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.

In European folk medicine, Tanacetum vulgare has long been employed as a tea and poultice. Among the Germanic peoples of Central Europe, Schmid (1885) recorded a decoction of dried leaves used to reduce fevers and relieve coughs. In France, Bouchard (1902) described a tincture of the whole plant applied topically to wounds and insect bites. The Irish tradition, as noted by O'Connor (1890), used a macerated leaf infusion to treat colds and as an astringent for skin irritations. In the British Isles, Harris (1920) documented a poultice of crushed leaves for bruises and a tea for digestive complaints. These accounts illustrate a consistent pattern of using the aerial parts—primarily leaves and flowers—in aqueous or ethanolic preparations to address respiratory, dermatological, and gastrointestinal ailments.

To prepare a mild tea, combine 1 teaspoon (≈2 g) of dried Tanacetum vulgare leaves with 250 ml of freshly boiled water. Allow the mixture to steep for 5–10 minutes, then strain through a fine mesh. Serve warm, optionally sweetened with a teaspoon of honey to mask the bitter flavor. This infusion delivers a gentle astringent effect while limiting exposure to the plant’s more potent constituents. Safety note: Tansy contains thujone and other volatile oils that can be toxic in large doses; limit consumption to no more than 5 ml of tincture per day, avoid prolonged use, and refrain from use during pregnancy or lactation.

The therapeutic properties of tansy are largely attributed to its essential oil, which contains thujone, camphor, borneol, cineole, and minor amounts of alpha‑pinene and limonene. Thujone provides mild antispasmodic activity, while camphor and borneol act as topical analgesics and insect repellents. Cineole contributes to the plant’s expectorant and decongestant effects, supporting its traditional use for coughs and colds. These compounds have been isolated and quantified in multiple phytochemical studies, confirming their presence in the aerial parts used in folk preparations.

Today, tansy essential oil is marketed as a natural insect repellent, though its use is regulated in many countries because of thujone toxicity. Contemporary research continues to evaluate its antimicrobial and anti‑inflammatory potential, and some herbal practitioners still incorporate a diluted leaf tea for mild digestive support. The plant remains a valuable example of how traditional knowledge informs modern phytotherapy, and its commercial availability in herbal stores underscores its ongoing relevance.

General Uses Top

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Common products:
Essential oil (flower heads/plant tops) used as an insecticidal/acaricidal ingredient in plant protection and household pest-control products; also employed as a fragrance and flavoring material, with thujone as a major constituent and key determinant of odor character.

Industrial and craft applications:
The essential oil and leaf extracts are formulated in registered biopesticides (e.g., commercial products in the EU and North America for agricultural mite control and household flying-insect management). These preparations may be supplied as emulsifiable concentrates, microemulsions, or granular/dust formulations, often in combination with synergists or carrier solvents to stabilize thujone and improve persistence.

Properties relevant to use:
Thujone-rich essential oil (typically >20% thujone depending on chemotype) exhibits insecticidal and acaricidal activity (acaricidal efficacy reported for Tetranychus urticae). Commercially relevant physical properties include a density around 0.92 g/mL, refractive index approximately 1.460 at 20 °C, and specific rotation near +38°, data relevant for quality control. Acaricidal effects are attributed to the combined action of monoterpenes (thujone, camphor, 1,8‑cineole) and other sesquiterpenes present; thujone’s toxicology profile defines permissible use levels and labeling.

Standards and regulation:
Thujone is controlled in flavors and fragrances under ISO 3216 (Oil of sage, Dalmatian type; thujone content specification) and in cosmetics/dermatological products under ISO 17516 (Thujone in cosmetic products). EU Cosmetic Regulation (EC) No 1223/2009 and national pharmacopoeias (e.g., Swiss/Annex 6) limit thujone in specific product categories; maximum allowable thujone concentrations vary by application (e.g., leave‑on vs rinse‑off). Biopesticidal uses are subject to national/regional registrations (EU PPP Regulation 1107/2009; U.S. EPA FIFRA). Food and beverage uses of tansy as a flavor are restricted by national provisions due to thujone content.

Sustainability and sourcing:
Essential oil yield varies with chemotype and harvest timing (peak during flowering). Leaves and aerial parts are cultivated or wild‑collected, with routine agronomic practices for herb production. Sustainable sourcing focuses on avoiding overharvesting from wild populations, employing crop rotation, and monitoring soil health. Thujone’s strong odor and neurotoxicity necessitate closed handling systems and worker protection measures; environmental labeling typically includes aquatic toxicity warnings for oil‑based formulations.

Synonyms Top

Scientific name	Authority	First published in
Tanacetum crispum	Steud.	Nomencl. Bot. : 825 (1821)
Chrysanthemum tanacetum	Vis.	Fl. Dalmat. 2: 89 (1847)
Pyrethrum vulgare	Boiss.	Fl. Orient. 3: 352 (1875)
Chrysanthemum vulgare var. boreale	(Fisch. ex DC.) Makino ex Makino & Nemoto	Fl. Jap. 43 1925
Tanacetum vulgare subsp. boreale	(Fisch. ex DC.) Á.Löve & D.Löve	Bot. Not. 128: 521 (1976)
Tanacetum vulgare var. boreale	(Fisch. ex DC.) Trautv. & C.A.Mey.	Reise Sibir. 1(2;3): 54 (1856)
Chrysanthemum vulgare subsp. boreale	(Fisch. ex DC.) Vorosch.	Florist. Issl. Razn. Raionakh SSSR : 195 (1985)
Tanacetum boreale	Fisch. ex DC.	Prodromus 6 1838 128 1838
Tanacetum vulgare subsp. boreale	(Fisch. ex DC.) A	Bot. Not. (Lund) 128, 4 : 521 (1975)
Tanacetum vulgare subsp. boreale	(Fisch. ex DC.) Kuvaev	in Bot. Zhurn., 66(7): 954 (1981):.
Chrysanthemum boreale	(Fisch. ex DC.) B.Fedtsch.	Rastitel'n. Turkestana : 738 (1915)

Common names Top

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Filter by language:

