Details Top

Internal ID UUID64400de9ea475821987124
Scientific name Bryonia alba
Authority L.
First published in Sp. Pl. : 1012 (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.

Bryonia alba, the white bryony, has a long history of use in European folk medicine, especially in the Russian Federation, Poland, and Germany. Among the Russian people, the dried root is boiled into a decoction that is taken for rheumatic pain and gout; Karpov et al. (2010) report that the root is simmered for 30 minutes and the liquid is drunk in small cups twice daily. In Poland, a similar root decoction is prescribed for urinary tract infections and bladder irritation; Kowalski (2015) documents that 10 g of powdered root are steeped in 500 ml of water for 20 minutes, then filtered and consumed as a mild tonic. German traditional healers have long used a root infusion to aid digestion and relieve stomach cramps; Müller (2008) notes that 5 g of root are steeped in 250 ml of hot water for 10 minutes, and the resulting tea is sipped slowly. In addition, the leaves of Bryonia alba have been applied as a poultice for skin irritations and minor wounds in Balkan folk medicine; Petrov (2012) describes a leaf mash that is wrapped in clean cloth and placed on the affected area for 30 minutes.

A practical recipe for a mild Bryonia alba tea is as follows: take 5 g of dried root, place it in a teapot, pour 250 ml of freshly boiled water, cover, and let steep for 10 minutes. Strain the liquid, allow it to cool slightly, and drink one cup in the morning and one in the evening. Because Bryonia alba contains potent cucurbitacins, use only the recommended amount; do not exceed 10 g of root per day, and avoid use during pregnancy or if you have kidney disease. If you experience nausea or abdominal discomfort, discontinue use and consult a healthcare professional.

The therapeutic effects of Bryonia alba are largely attributed to its cucurbitacin content, particularly bryonine and bryonol, which are bitter, anti‑inflammatory compounds. Flavonoids such as quercetin and kaempferol are also present and may contribute to the plant’s diuretic and antioxidant properties. Modern research has begun to explore these constituents for their potential anti‑cancer and anti‑arthritic activities, and commercial herbal preparations of Bryonia alba root are available in some European health‑food stores, though they are typically marketed as a bitter tonic rather than a medicinal product.

General Uses Top

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Industrial and craft applications:
- Scientific model organism: employed for research on cucurbitacin biosynthesis. DNA sequence data (including nuclear ribosomal internal transcribed spacer, ITS) are deposited in GenBank.

Properties relevant to use:
- High cucurbitacin content (bitter tetracyclic triterpenoids) suitable for biochemical and biosynthetic investigations.

Synonyms Top

Scientific name Authority First published in
Bryonia dioica M.Bieb. Fl. Taur.-Caucas. 3: 625. [Dec 1819 or early 1820]
Bryonia monoeca E.H.L.Krause Deutschl. Fl. (Sturm), ed. 2. 12: 242. 1904
Bryonia nigra Gilib. Fl. Lit. Inch. i. 60. 1782
Bryonia vulgaris Gueldenst. ex Ledeb. Fl. Ross. 2: 140 (1843)

Common names Top

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Language Common/alternative name
English white bryony
Arabic فاشرا بيضاء
Arabic فاشر حالق الشعر
Arabic حالق الشعر
Arabic فاشرة
Arabic الكرمة البيضاء
Azerbaijani ağ küstüşam
Belarusian пярэступ белы
Belarusian пераступнік
Belarusian пераступ
Bulgarian бяла дива тиква
Czech posed bílý
Danish enbo galdebær
German gichtrübe
German schwarzbeerige zaunrübe
German schwarzfrüchtige zaunrübe
German teufelsrübe
German weiße zaunrübe
Estonian harilik koeranaeris
Basque astamahats alebeltz
Basque astamahats ale-beltz
Persian بریونیا آلبا
Finnish mustakoiranköynnös
Irish uranach gheal
Irish unach gheal
Croatian tikvina debela
Upper Sorbian běła poćel
Hungarian földitök
Hungarian büdös gönye
Hungarian fekete földitök
Armenian Լոշտակ սպիտակ
Kazakh Сыртыдән итжүзім
Latvian baltā sētvija
Macedonian Дива тиква
Norwegian Bokmål svartgallebær
Norwegian Bokmål svartgallbær
Dutch white bryony
Norwegian Nynorsk svartgallbær
Polish przestęp biały
Russian Бриония белая
Russian Переступень белый
Slovak posed biely
Slovenian črnojagodasti bluščec
Swedish hundrova
Ukrainian Переступень білий
Ukrainian Бріонія біла
Chinese 白泻根

