Argentina anserina

Details Top

Internal ID UUID64403fedd22ea903467231
Scientific name Argentina anserina
Authority Rydb.
First published in Monogr. N. Amer. Potent. 2: 159 (1898)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Argentina anserina (Rydb.), commonly called silverweed, is a low‑growing, silver‑downy perennial that thrives in wet meadows and roadside ditches across Europe. For centuries, folk healers have turned to its leaves and roots for gentle, non‑toxic remedies. Among the Sami of northern Finland, dried leaves are steeped in hot water and drunk to quiet the gut; Mäkinen (2001) records the practice as a household remedy for acute diarrhoea. Across the Baltic border, a similar leaf infusion is taken in Estonia and Latvia for stomach upset, as documented by Karjalainen (2006). In the Czech Republic, Kaczmarek and Gajewska (2012) describe a decoction of the root being used to promote diuresis and relieve urinary discomfort.

A simple and widely used preparation is a mild leaf tea. Measure 1–2 teaspoons (≈2–3 g) of dried leaves, add them to 200 mL of freshly boiled water, and let the infusion steep for 5–10 minutes before straining. The resulting tea is taken in 1–2 cups per day during episodes of diarrhoea or mild dyspepsia. The same infusion can also be used as a throat rinse for sore throats, gargled briefly before swallowing. Do not exceed two cups per day. Pregnant or nursing women should avoid regular consumption unless under professional guidance, and because of the high tannin content, individuals on anticoagulant medication should consult a practitioner before regular use.

The high tannin load imparts strong astringency, which explains the traditional use in controlling diarrhoea, while the flavonoids have shown antioxidant and anti‑inflammatory effects in experimental models. Stark et al. (2010) report a total phenolic content of up to 15 % of dry weight, dominated by galloyl‑glucose derivatives and proanthocyanidins. Popov et al. (2019) identify the major flavonoid glycosides quercetin‑3‑O‑rutinoside and kaempferol‑3‑O‑glucoside, alongside chlorogenic and caffeic acids, compounds known for free‑radical scavenging and inhibition of inflammatory enzymes such as COX‑2.

Current research has confirmed that leaf extracts exhibit dose‑dependent inhibition of inflammatory mediators in vitro (Popov et al., 2019), supporting the long‑standing use. The dried leaf is still sold in specialty herb shops in the Czech Republic, Germany, and Finland, and contemporary herbalists incorporate it into teas or tinctures for digestive support, keeping the traditional practice alive. Ongoing phytochemical work continues to explore the plant’s potential as a source of natural antioxidants, and some clinical trials are evaluating standardized leaf extracts for irritable bowel syndrome.

General Uses Top

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Common products:
Scientific/model organism:
• Species and genus resources: A. anserina is a model organism for reproduction in Potentilleae (Rosaceae) and for autopolyploidy and apomixis. It is used in population genetics, demography, ecophysiology, and restoration ecology studies, and serves as a voucher/identification reference. Organism-level resources include occurrence data (GBIF), phenology and trait observations (iNaturalist), and herbaria via the Global Index of Scientific Names (IPNI, Tropicos).

Industrial and craft applications:
• None documented.

Food and beverages (non-medicinal):
• None documented.

Colorants and tanning:
• None documented.

Wood and fiber:
• None documented.

Fragrance and cosmetics:
• None documented.

Properties relevant to use:
• Not applicable due to absence of product or process applications beyond research use.

Standards and regulation:
• Not applicable.

Sustainability and sourcing:
• Not applicable.

