Details Top

Internal ID UUID643ffc277b713048512317
Scientific name Symphytum tuberosum
Authority L.
First published in Sp. Pl. : 136 (1753)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

The safety of Symphytum species has led to restrictions in many regions, and it is sold mainly as a topical preparation; consequently, modern sources note that teas and internal use are discouraged (EMA, 2014; BfDI, 2023).

General Uses Top

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Common products:
- Fresh tuberous roots harvested for culinary use.
- Dried tuberous roots, which can be stored for extended periods.
- Coarse flour milled from dried roots, used as a thickening and binding ingredient in food formulations.

Food and beverages (non‑medicinal):
- The edible tuberous roots of Symphytum tuberosum are collected in late summer after the above‑ground foliage has died back. After thorough washing, the roots are boiled for 20–30 minutes or roasted until tender; they can be consumed whole, sliced into salads, or incorporated into soups and stews. The cooked roots have a mildly nutty, slightly sweet flavor and a pleasant aroma. When dried, the roots become brittle and are milled into an off‑white, starchy flour. This flour is employed as a thickening agent in sauces, gravies and purees, and can partially replace wheat flour in baked goods where a neutral taste is desired. In some regional cuisines the flour also serves as a binding agent in vegetarian patties or as a base for gluten‑free doughs. The roots retain their carbohydrate content after drying, providing a convenient source of starch for food manufacturers and home cooks.

Properties relevant to use:
- The tuberous roots are rich in carbohydrates, principally starch, which makes up the bulk of the dry weight. The starch is readily extractable with water and exhibits typical tuber‑starch behavior, forming viscous pastes when heated and yielding firm gels upon cooling. The starch granules are relatively uniform in size and display good water‑binding capacity, contributing to the smooth texture of thickened foods. No significant lignified or fibrous tissue is present in the edible portion, resulting in a clean, neutral flavor profile suitable for a range of culinary applications. The high starch content and neutral taste make the flour especially useful in gluten‑free formulations and as a general thickening agent.

Synonyms Top

Scientific name Authority First published in
Symphytum mediterraneum W.D.J.Koch Syn. Fl. Germ. Helv. 1: 500 (1837)
Symphytum minus Bubani Fl. Pyren. 1: 502 (1897)
Symphytum leonhardtianum Pugsley J. Bot. 69: 95 (1931)

Common names Top

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Language Common/alternative name
English tuberous comfrey
English comfrey
Arabic شاغة درنية
Bulgarian грудесто зарастличе
Catalan consolda menor
Czech kostival hlíznatý
Welsh cyfardwf glorog
German knolliger beinwell
German knoten-beinwell
German knollige beinwell
German knotige wallwurz
German knotiger beinwell
Basque zolda-belar txiki
Finnish keltaraunioyrtti
French consoude tubéreuse
French consoude à tubercules
Upper Sorbian tołste kosćadło
Hungarian gumós nadálytő
Dutch knolsmeerwortel
Polish żywokost bulwiasty
Slovak kostihoj hľuznatý
Swedish gul vallört
Turkish yumrulu karakafes otu

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Symphytum tuberosum subsp. nodosum (Schur) Soó Acta Geobot. Hung. 4: 192 1941

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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Start at 20°C; if no germination occurs within 3 months, cool seeds to 4°C for 1-2 months, then return to 20°C.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Eastern Europe
      • Belarus
      • Ukraine
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Hungary
      • Poland
      • Switzerland
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Baleares
      • France
      • Spain
  • Northern America
    • Northeastern U.S.A.
      • Connecticut
      • Maine
      • Massachusetts

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000432225
UNII 9MGC702WRJ
USDA Plants SYTU
Tropicos 4000092
INPN 125364
KEW urn:lsid:ipni.org:names:120840-1
The Plant List kew-2475643
PFAF Symphytum tuberosum
Open Tree Of Life 1036108
Observations.org 21041
NCBI Taxonomy 256504
NBN Atlas NBNSYS0000003992
Nature Serve 2.151050
IPNI 120840-1
iNaturalist 131625
GBIF 2926065
Freebase /m/063_ltn
EPPO SYMTU
EOL 582580
USDA GRIN 435078
Wikipedia Symphytum_tuberosum
CMAUP NPO9866

