Potentilla anserina - Unknown
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Details Top

Internal ID UUID6440406f422b2272360227
Scientific name Potentilla anserina
Authority L.
First published in Sp. Pl. : 495 (1753)

Description Top

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Argentina anserina, also known as silverweed or silver cinquefoil, is a perennial flowering plant found in temperate regions of the Northern Hemisphere. It is a low-growing herbaceous plant with silvery leaves and yellow flowers. The plant was originally classified in the genus Potentilla, but was later reclassified into the genus Argentina. It is often found in sandy or gravelly soils and has been used for various purposes, such as absorbing sweat and as a food crop. The plant has a rich folklore and has been associated with legends and religious beliefs. Fossil records show that the plant has been present since the Pliocene era.

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
Argentina vulgaris Lam. Fl. Franç. 3: 119 (1779)
Potentilla anserina var. discolor Wallr. Schedulae criticae ; 1822 236 1822
Potentilla pratincola B.Boivin Canad. Field-Naturalist 65: 21 (1951)
Potentilla argentina Huds. Fl. Angl. : 195 (1762)
Potentilla pulchra Salisb. Prodr. Stirp. Chap. Allerton : 362 (1796)
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
Potentilla geminiflora Zimmeter ; 1884 6 1884
Potentilla anserina var. concolor Ser. Schedulae criticae ; 1822 236 1822
Potentilla anserina subsp. anserina L. Synopsis der Mitteleuropaischen Flora 6 1905

Common names Top

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Language Common/alternative name
English silverweed
Spanish anserina
Spanish argentina vulgaris
Spanish dactylophyllum anserina
Spanish dasiphora anserina
Spanish fragaria anserina
Spanish potentilla anserina subsp anserina
Spanish potentilla anserina subsp. anserina
Spanish potentilla argentina
Spanish potentilla pulchra
Spanish tormentilla anserina
Spanish argentina anserina
Arabic حشيشة الإوزة
Arabic عشبة القوى الإوزية
Arabic فضية إوزية
Azerbaijani qaz qaytarması
Azerbaijani Ördək qaytarması
azb قاز قایتارماسی
ba Ҡаҙ үләне
Belarusian Дуброўка гусіная
Bulgarian гъши очиболец
Catalan potentola
ceb argentina anserina
Czech mochna husí
Czech nátržník husí
Welsh dail arian
Welsh tansi wyllt
Danish gåse-potentil
Danish gåsepotentil
German gänse-fingerkraut
German gänsefingerkraut
German gänserich
German gänsewiß
German grensel
German krampfkraut
German säulkraut
German silberkraut
Estonian hanijalg
Basque argentina anserina
Persian آنسرینای آرژانتینی
Finnish ketohanhikki
Finnish argentina anserina
French potentille ansérine
French potentille des oies
French potentille anserine
Manx bossan argid
Croatian guščarski petoprst
Upper Sorbian husacy porstnik
Upper Sorbian rěbliki
Hungarian libapimpó
Hungarian rucafarok
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
mn Галуун гичгэнэ
Norwegian Bokmål gåsemure
Norwegian Bokmål argentina anserina
Dutch zilverschoon
Norwegian Nynorsk gåsemure
Norwegian Nynorsk argentina anserina
nv tʼąąʼdoolghasí
os Хъазы къах
pcd Àrjintine
pcd blanbò
pcd crassépoulhe
pcd fuëles`d àrjint
pcd iérpe à-qhu
pcd pate`d-ò
pcd peuplié
Polish pięciornik gęsi
Romanian coada racului
Russian Лапчатка гусиная
Russian гусиная лапка
Russian лапчатка гусиная
Yakutian Хаас кэйиҥэтэ
Slovak nátržník husí
Swedish gåsört
Swedish argentina anserina
Swedish silverört
tt Каз тәпие
Ukrainian Перстач гусячий
Ukrainian гусяча лапка
Ukrainian гусячі лапки
Ukrainian перстач гусячий
war argentina anserina
Chinese 人参果
Chinese 浮尸草
Chinese 蕨麻
Chinese 蕨麻(鹅绒萎陵菜)
Chinese 蕨麻草
Chinese 鹅绒委陵菜
Chinese 延寿草
Chinese 莲花菜
Chinese 蕨麻委陵菜

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Potentilla anserina subsp. groenlandica Tratt. Rosac. Monogr. 4: 13 (1824)

Varieties (abbr. var.) Top

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Name Authority First published in
Potentilla anserina var. lanata (B.Boivin) B.Boivin Naturaliste Canad. 93: 435. 1966

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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Name Authority First published in
Potentilla anserina f. sericea (Hayne) Hayek & Fernald Rhodora 35: 273 (1933)

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-0001016615
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

