Scientific name	Authority	First published in
Anthemis zephyrovii	Dobrocz.	Ukrayins'k. Bot. Zhurn. 18(2): 70 (1961)
Buphthalmum bipinnatum	Gilib.	Fl. Lit. Inch. 1: 213 (1782)
Chamaemelum tinctorium	Schreb.	Spic. Fl. Lips. : 145 (1771)
Anthemis discoidea	(All.) Vahl	Vahl. 1790. 74 1790
Anthemis maris-nigri	Fed.	Fl. URSS 26:866 (1961)
Anthemis kelwayi	hort. ex L.H.Bailey & N.Taylor	Stand. Cycl. Hort. 1: 299 (1914)
Anthemis tinctoria	L.	Sp. Pl. : 896. (1753)
Anthemis parnassica	(Boiss. & Heldr.) Nyman	Suppl. Syll. Fl. Eur. : 1 (1865)
Chamaemelum discoideum	All.	Fl. Pedem. 1: 188 (1785)
Anthemis brachyglossa	K.Koch	Linnaea 24: 318 (1851)
Anthemis tinctoria var. discoidea	(All.) DC.	Prodr. [A. P. de Candolle] 6: 11. 1838
Anthemis subtinctoria	Dobrocz.	Ukrayins'k. Bot. Zhurn. 18(2): 67 (1961)
Anthemis debilis	Fed.	Fl. URSS 26: 867 (1961)
Anthemis tinctoria subsp. subtinctoria	(Dobrocz.) Soó	Acta Bot. Acad. Sci. Hung. 12: 336 (1966)
Anacyclus tinctorius	(L.) Samp.	Ann. Sci. Acad. Polytecn. Porto 15: 162 (1921)
Anthemis tinctoria var. ramulosa	Thin	Fitologiya 22: 87 (1983)
Cota parnassica	Boiss. & Heldr.	Diagn. Pl. Orient. , ser. 2, 3: 20 (1856)
Cota tinctoria subsp. subtinctoria	(Dobroc.) Holub	Folia Geobot. Phytotax. 9: 270 (1974)
Anthemis tinctoria var. orientalis	Eig	Palestine J. Bot., Jerusalem Ser. 1: 211 (1938)
Anthemis tinctoria subsp. discoidea	(All.) Arcang.	Comp. Fl. Ital. : 357 (1882)
Anthemis tinctoria var. intermedia	Thin	Fitologiya 22: 87 (1983)
Anthemis tinctoria var. parviflora	Eig	Palestine J. Bot., Jerusalem Ser. 1: 211 (1938)
Anthemis tinctoria f. pectinata	Thin	Fitologiya 22: 87 (1983)
Anthemis tinctoria f. halophila	Thin	Fitologiya 22: 87 (1983)
Anthemis coarctata	Sm.	Fl. Graec. Prodr. 2(1): 191. 1813
Anthemis markhotensis	Fed.	Fl. URSS 26: 867 (1961)
Anthemis tinctoria subsp. parnassica	(Boiss. & Heldr.) Franzén	Mount. Fl. Greece 2: 430 (1991)
Anthemis chrysantha	Schur	Enum. Pl. Transsilv. 1: 331 (1866)
Anthemis parnassica	(Boiss. & Heldr.) R.Fernandes	15 1975
Anthemis coarctata	Sibth. & Sm.	Fl. Graec. ix. 68
Anthemis discoidea	(All.) Willd.	Sp. Pl., ed. 4 [Willdenow] 3(3): 2187. 1803 [Apr-Dec 1803]
Anthemis pallescens	Heldr. ex Nyman	Consp. Fl. Eur. 2: 359 (1879)

Common names Top

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Filter by language:

