Rosa gallica - Unknown
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Internal ID UUID64403e66d5fee455666176
Scientific name Rosa gallica
Authority L.
First published in Sp. Pl. : 492 (1753)

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Synonyms Top

Scientific name Authority First published in
Rosa heteracantha Chrshan. Bot. Žurn. (Kiev) 6(4): 92 (1949 publ. 1950)
Rosa crenulata Chrshan. Bot. Žurn. (Kiev) 6(4): 88 (1949 publ. 1950)
Rosa tauriae Chrshan. Sbornik nauchnykh trudov L'vovskogo veterinarnogo instituta ; 1948 250 1949
Rosa arvina Krock. Fl. Siles. (Krocker) ii. I. 150 (Quid ?). 1790
Rosa czackiana Besser Enum. Pl. Volh. : 66 (1822)
Rosa minimalis Chrshan. Bot. Žurn. (Kiev) 6(1): 61 (1949)
Rosa pumila Jacq. Flora austriacae sive Plantarum selectarum in Austriae Archiducatu sponte crescentium Icones ; 1773 59, t.198 1774
Rosa heteroacantha Chrshan. Bot. Žurn. (Kiev) 6(4): 92 (1949 publ. 1950)
Rosa austriaca Crantz Stirp. Austr. Fasc. 2: 33 (1763)
Rosa gallica var. czackiana (Besser) Heinr.Braun Flora von Nieder-™sterreich ; 1890 767 1892
Rosa tenuis Becker Fl. Frankfurt 1: 485 (1828)
Rosa provincialis Herrm. De Rosa : 9 (1762)
Rosa olympica Donn Hortus Cantabrig. , ed. 6: 144 (1811)
Rosa atropurpurea Boullu Ann. Soc. Bot. Lyon 9: 274 (1882)
Rosa pumila Scop. Fl. Carniol., ed. 2. 1: 353. 1771
Rosa cordifolia Host Fl. Austriac. [Host] 2: 23. 1831
Rosa rubra Lam. Fl. Franç. 3: 130 (1779)
Rosa belgica Brot. Fl. Lusit. 1: 338 (1804)
Rosa cordata Cariot Étude Fl. , ed. 5, 2: 180 (1872)
Rosa mirogojana Braun & Vuk. Sched. Fl. Exs. Austro-Hung. 3: 47 (1884)
Rosa gallica var. leiostyla Gelmi Prosperto della flora trentina ; 1893 58 1893
Rosa gallica subsp. leiostyla (Gelmi) Soó ; 1963 425 1963
Rosa pygmaea Krock. Fl. Siles. 2(1): 154 (1790)
Rosa gallica f. elata H.Christ Die Rosen der Schweiz ; 1873 199 1873
Rosa velutinaeflora Déségl. ; 1873 100 1873
Rosa repens Münchh. Hausvater 5(1): 281 (1770)
Rosa hispida Münchh. Hausvater 5: 281 (1770); Borck. Forstbot. ii. 1332.
Rosa virescens Déségl. Mém. Soc. Acad. Maine Loire 10: 73 (1861)
Rosa ruralis Déségl. Mém. Soc. Acad. Maine Loire 10: 79 (1861)
Rosa assimilis Déségl. Mém. Soc. Acad. Maine Loire 28: 103 (1873)
Rosa sylvatica Gaterau Descr. Pl. Montauban : 94 (1789)
Rosa grandiflora Salisb. Prodr. Stirp. Chap. Allerton : 358 (1796)
Rosa pinnatifida Andrews Roses 1: t. 41 (1820)
Rosa racemosa Andrews Roses 1: t. 49 (1805)
Rosa holosericea Du Roi Obs. Bot. : 20 (1771)
Rosa oligacantha Borbás Math. Term. Közlem. 16: 373 (1880 publ. 1881)
Rosa gallica var. pannonica Wiesb.
