Tanacetum parthenium, also known as feverfew, is a flowering plant in the daisy family that is often grown as an ornamental plant. It is a herbaceous perennial with pungently-scented leaves and daisy-like flowers. Native to Eurasia, it has spread around the world and is now found in Europe, North America, and Chile. In traditional medicine, feverfew has been used to treat headaches, but there is no scientific evidence to support this claim. It contains a compound called parthenolide, which is being studied for its potential anti-cancer properties. Feverfew is also used as a dietary supplement, but the amount of parthenolide in these supplements can vary greatly. Long-term use of feverfew may cause withdrawal symptoms and allergic reactions, and it should not be taken by pregnant women. The word "feverfew" comes from the Latin word for "fever reducer," although it is no longer used for this purpose. It has a long history of medicinal use, dating back to the first century, and is still used in traditional herbal medicine.

Synonyms Top

Scientific name	Authority	First published in
Pyrethrum persicum	Boiss.	Diagn. Pl. Orient. 6: 89 (1846)
Pontia matricaria	Bubani	Fl. Pyren. 2: 220 (1899)
Pyrethrum buschianum	Sosn.	Zhurn. Russk. Bot. Obshch. 14: 90 (1929)
Leucanthemum parthenium	Gren. & Godr.	Fl. France 2: 145 (1850)
Chrysanthemum praealtum	Vent.	Descr. Pl. Nouv. : t. 43 (1801)
Pyrethrum praealtum	(Vent.) Tzvelev	Fl. URSS xxvi. 208 (1961), in obs.
Matricaria pulverulenta	Poir.	Encycl. , Suppl. 3: 605 (1814)
Tanacetum partheniifolium	Sch.Bip.	Tanaceteen : 56 (1844)
Chrysanthemum parthenifolium	Pers.	Syn. Pl. 2(2): 462 (1807)
Chrysanthemum parthenium	(L.) Pers.	462 1807
Pyrethrum demetrii	Manden.	Zametki Sist. Geogr. Rast. 22: 60 (1961)
Pyrethrum parthenifolium	Willd.	Sp. Pl., ed. 4 , 3: 2156 (1803)
Tanacetum grossheimii	(Sosn.) Muradyan	Biol. Zhurn. Armenii 23(2): 90 (1970)
Pyrethrum glanduliferum	Sommier & Levier	Nuovo Giorn. Bot. Ital. , n.s., 2: 87 (1895)
Pyrethrum parthenium	(L.) J.E.Smith
Tanacetum demetrii	(Manden.) K.Bremer & Humphries	Bull. Nat. Hist. Mus. (London), Bot. 23(2): 102 (1993)
Matricaria eximia	hort.	Vilm. Blumengärtn. ed. 3 1: 509, in syn. (1894)
Tanacetum glanduliferum	(Sommier & Levier) K.Bremer & Humphries	Bull. Nat. Hist. Mus. (London), Bot. 23(2): 102 (1993)
Pyrethrum matricaria	gesn. ex Rupr.	Flora Ingrica 1: 573 1860
Matricaria praealta	Poir.	Encycl. , Suppl. 3: 602 (1814)
Chamaemelum parthenium	(L.) E.H.L.Krause	Deutschl. Fl. 13: 205 (1905)
Chrysanthemum parthenifolium	B.Fedtsch.	Rastit. Turkest. 737 (1915).
Pyrethrum grossheimii	Sosn.	Beih. Bot. Centralbl. 44(2): 243 (1927)
Tanacetum persicum	(Boiss.) Mozaff.	Iran. J. Bot. 11(1): 126 (2005)
Dendranthema parthenium	(L.) Des Moul.	Actes Soc. Linn. Bordeaux 20: 561 (1855)
Chrysanthemum parthenium	(L.) Bernh.	Syst. Verz. Erf. : 145 (1800)
Pyrethrum fruticosum	Spreng. ex DC.	Prodr. 6: 45 (1838)
Leucanthemum odoratum	Dulac	Fl. Hautes-Pyrénées : 504 (1867)
Pyrethrum latilobum	(Sosn.) Sosn.	Zametki Sist. Geogr. Rast. 15: 6 (1949)
Parthenium matricaria	Gueldenst.	Reis. Russland 2: 25 (1791)
Matricaria vulgaris	Gray	Nat. Arr. Brit. Pl. ii. 454
Pyrethrum parthenium	Sm.	Fl. Brit. 2: 900 (1800)
Pyrethrum sericeum var. divaricatum	(Sosn.) Sosn.	Sosn. in Grossgejm, Fl. Kavk. 4. 1934. 137 1934
Matricaria parthenium	L.	Sp. Pl. : 890 (1753)
Matricaria parthenifolia	Poir.	Encycl. , Suppl. 3: 608 (1814)
Tanacetum sevanense	(Sosn. ex Grossh.) K.Bremer & Humphries	Bull. Nat. Hist. Mus. (London), Bot. 23(2): 103 (1993)
Pyrethrum sevanense	Sosn. ex Grossh.	Fl. Kavkaza 4: 137 (1934)
Parthenium matricaria	gesn. ex Rupr.	Fl. Ingrica : 583 (1856)
Matricaria latifolia	Gilib.	Fl. Lit. Inch. 1: 220 (1782)
Matricaria alba	hort.	Vilm. Blumengärtn. ed. 3 1: 509, in syn. (1894)
Pyrethrum divaricatum	(Sosn.) Sosn.	Zametki Sist. Geogr. Rast. 15: 5 (1949)
Matricaria odorata	Lam.	Fl. Franç. 2: 136 (1779)
Pyrethrum eximium	hort.	Vilm. Blumengärtn. ed. 3 1: 509, in syn. (1894)
Matricaria florida	Salisb.	Prodr. Stirp. Chap. Allerton : 203 (1796)
Chrysanthemum parthenifolium f. sanguineum	Parsa	Fl. Iran 10: 64 (1980)
Tanacetum parthenium var. praealtum	(Vent.) B.Bock	Bull. Soc. Bot. Centre-Ouest 42: 274 (2012)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	feverfew
Spanish	hierba de altamira
Spanish	santa maría blanca
Spanish	santa maria blanca
Spanish	santa maría
Spanish	santa maria
Spanish	magarza amarilla
Spanish	madrehuela rosea
Spanish	madrehuela doble
Spanish	flor de santos
Spanish	flor de la calentura
Spanish	cochitzapotl
Spanish	artemiza
Spanish	chapote
Spanish	gamaza
ang	adreminte
Arabic	أقحوان زهرة الذهب
Belarusian	пірэтрум дзявочы
Catalan	botonets
Catalan	grande camomille
Catalan	segura
Czech	řimbaba obecná
Welsh	wermod wen
Danish	matrem
German	mutterkraut
German	zierkamille
German	fieberkraut
German	grande camomille
Estonian	lõhnav püreeter
Estonian	lõhnav neitsikummel
Persian	بابونهٔ گاوی
Persian	بابونه اروپایی
Persian	بابونه گاوی
Finnish	reunuspäivänkakkara
Finnish	reunuspietaryrtti
French	partenelle
French	pyrèthre doré
French	grande camomille
Irish	lus deartán
Manx	bossan pheddyr
Croatian	povratić
Hungarian	őszi margitvirág
Japanese	ナツシロギク
Lithuanian	grande camomille
Macedonian	дива камилица
Norwegian Bokmål	matrem
Dutch	moederkruid
pdc	meederle
Polish	wrotycz maruna
Quechua	santa mariya
Romanian	spilcuță
Romanian	spilcuţă
Russian	aphanostephus pinulensis
Russian	Пиретрум девичий
Russian	Пижма девичья
Slovak	rimbaba obyčajná
Swedish	mattram
Swedish	grande camomille
vec	maresina
vec	maresìna
Chinese	短舌匹菊

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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

Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Azores
  - Canary Islands
  - Cape Verde
  - Madeira
- Northeast Tropical Africa
  - Ethiopia
- Northern Africa
  - Algeria
  - Morocco
- Western Indian Ocean
  - Mauritius
  - Réunion

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - China Southeast
  - Hainan
  - Inner Mongolia
  - Manchuria
  - Qinghai
  - Tibet
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Western Asia
  - Afghanistan
  - Cyprus
  - East Aegean Islands
  - Iran
  - Iraq
  - Lebanon-Syria
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - India
  - Pakistan
  - West Himalaya
- Malesia
  - Borneo
  - Malaya
  - Philippines
  - Sulawesi
  - Sumatera

