Ageratina altissima, also known as white snakeroot, is a poisonous perennial herb found in eastern and central North America. It has white flowers and serrated leaves, and can grow up to 1.5 meters tall. The plant is native to the United States and Canada, and can adapt to different growing conditions. It blooms in the fall and attracts various insects. However, it contains a toxin called tremetol that can be harmful to humans and animals if consumed in large quantities. The plant was responsible for causing milk sickness in the early 19th century, and was only identified as the cause decades later. A cultivar with dark foliage is grown in gardens, and the plant's name is derived from Greek words meaning "un-aging" and "the tallest".

Synonyms Top

Scientific name	Authority	First published in
Ageratum altissimum	L.	Sp. Pl. : 839 (1753)
Batschia nivea	Moench	Methodus 567 (1794) (1794)
Eupatorium frasieri	Poir.	Encycl. , Suppl. 2: 600 (1812)
Eupatorium aboriginum	Greene	Pittonia 4(24): 277 (1901)
Eupatorium rugosum	Houtt.	Nat. Hist. 2(10): 558 (1779)
Eupatorium urticifolium var. angustatum	(A.Gray) B.L.Rob.	Proc. Amer. Acad. Arts 51: 537. 1916
Eupatorium boreale	Greene	Rhodora 3: 83 (1901)
Kyrstenia aboriginum	Greene	Leafl. Bot. Observ. Crit. 1: 8 (1903)
Kyrstenia borealis	Greene	Leafl. Bot. Observ. Crit. 1: 8 (1903)
Kyrstenia altissima	Greene	Leafl. Bot. Observ. Crit. 1: 8 (1903)
Eupatorium urticifolium	Reichard	Syst. Pl. 3: 719 (1780)
Eupatorium rugosum var. tomentellum	(B.L.Rob.) S.F.Blake	Rhodora 43(no. 515): 557 (1941)
Eupatorium rugosum var. villicaule	(Fernald) S.F.Blake	Rhodora 43: 558 (1941)
Ageratina ageratoides	Spach	Hist. Nat. Vég. (Spach) 10: 286 (1841)
Eupatorium rugosum var. chlorolepis	Fernald	Rhodora 44: 462, tab. 739 (1942)
Eupatorium urticifolium var. trifolium	Farw.	Rep. (Annual) Michigan Acad. Sci. 17: 170 (1916)
Eupatorium urticifolium var. tomentellum	B.L.Rob.	Proc. Amer. Acad. Arts 47: 195 (1911)
Eupatorium urticifolium var. villicaule	Fernald	Rhodora 10(no. 113): 87 (1908)
Ageratina altissima var. altissima	(L.) R.M.King & H.Rob.
Eupatorium ageratoides var. angustatum	A.Gray	Syn. Fl. N. Amer. 1(2): 101 (1884)
Eupatorium eurybiaefolium	Greene	Pittonia 4(24): 275 (1901)
Eupatorium urticifolium f. verticillatum	Vict.	Proc. & Trans. Roy. Soc. Canada, III, 20: 471 (1926)

Common names Top

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Filter by language:

Language	Common/alternative name
English	white snakeroot
Czech	nestarka bílá
Danish	eupatorium album
Danish	hvid hjortetrøst
Danish	hvid ageratina
Finnish	isovalkolatva
Finnish	valkolatva
Japanese	丸葉藤袴
Japanese	マルバフジバカマ
Korean	서양등골나물
Tamil	நாகசுவந்தை
Chinese	假白花草
Chinese	蛇根泽兰
Chinese	白蛇根

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Ageratina altissima var. angustata	(A.Gray) Clewell & Wooten	Brittonia 23: 138 (1971)

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Start at 4°C for 3 months, then warm to 20°C for another 3 months.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Southern Africa
  - Northern Provinces

Asia-temperate click to expand
- Eastern Asia
  - Korea

Europe click to expand
- Middle Europe
  - Austria
  - Belgium
  - Germany
  - Hungary
  - Poland

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Nova Scotia
  - Ontario
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Nebraska
  - North Dakota
  - Oklahoma
  - South Dakota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- South-central U.S.A.
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Arkansas
  - Delaware
  - District Of Columbia
  - Florida
  - Georgia
  - Kentucky
  - Louisiana
  - Maryland
  - Mississippi
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Subarctic America
  - Northwest Territorie