Rosa austriaca var. officinalis (Andrews) P.V.Heath Calyx 1: 167 (1992)
Rosa gallica var. subinermis (Chabert) R.Keller Synopsis rosarum spontanearum Europae mediae ; 1931 112 1931
Rosa gallica var. trichophylla R.Keller ; 1914 103 1914
Rosa gallica var. baldensis R.Keller ; 1912 8 1912
Rosa gallica var. cordifolia (Host) Heinr.Braun Flora von Nieder-™sterreich ; 1890 779 1892
Rosa gallica f. cordata (Cariot) R.Keller Synopsis der mitteleurop„ischen Flora ; 1896 49 1900
Rosa rubiginosa var. imitans R.Keller ; 1899 69 1899
Rosa gallica var. rosamundi Weston Botanicus universalis ; 1770 249 1770
Rosa gallica var. ruralis (Déségl.) Rouy Flore de France ; 1893 255 1900
Rosa arvina Krock. Fl. Siles. 2(1): 150 (1790)
Rosa gallica subsp. austriaca (Crantz) Nyman Conspectus florae europaeae ; 1878 231 1878
Rosa rhodanii Chabert ?tude des fleurs ; 1865 182 1865
Rosa gallica var. austriaca (Crantz) Heinr.Braun Flora von Nieder-™sterreich ; 1890 779 1892
Rosa gallica var. magnifica (Borbás) Heinr.Braun Flora von Nieder-™sterreich ; 1890 779 1892
Rosa gallica var. czakiana (Besser) Heinr.Braun Flora von Nieder-™sterreich ; 1890 780 1892
Rosa czakiana Besser Enumeratio plantarum hucusque in Volhynia, Podolia, gub. Kiiviensi, Bessarabia cis-tyraica et circa Odessam collectarum ; 1822 66 1822
Rosa gallica var. subglandulosa (Borbás) Heinr.Braun Flora von Nieder-™sterreich ; 1890 780 1892
Rosa austriaca var. subglandulosa Borbás Primitiae monographiae rosarum imperii Hungarici = A magyar birodalom vadon term” r¢zs i monographi j nak kis‚rlete ; 1881 372 1881
Rosa pumila var. holosericea (Du Roi) P.V.Heath Calyx 6: 76 (1999)
Rosa pumila var. rosamundi (Weston) P.V.Heath Calyx 6: 77 (1999)
Rosa pumila var. subnigra (Andrews) P.V.Heath Calyx 6: 76 (1999)
Rosa pumila var. tricolor (Andrews) P.V.Heath Calyx 6: 76 (1999)
Rosa pumila var. hispida (Münchh.) A.Rau Enumeratio rosarum circa Wirceburgum ; 1816 116 1816
Rosa austriaca var. leiophylla Borbás Primitiae monographiae rosarum imperii Hungarici = A magyar birodalom vadon term” r¢zs i monographi j nak kis‚rlete ; 1881 369 1881
Rosa gallica var. leiophylla (Borbás) R.Keller Synopsis rosarum spontanearum Europae mediae ; 1931 113 1931
Rosa centifolia var. subnigra hort. ex Andrews Roses ; 1805 t.43 1817
Rosa centifolia var. tricolor hort. ex Andrews Roses ; 1805 t.44 1822
Rosa austriaca var. cordifolia (Host) Borbás Primitiae monographiae rosarum imperii Hungarici = A magyar birodalom vadon term” r¢zs i monographi j nak kis‚rlete ; 1881 369 1881
Rosa flectidenta Gand. Tabulae rhodologicae europaeo-orientales locupletissimae ; 1881 56, no.351 1881
Rosa gallica var. grahovicensis R.Keller ; 1923 52 1923
Rosa gallica var. haplodonta (Borbás) Heinr.Braun Flora von Nieder-™sterreich ; 1890 779 1892
Rosa gallica var. pulchella R.Keller Synopsis rosarum spontanearum Europae mediae ; 1931 114 1931
Rosa gallica var. reinechei M.Schulze ; 1907 33 1907
Rosa gallica var. variegata hort. ex Andrews Roses ; 1805 t.46 1805
Rosa gallica var. subtomentella (Borbás) R.Keller Synopsis rosarum spontanearum Europae mediae ; 1931 114 1931
Rosa umbrosa H.Waldner Ueber Europaeische Rosentypen ; 1885 47 1885
Rosa gallica var. virescens (Déségl.) Degen Magyar fl¢ra ; 1924 548 1924
Rosa heteroacatha Chrshan. Bot. Žurn. (Kiev) 6(4): 92 (1949 publ. 1950)

Common names Top

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Language Common/alternative name
English gallica rose
English gallica
English french rose
Arabic ورد احمر
Arabic ورد غالي
Arabic ورد بروفانس
Arabic ورد فرنسي
Arabic حوجم
Arabic ورد غاليك
Azerbaijani fransa qızılgülü
Bulgarian галска роза
Bulgarian Галска роза
Czech růže galská
Czech růže nízká
Czech keltská růže
Czech růže keltská
Welsh rhosyn coch caerhirfryn
Danish fransk rose
German essig-rose
German essigrose
Esperanto vinagra rozo
Esperanto gaŭla rozo
Estonian äädika-kibuvits
Basque provinseko arrosa
Basque frantziar arrosa
Basque frantses arrosa
Persian رز گالیکا
Finnish ranskanruusu
Finnish gallianruusu
French rose de france
French rosier de provins
