Scientific name	Authority	First published in
Eupatorium riparium	Regel	Gartenflora 15 1866
Eupatorium riparium	Regel	Gartenflora xv. (1866) 324. I. 525.
Eupatorium harrisii	Urb.	Symb. Antill. 1(3): 460 (1899)
Ageratina ventillana	(Cuatrec.) R.M.King & H.Rob.	Phytologia 19: 217 (1970)
Fleischmannia repens	B.L.Rob.	Proc. Amer. Acad. Arts 54: 262 (1918)
Eupatorium ventillanum	Cuatrec.	Ann. Missouri Bot. Gard. 52: 305 (1965)
Ageratina repens	(B.L.Rob.) R.M.King & H.Rob.	Phytologia 19: 216 (1970)

Common names Top

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Filter by language:

Language	Common/alternative name
English	spreading snakeroot
English	creeping crofton weed
English	mist flower
Indonesian	teklan
jv	rara ireng
jv	tekelan
Ukrainian	Туманна квітка
Chinese	河岸泽兰
Chinese	河岸破坏草
Chinese	澤假藿香薊
Chinese	溪边紫茎泽兰
Chinese	雾花泽兰

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Canary Islands
  - Madeira
- Southern Africa
  - Kwazulu-Natal
- Western Indian Ocean
  - Mauritius
  - Rodrigues
  - Réunion

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - India
  - Sri Lanka
- Malesia
  - Jawa
  - Malaya

Australasia click to expand
- Australia
  - New South Wales
  - Norfolk Island
  - Queensland
- New Zealand
  - New Zealand North

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Southwest

Pacific click to expand
- North-central Pacific
  - Hawaii

Southern America click to expand
- Caribbean
  - Bermuda
  - Cuba
  - Jamaica
- Western South America
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000125911
USDA Plants	AGRI2
Tropicos	2709250
INPN	656287
KEW	urn:lsid:ipni.org:names:7013-2
The Plant List	gcc-86968
Open Tree Of Life	891088
Observations.org	199450
NCBI Taxonomy	287013
Nature Serve	2.155914
IPNI	7013-2
iNaturalist	158112
GBIF	5400790
Freebase	/m/043rj_3
EPPO	EUPRI
EOL	468162
USDA GRIN	317712
Wikipedia	Ageratina_riparia
CMAUP	NPO6147

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

Reproductive Parameters and Host Specificity of Eurytoma erythrinae (Hymenoptera: Eurytomidae), a Biological Control Agent of the Erythrina Gall Wasp, Quadrastichus erythrinae (Hymenoptera: Eulophidae)

Nagamine WT, Yalemar JA, Wright MG, Ramadan MM

Insects

03-Dec-2023

PMCID:	PMC10743454
doi:	10.3390/insects14120923
PMID:	38132597

Untapped potential of non-conventional rubus species: bioactivity, nutrition, and livelihood opportunities

Bhatt SC, Naik B, Kumar V, Gupta AK, Kumar S, Preet MS, Sharma N, Rustagi S

Plant Methods

27-Oct-2023

PMCID:	PMC10604922
doi:	10.1186/s13007-023-01094-y
PMID:	37891607

Screening antibiofilm activity of invasive plants growing at the Slope Merapi Mountain, Central Java, against Candida albicans

Desrini S, Girardot M, Imbert C, Mustofa M, Nuryastuti T

BMC Complement Med Ther

12-Jul-2023

PMCID:	PMC10339508
doi:	10.1186/s12906-023-04044-2
PMID:	37438777

Equine Crofton Weed (Ageratina spp.) Pneumotoxicity: What Do We Know and What Do We Need to Know?

Shapter FM, Granados-Soler JL, Stewart AJ, Bertin FR, Allavena R

Animals (Basel)

23-Jun-2023

PMCID:	PMC10339876
doi:	10.3390/ani13132082
PMID:	37443880

Thorectidiol A Isolated from the Marine Sponge Dactylospongia elegans Disrupts Interactions of the SARS-CoV-2 Spike Receptor Binding Domain with the Host ACE2 Receptor

Williams DE, Cassel J, Zhu JL, Yang JX, de Voogd NJ, Matainaho T, Salvino JM, Wang YA, Montaner LJ, Tietjen I, Andersen RJ

J Nat Prod

19-Jan-2023

PMCID:	PMC9885524
doi:	10.1021/acs.jnatprod.2c01030
PMID:	36657039

Plant pathogens as introduced weed biological control agents: Could antagonistic fungi be important factors determining agent success or failure?

