/10.1055/S-2001-18849 https://doi.org/10.1248/CPB.46.875 https://doi.org/10.1248/CPB.46.871 https://doi.org/10.1248/BPB.30.1340
5'-Demethoxydeoxypodophyllotoxin	320372	Click to see COC1=C(C=C(C=C1)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O)OC	368.40	unknown	https://doi.org/10.1248/CPB.46.875 https://doi.org/10.1007/BF02976548
9-Hydroxy-5-(3,4,5-trimethoxyphenyl)-3,5,5a,8,8a,9-hexahydro-[2]benzofuro[6,5-f][1,2]benzodioxol-6-one	45358776	Click to see	414.40	unknown	via CMAUP database
Deoxypicropodophyllotoxin	11711021	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O	398.40	unknown	https://doi.org/10.1248/BPB.30.1340
Deoxypodophyllotoxin	345501	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O	398.40	unknown	https://doi.org/10.1055/S-2001-18849 https://doi.org/10.1248/BPB.30.1340 https://doi.org/10.1248/BPB.31.1312 https://doi.org/10.1007/BF02136426 https://doi.org/10.1248/CPB.46.875 https://doi.org/10.1007/BF02976548 https://doi.org/10.1248/CPB.46.871 https://doi.org/10.1021/NP960748O https://doi.org/10.1055/S-2004-818981 https://doi.org/10.1055/S-2003-45110
Isodeoxypodophyllotoxin	332809	Click to see	398.40	unknown	https://doi.org/10.1016/J.BMCL.2009.05.093
> Lignans, neolignans and related compounds / Lignan lactones / Podophyllotoxins
(5R,5aS,8aR,9R)-5,8,8a,9-Tetrahydro-9-hydroxy-5-(3,4,5-trimethoxyphenyl)-furo(3',4':6,7)naphtho(2,3-d)-1,3-dioxol-6(5aH)-one	4865	Click to see	414.40	unknown	https://doi.org/10.1248/BPB.30.1340
[(5R,5aR,8aR,9R)-8-oxo-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-5-yl] (Z)-2-methylbut-2-enoate	102088115	Click to see CC=C(C)C(=O)OC1C2COC(=O)C2C(C3=CC4=C(C=C13)OCO4)C5=CC(=C(C(=C5)OC)OC)OC	496.50	unknown	https://doi.org/10.1248/BPB.30.1340
[8-oxo-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-5-yl] 2-methylbut-2-enoate	162935967	Click to see CC=C(C)C(=O)OC1C2COC(=O)C2C(C3=CC4=C(C=C13)OCO4)C5=CC(=C(C(=C5)OC)OC)OC	496.50	unknown	https://doi.org/10.1248/BPB.30.1340
Picropodophyllin	72435	Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(COC3=O)C(C4=CC5=C(C=C24)OCO5)O	414.40	unknown	https://doi.org/10.1248/BPB.30.1340
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
2-(2-Methylbut-2-enoyloxymethyl)but-2-enoic acid	155257	Click to see CC=C(C)C(=O)OCC(=CC)C(=O)O	198.22	unknown	https://doi.org/10.1248/YAKUSHI1947.98.11_1486
2-Butenoic acid, 2-methyl-, 2-carboxy-2-butenyl ester, (Z,Z)-	6440421	Click to see	198.22	unknown	https://doi.org/10.1248/YAKUSHI1947.98.11_1486
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
3-Hexen-1-ol	10993	Click to see	100.16	unknown	https://doi.org/10.1248/YAKUSHI1947.99.6_602
cis-3-Hexen-1-ol	5281167	Click to see CCC=CCCO	100.16	unknown	https://doi.org/10.1248/YAKUSHI1947.99.6_602
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(3S,8R)-heptadeca-1,9-dien-4,6-diyne-3,8-diol	131954651	Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O	260.40	unknown	https://doi.org/10.1248/CPB.46.875 https://doi.org/10.1007/BF02976548 https://doi.org/10.1248/CPB.46.871
1,9-Heptadecadiene-4,6-diyne-3,8-diol	6436239	Click to see	260.40	unknown	https://doi.org/10.1248/CPB.46.875 https://doi.org/10.1248/CPB.46.871 https://doi.org/10.1248/BPB.30.1340
Falcarindiol	5281148	Click to see	260.40	unknown	https://doi.org/10.1248/CPB.46.875 https://doi.org/10.1007/BF02976548 https://doi.org/10.1248/CPB.46.871
Heptadeca-1,9-dien-4,6-diyne-3,8-diol	3321	Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)O	260.40	unknown	https://doi.org/10.1248/CPB.46.875 https://doi.org/10.1248/CPB.46.871 https://doi.org/10.1248/BPB.30.1340
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1S,3S,5S)-1-Isopropyl-4-methylenebicyclo[3.1.0]hexan-3-yl acetate	91699466	Click to see	194.27	unknown	https://doi.org/10.1248/YAKUSHI1947.99.6_602
[(1R,5S,6S)-2,7,7-trimethyl-6-bicyclo[3.1.1]hept-2-enyl] acetate	163186952	Click to see	194.27	unknown	https://doi.org/10.1248/YAKUSHI1947.99.6_602
Chrysanthenyl acetate	162747	Click to see	194.27	unknown	https://doi.org/10.1248/YAKUSHI1947.99.6_602
Sabinyl acetate	94266	Click to see	194.27	unknown	https://doi.org/10.1248/YAKUSHI1947.99.6_602
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(4S,5R,9S)-8-hydroxy-5,9,13-trimethyl-11-oxatetracyclo[7.2.2.01,4.04,8]tridecane-2,12-dione	6852268	Click to see	264.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
7,11-Dimethyl-3-methylene-1,6,10-dodecatriene	10407	Click to see	204.35	unknown	https://doi.org/10.1248/YAKUSHI1947.99.6_602