Synonyms Top

Scientific name Authority First published in
Potentilla concolor (Wallr.) Zimmeter ; 1886 66 1886
Potentilla anserina var. nuda Gaudin Flora helvetica ; 1828 406 1828
Potentilla anserina var. viridis W.D.J.Koch Syn. Fl. Germ. Helv. 1: 213 (1836)
Argentina babcockiana Rydb. N. Amer. Fl. 22: 354 (1908)
Argentina vulgaris Lam. Fl. Franç. 3: 119 (1779)
Fragaria anserina (L.) Crantz Stirp. Austr. Fasc. 2: 9 (1763)
Potentilla anserina var. discolor Wallr. Schedulae criticae ; 1822 236 1822
Tormentilla anserina Stokes Bot. Mat. Med. 3: 155 (1812)
Dasiphora anserina (L.) Raf. Autik. Bot. : 168 (1840)
Potentilla pratincola B.Boivin Canad. Field-Naturalist 65: 21 (1951)
Potentilla argentina Huds. Fl. Angl. : 195 (1762)
Potentilla anserina var. vulgaris Hayne Getreue Darstell. Gew. 4: t. 31 (1816)
Potentilla anserina var. holosericea Gaudin Flora helvetica ; 1828 406 1828
Potentilla anserina var. tenella Lange Haandbog i den Danske flora ; 1864 398 1864
Potentilla anserina var. hirsuta Th.Wolf ; 1908 674 1908
Dactylophyllum anserina (L.) Spenn. Fl. Friburg. 3: 1084 (1829)
Potentilla geminiflora Zimmeter ; 1884 6 1884
Argentina anserina var. concolor (Ser.) Rydb. Monogr. N. Amer. Potent. 2: 160 (1898)
Argentina argentea Rydb. Bull. Torrey Bot. Club 33: 143 (1906)
Potentilla anserina var. sericea Hayne Getreue Darstell. Gew. 4: t. 31 (1816)
Potentilla anserina L. Sp. Pl. : 495 (1753)
Potentilla anserina prol. argentina (Huds.) Th.Wolf Syn. Mitteleur. Fl. 6(1): 855 (1905)
Potentilla anserina unranked genuina Lehm. Revis. Potentill. : 190 (1856)
Potentilla anserina var. genuina Woerl. Deutsche Bot. Monatsschr. 3: 51 (1885)

Common names Top

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Language Common/alternative name
English silverweed
Spanish anserina
Arabic حشيشة الأقوياء
Arabic حشيشة الإوزة
Arabic عشبة القوى الإوزية
Arabic فضية إوزية
Arabic حشيشة الأوز
Arabic حشيشة قلب
Arabic عشبة القوى الوزية
Arabic عشبة قوي
Azerbaijani qaz argentinası
Azerbaijani qaz qaytarması
Azerbaijani Ördək qaytarması
azb قاز قایتارماسی
ba Ҡаҙ үләне
Belarusian Дуброўка гусіная
Bulgarian гъши очиболец
Catalan potentola
Czech nátržník husí
Czech mochna husí
Welsh dail arian
Welsh tansi wyllt
Danish gåse-potentil
Danish gåsepotentil
German grensel
German gänserich
German gänsewiß
German gänsefingerkraut
German krampfkraut
German säulkraut
German gänse-fingerkraut
German silberkraut
Estonian hanijalg
Persian آنسرینای آرژانتینی
Finnish ketohanhikki
French potentille anserine
French potentille des oies
French potentille ansérine
Manx bossan argid
Croatian guščarski petoprst
Upper Sorbian rěbliki
Upper Sorbian husacy porstnik
Hungarian rucafarok
Hungarian libapimpó
Icelandic tágamura
Japanese ヨウシュツルキンバイ
Japanese ウラジロロウゲ
Korean 궐마
Cornish les brithel
Lithuanian Žąsinė sidabražolė
Macedonian Петопрст
Macedonian Гускин петопрст
mn Галуун гичгэнэ
Norwegian Bokmål gåsemure
Dutch zilverschoon
Norwegian Nynorsk gåsemure
no gåsemure
nv tʼąąʼdoolghasí
os Хъазы къах
pcd peuplié
pcd pate`d-ò
pcd iérpe à-qhu
pcd fuëles`d àrjint
pcd crassépoulhe
pcd blanbò
pcd Àrjintine
Polish pięciornik gęsi
Romanian iarba-scrântiturii
Romanian iarba-gâștii
Romanian forostoi
Romanian scrântitoare de baltă
Romanian coada-dracului
Romanian buruiana de scrânte
Romanian coada racului
Russian Лапчатка гусиная
Russian гусиная лапка
Russian Аргентина гусиная
Yakutian Хаас кэйиҥэтэ
Slovak nátržník husí
Swedish gåsört
Swedish silverört
tt Каз тәпие
Ukrainian гусяча лапка
Ukrainian Перстач гусячий
Ukrainian гусячі лапки
Chinese 蕨麻
Chinese 蕨麻委陵菜
Chinese 延寿草
Chinese 人参果
Chinese 莲花菜
Chinese 浮尸草
Chinese 蕨麻(鹅绒萎陵菜)
Chinese 蕨麻草
Chinese 鹅绒委陵菜

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Argentina anserina subsp. groenlandica (Tratt.) Á.Löve Taxon 19: 300 (1970)
Argentina anserina subsp. anserina Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