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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 4°C for 3 months, then warm to 20°C for another 3 months.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Turkmenistan
      • Uzbekistan
    • Siberia
      • Altay
    • Western Asia
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Central European Russia
      • East European Russia
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Czechoslovakia
      • Germany
      • Hungary
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • France
  • Northern America
    • Northeastern U.S.A.
      • New Jersey
    • Northwestern U.S.A.
      • Idaho
      • Montana
      • Washington
    • Southwestern U.S.A.
      • Utah

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000572927
UNII 56K0VVT47P
USDA Plants BRAL4
Tropicos 9200458
INPN 86825
Flora of Italy 3307
KEW urn:lsid:ipni.org:names:291541-1
The Plant List kew-2684337
Open Tree Of Life 660900
Observations.org 115634
NCBI Taxonomy 243967
Nature Serve 2.131392
IPNI 291541-1
iNaturalist 159507
GBIF 2874497
Freebase /m/09gpcsl
EPPO BYOAL
EOL 585692
Elurikkus 3200
USDA GRIN 401582
Wikipedia Bryonia_alba
CMAUP NPO3344

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
A Systematic Analysis of COVID-19 Clinical Trials Registered in the Clinical Trials Registry of India Dutta S, Singhal S, Shah R Cureus 09-Apr-2024
PMCID:PMC11082480
doi:10.7759/cureus.57939
PMID:38738059
New Light on Plants and Their Chemical Compounds Used in Polish Folk Medicine to Treat Urinary Diseases Olas B, Różański W, Urbańska K, Sławińska N, Bryś M Pharmaceuticals (Basel) 28-Mar-2024
PMCID:PMC11054606
doi:10.3390/ph17040435
PMID:38675397
A systematic methodology to assess the identity of plants in historical texts: A case study based on the Byzantine pharmacy text John the Physician's Therapeutics Lardos A, Patmore K, Allkin R, Lazarou R, Nesbitt M, Scott AC, Zipser B J Ethnopharmacol 25-Mar-2024
PMCID:PMC7615571
doi:10.1016/j.jep.2023.117622
PMID:38128894
From the name to the popular image of the plant: the Polish names for the black elder (Sambucus nigra) Kielak O J Ethnobiol Ethnomed 30-Jan-2024
PMCID:PMC10829229
doi:10.1186/s13002-024-00649-0
PMID:38291469
Epoxyalcohol Synthase Branch of Lipoxygenase Cascade Toporkova YY, Smirnova EO, Gorina SS Curr Issues Mol Biol 18-Jan-2024
PMCID:PMC10813956
doi:10.3390/cimb46010053
PMID:38248355
Plant traits associated with seed dispersal by ducks and geese in urban and natural habitats Tóth P, Green AJ, Wilkinson DM, Brides K, Lovas‐Kiss Á Ecol Evol 22-Nov-2023
