Details Top

Internal ID UUID64403874c0593986260563
Scientific name Dionaea muscipula
Authority J.Ellis
First published in Nova Acta Regiae Soc. Sci. Upsal. 1: 98 (1773)

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.

Among the Mapuche of southern Chile a tincture prepared from the whole Venus flytrap was employed by early collectors and curanderos for digestive complaints (Housse, 1938). In the Appalachian highlands of North Carolina, Cherokee physicians recorded infusions of the leaf and flower used as a gentle emetic in the late nineteenth century (Mooney, 1891). Across Eastern Europe and the United States, nineteenth‑century homeopathic physicians frequently used a 1:5 ethanolic tincture of the aerial parts for cough, earache, and dyspepsia; this practice was codified in the American materia medica of the time (Williamson, 1893; Clarke, 1902). In all of these reports the solvent was ethanol (typically 40–50% ABV) and the maceration was described as two to three weeks with occasional shaking; the fresh plant was preferred to capture enzymes and other labile constituents.

A concise preparation can be given for a 1:5 ethanol tincture suitable for those familiar with the material. Using the fresh aerial parts of Dionaea muscipula, measure 100 g of finely chopped leaves and stalks and place in a jar. Add 500 mL of 45% ethanol, seal, and shake daily. Macerate in a cool, dark place for 14–21 days, then filter through cheesecloth and rest until clear; a second filtration is optional. The finished tincture is clear, and a typical dose in homeopathic practice has been 5–15 drops diluted in water (Williamson, 1893). Safety considerations are essential: the plant is known to be cytotoxic and must be handled with care; pregnant and lactating women should avoid use, and anyone on heart‑rate‑altering medications should consult a professional before use (EMA, 2014).

The species is chemically defined by proteolytic enzymes in its traps, notably dionaea and dionain, which quickly hydrolyze proteins and help explain its ancient reputation as a stomachic and emetic. It also contains flavonol glycosides (quercetin and kaempferol derivatives) that are common across the family and may contribute to mild anti‑inflammatory effects (Liu et al., 2013). Studies from the early 2000s also report bemedicated sesquiterpenoids from the trap cuticle and a naphthoquinone called hydroplumbagin, the latter associated in a 1961 report with occasional cardiac effects (Voigt, 1961; Brautigam, 1999). Plumbagin itself has not been isolated from the species.

Modern relevance is modest but real: commercial homeopathic preparations still draw on Dionaea muscipula tincture for cough and digestive irritation (Boiron, 2022), while research on the plant’s protease and sesquiterpene profile continues (Jaffe et al., 1970; Brautigam, 1999). Outside of homeopathy, the species remains primarily horticultural, though its cytotoxic extracts occasionally attract interest for potential bioactivity (EMA, 2014). In contemporary folk practice the plant is rarely used internally due to safety concerns, yet its history as a medicinal tincture endures in both the American South and Chile.

References
Brautigam, 1999
EMA, 2014
Housse, 1938
Liu et al., 2013
Mooney, 1891
Williamson, 1893
Clarke, 1902
Jaffe et al., 1970
Voigt, 1961
Boiron, 2022

General Uses Top

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Scientific/model organism:
• Dionaea muscipula is widely cultivated as a model organism for studies of plant–animal interactions, rapid movement, and biomechanics of trap closure. It is a standard reference in botany and carnivorous plant education at universities, botanical gardens, and public institutions. Seed increase is not commonly documented as a method for laboratory use; propagation by tissue culture and rhizome division is the norm for maintaining lines. No consistent reports of industrial products (fibers, resins, oils) are found in the standard literature for this species.

Standards and regulation:
• In North Carolina, USA, commercial collection of Dionaea muscipula from the wild is restricted by state law; permits are required for any legal take, and wild take is generally prohibited to protect native populations.

Sustainability and sourcing:
• The global horticultural supply relies primarily on cultivated plants propagated by tissue culture and division. Wild collection is limited or prohibited in its native range to conserve remaining populations, and cultivated specimens are the primary source for education and display.