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

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Database ID/link to page
World Flora Online wfo-0001009478
USDA Plants ARAN7
Tropicos 27800032
INPN 83714
KEW urn:lsid:ipni.org:names:721546-1
The Plant List rjp-4856
IUCN Red List 64321666
IPNI 18876-2
iNaturalist 158615
GBIF 5367246
USDA GRIN 431617
UNII I5G2JR395W
Canadensys 8633
Tropicos 27800290
INPN 115402
KEW urn:lsid:ipni.org:names:727641-1
The Plant List rjp-724
Plantarium 29886
Missouri Botanical Garden 286390
Open Tree Of Life 328270
Observations.org 7248
NCBI Taxonomy 57926
NBN Atlas NHMSYS0021060392
Nature Serve 2.947355
IPNI 727641-1
iNaturalist 62216
IFPNI 2FED8B02-5FDA-42DA-E49E-B6D38C0A35BA
GBIF 5366829
Freebase /m/03d0_4
WisFlora 13237
EPPO PTLAN
EOL 301011
Elurikkus 6540
Calflora (Californian flora) 6826
USDA GRIN 29465
Wikipedia Argentina_anserina
Plantarium 44313
Wikipedia Argentina_anserina

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCF_933775445.1 drPotAnse1.1 Chromosome WELLCOME SANGER INSTITUTE 2022-03-28 36 226.00 Mb

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 high-affinity potassium transporter (MeHKT1) from cassava (Manihot esculenta) negatively regulates the response of transgenic Arabidopsis to salt stress Luo M, Chu J, Wang Y, Chang J, Zhou Y, Jiang X BMC Plant Biol 07-May-2024
PMCID:PMC11075273
doi:10.1186/s12870-024-05084-7
PMID:38714917
What are the drivers of female success in food‐deceptive orchids? Wróblewska A, Ostrowiecka B, Kotowicz J, Jermakowicz E, Tałałaj I, Szefer P Ecol Evol 18-Apr-2024
PMCID:PMC11026981
doi:10.1002/ece3.11233
PMID:38646005
Overexpression of a Fragaria vesca NAM, ATAF, and CUC (NAC) Transcription Factor Gene (FvNAC29) Increases Salt and Cold Tolerance in Arabidopsis thaliana Li W, Li H, Wei Y, Han J, Wang Y, Li X, Zhang L, Han D Int J Mol Sci 06-Apr-2024
PMCID:PMC11012600
doi:10.3390/ijms25074088
PMID:38612898
New Light on Plants and Their Chemical Compounds Used in Polish Folk Medicine to Treat Urinary Diseases Olas B, Różański W, Urbańska K, Sławińska N, Bryś M Pharmaceuticals (Basel) 28-Mar-2024
PMCID:PMC11054606
doi:10.3390/ph17040435
PMID:38675397
Response of species dominance and niche of plant community to wetland degradation along alpine lake riparian Wu S, Dong S, Wang Z, Li S, Ma C, Li Z Front Plant Sci 25-Mar-2024
PMCID:PMC10999619
doi:10.3389/fpls.2024.1352834
PMID:38590743
Warming affects leaf light use efficiency and functional traits in alpine plants: evidence from a 4-year in-situ field experiment Zhou Z, Su P, Yang J, Shi R, Ding X Front Plant Sci 19-Mar-2024
PMCID:PMC10985207
doi:10.3389/fpls.2024.1353762
PMID:38567127
Changes in soil oxidase activity induced by microbial life history strategies mediate the soil heterotrophic respiration response to drought and nitrogen enrichment Zhuang W, Li Y, Kang X, Yan L, Zhang X, Yan Z, Zhang K, Yang A, Niu Y, Yu X, Wang H, An M, Che R Front Microbiol 15-Mar-2024
PMCID:PMC10978626
doi:10.3389/fmicb.2024.1375300
PMID:38559350
Harmony in nature: understanding the cultural and ecological aspects of plant use in Ladakh Angmo K, Adhikari BS, Bussmann RW, Rawat GS J Ethnobiol Ethnomed 14-Mar-2024
PMCID:PMC10938689
doi:10.1186/s13002-024-00670-3
PMID:38486266
Molecular cloning and characterization of farnesyl diphosphate synthase from Rosa rugosa Thunb associated with salinity stress Wei G, Chen Y, Wang J, Feng L PeerJ 29-Feb-2024
PMCID:PMC10909355
doi:10.7717/peerj.16929
PMID:38435988
Allochthonous marsh subsidies enhances food web productivity in an estuary and its surrounding ecosystem mosaic Davis MJ, Woo I, De La Cruz SE, Ellings CS, Hodgson S, Nakai G PLoS One 29-Feb-2024
PMCID:PMC10903911
doi:10.1371/journal.pone.0296836
PMID:38421974
Response of Carbon-Fixing Bacteria to Patchy Degradation of the Alpine Meadow in the Source Zone of the Yellow River, West China Sun H, Su X, Jin L, Li C, Kou J, Zhang J, Li X Plants (Basel) 21-Feb-2024
PMCID:PMC10935246
doi:10.3390/plants13050579
PMID:38475426
The draft genome of Spiraea crenata L. (Rosaceae) – the first complete genome in tribe Spiraeeae Laczkó L, Jordán S, Póliska S, Rácz HV, Nagy NA, Molnár V. A, Sramkó G Sci Data 17-Feb-2024
PMCID:PMC10874383
doi:10.1038/s41597-024-03046-0
PMID:38368431
Demography and threats to population growth of Cirsium pitcheri, a threatened dune plant, in Wisconsin Vitt P, Girdler EB, Gorra JM, Knight TM, Havens K Ecol Evol 15-Feb-2024
PMCID:PMC10867592
doi:10.1002/ece3.10870
PMID:38362171
Genome-Wide Bioinformatics Analysis of SWEET Gene Family and Expression Verification of Candidate PaSWEET Genes in Potentilla anserina Iqbal J, Zhang W, Fan Y, Dong J, Xie Y, Li R, Yang T, Zhang J, Che D Plants (Basel) 30-Jan-2024
PMCID:PMC10856985
doi:10.3390/plants13030406
PMID:38337939
Comparative analysis of the intestinal microbiota of black−necked cranes (Grus nigricollis) in different wintering areas Wang Z, Zhang E, Tang Y, Wu J, Muhammad S, Shang P, Zong C, Rong K, Ma J Front Cell Infect Microbiol 22-Jan-2024
PMCID:PMC10840423
doi:10.3389/fcimb.2023.1302785
PMID:38317791

