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Galium mollugo

Galium mollugo - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Galium mollugo - 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 UUID64403c6e2df33167645763
Scientific name Galium mollugo
Authority L.
First published in Sp. Pl. : 107 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Rubia mollugo Baill. Hist. Pl. 7: 372 (1880)
Galium mollugo var. scabrum Tinant Fl. Luxemb. 89 1836
Galium lucidum var. viridulum (Jord.) Nyman Consp. Fl. Eur. Suppl. 2: 152. 1889
Galium mollugo var. elatum Tinant Fl. Luxemb. 89 1836
Galium elatum var. umbrosum Gren. & Godr. Fl. France 2: 22 1850
Galium gerardii var. falcatum Lange Prodr. Fl. Hispan. 2: 315 1868
Galium gerardii var. genuinum Rouy Bull. Assoc. Franç. Bot. 5: 149 1902
Galium gerardii var. tenuissimum Lange Prodr. Fl. Hispan. 2: 315 1868
Galium gerardii var. viridulum (Jord.) Rouy Bull. Assoc. Franç. Bot. 5: 149 1902
Galium mollugo var. elatum (Thuill.) DC. Prodr. 4: 596 1830
Galium mollugo subsp. gerardii (Vill.) Rouy Fl. France 8: 16 1903

Common names Top

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Language Common/alternative name
English false baby's breath
English hedge bedstraw
English hedge-bedstraw
English white bedstraw
Spanish rubia mansa
Spanish cerrillo
Spanish galio
Spanish galio blanco
Spanish presera castellana
Spanish rubia lisa
Spanish rubia silvestre
Arabic جويسئة بيضاء
Belarusian граднік
Belarusian маслянка
Belarusian урочнік белы
Belarusian маруна мяккая
Bulgarian меко еньовче
Catalan cua de rabosa
Catalan espunyidella blanca
Catalan espunyidera
Catalan espunyidera blanca
Catalan herba mosquera
Czech svízel povázka
Welsh briwydd y clawdd
Welsh briwydden syth
Danish hvid snerre
German wiesenlabkraut
German wiesen-labkraut
German weißes waldstroh
German weisses waldstroh
German kleinblütiges wiesen-labkraut
German klein-wiesen-labkraut
German grasstern
German gemeines labkraut
Estonian pehme madar
Finnish saksanmatara
Finnish etelänpaimenmatara
French caille-lait blanc
French gaillet mollugine
Irish rú fáil
gd màdar fàil
Upper Sorbian Łučny sydrik
Icelandic ljósamaðra
Italian caglio tirolese
Lithuanian paprastasis lipikas
Norwegian Bokmål stormaure
Dutch glad walstro
oc erbo dóu mèu
Polish przytulia zwyczajna
Polish przytulia pospolita
Russian Подмаренник мягкий
Slovak lipkavec mäkký
Slovenian navadna lakota
Swedish buskmåra
Ukrainian Підмаринник Бессерів
Ukrainian Підмаренник Бессерів

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Galium mollugo subsp. marmaricum Maire & Weiller
Galium mollugo subsp. mollugo

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Russian Far East
      • Kuril Islands
      • Magadan
      • Primorye
    • Siberia
      • Altay
      • Buryatiya
      • Irkutsk
      • West Siberia
  • 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
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Italy
      • Romania
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • Labrador
      • Newfoundland
    • North-central U.S.A.
      • Illinois
      • Minnesota
      • Wisconsin
    • Northeastern U.S.A.
      • New York
      • Vermont
    • Southeastern U.S.A.
      • Kentucky
      • Maryland
      • Tennessee
    • Southwestern U.S.A.