Den Breeyen A, Lange C, Fowler SV

Front Fungal Biol

26-Jul-2022

PMCID:	PMC10512343
doi:	10.3389/ffunb.2022.959753
PMID:	37746189

Life Histories and Host-Range Evaluation of Two Chrysomelid Beetles (Zygogramma spp.) Released against Tithonia rotundifolia in South Africa

Mawela KV, Simelane DO, Olckers T

Insects

08-Mar-2022

PMCID:	PMC8954993
doi:	10.3390/insects13030267
PMID:	35323565

Photosynthetic Properties of Co-Occurring Pioneer Species on Volcanically Devastated Sites in Miyake-jima Island, Japan

Zhang X, Li H, Hu X, Zheng P, Hirota M, Kamijo T

Plants (Basel)

18-Nov-2021

PMCID:	PMC8621165
doi:	10.3390/plants10112500
PMID:	34834865

Chloroplast DNA analysis of the invasive weed, Himalayan balsam (Impatiens glandulifera), in the British Isles

Kurose D, Pollard KM, Ellison CA

Sci Rep

03-Jul-2020

PMCID:	PMC7335094
doi:	10.1038/s41598-020-67871-0
PMID:	32620928

Classifying Hawaiian plant species along a habitat generalist-specialist continuum: Implications for species conservation under climate change

Ainsworth A, Drake DR

PLoS One

07-Feb-2020

PMCID:	PMC7006925
doi:	10.1371/journal.pone.0228573
PMID:	32032387

Natural 6-hydroxy-chromanols and -chromenols: structural diversity, biosynthetic pathways and health implications

Birringer M, Siems K, Maxones A, Frank J, Lorkowski S

RSC Adv

26-Jan-2018

PMCID:	PMC9078042
doi:	10.1039/c7ra11819h
PMID:	35539527

Processes affecting altitudinal distribution of invasive Ageratina adenophora in western Himalaya: The role of local adaptation and the importance of different life-cycle stages