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000080123
UNII	K6E0SZ79NY
Florida Plant Atlas	3674
Flora of Alabama	499
Canadensys	2777
USDA Plants	AGAL5
Tropicos	2709240
Flora of Italy	10042
KEW	urn:lsid:ipni.org:names:6815-2
The Plant List	gcc-36689
Missouri Botanical Garden	277391
PFAF	Ageratina altissima
Open Tree Of Life	345514
Observations.org	114008
NCBI Taxonomy	102750
Nature Serve	2.131913
IPNI	6815-2
iNaturalist	119048
GBIF	5400552
Freebase	/m/07hkv8
WisFlora	12817
EPPO	EUPRU
EOL	468507
USDA GRIN	317713
Wikipedia	Ageratina_altissima

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

Pharmaceutical characterization and exploration of Arkeshwara rasa in MDA-MB-231 cells

Jayakumar R, Dash MK, Kumar P, Sharma S, Gulati S, Pandey A, Cholke K, Fatima Z, Trigun SK, Joshi N

J Ayurveda Integr Med

30-Dec-2023

PMCID:	PMC10792653
doi:	10.1016/j.jaim.2023.100823
PMID:	38160612

Plant Invasion Ecology

Sukhorukov AP

Plants (Basel)

17-Nov-2023

PMCID:	PMC10674497
doi:	10.3390/plants12223887
PMID:	38005783

Distribution, Effect, and Control of Exotic Plants in Republic of Korea

Lim BS, Seok JE, Lim CH, Kim GS, Shin HC, Lee CS

Biology (Basel)

06-Jun-2023

PMCID:	PMC10294914
doi:	10.3390/biology12060826
PMID:	37372111

Role of priority effects in invasive plant species management: Early arrival of native seeds guarantees the containment of invasion by Giant ragweed

Byun C

Ecol Evol

26-Mar-2023

PMCID:	PMC10040727
doi:	10.1002/ece3.9940
PMID:	36993150

Green Synthesis of Bioinspired Nanoparticles Mediated from Plant Extracts of Asteraceae Family for Potential Biological Applications

Jaison JP, Balasubramanian B, Gangwar J, James N, Pappuswamy M, Anand AV, Al-Dhabi NA, Valan Arasu M, Liu WC, Sebastian JK

Antibiotics (Basel)

08-Mar-2023

PMCID:	PMC10044610
doi:	10.3390/antibiotics12030543
PMID:	36978410

Detection of Methicillin-Resistant Staphylococcus aureus in Clinical and Subclinical Mastitis in Ruminants and Studying the Effect of Novel Green Synthetized Nanoparticles as One of the Alternative Treatments

Mostafa Abdalhamed A, Zeedan GS, Ahmed Arafa A, Shafeek Ibrahim E, Sedky D, Abdel nabey Hafez A

Vet Med Int

22-Nov-2022

PMCID:	PMC9708356
doi:	10.1155/2022/6309984
PMID:	36457891

Diverse Host Plants of the First Instars of the Invasive Lycorma delicatula: Insights from eDNA Metabarcoding

McPherson C, Avanesyan A, Lamp WO

Insects

10-Jun-2022

PMCID:	PMC9225603
doi:	10.3390/insects13060534
PMID:	35735872

A Review on Green Synthesis of TiO2 NPs: Photocatalysis and Antimicrobial Applications

Verma V, Al-Dossari M, Singh J, Rawat M, Kordy MG, Shaban M

Polymers (Basel)

01-Apr-2022

PMCID:	PMC9002645
doi:	10.3390/polym14071444
PMID:	35406317

Competitive Interactions between Two Non-Native Species (Alliaria petiolata [M. Bieb.] Cavara & Grande and Hesperis matronalis L.) and a Native Species (Ageratina altissima [L.] R.M. King & H. Rob.)

