Ambrosia tenuifolia

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Collections

Details Top

Internal ID	UUID643fcde3a59a1456119069
Scientific name	Ambrosia tenuifolia
Authority	Spreng.
First published in	Syst. Veg., ed. 16 [Sprengel] 3: 851. 1826 [Jan-Mar 1826]

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Ambrosia longistylis	Nutt.	Trans. Amer. Philos. Soc. , ser. 2, 7: 344 (1840)
Ambrosia simulans	Shinners	Field & Lab. 17: 173 (1949)
Ambrosia maritima	Vell.	Fl. Flumin. 10: t. 26 (1831)
Xanthidium tenuifolium	Delpino	Studi Lign. Anemof. 62. 1871
Ambrosia fruticosa	DC.	Prodr. 5: 525 (1836)
Franseria tenuifolia	Harv. & A.Gray	Mem. Amer. Acad. Arts , ser. 2, 4(1): 80 (1849)

Common names Top

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Language	Common/alternative name
English	slimleaf bur ragweed
Arabic	دمسيسة هشة الأوراق
Chinese	细叶豚草
Chinese	細葉豚草

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Southern Africa
  - Cape Provinces
- Western Indian Ocean
  - Mauritius
  - Réunion

Asia-temperate click to expand
- Western Asia
  - Palestine
  - Turkey

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

Europe click to expand
- Middle Europe
  - Germany
- Southeastern Europe
  - Italy
  - Yugoslavia
- Southwestern Europe
  - Baleares
  - France
  - Spain

Northern America click to expand
- Southeastern U.S.A.
  - Louisiana

Southern America click to expand
- Brazil
  - Brazil South
- Caribbean
  - Puerto Rico
- Southern South America
  - Argentina Northeast
  - Argentina Northwest
  - Argentina South
  - Paraguay
  - Uruguay
- Western South America
  - Bolivia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000076429
UNII	006H22D6PZ
USDA Plants	AMTE5
Tropicos	2701653
INPN	82092
Flora of Italy	5571
KEW	urn:lsid:ipni.org:names:176136-1
The Plant List	gcc-33087
Open Tree Of Life	3899842
Observations.org	147366
NCBI Taxonomy	1532261
NBN Atlas	NHMSYS0000455852
Nature Serve	2.159408
IPNI	176136-1
iNaturalist	158270
GBIF	3110580
EPPO	AMBTE
EOL	468219
USDA GRIN	403696
CMAUP	NPO3718

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

The Essential Oil Compositions of Ambrosia acanthicarpa Hook., Artemisia ludoviciana Nutt., and Gutierrezia sarothrae (Pursh) Britton & Rusby (Asteraceae) from the Owyhee Mountains of Idaho

Swor K, Poudel A, Satyal P, Setzer WN

Molecules

20-Mar-2024

PMCID:	PMC10976104
doi:	10.3390/molecules29061383
PMID:	38543021

In vitro antimalarial activity of Syzygium cumini fruit fraction

Maslachah L, Purwitasari N

Open Vet J

30-Sep-2023

PMCID:	PMC10576581
doi:	10.5455/OVJ.2023.v13.i9.7
PMID:	37842099

The scenario of the studies on ragweed (Ambrosia Sp.) and related issues from its beginning to today: a useful tool for future goals in a one health approach

Albertini R, Veronesi L, Colucci ME, Pasquarella C

Acta Biomed

26-Oct-2022

PMCID:	PMC9686166
doi:	10.23750/abm.v93i5.13771
PMID:	36300205

The Application of Ultrasound in Honey: Antioxidant Activity, Inhibitory Effect on α-amylase and α-glucosidase, and In Vitro Digestibility Assessment

Peláez-Acero A, Garrido-Islas DB, Campos-Montiel RG, González-Montiel L, Medina-Pérez G, Luna-Rodríguez L, González-Lemus U, Cenobio-Galindo AD

Molecules

08-Sep-2022

PMCID:	PMC9504444
doi:	10.3390/molecules27185825
PMID:	36144558

In Vitro, In Vivo, and In Silico Studies of Cumanin Diacetate as a Potential Drug against Trypanosoma cruzi Infection