Datta A, Kühn I, Ahmad M, Michalski S, Auge H

PLoS One

10-Nov-2017

PMCID:	PMC5695283
doi:	10.1371/journal.pone.0187708
PMID:	29125852

Alien plant invasions of protected areas in Java, Indonesia

Padmanaba M, Tomlinson KW, Hughes AC, Corlett RT

Sci Rep

24-Aug-2017

PMCID:	PMC5570924
doi:	10.1038/s41598-017-09768-z
PMID:	28839224

Alien plant invasions and native plant extinctions: a six-threshold framework

Downey PO, Richardson DM

AoB Plants

02-Aug-2016

PMCID:	PMC4972473
doi:	10.1093/aobpla/plw047
PMID:	27422543

On the analysis of phylogenetically paired designs

Funk JL, Rakovski CS, Macpherson JM

Ecol Evol

30-Jan-2015

PMCID:	PMC4338975
doi:	10.1002/ece3.1406
PMID:	25750719

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
[(1R,2R,6S,10R,11R,13S,14R,15R)-13-acetyloxy-8-formyl-1-hydroxy-4,12,12,15-tetramethyl-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] 2-(methylamino)benzoate	162901456	Click to see CC1C(C2(C(C2(C)C)C3C1(C4C=C(C(=O)C4CC(=C3)C=O)C)O)OC(=O)C)OC(=O)C5=CC=CC=C5NC	521.60	unknown	https://doi.org/10.1016/0031-9422(92)80345-F
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)-	91104	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4S,5E,9E,11aS)-6,10-dimethyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-(hydroxymethyl)but-2-enoate	24838342	Click to see CC1=CC(C2C(CC(=CCC1)C)OC(=O)C2=C)OC(=O)C(=CCO)CO	362.40	unknown	via CMAUP database
> 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/10.1016/0031-9422(92)80345-F
[(4aR,6aS,6aR,6bR,8aR,12aS,14aS,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-yl] acetate	137704689	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/10.1016/0031-9422(92)80345-F
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	610148	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C	426.70	unknown	https://doi.org/10.1016/0031-9422(92)80345-F
Friedelinol	101341	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	via CMAUP database
Taraxasterol	115250	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C	426.70	unknown	https://doi.org/10.1016/0031-9422(92)80345-F
Taraxasterol Acetate	13889352	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/10.1016/0031-9422(92)80345-F
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/10.1016/0031-9422(92)80345-F
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(1R)-1-[(2S)-2-(hydroxymethyl)-7,8-dimethoxy-2-methylchromen-6-yl]ethanol	162999727	Click to see CC(C1=C(C(=C2C(=C1)C=CC(O2)(C)CO)OC)OC)O	280.32	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
1-[(2R)-2-(hydroxymethyl)-7,8-dimethoxy-2-methylchromen-6-yl]ethanone	162853317	Click to see CC(=O)C1=C(C(=C2C(=C1)C=CC(O2)(C)CO)OC)OC	278.30	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
1-[(2R)-7-hydroxy-2-(hydroxymethyl)-8-methoxy-2-methylchromen-6-yl]ethanone	163018154	Click to see CC(=O)C1=C(C(=C2C(=C1)C=CC(O2)(C)CO)OC)O	264.27	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
1-[(2S)-2-(hydroxymethyl)-8-methoxy-2-methylchromen-6-yl]ethanone	162966699	Click to see CC(=O)C1=CC2=C(C(=C1)OC)OC(C=C2)(C)CO	248.27	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
1-[(2S)-7-hydroxy-2-(hydroxymethyl)-2-methylchromen-6-yl]ethanone	13851478	Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)CO)O	234.25	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
1-[2-(Hydroxymethyl)-7,8-dimethoxy-2-methylchromen-6-yl]ethanol	162999726	Click to see CC(C1=C(C(=C2C(=C1)C=CC(O2)(C)CO)OC)OC)O	280.32	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
1-[2-(Hydroxymethyl)-7,8-dimethoxy-2-methylchromen-6-yl]ethanone	162853316	Click to see CC(=O)C1=C(C(=C2C(=C1)C=CC(O2)(C)CO)OC)OC	278.30	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
1-[2-(Hydroxymethyl)-8-methoxy-2-methylchromen-6-yl]ethanone	162966698	Click to see CC(=O)C1=CC2=C(C(=C1)OC)OC(C=C2)(C)CO	248.27	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
1-[7-Hydroxy-2-(hydroxymethyl)-2-methylchromen-6-yl]ethanone	13851477	Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)CO)O	234.25	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
1-[7-Hydroxy-2-(hydroxymethyl)-8-methoxy-2-methylchromen-6-yl]ethanone	163018153	Click to see CC(=O)C1=C(C(=C2C(=C1)C=CC(O2)(C)CO)OC)O	264.27	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(1R)-1-(7,8-dimethoxy-2,2-dimethylchromen-6-yl)ethanol	100945948	Click to see CC(C1=C(C(=C2C(=C1)C=CC(O2)(C)C)OC)OC)O	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
[2-(7-Hydroxy-2,2-dimethylchromen-6-yl)-2-oxoethyl] 2-methylpropanoate	101967015	Click to see CC(C)C(=O)OCC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)C)O	304.34	unknown	https://doi.org/10.1016/0031-9422(92)80345-F