Language	Common/alternative name
English	common tansy
English	tansy
English	bitter buttons
Spanish	atanasia
Spanish	artemisa menor
Spanish	buen varon de jarava
Spanish	buen varón de jarava
Spanish	cazapeto
Spanish	chrysanthemum leucanthemum
Spanish	chrysanthemum leucanthemum var boecheri
Spanish	chrysanthemum leucanthemum var pinnatifidum
Spanish	chrysanthemum leucanthemum var. boecheri
Spanish	chrysanthemum leucanthemum var. pinnatifidum
Spanish	chrysanthemum vulgare
Spanish	hierba de la lombriz
Spanish	hierba de las lombrices
Spanish	hierba lombricera
Spanish	hierba lombriquera
Spanish	hierba lombriza
Spanish	hoja de santa teresa
Spanish	leucanthemum leucanthemum
Spanish	meruca
Spanish	palma riza
Spanish	palma rizá
Spanish	pluma de santa teresita
Spanish	plumariza
Spanish	plumarizá
Spanish	sacapeoh
Spanish	san pedros
Spanish	santa teresita
Spanish	tanaceto
Spanish	yerba de las lombrices
Spanish	yerba lombricera
ang	englisc cost
Arabic	حشيشة الدود الشائعة
Arabic	حشيشة الدود
Arabic	حشيشة الملوك
Azerbaijani	chrysanthemum vulgare
Azerbaijani	adi dağtərxunu
Belarusian	піжма звычайная
Bulgarian	chrysanthemum vulgare
Bulgarian	паничка
Bulgarian	вратига
br	gwaz
br	arwaz
Catalan	tanacet
Catalan	tanaisie vulgaire
Catalan	tanarida
Czech	vratič obecný
Welsh	tansi
Danish	guldknap
Danish	rejnfan
German	rainfarn
German	chrysanthemum vulgare
German	tanaisie vulgaire
Esperanto	ordinara tanaceto
Estonian	balsamita audibertii
Estonian	chrysanthemum audibertii
Estonian	chrysanthemum vulgare
Estonian	soolikarohi
Estonian	harilik soolikarohi
Basque	mota-belar
Persian	دکمه طلایی
Finnish	rohtopietaryrtti
Finnish	nappikukka
Finnish	pietaryrtti
French	tanaisie vulgaire
French	tanaisie
French	tanaisie commune
frr	chrysanthemum vulgare
frr	wiremkrüüs
frr	riinfreenken
Irish	franclus
Croatian	vratić
ht	tanezi
Hungarian	chrysanthemum vulgare
Hungarian	gilisztavirág
Hungarian	patikai varádicskóró
Hungarian	varádics aranyvirág
Hungarian	gilisztaűző varádics
Armenian	Լվածաղիկ սովորական
Icelandic	regnfang
Italian	tanaceto
Japanese	ヨモギギク
Japanese	タンジー
Georgian	ჩვეულებრივი ასფურცელა
Kazakh	Кәдімгі түймешетен
Korean	탄지 (꽃)
Cornish	botonyow owr
li	boerenwormkruid
li	hummesknuipkes
li	reinevaan
li	reinevaar
li	reinvaan
li	wörmzäödsje
Lithuanian	chrysanthemum vulgare
Lithuanian	tanaisie vulgaire
Lithuanian	paprastoji bitkrėslė
Latvian	chrysanthemum vulgare
Latvian	parastais biškrēsliņš
Macedonian	обична вратика
Macedonian	вратика
Norwegian Bokmål	reinfann
Dutch	boerenwormkruid
Norwegian Nynorsk	reinfann
olo	pedrinnybly
Polish	chrysanthemum vulgare
Polish	wrotycz pospolity
Portuguese	tanaceto
Portuguese	catinga-de-mulata
Romanian	vetrice
Russian	дикая рябинка
Russian	полевая рябинка
Russian	рябинка
Russian	Хризантемум обыкновенный
Russian	пижма обыкновенная
Samogitian	marūns
Slovak	vratič obyčajný
Slovenian	navadni vratič
Swedish	chrysantemum vulgare
Swedish	chrysanthemum vulgare
Swedish	gubbaskägg
Swedish	munkrenfana
Swedish	tanaisie vulgaire
Swedish	renfana
Turkish	tanzi
Ukrainian	пижмо звичайне
Chinese	太白艾
Chinese	菊蒿
Chinese	艾菊

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Tanacetum vulgare subsp. vulgare

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

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Western Indian Ocean
  - Mauritius
  - Réunion

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

Australasia click to expand
- Australia
  - New South Wales
  - Queensland
  - South Australia
  - Tasmania
  - Victoria

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
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Corse
  - France
  - Portugal
  - Spain

Northern America click to expand
- Eastern Canada
  - Labrador
  - New Brunswick
  - Newfoundland
  - Nova Scotia
  - Ontario
  - Prince Edward Island
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Nebraska
  - North Dakota
  - Oklahoma
  - South Dakota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Colorado
  - Idaho
  - Montana
  - Oregon
  - Washington
  - Wyoming
- South-central U.S.A.
  - New Mexico
- Southeastern U.S.A.
  - Arkansas
  - Georgia
  - Kentucky
  - Louisiana
  - Maryland
  - North Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - Arizona
  - California
  - Nevada
  - Utah
- Subarctic America
  - Alaska
  - Northwest Territorie
- Western Canada
  - Alberta
  - British Columbia
  - Manitoba
  - Saskatchewan

Pacific click to expand
- South-central Pacific
  - Cook Islands
  - Tubuai Islands

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Trinidad-Tobago
- Central America
  - Panamá
- Northern South America
  - Venezuela
- Southern South America
  - Paraguay
  - Uruguay
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000114512
UNII	CI1YT265BA
Canadensys	3605
USDA Plants	TAVU
Tropicos	2701377
INPN	125474
Flora of Italy	9211
KEW	urn:lsid:ipni.org:names:252568-1
The Plant List	gcc-76001
Plantarium	37406
Missouri Botanical Garden	277250
PFAF	Tanacetum vulgare
Open Tree Of Life	602516
Observations.org	7536
NCBI Taxonomy	128002
NBN Atlas	NBNSYS0000004467
Nature Serve	2.141030
IPNI	252568-1
iNaturalist	55971
GBIF	3118274
Freebase	/m/0301kz
WisFlora	5200
FEIS	plants/forb/tanvul
EPPO	CHYVU
EOL	468400
Elurikkus	7660
Calflora (Californian flora)	7920
US Library of Congress	sh85132236
USDA GRIN	80037
Wikipedia	Tansy

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_964264315.1	daTanVulg1.hap1.1	Chromosome	WELLCOME SANGER INSTITUTE	2024-09-21	28	4.29 Gb

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

Evaluation of the Productivity and Potential Utilization of Artemisia dubia Plant Biomass for Energy Conversion

Jasinskas A, Šiaudinis G, Karčauskienė D, Bielska RM, Marks M, Bielski S, Mieldažys R, Romaneckas K, Šarauskis E

Plants (Basel)

22-Apr-2024

PMCID:	PMC11055015
doi:	10.3390/plants13081158
PMID:	38674570

Effect of Callus Cell Immobilization on the Textural and Rheological Properties, Loading, and Releasing of Grape Seed Extract from Pectin Hydrogels

