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Astragalus galegiformis

Astragalus galegiformis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fdf06d1bfa610741278
Scientific name Astragalus galegiformis
Authority L.
First published in Sp. Pl.: 756 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Astragalus galegifolius L.
Tragacantha galegiformis (L.) Kuntze Revis. Gen. Pl.2: 945 (1891)
Glycyphylla galegiformis (L.) Steven Bull. Soc. Imp. Naturalistes Moscou4: 266 (1832)
Onix galegiformis (L.) Medik. Vorles. Churpfälz. Phys.-Ökon. Ges.2: 378 (1787)

Common names Top

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Language Common/alternative name
Polish traganek rutwicowaty

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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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
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • Turkey
  • Europe
    • Eastern Europe
      • Ukraine
    • Middle Europe
      • Austria
    • Southeastern Europe
      • Romania

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000213560
USDA Plants ASGA10
Tropicos 13025933
KEW urn:lsid:ipni.org:names:477532-1
The Plant List ild-8627
Observations.org 126018
IPNI 477532-1
iNaturalist 557371
GBIF 5347136
EOL 704266
Elurikkus 523599
USDA GRIN 5788
Open Tree Of Life 530209

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)!
Title Authors Publication Released IDs
Flavonoid glycosides from Astragalus galegiformis leaves M. D. Alaniya, N. Sh. Kavtaradze, C. Bassarello, A. V. Skhirtladze, C. Pizza, I. Kutateladze Springer Science and Business Media LLC 21-Feb-2007
doi:10.1007/S10600-006-0251-Y
Cyclogaleginoside D from Astragalus galegiformis stems M. D. Alaniya, T. I. Gigoshvili, N. Sh. Kavtaradze Springer Science and Business Media LLC 15-Aug-2006
doi:10.1007/S10600-006-0107-5
Triterpenoids from the stems of Astragalus galegiformis T. I. Gigoshvili, M. D. Alaniya, �. P. Kemertelidze Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630136
Triterpene glycosides ofAstragalus and their genins. XVI. Cyclogaleginosides A and B fromAstraglus galegiformis M. D. Alaniya, M. I. Isaev, M. B. Gorovits, N. D. Abdullaev, É. P. Kemertelidze, N. K. Abubakirov Springer Science and Business Media LLC 21-Nov-2004
doi:10.1007/BF00574333
Triterpene glycosides of Astragalus and of their genins. X. Cyclogalegigenin from Astragalus galegiformis M. D. Alaniya, M. I. Isaev, M. B. Gorovits, N. D. Abdullaev, �. P. Kemertelidze, N. K. Abubakirov Springer Science and Business Media LLC 21-Nov-2004
doi:10.1007/BF00579768
Flavonoids from Astragalus galegifolius and A. maximus M. D. Alaniya, N. F. Komissarenko, É. P. Kemertelidze Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00564613
A study of the polyphenol compounds of Astragalus species of the flora of the northern Caucasus and Uzbekistan I N. A. Tsepkova, A. N. Svechnikova, V. A. Bandyukova, Kh. Kh. Khalmatov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00564334
Structure of Cyclogaleginoside E from<i>Astragalus galegiformis</i> T. I. Gigoshvili, M. D. Alaniya, V. G. Tsitsishvili, R. Foure, L. Debrauver, E. P. Kemertelidze Springer Science and Business Media LLC 25-Nov-2003
doi:10.1023/B:CONC.0000003419.24465.3F