Language	Common/alternative name
English	golden chamomile
English	oxeye chamomile
English	golden marguerite
English	yellow chamomile
English	dyer's chamomile
Spanish	camomila amarilla
Arabic	أقحوان أصفر
Arabic	عين الثور
Arabic	بابونج اصفر
Arabic	كوتا صبغية
Bulgarian	жълто подрумче
Czech	marunek barvířský
Welsh	camri melyn
Danish	farve-gåseurt
Danish	farvegåseurt
German	färberkamille
Estonian	kollane karikakar
Persian	بابونه زرد
Finnish	keltasauramo
French	camomille jaune
Hungarian	festő pipitér
Armenian	վայրի երիցուկ
Armenian	դեղին օշոշ
Armenian	ապրուկ-մեռնուկ
Armenian	ապրեմ-չապրեմ
Armenian	Ապրեմ-մեռնեմ
Italian	occhio di bue
Italian	camomilla dei tintori
Italian	bambayella
Lithuanian	geltonasis bobramunis
Norwegian Bokmål	gul gåseblom
Dutch	gele kamille
Polish	rumian żółty
Russian	пупавка красильная
Russian	пупавка желтоцветная
Russian	антемис красильный
Russian	Пупавка красильная
Slovenian	barvilna pasja kamilica
Swedish	färgkulla
Turkish	sarı papatya
Turkish	boyacı papatyası
Ukrainian	роман мархотський
Ukrainian	роман фарбувальний
Ukrainian	роман Зефірова
Chinese	春黄菊
Chinese	春黃菊

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Anthemis maritima subsp. bolosii	Benedí & Molero	Fontqueria 28: 1 (1990) (1990)
Anthemis maritima subsp. pseudopunctata	Oberpr.	Bocconea 9: 248 (1998) (1998)
Cota tinctoria subsp. australis	(R.Fern.) Oberpr. & Greuter	Willdenowia 33(1): 41 (2003) (2003)
Cota tinctoria subsp. euxina	(Boiss.) Oberpr. & Greuter	Willdenowia 33(1): 41 (2003) (2003)
Cota tinctoria subsp. fussii	(Griseb. & Schenk) Oberpr. & Greuter	Willdenowia 33(1): 41 (2003) (2003)
Cota tinctoria subsp. gaudium-solis	(Velen.) Oberpr. & Greuter	Willdenowia 33(1): 41 (2003) (2003)
Cota tinctoria subsp. parnassica	(Boiss. & Heldr.) Oberpr. & Greuter	Willdenowia 33(1): 41 (2003) (2003)
Cota tinctoria subsp. sancti-johannis	(Stoj., Stef. & Turrill) Oberpr. & Greuter	Willdenowia 33(1): 41 (2003) (2003)
Cota tinctoria subsp. tinctoria
Cota tinctoria subsp. virescens	(Bornm.) Oberpr. & Greuter	Willdenowia 33(1): 41 (2003) (2003)

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

Suggest a correction or add new data!

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
- Macaronesia
  - Canary Islands

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Uzbekistan
- Russian Far East
  - Amur
  - Kamchatka
  - Primorye
  - Sakhalin
- Siberia
  - Altay
  - Buryatiya
  - Chita
  - Irkutsk
  - Krasnoyarsk
  - West Siberia
  - Yakutskiya
- Western Asia
  - East Aegean Islands
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Turkey

Asia-tropical click to expand
- Malesia
  - Jawa

Australasia click to expand
- Australia
  - South Australia
  - Tasmania

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
  - Great Britain
  - Ireland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Corse
  - France
  - Sardegna

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Newfoundland
  - Nova Scotia
  - Ontario
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Minnesota
  - Missouri
  - North Dakota
  - South Dakota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Idaho
  - Oregon
  - Washington
  - Wyoming
- Southeastern U.S.A.
  - Arkansas
  - Maryland
  - Virginia
- Southwestern U.S.A.
  - California
  - Utah
- Subarctic America
  - Alaska
- Western Canada
  - Alberta
  - British Columbia
  - Manitoba
  - Saskatchewan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000076814
Canadensys	3019
Tropicos	2728728
INPN	92629
Flora of Italy	5593
KEW	urn:lsid:ipni.org:names:198407-1
The Plant List	gcc-33458
Plantarium	11415
Open Tree Of Life	1049246
NCBI Taxonomy	99028
IPNI	198407-1
iNaturalist	76456
GBIF	5390618
Freebase	/m/02_n_j
WisFlora	12935
EPPO	ANTTI
Calflora (Californian flora)	11547
USDA GRIN	462955
Wikipedia	Cota_tinctoria
CMAUP	NPO16801