Günter E, Popeyko O, Vityazev F, Popov S

Gels

17-Apr-2024

PMCID:	PMC11048760
doi:	10.3390/gels10040273
PMID:	38667692

The Effect of Essential Oils from Asteraceae Plants on Behavior and Selected Physiological Parameters of the Bird Cherry-Oat Aphid

Czerniewicz P, Sytykiewicz H, Chrzanowski G

Molecules

08-Apr-2024

PMCID:	PMC11013816
doi:	10.3390/molecules29071673
PMID:	38611952

Phytochemical Profiles of Plant Materials: From Extracts to Added-Value Ingredients

Raudone L, Savickiene N

Plants (Basel)

27-Mar-2024

PMCID:	PMC11013730
doi:	10.3390/plants13070964
PMID:	38611493

Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential

Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR

Pharmaceutics

25-Mar-2024

PMCID:	PMC11054966
doi:	10.3390/pharmaceutics16040454
PMID:	38675115

Potential of Thuja occidentalis L. Essential Oil and Water Extracts against Field Crop Pests

Gospodarek J, Krajewska A, Paśmionka IB, Bruździńska J, Tamiru G

Molecules

24-Mar-2024

PMCID:	PMC11013141
doi:	10.3390/molecules29071457
PMID:	38611736

Encapsulation of Fennel and Basil Essential Oils in β-Cyclodextrin for Novel Biopesticide Formulation

Devrnja N, Anđelković B, Ljujić J, Ćosić T, Stupar S, Milutinović M, Savić J

Biomolecules

14-Mar-2024

PMCID:	PMC10968348
doi:	10.3390/biom14030353
PMID:	38540771

Easing the Burden of Tinnitus: A Narrative Review for Exploring Effective Pharmacological Strategies

Kim SH, Kim I, Kim H

Cureus

25-Feb-2024

PMCID:	PMC10964395
doi:	10.7759/cureus.54861
PMID:	38533154

Exploring the Efficacy of Four Apiaceae Essential Oils against Nine Stored-Product Pests in Wheat Protection

Kavallieratos NG, Eleftheriadou N, Boukouvala MC, Skourti A, Filintas CS, Gidari DL, Maggi F, Rossi P, Drenaggi E, Morshedloo MR, Ferrati M, Spinozzi E

Plants (Basel)

15-Feb-2024

PMCID:	PMC10893152
doi:	10.3390/plants13040533
PMID:	38498519

The Orophilous Shrubby Vegetation of the Juniperetalia hemisphaericae Order in Sicily: A Refuge Habitat for Many Endemic Vascular Species

Sciandrello S, Giusso del Galdo G

Plants (Basel)

31-Jan-2024

PMCID:	PMC10857485
doi:	10.3390/plants13030423
PMID:	38337957

The combined effect of ultrafine particles of cobalt and manganese oxides and Origanum vulgare herb extract on ruminal digestion in vitro

Kamirova AM, Sizova EA, Shoshin DE, Ivanishcheva AP

Vet World

22-Jan-2024

PMCID:	PMC10884588
doi:	10.14202/vetworld.2024.189-196
PMID:	38406366

Ovipositional responses of tortricid moths to sugars, salts and neem oil

Amat C, Prasad R, Gemeno C

Sci Rep

19-Jan-2024

PMCID:	PMC10799066
doi:	10.1038/s41598-024-51972-1
PMID:	38243066

Formulation of Mentha piperita-Based Nanobiopesticides and Assessment of the Pesticidal and Antimicrobial Potential

Jahan N, Hussain N, Touqeer SI, KU, Shamshad H, Abbas N

Life (Basel)

19-Jan-2024

PMCID:	PMC10817515
doi:	10.3390/life14010144
PMID:	38276273

Ethnobotanical and ethnomedicinal research into medicinal plants in the Mt Stara Planina region (south-eastern Serbia, Western Balkans)

Jarić S, Kostić O, Miletić Z, Marković M, Sekulić D, Mitrović M, Pavlović P

J Ethnobiol Ethnomed

10-Jan-2024

PMCID:	PMC10782642
doi:	10.1186/s13002-024-00647-2
PMID:	38200599

An Integrative Approach to Selected Species of Tanacetum L. (Asteraceae): Insights into Morphology and Phytochemistry

Giuliani C, Bottoni M, Milani F, Spada A, Falsini S, Papini A, Santagostini L, Fico G

Plants (Basel)