Paulus KR, Marshall JM

Plants (Basel)

29-Jan-2022

PMCID:	PMC8839745
doi:	10.3390/plants11030374
PMID:	35161355

Assessment of the Spatial Invasion Risk of Intentionally Introduced Alien Plant Species (IIAPS) under Environmental Change in South Korea

Adhikari P, Lee YH, Park YS, Hong SH

Biology (Basel)

12-Nov-2021

PMCID:	PMC8614709
doi:	10.3390/biology10111169
PMID:	34827162

Environmental Status of Cryptococcus neoformans and Cryptococcus gattii in Colombia

Serna-Espinosa BN, Guzmán-Sanabria D, Forero-Castro M, Escandón P, Sánchez-Quitian ZA

J Fungi (Basel)

24-May-2021

PMCID:	PMC8225054
doi:	10.3390/jof7060410
PMID:	34073882

Titanium dioxide nanoparticles elicited agro-morphological and physicochemical modifications in wheat plants to control Bipolaris sorokiniana

Satti SH, Raja NI, Javed B, Akram A, Mashwani ZU, Ahmad MS, Ikram M

PLoS One

11-Feb-2021

PMCID:	PMC7877615
doi:	10.1371/journal.pone.0246880
PMID:	33571310

Plant associated fungal endophytes as a source of natural bioactive compounds

Rai N, Kumari Keshri P, Verma A, Kamble SC, Mishra P, Barik S, Kumar Singh S, Gautam V

Mycology

27-Jan-2021

PMCID:	PMC8451683
doi:	10.1080/21501203.2020.1870579
PMID:	34552808

Foliar fungal endophyte community structure is independent of phylogenetic relatedness in an Asteraceae common garden