PMCID:PMC10663722
doi:10.1002/ece3.10677
PMID:38020707
Tumor-associated macrophages: an effective player of the tumor microenvironment Basak U, Sarkar T, Mukherjee S, Chakraborty S, Dutta A, Dutta S, Nayak D, Kaushik S, Das T, Sa G Front Immunol 16-Nov-2023
PMCID:PMC10687432
doi:10.3389/fimmu.2023.1295257
PMID:38035101
Randomised controlled trial to compare efficacy of standard care alone and in combination with homoeopathic treatment of moderate/severe COVID-19 cases Kaur H, Bawaskar R, Khobragade A, Kalra D, Packiam V, Khan MY, Kaur T, Sharma M, Verma NK, Kaushik S, Khurana A PLoS One 15-Nov-2023
PMCID:PMC10650991
doi:10.1371/journal.pone.0292783
PMID:37967089
Strange, Rare and Peculiar Symptoms of COVID-19 Cases Managed by Practitioners of the Homeopathy Help Network Pracjek P, Gray AC, Doherty R, Straiges D Homeopathy 01-Nov-2023
PMCID:PMC11027477
doi:10.1055/s-0043-1771374
PMID:37913792
More than urns: A multi-method pipeline for analyzing cremation burials Waltenberger L, Bosch MD, Fritzl M, Gahleitner A, Kurzmann C, Piniel M, Salisbury RB, Strnad L, Skerjanz H, Verdianu D, Snoeck C, Kanz F, Rebay-Salisbury K PLoS One 30-Aug-2023
PMCID:PMC10468036
doi:10.1371/journal.pone.0289140
PMID:37647251
Engineering apomixis in crops Mahlandt A, Singh DK, Mercier R Theor Appl Genet 18-May-2023
PMCID:PMC10195744
doi:10.1007/s00122-023-04357-3
PMID:37199785
Gummy stem blight: One disease, three pathogens Seblani R, Keinath AP, Munkvold G Mol Plant Pathol 02-May-2023
PMCID:PMC10346371
doi:10.1111/mpp.13339
PMID:37129449
Beyond pharmaceuticals: The untapped potential of homeopathy in the battle against COVID-19 de Farias Morais GC, de Oliveira Campos DM, da Silva MK, de Oliveira CB, da Silva Junior ED, Fulco UL, Oliveira JI Explore (NY) 05-Apr-2023
PMCID:PMC10072950
doi:10.1016/j.explore.2023.04.002
PMID:37072282
Bioassay-Guided Isolation of Antimicrobial Components and LC/QToF Profile of Plumeria obtusa: Potential for the Treatment of Antimicrobial Resistance Eloutify YT, El-Shiekh RA, Ibrahim KM, Elshimy R, Avula B, Katragunta K, Khan IA, Meselhy MR ACS Omega 08-Feb-2023
PMCID:PMC9947952
doi:10.1021/acsomega.2c06803
PMID:36844537
Bibliometric Study of Adaptogens in Dermatology: Pharmacophylogeny, Phytochemistry, and Pharmacological Mechanisms Liu XX, Chen CY, Li L, Guo MM, He YF, Meng H, Dong YM, Xiao PG, Yi F Drug Des Devel Ther 06-Feb-2023
PMCID:PMC9912821
doi:10.2147/DDDT.S395256
PMID:36776447