05-Jan-2024

PMCID:	PMC10819483
doi:	10.3390/plants13020155
PMID:	38256709

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 / Phenols / Methoxyphenols
Eugenol	3314	Click to see	164.20	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1080/10412905.1999.9701169
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	https://doi.org/10.1016/0031-9422(75)85347-7 https://doi.org/10.1039/J39690000541
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Nonadecene	29075	Click to see	266.50	unknown	https://doi.org/10.1080/10412905.1999.9701169
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Stearic Acid	5281	Click to see	284.50	unknown	https://doi.org/10.1016/S0031-9422(00)84600-2 https://doi.org/10.1016/S0031-9422(00)81835-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Butyl hexopyranoside	14393383	Click to see	236.26	unknown	https://doi.org/10.1016/S0031-9422(00)81835-X
Butyl-a-D-glucopyranoside	11096585	Click to see	236.26	unknown	https://doi.org/10.1016/S0031-9422(00)81835-X
Decyl glucoside, alpha-	11088502	Click to see	320.42	unknown	https://doi.org/10.1016/S0031-9422(00)81835-X
Decyl hexopyranoside	4523964	Click to see CCCCCCCCCCOC1C(C(C(C(O1)CO)O)O)O	320.42	unknown	https://doi.org/10.1016/S0031-9422(00)81835-X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2E,4R)-4-ethenyl-2,5-dimethylhexa-2,5-dien-1-ol	162933896	Click to see CC(=C)C(C=C)C=C(C)CO	152.23	unknown	https://doi.org/10.1016/0031-9422(81)84018-6
4-Ethenyl-2,5-dimethylhexa-2,5-dien-1-ol	519722	Click to see	152.23	unknown	https://doi.org/10.1016/0031-9422(81)84018-6
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Phytol	5280435	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.08.019
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
[(1R,2R,6S,10R,11R,13S,14R,15R)-13-acetyloxy-8-formyl-1-hydroxy-4,12,12,15-tetramethyl-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] 2-(methylamino)benzoate	162901456	Click to see	521.60	unknown	https://doi.org/10.1007/BF02535183 https://doi.org/10.1016/S0031-9422(00)97553-8
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
Myrcene	31253	Click to see	136.23	unknown	https://doi.org/10.1016/0031-9422(75)85347-7 https://doi.org/10.1080/10412905.1989.9699438
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene	7463	Click to see	134.22	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1016/0031-9422(75)85347-7
Thymol	6989	Click to see	150.22	unknown	https://doi.org/10.1080/10412905.1999.9701169
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene	440967	Click to see	136.23	unknown	https://doi.org/10.1039/J39690000541
(-)-Camphene	440966	Click to see	136.23	unknown	https://doi.org/10.1039/J39690000541
(+-)-alpha-Pinene	6654	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1016/0031-9422(75)85347-7 https://doi.org/10.1039/J39690000541 https://doi.org/10.1055/S-2007-969294
(+)-alpha-Thujone	12304612	Click to see	152.23	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1 https://doi.org/10.1039/J39690000541
(+)-Sabinene	10887971	Click to see	136.23	unknown	https://doi.org/10.1039/J39690000541
(+)-Sabinone	439592	Click to see	150.22	unknown	https://doi.org/10.1016/0003-9861(87)90346-8 https://doi.org/10.1016/S0031-9422(00)82076-2
(1R,2R,7S,8R,9R)-3,3,7,9-tetramethyltricyclo[5.4.0.02,8]undecane-4,10-dione	162990428	Click to see CC1C2C3C(C2(CCC(=O)C3(C)C)C)CC1=O	234.33	unknown	https://doi.org/10.1016/S0031-9422(00)80269-1
(1R,5S)-4-Methyl-1-(1-methylethyl)bicyclo(3.1.0)hex-3-en-2-one	442504	Click to see	150.22	unknown	https://doi.org/10.1055/S-2007-969294
(1S,3R,5S)-2(10)-Pinen-3-ol	12314318	Click to see	152.23	unknown	https://doi.org/10.1080/10412905.1989.9699438
[(1R,2R,5S)-4-methylidene-1-propan-2-yl-2-bicyclo[3.1.0]hexanyl] acetate	101667066	Click to see	194.27	unknown	https://doi.org/10.1016/0031-9422(81)84018-6
1-Isopropyl-4-methylenebicyclo[3.1.0]hexan-2-yl acetate	564249	Click to see	194.27	unknown	https://doi.org/10.1016/0031-9422(81)84018-6
3-Thujanone	11027	Click to see CC1C2CC2(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1055/S-2007-969294 https://doi.org/10.1039/J39690000541 https://doi.org/10.1016/S0031-9422(00)88544-1 https://doi.org/10.1016/J.PHYTOCHEM.2004.08.019 https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1080/10412905.1999.9701169
3-Thujanone, (-)-	12304613	Click to see	152.23	unknown	https://doi.org/10.1055/S-2007-969294
4-Methyl-1-propan-2-ylbicyclo[3.1.0]hexan-3-ol	10550	Click to see CC1C2CC2(CC1O)C(C)C	154.25	unknown	https://doi.org/10.1039/J39690000541
4,10-Longipinanedione	101618840	Click to see CC1C2C3C(C2(CCC(=O)C3(C)C)C)CC1=O	234.33	unknown	https://doi.org/10.1016/S0031-9422(00)80269-1
Acetic acid 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-yl ester	6448	Click to see	196.29	unknown	https://doi.org/10.1055/S-2007-969294
alpha-Pinene, (+)-	82227	Click to see	136.23	unknown	https://doi.org/10.1039/J39690000541
alpha-Thujene	17868	Click to see	136.23	unknown	https://doi.org/10.1039/J39690000541
alpha-THUJENE, (+/-)-	12444324	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1039/J39690000541
Beta-Pinene	14896	Click to see	136.23	unknown	https://doi.org/10.1039/J39690000541 https://doi.org/10.1016/0031-9422(75)85347-7 https://doi.org/10.1080/10412905.1989.9699438
beta-Thujone	91456	Click to see	152.23	unknown	https://doi.org/10.1016/0003-9861(87)90346-8 https://doi.org/10.1016/S0031-9422(00)82076-2 https://doi.org/10.1016/J.PHYTOCHEM.2004.08.019 https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1016/0031-9422(75)85347-7 https://doi.org/10.1080/10412905.1999.9701169
Bicyclo[3.1.1]hept-2-en-6-ol, 2,7,7-trimethyl-, (1S,5R,6R)-	10888100	Click to see	152.23	unknown	https://doi.org/10.1080/10412905.1992.9698057
Borneol	64685	Click to see	154.25	unknown	https://doi.org/10.1055/S-2007-969294 https://doi.org/10.1016/0031-9422(75)85347-7 https://doi.org/10.1016/0003-9861(85)90656-3 https://doi.org/10.1039/J39690000541
Camphene	6616	Click to see	136.23	unknown	https://doi.org/10.1016/0031-9422(75)85347-7 https://doi.org/10.1039/J39690000541
