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Internal ID UUID643fd985d8c65979823043
Scientific name Astragalus robustus
Authority Bunge
First published in Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7, 11(16): 122 (1868)

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Synonyms Top

Scientific name Authority First published in
Astragalus robustus subsp. subrobustus (Boriss.) Ponert Feddes Repert.83: 632 (1972 publ. 1973)
Astragalus subrobustus Boriss. Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R.10: 55 (1947)
Tragacantha robusta (Bunge) Kuntze Revis. Gen. Pl.2: 947 (1891)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Western Asia
      • Iran
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000185970
Tropicos 13026755
KEW urn:lsid:ipni.org:names:479564-1
The Plant List ild-32304
Open Tree Of Life 127751
Observations.org 141540
NCBI Taxonomy 144147
IPNI 479564-1
GBIF 5343199
EOL 643667
Elurikkus 521947

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)!
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Title Authors Publication Released IDs
The Effect of Shen-Yuan-Dan Capsule on Autophagy-Related Gene Atg13 Promoter Methylation and Genomic Methylation Levels in Atherosclerotic Mice Lai X, Zhang Y, Li M, Shang J, Liu W, Zhou M, Liu H Acta Cardiol Sin 01-May-2020
PMCID:PMC7220961
doi:10.6515/ACS.202005_36(3).20190906B
PMID:32425441
Shen-Yuan-Dan Capsule Attenuates Atherosclerosis and Foam Cell Formation by Enhancing Autophagy and Inhibiting the PI3K/Akt/mTORC1 Signaling Pathway Zhou M, Ren P, Zhang Y, Li S, Li M, Li P, Shang J, Liu W, Liu H Front Pharmacol 31-May-2019
PMCID:PMC6554665
doi:10.3389/fphar.2019.00603
PMID:31214032
Phenolic compounds ofAstragalus subrobustus N. N. Guzhva, M. S. Luk'yanchikov, L. I. Dranik Springer Science and Business Media LLC 25-Nov-2004
doi:10.1007/BF00600855

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
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-O-Feruloylquinic acid 9799386 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2CC(CC(C2O)O)(C(=O)O)O)O 368.30 unknown https://doi.org/10.1007/BF00600855
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1007/BF00600855
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1007/BF00600855
> 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 https://doi.org/10.1007/BF00600855
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 https://doi.org/10.1007/BF00600855
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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 https://doi.org/10.1007/BF00600855
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00600855
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00600855
Hyperoside 5281643 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 https://doi.org/10.1007/BF00600855
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00600855

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