Salix caprea - Unknown
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Internal ID UUID6440369fb6614609494629
Scientific name Salix caprea
Authority L.
First published in Sp. Pl. : 1020 (1753)

Description Top

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Salix caprea, commonly known as goat willow, pussy willow, or great sallow, is a deciduous shrub or small tree native to Europe and western and central Asia. It grows to a height of 8-10 meters, rarely to 13 meters, and has leaves that are 3-12 cm long and 2-8 cm wide. It produces soft silky, silvery 3-7 cm long catkins in early spring before the new leaves appear. The male and female catkins are on different plants (dioecious). The fruit is a small capsule 5-10 mm long containing numerous minute seeds embedded in fine, cottony hairs. It is used as a browse for goats, and its leaves are used as a food resource by several species of Lepidoptera. It is also commonly eaten by browsing mammals. It is cultivated for garden use, and its bark is used to extract tannin and salicin. In Scandinavia, it is used to make willow flutes, and in Germany, Hungary, north of Slovakia, Poland and Ukraine, the just-opened catkins are used like the olive branches on Palm Sunday.

Synonyms Top

Scientific name Authority First published in
Nectopix caprea (L.) Raf. Alsogr. Amer. : 14 (1838)
Salix grandifolia Ser. Saules Suisse 6: no. 55. 1809
Salix lanata Vill. Hist. Pl. Dauphiné 3: 777 (1789)
Salix hultenii Flod. Ark. Bot. 20A(6): 51 (1926)
Salix ishidoyana Nakai Bot. Mag. (Tokyo) 31: 25 (1917)
Salix aurigerana Lapeyr. Hist. Pl. Pyrénées : 598 (1813)
Salix bakko Kimura Bot. Mag. (Tokyo) 42: 568 (1928)
Salix coaetanea Flod. Bot. Not. 1930: 331 (1930)
Salix caprea f. subglabra (Chang & Skvortzov) Kitag. Neolin. Fl. Manshur. 204. 1979
Salix ulmifolia Thuill. Fl. Env. Paris, ed. 2. 518. 1799 [24 Jun 1799]
Salix tomentosa Ser. Essai Saules Suisse 14. 1815 [Oct 1815]
Salix sphacelata Sm. Fl. Brit. 3: 1066 (1804)
Salix proteifolia J.Forbes Salict. Woburn. : 149 (1829)
Salix hallisanensis H.Lév. Repert. Spec. Nov. Regni Veg. 10: 435 (1912)
Salix raddeana var. subglabra Y.L.Chang & Skvortsov Ill. Man. Woody Pl. N.-E. Prov. 558 1955
Capraea vulgaris Opiz Seznam : 25 (1852)
Salix caprea subsp. hultenii Kom. Fl. Kamtschatka 2: 11 1929
Salix hultenii var. angustifolia Kimura J. Fac. Agr. Hokkaido Imp. Univ. Sapporo 26: 415 1934
Salix hultenii f. angustifolia (Kimura) Kimura Sci. Rep. Tohoku Imp. Univ., Ser. 4, Biol. 1962
Salix caprea f. elongata (Nakai) Kitag. Neolin. Fl. Manshur. : 204 (1979)
Salix hallisanensis f. elongata Nakai Fl. Sylv. Kor. 18: 135, t. 27 1930
Salix caprea var. lanatifolia Björnstr. Glasn. Zemaljsk. Muz. Bosne Hercegovine Sarajevu Prir. Nauke : 34 (1856)
Salix tomentosa var. androgyna Ser. Essai Saules Suisse : 16 (1815)
Salix tomentosa var. ternata Ser. Essai Saules Suisse : 16 (1815)
Salix tomentosa var. tenuifolia Ser. Essai Saules Suisse : 17 (1815)
Salix tomentosa var. rotundifolia Ser. Essai Saules Suisse : 17 (1815)
Salix tomentosa var. macrophylla Ser. Essai Saules Suisse : 17 (1815)
Salix caprea var. pendula T.Lang Gard. Chron. 1853: 85 (1853)