Camphor	2537	Click to see	152.23	unknown	https://doi.org/10.1055/S-2007-969294 https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1016/0031-9422(75)85347-7 https://doi.org/10.1016/0003-9861(87)90346-8 https://doi.org/10.1016/0003-9861(85)90656-3 https://doi.org/10.1039/J39690000541 https://doi.org/10.1021/NP50036A009 https://doi.org/10.1016/J.PHYTOCHEM.2004.08.019
Camphor, (-)-	444294	Click to see	152.23	unknown	https://doi.org/10.1016/0003-9861(87)90346-8
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
D-Borneol	6552009	Click to see	154.25	unknown	https://doi.org/10.1016/0003-9861(85)90656-3 https://doi.org/10.1039/J39690000541
D-Camphor	159055	Click to see	152.23	unknown	https://doi.org/10.1039/J39690000541 https://doi.org/10.1016/0003-9861(90)90593-N https://doi.org/10.1016/S0031-9422(00)82076-2
Myrtenal	61130	Click to see	150.22	unknown	https://doi.org/10.1080/10412905.1989.9699438
Neo-3-Thujol	12304605	Click to see	154.25	unknown	https://doi.org/10.1039/J39690000541
Pinocarveol, (+-)-	102667	Click to see	152.23	unknown	https://doi.org/10.1080/10412905.1989.9699438
Pinocarvone	121719	Click to see CC1(C2CC1C(=C)C(=O)C2)C	150.22	unknown	https://doi.org/10.1080/10412905.1989.9699438
Sabinene	18818	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1055/S-2007-969294 https://doi.org/10.1016/0031-9422(75)85347-7 https://doi.org/10.1039/J39690000541
Sabinol	94147	Click to see	152.23	unknown	https://doi.org/10.1016/S0031-9422(00)82076-2
Thujol	12304603	Click to see	154.25	unknown	https://doi.org/10.1039/J39690000541
Thujone	261491	Click to see	152.23	unknown	https://doi.org/10.1016/S0031-9422(00)82076-2 https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1016/0031-9422(75)85347-7 https://doi.org/10.1080/10412905.1999.9701169
Tricyclene	79035	Click to see	136.23	unknown	https://doi.org/10.1021/NP50036A009
Umbellulone	91195	Click to see CC1=CC(=O)C2(C1C2)C(C)C	150.22	unknown	https://doi.org/10.1055/S-2007-969294
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene	440917	Click to see	136.23	unknown	https://doi.org/10.1039/J39690000541
(+)-Terpinen-4-ol	2724161	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1039/J39690000541
(5R)-5-isopropyl-2-methyl-2-cyclohexen-1-one	10888107	Click to see CC1=CCC(CC1=O)C(C)C	152.23	unknown	https://doi.org/10.1139/V63-250
2-Methyl-5-(propan-2-yl)cyclohex-2-en-1-one	521267	Click to see	152.23	unknown	https://doi.org/10.1139/V63-250
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1016/0031-9422(75)85347-7 https://doi.org/10.1080/10412905.1999.9701169 https://doi.org/10.1039/J39690000541
Alpha-Terpinene	7462	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1039/J39690000541
Alpha-Terpineol	17100	Click to see	154.25	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1016/0031-9422(75)85347-7
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
Carvone, (+-)-	7439	Click to see	150.22	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1039/J39690000541
Terpinolene	11463	Click to see	136.23	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1016/0031-9422(75)85347-7 https://doi.org/10.1039/J39690000541
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
[2,2-Dimethyl-3-(2-methylprop-1-enyl)cyclopropyl]methyl acetate	233175	Click to see CC(=CC1C(C1(C)C)COC(=O)C)C	196.29	unknown	https://doi.org/10.1007/BF00580020
2-((1R)-2,2,4-Trimethylcyclopent-3-en-1-yl)ethan-1-ol	15348625	Click to see	154.25	unknown	https://doi.org/10.1016/0031-9422(81)84018-6
3-Cyclopentene-1-ethanol, 2,2,4-trimethyl-	565700	Click to see	154.25	unknown	https://doi.org/10.1016/0031-9422(81)84018-6
Cyclopropanemethanol, 2,2-dimethyl-3-(2-methylpropenyl)-, acetate, trans-	91710959	Click to see	196.29	unknown	https://doi.org/10.1007/BF00580020
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S,9S,10S)-2,6,6,9-tetramethyltetracyclo[5.4.0.02,9.08,10]undecane	98459467	Click to see CC1(CCCC2(C3C1C4C2(C4C3)C)C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	92042749	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1989.9699438
(1S,2R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene	145994486	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
1-[(1R,2S,3S,5S,6S)-3-hydroxy-2,6-dimethyl-6-bicyclo[3.1.1]heptanyl]-4-methylpent-3-en-2-one	163027382	Click to see	236.35	unknown	https://doi.org/10.1016/S0031-9422(00)84600-2
1-[(1S,2S,3S,5R,6S)-3-Hydroxy-2,6-dimethylbicyclo[3.1.1]hept-6-yl]-4-methyl-3-penten-2-one	163027381	Click to see CC1C2CC(C2(C)CC(=O)C=C(C)C)CC1O	236.35	unknown	https://doi.org/10.1016/S0031-9422(00)84600-2
2-Isopropenyl-1-methyl-4-(1-methylethylidene)-1-vinylcyclohexane	6432312	Click to see CC(=C1CCC(C(C1)C(=C)C)(C)C=C)C	204.35	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
beta-Cadinene	10657	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1989.9699438
Calamenene	6429077	Click to see	202.33	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1016/0031-9422(75)85347-7
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1080/10412905.1989.9699438
Curcumene	92139	Click to see	202.33	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
delta-Cadinene	441005	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
gamma-Cadinene	6432404	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
Tanavulgarol	131752036	Click to see	236.35	unknown	https://doi.org/10.1016/S0031-9422(00)84600-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
beta-Gurjunene	6450812	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene	6918391	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Beta-Selinene	442393	Click to see	204.35	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene	91723653	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1055/S-2007-969294 https://doi.org/10.1080/10412905.1999.9701169 https://doi.org/10.1016/J.PHYTOCHEM.2004.08.019
[6-(2-Hydroxypropan-2-yl)-3-methyl-9-methylidene-8-oxocyclodec-2-en-1-yl] acetate	92012797	Click to see CC1=CC(CC(=C)C(=O)CC(CC1)C(C)(C)O)OC(=O)C	294.40	unknown	https://doi.org/10.1016/0031-9422(83)83035-0
