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Aster auriculatus

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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 UUID643fcf96f229a253214525
Scientific name Aster auriculatus
Authority Franch.
First published in J. Bot. (Morot) 10: 379 (1896)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aster auriculatus f. crenatus Y.Ling Fl. Reipubl. Popularis Sin. 74: 144 (1985), without latin (1985)

Common names Top

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Language Common/alternative name
Chinese 蓑衣莲
Chinese 耳叶紫菀
Chinese 银线菊
Chinese 银钱菊

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
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Tibet

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000091694
Tropicos 2745756
KEW urn:lsid:ipni.org:names:180724-1
The Plant List gcc-4796
Open Tree Of Life 83905
NCBI Taxonomy 1196465
IPNI 180724-1
iNaturalist 933888
GBIF 5406537
USDA GRIN 433647

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
A new species, Aster yaoshanensis (Asteracae, Astereae), from Guangxi (China), based on morphology and molecular phylogenetic data Zheng X, Qin K, Li T, Qu T, Luo J, Zhang G, Li B, Li P, Fu Z Front Plant Sci 02-Apr-2024
PMCID:PMC11019006
doi:10.3389/fpls.2024.1367917
PMID:38628365
Gentiopicroside—An Insight into Its Pharmacological Significance and Future Perspectives Antoniadi L, Bartnik M, Angelis A, Wawruszak A, Halabalaki M, Kukula-Koch W, Skaltsounis LA Cells 29-Dec-2023
PMCID:PMC10778152
doi:10.3390/cells13010070
PMID:38201274
Auriculatone Sulfate Effectively Protects Mice Against Acetaminophen-Induced Liver Injury Lin L, Guan H, Li R, Liao X, Zhao F, Wang M, Li J, Xu G, He X, Zhang J, Li Y, Wang Y, Zhou M, Liao S Molecules 09-Oct-2019
PMCID:PMC6832223
doi:10.3390/molecules24203642
PMID:31600996
Role of Saponins in Plant Defense Against Specialist Herbivores Hussain M, Debnath B, Qasim M, Bamisile BS, Islam W, Hameed MS, Wang L, Qiu D Molecules 30-May-2019
PMCID:PMC6600540
doi:10.3390/molecules24112067
PMID:31151268
Phylogenetic relationships and generic delimitation of Eurasian Aster (Asteraceae: Astereae) inferred from ITS, ETS and trnL-F sequence data Li WP, Yang FS, Jivkova T, Yin GS Ann Bot 19-Apr-2012
PMCID:PMC3359916
doi:10.1093/aob/mcs054
PMID:22517812
Diterpenoid, sesquiterpenoid and secoiridoid glucosides from Aster auriculatus Wang Changzeng, Yu Dequan Elsevier BV 04-Mar-2003
doi:10.1016/S0031-9422(97)00156-8
Lignan and acetylenic glycosides from Aster auriculatus Chang Zeng Wang, De Quan Yu Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00019-3
Triterpenoid saponins from Aster auriculatus. Wang CZ, Yu DQ Planta Med 01-Feb-1998
doi:10.1055/S-2006-957365
PMID:17253218