French rosier de france
Croatian galska ruža
Upper Sorbian kisałowa róža
Hungarian parlagi rózsa
Hungarian bársonyrózsa
Japanese ロサ・ガリカ
Lithuanian prancūzinis erškėtis
Malayalam റോസ ഗാലിക
Norwegian Bokmål provinsrose
Dutch franse roos
Polish róża francuska
Punjab جلیقی گلاب
Russian Шиповник галльский
Russian Шиповник французский
Russian Шиповник крымский
Russian Роза французская
Russian Роза крымская
Russian Роза галльcкая
Slovak ruža galská
Swedish provinsros
Swedish gallicarosor
Swedish gallicaros
Turkish kırmızı frenk gülü
Ukrainian Шипшина французька
Chinese 法国蔷薇

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Rosa gallica var. officinalis Thory Roses 1: 75 (1818)
Rosa gallica var. pumila (Scop.) Thory Roses [Redoute] 1: 76. 1818

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Name Authority First published in
Rosa gallica f. versicolor (L.) Rehder Bibliography of cultivated trees and shrubs ; 1949 299 1949

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
    • Middle Asia
      • Tadzhikistan
    • Western Asia
      • Iraq
      • Turkey
  • Australasia
    • Australia
      • South Australia
    • New Zealand
      • New Zealand North
      • New Zealand South
  • Europe
    • Eastern Europe
      • Belarus
      • East European Russia
      • Krym
      • South European Russia
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Eastern Canada
      • Nova Scotia
      • Ontario
      • Québec
    • North-central U.S.A.
      • Illinois
      • Missouri
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000983164
UNII 71S8UE01P6
Canadensys 8896
USDA Plants ROGA
Tropicos 27800151
INPN 118192
Flora of Italy 1983
KEW urn:lsid:ipni.org:names:732569-1
The Plant List rjp-1000
Open Tree Of Life 333878
Observations.org 7329
NCBI Taxonomy 74632
NBN Atlas NBNSYS0000034283
Nature Serve 2.161166
IPNI 732569-1
iNaturalist 242657
iNaturalist 167982
GBIF 3002530
Freebase /m/06d1dh
WisFlora 7604
EPPO ROSGA
EOL 635719
Elurikkus 6913
USDA GRIN 5351
Wikipedia Rosa_gallica

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
Physicochemical Characterization of Pectic Polysaccharides from Rose Essential Oil Industry By-Products Slavov A, Chalova V Foods 15-Jan-2024
PMCID:PMC10814715
doi:10.3390/foods13020270
PMID:38254571
Beneficial medicinal effects and material applications of rose Wang H Heliyon 10-Dec-2023
PMCID:PMC10758878
doi:10.1016/j.heliyon.2023.e23530
PMID:38169957
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
Detailed Metabolic Characterization of Flowers and Hips of Rosa gallica L. Grown in Open Nature Kunc N, Hudina M, Mikulič-Petkovšek M, Bavcon J, Ravnjak B, Osterc G Plants (Basel) 18-Aug-2023
PMCID:PMC10457908
doi:10.3390/plants12162979
PMID:37631190
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
Phenolic Compounds of Rose Hips of Some Rosa Species and Their Hybrids Native Grown in the South-West of Slovenia during a Two-Year Period (2020–2021) Kunc N, Hudina M, Osterc G, Bavcon J, Ravnjak B, Mikulič-Petkovšek M Foods 11-May-2023
PMCID:PMC10217035
doi:10.3390/foods12101952
PMID:37238770
Skin Ageing: A Progressive, Multi-Factorial Condition Demanding an Integrated, Multilayer-Targeted Remedy Liang Y, Su W, Wang F Clin Cosmet Investig Dermatol 09-May-2023
PMCID:PMC10182820
doi:10.2147/CCID.S408765
PMID:37192990
Ergosterol extraction: a comparison of methodologies Wilkes TI Access Microbiol 28-Apr-2023
PMCID:PMC10202395
doi:10.1099/acmi.0.000490.v4
PMID:37223062
Natural Pigments Production and Their Application in Food, Health and Other Industries Di Salvo E, Lo Vecchio G, De Pasquale R, De Maria L, Tardugno R, Vadalà R, Cicero N Nutrients 16-Apr-2023
PMCID:PMC10144550
doi:10.3390/nu15081923
PMID:37111142
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
Comparative Chemical Profiling and Citronellol Enantiomers Distribution of Industrial-Type Rose Oils Produced in China Dobreva A, Nedeltcheva-Antonova D Molecules 28-Jan-2023
PMCID:PMC9919184
doi:10.3390/molecules28031281
PMID:36770946
