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Bryonia cretica

Bryonia cretica - 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 UUID64400dea34677509427579
Scientific name Bryonia cretica
Authority L.
First published in Sp. Pl. : 1013 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Bryonia cretica var. monoica Nábělek Iter Turc.-Pers. 1: 116 1923
Bryonia cretica f. monoica (Nábělek) Feinbrun Fl. Palaestina 3: 274 (1978)

Common names Top

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Language Common/alternative name
English cretan bryony
Finnish punakoiranköynnös
Hebrew דלעת-נחש מצויה
Croatian crveni bljuštac

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Bryonia cretica subsp. acuta (Desf.) Tutin Feddes Repert. 79(Heft 1-2): 61. 1968 [20 Aug 1968]
Bryonia cretica subsp. dioica (Jacq.) Tutin Feddes Repert. 79(Heft 1-2): 61. 1968 [20 Aug 1968]
Bryonia cretica subsp. marmorata (E.Petit) Jauzein Fl. Champs Cult. : 863 (1995)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Middle Asia
      • Kazakhstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Lebanon-Syria
      • Palestine
      • Turkey
  • Europe
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Kriti
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000572960
USDA Plants BRCR2
Tropicos 9200014
INPN 159572
KEW urn:lsid:ipni.org:names:291575-1
The Plant List kew-2684368
Open Tree Of Life 82976
Observations.org 115636
NCBI Taxonomy 61884
Nature Serve 2.148319
IPNI 291575-1
iNaturalist 55935
GBIF 2874496
EPPO BYOCR
EOL 594181
USDA GRIN 70132

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 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
Recent Advances in the Application of Cucurbitacins as Anticancer Agents Zieniuk B, Pawełkowicz M Metabolites 14-Oct-2023
PMCID:PMC10608718
doi:10.3390/metabo13101081
PMID:37887406
Determination of the Total Phenolics Content and Antioxidant Activity of Extracts from Parts of Plants from the Greek Island of Crete Kalpoutzakis E, Chatzimitakos T, Athanasiadis V, Mitakou S, Aligiannis N, Bozinou E, Gortzi O, Skaltsounis LA, Lalas SI Plants (Basel) 01-Mar-2023
PMCID:PMC10005234
doi:10.3390/plants12051092
PMID:36903954
New Weed Hosts for Tomato Brown Rugose Fruit Virus in Wild Mediterranean Vegetation Salem NM, Abumuslem M, Turina M, Samarah N, Sulaiman A, Abu-Irmaileh B, Ata Y Plants (Basel) 01-Sep-2022
PMCID:PMC9460064
doi:10.3390/plants11172287
PMID:36079668
Gastrointestinal, metabolic, and nutritional disorders: A plant-based ethnoveterinary meta-analysis in the Catalan linguistic area Cáceres F, Vallès J, Garnatje T, Parada M, Gras A Front Vet Sci 09-Aug-2022
PMCID:PMC9395657
doi:10.3389/fvets.2022.908491
PMID:36016807
Medicinal Plants Used Traditionally for Skin Related Problems in the South Balkan and East Mediterranean Region—A Review Tsioutsiou EE, Amountzias V, Vontzalidou A, Dina E, Stevanović ZD, Cheilari A, Aligiannis N Front Pharmacol 05-Jul-2022
PMCID:PMC9294246
doi:10.3389/fphar.2022.936047
PMID:35865952
Cancer and Traditional Plant Knowledge, an Interesting Field to Explore: Data from the Catalan Linguistic Area Gras A, Parada M, Pellicer J, Vallès J, Garnatje T Molecules 24-Jun-2022
PMCID:PMC9268183
doi:10.3390/molecules27134070
PMID:35807319
Ethnoveterinary Medicine and Ethnopharmacology in the Main Transhumance Areas of Castilla-La Mancha (Spain) Rivera D, Verde A, Fajardo Rodríguez J, Ríos S, Alcaraz F, Cárceles C, Ortíz J, Valdés A, Ruíz-Gallardo JR, García-Flores A, Palazón JA, Obón C Front Vet Sci 03-May-2022
PMCID:PMC9113055
doi:10.3389/fvets.2022.866132
PMID:35591874
Analysis of Active Compounds Using Target Protein Cofilin―Cucurbitacins in Cytotoxic Plant Bryonia cretica Nakashima S, Oda Y, Morita M, Ohta A, Morikawa T, Matsuda H, Nakamura S Toxins (Basel) 16-Mar-2022
PMCID:PMC8955846
doi:10.3390/toxins14030212
PMID:35324709
Food Behavior in Emergency Time: Wild Plant Use for Human Nutrition during the Conflict in Syria Sulaiman N, Pieroni A, Sõukand R, Polesny Z Foods 10-Jan-2022
PMCID:PMC8775266
doi:10.3390/foods11020177
PMID:35053908
Importance of natural land cover for plant species’ conservation: A nationwide study in The Netherlands Pan K, Moens M, Marshall L, Cieraad E, de Snoo GR, Biesmeijer K PLoS One 16-Nov-2021
PMCID:PMC8594855
doi:10.1371/journal.pone.0259255
PMID:34784365
Inventory of Medicinal Plants Used Traditionally to Manage Kidney Diseases in North-Eastern Morocco: Ethnobotanical Fieldwork and Pharmacological Evidence Bencheikh N, Elbouzidi A, Kharchoufa L, Ouassou H, Alami Merrouni I, Mechchate H, Es-safi I, Hano C, Addi M, Bouhrim M, Eto B, Elachouri M Plants (Basel) 20-Sep-2021
PMCID:PMC8468912
doi:10.3390/plants10091966
PMID:34579498
Potential Toxicity of Medicinal Plants Inventoried in Northeastern Morocco: An Ethnobotanical Approach Kharchoufa L, Bouhrim M, Bencheikh N, Addi M, Hano C, Mechchate H, Elachouri M Plants (Basel) 31-May-2021
PMCID:PMC8226742
doi:10.3390/plants10061108
PMID:34072709
Antiviral Activity of Ribosome-Inactivating Proteins Citores L, Iglesias R, Ferreras JM Toxins (Basel) 22-Jan-2021
PMCID:PMC7912582
doi:10.3390/toxins13020080
PMID:33499086
Population Dynamics of Drosophila suzukii in Coastal and Mainland Sweet Cherry Orchards of Greece Papanastasiou SA, Rodovitis VG, Bataka EP, Verykouki E, Papadopoulos NT Insects 10-Sep-2020
PMCID:PMC7564280
doi:10.3390/insects11090621
PMID:32927914

