Scientific name	Authority	First published in
Ageratum mexicanum	Sweet	The British Flower Garden 1 1825
Ageratum wendlandii	compactum nanum coeruleum vilm. ex Voss	Vilmorin's Blumengaertnerei . . . Dritte neubearbeite Auflage . . . 46 1894
Cacalia mentrasto	Vell.	Fl. Flumin. 339. 1829 [1825 publ. 7 Sep-28 Nov 1829] ; see also Fl. Flumin. Icon. 8: t. 69. 1831. [1827 publ. 29 Oct 1831]
Ageratum pinetorum	(L.O.Williams) R.M.King & H.Rob.	Phytologia 24: 115 (1972)
Carelia houstoniana	Kuntze	Revis. Gen. Pl. 1: 325 (1891)
Ageratum mexicanum	Sims	Bot. Mag. 52: t. 2524 (1824)
Cacalia mentrasto	Vell.Conc.	n. Flum. 339. 1825.
Ageratum conyzoides subsp. houstonianum	(Mill.) M.Sharma	Geobios, New Rep. 3(2): 152 (1984)
Ageratum wendlandii	Hort. ex Vilm.	Fl. Pl. Terre, Suppl. 2.
Ageratum wendlandii	Bailly	Suppl. Fl. Pleine Terre: 2 (1884)
Ageratum mexicanum var. nanum	Voss	Vilm. Blumengärtn. ed. 3, 2: 445 (1896)
Ageratum conyzoides var. mexicanum	(Sims) DC.	Prodr. 5: 108 (1836)
Ageratum conyzoides subsp. houstonianum	(Mill.) Sahu	Feddes Repert., 93(1–2): 64 (1982):.
Ageratum mexicanum f. caeruleum	Voss	Vilm. Blumengärtn. ed. 3, 2: 445 (1896)
Ageratum mexicanum f. wendlandii	Voss	Vilm. Blumengärtn. ed. 3, 2: 445 (1896)
Ageratum conyzoides var. houstonianum	(Mill.) T.R.Sahu	Feddes Repert. 93(1-2): 64 (1982)

Common names Top

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Filter by language:

Language	Common/alternative name
English	bluemink
English	mexican floss flower
Belarusian	агератум Хоўстана
Belarusian	агератум мексіканскі
Czech	nestařec americký
Welsh	ageratwm
German	gewöhnlicher leberbalsam
Finnish	meksikonsinitähtönen
Finnish	sinitähtönen
Armenian	Անծերի մեքսիկական
Japanese	オオカッコウアザミ
Korean	불로화
Lithuanian	meksikinis žydrūnis
Macedonian	Сина ѕвездичка
Norwegian Bokmål	blåkurv
Nepali	निलो गन्धे
Polish	Żeniszek meksykański
pwn	kaljaljuljalju
Russian	Агератум Гаустона
Slovak	agerát mexický
Serbian	Агератум
Swedish	leverbalsam
Chinese	臭草仔
Chinese	紫花藿香薊
Chinese	紫花毛麝香
Chinese	熊耳草
Chinese	斷血草
Chinese	墨西哥藍薊
Chinese	勝紅薊
Chinese	胜红蓟

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
  - Azores
  - Canary Islands
  - Madeira
- Northeast Tropical Africa
  - Chad
  - Ethiopia
  - Sudan
- Northern Africa
  - Egypt
- South Tropical Africa
  - Zimbabwe
- Southern Africa
  - Cape Provinces
  - Kwazulu-Natal
  - Northern Provinces
  - Swaziland
- West Tropical Africa
  - Benin
  - Mali
- West-central Tropical Africa
  - Cameroon
  - Zaïre
- Western Indian Ocean
  - Mauritius

Asia-temperate click to expand
- Caucasus
  - Transcaucasus
- China
  - China North-central
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Korea
  - Taiwan
- Middle Asia
  - Kazakhstan
  - Turkmenistan
  - Uzbekistan
- Russian Far East
  - Primorye