Common names Top

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Language Common/alternative name
English goat willow
English pussy willow
English great sallow
Spanish salix hultenii
Spanish zargatillo cabruno
Spanish sauce menor
Spanish sauce de cabras
Spanish sargatillo,
Spanish salix coaetanea
Spanish salix bakko
Spanish saliquera
Spanish salce pomal
Spanish sauce cabruno
Spanish salce cabruno
Arabic صفصاف المعز
Azerbaijani keçi söyüdü
Azerbaijani kolvari söyüd
azb کئچی سؤیودو
Belarusian Брэднік
Belarusian Вярба казіная
Bulgarian ива
Catalan gatsaule
Czech vrba jíva
Czech jíva
Welsh helygen ddeilgron
Danish seljepil
Danish selje-pil
German sal-weide
German palm-weide
German palmkätzchen
German saalweide
German salweide
Esperanto kapra saliko
Estonian raagremmelgas
Basque ahuntz-sahats
Persian بزبید
Finnish raita
Finnish metsäraita
French saule marsault
frr wilag
Irish sailchearnach
Galician salgueiro cabuxo
Hebrew ערבה קאפריאה
Croatian vrba iva
Upper Sorbian wšědna wjerba
Upper Sorbian jiwa
Hungarian kecskefűz
Armenian Այծուռենի
Armenian այծուռենի
Icelandic selja
Italian salice delle capre
Italian salcio di montagna
Italian salicone
Japanese バッコヤナギ
Georgian მდგნალი
Korean 호랑버들
Cornish helyk
Lithuanian blindė
Lithuanian paprastoji blindė
Latvian kazu vītols
Latvian blīgzna
Latvian pūpolvītols
Macedonian горска ива
Macedonian дива врба
Norwegian Bokmål silkeselje
Norwegian Bokmål selje
Dutch boswilg
Dutch waterwilg
Norwegian Nynorsk seljetre
Norwegian Nynorsk selje
Norwegian Nynorsk silju
os Талахæрис
Polish wierzba iwa
Portuguese salgueiro
Romanian salcie căprească
Romanian iovă
Russian козья ива
Russian бредина
Russian salix coaetanea
Russian Ива козья
Russian ива козья
Samogitian blindės
Slovak vŕba rakytová
Slovenian iva
smn räiđi
Swedish sälg
Swedish videung
Turkish keçi söğüdü
udm Кеч бадь
udm Бредина
Ukrainian верба козяча
Ukrainian Верба козяча
Walloon så mozale
Chinese 黃花柳
Chinese 黄花柳

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000929313
UNII R0G312197U
Cornell Woody Plants 229
Canadensys 9089
USDA Plants SACA22
UConn 445
Tropicos 28300146
INPN 119977
Flora of Italy 211
KEW urn:lsid:ipni.org:names:303599-2
The Plant List kew-5001859
Missouri Botanical Garden 286792
Open Tree Of Life 218600
Observations.org 7391
NCBI Taxonomy 172267
NBN Atlas NBNSYS0000003868
Nature Serve 2.133840
IUCN Red List 19620273
IPNI 777256-1
iNaturalist 55846
GBIF 5372952
Freebase /m/030h81
EPPO SAXCP
EOL 584270
Elurikkus 7006
USDA GRIN 32695
Wikipedia Salix_caprea