Australasia click to expand
- Australia
  - New South Wales
  - Northern Territory
  - Queensland
  - South Australia
  - Tasmania
  - Victoria
  - Western Australia
- New Zealand
  - Chatham Islands
  - New Zealand North
  - New Zealand South

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - East European Russia
  - Krym
  - North European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Belgium
  - Czechoslovakia
  - Germany
  - Hungary
  - Netherlands
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Northern America click to expand
- Eastern Canada
  - Newfoundland
  - Ontario
- Mexico
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southeast
  - Mexico Southwest
- North-central U.S.A.
  - Illinois
  - Minnesota
  - Missouri
  - 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
- Southeastern U.S.A.
  - Alabama
  - Delaware
  - Kentucky
  - Maryland
  - Mississippi
  - North Carolina
  - South Carolina
- Southwestern U.S.A.
  - Nevada
  - Utah
- Western Canada
  - British Columbia

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Cuba
  - Dominican Republic
- Central America
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Panamá
- Northern South America
  - Venezuela
- Southern South America
  - Argentina Northeast
  - Argentina Northwest
  - Argentina South
  - Chile Central
  - Chile North
  - Chile South
  - 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-0000079801
UNII	6GE7Z0761K
Flora of Alabama	1029
Canadensys	3604
USDA Plants	TAPA6
Tropicos	2701375
INPN	125469
Flora of Italy	5697
KEW	urn:lsid:ipni.org:names:252460-1
The Plant List	gcc-36373
Missouri Botanical Garden	277249
PFAF	Tanacetum parthenium
Open Tree Of Life	488828
Observations.org	7535
NCBI Taxonomy	127999
NBN Atlas	NHMSYS0000464153
Nature Serve	2.150432
IPNI	252460-1
iNaturalist	54520
GBIF	3118430
Freebase	/m/058sq5
WisFlora	5199
EPPO	CHYPA
EOL	468397
Elurikkus	7659
Calflora (Californian flora)	7919
USDA GRIN	104584
Wikipedia	Tanacetum_parthenium
CMAUP	NPO11429
CMAUP	NPO9049

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_964204775.1	daTanPart1.hap1.1	Chromosome	WELLCOME SANGER INSTITUTE	2024-07-27	54.0x	1.98 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

Edible Herbal Medicines as an Alternative to Common Medication for Sleep Disorders: A Review Article

Hosseini A, Mobasheri L, Rakhshandeh H, Rahimi VB, Najafi Z, Askari VR

Curr Neuropharmacol

22-Jun-2024

PMCID:	PMC10964091
doi:	10.2174/1570159X21666230621143944
PMID:	37345244

A critical assessment of Traditional Chinese Medicine databases as a source for drug discovery

Wang Y, Liu M, Jafari M, Tang J

Front Pharmacol

26-Apr-2024

PMCID:	PMC11082401
doi:	10.3389/fphar.2024.1303693
PMID:	38738181

Ferroptosis targeting natural compounds as a promising approach for developing potent liver cancer agents

Pandey P, Elsori D, Kumar R, Lakhanpal S, Rautela I, Alqahtani TM, Ahmad F, Iqbal D, Khan F

Front Pharmacol

26-Apr-2024

PMCID:	PMC11082342
doi:	10.3389/fphar.2024.1399677
PMID:	38738178

Anti‐inflammatory effect of Trichospira verticillata via suppression of the NLRP3 inflammasome in neutrophilic asthma

Yang H, Park G, Lee S, Lee S, Kim Y, Zamora NA, Yi D, Kim S, Choi CW, Choi S, Park YH

J Cell Mol Med

26-Apr-2024

PMCID:	PMC11048967
doi:	10.1111/jcmm.18356
PMID:	38668995

A Comparison between Bulgarian Tanacetum parthenium Essential Oil from Two Different Locations

Lechkova B, Benbassat N, Karcheva-Bahchevanska D, Ivanov K, Peychev L, Peychev Z, Dyankov S, Georgieva-Dimova Y, Kraev K, Ivanova S

Molecules

25-Apr-2024

PMCID:	PMC11085318
doi:	10.3390/molecules29091969
PMID:	38731460

Secondary metabolic profiling, antioxidant potential, enzyme inhibitory activities and in silico and ADME studies: a multifunctional approach to reveal medicinal and industrial potential of Tanacetum falconeri

Tousif MI, Abbas Z, Nazir M, Saleem M, Tauseef S, Hassan A, Ali S, Ahmed M, Khan J, Zengin G, Hashem A, Almutairi KF, Avila-Quezada GD, Abd-Allah EF

BMC Complement Med Ther

22-Apr-2024

PMCID:	PMC11034146
doi:	10.1186/s12906-024-04459-5
PMID:	38649994

Influence of Abiotic and Biotic Elicitors on Organogenesis, Biomass Accumulation, and Production of Key Secondary Metabolites in Asteraceae Plants

Petrova M, Miladinova-Georgieva K, Geneva M

Int J Mol Sci

10-Apr-2024

PMCID:	PMC11050642
doi:	10.3390/ijms25084197
PMID:	38673783

Nanoformulated herbal compounds: enhanced antibacterial efficacy of camphor and thymol-loaded nanogels

Abdollahi A, Fereydouni N, Moradi H, Karimivaselabadi A, Zarenezhad E, Osanloo M

BMC Complement Med Ther

02-Apr-2024

PMCID:	PMC10985855
doi:	10.1186/s12906-024-04435-z
PMID:	38566054

Hypocretenolides: collective total syntheses and activities toward metastatic colon cancer

Chen B, Zhang X, Yang Y, Xu D, Wu Q, Wang S, Bao S, Zhang X, Ding Y, Wang L, Chen Y

Chem Sci

28-Mar-2024

PMCID:	PMC11062092
doi:	10.1039/d4sc01469c
PMID:	38699277

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

Phytocompounds targeting epigenetic modulations: an assessment in cancer

Khan A, Khan A, Khan MA, Malik Z, Massey S, Parveen R, Mustafa S, Shamsi A, Husain SA

Front Pharmacol

26-Mar-2024

PMCID:	PMC11002180
doi:	10.3389/fphar.2023.1273993
PMID:	38596245

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

LC/MS/MS and GC/MS/MS metabolic profiling of Leontodon hispidulus, in vitro and in silico anticancer activity evaluation targeting hexokinase 2 enzyme

Abd-El-Aziz NM, Hifnawy MS, Lotfy RA, Younis IY

Sci Rep

22-Mar-2024

PMCID:	PMC10959984
doi:	10.1038/s41598-024-57288-4
PMID:	38519553

Functional analysis of CYP71AV1 reveals the evolutionary landscape of artemisinin biosynthesis

Chen FY, Mu QY, Xu BY, Lei YC, Liu HY, Fang X

Front Plant Sci

21-Mar-2024

PMCID:	PMC10991709
doi:	10.3389/fpls.2024.1361959
PMID:	38576787

Computational identification of natural senotherapeutic compounds that mimic dasatinib based on gene expression data

Meiners F, Hinz B, Boeckmann L, Secci R, Sueto S, Kuepfer L, Fuellen G, Barrantes I

