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Ambrosia arborescens

Ambrosia arborescens - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fcb15c4dfe901657405
Scientific name Ambrosia arborescens
Authority Mill.
First published in Gard. Dict. ed. 8 : n.° 5 (1768)

Description Top

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Synonyms Top

Scientific name Authority First published in
Franseria artemisioides Willd. Hort. Berol. 1(1): t. 2 (1803)
Xanthium fruticosum L.f. Suppl. Pl. : 418 (1782)
Gaertneria artemisiodes Kuntze Revis. Gen. Pl. 1: 339 (1891)
Xanthidium artemisioides Delpino Studi Lign. Anemof. 63. 1871
Franseria conwayi Rusby Bull. New York Bot. Gard. 8: 130 (1912)
Gaertneria meyeniana Kuntze Revis. Gen. Pl. 1: 339 (1891)
Xanthium artemisioides (Willd.) Delpino Studi Lign. Anem. Comp. Artem. 18 1871
Ambrosia fruticosa Medik. Hist. & Commentat. Acad. Elect. Sci. Theod.-Palat. iii. Phys. (1775) 247
Ambrosia frutescens Lam. Encyclopedie Methodique. Botanique . . . 1: 128 1783
Franseria arborescens Brandegee Zoe 5: 162 (1903)

Common names Top

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Language Common/alternative name
Arabic دمسيسة شجيرية

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Southern South America
      • Chile Central
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000043582
Tropicos 2728142
KEW urn:lsid:ipni.org:names:176055-1
The Plant List gcc-142156
Open Tree Of Life 7051541
NCBI Taxonomy 2067506
IPNI 176055-1
iNaturalist 327281
GBIF 3110705
USDA GRIN 416922
Wikipedia Ambrosia_arborescens

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
Traditional medicine in Incahuasi: An ethnobotanical study Morales Ramos JG, León-Figueroa DA, Picón Pérez MS, Arbulú Ballesteros MA, Llontop Ynga EG, Coaguila Cusicanqui LA, Morales Ramírez SM, Chirinos Ríos CA F1000Res 31-Aug-2023
PMCID:PMC10993006
doi:10.12688/f1000research.138398.1
PMID:38577227
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
Bioactive Molecules Derived from Plants in Managing Dengue Vector Aedes aegypti (Linn.) Priya SS, Vasantha-Srinivasan P, Altemimi AB, Keerthana R, Radhakrishnan N, Senthil-Nathan S, Kalaivani K, Chandrasekar N, Karthi S, Ganesan R, Alkanan ZT, Pal T, Verma OP, Proćków J Molecules 05-Mar-2023
PMCID:PMC10005433
doi:10.3390/molecules28052386
PMID:36903635
Green Nano-Biotechnology: A New Sustainable Paradigm to Control Dengue Infection Zohra T, Khalil AT, Saeed F, Latif B, Salman M, Ikram A, Ayaz M, Murthy HC Bioinorg Chem Appl 08-Aug-2022
PMCID:PMC9377959
doi:10.1155/2022/3994340
PMID:35979184
A comprehensive phytochemical and pharmacological review on sesquiterpenes from the genus Ambrosia Kovács B, Hohmann J, Csupor-Löffler B, Kiss T, Csupor D Heliyon 09-Jul-2022
PMCID:PMC9294060
doi:10.1016/j.heliyon.2022.e09884
PMID:35865986
Poorly Investigated Ecuadorian Medicinal Plants Armijos C, Ramírez J, Vidari G Plants (Basel) 16-Jun-2022
PMCID:PMC9229133
doi:10.3390/plants11121590
PMID:35736741
Enhanced Antimicrobial, Cytotoxicity, Larvicidal, and Repellence Activities of Brown Algae, Cystoseira crinita-Mediated Green Synthesis of Magnesium Oxide Nanoparticles Fouda A, Eid AM, Abdel-Rahman MA, EL-Belely EF, Awad MA, Hassan SE, AL-Faifi ZE, Hamza MF Front Bioeng Biotechnol 28-Feb-2022
PMCID:PMC8920522
doi:10.3389/fbioe.2022.849921
PMID:35295650
The Modulatory Influence of Plant-Derived Compounds on Human Keratinocyte Function Merecz-Sadowska A, Sitarek P, Zajdel K, Kucharska E, Kowalczyk T, Zajdel R Int J Mol Sci 19-Nov-2021
PMCID:PMC8618348
doi:10.3390/ijms222212488
PMID:34830374
Acute toxicity of aqueous extract of Ambrosia arborescens Mill. on biochemical and histopathological parameters in rats Silva-Correa CR, Villarreal-La Torre VE, González-Siccha AD, Cruzado-Razco JL, González-Blas MV, Sagástegui-Guarniz WA, Calderón-Peña AA, Aspajo-Villalaz CL, Hilario-Vargas J Toxicol Res 18-Sep-2021
PMCID:PMC8960535
doi:10.1007/s43188-021-00106-0
PMID:35419274
Cytotoxicity and molecular docking analysis of racemolactone I, a new sesquiterpene lactone isolated from Inula racemosa Alam P, Tyagi R, Farah MA, Rehman MT, Hussain A, AlAjmi MF, Siddiqui NA, Al-Anazi KM, Amin S, Mujeeb M, Mir SR Pharm Biol 11-Jul-2021
PMCID:PMC8274518
doi:10.1080/13880209.2021.1946090
PMID:35294328
Phylobioactive hotspots in plant resources used to treat Chagas disease Salm A, Krishnan SR, Collu M, Danton O, Hamburger M, Leonti M, Almanza G, Gertsch J iScience 15-Mar-2021
PMCID:PMC8040286
doi:10.1016/j.isci.2021.102310
PMID:33870129
Review of Whole Plant Extracts With Activity Against Herpes Simplex Viruses In Vitro and In Vivo Garber A, Barnard L, Pickrell C J Evid Based Integr Med 16-Feb-2021
PMCID:PMC7894602
doi:10.1177/2515690X20978394
PMID:33593082
Invasion history of Harmonia axyridis (Pallas, 1773) (Coleoptera: Coccinellidae) in Ecuador Cisneros-Heredia DF, Peñaherrera-Romero E PeerJ 27-Nov-2020
PMCID:PMC7703374
doi:10.7717/peerj.10461
PMID:33312773
Metal Nanoparticles: a Promising Treatment for Viral and Arboviral Infections Maduray K, Parboosing R Biol Trace Elem Res 07-Oct-2020
PMCID:PMC7540915
doi:10.1007/s12011-020-02414-2
PMID:33029761

