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Salix alba

Salix alba - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Salix alba - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Salix alba - 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 UUID6440369a507fc831555504
Scientific name Salix alba
Authority L.
First published in Sp. Pl. : 1021 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Salix caerulea Sm. Engl. Bot. 34: t. 2431 (1812)
Salix pameachiana Barratt Salices Amer. : 16 (1840)
Salix pallida Salisb. Prodr. Stirp. Chap. Allerton 394. 1796 [Nov-Dec 1796]
Salix regalis hort. ex Wesm. Bull. Congr. Bot. Bruxelles : 280 (1864)
Argorips alba (L.) Raf. Alsogr. Amer. : 13 (1838)
Argorips cerulea (Sm.) Raf. Alsogr. Amer. : 13 (1838)
Salix alba f. ovalis Wimm. Salic. Eur. : 18 (1866)
Salix alba subsp. caerulea (Sm.) Rech.f. Oesterr. Bot. Z. 110: 338 (1963)
Salix alba var. denudata Wimm. & Grab. Fl. Siles. 2(2): 361 (1829)

Common names Top

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Language Common/alternative name
English golden willow
English white willow
Spanish sauce blanco
Spanish arcazon
Spanish arcazón
Spanish azaoz
Spanish balaquera
Spanish blina
Spanish salguero blanco
Spanish salzo
Spanish sandisa
Spanish sarache
Spanish sauce blanco salado
Spanish sauce real
Spanish sauce relucinete
Spanish sauce triste
Arabic الصفصاف الأبيض
Arabic صفصاف أبيض
Arabic صفصاف
Arabic خلاف
Arabic اسبيدار
Azerbaijani ağ söyüd
azb آغ سؤیود
Belarusian Вярба
Belarusian Белалоз
Belarusian Вярба звычайная
Belarusian Вятла
Belarusian Вярба белая
Bulgarian Бяла върба
Bulgarian бяла върба
Catalan salze blanc
Catalan saulic
Catalan saule
Catalan saule blanc
Catalan vimera
Catalan vimetera groga o belga
Czech vrba bílá
cv Йăмра
Welsh helyg gwyn
Welsh helyg gwynion
Welsh helyg wen
Welsh helygen wen
Danish hvid-pil
Danish hvidpil
German silberweide
German silber-weide
German gelbe weide
German saule blanc
Greek Ιτέα η λευκή
Estonian hõberemmelgas
Estonian hõbepaju
Basque sahats zuri
Basque zume zuri
Persian بید سفید
Finnish valkopaju
Finnish valkosalava
French saule blanc
Irish saileach bhán
Galician salgueiro branco
Gujarati ઇંગ્લીશ વીલો
Hebrew ערבה לבנה
Hindi इंग्लिश विलो
Croatian bijela vrba
Upper Sorbian běła wjerba
Hungarian fehér fűz
Armenian Ուռենի սպիտակ
Indonesian dedalu putih
Italian salice bianco
Italian salice da pertiche
Japanese セイヨウシロヤナギ
Georgian წნორი
Kabyle tafsent
Kannada ಇಂಗ್ಲೀಷ್ ವಿಲೋ
Korean 흰버드나무
Cornish helyk gwynn
Lithuanian baltasis gluosnis
Lithuanian saule blanc
Latvian baltais vītols
mdf Акша каль
Macedonian бела врба
Malayalam വില്ലോമരം
myv Ашо каль
Norwegian Bokmål hvitpil
Norwegian Bokmål hengepil
Norwegian Bokmål kvitpil
Dutch schietwilg
Dutch witte wilg
os Урс хæрис
Polish wierzba biała
Portuguese salgueiro-branco
Portuguese salgueiro branco
Romansh salesch alv
Romanian salcie albă
Russian Ива белая
Russian ветла
Russian ива серебристая
Russian ива белая
Samogitian baltglousnis
Slovak vŕba biela
Slovenian bela vrba
Albanian shelgu i bardhë
Serbian Бела врба
Swedish vitpil
Swedish guldpil
Swedish gulpil
Swedish saule blanc
Swedish silverpil
Swedish vanlig vitpil
Telugu ఇంగ్లీష్ విల్లో
Turkish ak söğüt
tt Өянке
tyv Ак-тал
udm Тӧдьы бадь
Ukrainian Верба біла
Ukrainian верба біла
vec salež da manech
vep vauged raid
Chinese 白柳

