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Crepidiastrum sonchifolium

Crepidiastrum sonchifolium - 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 UUID643fcb9deeec3123278337
Scientific name Crepidiastrum sonchifolium
Authority (Bunge) Pak & Kawano
First published in Mem. Fac. Sci. Kyoto Univ., Ser. Biol. , n.s., 15(1-2): 58 (1992)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lactuca sonchifolia (Maxim.) Benth. & Hook.f. ex Debeaux Actes Soc. Linn. Bordeaux 31: 229. 1876
Paraixeris sonchifolia var. serotina (Maxim.) Kitag. Neolin. Fl. Manshur. 664. 1979
Ixeris denticulata subsp. elegans (Franch.) Stebbins Journal of Botany, British and Foreign 75: 48 1937

Common names Top

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Language Common/alternative name
English sonchus-leaf crepidiastrum
Korean 고들빼기
Chinese 抱茎小苦荬
Chinese 尖裂假还阳参
Chinese 抱茎苦荬菜

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Crepidiastrum sonchifolium subsp. pubescens (Stebbins) N.Kilian Fl. China 20-21: 266 (2011)
Crepidiastrum sonchifolium subsp. sonchifolium

Varieties (abbr. var.) Top

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No variety added yet.

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
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Korea
    • Mongolia
      • Mongolia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000049001
Tropicos 50117890
KEW urn:lsid:ipni.org:names:1178615-2
The Plant List gcc-147510
Open Tree Of Life 1011858
NCBI Taxonomy 77563
IPNI 1178615-2
iNaturalist 479773
GBIF 3145185
USDA GRIN 465878
Wikipedia Crepidiastrum_sonchifolium
CMAUP NPO13121

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
Cytotoxic Effects of Ardisiacrispin A from Labisia pumila on A549 Human Lung Cancer Cells Lee YG, Kim TH, Kwon JE, Kim H, Kang SC Life (Basel) 18-Feb-2024
PMCID:PMC10890250
doi:10.3390/life14020276
PMID:38398785
Flavonoids with Anti-Herpes Simplex Virus Properties: Deciphering Their Mechanisms in Disrupting the Viral Life Cycle Šudomová M, Hassan ST Viruses 29-Nov-2023
PMCID:PMC10748012
doi:10.3390/v15122340
PMID:38140581
Benefits of Combining Sonchus brachyotus DC. Extracts and Synbiotics in Alleviating Non-Alcoholic Fatty Liver Disease Huang W, Shen B, Li X, Zhang T, Zhou X Foods 11-Sep-2023
PMCID:PMC10530047
doi:10.3390/foods12183393
PMID:37761102
Evaluation of the Weeds around Capsicum annuum (CA) Cultivation Fields as Potential Habitats of CA-Infecting Viruses Choi MK Plant Pathol J 01-Aug-2023
PMCID:PMC10412962
doi:10.5423/PPJ.OA.04.2023.0066
PMID:37550983
Optimization of ultrasonic-assisted extraction of flavonoids from Lactuca indica L. cv. Mengzao and their antioxidant properties Hao J, Wang Z, Jia Y, Sun L, Fu Z, Zhao M, Li Y, Yuan N, Cong B, Zhao L, Ge G Front Nutr 15-Jun-2023
PMCID:PMC10308084
doi:10.3389/fnut.2023.1065662
PMID:37396124
Competition induces negative conspecific allelopathic effects on seedling recruitment Yuan L, Li J, van Kleunen M Ann Bot 13-Oct-2022
PMCID:PMC9758299
doi:10.1093/aob/mcac127
PMID:36227858
The Influence of Ixeris sonchifolia Hance Injection Combined with Isosorbide Mononitrate in Patients with Coronary Heart Disease and Diabetes Zhang L, Qin X Evid Based Complement Alternat Med 04-Jul-2022
PMCID:PMC9273379
doi:10.1155/2022/7503380
PMID:35832520
Chicoric Acid: Natural Occurrence, Chemical Synthesis, Biosynthesis, and Their Bioactive Effects Yang M, Wu C, Zhang T, Shi L, Li J, Liang H, Lv X, Jing F, Qin L, Zhao T, Wang C, Liu G, Feng S, Li F Front Chem 23-Jun-2022
PMCID:PMC9262330
doi:10.3389/fchem.2022.888673
PMID:35815211
Antioxidant Activity and Inhibitory Effects of Black Rice Leaf on the Proliferation of Human Carcinoma Cells Thepthanee C, Liu CC, Yu HS, Huang HS, Yen CH, Li YH, Lee MR, Liaw ET Biomed Res Int 11-Jun-2022
PMCID:PMC9206558
doi:10.1155/2022/7270782
PMID:35726317
Impacts of Heat Stress on Rabbit Immune Function, Endocrine, Blood Biochemical Changes, Antioxidant Capacity and Production Performance, and the Potential Mitigation Strategies of Nutritional Intervention Liang ZL, Chen F, Park S, Balasubramanian B, Liu WC Front Vet Sci 26-May-2022
PMCID:PMC9201964
doi:10.3389/fvets.2022.906084
PMID:35720853
Therapeutic potential of traditional Chinese medicine for vascular endothelial growth factor MAO Y, MENG L, LIU H, LU Y, YANG K, OUYANG G, BAN Y, CHEN S J Zhejiang Univ Sci B 15-May-2022
PMCID:PMC9110323
doi:10.1631/jzus.B2101055
PMID:35557037
Cardioprotective Effects and Possible Mechanisms of Luteolin for Myocardial Ischemia-Reperfusion Injury: A Systematic Review and Meta-Analysis of Preclinical Evidence Pan Q, Liu Y, Ma W, Kan R, Zhu H, Li D Front Cardiovasc Med 25-Apr-2022
PMCID:PMC9081501
doi:10.3389/fcvm.2022.685998
PMID:35548432
Effect of Fermentation Duration on the Quality Changes of Godulbaegi Kimchi Park JM, Zhang BZ, Kim JM Foods 31-Mar-2022
PMCID:PMC8997386
doi:10.3390/foods11071020
PMID:35407107
Flavonoids Target Human Herpesviruses That Infect the Nervous System: Mechanisms of Action and Therapeutic Insights Šudomová M, Berchová-Bímová K, Mazurakova A, Šamec D, Kubatka P, Hassan ST Viruses 13-Mar-2022
PMCID:PMC8949561
doi:10.3390/v14030592
PMID:35336999
The Role of PKC and HIF-1 and the Effect of Traditional Chinese Medicinal Compounds on Cerebral Ischemia-Reperfusion Injury Fang Z, Zhang Y, Zhao X, Jin W, Yu L Evid Based Complement Alternat Med 27-Feb-2022
PMCID:PMC8898791
doi:10.1155/2022/1835898
PMID:35265143