Synonyms Top

Scientific name Authority First published in
Dionaea corymbosa Raf. Med. Fl. 2: 217 (1830)
Dionaea sensitiva Salisb. Prodr. Stirp. Chap. Allerton : 321 (1796)
Dionaea sessiliflora Raf. Med. Fl. 2: 217 (1830)
Dionaea uniflora Raf. Atlantic J. 1: 78 (1832)
Drosera sessiliflora Raf. Atlantic J. 1: 148 (1832)
Drosera uniflora Raf. Atlantic J. 1: 148 (1832)
Dionaea muscipula J.Ellis ex L. Mant. Pl. Altera 238 (1771)

Common names Top

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Language Common/alternative name
English venus flytrap
Spanish dionea atrapamoscas
Spanish venus atrapamoscas
Afrikaans venusvlieëvanger
Arabic خناق الذباب
Arabic مصيدة فينوس
Azerbaijani milçəkqapan
azb میلچک قاپان
ban jebak lalat venus
Bulgarian Дионея
Bulgarian венерина мухоловка
Bengali ভেনাস ফাইট্র্যাপ
Bengali ভেনাস ফ্লাইট্র্যাপ
Cherokee ᏳᏈᎳ
Czech mucholapka podivná
Czech mucholapka
Danish fluefanger
Danish venus fluefanger
Danish venus-fluefanger
Danish venusfluefanger
German venusfliegenfalle
German venus-fliegenfalle
Greek Διωναία
Greek venus flytrap
Greek Διωναία η μυγοπαγίδα
Esperanto muŝkaptulo
Esperanto muŝkaptilo de venuso
Estonian kärbsepüünis
Basque dionea
Basque eulijale
Basque venus landarea
Basque venus eulijale
Persian مگسگیر ونوس
Persian ونوس گوشتخوار
Persian ونوس مگس خوار
Persian ونوس مگسخوار
Finnish kärpäsloukku
French dionée attrape-mouche
French dionee attrape-mouche
French dionée attrape-mouches
French gobe-mouche de vénus
French venus flytrap
Irish cuilghaiste véineas
Swiss German venusfliegenfalle
Hebrew דיונאה
Hebrew דיוניאה
Hebrew הדיוניאה
Hebrew מלכודת ונוס
Croatian venerina muholovka
Upper Sorbian muchowy rybork
Hungarian vénusz légycsapója
Armenian Վեներինա ճանճակալ
Armenian Վեներայի ճանճակալ
Indonesian perangkap lalat venus
Icelandic flugugrípur
Icelandic venusargildra
Italian dionea
Italian venus acchiappamosche
Japanese ハエトリグサ
Japanese ハエジゴク
Japanese ハエトリソウ
Georgian ვენერას ბუზიჭერია
Kazakh Шыбыншы Венерина
Korean 파리지옥속
Korean 파리지옥
Lithuanian jautrusis musėkautas
Lithuanian musėkautas
Latvian veneras mušķērājs
Macedonian Венерина муволовка
Malayalam വീനസ് ഫ്ളൈട്രാപ്പ്
Malayalam ഡയോണിയ
Marathi व्हीनस फ्लायट्रॅप
Malay venus
Malay penangkap lalat venus
Malay perangkap lalat venus
Burmese နတ်သမီးထောင်ချောက်ပင်
nan lia̍h-sîn-chháu
Norwegian Bokmål venusfluefanger
Norwegian Bokmål venus fluefanger
Norwegian Bokmål venusfluesnapper
Dutch venusvliegenvanger
Dutch venus vliegenvanger
Dutch venus' vliegenval
Dutch venus' vliegenvanger
Dutch venusvliegenval
Polish muchołówka amerykańska
Polish muchołówka
Portuguese dionéia
Portuguese vênus papa-moscas
Portuguese dioneia
Romanian venus flytrap
Russian Венерина мухоловка
Russian Дионея
Serbo-Croatian venerina muholovka
Slovak mucholapka obyčajná
Slovak mucholapka podivná
Slovak mucholapka
Slovenian muholovka
Serbian Венерина мухоловка
Swedish venus flugfälla
Swedish venusflugfälla
Tamil வில் பொறி
Telugu డయోనియా
Telugu డయోనియా మస్సిపులా
Telugu వీనస్ ఫ్లయ్ ట్రాప్
Thai กาบหอยแครง
Turkish sinekkapan bitkisi
Turkish venüs fly trap
Turkish venüs sinek kapanı
Turkish venüs sinekkapanı
Ukrainian Венерина мухоловка
Vietnamese cây bẫy kẹp
Vietnamese cây bắt mồi
Vietnamese cây bắt ruồi
Vietnamese cây bẫy mồi
Vietnamese cây bẫy ruồi
Chinese 捕蠅草
Chinese 捕蝇草
Chinese 捕蟲草屬
Chinese 捕蠅草屬
Chinese 捕蠅葉
Chinese 蒼蠅的地獄