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Bio-mordants: a review

Benli H

Environ Sci Pollut Res Int

23-Feb-2024

PMCID:	PMC10948525
doi:	10.1007/s11356-024-32174-8
PMID:	38396176

Exploring Plants with Flowers: From Therapeutic Nutritional Benefits to Innovative Sustainable Uses

Coyago-Cruz E, Moya M, Méndez G, Villacís M, Rojas-Silva P, Corell M, Mapelli-Brahm P, Vicario IM, Meléndez-Martínez AJ

Foods

08-Nov-2023

PMCID:	PMC10671036
doi:	10.3390/foods12224066
PMID:	38002124

Spatiotemporal environmental monitoring of the karst-related Almyros Wetland (Heraklion, Crete, Greece, Eastern Mediterranean)

Kokinou E, Zacharioudaki DE, Kokolakis S, Kotti M, Chatzidavid D, Karagiannidou M, Fanouraki E, Kontaxakis E

Environ Monit Assess

15-Jul-2023

PMCID:	PMC10349741
doi:	10.1007/s10661-023-11571-5
PMID:	37452883

Use of Multivariate Analysis to Unravel the Differences between Two Chamomile Varieties and Their Anticancer and Antioxidant Activities

Atoum D, Fernandez-Pastor I, Young L, Edrada-Ebel R

Plants (Basel)

12-Jun-2023

PMCID:	PMC10304069
doi:	10.3390/plants12122297
PMID:	37375922

Does Reproductive Success in Natural and Anthropogenic Populations of Generalist Epipactis helleborine Depend on Flower Morphology and Nectar Composition?

Brzosko E, Bajguz A, Burzyńska J, Chmur M

Int J Mol Sci

21-Feb-2023

PMCID:	PMC10001846
doi:	10.3390/ijms24054276
PMID:	36901705

Vertical Columns with Sustainable Green Cover: Meadow Plants in Urban Design

Stakelienė V, Pašakinskienė I, Ložienė K, Ryliškis D, Skridaila A

Plants (Basel)

01-Feb-2023

PMCID:	PMC9921580
doi:	10.3390/plants12030636
PMID:	36771721

Lutein Isomers: Preparation, Separation, Structure Elucidation, and Occurrence in 20 Medicinal Plants

Nagy V, Agócs A, Balázs VL, Purger D, Filep R, Sándor V, Turcsi E, Gulyás-Fekete G, Deli J

Molecules

25-Jan-2023

PMCID:	PMC9921531
doi:	10.3390/molecules28031187
PMID:	36770852

Edible Flowers Used in Some Countries of the Mediterranean Basin: An Ethnobotanical Overview

Motti R, Paura B, Cozzolino A, de Falco B

Plants (Basel)

28-Nov-2022

PMCID:	PMC9736219
doi:	10.3390/plants11233272
PMID:	36501312

Phytogeographic Characteristics of Montane Coniferous Forests of the Central Balkan Peninsula (SE Europe)

Ilić T, Kuzmanović N, Vukojičić S, Lakušić D

Plants (Basel)

22-Nov-2022

PMCID:	PMC9741231
doi:	10.3390/plants11233194
PMID:	36501234

An Ethnobotanical study of medicinal plants in Taşköprü (Kastamonu–Turkey)

Senkardes I, Dogan A, Emre G

Front Pharmacol

20-Oct-2022

PMCID:	PMC9630845
doi:	10.3389/fphar.2022.984065
PMID:	36339567

A Comprehensive Study of Therapeutic Applications of Chamomile

Sah A, Naseef PP, Kuruniyan MS, Jain GK, Zakir F, Aggarwal G

Pharmaceuticals (Basel)