Sci Rep

15-Mar-2024

PMCID:	PMC10943199
doi:	10.1038/s41598-024-55870-4
PMID:	38491064

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
Phenethyl acetate	7654	Click to see CC(=O)OCCC1=CC=CC=C1	164.20	unknown	https://doi.org/10.1007/S004030050433
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	https://doi.org/10.1007/S004030050433
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Methyl Salicylate	4133	Click to see COC(=O)C1=CC=CC=C1O	152.15	unknown	https://doi.org/10.1007/S004030050433
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
(2R,3R,4S,4aR,10bR)-3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one	6543710	Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)O)O)OC2=O)O	328.27	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Ethylbenzaldehyde	20861	Click to see CCC1=CC=C(C=C1)C=O	134.17	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
4-Methylbenzaldehyde	7725	Click to see CC1=CC=C(C=C1)C=O	120.15	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
Benzaldehyde	240	Click to see C1=CC=C(C=C1)C=O	106.12	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol	244	Click to see C1=CC=C(C=C1)CO	108.14	unknown	https://doi.org/10.1007/S004030050433
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate	8785	Click to see CC(=O)OCC1=CC=CC=C1	150.17	unknown	https://doi.org/10.1007/S004030050433
Benzyl isobutyrate	7646	Click to see CC(C)C(=O)OCC1=CC=CC=C1	178.23	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
Benzyl isovalerate	7651	Click to see CC(C)CC(=O)OCC1=CC=CC=C1	192.25	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
Benzyl propionate	31219	Click to see CCC(=O)OCC1=CC=CC=C1	164.20	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol	7127	Click to see COC1=C(C=C(C=C1)CC=C)OC	178.23	unknown	https://doi.org/10.1007/S004030050433
> Benzenoids / Fluorenes
Malfodicfsixpo-kouxddqnsa-	10573587	Click to see CC1CC(C(NC1)C(C)C2=C(C3=C(C=C2)C4CC=C5CC(CCC5(C4C3)C)O)C)O	409.60	unknown	via CMAUP database
Veratramine	6070	Click to see CC1CC(C(NC1)C(C)C2=C(C3=C(C=C2)C4CC=C5CC(CCC5(C4C3)C)O)C)O	409.60	unknown	via CMAUP database
Veratrosine	23616879	Click to see CC1CC(C(NC1)C(C)C2=C(C3=C(C=C2)C4CC=C5CC(CCC5(C4C3)C)OC6C(C(C(C(O6)CO)O)O)O)C)O	571.70	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenediols / Catechols
Hispidin	54685921	Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=O)O2)O)O)O	246.21	unknown	via CMAUP database
Hypholomine B	54730031	Click to see C1=CC(=C(C=C1C=CC2=CC3=C(C(C(O3)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=O)O5)O)C(=O)O2)O)O	490.40	unknown	via CMAUP database
Interfungin A	54726789	Click to see CC(=O)C=C(C(=CC1=CC(=C(C=C1)O)O)C2=C(C=C(OC2=O)C=CC3=CC(=C(C=C3)O)O)O)O	464.40	unknown	via CMAUP database
Phellinstatin	54728876	Click to see C1=CC(=C(C=C1C=CC2=CC(=C(C(=O)O2)C3=CC(=C(C=C3C=CC4=CC5=C(C(C(O5)C6=CC(=C(C=C6)O)O)C7=CC(=CC(=O)O7)O)C(=O)O4)O)O)O)O)O	734.60	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see COC1=C(C=CC(=C1)CC=C)O	164.20	unknown	https://doi.org/10.1007/S004030050433
Methyldavallialactone	54726724	Click to see CC1=CC(=O)C(C(O1)C2=CC(=C(C=C2)O)O)C3=C(C=C(OC3=O)C=CC4=CC(=C(C=C4)O)OC)O	478.40	unknown	via CMAUP database
> Hydrocarbon derivatives / Tropones
Colchicine	6167	Click to see CC(=O)NC1CCC2=CC(=C(C(=C2C3=CC=C(C(=O)C=C13)OC)OC)OC)OC	399.40	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Ethane	6324	Click to see CC	30.07	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene	7461	Click to see CC1=CCC(=CC1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1007/S004030050433 https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(2-Hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]non-3-en-8-yl) 3-methylbutanoate	163056799	Click to see CC#CC#CC=C1C=CC2(O1)CC(CO2)OC(=O)CC(C)C	300.30	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
[(2E,5S,8R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]non-3-en-8-yl] 3-methylbutanoate	163056801	Click to see CC#CC#CC=C1C=CC2(O1)CC(CO2)OC(=O)CC(C)C	300.30	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
[(2Z,5S,8R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]non-3-en-8-yl] 3-methylbutanoate	163056800	Click to see CC#CC#CC=C1C=CC2(O1)CC(CO2)OC(=O)CC(C)C	300.30	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
cis-3-Hexen-1-ol	5281167	Click to see CCC=CCCO	100.16	unknown	https://doi.org/10.1007/S004030050433
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Dehydrosaussurea lactone	556920	Click to see CC(=C)C1C2C(CCC1(C)C=C)C(=C)C(=O)O2	232.32	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1
Dehydrosaussurealactone	44409528	Click to see CC(=C)C1C2C(CCC1(C)C=C)C(=C)C(=O)O2	232.32	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)-	5281553	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1007/S004030050433
beta-Ocimene, (3Z)-	5320250	Click to see CC(=CCC=C(C)C=C)C	136.23	unknown	https://doi.org/10.1007/S004030050433
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1007/S004030050433
Linalyl propionate	61098	Click to see CCC(=O)OC(C)(CCC=C(C)C)C=C	210.31	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1007/S004030050433
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol	10364	Click to see CC1=C(C=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
Cuminaldehyde	326	Click to see CC(C)C1=CC=C(C=C1)C=O	148.20	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R https://doi.org/10.1007/S004030050433
Thymol	6989	Click to see CC1=CC(=C(C=C1)C(C)C)O	150.22	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphor	444294	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.1039/J39700002689
(1,7,7-Trimethyl-2-bicyclo[2.2.1]heptanyl) 2-methylbut-2-enoate	527422	Click to see CC=C(C)C(=O)OC1CC2CCC1(C2(C)C)C	236.35	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
(1,7,7-Trimethylbicyclo[2.2.1]heptan-2-yl)acetic acid	20327362	Click to see CC1(C2CCC1(C(C2)CC(=O)O)C)C	196.29	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene	6451618	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1989.9699438
(1S,5R,6S)-2,7,7-Trimethylbicyclo[3.1.1]hept-2-en-6-ol	71361104	Click to see CC1=CCC2C(C1C2(C)C)O	152.23	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
(2,7,7-Trimethyl-6-bicyclo[3.1.1]hept-2-enyl) 2-methylbut-2-enoate	163084257	Click to see CC=C(C)C(=O)OC1C2CC=C(C1C2(C)C)C	234.33	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
(4,6,6-Trimethyl-7-oxo-2-bicyclo[3.1.1]hept-3-enyl) acetate	101415502	Click to see CC1=CC(C2C(=O)C1C2(C)C)OC(=O)C	208.25	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
(S)-cis-Verbenol	87839	Click to see CC1=CC(C2CC1C2(C)C)O	152.23	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
[(1S,2S,4S)-1,7,7-trimethyl-2-bicyclo[2.2.1]heptanyl] (Z)-2-methylbut-2-enoate	162901484	Click to see CC=C(C)C(=O)OC1CC2CCC1(C2(C)C)C	236.35	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
[(1S,2S,5S)-4,6,6-trimethyl-7-oxo-2-bicyclo[3.1.1]hept-3-enyl] acetate	162846546	Click to see CC1=CC(C2C(=O)C1C2(C)C)OC(=O)C	208.25	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
[(1S,5R,6S)-2,7,7-trimethyl-6-bicyclo[3.1.1]hept-2-enyl] 3-methylbutanoate	162874495	Click to see CC1=CCC2C(C1C2(C)C)OC(=O)CC(C)C	236.35	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
[(1S,5R,6S)-2,7,7-trimethyl-6-bicyclo[3.1.1]hept-2-enyl] acetate	91753441	Click to see CC1=CCC2C(C1C2(C)C)OC(=O)C	194.27	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1007/S004030050433 https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
2,7,7-Trimethylbicyclo[3.1.1]hept-2-en-6-yl acetate	162747	Click to see CC1=CCC2C(C1C2(C)C)OC(=O)C	194.27	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
3-Carene	26049	Click to see CC1=CCC2C(C1)C2(C)C	136.23	unknown	https://doi.org/10.1007/S004030050433