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 36.0x 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
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
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
Effective population size mediates the impact of pollination services on pollen limitation Cisternas-Fuentes A, Koski MH Proc Biol Sci 10-Jan-2024
PMCID:PMC10777167
doi:10.1098/rspb.2023.1519
PMID:38196350
Optimization of Three Extraction Methods and Their Effect on the Structure and Antioxidant Activity of Polysaccharides in Dendrobium huoshanense Zhu H, Yi X, Jia SS, Liu CY, Han ZW, Han BX, Jiang GC, Ding ZF, Wang RL, Lv GP Molecules 08-Dec-2023
PMCID:PMC10745764
doi:10.3390/molecules28248019
PMID:38138509
The CsMYB123 and CsbHLH111 are involved in drought stress-induced anthocyanin biosynthesis in Chaenomeles speciosa Ren Y, Zhang S, Zhao Q, Wu Y, Li H Mol Hortic 22-Nov-2023
PMCID:PMC10664276
doi:10.1186/s43897-023-00071-2
PMID:37990285
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Effects of rainfall amount and frequencies on soil net nitrogen mineralization in Gahai wet meadow in the Qinghai-Tibetan Plateau Xu G, Li G, Wu J, Ma W, Wang H, Yuan J, Li X Sci Rep 08-Sep-2023
PMCID:PMC10491659
doi:10.1038/s41598-023-39267-3
PMID:37684356
Searching for Natural Plants with Antimelanogenesis and Antityrosinase Properties for Cosmeceutical or Nutricosmetics Applications: A Systematic Review Tung XY, Yip JQ, Gew LT ACS Omega 06-Sep-2023
PMCID:PMC10515176
doi:10.1021/acsomega.3c02994
PMID:37744793
Mass Spectrometric Fingerprint Mapping Reveals Species-Specific Differences in Plant Polyphenols and Related Bioactivities Vanhakylä S, Salminen JP Molecules 31-Aug-2023
PMCID:PMC10490256
doi:10.3390/molecules28176388
PMID:37687216
Optimum Reaction Conditions for the Synthesis of Selenized Ornithogalum caudatum Ait. (Liliaceae) Polysaccharides and Measurement of Their Antioxidant Activity In Vivo Sun R, Qu Z, Ji C, Yang X, Zhang Y, Zou X Molecules 07-Aug-2023
PMCID:PMC10420663
doi:10.3390/molecules28155929
PMID:37570899
Ecosystem multifunctionality and soil microbial communities in response to ecological restoration in an alpine degraded grassland Shu X, Liu W, Hu Y, Xia L, Fan K, Zhang Y, Zhang Y, Zhou W Front Plant Sci 01-Aug-2023
PMCID:PMC10431941
doi:10.3389/fpls.2023.1173962
PMID:37593047

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-tetrahydrobenzofuran-2(4H)-one 14334 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 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 CC1=CC(=O)CC(O1)(C)CC(=O)O 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 CC1=CC(=O)CC(O1)(C)CC(=O)O 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 COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1007/BF00629945
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1055/S-2006-958146
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1055/S-2006-958146
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Gallocatechin 65084 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1055/S-2006-958146
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[(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 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-[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 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 https://doi.org/10.1080/10286020.2010.489826
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 https://doi.org/10.1080/10286020.2010.489826
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
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
Vicenin-2 3084407 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 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/10.1055/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 C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 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 COC(=O)C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 492.40 unknown https://doi.org/10.1055/S-2006-958146
Myricetin 3-O-glucuronide 5487413 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 494.40 unknown https://doi.org/10.1055/S-2006-958146
Quercetin 3-glucuronide 12004528 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/10.1055/S-2006-958146
https://doi.org/10.1080/10286020.2010.489826
QUERCETIN 3-O-beta-D-GLUCURONIDE METHYL ESTER 21722016 Click to see COC(=O)C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 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 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
> 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 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
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2006-958146
https://doi.org/10.1080/10286020.2010.489826
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 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 https://doi.org/10.1055/S-2006-958146
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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 https://doi.org/10.1055/S-2006-958146
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
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 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 https://doi.org/10.1055/S-2006-958146
Isoquercitrin 5484006 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
Myricetin 3-rhamnoside 5352000 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1055/S-2006-958146
Myricitrin 5281673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O 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/10.1055/S-2006-958146
https://doi.org/10.1080/10286020.2010.489826
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2006-958146
https://doi.org/10.1080/10286020.2010.489826
Reynoutrin 5878729 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
Rutin 5280805 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)O)O 610.50 unknown https://doi.org/10.1080/10286020.2010.489826
Vitamin P 5293655 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)O)O 610.50 unknown https://doi.org/10.1080/10286020.2010.489826
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
acs.jmedchem.1c00409_ST.719 13345442 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1080/10286020.2010.489826
Luteolin 7-galactoside 5291488 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
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
Quercetin 3,7-diglucoside 10121947 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1080/10286020.2010.489826
Quercetin 7-O-glucoside 5381351 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1080/10286020.2010.489826
Quercimeritrin 5282160 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1080/10286020.2010.489826
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
4',5,7-Trihydroxy-8-(beta-D-glucopyranosyloxy)flavone 6420079 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)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-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 C1C(C(C(C(O1)OC2=C3C(=C(C(=C2O)OC4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 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 C1C(C(C(C(O1)OC2=C3C(=C(C(=C2O)OC4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O 596.50 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 C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O 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 C1=CC(=CC=C1C2C(C(C2C(=O)OCC3C(C(C(C(O3)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O)O)O)C(=O)OCC7C(C(C(C(O7)OC8=C(OC9=CC(=CC(=C9C8=O)O)O)C1=CC=C(C=C1)O)O)O)O)C1=CC=C(C=C1)O)O 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 C1=CC(=CC=C1C2C(C(C2C(=O)OCC3C(C(C(C(O3)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O)O)O)C(=O)OCC7C(C(C(C(O7)OC8=C(OC9=CC(=CC(=C9C8=O)O)O)C1=CC=C(C=C1)O)O)O)O)C1=CC=C(C=C1)O)O 1189.00 unknown https://doi.org/10.1080/10286020.2010.489826

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