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
4-Hydroxy-2-methoxybenzoic acid 12695575 Click to see COC1=C(C=CC(=C1)O)C(=O)O 168.15 unknown via CMAUP database
> Benzenoids / Indanes / Indanones
(2R-trans)-2,3-Dihydro-3-hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-1H-inden-1-one 169729 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)O 234.29 unknown via CMAUP database
(2R)-2-hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-3H-inden-1-one 46849571 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)O 234.29 unknown via CMAUP database
(2S-trans)-6-(2-Chloroethyl)-2,3-dihydro-3-hydroxy-2,5,7-trimethyl-1H-inden-1-one 148419 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCCl)C)O 252.73 unknown via CMAUP database
(2S,3R)-3-hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-2,3-dihydroinden-1-one 46850078 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)O 234.29 unknown via CMAUP database
(2S)-6-(2-hydroxyethyl)-2,5,7-trimethyl-2,3-dihydroinden-1-one 12314748 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCO)C 218.29 unknown via CMAUP database
(3R)-6-(2-chloroethyl)-3-hydroxy-2,2,5,7-tetramethyl-3H-inden-1-one 23260004 Click to see CC1=CC2=C(C(=C1CCCl)C)C(=O)C(C2O)(C)C 266.76 unknown via CMAUP database
(3S)-3-hydroxy-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-3H-inden-1-one 71361396 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)C 248.32 unknown via CMAUP database
(S)-2,3-Dihydro-2-(hydroxymethyl)-6-(2-methoxyethyl)-2,5,7-trimethyl-1H-inden-1-one 134443 Click to see CC1=CC2=C(C(=C1CCOC)C)C(=O)C(C2)(C)CO 262.34 unknown via CMAUP database
(S)-2,3-Dihydro-6-(2-hydroxyethyl)-2-(hydroxymethyl)-5,7-dimethyl-1H-inden-1-one 169739 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)CO 234.29 unknown via CMAUP database
(S)-2,3-Dihydro-6-(2-hydroxyethyl)-5-(hydroxymethyl)-2,7-dimethyl-1H-inden-1-one 151323 Click to see CC1CC2=CC(=C(C(=C2C1=O)C)CCO)CO 234.29 unknown via CMAUP database
1-Indanone 6735 Click to see C1CC(=O)C2=CC=CC=C21 132.16 unknown via CMAUP database
2S,3S-acetylpterosin C 21122778 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC(=O)C)C)O 276.33 unknown via CMAUP database
Epipterosin L 46848746 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)CO 264.32 unknown via CMAUP database
Pterosin A 135017 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)CO 248.32 unknown via CMAUP database
Pterosin B 115049 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCO)C 218.29 unknown via CMAUP database
Pterosin C 186209 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)O 234.29 unknown via CMAUP database
Pterosin D 147559 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)C 248.32 unknown via CMAUP database
Pterosin E 148588 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CC(=O)O)C 232.27 unknown via CMAUP database
Pterosin H 135029 Click to see CC1=CC2=C(C(=C1CCCl)C)C(=O)C(C2)(C)C 250.76 unknown via CMAUP database
Pterosin I 161891 Click to see CC1=CC2=C(C(=C1CCOC)C)C(=O)C(C2)(C)C 246.34 unknown via CMAUP database
Pterosin K 148420 Click to see CC1=CC2=C(C(=C1CCCl)C)C(=O)C(C2)(C)CO 266.76 unknown via CMAUP database
Pterosin L 21633068 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)CO 264.32 unknown via CMAUP database
Pterosin O 135255 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCOC)C 232.32 unknown via CMAUP database
Pterosin Z 134977 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)C 232.32 unknown via CMAUP database
Pterosinf 46849741 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCCl)C 236.73 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Pteridicacid A 11013967 Click to see CCC1C=CC2(C(C(C(C(O2)C(C)C=CC=CC(=O)O)C)O)C)OC1C 364.50 unknown via CMAUP database
Pteridicacid B 10883014 Click to see CCC1C=CC2(C(C(C(C(O2)C(C)C=CC=CC(=O)O)C)O)C)OC1C 364.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Tripalmitin 11147 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC 807.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Ptaquiloside Z 101242525 Click to see CC1=CC2(CC(C(=O)C2C(C13CC3)(C)O)(C)C)OC4C(C(C(C(O4)CO)O)O)O 412.50 unknown via CMAUP database
Pteridanoside 11795946 Click to see CC1(CC2C(C1=O)C3(CCC3=C(C2O)COC4C(C(C(C(O4)CO)O)O)O)C)C 412.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
20-Hydroxyecdysone 5459840 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
3alpha-Hydroxyecdysone 70686927 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
Pterosterone 441836 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)O 480.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
3-Epiecdysone 23724769 Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)O 464.60 unknown via CMAUP database
Ecdysone 19212 Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)O 464.60 unknown via CMAUP database