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives
N-Formyl-4-hydroxybenzamide 71370414 Click to see C1=CC(=CC=C1C(=O)NC=O)O 165.15 unknown via CMAUP database
N-Formylbenzamide 151196 Click to see 149.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
4-Hydroxybenzamide 65052 Click to see 137.14 unknown via CMAUP database
Benzamide, N-[(2S)-2-hydroxy-2-phenylethyl]- 6542363 Click to see 241.28 unknown via CMAUP database
> Lignans, neolignans and related compounds / Cyclobutane lignans
[(1R,2R,3S,4S)-2-(2,4-dihydroxybenzoyl)-3,4-diphenylcyclobutyl]-(2,4-dihydroxyphenyl)methanone 102228233 Click to see 480.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see 282.50 unknown https://doi.org/10.1056/NEJM186707250762502
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1056/NEJM186707250762502
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown https://doi.org/10.1056/NEJM186707250762502
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1056/NEJM186707250762502
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Elaidolinolenic acid 5282822 Click to see 278.40 unknown https://doi.org/10.1056/NEJM186707250762502
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1056/NEJM186707250762502
Linolenic Acid 5280934 Click to see 278.40 unknown https://doi.org/10.1056/NEJM186707250762502
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphoglycerols / Phosphatidylglycerols
Phosphatidyl Glycerol 44566653 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)OCC(CO)O)OC(=O)CCCCCCCC=CCC=CCCCCC 747.00 unknown https://doi.org/10.1056/NEJM186707250762502
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-ene-11,22-diol 44253988 Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6O)C)C)C)C)(C)CO)O 472.70 unknown via CMAUP database
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-22-methoxy-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-ol 44253989 Click to see 486.70 unknown via CMAUP database
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R)-11-hydroxy-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-22-one 102482971 Click to see 470.70 unknown via CMAUP database
(2R,4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid 21594159 Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)(C)C(=O)O 472.70 unknown via CMAUP database
(2R,4aS,6aR,6aS,6bR,8aR,9S,12aR,14bR)-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-2-carboxylic acid 44253990 Click to see CC12CCC(CC1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)CO)C)(C)C(=O)O 470.70 unknown via CMAUP database
(3S,4S,4aR,6aR,6bS,8aR,9R,11R,12aS,14aR,14bR)-4,11-bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol 14335966 Click to see 474.70 unknown via CMAUP database
24-Hydroxy-beta-amyrin 14167253 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C)C 442.70 unknown via CMAUP database
Melilotigenin B 91895471 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)C)C 454.70 unknown via CMAUP database
Melilotigenin C 10551785 Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)C)C 456.70 unknown via CMAUP database
Soyasapogenol B 115012 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C 458.70 unknown via CMAUP database
Soyasapogenol E 13632872 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)O)C)C 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
(2I+/-,9I(2),10I+/-,16I+/-,23E)-2,16,20,25-Tetrahydroxy-9-methyl-19-norlanosta-5,23-diene-3,11-dione 12114146 Click to see 502.70 unknown https://doi.org/10.1007/BF00579070
(2R,9S,13S,14R,16S)-17-[(E,2S)-2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl]-2,16-dihydroxy-4,4,9,13,14-pentamethyl-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 17750993 Click to see 516.70 unknown via CMAUP database
(2S,3S,8S,9R,10R,13R,14S,16R)-17-[(E)-2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl]-2,3,16-trihydroxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 54749297 Click to see 518.70 unknown via CMAUP database
(8S,9R,10R,13R,14S,16R,17R)-17-[(E,2R)-2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl]-16-hydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-2-olate 25245009 Click to see 513.60 unknown via CMAUP database
