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Astragalus caspicus

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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 UUID643fda8de37e6339066527
Scientific name Astragalus caspicus
Authority M.Bieb.
First published in Fl. Taur.-Caucas.2: 204 (1808)

Description Top

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Synonyms Top

Scientific name Authority First published in
Astracantha theodoriana (Fed. & Rzazade) Czerep.
Tragacantha caspica (M.Bieb.) Steven Bull. Soc. Imp. Naturalistes Moscou4: 269 (1832)
Ankylobus caspicus (M.Bieb.) Steven Bull. Soc. Imp. Naturalistes Moscou29(II): 148 (1856)
Astracantha caspica (M.Bieb.) Podlech Mitt. Bot. Staatssamml. München19: 7 (1983)

Common names Top

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Language Common/alternative name
Azerbaijani xəzər gəvəni

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Astragalus caspicus subsp. caspicus Unknown
Astragalus caspicus subsp. pseudocaspius (Fisch.) Zarre Syst. Revis. Astragalus sect.: 65 (1998)

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
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Western Asia
      • Iran
      • Iraq
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000190319
Tropicos 13025555
KEW urn:lsid:ipni.org:names:476684-1
Open Tree Of Life 465941
Observations.org 115294
NCBI Taxonomy 144079
IPNI 476684-1
GBIF 5353004
Elurikkus 525453

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
Phytocompounds as a source for the development of new drugs to treat respiratory viral infections Seibert JB, Amparo TR, Almeida TC, de Souza GH, dos Santos OD 23-May-2023
PMCID:PMC10204935
doi:10.1016/B978-0-323-91294-5.00007-5
Flower development of Goniorrhachis marginata reveals new insights into the evolution of the florally diverse detarioid legumes Prenner G, Cardoso D Ann Bot 26-Dec-2016
PMCID:PMC5314645
doi:10.1093/aob/mcw223
PMID:28025284
Cycloartane-type glycosides from the roots of Astragalus caspicus Bieb. Fathiazad F, Khosropanah MK, Movafeghi A Nat Prod Res 01-Jul-2010
doi:10.1080/14786410902975582
PMID:20552530

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
Cycloastragenol 13943286 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)O)O)C 490.70 unknown https://doi.org/10.1080/14786410902975582
Cyclogalegigenin 3664530 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)O)O)C 490.70 unknown https://doi.org/10.1080/14786410902975582
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2R,3R,4R,5R,6S)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-15-[(2R,5R)-5,6-dihydroxy-6-methylheptan-2-yl]-9-hydroxy-7,7,12,16-tetramethyl-14-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-methyloxane-3,4,5-triol 163056668 Click to see CC1C(C(C(C(O1)OC2CCC34CC35CCC6(C(C(CC6(C5CC(C4C2(C)C)O)C)OC7C(C(C(CO7)O)O)O)C(C)CCC(C(C)(C)O)O)C)O)O)O 771.00 unknown https://doi.org/10.1080/14786410902975582
(2R,3R,4S,5S,6R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-14-hydroxy-15-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-6-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-9-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162943407 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)O)C 785.00 unknown https://doi.org/10.1080/14786410902975582
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R)-3,5-dihydroxy-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-14-hydroxy-15-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-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]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162884354 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)OC9C(C(C(C(O9)CO)O)O)O)O)C 917.10 unknown https://doi.org/10.1080/14786410902975582
2-[[15-(5,6-Dihydroxy-6-methylheptan-2-yl)-9-hydroxy-7,7,12,16-tetramethyl-14-(3,4,5-trihydroxyoxan-2-yl)oxy-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-6-methyloxane-3,4,5-triol 163056667 Click to see CC1C(C(C(C(O1)OC2CCC34CC35CCC6(C(C(CC6(C5CC(C4C2(C)C)O)C)OC7C(C(C(CO7)O)O)O)C(C)CCC(C(C)(C)O)O)C)O)O)O 771.00 unknown https://doi.org/10.1080/14786410902975582
2-[3,5-Dihydroxy-2-[[14-hydroxy-15-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethyl-9-(3,4,5-trihydroxyoxan-2-yl)oxy-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]oxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162884353 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)OC9C(C(C(C(O9)CO)O)O)O)O)C 917.10 unknown https://doi.org/10.1080/14786410902975582
Cyclosiversioside F 500122 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)O)C 785.00 unknown https://doi.org/10.1080/14786410902975582

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