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R https://doi.org/10.1007/S004030050433
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R https://doi.org/10.1007/S004030050433
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)-	17868	Click to see CC1=CCC2(C1C2)C(C)C	136.23	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R https://doi.org/10.1080/10412905.1989.9699438
Bicyclo[3.1.1]hept-2-en-6-ol, 2,7,7-trimethyl-, (1S,5R,6R)-	10888100	Click to see CC1=CCC2C(C1C2(C)C)O	152.23	unknown	https://doi.org/10.1007/S004030050433
Bornyl acetate	6448	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1007/S004030050433 https://doi.org/10.1016/0031-9422(82)85253-9 https://doi.org/10.1080/10412905.1989.9699438
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R https://doi.org/10.1007/S004030050433
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.1007/S004030050433 https://doi.org/10.1039/J39700002689 https://doi.org/10.1016/S0031-9422(00)88544-1 https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
Camphor (synthetic)	159055	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1
Chrysanthenol	527032	Click to see CC1=CCC2C(C1C2(C)C)O	152.23	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R https://doi.org/10.1007/S004030050433 https://doi.org/10.1016/0031-9422(82)85253-9
Chrysanthenyl isovalerate	529750	Click to see CC1=CCC2C(C1C2(C)C)OC(=O)CC(C)C	236.35	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
CID 44630107	44630107	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1007/S004030050433
cis-Chrysanthenyl angelate	91751301	Click to see CC=C(C)C(=O)OC1C2CC=C(C1C2(C)C)C	234.33	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
Exo-1,7,7-trimethylbicyclo[2.2.1]hept-2-yl acetate	6950273	Click to see CC(=O)OC1CC2CCC1(C2(C)C)C	196.29	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
Pinocarvone	121719	Click to see CC1(C2CC1C(=C)C(=O)C2)C	150.22	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
Sabinen	18818	Click to see CC(C)C12CCC(=C)C1C2	136.23	unknown	https://doi.org/10.1007/S004030050433 https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
trans-Chrysanthenyl acetate	10899521	Click to see CC1=CCC2C(C1C2(C)C)OC(=O)C	194.27	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
Tricyclene	79035	Click to see CC1(C2CC3C1(C3C2)C)C	136.23	unknown	https://doi.org/10.1007/S004030050433
Verbenol	61126	Click to see CC1=CC(C2CC1C2(C)C)O	152.23	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)-	11230	Click to see CC1=CCC(CC1)(C(C)C)O	154.25	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1007/S004030050433 https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
alpha-PHELLANDRENE	7460	Click to see CC1=CCC(C=C1)C(C)C	136.23	unknown	https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1007/S004030050433
alpha-Terpinene	7462	Click to see CC1=CC=C(CC1)C(C)C	136.23	unknown	https://doi.org/10.1007/S004030050433 https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
Alpha-Terpineol	17100	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
Beta-Phellandrene	11142	Click to see CC(C)C1CCC(=C)C=C1	136.23	unknown	https://doi.org/10.1007/S004030050433
Limonene, (+/-)-	22311	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R https://doi.org/10.1007/S004030050433
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
(R,R)-chrysanthemol	2724508	Click to see CC(=CC1C(C1(C)C)CO)C	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1
Chrysanthemol	110685	Click to see CC(=CC1C(C1(C)C)CO)C	154.25	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-delta-Cadinene	441005	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1989.9699438
(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/10.1007/S004030050433
alpha-Curcumene	92139	Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C	202.33	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
Alpha-Farnesene	5281516	Click to see CC(=CCCC(=CCC=C(C)C=C)C)C	204.35	unknown	https://doi.org/10.1007/S004030050433
beta Farnesene	15228937	Click to see CCC(=C)CCC=C(C)CCC=C(C)C	206.37	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R https://doi.org/10.1080/10412905.1989.9699438 https://doi.org/10.1007/S004030050433
beta-CARYOPHYLLENE OXIDE	1742210	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1007/S004030050433
Cadina-1(10),4-diene	10223	Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C	204.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R https://doi.org/10.1007/S004030050433
Caryophyllene epoxide	14350	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	https://doi.org/10.1007/S004030050433
Copaene	19725	Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C	204.35	unknown	https://doi.org/10.1007/S004030050433 https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
Humulene	5281520	Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C	204.35	unknown	https://doi.org/10.1007/S004030050433 https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
Sesquichamene	97829	Click to see CC1=CCC2(CCCC(C23C1C3)(C)C)C	204.35	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Methyl 2-(4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalen-2-yl)prop-2-enoate	14707111	Click to see CC12CCCC(=C)C1CC(CC2)C(=C)C(=O)OC	248.36	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
Methyl-gamma-costate	14707110	Click to see CC12CCCC(=C)C1CC(CC2)C(=C)C(=O)OC	248.36	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1080/10412905.1989.9699438
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Epitaraxerol	344467	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1
Taraxerol	92097	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,2S,4R,7R,11S)-7-hydroxy-4-methyl-8,12-dimethylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradecan-13-one	15785646	Click to see CC12CCC(C(=C)CCC3C(C1O2)OC(=O)C3=C)O	264.32	unknown	https://doi.org/10.1055/S-2006-959596 https://doi.org/10.1039/P19960001979 https://doi.org/10.1002/PCA.2800030105 https://doi.org/10.1016/0031-9422(82)85253-9
(3aS,9R,10E,11aR)-9-hydroxy-10-methyl-3,6-dimethylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2,7-dione	162888070	Click to see CC1=CC2C(CCC(=C)C(=O)CC1O)C(=C)C(=O)O2	262.30	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
10-methyl-3,6-dimethylidene-7,8,11,11a-tetrahydro-3aH-cyclodeca[b]furan-2-one	163013751	Click to see CC1=CCCC(=C)C=CC2C(C1)OC(=O)C2=C	230.30	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1
4-Methyl-8,12-dimethylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradecane-7,13-dione	325152	Click to see CC12CCC(=O)C(=C)CCC3C(C1O2)OC(=O)C3=C	262.30	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
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/10.1016/0031-9422(82)85253-9
7-Hydroxy-4-methyl-8,12-dimethylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradecan-13-one	325150	Click to see CC12CCC(C(=C)CCC3C(C1O2)OC(=O)C3=C)O	264.32	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
9-Hydroxy-10-methyl-3,6-dimethylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2,7-dione	162888069	Click to see CC1=CC2C(CCC(=C)C(=O)CC1O)C(=C)C(=O)O2	262.30	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
Anhydroverlotorin epoxide	139597382	Click to see CC12CCC(=O)C(=C)CCC3C(C1O2)OC(=O)C3=C	262.30	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
Artemorin	5281428	Click to see CC1=CC2C(CCC(=C)C(CC1)O)C(=C)C(=O)O2	248.32	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
dimethyl (5R,5'S,6R,8S)-8-acetyloxy-5'-(furan-3-yl)-6-methyl-2'-oxospiro[2,3,4,6,7,8-hexahydronaphthalene-5,3'-oxolane]-1,1-dicarboxylate	101316809	Click to see CC1CC(C2=C(C13CC(OC3=O)C4=COC=C4)CCCC2(C(=O)OC)C(=O)OC)OC(=O)C	460.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(1S,2S,6S,9R,10R,12R,14S)-10-hydroxy-9,14-dimethyl-5-methylidene-3,13-dioxatetracyclo[7.5.0.02,6.012,14]tetradecan-4-one	101286231	Click to see CC12CCC3C(C1C4(C(O4)CC2O)C)OC(=O)C3=C	264.32	unknown	https://doi.org/10.1016/S0031-9422(96)00555-9