Sánchez Alberti A, Beer MF, Cerny N, Bivona AE, Fabian L, Morales C, Moglioni A, Malchiodi EL, Donadel OJ, Sülsen VP

ACS Omega

20-Dec-2021

PMCID:	PMC8757452
doi:	10.1021/acsomega.1c05560
PMID:	35036760

Study of Tissue-Specific Reactive Oxygen Species Formation by Cell Membrane Microarrays for the Characterization of Bioactive Compounds

Elexpe A, Nieto N, Fernández-Cuétara C, Domínguez-Fernández C, Morera-Herreras T, Torrecilla M, Miguélez C, Laso A, Ochoa E, Bailen M, González-Coloma A, Angulo-Barturen I, Astigarraga E, Barreda-Gómez G

Membranes (Basel)

29-Nov-2021

PMCID:	PMC8705675
doi:	10.3390/membranes11120943
PMID:	34940444

Natural-Product-Based Solutions for Tropical Infectious Diseases

Adegboye O, Field MA, Kupz A, Pai S, Sharma D, Smout MJ, Wangchuk P, Wong Y, Loiseau C

Clin Microbiol Rev

08-Sep-2021

PMCID:	PMC8673330
doi:	10.1128/CMR.00348-20
PMID:	34494873

Pest categorisation of Phenacoccus solenopsis

Bragard C, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Gregoire J, Malumphy C, Campese C, Czwienczek E, Kertesz V, Maiorano A, MacLeod A

EFSA J

18-Aug-2021

PMCID:	PMC8371560
doi:	10.2903/j.efsa.2021.6801
PMID:	34429782

Development of chloroplast microsatellite markers for giant ragweed (Ambrosia trifida)

Sharma H, Hyvönen J, Poczai P

Appl Plant Sci

22-Jan-2020

PMCID:	PMC6976888
doi:	10.1002/aps3.11313
PMID:	31993255

Interaction between fire and fragmentation in the successional stages of coastal dune grasslands of the southern Pampas, Argentina

Yezzi AL, Nebbia AJ, Zalba SM

Sci Rep

22-Oct-2019

PMCID:	PMC6805887
doi:	10.1038/s41598-019-51595-x
PMID:	31641186

Editorial: Ethnopharmacological Studies for the Development of Drugs With Special Reference to Asteraceae

Panda SK, da Silva LC, Sahal D, Leonti M

Front Pharmacol

03-Sep-2019

PMCID:	PMC6737279
doi:	10.3389/fphar.2019.00955
PMID:	31551771

Therapeutic Interventions for Countering Leishmaniasis and Chagas’s Disease: From Traditional Sources to Nanotechnological Systems

Souto EB, Dias-Ferreira J, Craveiro SA, Severino P, Sanchez-Lopez E, Garcia ML, Silva AM, Souto SB, Mahant S

Pathogens

01-Aug-2019

PMCID:	PMC6789685
doi:	10.3390/pathogens8030119
PMID:	31374930

Stress and defense responses in plant secondary metabolites production

Isah T

Biol Res

29-Jul-2019

PMCID:	PMC6661828
doi:	10.1186/s40659-019-0246-3
PMID:	31358053

Asteraceae Plants as Sources of Compounds Against Leishmaniasis and Chagas Disease

Moraes Neto RN, Setúbal RF, Higino TM, Brelaz-de-Castro MC, da Silva LC, Aliança AS

Front Pharmacol

08-May-2019

PMCID:	PMC6530400
doi:	10.3389/fphar.2019.00477
PMID:	31156427

Preparation of Sesquiterpene Lactone Derivatives: Cytotoxic Activity and Selectivity of Action

Beer MF, Bivona AE, Sánchez Alberti A, Cerny N, Reta GF, Martín VS, Padrón JM, Malchiodi EL, Sülsen VP, Donadel OJ