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 / Diterpenoids
(4aS,7S,8aS,10aR)-7-[(1R)-1,2-dihydroxyethyl]-1,1,4a,7-tetramethyl-3,4,6,8,8a,9,10,10a-octahydrophenanthren-2-one 46223441 Click to see CC1(C2CCC3CC(CC=C3C2(CCC1=O)C)(C)C(CO)O)C 320.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
(4aS,7S,8aS,10aR)-7-[(1S)-1,2-dihydroxyethyl]-1,1,4a,7-tetramethyl-3,4,6,8,8a,9,10,10a-octahydrophenanthren-2-one 46223442 Click to see CC1(C2CCC3CC(CC=C3C2(CCC1=O)C)(C)C(CO)O)C 320.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
7-(1,2-Dihydroxyethyl)-1,1,4a,7-tetramethyl-3,4,6,8,8a,9,10,10a-octahydrophenanthren-2-one 75154100 Click to see CC1(C2CCC3CC(CC=C3C2(CCC1=O)C)(C)C(CO)O)C 320.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,3S,7S,7aR)-1-acetyl-3-hydroxy-4-methyl-7-propan-2-yl-1,2,3,6,7,7a-hexahydroinden-5-one 46223443 Click to see CC1=C2C(CC(C2C(CC1=O)C(C)C)C(=O)C)O 250.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
1-Acetyl-3-hydroxy-4-methyl-7-propan-2-yl-1,2,3,6,7,7a-hexahydroinden-5-one 75154101 Click to see CC1=C2C(CC(C2C(CC1=O)C(C)C)C(=O)C)O 250.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
2-[(1S,5R)-5-methyl-4-(3-oxobutyl)cyclohept-3-en-1-yl]prop-2-enoic acid 154827895 Click to see CC1CCC(CC=C1CCC(=O)C)C(=C)C(=O)O 250.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
4-Oxobedfordiaic acid 14633035 Click to see CC1CCC(CC=C1CCC(=O)C)C(=C)C(=O)O 250.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1S,3S,4aR,5S,8aS)-5,8a-dimethyl-3-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene-1,5-diol 46223440 Click to see CC(=C)C1CC2C(CCCC2(C)O)(C(C1)O)C 238.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
(4aR,7R)-7-(3-hydroxyprop-1-en-2-yl)-4a-methyl-3,4,5,6,7,8-hexahydro-2H-naphthalene-1-carbaldehyde 162905051 Click to see CC12CCCC(=C1CC(CC2)C(=C)CO)C=O 234.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
4(15)-Eudesmene-1beta,7alpha-diol 11470456 Click to see CC(C)C1(CCC2(C(CCC(=C)C2C1)O)C)O 238.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
5,8a-Dimethyl-3-prop-1-en-2-yl-1,2,3,4,4a,6,7,8-octahydronaphthalene-1,5-diol 75154099 Click to see CC(=C)C1CC2C(CCCC2(C)O)(C(C1)O)C 238.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
7-(3-hydroxyprop-1-en-2-yl)-4a-methyl-3,4,5,6,7,8-hexahydro-2H-naphthalene-1-carbaldehyde 162905050 Click to see CC12CCCC(=C1CC(CC2)C(=C)CO)C=O 234.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
8a-methyl-4-methylidene-6-propan-2-yl-2,3,4a,5,7,8-hexahydro-1H-naphthalene-1,6-diol 72824221 Click to see CC(C)C1(CCC2(C(CCC(=C)C2C1)O)C)O 238.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
Platambin 613194 Click to see CC(C)C1CCC2(C(CCC(=C)C2C1O)O)C 238.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
Voleneol 14137570 Click to see CC(C)C1CCC2(C(CCC(=C)C2C1O)O)C 238.37 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Pseudoguaianes
Damcinic acid 11747064 Click to see CC1CCC(CC2(C1CCC2=O)C)C(=C)C(=O)O 250.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
(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/J.PHYTOCHEM.2010.02.002