      • California
  • Southern America
    • Southern South America
      • Argentina Northeast
      • Uruguay

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000969499
Canadensys 9009
USDA Plants GAMO
Tropicos 27900093
INPN 99473
Flora of Italy 4131
KEW urn:lsid:ipni.org:names:750253-1
The Plant List kew-86839
PFAF Galium mollugo
Open Tree Of Life 720440
NCBI Taxonomy 254777
NBN Atlas NBNSYS0000004308
Nature Serve 2.155400
IPNI 750253-1
iNaturalist 77206
GBIF 2915087
Freebase /m/0gnmw7
EPPO GALMO
EOL 1108055
Elurikkus 4837
Calflora (Californian flora) 3713
USDA GRIN 103278
Wikipedia Galium_mollugo
CMAUP NPO23286
GBIF 9039392

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
Land‐use affects pollinator‐specific resource availability and pollinator foraging behaviour Birkenbach M, Straub F, Kiesel A, Ayasse M, Wilfert L, Kuppler J Ecol Evol 07-Mar-2024
PMCID:PMC10918743
doi:10.1002/ece3.11061
PMID:38455145
Bumble bee microbiota shows temporal succession and increase of lactic acid bacteria when exposed to outdoor environments Weinhold A, Grüner E, Keller A Front Cell Infect Microbiol 04-Mar-2024
PMCID:PMC10945022
doi:10.3389/fcimb.2024.1342781
PMID:38500505
Soil Microbiome in Conditions of Oil Pollution of Subarctic Ecosystems Melekhina EN, Belykh ES, Kanev VA, Taskaeva AA, Tarabukin DV, Zinovyeva AN, Velegzhaninov IO, Rasova EE, Baturina OA, Kabilov MR, Markarova MY Microorganisms 30-Dec-2023
PMCID:PMC10820038
doi:10.3390/microorganisms12010080
PMID:38257907
LandS: Vegetation modeling based on Ellenberg's ecological indicator values Rumohr Q, Grimm V, Lennartz G, Schäffer A, Toschki A, Roß-Nickoll M, Hudjetz S MethodsX 13-Nov-2023
PMCID:PMC10709510
doi:10.1016/j.mex.2023.102486
PMID:38076710
Plant-based red colouration of shell beads 15,000 years ago in Kebara Cave, Mount Carmel (Israel) Davin L, Bellot-Gurlet L, Navas J PLoS One 25-Oct-2023
PMCID:PMC10599507
doi:10.1371/journal.pone.0292264
PMID:37878593
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
Examination of the Effects of Domestic Water Buffalo (Bubalus bubalis) Grazing on Wetland and Dry Grassland Habitats Fűrész A, Penksza K, Sipos L, Turcsányi-Járdi I, Szentes S, Fintha G, Penksza P, Viszló L, Szalai F, Wagenhoffer Z Plants (Basel) 31-May-2023
PMCID:PMC10255522
doi:10.3390/plants12112184
PMID:37299162
Edge Effects in the Distribution of Coleoptera in the Forests of the Center of the European Part of Russia Ruchin AB, Egorov LV, Khapugin AA Insects 10-Apr-2023
PMCID:PMC10144564
doi:10.3390/insects14040371
PMID:37103186
Characterization and phylogenetic analysis of the chloroplast genome of galium spurium Yin H, Huang K, Xie P, Mo P, Zhang N, Wang Y Mitochondrial DNA B Resour 29-Mar-2023
PMCID:PMC10062210
doi:10.1080/23802359.2023.2172971
PMID:37006957
Phytochemical Screening and Antioxidant Activity of Selected Estonian Galium Species Laanet PR, Saar-Reismaa P, Jõul P, Bragina O, Vaher M Molecules 22-Mar-2023
PMCID:PMC10056973
doi:10.3390/molecules28062867
PMID:36985838
Features of Natural Succession of Ex-Arable Forest Steppe Grassland (from Western Romania) under the Influence of Climate Sărățeanu V, Cotuna O, Paraschivu M, Cojocariu LL, Horablaga NM, Rechițean D, Mircov VD, Sălceanu C, Urlică AA, Copăcean L Plants (Basel) 07-Mar-2023
PMCID:PMC10059065
doi:10.3390/plants12061204
PMID:36986892
Long-Term Vegetation Changes and Socioeconomic Effects of River Engineering in Industrialized Areas (Southern Poland) Rahmonov O, Dragan W, Cabała J, Krzysztofik R Int J Environ Res Public Health 27-Jan-2023
PMCID:PMC9915360
doi:10.3390/ijerph20032255
PMID:36767623
Insect Feeding on Sorghum bicolor Pollen and Hymenoptera Attraction to Aphid-Produced Honeydew Harris-Shultz KR, Armstrong JS, Caballero M, Hoback WW, Knoll JE Insects 14-Dec-2022
PMCID:PMC9780982
doi:10.3390/insects13121152
PMID:36555062
Plant-Associated Bacteria as Sources for the Development of Bioherbicides Fang W, Liu F, Wu Z, Zhang Z, Wang K Plants (Basel) 06-Dec-2022
PMCID:PMC9737584
doi:10.3390/plants11233404