(3aR,5aS,6R,9aS,9bR)-6-hydroxy-5a-methyl-3,9-dimethylidene-3a,4,5,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-2-one	124708164	Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C	248.32	unknown	https://doi.org/10.1016/S0031-9422(00)85285-1
(3aS,5aS,6S,9aS,9bS)-6-hydroxy-5a,9-dimethyl-3-methylidene-4,5,6,7,9a,9b-hexahydro-3aH-benzo[g][1]benzofuran-2-one	163186658	Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O	248.32	unknown	https://doi.org/10.1016/S0031-9422(00)85285-1
1-beta-Hydroxyarbusculin A	60199554	Click to see CC12CCC3C(C1C(CCC2O)(C)O)OC(=O)C3=C	266.33	unknown	https://doi.org/10.1515/ZNC-2001-7-806
6-Hydroxy-5a-methyl-3,9-dimethylidenedecahydronaphtho[1,2-b]furan-2(3h)-one	98958	Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C	248.32	unknown	https://doi.org/10.1016/S0031-9422(00)85285-1 https://doi.org/10.1515/ZNC-2001-7-806 https://doi.org/10.1016/0031-9422(82)85253-9 https://doi.org/10.1016/S0031-9422(96)00555-9
Alantolactone	72724	Click to see CC1CCCC2(C1=CC3C(C2)OC(=O)C3=C)C	232.32	unknown	https://doi.org/10.1055/S-2006-957700
Armefolin	13944257	Click to see CC1=C2C3C(CCC2(C(CC1O)O)C)C(=C)C(=O)O3	264.32	unknown	https://doi.org/10.1515/ZNC-2001-7-806
Reynosin	482788	Click to see CC12CCC3C(C1C(=C)CCC2O)OC(=O)C3=C	248.32	unknown	https://doi.org/10.1515/ZNC-2001-7-806 https://doi.org/10.1016/0031-9422(82)85253-9 https://doi.org/10.1016/S0031-9422(96)00555-9
Santamarine	188297	Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O	248.32	unknown	https://doi.org/10.1515/ZNC-2001-7-806 https://doi.org/10.1016/S0031-9422(96)00555-9 https://doi.org/10.1016/J.JEP.2017.02.023
Sesquiterpene lactone CP-1	331391	Click to see CC1=CCC(C2(C1C3C(CC2)C(=C)C(=O)O3)C)O	248.32	unknown	https://doi.org/10.1016/J.JEP.2017.02.023 https://doi.org/10.1016/S0031-9422(00)85285-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1aR,7aS,10aS,10bS)-1a,5-dimethyl-8-methylidene-2,3,6,7,7a,8,10a,10b-octahydrooxireno[9,10]cyclodeca[1,2-b]furan-9(1aH)-one	6473881	Click to see CC1=CCCC2(C(O2)C3C(CC1)C(=C)C(=O)O3)C	248.32	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC538891/ https://doi.org/10.1016/0031-9422(82)85253-9
(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/10.1055/S-2006-957700 https://doi.org/10.1016/0021-9673(92)85036-S https://doi.org/10.1055/S-2006-959596 https://doi.org/10.1055/S-2002-33793 https://doi.org/10.1300/J133V04N01_04 https://doi.org/10.1111/J.1600-0536.1996.TB02217.X https://doi.org/10.1111/J.2042-7158.1997.TB06841.X https://doi.org/10.1021/NP50078A005 https://doi.org/10.1515/ZNC-2001-7-806 https://doi.org/10.1080/10575639508043219 https://doi.org/10.1021/NP50086A003 https://doi.org/10.1111/J.2042-7158.1988.TB07010.X https://doi.org/10.1002/(SICI)1099-1565(199603)7:2<86::AID-PCA287>3.0.CO;2-N https://doi.org/10.1016/0168-9452(96)04396-8 https://doi.org/10.1007/S004030050433 https://doi.org/10.1039/P19960001979 https://doi.org/10.1089/JMF.2006.9.55 https://doi.org/10.1093/JAOAC/83.4.789 https://doi.org/10.1111/J.2042-7158.1992.TB05510.X https://doi.org/10.1016/S0031-9422(96)00555-9 https://doi.org/10.1590/S0102-695X2008000300009 https://doi.org/10.1111/J.2042-7158.1992.TB03631.X https://doi.org/10.1021/JF980798U https://doi.org/10.1002/PCA.2800030105 https://doi.org/10.1055/S-2000-8637
(1S,2S,4R,5S,7E,11S)-5-hydroxy-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one	162941256	Click to see CC1=CCC(C2(C(O2)C3C(CC1)C(=C)C(=O)O3)C)O	264.32	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
(3aS,6E,9R,10E,11aR)-9-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one	12443214	Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)O	248.32	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
5-Hydroxy-4,8-dimethyl-12-methylidene-3,14-dioxatricyclo[9.3.0.02,4]tetradec-7-en-13-one	162941255	Click to see CC1=CCC(C2(C(O2)C3C(CC1)C(=C)C(=O)O3)C)O	264.32	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
9-Hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one	281981	Click to see CC1=CCC(C(=CC2C(CC1)C(=C)C(=O)O2)C)O	248.32	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
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)88544-1 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC538891/ https://doi.org/10.1254/JPHS.SC0060164 https://doi.org/10.1016/S0165-2478(01)00211-5 https://doi.org/10.1097/CMR.0B013E328333BBE4 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1573237/ https://doi.org/10.1016/J.CANLET.2007.03.002 https://doi.org/10.1093/CARCIN/BGI194 https://doi.org/10.1016/0031-9422(82)85253-9
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(14-Methyl-5,9-dimethylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-7-yl) 2-methylbut-2-enoate	163032959	Click to see CC=C(C)C(=O)OC1CC(=C)C2CC3C(C2C4C1C(=C)C(=O)O4)(O3)C	344.40	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
(14-Methyl-5,9-dimethylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-7-yl) 2-methylpropanoate	163042044	Click to see CC(C)C(=O)OC1CC(=C)C2CC3C(C2C4C1C(=C)C(=O)O4)(O3)C	332.40	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
(1R,2R,5S,9S,10S,11S)-2-hydroxy-2,11-dimethyl-6-methylidene-8,12,13-trioxatetracyclo[9.2.2.01,10.05,9]pentadec-14-en-7-one	10588629	Click to see CC1(CCC2C(C3C14C=CC3(OO4)C)OC(=O)C2=C)O	278.30	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
(1S,2R,5S,9S,10S,11R)-2-hydroxy-2,11-dimethyl-6-methylidene-8,12,13-trioxatetracyclo[9.2.2.01,10.05,9]pentadec-14-en-7-one	14219462	Click to see CC1(CCC2C(C3C14C=CC3(OO4)C)OC(=O)C2=C)O	278.30	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
(1S,2R,5S,9S,10S,11S)-2-hydroxy-2,11-dimethyl-6-methylidene-8,12,13-trioxatetracyclo[9.2.2.01,10.05,9]pentadec-14-en-7-one	14219461	Click to see CC1(CCC2C(C3C14C=CC3(OO4)C)OC(=O)C2=C)O	278.30	unknown	https://doi.org/10.1039/P19960001979 https://doi.org/10.1016/0031-9422(89)80150-5
(1S,2S,6R,7S,10R,12R,14S)-7-hydroxy-14-methyl-5,9-dimethylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-4-one	14829076	Click to see CC12C(O1)CC3C2C4C(C(CC3=C)O)C(=C)C(=O)O4	262.30	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
(1S,2S,6S,9R,10R,12S,14R)-9-hydroxy-9,14-dimethyl-5-methylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-4-one	102064887	Click to see CC1(CCC2C(C3C1CC4C3(O4)C)OC(=O)C2=C)O	264.32	unknown	https://doi.org/10.1016/S0031-9422(96)00555-9
(9-Hydroxy-9-methyl-3,6-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl) acetate	75596278	Click to see CC(=O)OC1CC(=C)C2CCC(C2C3C1C(=C)C(=O)O3)(C)O	306.40	unknown	https://doi.org/10.1111/J.2042-7158.1988.TB07010.X
[(1S,2S,6R,7S,10R,12R,14S)-14-methyl-5,9-dimethylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-7-yl] (Z)-2-methylbut-2-enoate	163032961	Click to see CC=C(C)C(=O)OC1CC(=C)C2CC3C(C2C4C1C(=C)C(=O)O4)(O3)C	344.40	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
[(1S,2S,6R,7S,10R,12R,14S)-14-methyl-5,9-dimethylidene-4-oxo-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-7-yl] 2-methylpropanoate	163042045	Click to see CC(C)C(=O)OC1CC(=C)C2CC3C(C2C4C1C(=C)C(=O)O4)(O3)C	332.40	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
2-Hydroxy-2,11-dimethyl-6-methylidene-8,12,13-trioxatetracyclo[9.2.2.01,10.05,9]pentadec-14-en-7-one	14219460	Click to see CC1(CCC2C(C3C14C=CC3(OO4)C)OC(=O)C2=C)O	278.30	unknown	https://doi.org/10.1002/PCA.2800030105 https://doi.org/10.1016/0031-9422(82)85253-9
9-Hydroxy-9,14-dimethyl-5-methylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradecan-4-one	162939147	Click to see CC1(CCC2C(C3C1CC4C3(O4)C)OC(=O)C2=C)O	264.32	unknown	https://doi.org/10.1016/S0031-9422(96)00555-9
