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Internal ID UUID643fdebfc4a45783185187
Scientific name Astragalus armatus
Authority Willd.
First published in Sp. Pl., ed. 4, 3: 1220 (1802)

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Synonyms Top

Scientific name Authority First published in
Astragalus fontanesii subsp. tragacanthoides (Pomel) Maire É.Jahandiez & al., Cat. Pl. Maroc2: 405 (1932)
Acanthyllis armata Batt. J.A.Battandier & L.C.Trabut, Fl. Algérie, Dicot.: 251 (1889)
Tragacantha armata (Willd.) Kuntze Revis. Gen. Pl.2: 943 (1891)
Acanthyllis tragacanthoides Pomel Nouv. Mat. Fl. Atl. 1: 179 (1874)
Anthyllis tragacanthoides Desf. Fl. Atlant. 2: 150 (1798)

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Language Common/alternative name
Arabic قتاد مسلح
Kabyle akdad

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Astragalus armatus subsp. armatus Willd. Unknown
Astragalus armatus subsp. numidicus (Murb.) Tietz Mitt. Bot. Staatssamml. München27: 251 (1988)

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000212439
Tropicos 13025376
KEW urn:lsid:ipni.org:names:476249-1
The Plant List ild-7512
Open Tree Of Life 471729
NCBI Taxonomy 512616
IPNI 476249-1
iNaturalist 498002
GBIF 5345597
EOL 703035
USDA GRIN 435719

Genomes (via NCBI) Top

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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
Five New Tamarixetin Glycosides from Astragalus thracicus Griseb. Including Some Substituted with the Rare 3-Hydroxy-3-methylglutaric Acid and Their Collagenase Inhibitory Effects In Vitro Vasilev H, Šmejkal K, Jusková S, Vaclavik J, Treml J ACS Omega 08-Apr-2024
PMCID:PMC11044239
doi:10.1021/acsomega.3c09677
PMID:38680358
Applications of tandem mass spectrometry (MS/MS) in antimicrobial peptides field: Current state and new applications Fang P, Yu S, Ma X, Hou L, Li T, Gao K, Wang Y, Sun Q, Shang L, Liu Q, Nie M, Yang J Heliyon 31-Mar-2024
PMCID:PMC11004759
doi:10.1016/j.heliyon.2024.e28484
PMID:38601527
Growth, productivity and phytochemicals of Coriander in responses to foliar application of Acacia saligna fruit extract as a biostimulant under field conditions Alkharpotly AA, Abd-Elkader DY, Salem MZ, Hassan HS Sci Rep 05-Feb-2024
PMCID:PMC10844193
doi:10.1038/s41598-024-53378-5
PMID:38316894
Ultrasound-Assisted Extraction, LC–MS/MS Analysis, Anticholinesterase, and Antioxidant Activities of Valuable Natural Metabolites from Astragalus armatus Willd.: In Silico Molecular Docking and In Vitro Enzymatic Studies Lekmine S, Bendjedid S, Benslama O, Martín-García AI, Boussekine S, Kadi K, Akkal S, Nieto G, Sami R, Al-Mushhin AA, Baakdah MM, Aljaadi AM, Alharthy SA Antioxidants (Basel) 09-Oct-2022
PMCID:PMC9598503
doi:10.3390/antiox11102000
PMID:36290723
Optimized Chemical Extraction Methods of Antimicrobial Peptides from Roots and Leaves of Extremophilic Plants: Anthyllis sericea and Astragalus armatus Collected from the Tunisian Desert Ben Brahim R, Ellouzi H, Fouzai K, Asses N, Neffati M, Sabatier JM, Bulet P, Regaya I Antibiotics (Basel) 24-Sep-2022
PMCID:PMC9599020
doi:10.3390/antibiotics11101302
PMID:36289960
Characterizing Biomass Yield and Nutritional Value of Selected Indigenous Range Species from Arid Tunisia Louhaichi M, Gamoun M, Hassan S, Abdallah MA Plants (Basel) 27-Sep-2021
PMCID:PMC8539911
doi:10.3390/plants10102031
PMID:34685840
Climatic Zone and Soil Properties Determine the Biodiversity of the Soil Bacterial Communities Associated to Native Plants from Desert Areas of North-Central Algeria Bona E, Massa N, Toumatia O, Novello G, Cesaro P, Todeschini V, Boatti L, Mignone F, Titouah H, Zitouni A, Lingua G, Vuolo F, Gamalero E Microorganisms 23-Jun-2021
PMCID:PMC8303931
doi:10.3390/microorganisms9071359
PMID:34201731
Ethnobotanical Study on Plant Used by Semi-Nomad Descendants’ Community in Ouled Dabbeb—Southern Tunisia Karous O, Ben Haj Jilani I, Ghrabi-Gammar Z Plants (Basel) 28-Mar-2021
PMCID:PMC8066878
doi:10.3390/plants10040642
PMID:33800664
Plant traits and phenotypic variability effect on the phytomass production of Stipagrostis ciliata (Desf.) De Winter Lobna MF, Kaouthar J, Naser AA, Chaieb M Saudi J Biol Sci 12-Mar-2020
PMCID:PMC7253882
doi:10.1016/j.sjbs.2020.03.010
PMID:32489293
Diversity of desert rangelands of Tunisia Gamoun M, Belgacem AO, Louhaichi M Plant Divers 20-Aug-2018
PMCID:PMC6224667
doi:10.1016/j.pld.2018.06.004
PMID:30740567
Mycobacterium terramassiliense, Mycobacterium rhizamassiliense and Mycobacterium numidiamassiliense sp. nov., three new Mycobacterium simiae complex species cultured from plant roots Bouam A, Armstrong N, Levasseur A, Drancourt M Sci Rep 18-Jun-2018
PMCID:PMC6006331
doi:10.1038/s41598-018-27629-1
PMID:29915369
Flavonoids from the Genus Astragalus: Phytochemistry and Biological Activity Bratkov VM, Shkondrov AM, Zdraveva PK, Krasteva IN Pharmacogn Rev 01-Jan-2016
PMCID:PMC4791984
doi:10.4103/0973-7847.176550
PMID:27041870
Endophytic Actinobacteria and the Interaction of Micromonospora and Nitrogen Fixing Plants Trujillo ME, Riesco R, Benito P, Carro L Front Microbiol 01-Dec-2015
PMCID:PMC4664631
doi:10.3389/fmicb.2015.01341
PMID:26648923
New data on aphid fauna (Hemiptera, Aphididae) in Algeria Laamari M, d’Acier AC, Jousselin E Zookeys 30-Jul-2013
PMCID:PMC3764523
doi:10.3897/zookeys.319.4340
PMID:24039520
Two New Acylated Tridesmosidic Saponins from <i>Astragalus armatus</i> Nabil Semmar, Miyamoto Tomofumi, Yassine Mrabet, Marie‐Aleth Lacaille‐Dubois Wiley 17-May-2010
doi:10.1002/HLCA.200900303