PMID:36501441
Mulching in lowland hay meadows drives an adaptive convergence of above- and below-ground traits reducing plasticity and improving biomass: A possible tool for enhancing phytoremediation Dalle Fratte M, Montagnoli A, Anelli S, Armiraglio S, Beatrice P, Ceriani A, Lipreri E, Miali A, Nastasio P, Cerabolini BE Front Plant Sci 24-Nov-2022
PMCID:PMC9746715
doi:10.3389/fpls.2022.1062911
PMID:36523619

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 / Anthracenes / Anthraquinones
1,3-Dimethoxyanthraquinone 361511 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C3=CC=CC=C3C2=O 268.26 unknown https://doi.org/10.1039/J39680000854
Anthraquinone 6780 Click to see C1=CC=C2C(=C1)C(=O)C3=CC=CC=C3C2=O 208.21 unknown https://doi.org/10.1093/JXB/36.3.485
Anthraquinone base + 2O, MeOH, O-Hex-Pen 21917783 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)C(=O)C5=CC=CC=C5C4=O)O)CO)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(00)80323-4
Lucidin primeveroside 160180 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)C(=O)C5=CC=CC=C5C4=O)O)CO)O)O)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(00)80323-4
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Purpurin 6683 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3O)O)O 256.21 unknown https://doi.org/10.1016/S0031-9422(00)80323-4
> Benzenoids / Benzene and substituted derivatives
1-Phenyl-5-heptene-1,3-diyne 5281154 Click to see CC=CC#CC#CC1=CC=CC=C1 166.22 unknown via CMAUP database
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown via CMAUP database
Phenylheptatriyne 77981 Click to see CC#CC#CC#CC1=CC=CC=C1 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
2-Butoxyethyl oleate 6436064 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCCOCCCC 382.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R)-1-hydroxytrideca-5,7,9,11-tetrayn-2-yl]oxyoxane-3,4,5-triol 54671425 Click to see CC#CC#CC#CC#CCCC(CO)OC1C(C(C(C(O1)CO)O)O)O 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
(2e)-7-Phenylhepta-2-en-4,6-diyn-1-yl acetate 23274467 Click to see CC(=O)OCC=CC#CC#CC1=CC=CC=C1 224.25 unknown via CMAUP database
7-Phenylhepta-2,4,6-triynyl acetate 11644243 Click to see CC(=O)OCC#CC#CC#CC1=CC=CC=C1 222.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2R)-7-phenylhepta-4,6-diyne-1,2-diol 101808987 Click to see C1=CC=C(C=C1)C#CC#CCC(CO)O 200.23 unknown via CMAUP database
(S)-7-Phenyl-4,6-heptadiyne-2-ol 101395939 Click to see CC(CC#CC#CC1=CC=CC=C1)O 184.23 unknown via CMAUP database
7-Phenyl-2,4,6-heptatriyn-1-ol 3085176 Click to see C1=CC=C(C=C1)C#CC#CC#CCO 180.20 unknown via CMAUP database
7-Phenylhept-2-en-4,6-diyn-1-ol 114662 Click to see C1=CC=C(C=C1)C#CC#CC=CCO 182.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
2-Butoxyethyl linoleate 87553426 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCCOCCCC 380.60 unknown via CMAUP database
2-Butoxyethyl linolenate 87552578 Click to see CCCCOCCOC(=O)CCCCCCCC=CCC=CCC=CCC 378.60 unknown via CMAUP database
Ethyl Linoleate 5282184 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC 308.50 unknown via CMAUP database
Ethyl linolenate 5367460 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OCC 306.50 unknown via CMAUP database
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
Methyl linolenate 5319706 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)OC 292.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Rrr-alpha-tocopherylquinone 46183941 Click to see CC1=C(C(=O)C(=C(C1=O)C)CCC(C)(CCCC(C)CCCC(C)CCCC(C)C)O)C 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E,7S,11S)-3,7,11,15-tetramethylhexadec-2-enoic acid 42433537 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CC(=O)O)C 310.50 unknown via CMAUP database
[(E,7R,11R)-3,7,11,15-tetramethylhexadec-2-enyl] heptanoate 101918983 Click to see CCCCCCC(=O)OCC=C(C)CCCC(C)CCCC(C)CCCC(C)C 408.70 unknown via CMAUP database