Characterization of the Slovene Autochthonous Rose Hybrid Rosa pendulina × spinosissima (Rosa reversa Waldst. and Kit) Using Biochemical Patterns of the Plant Blossoms Kunc N, Hudina M, Bavcon J, Vreš B, Luthar Z, Gostinčar K, Mikulič-Petkovšek M, Osterc G, Ravnjak B Plants (Basel) 22-Jan-2023
PMCID:PMC9920101
doi:10.3390/plants12030505
PMID:36771590
Evaluation of anti-oxidant and antimelanogenic effects of the essential oil and extracts of Rosa × damascena in B16F10 murine melanoma cell line Hadipour E, Rezazadeh Kafash M, Emami SA, Asili J, Boghrati Z, Tayarani-Najaran Z Iran J Basic Med Sci 01-Jan-2023
PMCID:PMC10440142
doi:10.22038/IJBMS.2023.69734.15182
PMID:37605721
Therapeutic Potential of Flavonoids and Tannins in Management of Oral Infectious Diseases—A Review Kováč J, Slobodníková L, Trajčíková E, Rendeková K, Mučaji P, Sychrová A, Bittner Fialová S Molecules 24-Dec-2022
PMCID:PMC9821998
doi:10.3390/molecules28010158
PMID:36615352
Plants as Modulators of Melanogenesis: Role of Extracts, Pure Compounds and Patented Compositions in Therapy of Pigmentation Disorders Merecz-Sadowska A, Sitarek P, Stelmach J, Zajdel K, Kucharska E, Zajdel R Int J Mol Sci 26-Nov-2022
PMCID:PMC9736547
doi:10.3390/ijms232314787
PMID:36499134

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
> Benzenoids / Benzene and substituted derivatives
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1016/0031-9422(88)84095-0
https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Docosane 12405 Click to see CCCCCCCCCCCCCCCCCCCCCC 310.60 unknown https://doi.org/10.1080/10412905.1995.9698472
Heneicosane 12403 Click to see CCCCCCCCCCCCCCCCCCCCC 296.60 unknown https://doi.org/10.1080/10412905.1995.9698472
https://doi.org/10.1002/JSFA.2740640408
Heptacosane 11636 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCC 380.70 unknown https://doi.org/10.1080/10412905.1995.9698472
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown https://doi.org/10.1080/10412905.1995.9698472
Hexacosane 12407 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC 366.70 unknown https://doi.org/10.1080/10412905.1995.9698472
Nonadecane 12401 Click to see CCCCCCCCCCCCCCCCCCC 268.50 unknown https://doi.org/10.1080/10412905.1995.9698472
https://doi.org/10.1002/JSFA.2740640408
Octadecane 11635 Click to see CCCCCCCCCCCCCCCCCC 254.50 unknown https://doi.org/10.1080/10412905.1995.9698472
Tetracosane 12592 Click to see CCCCCCCCCCCCCCCCCCCCCCCC 338.70 unknown https://doi.org/10.1080/10412905.1995.9698472
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown https://doi.org/10.1080/10412905.1995.9698472
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Nonadecene 29075 Click to see CCCCCCCCCCCCCCCCCC=C 266.50 unknown https://doi.org/10.1002/JSFA.2740640408
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(2E,6S)-6-hydroxy-2,6-dimethylocta-2,7-dienoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 11461715 Click to see CC(=CCCC(C)(C=C)O)COC1C(C(C(C(O1)CO)O)O)O 332.39 unknown https://doi.org/10.1021/JF970987X
(2R,3R,4S,5S,6R)-2-[(2Z,6S)-6-hydroxy-2,6-dimethylocta-2,7-dienoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 98789305 Click to see CC(=CCCC(C)(C=C)O)COC1C(C(C(C(O1)CO)O)O)O 332.39 unknown https://doi.org/10.1021/JF970987X
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2R)-4-[(4S)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]butan-2-yl]oxyoxane-3,4,5-triol 52316294 Click to see CC1=C(C(CC(C1)O)(C)C)CCC(C)OC2C(C(C(C(O2)CO)O)O)O 374.50 unknown https://doi.org/10.1021/JF970987X
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(2S)-4-[(4S)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]but-3-yn-2-yl]oxyoxane-3,4,5-triol 163186778 Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(C)OC2C(C(C(C(O2)CO)O)O)O 370.40 unknown https://doi.org/10.1021/JF970987X
2-(6-Hydroxy-2,6-dimethylocta-2,7-dienoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 72970728 Click to see CC(=CCCC(C)(C=C)O)COC1C(C(C(C(O1)CO)O)O)O 332.39 unknown https://doi.org/10.1021/JF970987X