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 / Benzoic acids and derivatives / Benzoic acid esters
[(1S,2S,5R,6S)-2-acetyloxy-5-benzoyloxy-1,6-dihydroxycyclohex-3-en-1-yl]methyl benzoate 16741795 Click to see CC(=O)OC1C=CC(C(C1(COC(=O)C2=CC=CC=C2)O)O)OC(=O)C3=CC=CC=C3 426.40 unknown https://doi.org/10.1248/CPB.58.747
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-hydroxy-9-[3-(4-hydroxyphenyl)prop-2-enoyloxymethyl]-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162976962 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)COC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1)C)C(=O)O)C 618.80 unknown https://doi.org/10.1248/CPB.58.747
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
(2S,8S,9R,10R,13R,14S,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-17-[(2R,5R)-2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl]-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 131884647 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C 534.70 unknown https://doi.org/10.1248/CPB.58.747
https://doi.org/10.1016/J.PHYTOL.2010.02.009
(2S,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]-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 46905998 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C 534.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.02.009
(3S,8S,9R,10R,13R,14S,16R,17R)-3,16-dihydroxy-4,4,9,13,14-pentamethyl-17-[(2R,5R)-2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl]-3,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-2,11-dione 162986737 Click to see CC1(C(C(=O)CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C)C)O)C 534.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.02.009
(3S,8S,9R,10R,13R,14S,16R,17R)-3,16-dihydroxy-4,4,9,13,14-pentamethyl-17-[(2R,5S)-2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl]-3,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-2,11-dione 162986736 Click to see CC1(C(C(=O)CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C)C)O)C 534.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.02.009
(8S,9R,10R,13R,14S,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-17-[(2R,5R)-2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl]-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthrene-3,11-dione 57402771 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2C=C(C1=O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C 532.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.02.009
(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 CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2C=C(C1=O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C 532.70 unknown https://doi.org/10.1248/CPB.58.747
(8S,9R,10S,13R,14S)-17-[(2R)-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 138113434 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 516.70 unknown https://doi.org/10.1002/(SICI)1099-1565(200003/04)11:2<121::AID-PCA493>3.0.CO;2-9
[6-(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 2885 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/10.1248/CPB.58.747
[6-(2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl)-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate 2887 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3C=C(C(=O)C4(C)C)O)C)C)C)O)O 556.70 unknown https://doi.org/10.1248/CPB.58.747
[6-(2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl)-6-hydroxy-2-methyl-5-oxoheptan-2-yl] acetate 73802899 Click to see CC(=O)OC(C)(C)CCC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3C=C(C(=O)C4(C)C)O)C)C)C)O)O 558.70 unknown https://doi.org/10.1248/CPB.58.747
[6-(3,16-dihydroxy-4,4,9,13,14-pentamethyl-2,11-dioxo-3,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-hydroxy-2-methyl-5-oxohept-3-en-2-yl] acetate 434841 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(=O)C(C4(C)C)O)C)C)C)O)O 558.70 unknown https://doi.org/10.1248/CPB.58.747
17-(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 2886 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 516.70 unknown https://doi.org/10.1248/CPB.58.747
17-(2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl)-3,16-dihydroxy-4,4,9,13,14-pentamethyl-3,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-2,11-dione 328200 Click to see CC1(C(C(=O)CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(=O)C=CC(C)(C)O)O)O)C)C)C)O)C 516.70 unknown https://doi.org/10.1248/CPB.58.747