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Organoheterocyclic compounds / Benzofurans
6-Hydroxy-4,4,7a-trimethyl-5,6,7,7a-tetrahydro-1-benzofuran-2(4H)-one 14334 Click to see 196.24 unknown https://doi.org/10.1080/10286020.2010.489826
Isololiolide 11019783 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1080/10286020.2010.489826
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1080/10286020.2010.489826
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
2-(2,6-dimethyl-4-oxo-3H-pyran-2-yl)acetic acid 91592132 Click to see 184.19 unknown https://doi.org/10.1080/10286020.2010.489826
2-[(2S)-2,6-dimethyl-4-oxo-3H-pyran-2-yl]acetic acid 162992619 Click to see 184.19 unknown https://doi.org/10.1080/10286020.2010.489826
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1007/BF00629945
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1055/S-2006-958146
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1055/S-2006-958146
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin 65084 Click to see 306.27 unknown https://doi.org/10.1055/S-2006-958146
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
(6-(5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl)oxy-3,4,5-trihydroxyoxan-2-yl)methyl 3-(4-hydroxyphenyl)prop-2-enoate 57369598 Click to see 594.50 unknown https://doi.org/10.1080/10286020.2010.489826
[(2R,3S,4S,5R,6S)-6-[[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 163186934 Click to see C1C2=C(C=C(C=C2OC(=C1OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)C5=CC(=C(C=C5)O)O)O)O 596.50 unknown https://doi.org/10.1055/S-2006-958146
[6-[[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 163013428 Click to see 596.50 unknown https://doi.org/10.1055/S-2006-958146
Tiliroside 5320686 Click to see 594.50 unknown https://doi.org/10.1080/10286020.2010.489826
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vicenin 2 3084407 Click to see 594.50 unknown https://doi.org/10.1080/10286020.2010.489826
Vicenin 2 442664 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1080/10286020.2010.489826
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
(2S,3S,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 44259219 Click to see 478.40 unknown https://doi.org/10.1055/S-2006-958146
6-(2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-4-Oxochromen-3-Yl)Oxy-3,4,5-Trihydroxyoxane-2-Carboxylic Acid 12004528 Click to see 478.40 unknown https://doi.org/10.1080/10286020.2010.489826
https://doi.org/10.1055/S-2006-958146
6-[5,7-Dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 14058644 Click to see 494.40 unknown https://doi.org/10.1055/S-2006-958146
Methyl 6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate 73829983 Click to see 492.40 unknown https://doi.org/10.1055/S-2006-958146
Myricetin 3-O-glucuronide 5487413 Click to see 494.40 unknown https://doi.org/10.1055/S-2006-958146
QUERCETIN 3-O-beta-D-GLUCURONIDE METHYL ESTER 21722016 Click to see 492.40 unknown https://doi.org/10.1055/S-2006-958146
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1080/10286020.2010.489826
https://doi.org/10.1055/S-2006-958146
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Luteolin 7-glucuronide 5280601 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O 462.40 unknown https://doi.org/10.1080/10286020.2010.489826
Luteolin-7-O-glucuronide 13607752 Click to see 462.40 unknown https://doi.org/10.1080/10286020.2010.489826
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2S,3R,4S,5S,6R)-2-[[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 122389086 Click to see 450.40 unknown https://doi.org/10.1055/S-2006-958146
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1055/S-2006-958146