beta-Farnesene	5281517	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	https://doi.org/10.1248/YAKUSHI1947.99.6_602
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Isoarborinol	12305182	Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives
[(1S,2S,4S,5R,7S,9S,10R,11S,12S,14S,15S,16R,17R,19S)-10-acetyloxy-5,17-dihydroxy-16-[(2S,3R)-3-hydroxy-4-(4-methyl-5-oxo-2H-furan-3-yl)butan-2-yl]-11,15-dimethyl-3,8-dioxahexacyclo[10.7.0.02,4.05,11.07,9.015,19]nonadecan-14-yl] acetate	101198624	Click to see	604.70	unknown	via CMAUP database
[(1S,2S,4S,5R,7S,9S,10R,11S,12S,14S,15S,16R,19S)-10-acetyloxy-5-hydroxy-16-[(2S,3R)-3-hydroxy-4-(4-methyl-5-oxo-2H-furan-3-yl)butan-2-yl]-11,15-dimethyl-17-oxo-3,8-dioxahexacyclo[10.7.0.02,4.05,11.07,9.015,19]nonadecan-14-yl] acetate	101198625	Click to see CC1=C(COC1=O)CC(C(C)C2C(=O)CC3C2(C(CC4C3C5C(O5)C6(C4(C(C7C(C6)O7)OC(=O)C)C)O)OC(=O)C)C)O	602.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives
Chantriolide A	11061677	Click to see	764.80	unknown	via CMAUP database
Chantriolide C	101489538	Click to see CC1=C(C(=O)OC(C1)C(C)C2CCC3C2(C(CC4C3C5C(O5)C6(C4(C(C7C(C6)O7)OC(=O)C)C)O)OC(=O)C)C)COC8C(C(C(C(O8)CO)O)O)O	750.80	unknown	via CMAUP database
Taccalonolide A	441685	Click to see	702.70	unknown	via CMAUP database
Taccalonolide Aa	53474112	Click to see CC1C=C2C(C3C1C4(C(C3OC(=O)C)C5C(C(C4OC(=O)C)OC(=O)C)C6(C(C7C(O7)CC6(C(=O)C5OC(=O)C)O)OC(=O)C)C)C)(C(C(=O)O2)(C)O)C	760.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Withanolides and derivatives / Withanolide glycosides and derivatives
(3S,4R,6R)-6-[(1S)-1-[(3S,8S,9S,10R,13S,14S,17R)-3-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]ethyl]-3,4-dimethyloxan-2-one	16203282	Click to see	1077.20	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(24R,25S)-3beta-[2-O-(4-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)-beta-D-glucopyranosyloxy]-26-[2-O-(4-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl)-6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyloxy]ergosta-5-ene	16203400	Click to see CC(CCC(C)C(C)COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)CO)O)O)O)O)O)C5CCC6C5(CCC7C6CC=C8C7(CCC(C8)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)CO)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C	1551.70	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[[(2R,3S,4S,5R,6R)-5-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[(2S,3R,6R)-6-[(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2,3-dimethylheptoxy]-3,4-dihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	21580610	Click to see	1227.40	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R,6S)-7-[(2R,3R,4S,5R,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	21580612	Click to see CC(CCC(C)C(C)COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)C5CCC6C5(CCC7C6CC=C8C7(CCC(C8)OC9C(C(C(C(O9)CO)O)O)O)C)C	1227.40	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R,6S)-7-[(2R,3R,4S,5S,6R)-3-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxyoxan-2-yl]oxy-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	21580608	Click to see	1389.50	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R,6S)-7-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	21580613	Click to see CC(CCC(C)C(C)COC1C(C(C(C(O1)CO)O)O)OC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)O)C4CCC5C4(CCC6C5CC=C7C6(CCC(C7)OC8C(C(C(C(O8)CO)O)O)O)C)C	1065.20	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R,6S)-7-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4R,5S,6R)-5-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxyoxan-2-yl]oxy-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	21580606	Click to see	1551.70	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R,6S)-7-[(2R,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	21580611	Click to see CC(CCC(C)C(C)COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)C5CCC6C5(CCC7C6CC=C8C7(CCC(C8)OC9C(C(C(C(O9)CO)O)O)O)C)C	1227.40	unknown	via CMAUP database