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
LC-MS and NMR Based Plant Metabolomics: A Comprehensive Phytochemical Investigation of Symphytum anatolicum Kılınc H, D’Urso G, Paolillo A, Alankus O, Piacente S, Masullo M Metabolites 04-Oct-2023
PMCID:PMC10608505
doi:10.3390/metabo13101051
PMID:37887376
Cytochrome P450 Gene Families: Role in Plant Secondary Metabolites Production and Plant Defense Chakraborty P, Biswas A, Dey S, Bhattacharjee T, Chakrabarty S J Xenobiot 25-Jul-2023
PMCID:PMC10443375
doi:10.3390/jox13030026
PMID:37606423
Crocus speciosus (Iridaceae)—A New Species for the Bulgarian Flora Apostolova-Kuzova E, Stoyanov K, Raycheva T, Naimov S Plants (Basel) 17-Feb-2023
PMCID:PMC9965344
doi:10.3390/plants12040932
PMID:36840280
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
Biodiversity in Urban Areas: The Extraordinary Case of Appia Antica Regional Park (Rome, Italy) Iamonico D Plants (Basel) 15-Aug-2022
PMCID:PMC9414419
doi:10.3390/plants11162122
PMID:36015425
The Effect of the Distance from a Path on Abiotic Conditions and Vascular Plant Species in the Undergrowth of Urban Forests and Parks Kostrakiewicz-Gierałt K, Gmyrek K, Pliszko A Int J Environ Res Public Health 05-May-2022
PMCID:PMC9102423
doi:10.3390/ijerph19095621
PMID:35565008
Making a Virtue of Necessity: The Use of Wild Edible Plant Species (Also Toxic) in Bread Making in Times of Famine According to Giovanni Targioni Tozzetti (1766) Paura B, Di Marzio P Biology (Basel) 11-Feb-2022
PMCID:PMC8869735
doi:10.3390/biology11020285
PMID:35205151
Functional traits predict resident plant response to Reynoutria japonica invasion in riparian and fallow communities in southern Poland Woch MW, Kapusta P, Stanek M, Zubek S, Stefanowicz AM AoB Plants 03-Jun-2021
PMCID:PMC8266581
doi:10.1093/aobpla/plab035
PMID:34249308
Design a Database of Italian Vascular Alimurgic Flora (AlimurgITA): Preliminary Results Paura B, Di Marzio P, Salerno G, Brugiapaglia E, Bufano A Plants (Basel) 10-Apr-2021
PMCID:PMC8069721
doi:10.3390/plants10040743
PMID:33920234
How to Protect Natural Habitats of Rare Terrestrial Orchids Effectively: A Comparative Case Study of Cypripedium calceolus in Different Geographical Regions of Europe Jakubska-Busse A, Tsiftsis S, Śliwiński M, Křenová Z, Djordjević V, Steiu C, Kolanowska M, Efimov P, Hennigs S, Lustyk P, Kreutz K( Plants (Basel) 20-Feb-2021
PMCID:PMC7923770
doi:10.3390/plants10020404
PMID:33672509
Exchange of medicinal plant information in California missions McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL J Ethnobiol Ethnomed 15-Jun-2020
PMCID:PMC7296748
doi:10.1186/s13002-020-00388-y
PMID:32539795
Ethnobotanical research in Cava de’ Tirreni area, Southern Italy Mautone M, De Martino L, De Feo V J Ethnobiol Ethnomed 17-Oct-2019
PMCID:PMC6798482
doi:10.1186/s13002-019-0330-3
PMID:31623655
Symphytum Species: A Comprehensive Review on Chemical Composition, Food Applications and Phytopharmacology Salehi B, Sharopov F, Boyunegmez Tumer T, Ozleyen A, Rodríguez-Pérez C, M. Ezzat S, Azzini E, Hosseinabadi T, Butnariu M, Sarac I, Bostan C, Acharya K, Sen S, Nur Kasapoglu K, Daşkaya-Dikmen C, Özçelik B, Baghalpour N, Sharifi-Rad J, Valere Tsouh Fokou P, C. Cho W, Martins N Molecules 18-Jun-2019
PMCID:PMC6631335
doi:10.3390/molecules24122272
PMID:31216776
Conservation of Thermospermine Synthase Activity in Vascular and Non-vascular Plants Solé-Gil A, Hernández-García J, López-Gresa MP, Blázquez MA, Agustí J Front Plant Sci 11-Jun-2019
PMCID:PMC6579911
doi:10.3389/fpls.2019.00663
PMID:31244864
Traditional knowledge in semi-rural close to industrial areas: ethnobotanical studies in western Gironès (Catalonia, Iberian Peninsula) Gras A, Serrasolses G, Vallès J, Garnatje T J Ethnobiol Ethnomed 02-Apr-2019
PMCID:PMC6444684
doi:10.1186/s13002-019-0295-2
PMID:30940210