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
Vertebrate Pollination of Angiosperms in the Mediterranean Area: A Review Valdés B Plants (Basel) 20-Mar-2024
PMCID:PMC10976121
doi:10.3390/plants13060895
PMID:38592907
Bottom‐up rather than top‐down mechanisms determine mesocarnivore interactions in Norway Cano‐Martínez R, Thorsen NH, Hofmeester TR, Odden J, Linnell J, Devineau O, Angoh SY, Odden M Ecol Evol 07-Mar-2024
PMCID:PMC10920318
doi:10.1002/ece3.11064
PMID:38463636
The genus Fomitopsis (Polyporales, Basidiomycota) reconsidered Spirin V, Runnel K, Vlasák J, Viner I, Barrett MD, Ryvarden L, Bernicchia A, Rivoire B, Ainsworth AM, Grebenc T, Cartabia M, Niemelä T, Larsson KH, Miettinen O Stud Mycol 22-Feb-2024
PMCID:PMC11003443
doi:10.3114/sim.2024.107.03
PMID:38600960
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Traditional Knowledge Evolution over Half of a Century: Local Herbal Resources and Their Changes in the Upper Susa Valley of Northwest Italy Sulaiman N, Zocchi DM, Borrello MT, Mattalia G, Antoniazzi L, Berlinghof SE, Bewick A, Häfliger I, Schembs M, Torri L, Pieroni A Plants (Basel) 22-Dec-2023
PMCID:PMC10780445
doi:10.3390/plants13010043
PMID:38202351
Biodiversity of Fungi in Freshwater Ecosystems of Italy Mirabile G, Ferraro V, Mancuso FP, Pecoraro L, Cirlincione F J Fungi (Basel) 07-Oct-2023
PMCID:PMC10607542
doi:10.3390/jof9100993
PMID:37888249
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
Bridging the gap: how to adopt opportunistic plant observations for phenology monitoring Katal N, Rzanny M, Mäder P, Römermann C, Wittich HC, Boho D, Musavi T, Wäldchen J Front Plant Sci 04-Oct-2023
PMCID:PMC10582721
doi:10.3389/fpls.2023.1150956
PMID:37860262
Rust Fungi on Medicinal Plants in Guizhou Province with Descriptions of Three New Species Wu Q, He M, Liu T, Hu H, Liu L, Zhao P, Li Q J Fungi (Basel) 21-Sep-2023
PMCID:PMC10532644
doi:10.3390/jof9090953
PMID:37755061
LiDAR GEDI derived tree canopy height heterogeneity reveals patterns of biodiversity in forest ecosystems Torresani M, Rocchini D, Alberti A, Moudrý V, Heym M, Thouverai E, Kacic P, Tomelleri E Ecol Inform 01-Sep-2023
PMCID:PMC10316066
doi:10.1016/j.ecoinf.2023.102082
PMID:37662896
Phenolic Compounds of the Medicinal Plants in an Anthropogenically Transformed Environment Vinogradova N, Vinogradova E, Chaplygin V, Mandzhieva S, Kumar P, Rajput VD, Minkina T, Seth CS, Burachevskaya M, Lysenko D, Singh RK Molecules 29-Aug-2023
PMCID:PMC10488847
doi:10.3390/molecules28176322
PMID:37687151
Physiological response mechanism of heavy metal‐resistant endophytic fungi isolated from the roots of Polygonatum kingianum Cao G, Li X, Zhang C, Xiong Y, Li X, Li T, He S, Cui Z, Yu J Environ Microbiol Rep 21-Aug-2023
PMCID:PMC10667662
doi:10.1111/1758-2229.13194
PMID:37604512
Commodity risk assessment of Fagus sylvatica plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 28-Jul-2023
PMCID:PMC10375364
doi:10.2903/j.efsa.2023.8118
PMID:37522095
Current Review of Increasing Animal Health Threat of Per- and Polyfluoroalkyl Substances (PFAS): Harms, Limitations, and Alternatives to Manage Their Toxicity Peritore AF, Gugliandolo E, Cuzzocrea S, Crupi R, Britti D Int J Mol Sci 20-Jul-2023
PMCID:PMC10380748
doi:10.3390/ijms241411707
PMID:37511474
Biological Activity and Structural Diversity of Steroids Containing Aromatic Rings, Phosphate Groups, or Halogen Atoms Dembitsky VM Molecules 20-Jul-2023
PMCID:PMC10384810
doi:10.3390/molecules28145549
PMID:37513423