2,16-dihydroxy-4,4,9,13,14-pentamethyl-17-(2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl)-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 4482416 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C 534.70 unknown https://doi.org/10.1248/CPB.58.747
https://doi.org/10.1016/J.PHYTOL.2010.02.009
23,24-dihydrocucurbitacin E 21577087 Click to see CC(=O)OC(C)(C)CCC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3C=C(C(=O)C4(C)C)O)C)C)C)O)O 558.70 unknown https://doi.org/10.1248/CPB.58.747
3-Epi-Isocucurbitacin B 6442968 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(=O)C(C4(C)C)O)C)C)C)O)O 558.70 unknown https://doi.org/10.1248/CPB.58.747
3-Epi-Isocucurbitacin D 57384018 Click to see CC1(C(C(=O)CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(=O)C=CC(C)(C)O)O)O)C)C)C)O)C 516.70 unknown https://doi.org/10.1248/CPB.58.747
3,16-dihydroxy-4,4,9,13,14-pentamethyl-17-(2,5,6-trihydroxy-6-methyl-3-oxoheptan-2-yl)-3,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-2,11-dione 77410148 Click to see CC1(C(C(=O)CC2C1=CCC3C2(C(=O)CC4(C3(CC(C4C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C)C)O)C 534.70 unknown https://doi.org/10.1016/J.PHYTOL.2010.02.009
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/10.1248/CPB.58.747
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/10.1248/CPB.58.747
Cucurbitacin D 5281318 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 516.70 unknown https://doi.org/10.1248/CPB.58.747
https://doi.org/10.1002/(SICI)1099-1565(200003/04)11:2<121::AID-PCA493>3.0.CO;2-9
Cucurbitacin E 5281319 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3C=C(C(=O)C4(C)C)O)C)C)C)O)O 556.70 unknown https://doi.org/10.1248/CPB.58.747
Cucurbitacin K 270061 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2C=C(C1=O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C 532.70 unknown https://doi.org/10.1248/CPB.58.747
https://doi.org/10.1016/J.PHYTOL.2010.02.009
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/10.1002/(SICI)1099-1565(200003/04)11:2<121::AID-PCA493>3.0.CO;2-9
Cucurbitacin R 180535 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)CCC(C)(C)O)O)O)C)C 518.70 unknown https://doi.org/10.1002/(SICI)1099-1565(200003/04)11:2<121::AID-PCA493>3.0.CO;2-9
https://doi.org/10.1248/CPB.58.747
Dihydrocucurbitacin B 267250 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/10.1248/CPB.58.747
Tetrahydrocucurbitacin I 270059 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)O)C)C)C(C)(C(=O)CCC(C)(C)O)O)O)C)C 518.70 unknown https://doi.org/10.1248/CPB.58.747
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
17-acetyl-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 56671290 Click to see CC(=O)C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)O)C)C)C)O 402.50 unknown https://doi.org/10.1248/CPB.58.747
hexanorcucurbitacin D 45272227 Click to see CC(=O)C1C(CC2(C1(CC(=O)C3(C2CC=C4C3CC(C(=O)C4(C)C)O)C)C)C)O 402.50 unknown https://doi.org/10.1248/CPB.58.747
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins / Cucurbitacin glycosides
(2S,3R,4R,5R,6S)-2-[(E,6S)-6-hydroxy-6-[(3S,8S,9R,10R,11S,13R,14S,17S)-11-hydroxy-4,4,9,13,14-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-3-en-2-yl]oxy-6-methyloxane-3,4,5-triol 46211015 Click to see CC1C(C(C(C(O1)OC(C)(C)C=CCC(C)(C2CCC3(C2(CC(C4(C3CC=C5C4CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)C)C)O)O)O)O 783.00 unknown https://doi.org/10.1248/CPB.58.747
(2S,8S,9R,10R,13R,14S,17S)-17-[(2R)-2-hydroxy-6-methyl-3-oxo-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-4,4,9,13,14-pentamethyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 101625614 Click to see CC1(C2=CCC3C4(CCC(C4(CC(=O)C3(C2CC(C1=O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)CCC(C)(C)OC6C(C(C(C(O6)CO)O)O)O)O)C)C 827.00 unknown https://doi.org/10.1002/(SICI)1099-1565(200003/04)11:2<121::AID-PCA493>3.0.CO;2-9
(3S,8S,9R,10R,13R,14S,17R)-17-[(2R,5R)-5-hydroxy-6-methyl-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-4,4,9,13,14-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 15143903 Click to see CC(CCC(C(C)(C)OC1C(C(C(C(O1)CO)O)O)O)O)C2CCC3(C2(CC(=O)C4(C3CC=C5C4CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)C 799.00 unknown https://doi.org/10.1002/(SICI)1099-1565(200003/04)11:2<121::AID-PCA493>3.0.CO;2-9
