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Astragalus corniculatus

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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 UUID643fdf060765b373186364
Scientific name Astragalus corniculatus
Authority M.Bieb.
First published in Fl. Taur.-Caucas.3: 492 (1819)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tragacantha corniculata (M.Bieb.) Kuntze Revis. Gen. Pl.2: 944 (1891)
Philammos corniculatus (M.Bieb.) Steven Bull. Soc. Imp. Naturalistes Moscou4: 268 (1832)

Common names Top

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Language Common/alternative name
Bulgarian рогчесто сграбиче
Ukrainian Астрагал ріжковий

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000213550
Tropicos 13025665
KEW urn:lsid:ipni.org:names:476921-1
The Plant List ild-8617
Open Tree Of Life 3925042
Observations.org 115341
NCBI Taxonomy 1632240
iNaturalist 897605
GBIF 5343049
EOL 704256
Elurikkus 521899

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
Lancemaside A, a major triterpene saponin of Codonopsis lanceolata enhances regulation of nitric oxide synthesis via eNOS activation Lee YS, Kim H, Kim J, Seol GH, Lee KW BMC Complement Altern Med 24-May-2019
PMCID:PMC6534936
doi:10.1186/s12906-019-2516-6
PMID:31126276
Therapeutic Potential of Plants and Plant Derived Phytochemicals against Acetaminophen-Induced Liver Injury Subramanya SB, Venkataraman B, Meeran MF, Goyal SN, Patil CR, Ojha S Int J Mol Sci 28-Nov-2018
PMCID:PMC6321362
doi:10.3390/ijms19123776
PMID:30486484
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
Triterpenoid Saponins from Astragalus corniculatus Ilina Krasteva, Stefan Nikolov, Maki Kaloga, Gisela Mayer Walter de Gruyter GmbH 16-Feb-2015
doi:10.1515/ZNB-2006-0919
Experimental liver protection of n-butanolic extract of Astragalus monspessulanus L. on carbon tetrachloride model of toxicity in rat Simeonova R, Bratkov VM, Kondeva-Burdina M, Vitcheva V, Manov V, Krasteva I Redox Rep 14-Nov-2014
PMCID:PMC6837432
doi:10.1179/1351000214Y.0000000115
PMID:25396696

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 glycosides / Triterpene glycosides / Triterpene saponins
(3R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-5-oxooxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163023811 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(=O)CO7)O)O)C)C 764.90 unknown https://doi.org/10.1515/ZNB-2006-0919
10-[3-(3,4-Dihydroxy-5-oxooxan-2-yl)oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163023810 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(=O)CO7)O)O)C)C 764.90 unknown https://doi.org/10.1515/ZNB-2006-0919
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R)-3,4-dihydroxy-5-oxooxan-2-yl]oxy-3-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162985986 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)OC6C(C(C(=O)CO6)O)O)C)C 602.80 unknown https://doi.org/10.1515/ZNB-2006-0919
(3R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-3,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 11420072 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)O)C)C 472.70 unknown https://doi.org/10.1515/ZNB-2006-0919
10-(3,4-Dihydroxy-5-oxooxan-2-yl)oxy-3-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162985985 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)OC6C(C(C(=O)CO6)O)O)C)C 602.80 unknown https://doi.org/10.1515/ZNB-2006-0919
3,10-Dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 12312627 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)O)C)C 472.70 unknown https://doi.org/10.1515/ZNB-2006-0919

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