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Scopolia carniolica

Scopolia carniolica - 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 UUID64404177a9d72368216871
Scientific name Scopolia carniolica
Authority Jacq.
First published in Observ. Bot.. 1: 32. t. 20. 1764.

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Scopolia carniolica var. hladnikiana (Frey ex W.D.J.Koch) Nyman
Scopolia hladnikiana Fleischm. ex Nyman Consp. Fl. Eur. 3: 524. 1881 [prob. Jul 1881]
Scopolia trichotoma Moench Methodus (Moench) 462. 1794 [4 May 1794]
Scopolia tubiflora Kreyer Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 12: 268. 1950
Scopolina atropoides Schult. Öster. Fl., ed. 2, 1: 383. 1814
Scopolina carniolica (Jacq.) Schur Enum. Pl. Transsilv. 479. 1866 [Apr-Jun 1866]
Scopolina hladnikiana Frey ex W.D.J.Koch Syn. Fl. Germ. Helv., ed. 2. 585. 1844

Common names Top

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Language Common/alternative name
English european scopolia
Spanish hyoscyamus chloranthus
Spanish scopolina atropoides
Spanish scopolina carniolica
Spanish scopolina hladnikiana
Spanish scopolina viridiflora
Azerbaijani karniol skopoliyası
azb کارنیول سکوپولیاسی
Czech pablen kraňský
German krainer tollkraut
German hyoscyamus scopolia
Finnish skopolia
Finnish euroopanskopolia
Croatian kranjski bijeli bun
Hungarian krajnai farkasbogyó
Icelandic flagðjurt
Georgian კავკასიური სკოპოლია
Norwegian Bokmål galnebær
Polish lulecznica kraińska
Slovak skopólia kranská
Slovenian kranjska bunika
Slovenian mala norica
Slovenian kranjski volčič
Serbian Бели бун
Swedish gul dårört
Swedish dårört
Swedish hyoscyamus scopolia
Ukrainian Скополія карніолійська

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Eastern Europe
      • Baltic States
      • Ukraine
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Hungary
      • Poland
    • Northern Europe
      • Denmark
    • Southeastern Europe
      • Italy
      • Romania
      • Yugoslavia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001025508
UNII XR0I456H79
Canadensys 9375
USDA Plants SCCA6
Tropicos 29604569
Flora of Italy 4698
KEW urn:lsid:ipni.org:names:817996-1
The Plant List kew-2579708
Open Tree Of Life 595763
Observations.org 104716
NCBI Taxonomy 258457
NBN Atlas NBNSYS0000034409
Nature Serve 2.138448
IPNI 817996-1
iNaturalist 168691
GBIF 5341850
Freebase /m/0cmcfb0
EPPO SLJCA
EOL 485031
USDA GRIN 400328
Wikipedia Scopolia_carniolica
CMAUP NPO10384
CMAUP NPO7625