Rel-(7S,11S,E)-3,7,11,15-tetramethylhexadec-2-en-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(2S)-2-[(3E)-4,8-dimethylnona-3,7-dienyl]-2,8-dimethyl-3,4-dihydrochromen-6-ol 163194297 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)C)O 328.50 unknown https://doi.org/10.1081/JLC-100101486
https://doi.org/10.1016/S0031-9422(00)84093-5
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin K compounds
2-Naphthalenecarboxylic acid, 1,4-dihydro-1,4-dioxo-3-(3-methyl-2-butenyl)-, methyl ester 617076 Click to see CC(=CCC1=C(C(=O)C2=CC=CC=C2C1=O)C(=O)OC)C 284.31 unknown https://doi.org/10.1039/C39810000334
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aR,7R,7aR)-7-hydroxy-4-methoxycarbonyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-7-carboxylic acid 162953421 Click to see COC(=O)C1=COC(C2C1C=CC2(C(=O)O)O)OC3C(C(C(C(O3)CO)O)O)O 418.30 unknown https://doi.org/10.1016/S0031-9422(00)80082-5
(1S,4aR,7R,7aS)-7-hydroxy-4-methoxycarbonyl-1-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-7-carboxylic acid 162953422 Click to see COC(=O)C1=COC(C2C1C=CC2(C(=O)O)O)OC3C(C(C(C(O3)CO)O)O)O 418.30 unknown https://doi.org/10.1016/S0031-9422(00)80082-5
(1S,4aS,7R,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid 3488508 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown https://doi.org/10.1016/S0031-9422(00)84093-5
(1S,4aS,7S,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid 162905353 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown https://doi.org/10.1016/S0031-9422(00)84093-5
(4aR,7aS)-5-acetyloxy-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid 138108972 Click to see CC(=O)OC1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 432.40 unknown https://doi.org/10.1081/JLC-100101486
10-Hydroxyloganin 443340 Click to see COC(=O)C1=COC(C2C1CC(C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 406.40 unknown https://doi.org/10.1016/S0031-9422(00)84093-5
https://doi.org/10.1016/0031-9422(96)00328-7
6alpha-Hydroxygeniposide; Deacetylasperulosidic acid methyl ester 3515876 Click to see COC(=O)C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown https://doi.org/10.1016/S0031-9422(00)84093-5
7-(Acetyloxymethyl)-5-hydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylic acid 13935238 Click to see CC(=O)OCC1=CC(C2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(00)84093-5
7-hydroxy-4-methoxycarbonyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-7-carboxylic acid 162953420 Click to see COC(=O)C1=COC(C2C1C=CC2(C(=O)O)O)OC3C(C(C(C(O3)CO)O)O)O 418.30 unknown https://doi.org/10.1016/S0031-9422(00)80082-5
Asperulosidic acid 11968867 Click to see CC(=O)OCC1=CC(C2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(00)84093-5
https://doi.org/10.1016/0031-9422(96)00328-7
Asperulosidicacid 145709477 Click to see CC(=O)OCC1=CC(C2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/S0031-9422(00)84093-5
https://doi.org/10.1081/JLC-100101486
https://doi.org/10.1016/0031-9422(96)00328-7
Daphylloside 21602024 Click to see CC(=O)OCC1=CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 446.40 unknown https://doi.org/10.1016/S0031-9422(00)84093-5
https://doi.org/10.1016/0031-9422(96)00328-7
Deacetylasperulosidic acid 12315350 Click to see C1=C(C2C(C1O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 390.34 unknown https://doi.org/10.1016/0031-9422(96)00328-7
Desacetyl asperulosidic acid 12315348 Click to see C1=C(C2C(C1O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 390.34 unknown https://doi.org/10.1016/0031-9422(96)00328-7
https://doi.org/10.1016/S0031-9422(00)84093-5
Galioside 185774 Click to see COC(=O)C1=COC(C2C1C=CC2(CO)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown https://doi.org/10.1002/JLAC.197619760716
https://doi.org/10.1016/S0031-9422(00)80082-5
Geniposidic Acid 443354 Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 374.34 unknown https://doi.org/10.1016/S0031-9422(00)84499-4
https://doi.org/10.1016/0031-9422(96)00328-7
https://doi.org/10.1081/JLC-100101486