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
- Indo-China
  - Myanmar
  - Vietnam
- Malesia
  - Jawa
  - Malaya
  - Philippines
  - Sumatera

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

Europe click to expand
- Eastern Europe
  - Belarus
  - Krym
  - South European Russia
  - Ukraine
- Middle Europe
  - Belgium
  - Germany
  - Hungary
  - Poland
- Northern Europe
  - Great Britain
- Southeastern Europe
  - Bulgaria
  - Italy
  - Yugoslavia
- Southwestern Europe
  - France
  - Portugal

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Northeast
  - Mexico Southeast
  - Mexico Southwest
- Northeastern U.S.A.
  - Connecticut
  - Massachusetts
  - New York
- South-central U.S.A.
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Florida
  - Georgia
  - North Carolina
  - South Carolina

Pacific click to expand
- North-central Pacific
  - Hawaii
- South-central Pacific
  - Society Islands
- Southwestern Pacific
  - Fiji
  - New Caledonia

Southern America click to expand
- Caribbean
  - Cuba
  - Jamaica
  - Trinidad-Tobago
- Central America
  - Belize
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua
  - Panamá
- Northern South America
  - Suriname
  - Venezuela
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000017628
Florida Plant Atlas	286
Flora of Alabama	5493
USDA Plants	AGHO3
Tropicos	2700027
INPN	80390
Flora of Italy	8387
KEW	urn:lsid:ipni.org:names:175500-1
The Plant List	gcc-11706
Missouri Botanical Garden	277131
Open Tree Of Life	1071119
Observations.org	128452
NCBI Taxonomy	55598
NBN Atlas	NHMSYS0000455641
Nature Serve	2.157143
IPNI	175500-1
iNaturalist	120944
GBIF	5401760
Freebase	/m/0d55w2
EPPO	AGEHO
EOL	468158
Elurikkus	2584
USDA GRIN	1761
Wikipedia	Ageratum_houstonianum
CMAUP	NPO24969

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

ZnO nanostructured matrix as nexus catalysts for the removal of emerging pollutants

Matei E, Șăulean AA, Râpă M, Constandache A, Predescu AM, Coman G, Berbecaru AC, Predescu C

Environ Sci Pollut Res Int

03-Nov-2023

PMCID:	PMC10682326
doi:	10.1007/s11356-023-30713-3
PMID:	37919505

Reconstructed Global Invasion and Spatio-Temporal Distribution Pattern Dynamics of Sorghum halepense under Climate and Land-Use Change

Yang M, Zhao H, Xian X, Qi Y, Li Q, Guo J, Chen L, Liu W

Plants (Basel)

31-Aug-2023

PMCID:	PMC10489930
doi:	10.3390/plants12173128
PMID:	37687374

Biogenic Nanoparticles Silver and Copper and Their Composites Derived from Marine Alga Ulva lactuca: Insight into the Characterizations, Antibacterial Activity, and Anti-Biofilm Formation

Hamouda RA, Alharthi MA, Alotaibi AS, Alenzi AM, Albalawi DA, Makharita RR

Molecules

29-Aug-2023

PMCID:	PMC10489668
doi:	10.3390/molecules28176324
PMID:	37687153

Hippophae rhamnoides L. (sea buckthorn) mediated green synthesis of copper nanoparticles and their application in anticancer activity

Dadhwal P, Dhingra HK, Dwivedi V, Alarifi S, Kalasariya H, Yadav VK, Patel A

Front Mol Biosci

24-Aug-2023

PMCID:	PMC10484619
doi:	10.3389/fmolb.2023.1246728
PMID:	37692067

Biogenic Synthesis of Copper Nanoparticles: A Systematic Review of Their Features and Main Applications

Luque-Jacobo CM, Cespedes-Loayza AL, Echegaray-Ugarte TS, Cruz-Loayza JL, Cruz I, de Carvalho JC, Goyzueta-Mamani LD

Molecules

18-Jun-2023

PMCID:	PMC10301071
doi:	10.3390/molecules28124838
PMID:	37375393

Patterns of understory invasion in invasive timber stands of a tropical sky island

Jobin V, Das A, Harikrishnan CP, Chanda R, Lawrence S, Robin VV

Ecol Evol

13-Apr-2023

PMCID:	PMC10099487
doi:	10.1002/ece3.9995
PMID:	37066061

Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India?