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
Hairy root culture: a potent method for improved secondary metabolite production of Solanaceous plants Biswas D, Chakraborty A, Mukherjee S, Ghosh B Front Plant Sci 04-Sep-2023
PMCID:PMC10507345
doi:10.3389/fpls.2023.1197555
PMID:37731987
From Plants to Psycho-Neurology: Unravelling the Therapeutic Benefits of Bioactive Compounds in Brain Disorders Grosso C, Santos M, Barroso MF Antioxidants (Basel) 11-Aug-2023
PMCID:PMC10451187
doi:10.3390/antiox12081603
PMID:37627598
Response Surface Optimization of Extraction Conditions for the Active Components with High Acetylcholinesterase Inhibitory Activity and Identification of Key Metabolites from Acer truncatum Seed Oil Residue Meng R, Ou K, Chen L, Jiao Y, Jiang F, Gu R Foods 23-Apr-2023
PMCID:PMC10177952
doi:10.3390/foods12091751
PMID:37174291
Natural Coumarin Derivatives Activating Nrf2 Signaling Pathway as Lead Compounds for the Design and Synthesis of Intestinal Anti-Inflammatory Drugs Di Stasi LC Pharmaceuticals (Basel) 30-Mar-2023
PMCID:PMC10142712
doi:10.3390/ph16040511
PMID:37111267
Natural Inhibitors of Cholinesterases: Chemistry, Structure–Activity and Methods of Their Analysis Smyrska-Wieleba N, Mroczek T Int J Mol Sci 01-Feb-2023
PMCID:PMC9916849
doi:10.3390/ijms24032722
PMID:36769043
Phytogeographic Characteristics of Montane Coniferous Forests of the Central Balkan Peninsula (SE Europe) Ilić T, Kuzmanović N, Vukojičić S, Lakušić D Plants (Basel) 22-Nov-2022
PMCID:PMC9741231
doi:10.3390/plants11233194
PMID:36501234
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
Natural compounds as safe therapeutic options for ulcerative colitis Gupta M, Mishra V, Gulati M, Kapoor B, Kaur A, Gupta R, Tambuwala MM Inflammopharmacology 25-Feb-2022
PMCID:PMC8948151
doi:10.1007/s10787-022-00931-1
PMID:35212849
Pipes and Potions: Testing the Efficacy of European Folk Preparation Methods for Anticholinergic Solanaceae Plants Fatur K, Ravnikar M, Fras V, Kreft S Plants (Basel) 04-Jan-2022
PMCID:PMC8747641
doi:10.3390/plants11010126
PMID:35009129
Scopolia carniolica var. hladnikiana: Alkaloidal Analysis and Potential Taxonomical Implications Fatur K, Ravnikar M, Kreft S Plants (Basel) 10-Aug-2021
PMCID:PMC8401577
doi:10.3390/plants10081643
PMID:34451686
Nixing the nightshades: Traditional knowledge of intoxicating members of the Solanaceae among hallucinogenic plant and mushroom users in Slovenia Fatur K, Kreft S PLoS One 22-Feb-2021
PMCID:PMC7899348
doi:10.1371/journal.pone.0247688
PMID:33617573
Fungal Endophytes as Efficient Sources of Plant-Derived Bioactive Compounds and Their Prospective Applications in Natural Product Drug Discovery: Insights, Avenues, and Challenges Singh A, Singh DK, Kharwar RN, White JF, Gond SK Microorganisms 19-Jan-2021
PMCID:PMC7833388
doi:10.3390/microorganisms9010197
PMID:33477910
Peculiar plants and fantastic fungi: An ethnobotanical study of the use of hallucinogenic plants and mushrooms in Slovenia Fatur K PLoS One 07-Jan-2021
PMCID:PMC7790546
doi:10.1371/journal.pone.0245022
PMID:33412556
Coumarin derivatives as acetyl- and butyrylcholinestrase inhibitors: An in vitro, molecular docking, and molecular dynamics simulations study Abu-Aisheh MN, Al-Aboudi A, Mustafa MS, El-Abadelah MM, Ali SY, Ul-Haq Z, Mubarak MS Heliyon 28-Apr-2019
PMCID:PMC6488543
doi:10.1016/j.heliyon.2019.e01552
PMID:31183424
Scopolin ameliorates high-fat diet induced hepatic steatosis in mice: potential involvement of SIRT1-mediated signaling cascades in the liver Yoo A, Narayan VP, Hong EY, Whang WK, Park T Sci Rep 22-May-2017
PMCID:PMC5440403
doi:10.1038/s41598-017-02416-6
PMID:28533555