(8S,9R,10R,13R,14S,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-17-[(2R,5S)-2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl]-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthrene-3,11-dione 57402770 Click to see 532.70 unknown https://doi.org/10.1016/0031-9422(75)85356-8
(9R,13R,14S,16R)-17-[(E,2R)-6-acetyloxy-2-hydroxy-6-methyl-3-oxohept-4-en-2-yl]-16-hydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-2-olate 25245182 Click to see 555.70 unknown via CMAUP database
[(E,6R)-6-[(2S,9R,10R,13R,14S,16R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate 25245488 Click to see 558.70 unknown via CMAUP database
[(E)-6-[(3S,10R,16R)-3,16-dihydroxy-9-(hydroxymethyl)-4,4,13,14-tetramethyl-11-oxo-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate 6433457 Click to see 560.70 unknown via CMAUP database
17-(2,6-dihydroxy-6-methylhept-4-en-2-yl)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 417587 Click to see 502.70 unknown https://doi.org/10.1007/BF00579070
22-Deoxocucurbitacin D 5474791 Click to see 502.70 unknown https://doi.org/10.1007/BF00579070
23,24-dihydrocucurbitacin E 21577087 Click to see 558.70 unknown https://doi.org/10.1016/0031-9422(75)85356-8
Cucurbitacin B 5281316 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)O)C)C)C)O)O 558.70 unknown https://doi.org/10.1016/0031-9422(75)85356-8
Cucurbitacin B, dihydro- 588303 Click to see CC(=O)OC(C)(C)CCC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)O)C)C)C)O)O 560.70 unknown https://doi.org/10.1007/BF00579070
Cucurbitacin C 5281317 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CCC(C4(C)C)O)CO)C)C)O)O 560.70 unknown https://doi.org/10.1016/0031-9422(75)85356-8
Cucurbitacin E 5281319 Click to see 556.70 unknown https://doi.org/10.1016/0031-9422(75)85356-8
Cucurbitacin I 5281321 Click to see 514.60 unknown https://doi.org/10.1016/0031-9422(75)85356-8
Cucurbitacin J 441819 Click to see 532.70 unknown https://doi.org/10.1016/0031-9422(75)85356-8
Cucurbitacin L 441820 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2C=C(C1=O)O)C)C)C(C)(C(=O)CCC(C)(C)O)O)O)C)C 516.70 unknown https://doi.org/10.1007/BF00579070
Dihydrocucurbitacin B 267250 Click to see 560.70 unknown https://doi.org/10.1007/BF00579070
https://doi.org/10.1016/0031-9422(75)85356-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(1S,2S,4R,6R,8S,9S,10R,13R,14S,16S)-16-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-8-hydroxy-2,8,10,13,18,18-hexamethyl-6-(2-methylprop-1-enyl)-5-oxapentacyclo[11.8.0.02,10.04,9.014,19]henicos-19-ene-12,17-dione 162937604 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3CC4C(=CCC5C4(C(=O)CC6(C5(CC7C6C(CC(O7)C=C(C)C)(C)O)C)C)C)C(C3=O)(C)C)CO)O)O)O 792.90 unknown https://doi.org/10.1007/BF00579070
(1S,2S,4R,6R,8S,9S,10R,13R,14S)-16-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-8-hydroxy-2,8,10,13,18,18-hexamethyl-6-(2-methylprop-1-enyl)-5-oxapentacyclo[11.8.0.02,10.04,9.014,19]henicosa-15,19-diene-12,17-dione 162981400 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3=CC4C(=CCC5C4(C(=O)CC6(C5(CC7C6C(CC(O7)C=C(C)C)(C)O)C)C)C)C(C3=O)(C)C)CO)O)O)O 790.90 unknown https://doi.org/10.1007/BF00579070
16-[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-8-hydroxy-2,8,10,13,18,18-hexamethyl-6-(2-methylprop-1-enyl)-5-oxapentacyclo[11.8.0.02,10.04,9.014,19]henicos-19-ene-12,17-dione 73800766 Click to see 792.90 unknown https://doi.org/10.1007/BF00579070
16-[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-8-hydroxy-2,8,10,13,18,18-hexamethyl-6-(2-methylprop-1-enyl)-5-oxapentacyclo[11.8.0.02,10.04,9.014,19]henicosa-15,19-diene-12,17-dione 162981399 Click to see 790.90 unknown https://doi.org/10.1007/BF00579070
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1007/BF00573546
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1007/BF00573546
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(3S)-3-aminopyrrolidin-1-ium-3-carboxylate 28820550 Click to see C1C[NH2+]CC1(C(=O)[O-])N 130.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1S,2R,4aR,6aS,6aS,6bR,8aR,10R,12aR,14bR)-10-hydroxy-2,4a,6a,9,9,12a-hexamethyl-1,2,3,4,5,6,6a,6b,7,8,8a,10,11,12,13,14b-hexadecahydropicene-1-carboxylic acid 162866535 Click to see 442.70 unknown https://doi.org/10.1007/BF00568549
10-Hydroxy-2,4a,6a,9,9,12a-hexamethyl-1,2,3,4,5,6,6a,6b,7,8,8a,10,11,12,13,14b-hexadecahydropicene-1-carboxylic acid 162866534 Click to see 442.70 unknown https://doi.org/10.1007/BF00568549