(2S,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6R)-6-[[(2R,3S,4S,5R,6R)-5-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-[(2S,3R,6R)-6-[(3S,8S,9S,10R,13R,14S,17R)-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2,3-dimethylheptoxy]oxan-2-yl]methoxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	21580609	Click to see CC(CCC(C)C(C)COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)O)O)O)OC4C(C(C(C(O4)CO)OC5C(C(C(C(O5)CO)O)O)O)O)O)C6CCC7C6(CCC8C7CC=C9C8(CCC(C9)O)C)C	1227.40	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-3-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxyoxan-2-yl] (2S,3R,6R)-6-[(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2,3-dimethylheptanoate	11251919	Click to see	1403.50	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4R,5S,6R)-5-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxyoxan-2-yl] (2S,3R,6R)-6-[(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2,3-dimethylheptanoate	11320871	Click to see	1565.60	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl] (2S,3R,6R)-6-[(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2,3-dimethylheptanoate	11309354	Click to see CC(CCC(C)C(C)C(=O)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)OC3C(C(C(C(O3)CO)O)O)O)O)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)C5CCC6C5(CCC7C6CC=C8C7(CCC(C8)OC9C(C(C(C(O9)CO)O)O)O)C)C	1241.40	unknown	via CMAUP database
1-[(3S,8R,9S,10R,13S,14S)-3-[(2R,3R,4S,5R,6R)-4-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15-decahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone	11115684	Click to see	931.00	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(25S)-3beta-[3-O-(4-O-beta-D-Glucopyranosyl-alpha-L-rhamnopyranosyl)-beta-D-glucopyranosyloxy]spirosta-5-ene	101204873	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C)OC1	885.00	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-3-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol	11828974	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)C)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1	869.00	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol	44429637	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)C)O)O)O)O)C)C)C)OC1	722.90	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-4-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-2-[(1S,2S,4S,4'S,5'R,6R,7S,8R,9S,12S,13R,16S)-4'-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101204871	Click to see CC1COC2(CC1O)C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)O)O)OC1C(C(C(C(O1)C)O)O)O)C)C)C	1047.20	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-4-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-2-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	44474895	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)O)O)OC2C(C(C(C(O2)C)O)O)O)C)C)C)OC1	1031.20	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-4-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-2-[(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol	101204872	Click to see	1031.20	unknown	via CMAUP database
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-4-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-2-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-methoxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol	11094424	Click to see	1225.40	unknown	via CMAUP database
[(25S)-26-(6-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyloxy)-22alpha-methoxyfurosta-5-ene-3beta-yl]2-O-alpha-L-rhamnopyranosyl-3-O-(4-O-beta-D-glucopyranosyl-alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside	10866184	Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)C)OC8C(C(C(C(O8)CO)O)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)OC1(CCC(C)COC1C(C(C(C(O1)COC1C(C(C(C(O1)CO)O)O)O)O)O)O)OC	1387.50	unknown	via CMAUP database
[(25S)-26-(beta-D-Glucopyranosyloxy)furosta-5,20(22)-diene-3beta-yl]2-O-alpha-L-rhamnopyranosyl-3-O-(4-O-beta-D-glucopyranosyl-alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside	10887699	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC6(C(C5CC=C4C3)CC7C6C(=C(O7)CCC(C)COC8C(C(C(C(O8)CO)O)O)O)C)C)C)CO)O)OC9C(C(C(C(O9)C)OC1C(C(C(C(O1)CO)O)O)O)O)O)O)O)O	1193.30	unknown	via CMAUP database
[(2R,3R,4S,5R,6R)-4-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(1S,2S,4S,8S,9S,12S,13R,16S)-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-6,18-dien-16-yl]oxy]oxan-2-yl]methyl acetate	11126072	Click to see	1235.40	unknown	via CMAUP database
[(2R,3R,4S,5R,6R)-4-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-6-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-methoxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl acetate	10996873	Click to see	1267.40	unknown	via CMAUP database
[(3S,8S,9S,10R,13S,14S,16S,17R)-17-acetyl-3-[(2R,3R,4S,5R,6R)-4-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-16-yl] (4S)-4-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypentanoate	11137002	Click to see	1225.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1055/S-2003-45110
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1055/S-2003-45110