2-(Hydroxymethyl)-6-[4-(4-hydroxy-2,6,6-trimethylcyclohexen-1-yl)butan-2-yloxy]oxane-3,4,5-triol 75614558 Click to see CC1=C(C(CC(C1)O)(C)C)CCC(C)OC2C(C(C(C(O2)CO)O)O)O 374.50 unknown https://doi.org/10.1021/JF970987X
5-Megastigmen-7-yne-3,9-diol 9-glucoside 85258909 Click to see CC1=C(C(CC(C1)O)(C)C)C#CC(C)OC2C(C(C(C(O2)CO)O)O)O 370.40 unknown https://doi.org/10.1021/JF970987X
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellyl acetate 9017 Click to see CC(CCC=C(C)C)CCOC(=O)C 198.30 unknown https://doi.org/10.1080/10412905.1993.9698225
https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1993.9698225
https://doi.org/10.1080/10412905.1995.9698472
https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
Neryl acetate 1549025 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1995.9698472
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3S,5E)-3,7-Dimethyl-5-octene-1,7-diol 10035064 Click to see CC(CCO)CC=CC(C)(C)O 172.26 unknown https://doi.org/10.1021/JF970987X
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
3-Hexen-1-ol 10993 Click to see CCC=CCCO 100.16 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
3,7-Dimethyloct-5-ene-1,7-diol 54416293 Click to see CC(CCO)CC=CC(C)(C)O 172.26 unknown https://doi.org/10.1021/JF970987X
Nonan-1-ol 8914 Click to see CCCCCCCCCO 144.25 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Citronellol 7793 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1007/BF00565540
(2E,6S)-2,6-dimethylocta-2,7-diene-1,6-diol 11206026 Click to see CC(=CCCC(C)(C=C)O)CO 170.25 unknown https://doi.org/10.1021/JF970987X
2,6-Dimethylocta-2,7-diene-1,6-diol 188028 Click to see CC(=CCCC(C)(C=C)O)CO 170.25 unknown https://doi.org/10.1021/JF970987X
3,7-Dimethyl-2,6-octadien-1-al 8843 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.1995.9698472
3,7-Dimethyl-2,6-octadien-1-ol 4458 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1007/BF00565540
3,7-Dimethyl-6-octene-1,3-diol 13665263 Click to see CC(=CCCC(C)(CCO)O)C 172.26 unknown https://doi.org/10.1021/JF970987X
6-Octene-1,3-diol, 3,7-dimethyl-, (3R)- 11805222 Click to see CC(=CCCC(C)(CCO)O)C 172.26 unknown https://doi.org/10.1021/JF970987X
beta-CITRONELLOL, (+/-)- 8842 Click to see CC(CCC=C(C)C)CCO 156.26 unknown https://doi.org/10.1080/10412905.1993.9698225
https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
https://doi.org/10.1002/JSFA.2740640408
https://doi.org/10.1007/BF00565540
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1016/S0031-9422(00)81688-X
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
https://doi.org/10.1080/10412905.1993.9698225
https://doi.org/10.1002/JSFA.2740640408
https://doi.org/10.1007/BF00565540
Linalool, (+)- 67179 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1007/BF00565540
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1007/BF00565540
https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
https://doi.org/10.1080/10412905.1993.9698225
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown https://doi.org/10.1080/10412905.1995.9698472
https://doi.org/10.1016/S0031-9422(00)81688-X
https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1993.9698225
https://doi.org/10.1080/10412905.1995.9698472
https://doi.org/10.1016/S0031-9422(00)81688-X
https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
https://doi.org/10.1002/JSFA.2740640408
https://doi.org/10.1007/BF00565540
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
Carvone, (+/-)- 7439 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(E,Z)-farnesol 1549109 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1080/10412905.1995.9698472
Farnesol 3327 Click to see CC(=CCCC(=CCCC(=CCO)C)C)C 222.37 unknown https://doi.org/10.1080/10412905.1995.9698472
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(S)-4-[(4R)-2,6,6-Trimethyl-4beta-(beta-D-glucopyranosyloxy)-1-cyclohexenyl]-2-butanol 10904843 Click to see CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)CCC(C)O 374.50 unknown https://doi.org/10.1021/JF970987X
2-(8-Hydroxy-3,7-dimethylocta-2,6-dienoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 72738565 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)CCC=C(C)CO 332.39 unknown https://doi.org/10.1021/JF970987X