Whitaker BK, Christian N, Chai Q, Clay K

Ecol Evol

26-Nov-2020

PMCID:	PMC7771118
doi:	10.1002/ece3.6983
PMID:	33391689

N/A

Saunders Comprehensive Veterinary Dictionary

16-Oct-2020

PMCID:	PMC9771675
doi:	10.1016/B978-0-7020-7463-9.50027-6

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 / Benzoic acids and derivatives / Benzoic acid esters
Diethylhexylphthalate	7057919	Click to see CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC	390.60	unknown	https://doi.org/10.1515/ZNB-2005-0916
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Octadecane	11635	Click to see CCCCCCCCCCCCCCCCCC	254.50	unknown	https://doi.org/10.1515/ZNB-2005-0916
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Phytol	5280435	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	https://doi.org/10.1016/S0031-9422(00)81232-7
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Bisabolol	10586	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	https://doi.org/10.1016/S0031-9422(00)81232-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4R,6E,9R,10E,11aR)-9-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-acetyloxy-2-methylbut-2-enoate	163189642	Click to see CC1=CCC(C(=CC2C(C(C1)OC(=O)C(=CCOC(=O)C)C)C(=C)C(=O)O2)C)O	404.50	unknown	https://doi.org/10.1016/S0031-9422(00)81232-7
[(3aR,4R,6E,9R,10Z,11aS)-9-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-(hydroxymethyl)but-2-enoate	163015367	Click to see CC1=CCC(C(=CC2C(C(C1)OC(=O)C(=CCO)CO)C(=C)C(=O)O2)C)O	378.40	unknown	https://doi.org/10.1016/S0031-9422(00)81232-7
[(3aR,4R,6E,9S,10Z,11aS)-9-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-methylbut-2-enoate	162983846	Click to see CC1=CCC(C(=CC2C(C(C1)OC(=O)C(=CCO)C)C(=C)C(=O)O2)C)O	362.40	unknown	https://doi.org/10.1016/S0031-9422(00)81232-7
Chromolaenide	11953932	Click to see CC1=CCC(C(=CC2C(C(C1)OC(=O)C(=CCO)C)C(=C)C(=O)O2)C)OC(=O)C	404.50	unknown	https://doi.org/10.1016/S0031-9422(00)81232-7
CID 77985613	77985613	Click to see CC1=CCC(C(=CC2C(C(C1)OC(=O)C(=CCO)C)C(=C)C(=O)O2)C)O	362.40	unknown	https://doi.org/10.1016/S0031-9422(00)81232-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(7-hydroxy-9-methyl-3-methylidene-2-oxospiro[4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-6,2'-oxirane]-4-yl) 4-hydroxy-2-(hydroxymethyl)but-2-enoate	163014923	Click to see CC1=CC(C2C1C3C(C(CC24CO4)OC(=O)C(=CCO)CO)C(=C)C(=O)O3)O	392.40	unknown	https://doi.org/10.1016/S0031-9422(00)81232-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(6aR,6bR,8aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol	145706026	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)81232-7
2-(10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-4a-yl)acetic acid	72999920	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)CC(=O)O)C	470.70	unknown	https://doi.org/10.1515/ZNB-2005-0916
Lup-20(29)-en-3-ol, (3beta)-	521518	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)91316-5
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)81232-7
Taraxasterol, acetate	344468	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C	468.80	unknown	https://doi.org/10.1016/S0031-9422(00)81232-7
> Lipids and lipid-like molecules / Saccharolipids
(3S)-5-[[(2R,3S,4S,5R,6R)-6-[[(2R)-6-acetyl-2-methylchromen-2-yl]methoxy]-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-hydroxy-3-methyl-5-oxopentanoic acid	162983385	Click to see CC(=O)C1=CC2=C(C=C1)OC(C=C2)(C)COC3C(C(C(C(O3)COC(=O)CC(C)(CC(=O)O)O)O)O)O	524.50	unknown	https://doi.org/10.1016/0031-9422(88)80802-1
5-[[6-[(6-Acetyl-2-methylchromen-2-yl)methoxy]-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-hydroxy-3-methyl-5-oxopentanoic acid	14162653	Click to see CC(=O)C1=CC2=C(C=C1)OC(C=C2)(C)COC3C(C(C(C(O3)COC(=O)CC(C)(CC(=O)O)O)O)O)O	524.50	unknown	https://doi.org/10.1016/0031-9422(88)80802-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
[(3S,5S,9R,10S,13R,14R,17R)-10,13,14-trimethyl-17-[(2R)-6-methylhept-5-en-2-yl]-1,2,3,4,5,6,9,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate	162937272	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4)OC(=O)C)C)C)C	440.70	unknown	https://doi.org/10.1515/ZNB-2005-0916
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1515/ZNB-2005-0916
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0031-9422(00)81232-7
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/S0031-9422(00)81232-7
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/10.1515/ZNB-2005-0916
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
1-[(2R)-2-methyl-2-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]chromen-6-yl]ethanone	162871694	Click to see CC(=O)C1=CC2=C(C=C1)OC(C=C2)(C)COC3C(C(C(C(O3)CO)O)O)O	380.40	unknown	https://doi.org/10.1016/0031-9422(88)80802-1
1-[2-Methyl-2-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]chromen-6-yl]ethanone	14162655	Click to see CC(=O)C1=CC2=C(C=C1)OC(C=C2)(C)COC3C(C(C(C(O3)CO)O)O)O	380.40	unknown	https://doi.org/10.1016/0031-9422(88)80802-1