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
(1S,3R,6S,8S,9S,11R,12S,14S,15R,16R)-15-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-6,9,14-triol 162971719 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/10.1007/BF00579768
(6S,9S,11S,12S,14S,15R,16R)-15-[(2S,5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-6,9,14-triol 44144539 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/10.1007/BF00630136
https://doi.org/10.1007/BF00579768
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/10.1007/BF00579768
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2S,3R,4S,5R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-9,14-dihydroxy-15-[(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]oxane-3,4,5-triol 14241104 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)O)OC7C(C(C(CO7)O)O)O)C 622.80 unknown https://doi.org/10.1007/BF00574333
(2S,3R,4S,5S,6R)-2-[2-[(2R,5S)-5-[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-9,14-dihydroxy-7,7,12,16-tetramethyl-6-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-5-methyloxolan-2-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162964721 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)OC7C(C(C(C(O7)CO)O)O)O)C)O)C)C)O)OC8C(C(C(CO8)O)O)O)C 785.00 unknown https://doi.org/10.1023/B:CONC.0000003419.24465.3F
[(2S,3R,4S,5R)-2-[[(1S,3R,6S,8R,9S,11S,12S,14S,15R,16R)-9,14-dihydroxy-7,7,12,16-tetramethyl-15-[(2S,5R)-2-methyl-5-[2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]oxolan-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-4,5-dihydroxyoxan-3-yl] acetate 163053551 Click to see CC(=O)OC1C(C(COC1OC2CCC34CC35CCC6(C(C(CC6(C5CC(C4C2(C)C)O)C)O)C7(CCC(O7)C(C)(C)OC8C(C(C(C(O8)CO)O)O)O)C)C)O)O 827.00 unknown https://doi.org/10.1007/S10600-006-0107-5
[2-[[9,14-Dihydroxy-15-[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-dihydroxyoxan-3-yl] acetate 3767285 Click to see CC(=O)OC1C(C(COC1OC2CCC34CC35CCC6(C(C(CC6(C5CC(C4C2(C)C)O)C)O)C7(CCC(O7)C(C)(C)O)C)C)O)O 664.90 unknown https://doi.org/10.1007/BF00574333
[2-[[9,14-Dihydroxy-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]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]oxy]-4,5-dihydroxyoxan-3-yl] acetate 163053550 Click to see CC(=O)OC1C(C(COC1OC2CCC34CC35CCC6(C(C(CC6(C5CC(C4C2(C)C)O)C)O)C7(CCC(O7)C(C)(C)OC8C(C(C(C(O8)CO)O)O)O)C)C)O)O 827.00 unknown https://doi.org/10.1007/S10600-006-0107-5
2-[[9,14-Dihydroxy-15-[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]oxane-3,4,5-triol 3826638 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)O)C)O)C)C)O)OC7C(C(C(CO7)O)O)O)C 622.80 unknown https://doi.org/10.1007/BF00574333
2-[2-[5-[9,14-Dihydroxy-7,7,12,16-tetramethyl-6-(3,4,5-trihydroxyoxan-2-yl)oxy-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]-5-methyloxolan-2-yl]propan-2-yloxy]-6-(hydroxymethyl)oxane-3,4,5-triol 137796355 Click to see CC1(C(CCC23C1C(CC4C2(C3)CCC5(C4(CC(C5C6(CCC(O6)C(C)(C)OC7C(C(C(C(O7)CO)O)O)O)C)O)C)C)O)OC8C(C(C(CO8)O)O)O)C 785.00 unknown https://doi.org/10.1023/B:CONC.0000003419.24465.3F
20(R),24(S)-epoxycycloartane-3beta,6alpha,16beta,25-tetraol-3beta-O-D-(2-O-acetyl)-xylopyranoside 13996714 Click to see CC(=O)OC1C(C(COC1OC2CCC34CC35CCC6(C(C(CC6(C5CC(C4C2(C)C)O)C)O)C7(CCC(O7)C(C)(C)O)C)C)O)O 664.90 unknown https://doi.org/10.1007/BF00574333
Cyclogaleginoside A 133550435 Click to see CC(=O)OC1C(C(COC1OC2CCC34CC35CCC6(C(C(CC6(C5CC(C4C2(C)C)O)C)O)C7(CCC(O7)C(C)(C)O)C)C)O)O 664.90 unknown https://doi.org/10.1007/BF00630136
> 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/S10600-006-0251-Y
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2S,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 124708157 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 450.40 unknown https://doi.org/10.1007/BF00564613
3-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 162926601 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)OC6C(C(C(CO6)O)O)O)O 742.60 unknown https://doi.org/10.1007/S10600-006-0251-Y
3-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one 162950318 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(CO4)O)OC5C(C(C(CO5)O)O)O)O)O 580.50 unknown https://doi.org/10.1007/S10600-006-0251-Y
3-[3,5-Dihydroxy-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)chromen-4-one 162950317 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(CO4)O)OC5C(C(C(CO5)O)O)O)O)O 580.50 unknown https://doi.org/10.1007/S10600-006-0251-Y
3-[6-[[3,5-Dihydroxy-6-methyl-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 73170068 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)OC6C(C(C(CO6)O)O)O)O 742.60 unknown https://doi.org/10.1007/S10600-006-0251-Y
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/BF00564334
https://doi.org/10.1007/S10600-006-0251-Y
https://doi.org/10.1007/BF00564613
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/S10600-006-0251-Y
https://doi.org/10.1007/BF00564334
Dihydrokaempferol-3-glucoside 14354979 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 450.40 unknown https://doi.org/10.1007/BF00564613
kaempferol 3-O-beta-L-glucopyranoside 9911508 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/BF00564613
https://doi.org/10.1007/BF00564334
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(1R,18R,21R)-4,5,6,9-tetramethoxy-21-methyl-11,13,20-trioxapentacyclo[16.2.1.02,7.08,16.010,14]henicosa-2,4,6,8,10(14),15-hexaene 101099883 Click to see CC1C2CC3=CC4=C(C(=C3C5=C(C(=C(C=C5C1OC2)OC)OC)OC)OC)OCO4 414.40 unknown https://doi.org/10.1007/BF00579768
https://doi.org/10.1007/BF00630136

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