Artecanin	442147	Click to see CC1(CCC2C(C3C14C(O4)C5C3(O5)C)OC(=O)C2=C)O	278.30	unknown	https://doi.org/10.1515/ZNC-2001-7-806 https://doi.org/10.1039/P19960001979 https://doi.org/10.1055/S-2006-959596 https://doi.org/10.1002/PCA.2800030105
Canin	442175	Click to see CC1(CCC2C(C3C14C(O4)C5C3(O5)C)OC(=O)C2=C)O	278.30	unknown	https://doi.org/10.1016/0031-9422(89)80150-5 https://doi.org/10.1515/ZNC-2001-7-806 https://doi.org/10.1039/P19960001979 https://doi.org/10.1055/S-2006-959596 https://doi.org/10.1002/PCA.2800030105
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(3S,4R,5S,6S)-2-[(3S,6E,8E,10E,12E,14E,16E,18E,20E,22E,24E)-2-hydroxy-25-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-2,6,10,14,19,23-hexamethylpentacosa-6,8,10,12,14,16,18,20,22,24-decaen-3-yl]oxy-6-methyloxane-3,4,5-triol	139585140	Click to see CC1C(C(C(C(O1)OC(CCC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C)C)C(C)(C)O)O)O)O	733.00	unknown	https://doi.org/10.1016/S0031-9422(96)00555-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(13alpha)-3alpha-(Benzoyloxy)-12beta-hydroxyursane-28-oic acid 28,12-lactone	100973316	Click to see CC1CCC23CCC4(C(C2C1C)C(CC5C4(CCC6C5(CCC(C6(C)C)OC(=O)C7=CC=CC=C7)C)C)OC3=O)C	560.80	unknown	via CMAUP database
(13alpha)-3alpha-Hydroxyursan-28-oic acid	100973318	Click to see CC1CCC2(CCC3(C(C2C1C)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C(=O)O	458.70	unknown	via CMAUP database
(1R,3aR,5aR,5bR,7aS,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol	7092625	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
(1R,4S,5S,8S,9R,10S,13S,14R,16R,17S,22R)-8-hydroxy-4,9,10,14,17,20,20-heptamethyl-24-oxahexacyclo[14.6.2.01,14.04,13.05,10.017,22]tetracosan-23-one	11070498	Click to see CC1C(CCC2C1(CCC3C2(CCC45C3(CC(C6(C4CC(CC6)(C)C)C)OC5=O)C)C)C)O	456.70	unknown	via CMAUP database
(1R,4S,5S,9R,10S,13S,14R,16R,17S,22R)-4,9,10,14,17,20,20-heptamethyl-24-oxahexacyclo[14.6.2.01,14.04,13.05,10.017,22]tetracosane-8,23-dione	10928543	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC45C3(CC(C6(C4CC(CC6)(C)C)C)OC5=O)C)C)C	454.70	unknown	via CMAUP database
[(1S,4R,5R,8R,10R,13R,14R,16R,17S,18S,19S,20R,23R)-23-methoxy-4,5,9,9,13,19,20-heptamethyl-24-oxahexacyclo[14.6.2.01,18.04,17.05,14.08,13]tetracosan-10-yl] benzoate	100973317	Click to see CC1CCC23CCC4(C(C2C1C)C(CC5C4(CCC6C5(CCC(C6(C)C)OC(=O)C7=CC=CC=C7)C)C)OC3OC)C	576.80	unknown	via CMAUP database
3alpha-(Benzoyloxy)-16alpha-hydroxy-D:A-friedoolean-27-oic acid 27,16-lactone	11060762	Click to see CC1C(CCC2C1(CCC3C2(CCC45C3(CC(C6(C4CC(CC6)(C)C)C)OC5=O)C)C)C)OC(=O)C7=CC=CC=C7	560.80	unknown	via CMAUP database
Friedelin	91472	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C	426.70	unknown	via CMAUP database
Methyl Ursolate	636516	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC	470.70	unknown	via CMAUP database
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
Ergosterol peroxide	5351516	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C	428.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
22,23-Dihydrobrassicasterol	5283637	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/S0031-9422(00)97553-8 https://doi.org/10.1016/0031-9422(96)00156-2
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/0031-9422(96)00156-2 https://doi.org/10.1016/S0031-9422(00)97553-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
Ethinyl Estradiol	5991	Click to see CC12CCC3C(C1CCC2(C#C)O)CCC4=C3C=CC(=C4)O	296.40	unknown	https://doi.org/10.1002/(SICI)1099-1026(199611)11:6<367::AID-FFJ598>3.0.CO;2-R
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / 22,26-epiminocholestanes
(3S,8R,9S,10R,12S,13S,14S,17R)-10,13-dimethyl-17-[(1S)-1-[(3S)-3-methyl-2,3,4,5-tetrahydropyridin-6-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,12-diol	101861833	Click to see CC1CCC(=NC1)C(C)C2CCC3C2(C(CC4C3CC=C5C4(CCC(C5)O)C)O)C	413.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,18S,19S,22S,23R,25R)-10,12,13,14,23-pentahydroxy-6,10,19-trimethyl-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] 3,4-dimethoxybenzoate	23620249	Click to see CC1CCC2C(C3C(CN2C1)C4CC56C(C4(C(C3O)O)O)CCC7C5(CCC(C7(O6)O)OC(=O)C8=CC(=C(C=C8)OC)OC)C)(C)O	657.80	unknown	via CMAUP database
Germerine	91800232	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C(C)(CC)O)O)C)O)O)O	693.90	unknown	via CMAUP database
Germidine	90478953	Click to see CCC(C)C(=O)OC1C(C2C(CN3CC(CCC3C2(C)O)C)C4C1(C5C(CC6C7(C5(C4)OC6(C(CC7)OC(=O)C)O)C)O)O)O	635.80	unknown	via CMAUP database
Zygacine	21573746	Click to see CC1CCC2C(C3C(CN2C1)C4CC56C(C4(C(C3O)O)O)CCC7C5(CCC(C7(O6)O)OC(=O)C)C)(C)O	535.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Jerveratrum-type alkaloids
(1R,3S,3'R,3'aS,4aR,6'S,6aS,6bS,7'aR,9R,11aS,11bS)-1,3-dihydroxy-3',6',10,11b-tetramethylspiro[1,2,3,4,4a,5,6,6a,6b,7,8,11a-dodecahydrobenzo[a]fluorene-9,2'-3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine]-11-one	16723933	Click to see CC1CC2C(C(C3(O2)CCC4C5CCC6CC(CC(C6(C5C(=O)C4=C3C)C)O)O)C)NC1	443.60	unknown	via CMAUP database
(3S,3'R,3'aS,6'S,6aS,6bS,7'aR,9S,11aS,11bR)-3',6',10,11b-tetramethylspiro[2,3,4,6,6a,6b,7,8,11,11a-decahydro-1H-benzo[a]fluorene-9,2'-3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine]-3-ol	86287406	Click to see CC1CC2C(C(C3(O2)CCC4C5CC=C6CC(CCC6(C5CC4=C3C)C)O)C)NC1	411.60	unknown	via CMAUP database
23-Methoxycyclopamine	101844722	Click to see CC1CC2(C(C(C3(O2)CCC4C5CC=C6CC(CCC6(C5CC4=C3C)C)O)C)NC1)OC	441.60	unknown	via CMAUP database
Jervine	10098	Click to see CC1CC2C(C(C3(O2)CCC4C5CC=C6CC(CCC6(C5C(=O)C4=C3C)C)O)C)NC1	425.60	unknown	via CMAUP database
methyl (3S,3'R,3'aS,6'S,6aS,6bS,7'aR,9R,11S,11aS,11bR)-3,11-dihydroxy-3',6',10,11b-tetramethylspiro[2,3,4,6,6a,6b,7,8,11,11a-decahydro-1H-benzo[a]fluorene-9,2'-3,3a,5,6,7,7a-hexahydrofuro[3,2-b]pyridine]-4'-carboxylate	16723827	Click to see CC1CC2C(C(C3(O2)CCC4C5CC=C6CC(CCC6(C5C(C4=C3C)O)C)O)C)N(C1)C(=O)OC	485.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
Rubijervine	253295	Click to see CC1CCC2C(C3C(N2C1)CC4C3(C(CC5C4CC=C6C5(CCC(C6)O)C)O)C)C	413.60	unknown	via CMAUP database
Solanidine	65727	Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C	397.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
10,13-dimethyl-17-(5-propan-2-ylhept-5-en-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86747	Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)97553-8 https://doi.org/10.1016/0031-9422(96)00156-2
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 CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/0031-9422(96)00156-2 https://doi.org/10.1016/S0031-9422(00)97553-8
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/10.1016/0031-9422(96)00156-2 https://doi.org/10.1016/S0031-9422(00)97553-8
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(96)00156-2 https://doi.org/10.1016/S0031-9422(00)97553-8
Fucosterol	5281328	Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/0031-9422(96)00156-2 https://doi.org/10.1016/S0031-9422(00)97553-8
Isofucosterol	5281326	Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/0031-9422(96)00156-2 https://doi.org/10.1016/S0031-9422(00)97553-8
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1 https://doi.org/10.1016/0031-9422(96)00156-2
> Nucleosides, nucleotides, and analogues / Purine nucleosides
(2R,3S,4R,5R)-2-(hydroxymethyl)-5-[6-[hydroxy(methyl)amino]purin-9-yl]oxolane-3,4-diol	101518	Click to see CN(C1=NC=NC2=C1N=CN2C3C(C(C(O3)CO)O)O)O	297.27	unknown	via CMAUP database
Adenosine	60961	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Protocatechualdehyde	8768	Click to see C1=CC(=C(C=C1C=O)O)O	138.12	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