methyl (1S,4aR,7S,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate 161728207 Click to see COC(=O)C1=COC(C2C1C=CC2(CO)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown https://doi.org/10.1002/JLAC.197619760716
Methyl 6-hydroxy-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 4490437 Click to see COC(=O)C1=COC(C2C1CC(C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 406.40 unknown https://doi.org/10.1016/0031-9422(96)00328-7
https://doi.org/10.1016/S0031-9422(00)84093-5
Methyl 7-(acetyloxymethyl)-5-hydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-4-carboxylate 12309039 Click to see CC(=O)OCC1=CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 446.40 unknown https://doi.org/10.1016/0031-9422(96)00328-7
https://doi.org/10.1016/S0031-9422(00)84093-5
Monotropein 73466 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown https://doi.org/10.1016/S0031-9422(00)80082-5
https://doi.org/10.1016/S0031-9422(00)84093-5
https://doi.org/10.1081/JLC-100101486
Scandoside methyl ester 442433 Click to see COC(=O)C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 404.40 unknown https://doi.org/10.1016/S0031-9422(00)84093-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
alpha-Spinasterin 5281331 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Schottenol 441837 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
3-(1-Carboxyethenoxy)-4-hydroxycyclohexa-1,5-diene-1-carboxylic acid 306 Click to see C=C(C(=O)O)OC1C=C(C=CC1O)C(=O)O 226.18 unknown https://doi.org/10.1007/S004250050120
Butanedioate;hydron 21952380 Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-] 118.09 unknown via CMAUP database
Chorismic acid 12039 Click to see C=C(C(=O)O)OC1C=C(C=CC1O)C(=O)O 226.18 unknown https://doi.org/10.1007/S004250050120
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
5-[(1-Carboxyethenyl)oxy]-6-hydroxycyclohexa-1,3-diene-1-carboxylic acid 809 Click to see C=C(C(=O)O)OC1C=CC=C(C1O)C(=O)O 226.18 unknown https://doi.org/10.1007/S004250050120
Isochorismic acid 189062 Click to see C=C(C(=O)O)OC1C=CC=C(C1O)C(=O)O 226.18 unknown https://doi.org/10.1007/S004250050120
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-3,4-bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid 460890 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
(1S,3R,4R,5R)-3,4-Bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid 153946 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
3,4-Dicaffeoylquinic acid 6474309 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[5-(hexopyranosyloxy)-1-oxo-2a,4a,5,7b-tetrahydro-1H-2,6-dioxacyclopenta[cd]inden-4-yl]methyl acetate 233330 Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O 414.40 unknown https://doi.org/10.1081/JLC-100101486
https://doi.org/10.3891/ACTA.CHEM.SCAND.30B-0743
https://doi.org/10.1016/S0031-9422(00)84093-5
10-Hydroxymorroniside 443341 Click to see COC(=O)C1=COC(C2C1CC(OC2CO)O)OC3C(C(C(C(O3)CO)O)O)O 422.40 unknown https://doi.org/10.1016/S0031-9422(00)84093-5
Asperuloside 84298 Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O 414.40 unknown https://doi.org/10.1081/JLC-100101486
https://doi.org/10.1016/S0031-9422(00)84093-5
Deacetylasperuloside 44593378 Click to see C1=C(C2C3C1OC(=O)C3=COC2OC4C(C(C(C(O4)CO)O)O)O)CO 372.32 unknown https://doi.org/10.1081/JLC-100101486
methyl (1R,3R,4aS,8S,8aS)-3-hydroxy-1-(hydroxymethyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,4a,8,8a-hexahydropyrano[3,4-c]pyran-5-carboxylate 163047522 Click to see COC(=O)C1=COC(C2C1CC(OC2CO)O)OC3C(C(C(C(O3)CO)O)O)O 422.40 unknown https://doi.org/10.1016/S0031-9422(00)84093-5
methyl (1R,3S,4aS,8S,8aS)-3-hydroxy-1-(hydroxymethyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,4a,8,8a-hexahydropyrano[3,4-c]pyran-5-carboxylate 163047521 Click to see COC(=O)C1=COC(C2C1CC(OC2CO)O)OC3C(C(C(C(O3)CO)O)O)O 422.40 unknown https://doi.org/10.1016/0031-9422(96)00328-7
https://doi.org/10.1016/S0031-9422(00)84093-5
methyl (1S,2S,3S,7S,9S,11R)-11-hydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,10,12-trioxatricyclo[7.2.1.02,7]dodec-5-ene-6-carboxylate 162890620 Click to see COC(=O)C1=COC(C2C1CC3OC2C(O3)O)OC4C(C(C(C(O4)CO)O)O)O 420.40 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.30B-0743