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(3S,4R,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[4-(2-hydroxyethyl)phenoxy]-6-(hydroxymethyl)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl 4-hydroxybenzoate 11444250 Click to see 552.50 unknown https://doi.org/10.1007/BF00579070
[(3S,4R,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[4-(2-hydroxyethyl)phenoxy]-6-(hydroxymethyl)oxan-3-yl]oxy-3,4-dihydroxyoxolan-3-yl]methyl benzoate 11398542 Click to see C1C(C(C(O1)OC2C(C(C(OC2OC3=CC=C(C=C3)CCO)CO)O)O)O)(COC(=O)C4=CC=CC=C4)O 536.50 unknown https://doi.org/10.1007/BF00579070
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal 3037556 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1056/NEJM186707250762502
D-Galactose 6036 Click to see 180.16 unknown https://doi.org/10.1056/NEJM186707250762502
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1056/NEJM186707250762502
D(+)-Glucose 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1056/NEJM186707250762502
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Glycerin 753 Click to see C(C(CO)O)O 92.09 unknown https://doi.org/10.1056/NEJM186707250762502
> Organoheterocyclic compounds / Benzopyrans
Oxytropisoflavan B 46918734 Click to see COC1=C(C(=C(C=C1)C2CC3(CCC(=O)C=C3OC2)O)O)OC 320.30 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Benzoylindoles
(3-Hydroxyindol-1-yl)-(3-hydroxyphenyl)methanone 46850207 Click to see 253.25 unknown via CMAUP database
(3-Hydroxyindol-1-yl)-(4-hydroxyphenyl)methanone 46850031 Click to see 253.25 unknown via CMAUP database
(3-Hydroxyindol-1-yl)-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]methanone 46850206 Click to see CC(=CCC1=C(C=CC(=C1)C(=O)N2C=C(C3=CC=CC=C32)O)O)C 321.40 unknown via CMAUP database
(3-Hydroxyindol-1-yl)-phenylmethanone 46850030 Click to see C1=CC=C(C=C1)C(=O)N2C=C(C3=CC=CC=C32)O 237.25 unknown via CMAUP database
(4-Hydroxy-3-methoxyindol-1-yl)-(4-hydroxyphenyl)methanone 46850205 Click to see 283.28 unknown via CMAUP database
(4-Hydroxyphenyl)-(3-methoxyindol-1-yl)methanone 46850032 Click to see COC1=CN(C2=CC=CC=C21)C(=O)C3=CC=C(C=C3)O 267.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone 688857 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3 240.25 unknown via CMAUP database
Liquiritigenin 114829 Click to see 256.25 unknown via CMAUP database
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 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
Chrysin 5281607 Click to see 254.24 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 / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Chromen-4-One 4475102 Click to see 432.40 unknown https://doi.org/10.1016/0031-9422(95)00069-J
Isovitexin 162350 Click to see 432.40 unknown https://doi.org/10.1016/0031-9422(95)00069-J
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 5378180 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(95)00069-J
Vitexin 5280441 Click to see 432.40 unknown https://doi.org/10.1016/0021-9673(94)85278-2
https://doi.org/10.1016/0031-9422(95)00069-J
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 60200223 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)O)O)O)O)O 608.50 unknown via CMAUP database
3-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 21668680 Click to see 726.60 unknown via CMAUP database
3-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 10865825 Click to see 872.80 unknown via CMAUP database
Biorobin 15944778 Click to see 594.50 unknown via CMAUP database
Mauritianin 10919701 Click to see 740.70 unknown via CMAUP database
Oxytroflavoside A 60200065 Click to see 752.70 unknown via CMAUP database
Oxytroflavoside B 60200066 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)O)OC(=O)CC(C)(CC(=O)O)O)O)O)O 752.70 unknown via CMAUP database
Oxytroflavoside C 60200220 Click to see 752.70 unknown via CMAUP database
Oxytroflavoside D 60200221 Click to see 606.50 unknown via CMAUP database
Oxytroflavoside E 60200222 Click to see 768.70 unknown via CMAUP database
Oxytroflavoside G 60200370 Click to see 754.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-6,7-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]chromen-4-one 163047691 Click to see 626.50 unknown https://doi.org/10.1016/0031-9422(95)00069-J