Kumar BM

Agrofor Syst

07-Apr-2023

PMCID:	PMC10081327
doi:	10.1007/s10457-023-00821-7
PMID:	37193256

One-Pot Synthesis of Silver Nanoparticles Derived from Aqueous Leaf Extract of Ageratum conyzoides and Their Biological Efficacy

Paramasivam D, Balasubramanian B, Suresh R, Kumaravelu J, Vellingiri MM, Liu WC, Meyyazhagan A, Alanazi AM, Rengasamy KR, Arumugam VA

Antibiotics (Basel)

01-Apr-2023

PMCID:	PMC10135330
doi:	10.3390/antibiotics12040688
PMID:	37107050

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

Phytochemical Profiling of Sambucus nigra L. Flower and Leaf Extracts and Their Antimicrobial Potential against Almond Tree Pathogens

Sánchez-Hernández E, Balduque-Gil J, González-García V, Barriuso-Vargas JJ, Casanova-Gascón J, Martín-Gil J, Martín-Ramos P

Int J Mol Sci

06-Jan-2023

PMCID:	PMC9866908
doi:	10.3390/ijms24021154
PMID:	36674670

Larvicidal and repellent potential of Ageratum houstonianum against Culex pipiens

Hadidy DE, El Sayed AM, Tantawy ME, Alfy TE, Farag SM, Haleem DR

Sci Rep

10-Dec-2022

PMCID:	PMC9741651
doi:	10.1038/s41598-022-25939-z
PMID:	36496475

β-Caryophyllene Ameliorates 2,4-Dinitrochlorobenzene-Induced Atopic Dermatitis through the Downregulation of Mitogen-Activated Protein Kinase/EGR1/TSLP Signaling Axis

Ahn SS, Yeo H, Jung E, Ou S, Lee YH, Lim Y, Shin SY

Int J Mol Sci

28-Nov-2022

PMCID:	PMC9740728
doi:	10.3390/ijms232314861
PMID:	36499191

Pomelo seed oil: Natural insecticide against cowpea aphid

Ling W, Kaliaperumal K, Huang M, Liang Y, Ouyang Z, Zhou Z, Jiang Y, Zhang J

Front Plant Sci

08-Nov-2022

PMCID:	PMC9681153
doi:	10.3389/fpls.2022.1048814
PMID:	36426147

Edible Flower Species as a Promising Source of Specialized Metabolites

Dujmović M, Radman S, Opačić N, Fabek Uher S, Mikuličin V, Voća S, Šic Žlabur J

Plants (Basel)

27-Sep-2022

PMCID:	PMC9570977
doi:	10.3390/plants11192529
PMID:	36235395

Editorial: Edible flowers: Understanding the effect of genotype, preharvest, and postharvest on quality, safety, and consumption