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 / Sesquiterpene lactones / Germacranolides and derivatives
[(3aS,4R,5R,6E,10E,11aR)-4-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-5-yl] (Z)-2-methylbut-2-enoate 14138845 Click to see 388.50 unknown https://doi.org/10.1002/HLCA.200900303
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2R,3R,4S,5S,6R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-6-[(2S,3R,4S,5R)-4,5-dihydroxy-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-15-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162900613 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(CO8)O)O)OC9C(C(C(CO9)O)O)O)C 917.10 unknown https://doi.org/10.1002/HLCA.200900303
(2S,3R,4S,5R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-6-[(2S,3R,4S,5R)-4,5-dihydroxy-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-14-hydroxy-15-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxane-3,4,5-triol 21630099 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)OC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)OC9C(C(C(CO9)O)O)O)C 887.10 unknown https://doi.org/10.1002/HLCA.200900303
[(2S,3R,4S,5R)-3-acetyloxy-5-hydroxy-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-14-hydroxy-7,7,12,16-tetramethyl-15-[(2R,5S)-2-methyl-5-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]oxolan-2-yl]-9-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxan-4-yl] acetate 162938395 Click to see 1001.20 unknown https://doi.org/10.1002/HLCA.200900303
[(2S,3R,4S,5R)-4,5-dihydroxy-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-14-hydroxy-7,7,12,16-tetramethyl-15-[(2R,5S)-2-methyl-5-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]oxolan-2-yl]-9-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxan-3-yl] acetate 162880751 Click to see CC(=O)OC1C(C(COC1OC2CCC34CC35CCC6(C(C(CC6(C5CC(C4C2(C)C)OC7C(C(C(CO7)O)O)O)C)O)C8(CCC(O8)C(C)(C)OC9C(C(C(C(O9)CO)O)O)O)C)C)O)O 959.10 unknown https://doi.org/10.1002/HLCA.200900303
[3-Acetyloxy-5-hydroxy-2-[[14-hydroxy-7,7,12,16-tetramethyl-15-[2-methyl-5-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]oxolan-2-yl]-9-(3,4,5-trihydroxyoxan-2-yl)oxy-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxan-4-yl] acetate 162938394 Click to see CC(=O)OC1C(COC(C1OC(=O)C)OC2CCC34CC35CCC6(C(C(CC6(C5CC(C4C2(C)C)OC7C(C(C(CO7)O)O)O)C)O)C8(CCC(O8)C(C)(C)OC9C(C(C(C(O9)CO)O)O)O)C)C)O 1001.20 unknown https://doi.org/10.1002/HLCA.200900303
[4,5-Dihydroxy-2-[[14-hydroxy-7,7,12,16-tetramethyl-15-[2-methyl-5-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]oxolan-2-yl]-9-(3,4,5-trihydroxyoxan-2-yl)oxy-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxan-3-yl] acetate 162880750 Click to see 959.10 unknown https://doi.org/10.1002/HLCA.200900303
2-[[6-[4,5-Dihydroxy-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-14-hydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162900612 Click to see 917.10 unknown https://doi.org/10.1002/HLCA.200900303

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