19-Oct-2022

PMCID:	PMC9611340
doi:	10.3390/ph15101284
PMID:	36297396

Initial assemblage characteristics determine the functional dynamics of flower‐strip plant communities

Gardarin A, Valantin‐Morison M

Ecol Evol

18-Oct-2022

PMCID:	PMC9579737
doi:	10.1002/ece3.9435
PMID:	36267684

A recent (2009–2021) perspective on sustainable color and textile coloration using natural plant resources

Che J, Yang X

Heliyon

11-Oct-2022

PMCID:	PMC9587285
doi:	10.1016/j.heliyon.2022.e10979
PMID:	36281409

Floral Volatile Organic Compounds and a List of Pollinators of Fallopia baldschuanica (Polygonaceae)

Jakubska-Busse A, Dziadas M, Gruss I, Kobyłka MJ

Insects

05-Oct-2022

PMCID:	PMC9604458
doi:	10.3390/insects13100904
PMID:	36292852

The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature

Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR

Vet Med Sci

29-Aug-2022

PMCID:	PMC9677405
doi:	10.1002/vms3.912
PMID:	36037401

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
2-(Hydroxymethyl)-6-[[18-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraen-17-yl]oxy]oxane-3,4,5-triol	14539284	Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5OC6C(C(C(C(O6)CO)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)OCO4	611.60	unknown	https://doi.org/10.1002/CBER.19660990531
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
Dihydrochelerythrine	485077	Click to see CN1CC2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5	349.40	unknown	via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Arnottianamide	3085181	Click to see CN(C=O)C1=C(C=CC2=CC3=C(C=C21)OCO3)C4=C(C(=C(C=C4)OC)OC)O	381.40	unknown	via CMAUP database
> Alkaloids and derivatives / Harmala alkaloids
methyl 9H-pyrido[3,4-b]indole-1-carboxylate	597266	Click to see COC(=O)C1=NC=CC2=C1NC3=CC=CC=C23	226.23	unknown	via CMAUP database
> 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
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl 4-hydroxy-3,5-dimethoxybenzoate	70164	Click to see COC1=CC(=CC(=C1O)OC)C(=O)OC	212.20	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate	7428	Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O	184.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl vanillate	19844	Click to see COC1=C(C=CC(=C1)C(=O)OC)O	182.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben	7456	Click to see COC(=O)C1=CC=C(C=C1)O	152.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
3,4,5-Trimethoxybenzyl alcohol	77449	Click to see COC1=CC(=CC(=C1OC)OC)CO	198.22	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(3-Methylbut-2-enyl)-4-(2-methylbut-3-en-2-yl)phenol	333664	Click to see CC(=CCC1=C(C=CC(=C1)C(C)(C)C=C)O)C	230.34	unknown	https://doi.org/10.1002/CBER.19660990705
> Benzenoids / Naphthalenes / Naphthols and derivatives
Vitexdoin C	44478949	Click to see COC1=C(C=CC(=C1)C2=C(C=CC3=CC(=C(C=C32)O)OC)C=O)O	324.30	unknown	https://doi.org/10.1002/CBER.19630960603
> Benzenoids / Phenols / Methoxyphenols
4-Hydroxy-3-methoxycinnamaldehyde	5280536	Click to see COC1=C(C=CC(=C1)C=CC=O)O	178.18	unknown	via CMAUP database
N-Trans-feruloyltramine	5280537	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O	313.30	unknown	via CMAUP database
Syringaldehyde	8655	Click to see COC1=CC(=CC(=C1O)OC)C=O	182.17	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(3-Oxo-9-thiophen-2-ylnon-6-en-8-yn-4-yl) 3-methylbutanoate	162916072	Click to see CCC(=O)C(CC=CC#CC1=CC=CS1)OC(=O)CC(C)C	318.40	unknown	https://doi.org/10.1002/CBER.19660990531