Scariot V, Ferrante A, Romano D

Front Plant Sci

13-Sep-2022

PMCID:	PMC9513602
doi:	10.3389/fpls.2022.1025196
PMID:	36176674

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
(7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-hydroxy-2,3-dimethylbutanoate	22297469	Click to see CC(C)C(C)(C(=O)OCC1=CCN2C1C(CC2)O)O	269.34	unknown	https://doi.org/10.1016/S0031-9422(01)00192-3
[(1R,8R)-7-(hydroxymethyl)-2,3,5,8-tetrahydro-1H-pyrrolizin-1-yl] (2S)-2-hydroxy-2,3-dimethylbutanoate	162994979	Click to see CC(C)C(C)(C(=O)OC1CCN2C1C(=CC2)CO)O	269.34	unknown	https://doi.org/10.1016/S0031-9422(01)00192-3
[(1R,8S)-7-(hydroxymethyl)-2,3,5,8-tetrahydro-1H-pyrrolizin-1-yl] (2S)-2-hydroxy-2,3-dimethylbutanoate	162994980	Click to see CC(C)C(C)(C(=O)OC1CCN2C1C(=CC2)CO)O	269.34	unknown	https://doi.org/10.1016/S0031-9422(01)00192-3
[(1R,8S)-7-(hydroxymethyl)-2,3,5,8-tetrahydro-1H-pyrrolizin-1-yl]methyl (2S)-2-hydroxy-2,3-dimethylbutanoate	102019615	Click to see CC(C)C(C)(C(=O)OCC1CCN2C1C(=CC2)CO)O	283.36	unknown	https://doi.org/10.1016/S0031-9422(01)00192-3
[(7S,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2-hydroxy-2,3-dimethylbutanoate	12972112	Click to see CC(C)C(C)(C(=O)OCC1=CCN2C1C(CC2)O)O	269.34	unknown	https://doi.org/10.1016/S0031-9422(01)00192-3
[7-(hydroxymethyl)-2,3,5,8-tetrahydro-1H-pyrrolizin-1-yl] 2-hydroxy-2,3-dimethylbutanoate	162994978	Click to see CC(C)C(C)(C(=O)OC1CCN2C1C(=CC2)CO)O	269.34	unknown	https://doi.org/10.1016/S0031-9422(01)00192-3
Echinatine	22384	Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O	299.36	unknown	https://doi.org/10.1016/S0031-9422(01)00192-3
Intermedine, (+)-	114843	Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O	299.36	unknown	https://doi.org/10.1016/S0031-9422(01)00192-3
Lycopsamine	107938	Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O	299.36	unknown	https://doi.org/10.1016/S0031-9422(01)00192-3
Retrohoustine	636922	Click to see CC(C)C(C)(C(=O)OCC1=CCN2C1C(CC2)O)O	269.34	unknown	https://doi.org/10.1016/S0031-9422(01)00192-3
> 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 / Tetralins
(4S)-10-Nor-calamenen-10-one	73350586	Click to see CC1=CC2=C(C=C1)C(=O)CCC2C(C)C	202.29	unknown	via CMAUP database
Oxyphyllenotriol A	51041015	Click to see CC(C)C1=C2C(C(CCC2=C(C=C1)O)(C)O)O	236.31	unknown	via CMAUP database
Oxyphyllone G	51041016	Click to see CC1=C(C2=C(C=C1)C(=O)CCC2C(C)C)O	218.29	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid	445639	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Palmitoleic Acid	445638	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Tetracosanoic acid	11197	Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O	368.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid	5280934	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O	278.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Labda-8(17),12-diene-15,16-dial	11077520	Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C	302.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1r,2r)-p-Menth-3-en-1,2-diol	71423340	Click to see CC(C)C1=CC(C(CC1)(C)O)O	170.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2R,3R,6S,7S)-1-hydroxy-3,7-dimethyl-10-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undec-9-en-8-one	76285513	Click to see CC1CCC2C1C3(C(=CC(=O)C2(O3)C)C(C)C)O	250.33	unknown	via CMAUP database
Oxyphyllanene D	57396910	Click to see CC(=C)C1(CCC2(CCC(=O)C3(C2(C1)O3)C)C)O	250.33	unknown	via CMAUP database