Ponasterone A 115127 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O 464.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
Ponasteroside A 12314455 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)OC5C(C(C(C(O5)CO)O)O)O)O)C)C)O)O)O 626.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron 21883788 Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-] 116.07 unknown via CMAUP database
Butanedioate;hydron 21952380 Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-] 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Prunasin 119033 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3R)-3-hydroxy-2,5,7-trimethyl-6-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-2,3-dihydroinden-1-one 46848577 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C)O 396.40 unknown via CMAUP database
(2S,3S)-6-(2-hydroxyethyl)-2,5,7-trimethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydroinden-1-one 23260007 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)OC3C(C(C(C(O3)CO)O)O)O 396.40 unknown via CMAUP database
(2S)-2,5,7-trimethyl-6-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-2,3-dihydroinden-1-one 46848576 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C 380.40 unknown via CMAUP database
(3R)-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3H-inden-1-one 46848743 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2OC3C(C(C(C(O3)CO)O)O)O)(C)C 410.50 unknown via CMAUP database
Ptaquiloside 13962857 Click to see CC1CC2(C=C(C3(CC3)C(C2C1=O)(C)O)C)OC4C(C(C(C(O4)CO)O)O)O 398.40 unknown via CMAUP database
Pteroside A 169727 Click to see CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2)(C)CO 410.50 unknown via CMAUP database
Pteroside B 134279 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C 380.40 unknown via CMAUP database
Pteroside C 169728 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C)O 396.40 unknown via CMAUP database
Pteroside D 169738 Click to see CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2O)(C)C 410.50 unknown via CMAUP database
Pteroside P 148715 Click to see CC1CC2=CC(=C(C(=C2C1=O)C)CCOC3C(C(C(C(O3)CO)O)O)O)CO 396.40 unknown via CMAUP database
Pteroside Z 169737 Click to see CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2)(C)C 394.50 unknown via CMAUP database
pterosin C 3-O-glucoside 44201982 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C)O 396.40 unknown via CMAUP database
Pterosin D 3-O-glucoside 21670079 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2OC3C(C(C(C(O3)CO)O)O)O)(C)C 410.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-Ethenylphenyl beta-D-glucopyranoside 182338 Click to see C=CC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 282.29 unknown via CMAUP database
beta-D-Glucopyranoside, 4-ethenylphenyl 6-O-beta-D-xylopyranosyl- 185053 Click to see C=CC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O 414.40 unknown via CMAUP database
Ptelatoside b 130179 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC=C(C=C3)C=C)CO)O)O)O)O)O 428.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidones / Pyrrolidine-2-ones
(5R)-5-methoxypyrrolidin-2-one 643445 Click to see COC1CCC(=O)N1 115.13 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
5-Caffeoylshikimic acid 5281762 Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 336.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
> 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 via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
kaempferol 3-O-(6"-O-feruloyl)-glucoside 23265189 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O 624.50 unknown via CMAUP database
Tiliroside 5320686 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
kaempferol 5-O-beta-L-glucopyranoside 72551435 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxychromen-4-one 101714010 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC(=C(C=C5)O)O)O 640.50 unknown via CMAUP database
3-[(3-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-1-benzopyran-4-one 101683505 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 640.50 unknown via CMAUP database
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 via CMAUP database
Isoquercetin 5280804 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 via CMAUP database
Isoquercitin 10813969 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 via CMAUP database
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 via CMAUP database
Quercetin 3-laminaribioside 101683504 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)OC5C(C(C(C(O5)CO)O)O)O)O)O)O 626.50 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol 7-O-alpha-L-rhamnopyranoside-4'-O-beta-D-glucopyranoside 101949540 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 594.50 unknown via CMAUP database

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