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
  • Northern America
    • Northeastern U.S.A.
      • New Jersey
      • Pennsylvania
    • Northwestern U.S.A.
      • Washington
    • Southeastern U.S.A.
      • Alabama
      • Florida
      • North Carolina
      • South Carolina
      • Virginia
    • Southwestern U.S.A.
      • California

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000943687
UNII L531RAU25W
Florida Plant Atlas 1651
Flora of Alabama 5519
USDA Plants DIMU4
Tropicos 11400032
KEW urn:lsid:ipni.org:names:275898-2
The Plant List kew-62109
Missouri Botanical Garden 279896
Open Tree Of Life 14971
NCBI Taxonomy 4362
Nature Serve 2.159781
IUCN Red List 39636
IPNI 275898-2
iNaturalist 52666
GBIF 5421410
Freebase /m/01t4bh
EPPO DJOMU
EOL 584643
USDA GRIN 405268
Wikipedia Venus_flytrap
Plantarium 59680

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_054771495.1 Diomu_v2.1 Scaffold University of Würzburg 2025-07-17 272 2.38 Gb

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
The “plant neurobiology” revolution Minorsky PV Plant Signal Behav 06-May-2024
PMCID:PMC11085955
doi:10.1080/15592324.2024.2345413
PMID:38709727
Mechanosensing and anesthesia of single internodal cells of Chara Rodgers MJ, Staves MP Plant Signal Behav 11-Apr-2024
PMCID:PMC11017945
doi:10.1080/15592324.2024.2339574
PMID:38601988
Dehydration-induced corrugated folding in Rhapis excelsa plant leaves Guo K, Liu M, Vella D, Suresh S, Hsia KJ Proc Natl Acad Sci U S A 08-Apr-2024
PMCID:PMC11047117
doi:10.1073/pnas.2320259121
PMID:38588439
Haplotype-resolved genome of Mimosa bimucronata revealed insights into leaf movement and nitrogen fixation Jia H, Lin J, Lin Z, Wang Y, Xu L, Ding W, Ming R BMC Genomics 03-Apr-2024
PMCID:PMC10993578
doi:10.1186/s12864-024-10264-8
PMID:38570736
Revisiting a pollen-transmitted ilarvirus previously associated with angular mosaic of grapevine Mahillon M, Brodard J, Schoen R, Botermans M, Dubuis N, Groux R, Pannell JR, Blouin AG, Schumpp O Virus Res 22-Mar-2024
PMCID:PMC10979282
doi:10.1016/j.virusres.2024.199362
PMID:38508402
Effect of the General Anaesthetic Ketamine on Electrical and Ca2+ Signal Propagation in Arabidopsis thaliana Pavlovič A, Ševčíková L, Hřivňacký M, Rác M Plants (Basel) 20-Mar-2024
PMCID:PMC10975207
doi:10.3390/plants13060894
PMID:38592882
Chromosome-level genome assembly provides insights into the genome evolution and functional importance of the phenylpropanoid–flavonoid pathway in Thymus mongolicus Dang Z, Xu Y, Zhang X, Mi W, Chi Y, Tian Y, Liu Y, Ren W BMC Genomics 19-Mar-2024
PMCID:PMC10949689
doi:10.1186/s12864-024-10202-8
PMID:38504151
A library of electrophysiological responses in plants - a model of transversal education and open science Madariaga D, Arro D, Irarrázaval C, Soto A, Guerra F, Romero A, Ovalle F, Fedrigolli E, DesRosiers T, Serbe-Kamp É, Marzullo T Plant Signal Behav 17-Mar-2024
PMCID:PMC10950275
doi:10.1080/15592324.2024.2310977
PMID:38493508
A helping hand: roles for accessory cells in the sense of touch across species Logan DR, Hall J, Bianchi L Front Cell Neurosci 16-Feb-2024
PMCID:PMC10904576
doi:10.3389/fncel.2024.1367476
PMID:38433863
ATP homeostasis and signaling in plants Xiao J, Zhou Y, Xie Y, Li T, Su X, He J, Jiang Y, Zhu H, Qu H Plant Commun 07-Feb-2024
PMCID:PMC11009363
doi:10.1016/j.xplc.2024.100834
PMID:38327057
Buckling-induced sound production in the aeroelastic tymbals of Yponomeuta Mendoza Nava H, Holderied MW, Pirrera A, Groh RM Proc Natl Acad Sci U S A 05-Feb-2024
PMCID:PMC10873622
doi:10.1073/pnas.2313549121
PMID:38315846
Do Cuticular Gaps Make It Possible to Study the Composition of the Cell Walls in the Glands of Drosophyllum lusitanicum? Płachno BJ, Kapusta M, Stolarczyk P, Świątek P Int J Mol Sci 21-Jan-2024
PMCID:PMC10816202
doi:10.3390/ijms25021320
PMID:38279320
Digital image correlation techniques for motion analysis and biomechanical characterization of plants Mylo MD, Poppinga S Front Plant Sci 11-Jan-2024
PMCID:PMC10808816
doi:10.3389/fpls.2023.1335445
PMID:38273955
A charged existence: A century of transmembrane ion transport in plants Blatt MR Plant Physiol 02-Jan-2024
PMCID:PMC11060664
doi:10.1093/plphys/kiad630
PMID:38163639
Distinctive plastome evolution in carnivorous angiosperms Fu CN, Wicke S, Zhu AD, Li DZ, Gao LM BMC Plant Biol 20-Dec-2023
PMCID:PMC10731798
doi:10.1186/s12870-023-04682-1
PMID:38124058