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
Cuscohygrine 1201543 Click to see CN1CCCC1CC(=O)CC2CCCN2C 224.34 unknown https://doi.org/10.1002/JPS.2600551039
Cuskhygrine 441070 Click to see CN1CCCC1CC(=O)CC2CCCN2C 224.34 unknown https://doi.org/10.1002/JPS.2600551039
> Alkaloids and derivatives / Tropane alkaloids
(+)-Hyoscyamine 637577 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown via CMAUP database
(1R,2S,3R,4R)-8-azabicyclo[3.2.1]octane-1,2,3,4-tetrol 45109805 Click to see C1CC2(C(C(C(C1N2)O)O)O)O 175.18 unknown via CMAUP database
Atropine 174174 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1002/JPS.2600551039
Atropine sulfate 3661 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1002/ARDP.18902280209
https://doi.org/10.1002/ARDP.18902280904
https://doi.org/10.1002/ARDP.18882260504
Benzeneacetic acid, alpha-(hydroxymethyl)-, 8-methyl-8-azabicyclo(3.2.1)oct-3-yl ester, (3(R)-endo)- 25817 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown via CMAUP database
Calystegine B4 10559162 Click to see C1CC2(C(C(C(C1N2)O)O)O)O 175.18 unknown via CMAUP database
Hyoscyamine 154417 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1002/JPS.2600551039
L-Hyoscyamine 64692 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown via CMAUP database
Levsin 5318386 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown via CMAUP database
Pseudotropine 8424 Click to see CN1C2CCC1CC(C2)O 141.21 unknown https://doi.org/10.1002/JPS.2600551039
https://doi.org/10.1002/JPS.2600551039
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
3-Galloylshikimic acid 10449030 Click to see C1C(C(C(C=C1C(=O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)O)O 326.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4R,4aS,6aR,6bS,8S,8aR,12aS,14aS,14bS)-8a-[(2R,3S,4R,5S)-3-[(2R,3S,4S,5S,6S)-5-acetyloxy-3-hydroxy-6-methyl-4-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxycarbonyl-2,8-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 162963026 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC(=O)C34CCC(CC3C5=CCC6C(C5(CC4O)C)(CCC7C6(CC(C(C7(C)C(=O)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)(C)C)O)O)O)OC9C(C(C(CO9)O)O)O)OC(=O)C 1133.20 unknown https://doi.org/10.1002/JPS.2600551039
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(-)-Scopolamine 5184 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown https://doi.org/10.1002/ARDP.18902280904
(+)-Scopolamine 673473 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown via CMAUP database
[(1R,2S,4S,5S)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl] (2S)-3-hydroxy-2-phenylpropanoate 11968014 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown via CMAUP database
6-beta,7-beta-Epoxy-3-alpha-tropanyl S-(-)-tropate 6432494 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown via CMAUP database
Atroscine 452977 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown via CMAUP database
Isoptpo Hyoscine 5284456 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown via CMAUP database
Scopalamine 6451257 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown via CMAUP database
Scopolamine 3000322 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown via CMAUP database
Sdccgsbi-0051046.P002 2723877 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown via CMAUP database
Transderm-V 5809 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown via CMAUP database
Tropic acid ester with scopine 153311 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown https://doi.org/10.1002/ARDP.18902280904
https://doi.org/10.1002/JPS.2600551039
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
1alpha,3beta-Dihydroxy-4alpha,5alpha-bis(galloyloxy)cyclohexanecarboxylic acid 13270012 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O 496.40 unknown via CMAUP database
3,4-Di-O-galloylquinic acid 460895 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O 496.40 unknown via CMAUP database
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
cis-Chlorogenic acid 1794425 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
Nigericin 34230 Click to see CC1CCC(OC1C(C)C(=O)O)CC2CC(C(C3(O2)C(CC(O3)(C)C4CCC(O4)(C)C5C(CC(O5)C6C(CC(C(O6)(CO)O)C)C)C)C)C)OC 725.00 unknown https://doi.org/10.1002/ARDP.18882260504
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Fabiatrin 10994544 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O 486.40 unknown via CMAUP database
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Procyanidin B3 146798 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin C2 11182062 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown via CMAUP database
Procyanidin tetramer 101228664 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C(C(=CC(=C56)O)O)C7C(C(OC8=CC(=CC(=C78)O)O)C9=CC(=C(C=C9)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1155.00 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Leucocianidol 440833 Click to see C1=CC(=C(C=C1C2C(C(C3=C(C=C(C=C3O2)O)O)O)O)O)O 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Gallocatechin 9882981 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Delphinidin 3-O-glucoside cation 443650 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 465.40 unknown via CMAUP database
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
3',5'-Dimethoxy-4',7-dihydroxy-5-(beta-D-glucopyranosyloxy)-3-[(6-O-acetyl-beta-D-glucopyranosyl)oxy]flavylium 101918997 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C([O+]=C3C=C(C=C(C3=C2)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC(=C(C(=C5)OC)O)OC)O)O)O 697.60 unknown via CMAUP database
Cyanin 441688 Click to see C1=CC(=C(C=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 611.50 unknown via CMAUP database
Malvidin-3,5-diglucoside 441765 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 655.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl]Oxy-Chromen-4-one 12304323 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 via CMAUP database
Hyperoside 5281643 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 via CMAUP database
kaempferol 3-O-beta-L-glucopyranoside 9911508 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 via CMAUP database
Quercetin 3-O-(6''-galloyl)-beta-D-galactopyranoside 5491814 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O 616.50 unknown via CMAUP database
Quercetin 3-O-(6''-galloyl)-beta-D-glucopyranoside 9830456 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O 616.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(4-Hydroxyphenyl)-5-hydroxy-3-(2-O-beta-D-glucopyranosyl-beta-D-galactopyranosyloxy)-7-(beta-D-glucopyranosyloxy)-4H-1-benzopyran-4-one 12960461 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)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)O 772.70 unknown via CMAUP database
3-[(2R,3S,4S,5S)-3,4-dihydroxy-5-[(1S)-1-hydroxyethyl]oxolan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 162890784 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(O4)C(C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown https://doi.org/10.1002/JPS.2600551039
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
(1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylic acid 102004656 Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)O 292.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
(2R,3R,4S,5R,6R)-6-(((3,4,5-Trihydroxybenzoyl)oxy)methyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetrakis(3,4,5-trihydroxybenzoate) 9876301 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(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(=C6)O)O)O 940.70 unknown via CMAUP database
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database
NP-003686 73178 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(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)O 788.60 unknown via CMAUP database
Pentagalloylglucose 65238 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(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(=C6)O)O)O 940.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
1,2-Di-O-galloyl-4,6-O-(S)-hexahydroxydiphenoyl-beta-D-glucopyranose 101259865 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)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown via CMAUP database
3-O-digalloyl-1,2,4,6-tetra-O-beta-D-galloylglucose 16164119 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(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)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 1092.80 unknown via CMAUP database
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown via CMAUP database
Geraniin 3001497 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 952.60 unknown via CMAUP database
Xcxwmhrrisfuff-xngpzlstsa- 21636130 Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C9C(C(COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O9)O)O)O)O)O)O)OC8OC(=O)C1=CC(=C(C(=C1)O)O)O)OC5=O)O)O)O)O)O)O 1110.80 unknown via CMAUP database

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