methyl (1S,2S,3S,7S,9S,11S)-11-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,10,12-trioxatricyclo[7.2.1.02,7]dodec-5-ene-6-carboxylate 162890619 Click to see COC(=O)C1=COC(C2C1CC3OC2C(O3)O)OC4C(C(C(C(O4)CO)O)O)O 420.40 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.30B-0743
Methyl 11-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,10,12-trioxatricyclo[7.2.1.02,7]dodec-5-ene-6-carboxylate 4490615 Click to see COC(=O)C1=COC(C2C1CC3OC2C(O3)O)OC4C(C(C(C(O4)CO)O)O)O 420.40 unknown https://doi.org/10.1016/S0031-9422(00)84093-5
https://doi.org/10.3891/ACTA.CHEM.SCAND.30B-0743
Methyl 3-hydroxy-1-(hydroxymethyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,4a,8,8a-hexahydropyrano[3,4-c]pyran-5-carboxylate 4490438 Click to see COC(=O)C1=COC(C2C1CC(OC2CO)O)OC3C(C(C(C(O3)CO)O)O)O 422.40 unknown https://doi.org/10.1016/S0031-9422(00)84093-5
Secogalioside 443355 Click to see COC(=O)C1=COC(C2C1CC3OC2C(O3)O)OC4C(C(C(C(O4)CO)O)O)O 420.40 unknown https://doi.org/10.1016/S0031-9422(00)84093-5
https://doi.org/10.1016/0031-9422(96)00328-7
https://doi.org/10.1016/S0031-9422(00)84499-4
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(E)-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-enoic acid 15071011 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)C=CC(=O)O)O)O)O)O 472.40 unknown via CMAUP database
2-(Hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol 346 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.30B-0743
2-Carbomethoxy-3-prenyl-1,4-naphthohydroquinone-di-O-beta-D-glucoside 14539974 Click to see CC(=CCC1=C(C2=CC=CC=C2C(=C1C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)C 610.60 unknown https://doi.org/10.1016/S0031-9422(00)80323-4
4-[[2-O-Acetyl-6-O-[3-(4-hydroxyphenyl)-1-oxo-2-propenyl]-beta-D-glucopyranosyl]oxy]benzeneacrylic acid 15071014 Click to see CC(=O)OC1C(C(C(OC1OC2=CC=C(C=C2)C=CC(=O)O)COC(=O)C=CC3=CC=C(C=C3)O)O)O 514.50 unknown via CMAUP database
Methyl 1,4-bisglucosyloxy-3-prenyl-2-naphthoate 10031663 Click to see CC(=CCC1=C(C2=CC=CC=C2C(=C1C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)C 610.60 unknown https://doi.org/10.1016/S0031-9422(00)80323-4
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
2-Acetylthiophene 6920 Click to see CC(=O)C1=CC=CS1 126.18 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
2-Succinylbenzoate 955 Click to see C1=CC=C(C(=C1)C(=O)CCC(=O)O)C(=O)O 222.19 unknown https://doi.org/10.1016/0031-9422(91)85259-3
> Organoheterocyclic compounds / Naphthofurans
Furomollugin 10354359 Click to see COC(=O)C1=C(C2=CC=CC=C2C3=C1C=CO3)O 242.23 unknown https://doi.org/10.1002/JLAC.197619760716
> Organoheterocyclic compounds / Naphthopyrans
Mollugin 124219 Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3C(=C2C(=O)OC)O)C 284.31 unknown https://doi.org/10.1016/S0031-9422(00)80323-4
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
5-(Phenylethynyl)thiophene-2-methanol 2822242 Click to see C1=CC=C(C=C1)C#CC2=CC=C(S2)CO 214.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Aurone flavonoids
(Z)-7-[[beta-D-Glucopyranosyl]oxy]-3',4',6-trihydroxyaurone 15071008 Click to see C1=CC(=C(C=C1C=C2C(=O)C3=C(O2)C(=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, ethyl ester 66883 Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O 208.21 unknown via CMAUP database
Ethyl caffeate 5317238 Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O 208.21 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
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
[(2R,3R,4R,5R,6S)-3,4-diacetyloxy-6-[4-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]-2,3-dihydroxyphenoxy]-5-hydroxyoxan-2-yl]methyl acetate 14861259 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)OC(=O)C)OC(=O)C 576.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[4-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]-2,3-dihydroxyphenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 14213555 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)O 492.40 unknown via CMAUP database