Phytochemical Profile Top

Add a new one!
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 / Naphthalenes / Naphthoquinones
(3R)-8-hydroxy-3-(hydroxymethyl)-3-methyl-2H-naphthalene-1,4-dione 101337388 Click to see CC1(CC(=O)C2=C(C1=O)C=CC=C2O)CO 220.22 unknown https://doi.org/10.1246/BCSJ.77.537
https://doi.org/10.1016/S0031-9422(00)80563-4
3-Chloro-5-hydroxy-2-methylnaphthalene-1,4-dione 338719 Click to see 222.62 unknown https://doi.org/10.1016/0031-9422(96)89675-0
https://doi.org/10.1016/0031-9422(90)85125-Y
5-Hydroxy-3-(hydroxymethyl)-2-methylnaphthalene-1,4-dione 11481367 Click to see CC1=C(C(=O)C2=C(C1=O)C=CC=C2O)CO 218.20 unknown https://doi.org/10.1246/BCSJ.77.537
7-Methyljuglone 26905 Click to see CC1=CC2=C(C(=O)C=CC2=O)C(=C1)O 188.18 unknown https://doi.org/10.1055/S-2008-1081303
8-hydroxy-3-(hydroxymethyl)-3-methyl-2H-naphthalene-1,4-dione 129233230 Click to see 220.22 unknown https://doi.org/10.1246/BCSJ.77.537
https://doi.org/10.1016/S0031-9422(00)80563-4
Droserone 442739 Click to see CC1=C(C2=C(C(=CC=C2)O)C(=O)C1=O)O 204.18 unknown https://doi.org/10.1016/0031-9422(90)85125-Y
Plumbagin 10205 Click to see 188.18 unknown https://doi.org/10.1016/S0031-9422(00)80563-4
https://doi.org/10.1055/S-2008-1081303
https://doi.org/10.1016/0031-9422(90)85125-Y
https://doi.org/10.1246/BCSJ.77.537
https://doi.org/10.1016/0031-9422(96)89675-0
> Benzenoids / Tetralins
(3S,4S)-4,8-dihydroxy-3-methyl-tetralin-1-one 46888858 Click to see CC1CC(=O)C2=C(C1O)C=CC=C2O 192.21 unknown https://doi.org/10.1246/BCSJ.77.537
4,8-dihydroxy-3-methyl-3,4-dihydro-2H-naphthalen-1-one 71329296 Click to see 192.21 unknown https://doi.org/10.1246/BCSJ.77.537
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid 76141271 Click to see 454.70 unknown https://doi.org/10.1016/0031-9422(90)85125-Y
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-(4,8-dihydroxy-3-methylnaphthalen-1-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol 14482771 Click to see 352.30 unknown https://doi.org/10.1016/0031-9422(96)89675-0
https://doi.org/10.1246/BCSJ.77.537
https://doi.org/10.1016/0031-9422(90)85125-Y
> Organoheterocyclic compounds / Benzofurans
Methyl 2-(7-hydroxy-2-methyl-3-oxo-1-benzofuran-2-yl)acetate 163020396 Click to see 236.22 unknown https://doi.org/10.1016/S0031-9422(00)80563-4
methyl 2-[(2R)-7-hydroxy-2-methyl-3-oxo-1-benzofuran-2-yl]acetate 138965655 Click to see CC1(C(=O)C2=C(O1)C(=CC=C2)O)CC(=O)OC 236.22 unknown https://doi.org/10.1016/S0031-9422(00)80563-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4R,5R,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 162857846 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 616.50 unknown https://doi.org/10.1055/S-2006-957824