Oxyphyllol E	51041018	Click to see CC(=C)C1(CCC2(CCC(=O)C3(C2(C1)O3)C)C)O	250.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(11S)-Nootkatone-11,12-diol	15601439	Click to see CC1CC(=O)C=C2C1(CC(CC2)C(C)(CO)O)C	252.35	unknown	via CMAUP database
(1S)-1,2,3,4,4a,5,6,7-Octahydro-4beta,4abeta-dimethyl-6alpha-(1-methylethenyl)naphthalene-1beta-ol	44576208	Click to see CC1CCC(C2=CCC(CC12C)C(=C)C)O	220.35	unknown	via CMAUP database
(3S,4aS,5R)-4a,5-dimethyl-3-prop-1-en-2-yl-3,4,5,6-tetrahydro-2H-naphthalene-1,7-dione	72715093	Click to see CC1CC(=O)C=C2C1(CC(CC2=O)C(=C)C)C	232.32	unknown	via CMAUP database
(4R,4aR)-6-acetyl-4,4a-dimethyl-3,4,7,8-tetrahydronaphthalen-2-one	117654813	Click to see CC1CC(=O)C=C2C1(C=C(CC2)C(=O)C)C	218.29	unknown	via CMAUP database
(4R,4aS,6R)-6-(2-hydroxypropan-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one	89960876	Click to see CC1CC(=O)C=C2C1(CC(CC2)C(C)(C)O)C	236.35	unknown	via CMAUP database
(4R,4aS,6R)-6-(3-hydroxyprop-1-en-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one	53249021	Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)CO)C	234.33	unknown	via CMAUP database
(4R)-4beta,4abeta-Dimethyl-6alpha-isopropenyl-8alpha-hydroxy-2,3,4,4a,5,6,7,8-octahydronaphthalene-2-one	11651584	Click to see CC1CC(=O)C=C2C1(CC(CC2O)C(=C)C)C	234.33	unknown	via CMAUP database
Nootkatene	25200342	Click to see CC1CC=CC2=CCC(CC12C)C(=C)C	202.33	unknown	via CMAUP database
Nootkatol	182645	Click to see CC1CC(C=C2C1(CC(CC2)C(=C)C)C)O	220.35	unknown	via CMAUP database
Nootkatone	1268142	Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C)C	218.33	unknown	via CMAUP database
oxyphyllol C	10857540	Click to see CC1CCC(C2(C1(CC(CC2)C(=C)C)C)O)O	238.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4aR,7R,8aS)-1,4a-dimethyl-7-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol	15560338	Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C	222.37	unknown	via CMAUP database
(2R,4aS,7R,8aR)-4a-Methyl-1-methylidene-7-(prop-1-en-2-yl)decahydronaphthalen-2-ol	14076604	Click to see CC(=C)C1CCC2(CCC(C(=C)C2C1)O)C	220.35	unknown	via CMAUP database
(4aS,7S,8R)-8-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one	57393410	Click to see CC1=C2C(C(CCC2(CCC1=O)C)C(=C)C)O	234.33	unknown	via CMAUP database
(4aS,7S)-7-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-4,5,6,8-tetrahydro-3H-naphthalen-2-one	57335617	Click to see CC1=C2CC(CCC2(CCC1=O)C)(C(=C)C)O	234.33	unknown	via CMAUP database
7-Epi-Teucrenone B	57393409	Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C	234.33	unknown	via CMAUP database
Ligucyperonol	14681770	Click to see CC1=C2CC(CCC2(C(CC1=O)O)C)C(=C)C	234.33	unknown	via CMAUP database
Oxyphyllol A	637451	Click to see CC(=C)C1CCC2(CCCC(C2=C1)(C)O)C	220.35	unknown	via CMAUP database
Rel-Oxyphyllanene E	57400339	Click to see CC(=C)C1(CCC2(CCC(C(=C)C2C1)O)C)O	236.35	unknown	via CMAUP database
Teucrenone	10105443	Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C	234.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(4aS,8aR,9aR)-3,5,8a-trimethyl-4a,8,9,9a-tetrahydro-4H-benzo[f][1]benzofuran-2,7-dione	71681246	Click to see CC1=CC(=O)CC2(C1CC3=C(C(=O)OC3C2)C)C	246.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Sitosteryl palmitate	9852570	Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C	653.10	unknown	via CMAUP database
Epifriedelanol	119242	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	https://doi.org/10.1016/S0031-9422(00)97171-1