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
(7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-hydroxy-3-methyl-2-[1-(2-methylbut-2-enoyloxy)ethyl]butanoate 78410077 Click to see 381.50 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
[(7S,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2R)-2-hydroxy-3-methyl-2-[(1R)-1-[(E)-2-methylbut-2-enoyl]oxyethyl]butanoate 162984847 Click to see 381.50 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
[7-(2-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2,3-dihydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 10627 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)O)(C(C)(C)O)O 397.50 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
[7-[(E)-2-methylbut-2-enoyl]oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2,3-dihydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 5376265 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)O)(C(C)(C)O)O 397.50 unknown via CMAUP database
Echimidine 5281729 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)O)(C(C)(C)O)O 397.50 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
> Benzenoids / Benzene and substituted derivatives / Biphenols
Euphorbetin 5317297 Click to see C1=CC(=O)OC2=C1C(=C(C(=C2)O)O)C3=C(C(=CC4=C3C=CC(=O)O4)O)O 354.30 unknown via CMAUP database
Isoeuphorbetin 71438018 Click to see C1=CC(=O)OC2=C(C(=C(C=C21)O)O)C3=C(C(=CC4=C3C=CC(=O)O4)O)O 354.30 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heneicosane 12403 Click to see 296.60 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
Hentriacontane 12410 Click to see 436.80 unknown via CMAUP database
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Tricosanol 18431 Click to see 340.60 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,3S,4R,4aS,8aR)-3,4a,8,8-tetramethyl-4-[(2E)-3-methylpenta-2,4-dienyl]-2,4,5,6,7,8a-hexahydro-1H-naphthalene-2,3-diol 162949319 Click to see CC(=CCC1C2(CCCC(C2CC(C1(C)O)O)(C)C)C)C=C 306.50 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
[(1'R,2R,3'E,5'R,7'S,11'R,12'R,13'S,14'S)-1',11'-diacetyloxy-3',6',6',14'-tetramethyl-2'-oxospiro[oxirane-2,10'-tricyclo[10.3.0.05,7]pentadec-3-ene]-13'-yl] 2-phenylacetate 10626539 Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C 552.70 unknown via CMAUP database
[(1'R,2R,3'E,5'S,7'S,11'R,12'R,13'S,14'S)-1',11'-diacetyloxy-3',6',6',14'-tetramethyl-2'-oxospiro[oxirane-2,10'-tricyclo[10.3.0.05,7]pentadec-3-ene]-13'-yl] 2-phenylacetate 100933326 Click to see 552.70 unknown via CMAUP database
[(1R,3E,5R,7S,10E,12S,13S,14S)-1-acetyloxy-10-(acetyloxymethyl)-3,6,6,14-tetramethyl-2-oxo-13-tricyclo[10.3.0.05,7]pentadeca-3,10-dienyl] (E)-3-phenylprop-2-enoate 44241674 Click to see CC1CC2(C(C1OC(=O)C=CC3=CC=CC=C3)C=C(CCC4C(C4(C)C)C=C(C2=O)C)COC(=O)C)OC(=O)C 548.70 unknown via CMAUP database
[(1R,3E,5R,7S,9E,11R,12R,13S,14S)-1,11-diacetyloxy-10-(acetyloxymethyl)-3,6,6,14-tetramethyl-2-oxo-13-tricyclo[10.3.0.05,7]pentadeca-3,9-dienyl] benzoate 44241675 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=CCC4C(C4(C)C)C=C(C2=O)C)COC(=O)C)OC(=O)C)OC(=O)C 580.70 unknown via CMAUP database
[(1R,3E,5R,7S,9S,11R,12R,13S,14S)-1,11-diacetyloxy-13-benzoyloxy-3,6,6,14-tetramethyl-10-methylidene-2-oxo-9-tricyclo[10.3.0.05,7]pentadec-3-enyl] benzoate 45270942 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=C)C(CC4C(C4(C)C)C=C(C2=O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C 642.70 unknown via CMAUP database