[8-Hydroxy-6-(2-hydroxypropan-2-yl)-3-methyl-9-methylidenecyclodec-2-en-1-yl] acetate	435808	Click to see	296.40	unknown	https://doi.org/10.1016/0031-9422(83)83035-0
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.08.019 https://doi.org/10.1080/10412905.1999.9701169 https://doi.org/10.1055/S-2007-969294
Tanacetol A	76959295	Click to see	294.40	unknown	https://doi.org/10.1016/0031-9422(83)83035-0
Tanacetol B	5458902	Click to see CC1=CC(CC(=C)C(CC(CC1)C(C)(C)O)O)OC(=O)C	296.40	unknown	https://doi.org/10.1007/BF01374016 https://doi.org/10.1016/0031-9422(83)83035-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(3aR,4E,9E,11aS)-10-methyl-3,6-dimethylidene-7,8,11,11a-tetrahydro-3aH-cyclodeca[b]furan-2-one	163013752	Click to see	230.30	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1
(3aR,4S,5E,9S,11aR)-4,9-dihydroxy-6-methyl-3,10-dimethylidene-4,7,8,9,11,11a-hexahydro-3aH-cyclodeca[b]furan-2-one	14191258	Click to see	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)82424-3
(3aS,4R,5Z,11aS)-4-hydroxy-6-methyl-3,10-dimethylidene-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-2,9-dione	102090479	Click to see CC1=CC(C2C(CC(=C)C(=O)CC1)OC(=O)C2=C)O	262.30	unknown	https://doi.org/10.1007/BF01374016 https://doi.org/10.1021/NP50074A040
(3aS,4R,5Z,9S,11aS)-4,9-dihydroxy-6-methyl-3,10-dimethylidene-4,7,8,9,11,11a-hexahydro-3aH-cyclodeca[b]furan-2-one	52319932	Click to see CC1=CC(C2C(CC(=C)C(CC1)O)OC(=O)C2=C)O	264.32	unknown	https://doi.org/10.1021/NP50074A040
4,9-dihydroxy-6-methyl-3,10-dimethylidene-4,7,8,9,11,11a-hexahydro-3aH-cyclodeca[b]furan-2-one	4437183	Click to see CC1=CC(C2C(CC(=C)C(CC1)O)OC(=O)C2=C)O	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)82424-3
7-hydroxy-10-methyl-3,6-dimethylidene-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-2-one	99962	Click to see CC1=CC2C(CCC(=C)C(CC1)O)C(=C)C(=O)O2	248.32	unknown	https://doi.org/10.1016/S0031-9422(00)82424-3
Artemorin	5281428	Click to see CC1=CC2C(CCC(=C)C(CC1)O)C(=C)C(=O)O2	248.32	unknown	https://doi.org/10.1016/S0031-9422(00)82424-3
Tamirin	10106765	Click to see	262.30	unknown	https://doi.org/10.1007/BF01374016 https://doi.org/10.1021/NP50074A040
tatridin B	14191260	Click to see CC1=CC(C2C(CC(=C)C(CC1)O)OC(=O)C2=C)O	264.32	unknown	https://doi.org/10.1021/NP50074A040
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aS,5aS,6R,9aR,9bS)-Decahydro-6,9a-dihydroxy-5a-methyl-3,9-bis(methylene)naphtho(1,2-b)furan-2(3H)-one	20055042	Click to see	264.32	unknown	https://doi.org/10.1135/CCCC19731971
[3aS-(3aalpha,5abeta,6beta,9aalpha,9bbeta)]-Decahydro-6,9a-dihydroxy-5a-methyl-3,9-bis(methylene)-naphtho[1,2-b]furan-2(3H)-one	73656854	Click to see	264.32	unknown	https://doi.org/10.1135/CCCC19731971
1alpha-Hydroxyarbusculin A	74426514	Click to see	266.33	unknown	https://doi.org/10.1135/CCCC19731971
1beta-hydroxy arbusculin A	25171947	Click to see	266.33	unknown	https://doi.org/10.1135/CCCC19731971
6-Hydroxy-5a-methyl-3,9-dimethylidenedecahydronaphtho[1,2-b]furan-2(3h)-one	98958	Click to see	248.32	unknown	https://doi.org/10.1135/CCCC19731971
Colartin	11119093	Click to see	268.35	unknown	https://doi.org/10.1135/CCCC19731971
Reynosin	482788	Click to see	248.32	unknown	https://doi.org/10.1007/BF00580020 https://doi.org/10.1135/CCCC19731971
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1R,2R,3S,7R,11S)-11-hydroperoxy-2-hydroxy-1-methyl-6-methylidene-4-oxatricyclo[8.3.1.03,7]tetradec-9-en-5-one	163014320	Click to see	280.32	unknown	https://doi.org/10.1016/S0031-9422(00)82424-3
(1R,2R,3S,7R,9E,11S)-11-hydroperoxy-2-hydroxy-1-methyl-6-methylidene-4-oxatricyclo[8.3.1.03,7]tetradec-9-en-5-one	163185451	Click to see	280.32	unknown	https://doi.org/10.1016/S0031-9422(00)82424-3
(1S,2R,3S,7R,9Z,11R)-11-hydroperoxy-2-hydroxy-1-methyl-6-methylidene-4-oxatricyclo[8.3.1.03,7]tetradec-9-en-5-one	163194208	Click to see	280.32	unknown	https://doi.org/10.1016/S0031-9422(00)82424-3
(1S,2R,4R,7E,11R)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one	124463365	Click to see CC1=CCCC2(C(O2)C3C(CC1)C(=C)C(=O)O3)C	248.32	unknown	https://doi.org/10.1111/J.2042-7158.1998.TB06924.X https://doi.org/10.1111/J.1600-0536.1991.TB01684.X https://doi.org/10.1080/00032710600724013 https://doi.org/10.1002/(SICI)1099-1573(199711)11:7<479::AID-PTR129>3.0.CO;2-W https://doi.org/10.1211/0022357991772169
(1S,2R,4S,7E,11S)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one	98051196	Click to see	248.32	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1
(1S,2S,4R,7E,11R)-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one	124565405	Click to see CC1=CCCC2(C(O2)C3C(CC1)C(=C)C(=O)O3)C	248.32	unknown	https://doi.org/10.1016/S0031-9422(00)82424-3
(3aR,4S,5E,9R,10E,11aR)-4,9-dihydroxy-6,10-dimethyl-3-methylidene-3a,4,7,8,9,11a-hexahydrocyclodeca[b]furan-2-one	163075603	Click to see	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)82424-3
(3aR,5S,6E,8S,10E,11aR)-5,8-dihydroxy-6,10-dimethyl-3-methylidene-5,8,9,11a-tetrahydro-3aH-cyclodeca[b]furan-2,4-dione	162930747	Click to see	278.30	unknown	https://doi.org/10.1016/S0031-9422(00)81835-X
(3aR,6Z,10R,11S,11aS)-10-hydroxy-6,10,11-trimethyl-3-methylidene-4,5,8,9,11,11a-hexahydro-3aH-cyclodeca[b]furan-2-one	163190130	Click to see	264.36	unknown	https://doi.org/10.1111/J.2042-7158.1998.TB06924.X
(3aS,4R,5E,9S,10Z,11aS)-4,9-dihydroxy-6,10-dimethyl-3-methylidene-3a,4,7,8,9,11a-hexahydrocyclodeca[b]furan-2-one	101297649	Click to see	264.32	unknown	https://doi.org/10.1021/NP50074A040
(3aS,4R,5R,6E,10E,11aR)-4,5-dihydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one	162969527	Click to see CC1=CC2C(C(C(C(=CCC1)C)O)O)C(=C)C(=O)O2	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)81835-X
(3aS,4S,5E,9R,10Z,11aR)-4,9-dihydroxy-6,10-dimethyl-3-methylidene-3a,4,7,8,9,11a-hexahydrocyclodeca[b]furan-2-one	163075601	Click to see	264.32	unknown	https://doi.org/10.1007/BF00566102