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
(2S,4R)-Pentane-1,2,3,4,5-Pentol	6912	Click to see	152.15	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Evelynin	46938776	Click to see COC1=C(C=C(C=C1)C(=O)CCC2=C(C(=O)C(=CC2=O)OC)OC)OC	360.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
3-(7-Methoxy-1,3-benzodioxol-5-yl)prop-2-enyl 2-(2-methylbut-2-enoyloxymethyl)but-2-enoate	194241	Click to see CC=C(C)C(=O)OCC(=CC)C(=O)OCC=CC1=CC2=C(C(=C1)OC)OCO2	388.40	unknown	https://doi.org/10.1248/CPB.46.871
4-Methoxy-6-(1-methoxyprop-2-enyl)-1,3-benzodioxole	10198380	Click to see	222.24	unknown	https://doi.org/10.1248/CPB.46.871
4-Methoxy-6-(3-methoxyprop-1-enyl)-1,3-benzodioxole	86022942	Click to see COCC=CC1=CC2=C(C(=C1)OC)OCO2	222.24	unknown	https://doi.org/10.1248/CPB.46.871
4-methoxy-6-[(1R)-1-methoxyprop-2-enyl]-1,3-benzodioxole	162871452	Click to see	222.24	unknown	https://doi.org/10.1248/CPB.46.871
Anthriscinol methyl ether	12851551	Click to see	222.24	unknown	https://doi.org/10.1248/CPB.46.871
Anthriscusin	6443833	Click to see	388.40	unknown	https://doi.org/10.1248/CPB.46.871 https://doi.org/10.1055/S-2003-45110
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
2-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2,3-dihydrofuro[3,2-g]chromen-7-one	5319288	Click to see	408.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten	2355	Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3	216.19	unknown	https://doi.org/10.1248/BPB.30.1340
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin	69894	Click to see	192.17	unknown	https://doi.org/10.1248/BPB.30.1340
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see	192.17	unknown	https://doi.org/10.1248/BPB.30.1340
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2R,3R,4S,5S,6R)-2-[(3R,5R)-1-(3,4-dihydroxyphenyl)-5-hydroxy-7-(4-hydroxyphenyl)heptan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	11071056	Click to see	494.50	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(3R,5R)-1,7-bis(3,4-dihydroxyphenyl)-5-hydroxyheptan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	10896495	Click to see	510.50	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(3R,5R)-7-(3,4-dihydroxyphenyl)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)heptan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	11005885	Click to see	524.60	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(3R,5R)-7-(3,4-dihydroxyphenyl)-5-hydroxy-1-(4-hydroxyphenyl)heptan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	11005529	Click to see C1=CC(=CC=C1CCC(CC(CCC2=CC(=C(C=C2)O)O)O)OC3C(C(C(C(O3)CO)O)O)O)O	494.50	unknown	via CMAUP database
3,5-Dihydroxy-1,7-bis(3,4-dihydroxyphenyl)heptane	11131830	Click to see C1=CC(=C(C=C1CCC(CC(CCC2=CC(=C(C=C2)O)O)O)O)O)O	348.40	unknown	via CMAUP database
4-[(3R,5R)-3,5-dihydroxy-7-(4-hydroxyphenyl)heptyl]benzene-1,2-diol	636849	Click to see	332.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(2R,3R,4S,5S,6R)-2-[(3R,5R)-5-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-7-(4-hydroxyphenyl)heptan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	10973237	Click to see	508.60	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(3R,5R)-5-hydroxy-1,7-bis(4-hydroxy-3-methoxyphenyl)heptan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	11731236	Click to see COC1=C(C=CC(=C1)CCC(CC(CCC2=CC(=C(C=C2)O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O	538.60	unknown	via CMAUP database
(2R,3R,4S,5S,6R)-2-[(3R,5R)-5-hydroxy-1,7-bis(4-hydroxyphenyl)heptan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	10896097	Click to see	478.50	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	https://doi.org/10.1007/BF02517954
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	https://doi.org/10.1007/BF02517954
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	Click to see	610.50	unknown	https://doi.org/10.1007/BF02517954
Vitamin P	5293655	Click to see	610.50	unknown	https://doi.org/10.1007/BF02517954
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retro-dihydrochalcones
Taccabulin A	72702319	Click to see	346.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(4-hydroxy-3,5-dimethoxybenzoyl)oxymethyl]oxan-2-yl]oxybenzoic acid	16203399	Click to see COC1=CC(=CC(=C1O)OC)C(=O)OCC2C(C(C(C(O2)OC3=C(C=C(C=C3)C(=O)O)OC)O)O)O	510.40	unknown	via CMAUP database

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Anthriscus sylvestris

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