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 / Anthracenes / Anthraquinones
Fragilin 15559331 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C(=C(C=C3C2=O)OC)Cl)O 318.71 unknown https://doi.org/10.1016/0031-9422(86)88020-7
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Salicyl alcohol 5146 Click to see C1=CC=C(C(=C1)CO)O 124.14 unknown https://doi.org/10.1007/BF00605218
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
2'-Hydroxyaucuparin 46879744 Click to see COC1=CC(=CC(=C1O)OC)C2=CC=CC=C2O 246.26 unknown https://doi.org/10.1515/ZNB-1985-0629
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Sachaliside 14048613 Click to see C1=CC(=CC=C1C=CCOC2C(C(C(C(O2)CO)O)O)O)O 312.31 unknown https://doi.org/10.1016/S0031-9422(00)85563-6
Vimalin 14048616 Click to see COC1=CC=C(C=C1)C=CCOC2C(C(C(C(O2)CO)O)O)O 326.34 unknown https://doi.org/10.1016/S0021-9673(01)81312-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[2-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl 1-hydroxy-6-oxocyclohex-2-ene-1-carboxylate 133554354 Click to see C1CC(=O)C(C=C1)(C(=O)OCC2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)O)O 424.40 unknown https://doi.org/10.1016/S0031-9422(00)85563-6
2-(4-Hydroxyphenoxy)-6-[3-(4-hydroxyphenyl)prop-2-enoxymethyl]oxane-3,4,5-triol 162890773 Click to see C1=CC(=CC=C1C=CCOCC2C(C(C(C(O2)OC3=CC=C(C=C3)O)O)O)O)O 404.40 unknown https://doi.org/10.1016/S0031-9422(00)85563-6
https://doi.org/10.1016/S0031-9422(00)88609-4
Picein 92123 Click to see CC(=O)C1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 298.29 unknown https://doi.org/10.1016/0031-9422(86)88020-7
Salicin 439503 Click to see C1=CC=C(C(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown https://doi.org/10.1007/BF00605218
https://doi.org/10.1016/S0021-9673(01)81312-1
https://doi.org/10.1016/S0031-9422(00)88609-4
Salicortin 115158 Click to see C1CC(=O)C(C=C1)(C(=O)OCC2=CC=CC=C2OC3C(C(C(C(O3)CO)O)O)O)O 424.40 unknown https://doi.org/10.1016/S0031-9422(00)85563-6
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Procyanidin B3 146798 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1021/JF981380Z
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
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/10.1021/JF981380Z
https://doi.org/10.1021/NP50040A007
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/NP50040A007
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/NP50040A007
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1021/NP50040A007
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1021/NP50040A007
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1021/NP50040A007
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF00605218
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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 https://doi.org/10.1007/BF00605218
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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/10.1007/S10600-010-9747-6
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/S10600-010-9747-6
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/S10600-010-9747-6
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/10.1007/S10600-010-9747-6
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/10.1007/BF00605218
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,5-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 12302035 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1007/S10600-010-9747-6
4',5-Dihydroxy-7-glucosyloxyflavanone 124300887 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1021/NP50040A007
Isorhamnetin 7-glucoside 6455477 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1007/S10600-010-9747-6
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/10.1007/BF00563763
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/10.1007/BF00605218
https://doi.org/10.1007/BF00563763
Prunin 92794 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1021/NP50040A007
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/10.1007/BF00579442
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/10.1007/BF00579442
https://doi.org/10.1007/S10600-010-9747-6
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/10.1007/BF00579442
https://doi.org/10.1007/S10600-010-9747-6
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
3,3',4',5,5',7-Hexahydroxyflavylium 128853 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O 303.24 unknown https://doi.org/10.1016/S0031-9422(00)88609-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Flavanone, 3,5,7-trihydroxy-4'-methoxy- 586387 Click to see COC1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1021/NP50040A007

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