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Astragalus peregrinus

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fdec5eef62895401093
Scientific name Astragalus peregrinus
Authority Vahl
First published in Symb. Bot.1: 57 (1790)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Tragacantha peregrina (Vahl) Kuntze Revis. Gen. Pl.2: 947 (1891)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Astragalus peregrinus subsp. peregrinus Vahl Unknown
Astragalus peregrinus subsp. warionis (Gand.) Maire Bull. Soc. Hist. Nat. Afrique N.39: 133 (1949)

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
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
    • Western Asia
      • Palestine
      • Sinai
  • Europe
    • Southeastern Europe
      • Kriti
      • Sicilia
    • Southwestern Europe
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000212549
KEW urn:lsid:ipni.org:names:479170-1
The Plant List ild-7627
Open Tree Of Life 3925060
Observations.org 138208
NCBI Taxonomy 2014710
IPNI 479170-1
GBIF 5346176
EPPO ASAPS
EOL 703086
Elurikkus 523154

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
Interspecific variations in the habitats of Reichardia tingitana (L.) Roth leading to changes in its bioactive constituents and allelopathic activity Abd-ElGawad AM, El-Amier YA, Assaeed AM, Al-Rowaily SL Saudi J Biol Sci 25-Nov-2019
PMCID:PMC6933205
doi:10.1016/j.sjbs.2019.11.015
PMID:31889875
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
A New Isoflavone from Astragalus peregrinus R. R. Abd El-Latif, M. H. Shabana, A. H. El-Gandour, R. M. Mansour, M. Sharaf Springer Science and Business Media LLC 03-Mar-2004
doi:10.1023/B:CONC.0000018105.23722.7D
Cycloartane saponins from Astragalus peregrinus as modulators of lymphocyte proliferation. Verotta L, Guerrini M, El-Sebakhy NA, Asaad AM, Toaima SM, Abou-Sheer ME, Luo YD, Pezzuto JM Fitoterapia 01-Dec-2001
doi:10.1016/S0367-326X(01)00339-2
PMID:11731114

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 / Steroids and steroid derivatives / Steroidal glycosides
(2R,3R,4S,5S,6R)-2-[[(1S,3R,6S,8R,9S,11R,12S,13R,14R,16R)-9,13-dihydroxy-14-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162985789 Click to see 652.90 unknown https://doi.org/10.1016/S0367-326X(01)00339-2
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-2-[[(1S,3R,6S,8R,9S,11R,12S,13R,14R,16R)-9,13-dihydroxy-14-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162887389 Click to see 799.00 unknown https://doi.org/10.1016/S0367-326X(01)00339-2
(2S,3R,4R,5R,6S)-2-[(2R,3S,4R,5R,6R)-6-[[(1S,3R,6S,8R,9S,11R,12S,13R,14R,16R)-9,13-dihydroxy-14-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162844555 Click to see 799.00 unknown https://doi.org/10.1016/S0367-326X(01)00339-2
[(2R,3S,4S,5R,6R)-6-[[(1S,3R,6S,8R,9S,11R,12S,13R,14R,16R)-14-[(2R,5S)-5-acetyloxy-2,6,6-trimethyloxan-2-yl]-9,13-dihydroxy-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl acetate 162881466 Click to see 883.10 unknown https://doi.org/10.1016/S0367-326X(01)00339-2
[6-[[14-(5-Acetyloxy-2,6,6-trimethyloxan-2-yl)-9,13-dihydroxy-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-3,4-dihydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl acetate 162881465 Click to see 883.10 unknown https://doi.org/10.1016/S0367-326X(01)00339-2
2-[[9,13-Dihydroxy-14-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162985788 Click to see 652.90 unknown https://doi.org/10.1016/S0367-326X(01)00339-2
2-[2-[[9,13-Dihydroxy-14-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162887388 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC45CC46CCC7(CC(C(C7(C6CC(C5C3(C)C)O)C)O)C8(CCC(O8)C(C)(C)O)C)C)CO)O)O)O)O)O 799.00 unknown https://doi.org/10.1016/S0367-326X(01)00339-2
2-[6-[[9,13-Dihydroxy-14-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162844554 Click to see 799.00 unknown https://doi.org/10.1016/S0367-326X(01)00339-2
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1023/B:CONC.0000018105.23722.7D
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1023/B:CONC.0000018105.23722.7D
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin-7-O-neohesperidoside 5459217 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1023/B:CONC.0000018105.23722.7D
Rhoifolin 5282150 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1023/B:CONC.0000018105.23722.7D
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
7-Hydroxy-3',5'-dimethoxyisoflavone 11208735 Click to see COC1=CC(=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)OC 298.29 unknown https://doi.org/10.1023/B:CONC.0000018105.23722.7D

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