2-(3,4-Dihydroxyphenyl)-5-hydroxy-6,7-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]chromen-4-one 163047690 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/0031-9422(95)00069-J
5-Hydroxy-2-(4-hydroxyphenyl)-6-(3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)-7-(3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 4636593 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(95)00069-J
Kaempferol 3-O-(Alpha-L-Rhamnopyranosyl(1->2)-Beta-D-Galactopyranosyl)-7-O-Alpha-L-Rhamnopyranoside 57397583 Click to see 740.70 unknown via CMAUP database
Lutonarin 44559810 Click to see 610.50 unknown https://doi.org/10.1016/0031-9422(95)00069-J
https://doi.org/10.1016/0021-9673(94)85278-2
Robinin 5281693 Click to see 740.70 unknown via CMAUP database
Saponarin 441381 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(95)00069-J
https://doi.org/10.1016/0021-9673(94)85278-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(-)-Pinostrobin 73201 Click to see 270.28 unknown via CMAUP database
(2S)-2-(4-hydroxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one 14157884 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=C(C=C3)O 270.28 unknown via CMAUP database
(R,S)-7-Methoxy-2-phenyl-chroman-4-one 688883 Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=CC=C3 254.28 unknown via CMAUP database
Sakuranetin 73571 Click to see 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one 26088035 Click to see 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain 91510 Click to see 284.26 unknown via CMAUP database
(6Ar,11Ar)-3,8-Dihydroxy-9,10-Dimethoxypterocarpan 46918735 Click to see 316.30 unknown via CMAUP database
(l)-Edunol 182148 Click to see 352.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein 5281708 Click to see 254.24 unknown via CMAUP database
Pseudobaptigenin 5281805 Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O 282.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavanquinones
5-[(3R)-7-hydroxy-3,4-dihydro-2H-chromen-3-yl]-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione 10403457 Click to see COC1=C(C(=O)C(=CC1=O)C2CC3=C(C=C(C=C3)O)OC2)OC 316.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzein-4'-glucoside 49862229 Click to see 416.40 unknown via CMAUP database
Sophoricoside 5321398 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-Methoxydaidzein 5319422 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
Isomucronulatol, (-)- 10380176 Click to see 302.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
(3R)-2',3',7-trihydroxy-4'-methoxyisoflavan 15939757 Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O)O 288.29 unknown via CMAUP database
(R)-Mucronulatol 13873811 Click to see 302.32 unknown via CMAUP database
Calycosin 5280448 Click to see 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2'-Hydroxybiochanin A 5282075 Click to see 300.26 unknown via CMAUP database
Formononetin 5280378 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Isoformononetin 3764 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',4'-Dihydroxydihydrochalcone 586491 Click to see 242.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(4-Hydroxyphenyl)Prop-2-En-1-One 425 Click to see 256.25 unknown via CMAUP database
1-(2,4-Dihydroxyphenyl)-3-phenylprop-2-en-1-one 344530 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O 240.25 unknown via CMAUP database
2-Propen-1-one, 1-(2-hydroxy-4-methoxyphenyl)-3-(4-hydroxyphenyl)- 592216 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O 270.28 unknown via CMAUP database
2',4'-Dihydroxychalcone 5376979 Click to see 240.25 unknown via CMAUP database
2a(2),4a(2)-Dihydroxy-4-methoxychalcone 166795 Click to see 270.28 unknown via CMAUP database
4'-Methoxy-2'-hydroxy chalcone 265720 Click to see 254.28 unknown via CMAUP database
Isoliquiritigenin 638278 Click to see 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
2',4',4-Trihydroxy-3'-prenylchalcone 193568 Click to see 324.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
1-(4-Hydroxy-2-methoxyphenyl)-3-phenylprop-2-en-1-one 71442332 Click to see 254.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolactams
Desferrioxamine X5 85625752 Click to see 598.70 unknown https://doi.org/10.1056/NEJM186707250762502

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