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Salix alba subsp. micans (Andersson) Rech.f. Oesterr. Bot. Z. 110: 338 (1963)

Varieties (abbr. var.) Top

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Name Authority First published in
Salix alba var. caerulea (Sm.) W.D.J.Koch Syn. Fl. Germ. Helv. 644. 1837 [1-7 Oct 1837]

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Arabian Peninsula
      • Yemen
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • Inner Mongolia
      • Qinghai
      • Tibet
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Siberia
      • Altay
      • Krasnoyarsk
      • West Siberia
    • Western Asia
      • Afghanistan
      • Cyprus
      • East Aegean Islands
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Australasia
    • Australia
      • New South Wales
      • South Australia
      • Tasmania
      • Victoria
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Romania
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Ontario
      • Québec
    • North-central U.S.A.
      • Illinois
      • Minnesota
      • Missouri
      • Nebraska
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Northwestern U.S.A.
      • Colorado
      • Idaho
      • Montana
    • Southeastern U.S.A.
      • Arkansas
      • Delaware
      • District Of Columbia
      • Georgia
      • Kentucky
      • Maryland
      • North Carolina
      • Tennessee
      • Virginia
    • Southwestern U.S.A.
      • Arizona
      • California
      • Nevada
    • Western Canada
      • Saskatchewan
  • Southern America
    • Southern South America
      • Argentina Northwest
      • Chile Central

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000929085
UNII V8UV0R324S
Flora of Alabama 5474
Canadensys 9066
USDA Plants SAAL2
UConn 443
Tropicos 28300135
INPN 119915
Flora of Italy 186
KEW urn:lsid:ipni.org:names:776974-1
The Plant List kew-5001521
Plantarium 32959
Missouri Botanical Garden 286791
PFAF Salix alba
Open Tree Of Life 164209
Observations.org 7389
NCBI Taxonomy 75704
NBN Atlas NBNSYS0000003859
Nature Serve 2.152740
IUCN Red List 203465
IPNI 776974-1
iNaturalist 54841
GBIF 5372513
Freebase /m/02zfch
WisFlora 4941
EPPO SAXAL
Elurikkus 6999
Calflora (Californian flora) 7260
US Library of Congress sh85116812
USDA GRIN 32674
Wikipedia Salix_alba
CMAUP NPO3277