(7-Oxo-1-thiophen-2-ylnon-3-en-1-yn-5-yl) 3-methylbutanoate	162885663	Click to see CCC(=O)CC(C=CC#CC1=CC=CS1)OC(=O)CC(C)C	318.40	unknown	https://doi.org/10.1002/CBER.19660990531
[(E,4S)-3-oxo-9-thiophen-2-ylnon-6-en-8-yn-4-yl] 3-methylbutanoate	163186129	Click to see CCC(=O)C(CC=CC#CC1=CC=CS1)OC(=O)CC(C)C	318.40	unknown	https://doi.org/10.1002/CBER.19660990531
[(E,5R)-7-oxo-1-thiophen-2-ylnon-3-en-1-yn-5-yl] 3-methylbutanoate	163188281	Click to see CCC(=O)CC(C=CC#CC1=CC=CS1)OC(=O)CC(C)C	318.40	unknown	https://doi.org/10.1002/CBER.19660990531
2-Decene-4,6,8-triynoic acid, methyl ester, (Z)-	5281309	Click to see CC#CC#CC#CC=CC(=O)OC	172.18	unknown	https://doi.org/10.1002/CBER.19630960603
methyl (2E,4Z)-4-methylsulfanyldeca-2,4-dien-6,8-diynoate	101417344	Click to see CC#CC#CC=C(C=CC(=O)OC)SC	220.29	unknown	https://doi.org/10.1002/CBER.19660990705
methyl (2E,8E)-9-methylsulfanyldeca-2,8-dien-4,6-diynoate	101417343	Click to see CC(=CC#CC#CC=CC(=O)OC)SC	220.29	unknown	https://doi.org/10.1002/CBER.19650980538
methyl (2E,8Z)-9-methylsulfanyldeca-2,8-dien-4,6-diynoate	13167539	Click to see CC(=CC#CC#CC=CC(=O)OC)SC	220.29	unknown	https://doi.org/10.1002/CBER.19630960603
Methyl 2-decene-4,6,8-triynoate	75958	Click to see CC#CC#CC#CC=CC(=O)OC	172.18	unknown	https://doi.org/10.1002/CBER.19630960603
Methyl 4-methylsulfanyldeca-2,4-dien-6,8-diynoate	86006055	Click to see CC#CC#CC=C(C=CC(=O)OC)SC	220.29	unknown	https://doi.org/10.1002/CBER.19660990705
Methyl 9-methylsulfanyldeca-2,8-dien-4,6-diynoate	162997947	Click to see CC(=CC#CC#CC=CC(=O)OC)SC	220.29	unknown	https://doi.org/10.1002/CBER.19650980538 https://doi.org/10.1002/CBER.19630960603
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid	2969	Click to see CCCCCCCCCC(=O)O	172.26	unknown	https://doi.org/10.1080/10412905.2000.9712198
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3S,6E,12E)-tetradeca-6,12-dien-8,10-diyn-3-ol	162956999	Click to see CCC(CCC=CC#CC#CC=CC)O	202.29	unknown	https://doi.org/10.1002/CBER.19660990531
Tetradeca-6,12-dien-8,10-diyn-3-ol	129684543	Click to see CCC(CCC=CC#CC#CC=CC)O	202.29	unknown	https://doi.org/10.1002/CBER.19660990531
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(2Z,9Z)-heptadeca-2,9,16-trien-4,6-diyn-1-ol	92033826	Click to see C=CCCCCCC=CCC#CC#CC=CCO	242.36	unknown	https://doi.org/10.1002/CBER.19660990705
Heptadeca-2,9,16-triene-4,6-diyn-1-ol	71399337	Click to see C=CCCCCCC=CCC#CC#CC=CCO	242.36	unknown	https://doi.org/10.1002/CBER.19660990705
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1080/10412905.2000.9712198
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	unknown	https://doi.org/10.1080/10412905.2000.9712198
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Isotaraxerol	12443227	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	via CMAUP database
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	via CMAUP database
Taraxerone	92785	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C	424.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(2S,3E,5R)-10-[(1S,3S,6S)-6-acetyloxy-3-hydroxy-2,2,6-trimethylcyclohexyl]-5-hydroxy-1-[(1S,2S)-2-hydroxy-2,6,6-trimethyl-5-oxocyclohex-3-en-1-yl]-3,8-dimethyldeca-3,7-dien-2-yl] acetate	162958017	Click to see CC(=CCC(C=C(C)C(CC1C(C(=O)C=CC1(C)O)(C)C)OC(=O)C)O)CCC2C(C(CCC2(C)OC(=O)C)O)(C)C	590.80	unknown	https://doi.org/10.1002/CBER.19660990705
beta-Amyrin acetate	92156	Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C	468.80	unknown	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