Molecules

20-Mar-2019

PMCID:	PMC6471591
doi:	10.3390/molecules24061113
PMID:	30897836

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
3-(8-Hydroxy-6,8-dimethyl-3-methylidene-2-oxo-3a,4,5,8a-tetrahydrocyclohepta[b]furan-7-yl)propanoic acid	72746098	Click to see CC1=C(C(C2C(CC1)C(=C)C(=O)O2)(C)O)CCC(=O)O	280.32	unknown	https://doi.org/10.1016/S0031-9422(00)81289-3
Altamisic acid	15143694	Click to see CC1=C(C(C2C(CC1)C(=C)C(=O)O2)(C)O)CCC(=O)O	280.32	unknown	https://doi.org/10.1016/S0031-9422(00)81289-3
Ethyl 3-(8-hydroxy-6,8-dimethyl-3-methylidene-2-oxo-3a,4,5,8a-tetrahydrocyclohepta[b]furan-7-yl)propanoate	162844048	Click to see CCOC(=O)CCC1=C(CCC2C(C1(C)O)OC(=O)C2=C)C	308.40	unknown	https://doi.org/10.1016/0031-9422(92)80029-E https://doi.org/10.1016/S0031-9422(00)81289-3
ethyl 3-[(3aS,8R,8aR)-8-hydroxy-6,8-dimethyl-3-methylidene-2-oxo-3a,4,5,8a-tetrahydrocyclohepta[b]furan-7-yl]propanoate	15143692	Click to see CCOC(=O)CCC1=C(CCC2C(C1(C)O)OC(=O)C2=C)C	308.40	unknown	https://doi.org/10.1016/0031-9422(92)83280-C https://doi.org/10.1016/0031-9422(90)87098-F https://doi.org/10.1016/0031-9422(92)80029-E https://doi.org/10.1007/978-3-642-58062-8_3 https://doi.org/10.1016/S0031-9422(00)81289-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
(1R,2R,6R,9S,10S)-1,9-dimethyl-5-methylidene-3,14-dioxatricyclo[8.4.0.02,6]tetradecane-4,13-dione	163029766	Click to see CC1CCC2C(C3(C1CCC(=O)O3)C)OC(=O)C2=C	264.32	unknown	https://doi.org/10.1016/0031-9422(92)80029-E
(1R,2R,6S,9S,10S)-1,9-dimethyl-5-methylidene-3,14-dioxatricyclo[8.4.0.02,6]tetradecane-4,13-dione	5320769	Click to see CC1CCC2C(C3(C1CCC(=O)O3)C)OC(=O)C2=C	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)81289-3
(3aR,5S,5aS,7S,8R,8aS,9aR)-7,8-dihydroxy-5,5a,8a-trimethyl-1-methylidene-3a,4,5,6,7,8,9,9a-octahydroazuleno[6,5-b]furan-2-one	162917622	Click to see CC1CC2C(CC3(C1(CC(C3O)O)C)C)C(=C)C(=O)O2	280.36	unknown	https://doi.org/10.1016/S0031-9422(00)81289-3
(3aS,6S,7R,8R,8aR)-8-hydroxy-6,8-dimethyl-3-methylidenespiro[4,5,6,8a-tetrahydro-3aH-cyclohepta[b]furan-7,5'-oxolane]-2,2'-dione	12314732	Click to see CC1CCC2C(C(C13CCC(=O)O3)(C)O)OC(=O)C2=C	280.32	unknown	https://doi.org/10.1016/0031-9422(92)80029-E
1,9-Dimethyl-5-methylidene-3,14-dioxatricyclo[8.4.0.02,6]tetradec-9-ene-4,13-dione	98332	Click to see CC1=C2CCC(=O)OC2(C3C(CC1)C(=C)C(=O)O3)C	262.30	unknown	https://doi.org/10.1016/0031-9422(92)83280-C https://doi.org/10.1016/S0031-9422(00)81289-3 https://doi.org/10.1016/0031-9422(92)80029-E https://doi.org/10.1007/978-3-642-58062-8_3
7,8-Dihydroxy-5,5a,8a-trimethyl-1-methylidene-3a,4,5,6,7,8,9,9a-octahydroazuleno[6,5-b]furan-2-one	162917621	Click to see CC1CC2C(CC3(C1(CC(C3O)O)C)C)C(=C)C(=O)O2	280.36	unknown	https://doi.org/10.1016/S0031-9422(00)81289-3
Cordilin	98331	Click to see CC1CCC2C(C(C13CCC(=O)O3)(C)O)OC(=O)C2=C	280.32	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2443877/ https://doi.org/10.1016/S0031-9422(00)81289-3 https://doi.org/10.1016/0031-9422(92)80029-E
Cumanin	353378	Click to see CC1CC2C(CC3(C1CC(C3O)O)C)C(=C)C(=O)O2	266.33	unknown	https://doi.org/10.1016/S0031-9422(00)81289-3