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
Effects on keratinocytes of the traditional combination of herb extract (Royal Oji Complex) implicated the improvement of young children's skin moisture and barrier Trinh TT, Choi JH, Yang J, Kim WH, Chien PN, Le LT, Ngan‐Giang N, Nga PT, Nam S, Heo C Skin Res Technol 14-Apr-2024
PMCID:PMC11016816
doi:10.1111/srt.13682
PMID:38616504
Exogenous application of salicylic acid ameliorates salinity stress in barley (Hordeum vulgare L.) Hanif S, Mahmood A, Javed T, Bibi S, Zia MA, Asghar S, Naeem Z, Ercisli S, Rahimi M, Ali B BMC Plant Biol 11-Apr-2024
PMCID:PMC11008038
doi:10.1186/s12870-024-04968-y
PMID:38605311
The influence of tree genus, phylogeny, and richness on the specificity, rarity, and diversity of ectomycorrhizal fungi Tedersoo L, Drenkhan R, Abarenkov K, Anslan S, Bahram M, Bitenieks K, Buegger F, Gohar D, Hagh‐Doust N, Klavina D, Makovskis K, Zusevica A, Pritsch K, Padari A, Põlme S, Rahimlou S, Rungis D, Mikryukov V Environ Microbiol Rep 04-Apr-2024
PMCID:PMC10994715
doi:10.1111/1758-2229.13253
PMID:38575147
Apple crown and collar canker and necrosis caused by Cytospora balanejica sp. nov. in Iran Azizi R, Ghosta Y, Ahmadpour A Sci Rep 19-Mar-2024
PMCID:PMC10951349
doi:10.1038/s41598-024-57235-3
PMID:38504125
Green solution to riparian pollution: Populus alba L. potential for phytoremediation and bioindication of PTEs along the Sava river Miletić Z, Jonjev M, Jarić S, Kostić O, Sekulić D, Mitrović M, Pavlović P Heliyon 18-Mar-2024
PMCID:PMC10981065
doi:10.1016/j.heliyon.2024.e28183
PMID:38560157
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
Plant-Based Films and Hydrogels for Wound Healing Lopes AI, Pintado MM, Tavaria FK Microorganisms 21-Feb-2024
PMCID:PMC10972459
doi:10.3390/microorganisms12030438
PMID:38543489
Morphology and Phylogeny Reveal Three New Species of Cytospora Associated with Tree Cankers in China Wang S, Jiang N, Ma R J Fungi (Basel) 09-Feb-2024
PMCID:PMC10890096
doi:10.3390/jof10020139
PMID:38392811
Quantitative distribution of flavan-3-ols, procyanidins, flavonols, flavanone and salicylic acid in five varieties of organic winter dormant Salix spp. by LC-MS/MS Curtasu MV, Nørskov NP Heliyon 01-Feb-2024
PMCID:PMC10850552
doi:10.1016/j.heliyon.2024.e25129
PMID:38333780
Influence of meteorological and ambient air quality factors on Artemisia pollen counts in Urumqi, Northwest China Jiapaer K, Halik Ü, Keyimu M, Bilal I, Shi L, Mumin R Heliyon 26-Jan-2024
PMCID:PMC10847607
doi:10.1016/j.heliyon.2024.e25124
PMID:38327407
Comparative Analysis of a Secondary Metabolite Profile from Roots and Leaves of Iostephane heterophylla by UPLC-MS and GC-MS Navarrete-Carriola DV, Paz-González AD, Vázquez-Jiménez LK, De Luna-Santillana E, Cruz-Hernández MA, Bandyopadhyay D, Rivera G ACS Omega 25-Jan-2024
PMCID:PMC10851369
doi:10.1021/acsomega.3c06800
PMID:38343925
Ethnobotanical and ethnomedicinal research into medicinal plants in the Mt Stara Planina region (south-eastern Serbia, Western Balkans) Jarić S, Kostić O, Miletić Z, Marković M, Sekulić D, Mitrović M, Pavlović P J Ethnobiol Ethnomed 10-Jan-2024
PMCID:PMC10782642
doi:10.1186/s13002-024-00647-2
PMID:38200599
Psyllids in Natural Habitats as Alternative Resources for Key Natural Enemies of the Pear Psyllids (Hemiptera: Psylloidea) Horton DR Insects 06-Jan-2024
PMCID:PMC10816694
doi:10.3390/insects15010037
PMID:38249044
Unveiling the Dual Nature of Heavy Metals: Stressors and Promoters of Phenolic Compound Biosynthesis in Basilicum polystachyon (L.) Moench In Vitro Das S, Sultana KW, Mondal M, Chandra I, Ndhlala AR Plants (Basel) 28-Dec-2023
PMCID:PMC10780674
doi:10.3390/plants13010098
PMID:38202406
PhytoPipe: a phytosanitary pipeline for plant pathogen detection and diagnosis using RNA-seq data Hu X, Hurtado-Gonzales OP, Adhikari BN, French-Monar RD, Malapi M, Foster JA, McFarland CD BMC Bioinformatics 13-Dec-2023
PMCID:PMC10717670
doi:10.1186/s12859-023-05589-2
PMID:38093207