1-(7-Hydroxy-8-methoxy-2,2-dimethylchromen-6-yl)ethanone	12314885	Click to see CC(=O)C1=C(C(=C2C(=C1)C=CC(O2)(C)C)OC)O	248.27	unknown	https://doi.org/10.1016/0031-9422(92)80345-F https://doi.org/10.1016/S0031-9422(00)80693-7
1-(8-Methoxy-2,2-dimethyl-2H-1-benzopyran-6-yl)ethan-1-one	10466473	Click to see CC(=O)C1=CC2=C(C(=C1)OC)OC(C=C2)(C)C	232.27	unknown	https://doi.org/10.1002/CBER.19771100132 https://doi.org/10.1016/S0031-9422(00)80693-7 https://doi.org/10.1016/0031-9422(71)85045-8
2-(7-Hydroxy-2,2-dimethyl-2H-1-benzopyran-6-yl)-2-oxoethyl acetate	71359087	Click to see CC(=O)OCC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)C)O	276.28	unknown	https://doi.org/10.1016/0031-9422(92)80345-F https://doi.org/10.1016/S0031-9422(00)80693-7
6-(1-Hydroxyethyl)-7,8-dimethoxy-2,2-dimethyl-2h-1-benzopyran	10706737	Click to see CC(C1=C(C(=C2C(=C1)C=CC(O2)(C)C)OC)OC)O	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
7,8-Dimethoxy-2,2-dimethylchromen-6-ol	86146315	Click to see CC1(C=CC2=CC(=C(C(=C2O1)OC)OC)O)C	236.26	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
Desacetylripariochromene B	14282640	Click to see CC1(C=CC2=CC(=C(C=C2O1)O)C(=O)CO)C	234.25	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
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(92)80345-F https://doi.org/10.1016/S0031-9422(00)80693-7
Methylripariochromene A	177148	Click to see CC(=O)C1=C(C(=C2C(=C1)C=CC(O2)(C)C)OC)OC	262.30	unknown	https://doi.org/10.1016/0031-9422(71)85045-8 https://doi.org/10.1016/0031-9422(92)80345-F https://doi.org/10.1016/S0031-9422(00)80693-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
(6R)-17,18-dimethoxy-6-prop-1-en-2-yl-2,7,14,21-tetraoxapentacyclo[11.9.0.03,11.04,8.015,20]docosa-1(13),3(11),4(8),9,15,17,19-heptaen-12-one	10501591	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)OC5=CC(=C(C=C5OC4)OC)OC	408.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
13-Homo-13-oxa-6a,12a-dehydrodeguelin	10092854	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)OC5=CC(=C(C=C5OC4)OC)OC)C	408.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(6-Acetyl-7-hydroxy-2-methylchromen-2-yl)methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	163075502	Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O	410.40	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
(6-Acetyl-8-methoxy-2-methylchromen-2-yl)methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	162900071	Click to see CC(=O)C1=CC2=C(C(=C1)OC)OC(C=C2)(C)COC(=O)C=CC3=CC(=C(C=C3)O)OC	424.40	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
[(2R)-6-acetyl-7-hydroxy-2-methylchromen-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	163187190	Click to see CC(=O)C1=C(C=C2C(=C1)C=CC(O2)(C)COC(=O)C=CC3=CC(=C(C=C3)O)OC)O	410.40	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
[(2R)-6-acetyl-8-methoxy-2-methylchromen-2-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	163186318	Click to see CC(=O)C1=CC2=C(C(=C1)OC)OC(C=C2)(C)COC(=O)C=CC3=CC(=C(C=C3)O)OC	424.40	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-6-(Gamma,Gamma-Dimethylallyl)-5-Hydroxy-3',4'-Dimethoxy-6'',6''-Dimethylpyran(2'',3'':7,8)Flavanone	44559036	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC(=C(C=C4)OC)OC)O)C	450.50	unknown	via CMAUP database
(2S)-6-(gamma,gamma-dimethylallyl)-5,3'-dihydroxy-4'-methoxy-6'',6''-dimethylpyran[2'',3'':7,8]flavanone	44559037	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC(=C(C=C4)OC)O)O)C	436.50	unknown	via CMAUP database
(2S)-6-(gamma,gamma-dimethylallyl)-5,4'-dihydroxy-3'-methoxy-6'',6''-dimethylpyran[2'',3'':7,8]flavanone	44559077	Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC(=C(C=C4)O)OC)O)C	436.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Anhydropisatin	11822566	Click to see COC1=CC2=C(C=C1)C3=C(CO2)C4=CC5=C(C=C4O3)OCO5	296.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids
Rotenonone	442819	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=O)OC)OC	406.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(1)Benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(12H)-one, 1,2-dihydro-8,9-dimethoxy-2-(1-methylethenyl)-, (R)-	99190	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC	392.40	unknown	via CMAUP database
(1R,13R)-6-acetyl-13-hydroxy-16,17-dimethoxy-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),5,9,14,16,18-heptaen-12-one	10549503	Click to see CC(=O)C1=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC	410.40	unknown	via CMAUP database