Peruvin	52944698	Click to see CC1CC2C(CC3(C1(CCC3=O)O)C)C(=C)C(=O)O2	264.32	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2443877/ https://doi.org/10.1016/S0031-9422(00)81289-3
Psilostachyin	71586746	Click to see CC1CCC2C(C(C13CCC(=O)O3)(C)O)OC(=O)C2=C	280.32	unknown	https://doi.org/10.1016/0031-9422(90)87098-F https://doi.org/10.1016/0031-9422(92)83280-C https://doi.org/10.1016/S0031-9422(00)81289-3 https://doi.org/10.1007/978-3-642-58062-8_3
Psilostachyin A	5320767	Click to see CC1CCC2C(C(C13CCC(=O)O3)(C)O)OC(=O)C2=C	280.32	unknown	https://doi.org/10.1016/0031-9422(92)80029-E https://doi.org/10.1016/0031-9422(92)83280-C https://doi.org/10.1016/0031-9422(90)87098-F https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2443877/ https://doi.org/10.1007/978-3-642-58062-8_3 https://doi.org/10.1016/S0031-9422(00)81289-3
Psilostachyin B	5320768	Click to see CC1=C2CCC(=O)OC2(C3C(CC1)C(=C)C(=O)O3)C	262.30	unknown	https://doi.org/10.1016/S0031-9422(00)81289-3 https://doi.org/10.1016/0031-9422(92)83280-C https://doi.org/10.1016/0031-9422(92)80029-E https://doi.org/10.1007/978-3-642-58062-8_3
Psilostachyin C	97213	Click to see CC1CCC2C(C3(C1CCC(=O)O3)C)OC(=O)C2=C	264.32	unknown	https://doi.org/10.1007/978-3-642-58062-8_3 https://doi.org/10.1016/0031-9422(92)80029-E https://doi.org/10.1016/S0031-9422(00)81289-3 https://doi.org/10.1016/0031-9422(90)87098-F
Sequiterpene lactone 326	338659	Click to see CC1CC2C(CC3(C1(CCC3=O)O)C)C(=C)C(=O)O2	264.32	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2443877/ https://doi.org/10.1016/S0031-9422(00)81289-3
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	via CMAUP database
Stigmasterol acetate	6437330	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C	454.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
alpha-Spinasterin	5281331	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(1R,2R,5R,6S,9S,10S)-1,5,9-trimethyl-3,14-dioxatricyclo[8.4.0.02,6]tetradecane-4,13-dione	162923937	Click to see CC1CCC2C(C(=O)OC2C3(C1CCC(=O)O3)C)C	266.33	unknown	https://doi.org/10.1016/S0031-9422(00)81289-3
1,5,9-Trimethyl-3,14-dioxatricyclo[8.4.0.02,6]tetradecane-4,13-dione	162923936	Click to see CC1CCC2C(C(=O)OC2C3(C1CCC(=O)O3)C)C	266.33	unknown	https://doi.org/10.1016/S0031-9422(00)81289-3
> Organoheterocyclic compounds / Oxanes
(3aR)-2,3,4,5,6,7,8,8a-Octahydro-4beta,8abeta-dimethyl-alpha-methylene-1-oxo-1H-3a,6alpha-epoxyazulene-7beta-acetic acid	156603030	Click to see CC1CC2C(CC3(C1(O2)CCC3=O)C)C(=C)C(=O)O	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)81289-3
Ambrosic acid	75368818	Click to see CC1CC2C(CC3(C1(O2)CCC3=O)C)C(=C)C(=O)O	264.32	unknown	https://doi.org/10.1016/S0031-9422(00)81289-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	via CMAUP database
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin	5280804	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	via CMAUP database

Biological Material Top

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Ambrosia tenuifolia

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top