(3S,8S,9R,10R,13R,14S,17R)-17-[(2R,5R)-5-hydroxy-6-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyheptan-2-yl]-4,4,9,13,14-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 15143904 Click to see CC(CCC(C(C)(C)OC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)O)C3CCC4(C3(CC(=O)C5(C4CC=C6C5CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)O)O)C)C)C 961.10 unknown https://doi.org/10.1002/(SICI)1099-1565(200003/04)11:2<121::AID-PCA493>3.0.CO;2-9
(3S,8S,9R,10R,13R,14S,17R)-17-[(2R,5R)-6-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-methylheptan-2-yl]-3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 101625613 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4C(=CCC5C4(C(=O)CC6(C5(CCC6C(C)CCC(C(C)(C)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C)C3(C)C)CO)O)O)O)O)O 1107.30 unknown https://doi.org/10.1002/(SICI)1099-1565(200003/04)11:2<121::AID-PCA493>3.0.CO;2-9
(3S,8S,9R,10R,13R,14S,17R)-3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-17-[(2R,5R)-5-hydroxy-6-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-4,4,9,13,14-pentamethyl-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 101625612 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4C(=CCC5C4(C(=O)CC6(C5(CCC6C(C)CCC(C(C)(C)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C)C3(C)C)CO)O)O)O)O)O 945.10 unknown https://doi.org/10.1002/(SICI)1099-1565(200003/04)11:2<121::AID-PCA493>3.0.CO;2-9
(3S,8S,9R,10R,13R,14S,17S)-17-[(E,2S)-2-hydroxy-6-methyl-6-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyhept-4-en-2-yl]-4,4,9,13,14-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 46211014 Click to see CC1C(C(C(C(O1)OC(C)(C)C=CCC(C)(C2CCC3(C2(CC(=O)C4(C3CC=C5C4CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)C)O)O)O)O 781.00 unknown https://doi.org/10.1248/CPB.58.747
[6-hydroxy-6-[16-hydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methyl-5-oxohept-3-en-2-yl] acetate 72968961 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)OC5C(C(C(C(O5)CO)O)O)O)C)C)C)O)O 720.80 unknown https://doi.org/10.1248/CPB.58.747
17-(2,6-dihydroxy-6-methyl-3-oxohept-4-en-2-yl)-16-hydroxy-4,4,9,13,14-pentamethyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,7,8,10,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthrene-3,11-dione 73804168 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 678.80 unknown https://doi.org/10.1248/CPB.58.747
17-[2-Hydroxy-6-methyl-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyhept-4-en-2-yl]-4,4,9,13,14-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,7,8,10,12,15,16,17-decahydrocyclopenta[a]phenanthren-11-one 75149673 Click to see CC1C(C(C(C(O1)OC(C)(C)C=CCC(C)(C2CCC3(C2(CC(=O)C4(C3CC=C5C4CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)C)O)O)O)O 781.00 unknown https://doi.org/10.1248/CPB.58.747
2-[6-hydroxy-6-[11-hydroxy-4,4,9,13,14-pentamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-3-en-2-yl]oxy-6-methyloxane-3,4,5-triol 75149674 Click to see CC1C(C(C(C(O1)OC(C)(C)C=CCC(C)(C2CCC3(C2(CC(C4(C3CC=C5C4CCC(C5(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)C)C)O)O)O)O 783.00 unknown https://doi.org/10.1248/CPB.58.747
Arvenin I 6441104 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)OC5C(C(C(C(O5)CO)O)O)O)C)C)C)O)O 720.80 unknown https://doi.org/10.1248/CPB.58.747
arvenin III 21579640 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2CC(C1=O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 678.80 unknown https://doi.org/10.1248/CPB.58.747
https://doi.org/10.1002/(SICI)1099-1565(200003/04)11:2<121::AID-PCA493>3.0.CO;2-9
cucurbitacin I 2-O-beta-D-glucopyranoside 6441519 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2C=C(C1=O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)C=CC(C)(C)O)O)O)C)C 676.80 unknown https://doi.org/10.1248/CPB.58.747
cucurbitacin K 2-O-beta-D-glucopyranoside 6324997 Click to see CC1(C2=CCC3C4(CC(C(C4(CC(=O)C3(C2C=C(C1=O)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)(C(=O)CC(C(C)(C)O)O)O)O)C)C 694.80 unknown https://doi.org/10.1248/CPB.58.747

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