6-Methyl-5-hepten-2-one	9862	Click to see CC(=CCCC(=O)C)C	126.20	unknown	https://doi.org/10.1007/S004030050433
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2-Hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]non-3-en-8-yl) acetate	129682131	Click to see CC#CC#CC=C1C=CC2(O1)CC(CO2)OC(=O)C	258.27	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
(2E,5R)-2-hexa-2,4-diynylidene-1,10-dioxaspiro[4.5]dec-3-ene	10846300	Click to see CC#CC#CC=C1C=CC2(O1)CCCCO2	214.26	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
(2E,5R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]non-3-ene	44575220	Click to see CC#CC#CC=C1C=CC2(O1)CCCO2	200.23	unknown	https://doi.org/10.1016/S0031-9422(97)87091-4
(2E,5S)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]non-3-ene	76961451	Click to see CC#CC#CC=C1C=CC2(O1)CCCO2	200.23	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1 https://doi.org/10.1016/0031-9422(82)85253-9
(2Z,5R)-2-hexa-2,4-diynylidene-1,10-dioxaspiro[4.5]dec-3-ene	10608668	Click to see CC#CC#CC=C1C=CC2(O1)CCCCO2	214.26	unknown	https://doi.org/10.1016/S0031-9422(97)87091-4 https://doi.org/10.1016/0031-9422(82)85253-9
(2Z,5R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]non-3-ene	76960595	Click to see CC#CC#CC=C1C=CC2(O1)CCCO2	200.23	unknown	https://doi.org/10.1016/S0031-9422(97)87091-4
(2Z,5S)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]non-3-ene	76960596	Click to see CC#CC#CC=C1C=CC2(O1)CCCO2	200.23	unknown	https://doi.org/10.1016/S0031-9422(00)88544-1 https://doi.org/10.1016/0031-9422(82)85253-9
[(2E,5S,8R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]non-3-en-8-yl] acetate	162940570	Click to see CC#CC#CC=C1C=CC2(O1)CC(CO2)OC(=O)C	258.27	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
[(2Z,5S,8R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]non-3-en-8-yl] acetate	162940569	Click to see CC#CC#CC=C1C=CC2(O1)CC(CO2)OC(=O)C	258.27	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
1,6-Dioxaspiro(4.5)dec-3-ene, 2-(2,4-hexadiynylidene)-, (E)-	327391	Click to see CC#CC#CC=C1C=CC2(O1)CCCCO2	214.26	unknown	https://doi.org/10.1016/S0031-9422(97)87091-4 https://doi.org/10.1016/0031-9422(82)85253-9
2-(2,4-Hexadiynylidene)-1,6-dioxaspiro[4.4]non-3-ene	103031	Click to see CC#CC#CC=C1C=CC2(O1)CCCO2	200.23	unknown	https://doi.org/10.1016/S0031-9422(97)87091-4 https://doi.org/10.1016/S0031-9422(00)88544-1 https://doi.org/10.1016/0031-9422(82)85253-9
> Organoheterocyclic compounds / Azoles / Pyrazoles / Phenylpyrazoles
4-(5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)phenol	71607972	Click to see C1CC2=C(C=NN2C1)C3=CC=C(C=C3)O	200.24	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
Cannabichromene	30219	Click to see CCCCCC1=CC(=C2C=CC(OC2=C1)(C)CCC=C(C)C)O	314.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Furopyrans
Phellifuropyranone A	24770409	Click to see C1=CC(=C(C=C1C=CC2=CC3=C(C=C(O3)C4=CC(=C(C=C4)O)O)C(=O)O2)O)O	378.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole	798	Click to see C1=CC=C2C(=C1)C=CN2	117.15	unknown	https://doi.org/10.1007/S004030050433
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3aS,6R,9aS,9bS)-6-hydroxy-6,9-dimethyl-3-methylidene-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-2-one	15406669	Click to see CC1=CC=C2C1C3C(CCC2(C)O)C(=C)C(=O)O3	246.30	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
(3R,3aS,9aS,9bS)-3,6,9-trimethyl-3,3a,4,5,9a,9b-hexahydroazuleno[4,5-b]furan-2,7-dione	442139	Click to see CC1C2CCC(=C3C(C2OC1=O)C(=CC3=O)C)C	246.30	unknown	https://doi.org/10.1515/ZNC-2001-7-806
(3R,4R,5S)-5-[(1S,2R)-2-hydroxy-2-methyl-5-oxocyclopent-3-en-1-yl]-3-methyl-4-(3-oxobutyl)oxolan-2-one	162842017	Click to see CC1C(C(OC1=O)C2C(=O)C=CC2(C)O)CCC(=O)C	280.32	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
(3R,4R,5S)-5-[(1S,2S)-2-hydroxy-2-methyl-5-oxocyclopent-3-en-1-yl]-3-methyl-4-(3-oxobutyl)oxolan-2-one	162842016	Click to see CC1C(C(OC1=O)C2C(=O)C=CC2(C)O)CCC(=O)C	280.32	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
3-O-methyl-isosecotanapartholide	70697791	Click to see CC1=C(C(=O)CC1OC)C2C(C(=C)C(=O)O2)CCC(=O)C	292.33	unknown	https://doi.org/10.1016/0031-9422(90)80039-J
5-(2-Hydroxy-2-methyl-5-oxocyclopent-3-en-1-yl)-3-methyl-4-(3-oxobutyl)oxolan-2-one	162842015	Click to see CC1C(C(OC1=O)C2C(=O)C=CC2(C)O)CCC(=O)C	280.32	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
6-hydroxy-6,9-dimethyl-3-methylidene-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-2-one	162906721	Click to see CC1=CC=C2C1C3C(CCC2(C)O)C(=C)C(=O)O3	246.30	unknown	https://doi.org/10.1016/0031-9422(82)85253-9
Achillin	291264	Click to see CC1C2CCC(=C3C(C2OC1=O)C(=CC3=O)C)C	246.30	unknown	https://doi.org/10.1515/ZNC-2001-7-806
Secotanapartholide A	10356188	Click to see CC(=O)CCC1C(OC(=O)C1=C)C2C(=O)C=CC2(C)O	278.30	unknown	https://doi.org/10.1039/P19960001979 https://doi.org/10.1515/ZNC-2001-7-806 https://doi.org/10.1016/0031-9422(89)80150-5
secotanapartholide B	10265551	Click to see CC(=O)CCC1C(OC(=O)C1=C)C2C(=O)C=CC2(C)O	278.30	unknown	https://doi.org/10.1039/P19960001979 https://doi.org/10.1016/0031-9422(89)80150-5
Teucvin	179592	Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2	328.40	unknown	via CMAUP database
Teuflin	13071598	Click to see CC1CC2C3=C(CCCC3C14CC(OC4=O)C5=COC=C5)C(=O)O2	328.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / 3-pyridinecarbonitriles
Mallorepine	13027	Click to see CN1C=CC(=O)C(=C1)C#N	134.14	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Dihydropyridines
1-Methyl-4-oxo-1,4-dihydropyridine-2-carbonitrile	45087607	Click to see CN1C=CC(=O)C=C1C#N	134.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-[4-(1,3-Dihydroxypropan-2-yloxy)-3-methoxyphenyl]prop-2-enal	162920423	Click to see COC1=C(C=CC(=C1)C=CC=O)OC(CO)CO	252.26	unknown	https://doi.org/10.1016/S0031-9422(98)00607-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-[[(1S,4aR,6S,8aS)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]-6,8-dimethoxychromen-2-one	102328535	Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)COC3=C(C=C4C=CC(=O)OC4=C3OC)OC)C	442.50	unknown	https://doi.org/10.1016/S0031-9422(97)87091-4
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Isofraxidin	5318565	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)O	222.19	unknown	https://doi.org/10.1016/S0031-9422(98)00607-4 https://doi.org/10.1016/S0031-9422(00)88544-1 https://doi.org/10.1016/S0031-9422(97)87091-4
> 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/S0031-9422(99)00474-4 https://doi.org/10.1089/JMF.2006.9.55
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)00474-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
(2S,3S,4S,5R,6S)-6-[(2S,3R,4S,5S,6S)-6-carboxy-3,4,5-trihydroxyoxan-2-yl]oxy-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxane-2-carboxylic acid	145925705	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)C4(C(C(C(C(O4)C(=O)O)O)O)O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O	622.50	unknown	https://doi.org/10.1016/S0031-9422(99)00021-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid	154496169	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	446.40	unknown	https://doi.org/10.1016/S0031-9422(99)00021-7
(2S,3S,4S,5R,6R)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	25202164	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carbonyl]oxyoxane-2-carboxylic acid	162994883	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O)O)O)O	622.50	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4
(2S,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-3,5,6-trihydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	162971935	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O)O)O	494.40	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4