2,3-Dihydroxy-4-[(E)-3-(3,4-dihydroxyphenyl)acryloyl]phenyl 4-O,6-O-diacetyl-beta-D-glucopyranoside 10840030 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C(=C(C=C2)C(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O)OC(=O)C 534.50 unknown via CMAUP database
3',4'-Di(beta-D-glucopyranosyloxy)-2',3,4-trihydroxychalcone 102149400 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 612.50 unknown via CMAUP database
4'-[(6-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy]-2',3,3',4-tetrahydroxychalcone 14213552 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C(=C(C=C2)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)O)O)O)O 612.50 unknown via CMAUP database
chrysosplenosid-C 118856019 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC4C(C(C(C(O4)CO)O)O)O)O)OC)O 522.50 unknown via CMAUP database
Marein 6441269 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C(=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O)O 450.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Aurone O-glycosides
(2Z)-2-(3,4-Dihydroxybenzylidene)-6-[(4-O,6-O-diacetyl-beta-D-glucopyranosyl)oxy]-7-hydroxybenzofuran-3(2H)-one 101669623 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=O)C(=CC4=CC(=C(C=C4)O)O)O3)O)O)O)OC(=O)C 532.40 unknown via CMAUP database
(Z)-6-[[6-O-[3-(4-Hydroxyphenyl)-1-oxo-2-propenyl]-beta-D-glucopyranosyl]oxy]-3',4',7-trihydroxyaurone 15071009 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(C4=C(C=C3)C(=O)C(=CC5=CC(=C(C=C5)O)O)O4)O)O)O)O)O 594.50 unknown via CMAUP database
[(2R,3R,4R,5R,6S)-3,4-diacetyloxy-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-5-hydroxyoxan-2-yl]methyl acetate 10603216 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=O)C(=CC4=CC(=C(C=C4)O)O)O3)O)O)OC(=O)C)OC(=O)C 574.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-6-[[(2Z)-2-[(3,4-dihydroxyphenyl)methylidene]-7-hydroxy-3-oxo-1-benzofuran-6-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 15071010 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=O)C(=CC4=CC(=C(C=C4)O)O)O3)O)O)O)O 490.40 unknown via CMAUP database
2-[(alphaZ)-3,4-Dihydroxybenzylidene]-6-(2-O,4-O,6-O-triacetyl-beta-D-glucopyranosyloxy)-7-hydroxybenzofuran-3(2H)-one 10674637 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C3=C(C=C2)C(=O)C(=CC4=CC(=C(C=C4)O)O)O3)O)OC(=O)C)O)OC(=O)C 574.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3,3'-Dimethoxy-4',5-dihydroxy-7-(beta-D-glucopyranosyloxy)flavone 13344657 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)OC)O 492.40 unknown via CMAUP database
5-hydroxy-2-(3-hydroxy-4-methoxy-phenyl)-3-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxymethyl]tetrahydropyran-2-yl]oxy-chromen-4-one 5495545 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=C(C4=O)OC)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 638.60 unknown via CMAUP database
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 102316697 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=C(C4=O)OC)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O)O 638.60 unknown via CMAUP database
5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,6-dimethoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11577257 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)OC)O)OC)O 522.50 unknown via CMAUP database
Axillaroside 101243893 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC4C(C(C(C(O4)CO)O)O)O 508.40 unknown via CMAUP database
Centaurein 5489090 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)OC)O)OC)O 522.50 unknown via CMAUP database
Hesperetin-rutinoside 53477767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Jaceidin 5464461 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Okanin 5281294 Click to see C1=CC(=C(C=C1C=CC(=O)C2=C(C(=C(C=C2)O)O)O)O)O 288.25 unknown via CMAUP database

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