Phytochemical Profile Top

Add a new one!
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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> 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/10.1093/JAOAC/81.4.757
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown via CMAUP database
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
9,9'-Di-O-(E)-feruloylsecoisolariciresinol 10439806 Click to see COC1=C(C=CC(=C1)CC(COC(=O)C=CC2=CC(=C(C=C2)O)OC)C(CC3=CC(=C(C=C3)O)OC)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O 714.80 unknown via CMAUP database
Di-(Z)-feruloylsecoisolariciresinol 24898244 Click to see COC1=C(C=CC(=C1)CC(COC(=O)C=CC2=CC(=C(C=C2)O)OC)C(CC3=CC(=C(C=C3)O)OC)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O 714.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Eicosanoids / Prostaglandins and related compounds
Methyl 15-hydroxy-9-oxoprosta-5,10,13-trien-1-oate 53393996 Click to see CCCCCC(C=CC1C=CC(=O)C1CC=CCCCC(=O)OC)O 348.50 unknown https://doi.org/10.1016/S0008-6215(00)83977-4
> 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/10.1007/BF00564031
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
triptogelin C-1 10459206 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)C)OC(=O)C)OC(=O)C 516.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
11alpha-Methoxyurs-12-ene-3beta,16beta-diol 44235666 Click to see CC1CCC2(C(CC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)C)O)C)C)OC)C2C1C)C)O)C 472.70 unknown via CMAUP database
12,23-Dihydroxy-11alpha-methoxyurs-12-ene-3-one 44235900 Click to see CC1CCC2(CCC3(C(=C(C(C4C3(CCC5C4(CCC(=O)C5(C)CO)C)C)OC)O)C2C1C)C)C 486.70 unknown via CMAUP database
13beta,28-Epoxy-23-hydroxyursane-3,12-dione 101485480 Click to see CC1CCC23CCC4(C5(CCC6C(C5CC(=O)C4(C2C1C)OC3)(CCC(=O)C6(C)CO)C)C)C 470.70 unknown via CMAUP database
13beta,28-Epoxy-3beta-hydroxy-12-oxoursane-23-al 101485479 Click to see CC1CCC23CCC4(C5(CCC6C(C5CC(=O)C4(C2C1C)OC3)(CCC(C6(C)C=O)O)C)C)C 470.70 unknown via CMAUP database
3beta,12-Dihydroxy-11alpha-methoxyurs-12-ene-23-al 44235896 Click to see CC1CCC2(CCC3(C(=C(C(C4C3(CCC5C4(CCC(C5(C)C=O)O)C)C)OC)O)C2C1C)C)C 486.70 unknown via CMAUP database
6beta,12-Dihydroxy-11alpha-methoxy-24-norurs-12-ene-3-one 44235898 Click to see CC1CCC2(CCC3(C(=C(C(C4C3(CC(C5C4(CCC(=O)C5C)C)O)C)OC)O)C2C1C)C)C 472.70 unknown via CMAUP database
Microtropioside B 101506966 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CCC(O3)(C)C(CO)O)C)C 502.60 unknown via CMAUP database
Microtropioside C 101506967 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CCC(O3)(C)C(CO)OC5C(C(C(C(O5)CO)O)O)O)C)C 664.80 unknown via CMAUP database
Microtropioside D 101506968 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CCC(O3)(C)C(COC5C(C(C(C(O5)CO)O)O)O)O)C)C 664.80 unknown via CMAUP database
Microtropioside E 101506969 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CC(C(O3)(C)C=C)OC5C(C(C(C(O5)CO)O)O)O)C)C 646.80 unknown via CMAUP database
Microtropioside F 101506970 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)CC(C(O3)(C)C=C)OC5C(C(C(C(O5)CO)O)O)O)C)C 646.80 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids
Microtropin A 102448004 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C(C)C#N)O)O)O)O 391.40 unknown via CMAUP database
Microtropin B 102448005 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C(C)C#N)O)O)O)O 391.40 unknown via CMAUP database
Microtropin C 102448006 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C(C)C#N)O)O)O)O 391.40 unknown via CMAUP database
Microtropin D 102448007 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OCC=C(CO)C#N)O)O)O)O 405.40 unknown via CMAUP database