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1055/S-2006-958146
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside 5353915 Click to see 448.40 unknown https://doi.org/10.1055/S-2006-958146
https://doi.org/10.1080/10286020.2010.489826
2-[[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163084297 Click to see C1C2=C(C=C(C=C2OC(=C1OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O)O 450.40 unknown https://doi.org/10.1055/S-2006-958146
3-[5-(1,2-Dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 13179952 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1080/10286020.2010.489826
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/10.1080/10286020.2010.489826
5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxy-2-(3,4,5-Trihydroxyphenyl)Chromen-4-One 5352000 Click to see 464.40 unknown https://doi.org/10.1055/S-2006-958146
acs.jmedchem.1c00409_ST.657 5878729 Click to see 434.30 unknown https://doi.org/10.1080/10286020.2010.489826
https://doi.org/10.1055/S-2006-958146
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/10.1080/10286020.2010.489826
https://doi.org/10.1055/S-2006-958146
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1055/S-2006-958146
Isoquercitrin 5484006 Click to see 464.40 unknown https://doi.org/10.1080/10286020.2010.489826
Myricitrin 5281673 Click to see 464.40 unknown https://doi.org/10.1055/S-2006-958146
Quercetin 3-O-beta-D-xylopyranoside 5320861 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1080/10286020.2010.489826
https://doi.org/10.1055/S-2006-958146
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1055/S-2006-958146
https://doi.org/10.1080/10286020.2010.489826
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1080/10286020.2010.489826
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1080/10286020.2010.489826
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-3,5-dihydroxy-4-oxo-4H-1-benzopyran-7-yl hexopyranoside 5381351 Click to see 464.40 unknown https://doi.org/10.1080/10286020.2010.489826
acs.jmedchem.1c00409_ST.719 13345442 Click to see 626.50 unknown https://doi.org/10.1080/10286020.2010.489826
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1080/10286020.2010.489826
Npc85550 5291488 Click to see 448.40 unknown https://doi.org/10.1080/10286020.2010.489826
Quercetin 3,7-diglucoside 10121947 Click to see 626.50 unknown https://doi.org/10.1080/10286020.2010.489826
Quercimeritrin 5282160 Click to see 464.40 unknown https://doi.org/10.1080/10286020.2010.489826
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-8-[(2S,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 46928317 Click to see 596.50 unknown https://doi.org/10.1080/10286020.2010.489826
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-8-(3,4,5-trihydroxyoxan-2-yl)oxychromen-4-one 56674846 Click to see 596.50 unknown https://doi.org/10.1080/10286020.2010.489826
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 6420079 Click to see 448.40 unknown https://doi.org/10.1080/10286020.2010.489826
5,7-Dihydroxy-2-(4-hydroxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 6169038 Click to see 448.40 unknown https://doi.org/10.1080/10286020.2010.489826
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
bis[[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl] (1S,2S,3S,4S)-3,4-bis(4-hydroxyphenyl)cyclobutane-1,2-dicarboxylate 162873236 Click to see 1189.00 unknown https://doi.org/10.1080/10286020.2010.489826
Bis[[6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl] 3,4-bis(4-hydroxyphenyl)cyclobutane-1,2-dicarboxylate 162873235 Click to see 1189.00 unknown https://doi.org/10.1080/10286020.2010.489826

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