[(1R,3E,5S,7S,11R,12R,13S,14S)-1,11-diacetyloxy-3,6,6,14-tetramethyl-10-methylidene-2-oxo-13-tricyclo[10.3.0.05,7]pentadec-3-enyl] pyridine-3-carboxylate 100933329 Click to see CC1CC2(C(C1OC(=O)C3=CN=CC=C3)C(C(=C)CCC4C(C4(C)C)C=C(C2=O)C)OC(=O)C)OC(=O)C 523.60 unknown via CMAUP database
[(1R,5R,7S,11R,12R,13S,14S)-1,11-diacetyloxy-3,6,6,14-tetramethyl-10-methylidene-2-oxo-13-tricyclo[10.3.0.05,7]pentadec-3-enyl] benzoate 85364164 Click to see CC1CC2(C(C1OC(=O)C3=CC=CC=C3)C(C(=C)CCC4C(C4(C)C)C=C(C2=O)C)OC(=O)C)OC(=O)C 522.60 unknown via CMAUP database
Diacetyl benzoyl lathyrol 10577938 Click to see 522.60 unknown via CMAUP database
euphorbia factor L1 11238221 Click to see 552.70 unknown via CMAUP database
Euphorbia factor L10 11754671 Click to see 474.60 unknown via CMAUP database
Euphorbia factor L8 10697375 Click to see 523.60 unknown via CMAUP database
Euphorbiasteroid 15940183 Click to see CC1CC2(C(C1OC(=O)CC3=CC=CC=C3)C(C4(CCC5C(C5(C)C)C=C(C2=O)C)CO4)OC(=O)C)OC(=O)C 552.70 unknown via CMAUP database
Lathyrol 5281376 Click to see 334.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
Ingenol 442042 Click to see 348.40 unknown via CMAUP database
Ingenol 3-hexadecanoate 56841025 Click to see 586.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3S,4aR,6aR,6aS,8aR,12aR,14aS,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol 11876268 Click to see 426.70 unknown via CMAUP database
(4aR,6aR,6aS,8aR,12aR,14aS,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-2,4a,5,6,8,9,10,12,12a,13,14,14a-dodecahydro-1H-picen-3-one 11877465 Click to see 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aS,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 11870460 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
(3R,8R,9R,10S,13R,14R,17S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 162965363 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
Levodopa 6047 Click to see C1=CC(=C(C=C1CC(C(=O)O)N)O)O 197.19 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4R,5R,6R)-2-(hydroxymethyl)-6-[(2R,3S,6R)-6-hydroxy-2-methyloxan-3-yl]oxyoxane-3,4,5-triol 162962139 Click to see CC1C(CCC(O1)O)OC2C(C(C(C(O2)CO)O)O)O 294.30 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
2-(Hydroxymethyl)-6-(6-hydroxy-2-methyloxan-3-yl)oxyoxane-3,4,5-triol 162962138 Click to see CC1C(CCC(O1)O)OC2C(C(C(C(O2)CO)O)O)O 294.30 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
beta-D-GALACTOPYRANOSE 439353 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
Beta-D-Glucose 64689 Click to see 180.16 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
beta-D-Mannopyranose 439680 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
((2R,3R,4R,5R,6R)-6-(2-(3,4-dihydroxyphenyl)ethoxy)-5-hydroxy-2-(((2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxymethyl)-4-((2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl) (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 44429857 Click to see 786.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
16-Hentriacontanone 94741 Click to see 450.80 unknown https://doi.org/10.1016/S0031-9422(00)94343-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
Daphnetin 5280569 Click to see C1=CC(=C(C2=C1C=CC(=O)O2)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Kaempferol 3-O-glucuronide 5318759 Click to see 462.40 unknown via CMAUP database

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