Friedelinol	348029	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	https://doi.org/10.1016/S0031-9422(00)97171-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,8R,9R,10S,13R,14R,17S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	162965363	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)97171-1
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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Pubescone	102054514	Click to see CC(C)C1C2C(C2CCC(=O)C)CCC1=O	222.32	unknown	via CMAUP database
Spiro[4.4]nonan-2-one	549163	Click to see C1CCC2(C1)CCC(=O)C2	138.21	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4aR,6S,8aS)-6-acetyl-4a-hydroxy-4,8a-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-2-one	71681103	Click to see CC1=CC(=O)CC2(C1(CC(CC2)C(=O)C)O)C	236.31	unknown	via CMAUP database
(4aR)-7-acetyl-1,4a-dimethyl-3,4,5,6-tetrahydronaphthalen-2-one	71681245	Click to see CC1=C2C=C(CCC2(CCC1=O)C)C(=O)C	218.29	unknown	via CMAUP database
4-Hydroxy-11,12,13-trinor-5-eudesmen-7-one	15153217	Click to see CC12CCCC(C1=CC(=O)CC2)(C)O	194.27	unknown	via CMAUP database
OxyphyllaneneA	122402647	Click to see CC1=CC(=O)CC2(C1CC(=O)CC2)C	192.25	unknown	via CMAUP database
Oxyphyllenodiol A	10082923	Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O	238.32	unknown	via CMAUP database
Oxyphyllenodiol B	5279294	Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O	238.32	unknown	via CMAUP database
Oxyphyllenone A	10262534	Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O	210.27	unknown	via CMAUP database
Oxyphyllenone B	44310512	Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O	210.27	unknown	via CMAUP database
Oxyphyllone C	44255203	Click to see CC(C)C1CCC(=O)C2=C1C3C(O3)(CC2)C	220.31	unknown	via CMAUP database
Teuhetenone A	15153216	Click to see CC12CCCC(C1=CC(=O)CC2)(C)O	194.27	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
[(2S)-2-(6-acetyl-5-hydroxy-1-benzofuran-2-yl)propyl] 3-methylbutanoate	163049926	Click to see CC(C)CC(=O)OCC(C)C1=CC2=CC(=C(C=C2O1)C(=O)C)O	318.40	unknown	https://doi.org/10.1016/0031-9422(88)83072-3
1-[5-Hydroxy-2-(1-hydroxyprop-1-enyl)-1-benzofuran-6-yl]ethanone	163192816	Click to see CC=C(C1=CC2=CC(=C(C=C2O1)C(=O)C)O)O	232.23	unknown	https://doi.org/10.1016/S0031-9422(00)84592-6
1-[5-Hydroxy-2-(prop-1-en-2-yl)-1-benzofuran-6-yl]ethan-1-one	71336886	Click to see CC(=C)C1=CC2=CC(=C(C=C2O1)C(=O)C)O	216.23	unknown	https://doi.org/10.1016/S0031-9422(00)84592-6
2-(5-Acetyl-6-hydroxy-1-benzofuran-2-yl)prop-2-enyl acetate	90470827	Click to see CC(=O)C1=C(C=C2C(=C1)C=C(O2)C(=C)COC(=O)C)O	274.27	unknown	https://doi.org/10.3891/ACTA.CHEM.SCAND.24-0721 https://doi.org/10.1016/S0031-9422(00)84592-6
2-(6-Acetyl-5-hydroxy-1-benzofuran-2-yl)propyl 3-methylbutanoate	14186903	Click to see CC(C)CC(=O)OCC(C)C1=CC2=CC(=C(C=C2O1)C(=O)C)O	318.40	unknown	https://doi.org/10.1016/0031-9422(88)83072-3
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Precocene II	12565	Click to see CC1(C=CC2=CC(=C(C=C2O1)OC)OC)C	220.26	unknown	https://doi.org/10.1016/0031-9422(90)83022-S https://doi.org/10.3891/ACTA.CHEM.SCAND.09-1725
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans / Precocenes
Precocene I	28619	Click to see CC1(C=CC2=C(O1)C=C(C=C2)OC)C	190.24	unknown	https://doi.org/10.1016/0031-9422(90)83022-S
> Organoheterocyclic compounds / Epoxides