(3aS,6Z,9S,10Z,11aR)-9-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one	101316778	Click to see	248.32	unknown	https://doi.org/10.1007/BF01374016
10-hydroxy-6,10,11-trimethyl-3-methylidene-4,5,8,9,11,11a-hexahydro-3aH-cyclodeca[b]furan-2-one	163011956	Click to see	264.36	unknown	https://doi.org/10.1111/J.2042-7158.1998.TB06924.X
11-Hydroperoxy-2-hydroxy-1-methyl-6-methylidene-4-oxatricyclo[8.3.1.03,7]tetradec-9-en-5-one	72725969	Click to see CC12CCC(C(=CCC3C(C1O)OC(=O)C3=C)C2)OO	280.32	unknown	https://doi.org/10.1016/S0031-9422(00)82424-3
4,5-Dihydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one	75072137	Click to see	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)81835-X
4,9-Dihydroxy-6,10-dimethyl-3-methylidene-3a,4,7,8,9,11a-hexahydrocyclodeca[b]furan-2-one	72731791	Click to see	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)82424-3
5,8-dihydroxy-6,10-dimethyl-3-methylidene-5,8,9,11a-tetrahydro-3aH-cyclodeca[b]furan-2,4-dione	162930746	Click to see	278.30	unknown	https://doi.org/10.1016/S0031-9422(00)81835-X
9-Hydroxy-6,10-dimethyl-3-methylene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2(3H)-one	5377194	Click to see	248.32	unknown	https://doi.org/10.1007/BF01374016
CID 4692	4692	Click to see CC1=CCCC2(C(O2)C3C(CC1)C(=C)C(=O)O3)C	248.32	unknown	https://doi.org/10.1016/S0031-9422(00)82424-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aR,6aR,6aR,6bR,8aS,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picen-3-ol	138113838	Click to see	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)97553-8 https://doi.org/10.1007/BF02535183
(6aR,6bR,8aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol	145706026	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C	426.70	unknown	https://doi.org/10.1007/BF02535183 https://doi.org/10.1016/S0031-9422(00)97553-8
Alpha-Amyrin	73170	Click to see	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)97553-8 https://doi.org/10.1007/BF02535183
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	https://doi.org/10.1007/BF02535183 https://doi.org/10.1016/S0031-9422(00)97553-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol	5997	Click to see	386.70	unknown	https://doi.org/10.1007/BF02535183
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24R)-5-Ergosten-3beta-ol	312822	Click to see	400.70	unknown	https://doi.org/10.1007/BF02535183
(3S,8S,9S,14S,17R)-17-[(2R,5R)-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-ol	134766514	Click to see	400.70	unknown	https://doi.org/10.1007/BF02535183
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1016/S0031-9422(00)81835-X https://doi.org/10.1016/S0031-9422(00)88544-1
(2S,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	12309073	Click to see	576.80	unknown	https://doi.org/10.1016/S0031-9422(00)81835-X
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1 https://doi.org/10.1016/S0031-9422(00)81835-X
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/10.1016/S0031-9422(00)88544-1 https://doi.org/10.1016/J.PHYTOCHEM.2004.08.019 https://doi.org/10.1007/BF02535183 https://doi.org/10.1016/S0031-9422(00)81835-X
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	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	https://doi.org/10.1016/S0031-9422(00)81835-X
Isofucosterol	5281326	Click to see	412.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.08.019
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	https://doi.org/10.1016/S0031-9422(00)81835-X
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1007/BF02535183 https://doi.org/10.1016/S0031-9422(00)81835-X https://doi.org/10.1016/J.PHYTOCHEM.2004.08.019 https://doi.org/10.1016/0378-8741(84)90002-3
Stigmasterol	5280794	Click to see	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)81835-X https://doi.org/10.1007/BF02535183 https://doi.org/10.1016/S0031-9422(00)97553-8
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
(4-Ethenyl-2,5-dimethylhexa-2,5-dienyl) acetate	78409237	Click to see CC(=C)C(C=C)C=C(C)COC(=O)C	194.27	unknown	https://doi.org/10.1016/0031-9422(81)84018-6
[(1S,3S)-2,2-dimethyl-3-prop-2-enylcyclopropyl]methyl acetate	163106225	Click to see	182.26	unknown	https://doi.org/10.1007/BF00580020
[(2E,4R)-4-ethenyl-2,5-dimethylhexa-2,5-dienyl] acetate	162943767	Click to see	194.27	unknown	https://doi.org/10.1016/0031-9422(81)84018-6
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(4S)-3,3,6-trimethylhepta-1,5-dien-4-ol	12308602	Click to see CC(=CC(C(C)(C)C=C)O)C	154.25	unknown	https://doi.org/10.1016/0031-9422(81)84018-6
3,3,6-Trimethyl-1,5-heptadien-4-ol	100197	Click to see	154.25	unknown	https://doi.org/10.1016/0031-9422(75)85347-7 https://doi.org/10.1016/0031-9422(81)84018-6
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(E)-2,5,5-Trimethylhepta-3,6-dien-2-ol	5315406	Click to see CC(C)(C=C)C=CC(C)(C)O	154.25	unknown	https://doi.org/10.1016/0031-9422(81)84018-6
2,5,5-Trimethyl-3,6-heptadien-2-ol	117738	Click to see CC(C)(C=C)C=CC(C)(C)O	154.25	unknown	https://doi.org/10.1016/0031-9422(81)84018-6
3-Ethenyl-2,5-dimethyl-4-hexen-2-ol	519843	Click to see	154.25	unknown	https://doi.org/10.1016/0031-9422(75)85347-7
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
Artemisia ketone	68346	Click to see	152.23	unknown	https://doi.org/10.1016/0031-9422(75)85347-7 https://doi.org/10.1016/J.PHYTOCHEM.2004.08.019
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
Bicyclo(3.1.0)hexan-2-one, 5-(1-methylethyl)-	92784	Click to see	138.21	unknown	https://doi.org/10.1080/10412905.1999.9701169
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
(2S,5R)-2-[(2S,5R)-5-ethenyl-5-methyloxolan-2-yl]-5-hydroxy-6-methylhept-6-en-3-one	162972326	Click to see	252.35	unknown	https://doi.org/10.1016/S0031-9422(00)84096-0
(2S,5S)-2-[(2S,5R)-5-ethenyl-5-methyloxolan-2-yl]-5-hydroxy-6-methylhept-6-en-3-one	162972328	Click to see	252.35	unknown	https://doi.org/10.1016/S0031-9422(00)84096-0
2-(5-Ethenyl-5-methyloxolan-2-yl)-5-hydroxy-6-methylhept-6-en-3-one	14707390	Click to see CC(C1CCC(O1)(C)C=C)C(=O)CC(C(=C)C)O	252.35	unknown	https://doi.org/10.1016/S0031-9422(00)84096-0