N-[(1S,3R,6S,8R,11S,12S,15S,16R)-7,7,12,16-tetramethyl-15-[(1S)-1-(methylamino)ethyl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]acetamide	162919434	Click to see CC(C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)NC(=O)C)C)C)NC	414.70	unknown	https://doi.org/10.1002/CBER.19660990705
Squalene	638072	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C	410.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Limonin	179651	Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C	470.50	unknown	via CMAUP database
methyl 2-[(1R,2R,5R,6R,11R,12R,13R,14S,16S)-12,14-diacetyloxy-6-(furan-3-yl)-13-hydroxy-1,5,15,15-tetramethyl-8,17-dioxo-11-propan-2-yloxycarbonyloxy-7-oxatetracyclo[11.3.1.02,11.05,10]heptadec-9-en-16-yl]acetate	101130201	Click to see CC(C)OC(=O)OC12C(CCC3(C1=CC(=O)OC3C4=COC=C4)C)C5(C(C(C(C(C2OC(=O)C)(C5=O)O)OC(=O)C)(C)C)CC(=O)OC)C	688.70	unknown	https://doi.org/10.1002/CBER.19660990531
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
CID 9848259	9848259	Click to see CC1(C2C(=O)C(C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)O)C	486.50	unknown	via CMAUP database
Evodol	185481	Click to see CC1(C2=C(C(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)O)C	484.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
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 / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Methyl chlorogenate	6476139	Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O	368.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see C1=CC(=CC=C1C=O)O	122.12	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2S)-2-hydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one	12181418	Click to see CC(C(=O)C1=CC(=C(C=C1)O)OC)O	196.20	unknown	via CMAUP database
Paeonol	11092	Click to see CC(=O)C1=C(C=C(C=C1)OC)O	166.17	unknown	via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
(4Z)-9-(2-Thienyl)-4,6-nonadiene-8-yne-3-one	101416675	Click to see CCC(=O)C=CC=CC#CC1=CC=CS1	216.30	unknown	https://doi.org/10.1002/CBER.19660990531
(E,3S)-9-thiophen-2-ylnon-6-en-8-yn-3-ol	163188840	Click to see CCC(CCC=CC#CC1=CC=CS1)O	220.33	unknown	https://doi.org/10.1002/CBER.19660990531
(E)-5-thiophen-2-ylpent-2-en-4-ynal	14434944	Click to see C1=CSC(=C1)C#CC=CC=O	162.21	unknown	https://doi.org/10.1002/CBER.19660990531
5-(Thiophen-2-yl)pent-2-en-4-ynal	71382431	Click to see C1=CSC(=C1)C#CC=CC=O	162.21	unknown	https://doi.org/10.1002/CBER.19660990531
9-Thiophen-2-ylnon-6-en-8-yn-3-ol	162889859	Click to see CCC(CCC=CC#CC1=CC=CS1)O	220.33	unknown	https://doi.org/10.1002/CBER.19660990531
9-Thiophen-2-ylnona-4,6-dien-8-yn-3-ol	85195426	Click to see CCC(C=CC=CC#CC1=CC=CS1)O	218.32	unknown	https://doi.org/10.1002/CBER.19660990531
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
1H-Pyrido(3,4-b)indol-1-one, 2,3,4,9-tetrahydro-2-methyl-	162871	Click to see CN1CCC2=C(C1=O)NC3=CC=CC=C23	200.24	unknown	via CMAUP database
Hortiacine	378227	Click to see COC1=CC2=C(C=C1)NC3=C2CCN4C3=NC5=CC=CC=C5C4=O	317.30	unknown	via CMAUP database
Rutaecarpine	65752	Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C4=C1C5=CC=CC=C5N4	287.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Isobenzofurans
Epi-Velatumolide	53466548	Click to see CC1CCCC2C1(C(OC2=O)C3=C(COC3=O)C)C	264.32	unknown	https://doi.org/10.1002/CBER.19630960603
> Organoheterocyclic compounds / Naphthofurans
(4-chloro-6,6,9a-trimethyl-3-oxo-4,5,5a,7,8,9-hexahydro-1H-benzo[e][2]benzofuran-9-yl) 2-acetamido-3-methylbutanoate	163064236	Click to see CC(C)C(C(=O)OC1CCC(C2C1(C3=C(C(C2)Cl)C(=O)OC3)C)(C)C)NC(=O)C	425.90	unknown	https://doi.org/10.1002/CBER.19660990705