3,7-Dimethyl-8-hydroxy-2,6-octadienyl beta-D-glucopyranoside 14729929 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)CCC=C(C)CO 332.39 unknown https://doi.org/10.1021/JF970987X
Tsangane L 3-glucoside 73981648 Click to see CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)CCC(C)O 374.50 unknown https://doi.org/10.1021/JF970987X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
1,3,4,5-Tetrahydroxycyclohexanecarboxylic acid 1064 Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O 192.17 unknown https://doi.org/10.1006/BBRC.1996.1759
Quinic acid 6508 Click to see C1C(C(C(CC1(C(=O)O)O)O)O)O 192.17 unknown https://doi.org/10.1006/BBRC.1996.1759
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(Hydroxymethyl)-6-phenylmethoxyoxane-3,4,5-triol 4984739 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1021/JF970987X
2-phenylethyl beta-D-glucopyranoside 468284 Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O 284.30 unknown https://doi.org/10.1007/BF00568490
https://doi.org/10.1021/JF970987X
Benzyl beta-d-glucopyranoside 188977 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1021/JF970987X
Phenethyl beta-D-galactopyranoside 84675 Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O 284.30 unknown https://doi.org/10.1021/JF970987X
Phenylethyl beta-D-glucopyranoside 11289099 Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O 284.30 unknown https://doi.org/10.1007/BF00568490
https://doi.org/10.1021/JF970987X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Valeraldehyde 8063 Click to see CCCCC=O 86.13 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
Decanal 8175 Click to see CCCCCCCCCC=O 156.26 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
Heptanal 8130 Click to see CCCCCCC=O 114.19 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
Damascenone 5366074 Click to see CC=CC(=O)C1=C(C=CCC1(C)C)C 190.28 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
9-Hentriacontanone 129820665 Click to see CCCCCCCCCCCCCCCCCCCCCCC(=O)CCCCCCCC 450.80 unknown https://doi.org/10.1016/S0031-9422(00)86320-7
> Organoheterocyclic compounds / Heteroaromatic compounds
3-(4-Methylpent-3-enyl)thiophene 566107 Click to see CC(=CCCC1=CSC=C1)C 166.29 unknown https://doi.org/10.1271/BBB1961.51.3421
> Organoheterocyclic compounds / Oxanes
Rose oxide 27866 Click to see CC1CCOC(C1)C=C(C)C 154.25 unknown https://doi.org/10.1080/10412905.1993.9698225
https://doi.org/10.1080/10412905.1995.9698472
https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
trans-Rose oxide 7093102 Click to see CC1CCOC(C1)C=C(C)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9698472
https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
> Phenylpropanoids and polyketides / Cinnamaldehydes
3-Phenyl-propenal 307 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
Cinnamaldehyde 637511 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown https://doi.org/10.1111/J.1600-0536.1991.TB01726.X
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1006/BBRC.1996.1759
https://doi.org/10.1007/BF00579444
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/10.1006/BBRC.1996.1759
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
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/10.1007/BF00563465
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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/10.1021/JF00003A007
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one 5317364 Click to see C1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 436.40 unknown https://doi.org/10.1021/JF00003A007
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/10.1021/JF903515F
3-[(2R,3S,4S,5S)-3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 163001527 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)OC5C(C(C(C(O5)CO)O)O)O 580.50 unknown https://doi.org/10.1021/JF903515F
3-[3,4-Dihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 75058672 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)OC5C(C(C(C(O5)CO)O)O)O 580.50 unknown https://doi.org/10.1021/JF903515F