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
1-(2,2-Dimethylchromen-6-yl)ethanone	177040	Click to see CC(=O)C1=CC2=C(C=C1)OC(C=C2)(C)C	202.25	unknown	https://doi.org/10.1016/0031-9422(88)80802-1
Encecalin	114703	Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)C)OC	232.27	unknown	https://doi.org/10.1016/0031-9422(88)80802-1
Eupatoriochromene	100768	Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)C)O	218.25	unknown	https://doi.org/10.1016/0031-9422(88)80802-1
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferide	5281666	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.3987/COM-08-S(F)79
Rhamnetin	5281691	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O	316.26	unknown	https://doi.org/10.3987/COM-08-S(F)79
Tamarixetin	5281699	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	316.26	unknown	https://doi.org/10.3987/COM-08-S(F)79
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
5,7-Dihydroxy-2-(3-hydroxy-5-methoxyphenyl)-2,3-dihydrochromen-4-one	74819362	Click to see COC1=CC(=CC(=C1)O)C2CC(=O)C3=C(C=C(C=C3O2)O)O	302.28	unknown	https://doi.org/10.3987/COM-08-S(F)79
5,7,3'-Trihydroxy-5'-methoxyflavanone	42607889	Click to see COC1=CC(=CC(=C1)O)C2CC(=O)C3=C(C=C(C=C3O2)O)O	302.28	unknown	https://doi.org/10.3987/COM-08-S(F)79
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
5,7-Dihydroxy-3',4'-dimethoxyflavone	5351234	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC	314.29	unknown	https://doi.org/10.3987/COM-08-S(F)79
5,7-Dihydroxy-4'-methoxyflavanone	5118250	Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O	286.28	unknown	https://doi.org/10.3987/COM-08-S(F)79
Dihydrokaempferide	21721857	Click to see COC1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O	302.28	unknown	https://doi.org/10.3987/COM-08-S(F)79
Isosakuranetin	160481	Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O	286.28	unknown	https://doi.org/10.3987/COM-08-S(F)79
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
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/10.1515/ZNC-1996-11-1219
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-8-hydroxy-6,7-dimethoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one	42599499	Click to see COC1=CC=C(C=C1)C2CC(=O)C3=CC(=C(C(=C3O2)O)OC)OC	330.30	unknown	https://doi.org/10.3987/COM-08-S(F)79
3,3',5-Trihydroxy-4',7-dimethoxyflavanone	11256019	Click to see COC1=C(C=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)OC)O)O)O	332.30	unknown	https://doi.org/10.3987/COM-08-S(F)79
8-Hydroxy-6,7-dimethoxy-2-(4-methoxyphenyl)-2,3-dihydrochromen-4-one	74827138	Click to see COC1=CC=C(C=C1)C2CC(=O)C3=CC(=C(C(=C3O2)O)OC)OC	330.30	unknown	https://doi.org/10.3987/COM-08-S(F)79
Aromadendrin 7-methyl ether	181132	Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=C(C=C3)O)O	302.28	unknown	https://doi.org/10.3987/COM-08-S(F)79
Folerogenin	5319509	Click to see COC1=CC(=C2C(=C1)OC(C(C2=O)O)C3=CC=C(C=C3)O)O	302.28	unknown	https://doi.org/10.3987/COM-08-S(F)79
Tetramethylscutellarein	96118	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC	342.30	unknown	https://doi.org/10.3987/COM-08-S(F)79
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2S)-2-(3-hydroxy-4-methoxyphenyl)-6,7,8-trimethoxy-2,3-dihydrochromen-4-one	42599498	Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=CC(=C(C(=C3O2)OC)OC)OC)O	360.40	unknown	https://doi.org/10.3987/COM-08-S(F)79
2-(3-Hydroxy-4-methoxyphenyl)-6,7,8-trimethoxy-2,3-dihydrochromen-4-one	74827137	Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=CC(=C(C(=C3O2)OC)OC)OC)O	360.40	unknown	https://doi.org/10.3987/COM-08-S(F)79
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one	11602329	Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC	328.27	unknown	https://doi.org/10.1515/ZNB-2005-0916
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
4,2'-Dihydroxy-4',5',6'-trimethoxychalcone	253005	Click to see COC1=C(C(=C(C(=C1)O)C(=O)C=CC2=CC=C(C=C2)O)OC)OC	330.30	unknown	https://doi.org/10.3987/COM-08-S(F)79
4,6'-Dihydroxy-2',3',4'-trimethoxychalcone	5357334	Click to see COC1=C(C(=C(C(=C1)O)C(=O)C=CC2=CC=C(C=C2)O)OC)OC	330.30	unknown	https://doi.org/10.3987/COM-08-S(F)79
> Phenylpropanoids and polyketides / Macrolides and analogues
3,13,15,25,35,37-Hexahydroxy-11,33-bis[3-hydroxy-6-(4-methoxy-6-methyloxan-2-yl)-4-methylhexan-2-yl]-17,39-dimethoxy-6,12,16,28,34,38-hexamethyl-10,32,45,46-tetraoxatricyclo[39.3.1.119,23]hexatetraconta-5,7,21,27,29,43-hexaene-9,31-dione	73309078	Click to see CC1CC(CC(O1)CCC(C)C(C(C)C2C(C(CC(C(C(CC3CC=CC(O3)CC(CC=C(C=CC(=O)OC(C(C(CC(C(C(CC4CC=CC(O4)CC(CC=C(C=CC(=O)O2)C)O)OC)C)O)O)C)C(C)C(C(C)CCC5CC(CC(O5)C)OC)O)C)O)OC)C)O)O)C)O)OC	1389.90	unknown	https://doi.org/10.1016/S0031-9422(00)81232-7

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Ageratina altissima

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