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Decarine	179640	Click to see COC1=C(C=CC2=C3C=CC4=CC5=C(C=C4C3=NC=C21)OCO5)O	319.30	unknown	via CMAUP database
Norchelerythrine	443719	Click to see COC1=C(C2=CN=C3C(=C2C=C1)C=CC4=CC5=C(C=C43)OCO5)OC	333.30	unknown	via CMAUP database
Oxychelerythrine	147279	Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=C(C1=O)C(=C(C=C5)OC)OC	363.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine	68085	Click to see COC1=C2C=COC2=NC3=CC=CC=C31	199.20	unknown	via CMAUP database
Gamma-Fagarine	107936	Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3	229.23	unknown	via CMAUP database
Robustine	164950	Click to see COC1=C2C=COC2=NC3=C1C=CC=C3O	215.20	unknown	via CMAUP database
Skimmianine	6760	Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC	259.26	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methylquinolin-2-one	182073	Click to see CN1C2=CC=CC=C2C(=CC1=O)OC	189.21	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
n-cis-Feruloyltyramine	6440659	Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O	313.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
cis-N-p-coumaroyltyramine	13939145	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O	283.32	unknown	via CMAUP database
Paprazine	5372945	Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O	283.32	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Methyl 4-hydroxycinnamate	5319562	Click to see COC(=O)C=CC1=CC=C(C=C1)O	178.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Evofolin C	44445795	Click to see CC(=CCOC1=CC=C(C=C1)C=CCO)C	218.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Fraxin	5273568	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O	370.31	unknown	via CMAUP database
Isofraxoside	11508953	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O	370.31	unknown	via CMAUP database
Skimmin	99693	Click to see C1=CC(=CC2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O	324.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin	5280460	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O	192.17	unknown	via CMAUP database
Umbelliferone	5281426	Click to see C1=CC(=CC2=C1C=CC(=O)O2)O	162.14	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Sophoraflavone B	5491513	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O	416.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
4',5,7-Trihydroxy-3-(alpha-D-arabinopyranosyloxy)flavone	11625890	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	418.30	unknown	via CMAUP database
kaempferol 3-O-beta-D-xyloside	21310440	Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	418.30	unknown	via CMAUP database
Kaempferol-3-O-rutinoside	5318767	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O	594.50	unknown	via CMAUP database
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Patuletin 7-glucoside	14157911	Click to see COC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	494.40	unknown	https://doi.org/10.1007/BF00567717
Patulitrin	5320435	Click to see COC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)OC4C(C(C(C(O4)CO)O)O)O	494.40	unknown	https://doi.org/10.1007/BF00567717
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
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/10.1055/S-0029-1185942
> Phenylpropanoids and polyketides / Stilbenes
(-)-Evofolin B	46229015	Click to see COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O	318.32	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
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

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Cota tinctoria

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