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/BF00579444
Afzelin 5316673 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 432.40 unknown https://doi.org/10.1021/JF903515F
https://doi.org/10.1007/BF00563465
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/10.1006/BBRC.1996.1759
https://doi.org/10.1007/BF00579444
https://doi.org/10.1007/BF00563465
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/10.1021/JF903515F
Juglanin 5318717 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O 418.30 unknown https://doi.org/10.1021/JF00003A007
https://doi.org/10.1007/BF00563465
Kaempferol-3-O-rhamnoside 5835713 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 432.40 unknown https://doi.org/10.1021/JF903515F
Quercetin 3-gentiobioside 5320834 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O 626.50 unknown https://doi.org/10.1021/JF903515F
Quercetin-3-gentiobioside 13915961 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O 626.50 unknown https://doi.org/10.1021/JF903515F
Trifolin 5282149 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/BF00563465
https://doi.org/10.1007/BF00579444
> 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/10.1006/BBRC.1996.1759
kaempferol 7-O-glucoside 10095180 Click to see C1=CC(=CC=C1C2=C(C(=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/10.1006/BBRC.1996.1759
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/10.1006/BBRC.1996.1759
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(3,4,5,11,12,21,22,23-Octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl) 3,4,5-trihydroxybenzoate 13917511 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1007/S11418-010-0402-0
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate 5153915 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1007/S11418-010-0402-0
[3,4,5,21,22,23-Hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 3,4,5-trihydroxy-2-[[3,4,5,22,23-pentahydroxy-8,18-dioxo-11,12,13-tris[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]benzoate 16130312 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C(C(C(O6)OC(=O)C7=CC(=C(C(=C7)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1875.30 unknown https://doi.org/10.1007/S11418-010-0402-0
1-Desgalloyleugeniin 9918701 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1007/S11418-010-0402-0
1-O-Galloylpedunculagin 452242 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 936.60 unknown https://doi.org/10.1007/S11418-010-0402-0
3,4,5-Trihydroxy-2-[(5,7,12,13,14-pentahydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(14),4(16),5,7,11(15),12-hexaen-6-yl)oxy]benzoic acid 162944385 Click to see C1=C(C(=C(C(=C1O)O)O)OC2=C(C3=C4C5=C(C(=C(C(=C5OC3=O)O)O)O)C(=O)OC4=C2O)O)C(=O)O 502.30 unknown https://doi.org/10.1007/S11418-010-0402-0
Casuarictin 73644 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 936.60 unknown https://doi.org/10.1007/S11418-010-0402-0
CID 16170073 16170073 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)O)O)O)O)O)O)O)O)O 1106.80 unknown https://doi.org/10.1007/S11418-010-0402-0
Eugeniin 442679 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown https://doi.org/10.1007/S11418-010-0402-0
Isostrictinin 13917513 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1007/S11418-010-0402-0
Rugosin A 16132354 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)O)O)O)O)O)O)O)O)O 1106.80 unknown https://doi.org/10.1007/S11418-010-0402-0
Rugosin D 16129626 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C(C(C(O6)OC(=O)C7=CC(=C(C(=C7)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1875.30 unknown https://doi.org/10.1007/S11418-010-0402-0
Sanguiin H4 13917512 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1007/S11418-010-0402-0
Strictinin 73330 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1007/S11418-010-0402-0
Tellimagrandin II 151590 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown https://doi.org/10.1007/S11418-010-0402-0

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