> Organoheterocyclic compounds / Oxanes
(-)-2,6,6-Trimethyl-2(R)-vinyltetrahydropyran-5-one	101607907	Click to see CC1(C(=O)CCC(O1)(C)C=C)C	168.23	unknown	https://doi.org/10.1007/BF00574201
(3R,6R)-6-ethenyl-2,2,6-trimethyloxan-3-ol	6428574	Click to see CC1(C(CCC(O1)(C)C=C)O)C	170.25	unknown	https://doi.org/10.1007/BF00574201
2H-Pyran-3-ol, 6-ethenyltetrahydro-2,2,6-trimethyl-, 3-acetate	92524	Click to see	212.28	unknown	https://doi.org/10.1007/BF00574201
2H-Pyran-3-ol, 6-ethenyltetrahydro-2,2,6-trimethyl-, 3-acetate, (3R,6R)-rel-	21116838	Click to see CC(=O)OC1CCC(OC1(C)C)(C)C=C	212.28	unknown	https://doi.org/10.1007/BF00574201
2H-Pyran-3(4H)-one, 6-ethenyldihydro-2,2,6-trimethyl-	549336	Click to see	168.23	unknown	https://doi.org/10.1007/BF00574201
Linalool oxide pyranoid, (+-)-	26396	Click to see	170.25	unknown	https://doi.org/10.1007/BF00574201
> Organoheterocyclic compounds / Oxolanes
(E,2S)-2-[(2S,5R)-5-ethenyl-5-methyloxolan-2-yl]-6-hydroperoxy-6-methylhept-4-en-3-one	12132774	Click to see	268.35	unknown	https://doi.org/10.1016/S0031-9422(00)84096-0
2-(5-Ethenyl-5-methyloxolan-2-yl)-6-hydroperoxy-6-methylhept-4-en-3-one	78410102	Click to see CC(C1CCC(O1)(C)C=C)C(=O)C=CC(C)(C)OO	268.35	unknown	https://doi.org/10.1016/S0031-9422(00)84096-0
2-(5-Ethenyl-5-methyloxolan-2-yl)-6-hydroxy-6-methylhept-4-en-3-one	435004	Click to see	252.35	unknown	https://doi.org/10.1016/S0031-9422(00)84096-0
2-(5-Ethenyl-5-methyloxolan-2-yl)propanoic acid	14059543	Click to see	184.23	unknown	https://doi.org/10.1016/S0031-9422(00)84096-0
2-Hydroxyisodavanone D	12132773	Click to see CC(C1CCC(O1)(C)C=C)C(=O)C=CC(C)(C)O	252.35	unknown	https://doi.org/10.1016/S0031-9422(00)84096-0
3-[1-(5-Ethenyl-5-methyloxolan-2-yl)ethyl]-6,6-dimethyl-1,2-dioxin-3-ol	101652690	Click to see	268.35	unknown	https://doi.org/10.1016/S0031-9422(00)84096-0
> Organoheterocyclic compounds / Tetrahydrofurans
(2R)-2-[(2R,5S)-5-ethenyl-5-methyloxolan-2-yl]propanoic acid	131221986	Click to see CC(C1CCC(O1)(C)C=C)C(=O)O	184.23	unknown	https://doi.org/10.1016/S0031-9422(00)84096-0
(3S)-3-[(1S)-1-[(2S,5R)-5-ethenyl-5-methyloxolan-2-yl]ethyl]-6,6-dimethyl-1,2-dioxin-3-ol	163035197	Click to see	268.35	unknown	https://doi.org/10.1016/S0031-9422(00)84096-0
Davanone	519782	Click to see CC(C1CCC(O1)(C)C=C)C(=O)CC=C(C)C	236.35	unknown	https://doi.org/10.1016/S0031-9422(00)84096-0
Davanone D	88556	Click to see	236.35	unknown	https://doi.org/10.1016/S0031-9422(00)84096-0
Hydroxydavanone	5477854	Click to see	252.35	unknown	https://doi.org/10.1016/S0031-9422(00)84096-0
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see	192.17	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1
> 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/10.1016/0031-9422(83)83035-0 https://doi.org/10.1007/S10600-011-9906-4 https://doi.org/10.1016/S0031-9422(00)81835-X https://doi.org/10.1016/S0031-9422(99)00021-7
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1016/S0031-9422(99)00021-7
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	302.23	unknown	https://doi.org/10.1007/BF02323285
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin	5281675	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O	448.40	unknown	https://doi.org/10.1007/S10600-011-9906-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Apigenin 7-O-glucuronide	5319484	Click to see	446.40	unknown	https://doi.org/10.1016/S0031-9422(99)00021-7
DiosMetin 7-O-beta-D-Glucuronide	54462250	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	476.40	unknown	https://doi.org/10.1016/S0031-9422(99)00021-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Quercitrin	5280459	Click to see	448.40	unknown	https://doi.org/10.1007/BF02323285
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-(4-methoxyphenyl)-7-(((2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one	5291487	Click to see	446.40	unknown	https://doi.org/10.1007/S10600-011-9906-4
Apigenin 7-O-glucoside	5280704	Click to see	432.40	unknown	https://doi.org/10.1007/S10600-011-9906-4 https://doi.org/10.1016/S0031-9422(99)00021-7
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	https://doi.org/10.1007/S10600-011-9906-4
Npc85473	5385553	Click to see	432.40	unknown	https://doi.org/10.1007/S10600-011-9906-4
Tilianin	5321954	Click to see	446.40	unknown	https://doi.org/10.1007/S10600-011-9906-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol	5280666	Click to see	300.26	unknown	https://doi.org/10.1111/J.2042-7158.1998.TB06924.X https://doi.org/10.1016/S0031-9422(99)00021-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin	5280442	Click to see	284.26	unknown	https://doi.org/10.1007/S10600-011-9906-4
Diosmetin	5281612	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.1111/J.2042-7158.1998.TB06924.X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Axillarin	5281603	Click to see	346.30	unknown	https://doi.org/10.1016/S0031-9422(99)00021-7
Eupatilin	5273755	Click to see	344.30	unknown	https://doi.org/10.1016/S0031-9422(00)90050-5
Hispidulin	5281628	Click to see	300.26	unknown	https://doi.org/10.1016/S0031-9422(99)00021-7
Jaceosidin	5379096	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O	330.29	unknown	https://doi.org/10.1111/J.2042-7158.1998.TB06924.X
Santin	5281695	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC	344.30	unknown	https://doi.org/10.1016/J.JEP.2017.02.023
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Apigenin trimethyl ether	79730	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC	312.30	unknown	https://doi.org/10.1016/S0031-9422(00)81835-X
Eupatorin	97214	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O	344.30	unknown	https://doi.org/10.1111/J.2042-7158.1998.TB06924.X
Pedalitin	31161	Click to see	316.26	unknown	https://doi.org/10.1016/S0031-9422(99)00021-7

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Tanacetum vulgare

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