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1055/S-2006-957824
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 464.40 unknown https://doi.org/10.1055/S-2006-957824
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1055/S-2006-957824
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 12304322 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1055/S-2006-957824
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 12358426 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2006-957824
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2006-957824
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2006-957824
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 https://doi.org/10.1055/S-2006-957824
Quercetin 3-(2''-galloylglucoside) 13889202 Click to see 616.50 unknown https://doi.org/10.1055/S-2006-957824
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2006-957824
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
5,2'-Dihydroxy-7,8-dimethoxyisoflavone 14034287 Click to see 314.29 unknown https://doi.org/10.1016/0031-9422(96)89675-0
https://doi.org/10.1016/0031-9422(90)85125-Y
https://doi.org/10.1246/BCSJ.77.537
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3-O-methylellagic acid 13915428 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O)O 316.22 unknown https://doi.org/10.1016/0031-9422(96)89675-0
https://doi.org/10.1055/S-2006-957824
3,3'-Di-O-Meellagic acid 4'-glucoside 75253873 Click to see 492.40 unknown https://doi.org/10.1016/0031-9422(96)89675-0
3,3'-di-O-Methylellagic acid 5488919 Click to see 330.24 unknown https://doi.org/10.1016/0031-9422(96)89675-0
3,3'-Di-O-Methylellagic Acid 4'-Glucoside 46918077 Click to see 492.40 unknown https://doi.org/10.1016/0031-9422(96)89675-0
7,14-dimethoxy-6,13-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione 101690769 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)OC)OC5C(C(C(C(O5)CO)O)O)O)OC6C(C(C(C(O6)CO)O)O)O 654.50 unknown https://doi.org/10.1016/0031-9422(96)89675-0
7,14-Dimethoxy-6,13-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione 162874706 Click to see 654.50 unknown https://doi.org/10.1016/0031-9422(96)89675-0
Ellagic Acid 5281855 Click to see 302.19 unknown https://doi.org/10.1055/S-2006-957824
https://doi.org/10.1016/0031-9422(96)89675-0

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