(1S,4S,6S,8E,12S)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.04,6]tridec-8-ene	12014673	Click to see CC1(CC2C(O2)(CCC3C(O3)(CC=C1)C)C)C	236.35	unknown	via CMAUP database
> Organoheterocyclic compounds / Oxepanes
Oxyphyllanene C	57335616	Click to see CC1=C2C3C(O3)(CCC2(CCC1=O)C)C(=O)C	234.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E)-1-(4-Hydroxy-3-methoxyphenyl)-7-phenyl-1-hepten-3-one	6440365	Click to see COC1=C(C=CC(=C1)C=CC(=O)CCCCC2=CC=CC=C2)O	310.40	unknown	via CMAUP database
1-(2,4-Dihydroxy-3-methoxyphenyl)-7-(4-methoxyphenyl)heptan-3-one	72708396	Click to see COC1=CC=C(C=C1)CCCCC(=O)CCC2=C(C(=C(C=C2)O)OC)O	358.40	unknown	via CMAUP database
1-(3,5-Dihydroxy-4-methoxyphenyl)-7-phenylheptan-3-one	72708395	Click to see COC1=C(C=C(C=C1O)CCC(=O)CCCCC2=CC=CC=C2)O	328.40	unknown	via CMAUP database
Yakuchinone-A	133145	Click to see COC1=C(C=CC(=C1)CCC(=O)CCCCC2=CC=CC=C2)O	312.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin	68071	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin	5281607	Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	254.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5-Dihydroxy-7-methoxy-2-(4-methoxyphenyl)-4H-chromen-4-one	5378823	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)O	314.29	unknown	via CMAUP database
Izalpinin	5318691	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O	284.26	unknown	via CMAUP database
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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,6,7,3',4',5'-Hexamethoxyflavone	185670	Click to see COC1=CC(=CC(=C1OC)OC)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC	402.40	unknown	https://doi.org/10.1016/S0031-9422(00)81761-6
Agehoustin B	389484	Click to see COC1=C(C(=C(C(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC)OC)OC	432.40	unknown	https://doi.org/10.1016/0031-9422(82)85260-6
Agehoustin G	13939321	Click to see COC1=CC(=C(C=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC	388.40	unknown	https://doi.org/10.1016/S0031-9422(00)81761-6
Tectochrysin	5281954	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Agecorynin C	256420	Click to see COC1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC)OC	432.40	unknown	https://doi.org/10.1016/0031-9422(82)85260-6
Agehoustin A	389483	Click to see COC1=C(C(=C(C(=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC)OC)OC	462.40	unknown	https://doi.org/10.1016/0031-9422(82)85260-6
Agehoustin C	13914992	Click to see COC1=C(C(=C(C(=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC)O)OC	448.40	unknown	https://doi.org/10.1016/S0031-9422(00)83188-X
Agehoustin D	13914993	Click to see COC1=C(C(=C(C(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O)OC	434.40	unknown	https://doi.org/10.1016/S0031-9422(00)83188-X
Agehoustin E	13939319	Click to see COC1=CC(=C(C=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)OC	418.40	unknown	https://doi.org/10.1016/S0031-9422(00)81761-6
Agehoustin F	13939320	Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O)OC	404.40	unknown	https://doi.org/10.1016/S0031-9422(00)81761-6
Eupalestin	331149	Click to see COC1=CC(=CC2=C1OCO2)C3=CC(=O)C4=C(O3)C(=C(C(=C4OC)OC)OC)OC	416.40	unknown	https://doi.org/10.1016/0031-9422(82)85260-6
Linderoflavone B	97151	Click to see COC1=C(C(=C(C2=C1C(=O)C=C(O2)C3=CC4=C(C=C3)OCO4)OC)OC)OC	386.40	unknown	https://doi.org/10.1016/0031-9422(82)85260-6

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Ageratum houstonianum

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