Microtropin E 102448008 Click to see CCC(C(C)O)(C(=O)OCC1C(C(C(C(O1)OC(C)C)O)O)O)O 352.38 unknown via CMAUP database
Microtropin F 102448009 Click to see CCC(COC1C(C(C(C(O1)COC(=O)C(CC)(C(C)O)O)O)O)O)O 382.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
28-Hydroxy-2,3-secooleana-12-ene 2,3-dioic acid 3-methyl ester 44235899 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC(C4(C)CC(=O)O)C(C)(C)C(=O)OC)C)C2C1)C)CO)C 502.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
[(1S,2R,4S,5R,6S,7R,8S,9R,12R)-4,5,12-triacetyloxy-7,8-dibenzoyloxy-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-6-yl]methyl benzoate 24898243 Click to see CC1CC(C(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C(O3)(C)C)OC(=O)C)COC(=O)C6=CC=CC=C6)OC(=O)C)OC(=O)C 756.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(1S,2R,4S,5R,6R,7S,9R,12R)-4,5,12-triacetyloxy-6-(acetyloxymethyl)-2,10,10-trimethyl-11-oxatricyclo[7.2.1.01,6]dodecan-7-yl] benzoate 14414924 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C 574.60 unknown via CMAUP database
15-Acetoxyorbiculin G 24898039 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C5=CC=CC=C5)COC(=O)C)OC(=O)C)OC(=O)C6=CC=CC=C6 698.80 unknown via CMAUP database
1alpha,2alpha-Diacetoxy-6beta,9beta,15-tribenzoyloxy-beta-dihydroagarofuran 16109789 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C5=CC=CC=C5)COC(=O)C6=CC=CC=C6)OC(=O)C)OC(=O)C 698.80 unknown via CMAUP database
Mutangin 44419602 Click to see CC1CC(C(C2(C13C(C(CC2OC(=O)C4=CC=CC=C4)C(O3)(C)C)OC(=O)C)COC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C 636.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Salidroside 159278 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown https://doi.org/10.1016/S0031-9422(00)88609-4
https://doi.org/10.1016/S0031-9422(00)85563-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
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/10.1016/S0021-9673(01)87884-5
https://doi.org/10.1007/BF00564031
https://doi.org/10.1016/0031-9422(86)88020-7
https://doi.org/10.1016/S0021-9673(97)00492-5
Salireposide 117440 Click to see C1=CC=C(C=C1)C(=O)OCC2=C(C=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(00)85563-6
Tremuloidin 3083619 Click to see C1=CC=C(C=C1)C(=O)OC2C(C(C(OC2OC3=CC=CC=C3CO)CO)O)O 390.40 unknown https://doi.org/10.1016/0031-9422(86)88020-7
https://doi.org/10.1016/S0031-9422(00)88609-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Ethyl vanillin 8467 Click to see CCOC1=C(C=CC(=C1)C=O)O 166.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-1-propanone 75142 Click to see COC1=C(C=CC(=C1)C(=O)CCO)O 196.20 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Microtropioside A 101506965 Click to see CC1(C2CCC34COCC(C(O3)(CCC4C2(CCC1OC5C(C(C(C(O5)CO)O)O)O)C)C)O)C 500.60 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolidines / N-alkylpyrrolidines
1-Methyl-2-pyrrolidinone 13387 Click to see CN1CCCC1=O 99.13 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163042195 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O 492.40 unknown https://doi.org/10.1016/S0040-4039(00)61980-9
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/BF00579442
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/BF00579442
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44259225 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
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/10.1007/BF00579442
> 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)85563-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(-)-Evofolin B 46229015 Click to see COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O 318.32 unknown via CMAUP database

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