(3aS,6R,6aR,9aR,9bR)-6-hydroxy-6,9a-dimethyl-3-methylidene-4,5,6a,7,8,9b-hexahydro-3aH-azuleno[8,7-b]furan-2,9-dione 163017996 Click to see CC1(CCC2C(C3(C1CCC3=O)C)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
(3S,3aS,6R,6aS,9S,9aR,9bR)-3,6,9a-trimethyl-9-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,3a,4,5,6,6a,7,8,9,9b-decahydroazuleno[4,5-b]furan-2-one 162887710 Click to see CC1CCC2C(C(=O)OC2C3(C1CCC3OC4C(C(C(C(O4)CO)O)O)O)C)C 414.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
(3S,3aS,6S,6aR,9aS,9bR)-6a-hydroxy-3,6,9a-trimethyl-3,3a,4,5,6,7,8,9b-octahydroazuleno[8,7-b]furan-2,9-dione 11780449 Click to see CC1CCC2C(C(=O)OC2C3(C1(CCC3=O)O)C)C 266.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
(6S,6aR,9aR,9bR)-3-(hydroxymethyl)-6,9a-dimethyl-5,6,6a,7,8,9b-hexahydro-4H-azuleno[8,7-b]furan-2,9-dione 162968825 Click to see CC1CCC2=C(C(=O)OC2C3(C1CCC3=O)C)CO 264.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
3-(hydroxymethyl)-6,9a-dimethyl-5,6,6a,7,8,9b-hexahydro-4H-azuleno[8,7-b]furan-2,9-dione 162968823 Click to see CC1CCC2=C(C(=O)OC2C3(C1CCC3=O)C)CO 264.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
3,6,9a-Trimethyl-9-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,3a,4,5,6,6a,7,8,9,9b-decahydroazuleno[4,5-b]furan-2-one 75154103 Click to see CC1CCC2C(C(=O)OC2C3(C1CCC3OC4C(C(C(C(O4)CO)O)O)O)C)C 414.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
6-hydroxy-6,9a-dimethyl-3-methylidene-4,5,6a,7,8,9b-hexahydro-3aH-azuleno[8,7-b]furan-2,9-dione 163017995 Click to see CC1(CCC2C(C3(C1CCC3=O)C)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
6a-Hydroxy-3,6,9a-trimethyl-3,3a,4,5,6,7,8,9b-octahydroazuleno[8,7-b]furan-2,9-dione 72742677 Click to see CC1CCC2C(C(=O)OC2C3(C1(CCC3=O)O)C)C 266.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
Cordilin 98331 Click to see CC1CCC2C(C(C13CCC(=O)O3)(C)O)OC(=O)C2=C 280.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
Coronopilin 257278 Click to see CC1CCC2C(C3(C1(CCC3=O)O)C)OC(=O)C2=C 264.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
Coronopolin 457959 Click to see CC1CCC2C(C3(C1(CCC3=O)O)C)OC(=O)C2=C 264.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
Damsin 14631 Click to see CC1CCC2C(C3(C1CCC3=O)C)OC(=O)C2=C 248.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
Damsine 457960 Click to see CC1CCC2C(C3(C1CCC3=O)C)OC(=O)C2=C 248.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
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/J.PHYTOCHEM.2010.02.002
Psilostachyin C 97213 Click to see CC1CCC2C(C3(C1CCC(=O)O3)C)OC(=O)C2=C 264.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
3-Methyl-2-pentanol 11261 Click to see CCC(C)C(C)O 102.17 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3S,3aS,6R,7S,8R,8aR)-6,8-dihydroxy-3,6,8-trimethylspiro[3a,4,5,8a-tetrahydro-3H-cyclohepta[b]furan-7,5'-oxolane]-2,2'-dione 162919704 Click to see CC1C2CCC(C3(CCC(=O)O3)C(C2OC1=O)(C)O)(C)O 298.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002
6,8-dihydroxy-3,6,8-trimethylspiro[3a,4,5,8a-tetrahydro-3H-cyclohepta[b]furan-7,5'-oxolane]-2,2'-dione 75154102 Click to see CC1C2CCC(C3(CCC(=O)O3)C(C2OC1=O)(C)O)(C)O 298.33 unknown https://doi.org/10.1016/J.PHYTOCHEM.2010.02.002

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