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
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-7-epi-Syringaresinol 4'-glucoside 4486984 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 580.60 unknown https://doi.org/10.1016/S0031-9422(98)00019-3
(2S,3R,4S,5S,6R)-2-[4-[(1R,2R)-2-[4-[(3R,3aS,6R,6aS)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-1,3-dihydroxypropyl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162889844 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC(CO)C(C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC)O)OC 806.80 unknown https://doi.org/10.1016/S0031-9422(98)00019-3
2-[4-[1,3-Dihydroxy-2-[4-[3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]propyl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162889843 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC(CO)C(C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC)O)OC 806.80 unknown https://doi.org/10.1016/S0031-9422(98)00019-3
Episyringaresinol 4'-O-beta-D-glncopyranoside 45482321 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 580.60 unknown https://doi.org/10.1016/S0031-9422(98)00019-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(E)-dec-2-en-4,6-diynoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 102316652 Click to see CCCC#CC#CC=CCOC1C(C(C(C(O1)CO)O)O)O 310.34 unknown https://doi.org/10.1016/S0031-9422(98)00019-3
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-2-[(E)-dec-8-en-4,6-diynoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 102316631 Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)CO)O)O)OC2C(C(C(C(O2)CO)O)O)O 472.50 unknown https://doi.org/10.1016/S0031-9422(98)00019-3
2-[2-Dec-8-en-4,6-diynoxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 163054024 Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)CO)O)O)OC2C(C(C(C(O2)CO)O)O)O 472.50 unknown https://doi.org/10.1016/S0031-9422(98)00019-3
2-Dec-2-en-4,6-diynoxy-6-(hydroxymethyl)oxane-3,4,5-triol 162880264 Click to see CCCC#CC#CC=CCOC1C(C(C(C(O1)CO)O)O)O 310.34 unknown https://doi.org/10.1016/S0031-9422(98)00019-3
2-Dec-8-en-4,6-diynoxy-6-(hydroxymethyl)oxane-3,4,5-triol 73802885 Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)CO)O)O)O 310.34 unknown https://doi.org/10.1016/S0031-9422(98)00019-3
Bidenoside C 70695725 Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)CO)O)O)O 310.34 unknown https://doi.org/10.1016/S0031-9422(98)00019-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(3aR,4S,6aR,8S,9aR,9bR)-8-hydroxy-3,6,9-trimethylidene-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydro-1H-cyclopenta[e]azulen-2-one 162923814 Click to see C=C1CC(C2C(CC(=O)C2=C)C3C1CC(C3=C)O)OC4C(C(C(C(O4)CO)O)O)O 422.50 unknown https://doi.org/10.1016/S0031-9422(97)00156-8
[(2R,3S,4S,5R,6R)-6-[[(3aR,4S,6aR,8S,9aR,9bR)-8-hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydro-1H-cyclopenta[e]azulen-4-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl formate 163092130 Click to see C=C1CC(C2C(CC(=O)C2=C)C3C1CC(C3=C)O)OC4C(C(C(C(O4)COC=O)O)O)O 450.50 unknown https://doi.org/10.1016/S0031-9422(97)00156-8
[3,4,5-trihydroxy-6-[(8-hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydro-1H-cyclopenta[e]azulen-4-yl)oxy]oxan-2-yl]methyl formate 163092129 Click to see C=C1CC(C2C(CC(=O)C2=C)C3C1CC(C3=C)O)OC4C(C(C(C(O4)COC=O)O)O)O 450.50 unknown https://doi.org/10.1016/S0031-9422(97)00156-8
8-hydroxy-3,6,9-trimethylidene-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydro-1H-cyclopenta[e]azulen-2-one 162923813 Click to see C=C1CC(C2C(CC(=O)C2=C)C3C1CC(C3=C)O)OC4C(C(C(C(O4)CO)O)O)O 422.50 unknown https://doi.org/10.1016/S0031-9422(97)00156-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2S,3R,4S,5S,6R)-2-[[(4aR,4bS,5S,7R,8aR,9S,10aS)-7-ethenyl-5,8a-dihydroxy-4a-(hydroxymethyl)-1,1,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthren-9-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101713125 Click to see CC1(CCCC2(C1CC(C3(C2C(CC(C3)(C)C=C)O)O)OC4C(C(C(C(O4)CO)O)O)O)CO)C 500.60 unknown https://doi.org/10.1016/S0031-9422(97)00156-8
[(4aR,4bS,5R,7R,8aR,9S,10aS)-7-ethenyl-5,8a-dihydroxy-1,1,7-trimethyl-9-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthren-4a-yl]methyl 3-hydroxy-3-methylbutanoate 101713126 Click to see CC1(CCCC2(C1CC(C3(C2C(CC(C3)(C)C=C)O)O)OC4C(C(C(C(O4)CO)O)O)O)COC(=O)CC(C)(C)O)C 600.70 unknown https://doi.org/10.1016/S0031-9422(97)00156-8
[7-Ethenyl-5,8a-dihydroxy-1,1,7-trimethyl-9-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthren-4a-yl]methyl 3-hydroxy-3-methylbutanoate 162992737 Click to see CC1(CCCC2(C1CC(C3(C2C(CC(C3)(C)C=C)O)O)OC4C(C(C(C(O4)CO)O)O)O)COC(=O)CC(C)(C)O)C 600.70 unknown https://doi.org/10.1016/S0031-9422(97)00156-8
2-[[7-Ethenyl-5,8a-dihydroxy-4a-(hydroxymethyl)-1,1,7-trimethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthren-9-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162962753 Click to see CC1(CCCC2(C1CC(C3(C2C(CC(C3)(C)C=C)O)O)OC4C(C(C(C(O4)CO)O)O)O)CO)C 500.60 unknown https://doi.org/10.1016/S0031-9422(97)00156-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8R,8aR,12aS,14aR,14bR)-8a-(carboxymethoxycarbonyl)-8-hydroxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 101935946 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C(=O)OCC(=O)O)C 706.90 unknown https://doi.org/10.1055/S-2006-957365
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8R,8aS,12aS,14aR,14bR)-8-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 101935945 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2OC(=O)C=CC6=CC(=C(C=C6)O)OC)C)C)(C)C)OC7C(C(C(C(O7)C(=O)O)O)O)O)C)C)C 795.00 unknown https://doi.org/10.1055/S-2006-957365
2-[(4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carbonyl]oxyacetic acid 162956798 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C(=O)OCC(=O)O)C 692.90 unknown https://doi.org/10.1055/S-2006-957365
2-[5-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carbonyl]oxyacetic acid 162956797 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C(=O)OCC(=O)O)C 692.90 unknown https://doi.org/10.1055/S-2006-957365
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8-oxo-1,2,3,4a,5,6,7,8a,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 101935943 Click to see CC1(CCC2C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2=O)C)C)(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C 602.80 unknown https://doi.org/10.1055/S-2006-957365
6-[(4,4,6a,6b,11,11,14b-Heptamethyl-8-oxo-1,2,3,4a,5,6,7,8a,9,10,12,12a,14,14a-tetradecahydropicen-3-yl)oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 163031928 Click to see CC1(CCC2C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2=O)C)C)(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C 602.80 unknown https://doi.org/10.1055/S-2006-957365
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(3S,4R,5R)-3,4-diacetyloxy-5-[[(2R,3R,4S,5R,6R)-3,4,5-triacetyloxy-6-[(E)-dec-8-en-4,6-diynoxy]oxan-2-yl]methoxy]oxolan-3-yl]methyl acetate 163020904 Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)COC2C(C(CO2)(COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 694.70 unknown https://doi.org/10.1016/S0031-9422(98)00019-3
[3,4-Diacetyloxy-5-[(3,4,5-triacetyloxy-6-dec-8-en-4,6-diynoxyoxan-2-yl)methoxy]oxolan-3-yl]methyl acetate 163020903 Click to see CC=CC#CC#CCCCOC1C(C(C(C(O1)COC2C(C(CO2)(COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 694.70 unknown https://doi.org/10.1016/S0031-9422(98)00019-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Gentiopicrin 88708 Click to see C=CC1C(OC=C2C1=CCOC2=O)OC3C(C(C(C(O3)CO)O)O)O 356.32 unknown https://doi.org/10.1016/S0031-9422(97)00156-8

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