(2S,3S,4S,5R)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	5488307	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	https://doi.org/10.1016/S0031-9422(99)00021-7 https://doi.org/10.1016/0031-9422(94)00609-W
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylate	163075239	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O	608.50	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylate	163075238	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O	608.50	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4
3,4,5-Trihydroxy-6-[3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carbonyl]oxyoxane-2-carboxylic acid	162994882	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)OC5C(C(C(C(O5)C(=O)O)O)O)O)O)O)O)O)O	622.50	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4
3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid	5387370	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	446.40	unknown	https://doi.org/10.1016/0031-9422(94)00609-W https://doi.org/10.1016/S0031-9422(99)00474-4
6-[2-(3,4-Dihydroxyphenyl)-3,5,6-trihydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid	131834509	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O)O)O	494.40	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4
Apigenin 7-glucuronide	5319484	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	446.40	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4 https://doi.org/10.1016/0031-9422(94)00609-W
Chrysoeriol 7-glucuronide	14630700	Click to see COC1=C(C=CC(=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/10.1016/0031-9422(94)00609-W
Chrysoeriol glucuronide	14630703	Click to see COC1=C(C=CC(=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 https://doi.org/10.1016/0031-9422(94)00609-W
CID 44259227	44259227	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1016/S0031-9422(99)00021-7
Luteolin 7-glucuronide	5280601	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	https://doi.org/10.1016/S0031-9422(99)00021-7 https://doi.org/10.1016/0031-9422(94)00609-W
Luteolin-7-o-glucuronide	13607752	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O	462.40	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4 https://doi.org/10.1016/S0031-9422(99)00021-7 https://doi.org/10.1016/0031-9422(94)00609-W
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	13093776	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/10.1016/S0031-9422(99)00474-4
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one	12304095	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4
Apigenin 7-O-glucoside	5385553	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4
Luteolin 7-galactoside	5291488	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/10.1016/0031-9422(94)00609-W https://doi.org/10.1016/S0031-9422(99)00474-4
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/10.1016/0031-9422(94)00609-W https://doi.org/10.1016/S0031-9422(99)00021-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
4',5,7-Trihydroxy-3,6-dimethoxyflavone	5352032	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O	330.29	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4 https://doi.org/10.1016/S0031-9422(99)00021-7
5,7-Dihydroxy-3,6,3',4'-tetramethoxyflavone	5379563	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)OC	374.30	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4
Axillarin	5281603	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O	346.30	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4
Centaureidin	5315773	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O	360.30	unknown	https://doi.org/10.1016/S0031-9422(03)00208-5 https://doi.org/10.1016/S0031-9422(99)00474-4 https://doi.org/10.1002/CHIN.200402242 https://doi.org/10.1016/S0031-9422(99)00021-7
Eupafolin	5317284	Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O	316.26	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4
Hispidulin	5281628	Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O	300.26	unknown	https://doi.org/10.1016/S0031-9422(99)00474-4
Jaceidin	5464461	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O	360.30	unknown	https://doi.org/10.1016/S0031-9422(03)00208-5 https://doi.org/10.1016/S0031-9422(99)00474-4 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/10.1016/S0031-9422(99)00474-4
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/S0031-9422(03)00208-5 https://doi.org/10.1016/S0031-9422(99)00474-4 https://doi.org/10.1002/CHIN.200402242 https://doi.org/10.1590/S0102-695X2008000300009
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,6-Dihydroxy-3,7,4'-trimethoxyflavone	10043097	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)O)O)OC	344.30	unknown	https://doi.org/10.1016/0031-9422(94)00609-W
5,6,4'-Trihydroxy-3,7-dimethoxyflavone	13983730	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)O	330.29	unknown	https://doi.org/10.1016/0031-9422(94)00609-W
Chrysosplenol C	189065	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)O)O)OC)O	360.30	unknown	https://doi.org/10.1016/0031-9422(94)00609-W
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/10.1016/S0031-9422(99)00474-4
Tomentin	148856	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)O	346.30	unknown	https://doi.org/10.1016/0031-9422(94)00609-W
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
(1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylic acid	102004656	Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)O	292.20	unknown	via CMAUP database
Phelligridin C	10248188	Click to see C1=CC(=CC=C1C=CC2=CC3=C(C4=CC(=C(C=C4C(=O)O3)O)O)C(=O)O2)O	364.30	unknown	via CMAUP database
Phelligridin D	10339712	Click to see C1=CC(=C(C=C1C=CC2=CC3=C(C4=CC(=C(C=C4C(=O)O3)O)O)C(=O)O2)O)O	380.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2-methoxybenzene-1,3-diol	5315205	Click to see COC1=C(C=CC(=C1O)C=CC2=CC(=CC(=C2)O)O)O	274.27	unknown	via CMAUP database
Resveratrol	445154	Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O	228.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins
beta-Glucogallin	124021	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O	332.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(Z)-3-[(3S,4R)-3-carboxy-5,6,7-trihydroxy-1-oxo-3,4-dihydroisochromen-4-yl]-4-[[(1R,19R,21S,22R,23R)-6-(6-carboxy-2,3,4-trihydroxyphenoxy)-7,8,11,12,13,22-hexahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl]oxy]-4-oxobut-2-enoate	21672437	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)OC6=C(C(=C(C=C6C(=O)O)O)O)O)OC(=O)C(=CC(=O)[O-])C7C(OC(=O)C8=CC(=C(C(=C78)O)O)O)C(=O)O	1137.80	unknown	via CMAUP database
(Z)-3-[(3S,4R)-3-carboxy-5,6,7-trihydroxy-1-oxo-3,4-dihydroisochromen-4-yl]-4-[[(1R,19R,21S,22R,23R)-6,7,8,11,12,13,22-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl]oxy]-4-oxobut-2-enoate	21672435	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)OC(=O)C(=CC(=O)[O-])C6C(OC(=O)C7=CC(=C(C(=C67)O)O)O)C(=O)O	969.60	unknown	via CMAUP database
Corilagin	73568	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O	634.50	unknown	via CMAUP database
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	via CMAUP database
Eugeniin	442679	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	938.70	unknown	via CMAUP database
Mallotinic Acid	10056140	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)OC6=C(C(=C(C=C6C(=O)O)O)O)O)O	802.60	unknown	via CMAUP database
Punicafolin	5320800	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O	938.70	unknown	via CMAUP database
Wutxioakrfkqhk-bwpkhyersa-	21672436	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)OC(=O)C(=CC(=O)O)C6C(OC(=O)C7=CC(=C(C(=C67)O)O)O)C(=O)O	970.70	unknown	via CMAUP database

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Tanacetum parthenium

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top