(1R,14R)-14,17,18-trimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one	100970022	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)OC)OC)OC)C	424.40	unknown	via CMAUP database
(1R,14S)-14-hydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),5,10,15,17,19-heptaen-13-one	11962145	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C	410.40	unknown	via CMAUP database
(1R,5R,6S,14R)-5,6,14-trihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),10,15,17,19-hexaen-13-one	11797541	Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C	444.40	unknown	via CMAUP database
(1R,5S,6R,14R)-5,6,14-trihydroxy-17,18-dimethoxy-7,7-dimethyl-2,8,21-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-3(12),4(9),10,15,17,19-hexaen-13-one	10049103	Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C	444.40	unknown	via CMAUP database
(1R,6R,13R)-13,16,17-trimethoxy-6-prop-1-en-2-yl-2,7,20-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-3(11),4(8),9,14,16,18-hexaen-12-one	100970024	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)OC)OC)OC	424.40	unknown	via CMAUP database
(1R)-1beta,2beta,7aalpha-Trihydroxy-9,10-dimethoxy-3,3-dimethyl-1,2,13,13aalpha-tetrahydro-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one	10694586	Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C	444.40	unknown	via CMAUP database
(1S)-1alpha,2alpha,7aalpha-Trihydroxy-9,10-dimethoxy-3,3-dimethyl-1,2,13,13aalpha-tetrahydro-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one	10789429	Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C	444.40	unknown	via CMAUP database
(2R)-1,2,12,12aalpha-Tetrahydro-6abeta-methoxy-2alpha-isopropenyl-8,9-dimethoxy-[1]benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-one	100970021	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)OC)OC)OC	424.40	unknown	via CMAUP database
(6Ar,12aR)-9,12a-dihydroxy-2,3-dimethoxy-8-(3-methylbut-2-enyl)-6,6a-dihydrochromeno[3,4-b]chromen-12-one	51136534	Click to see CC(=CCC1=C(C=CC2=C1OC3COC4=CC(=C(C=C4C3(C2=O)O)OC)OC)O)C	412.40	unknown	via CMAUP database
(7aS)-13,13aalpha-Dihydro-7abeta-methoxy-9,10-dimethoxy-3,3-dimethyl-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one	100970023	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)OC)OC)OC)C	424.40	unknown	via CMAUP database
11-Hydroxytephrosin	155725	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C	426.40	unknown	via CMAUP database
alpha-Toxicarol	442826	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C	410.40	unknown	via CMAUP database
Deguelin	107935	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C	394.40	unknown	via CMAUP database
Dehydrodeguelin	3083803	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)C	392.40	unknown	via CMAUP database
Dehydrotoxicarol	5491616	Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)O)C	408.40	unknown	via CMAUP database
rel-(7aR,13aR)-9,10-Dimethoxy-3,3-dimethyl-13,13a-dihydro-3H-pyrano[2,3-c:6,5-f']dichromen-7(7aH)-one	184223	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C	394.40	unknown	via CMAUP database
Rotenolon II	99189	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC	410.40	unknown	via CMAUP database
Rotenolone	68184	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC	410.40	unknown	via CMAUP database
Rotenone	6758	Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC	394.40	unknown	via CMAUP database
Tephrosin	114909	Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C	410.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Isobavachromene	5889042	Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C	322.40	unknown	via CMAUP database
Pongachalcone II	10712965	Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC(=C(C=C3)O)OC)C	352.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
2,2-dimethyl-7-[(E)-2-(3,4,5-trimethoxyphenyl)ethenyl]chromene	10689330	Click to see CC1(C=CC2=C(O1)C=C(C=C2)C=CC3=CC(=C(C(=C3)OC)OC)OC)C	352.40	unknown	via CMAUP database
4-[(E)-2-(5-methoxy-2,2-dimethylchromen-7-yl)ethenyl]phenol	10542828	Click to see CC1(C=CC2=C(O1)C=C(C=C2OC)C=CC3=CC=C(C=C3)O)C	308.40	unknown	via CMAUP database
5-Methoxy-2,2-dimethyl-7-[2-(4-hydroxy-3-methoxyphenyl)ethenyl]-2H-1-benzopyran	10520980	Click to see CC1(C=CC2=C(O1)C=C(C=C2OC)C=CC3=CC(=C(C=C3)O)OC)C	338.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
5-(6-Hydroxy-7,8-dimethoxy-2,2-dimethylchromen-5-yl)-7,8-dimethoxy-2,2-dimethylchromen-6-ol	163046779	Click to see CC1(C=CC2=C(C(=C(C(=C2O1)OC)OC)O)C3=C4C=CC(OC4=C(C(=C3O)OC)OC)(C)C)C	470.50	unknown	https://doi.org/10.1016/S0031-9422(00)80693-7

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Ageratina riparia

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