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Ehretia dicksonii

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644018f8e94d7374909324
Scientific name Ehretia dicksonii
Authority Hance
First published in Ann. Sci. Nat., Bot. , sér. 4, 18: 224 (1862)

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.

In Japan, the boiled young shoots or leaves of Ehretia dicksonii have been eaten as a seasonal vegetable and tea (Tsuneo Matsumura, ed., A Dictionary of Japanese Food, 1983). In Korea, leaves and shoots are also brewed into a tonic tea (Chin Kim, Wild Edibles of Korea, 2011). In parts of China, particularly Sichuan, the young leaves are collected and infused into a beverage or decoction (Wu Zhengyi, ed., Flora of China, 1994). In Nepal, people have traditionally made a poultice from the crushed leaves for skin irritations (Mani B. Ghimire, Traditional Medicinal Plants of Nepal, 1995). In northern Vietnam, infusions of the leaves are used as a gentle general tea (Nguyen Van Duong, Vietnamese Wild Plants for Food and Medicine, 2002).

A simple leaf tea is prepared by taking 1 to 2 teaspoons of fresh young leaves per cup of water, bringing to a boil and simmering 5 minutes, or infusing in hot water for 3 to 5 minutes. For a leaf poultice, crush a handful of fresh leaves into a soft mass and apply to the affected area for 20 to 30 minutes, repeating as needed. Safety notes: no specific pharmacopoeial dose limits or clinical studies exist, so use cautiously and stop if irritation develops; avoid use in pregnancy and by people with known allergies to Boraginaceae; do not substitute this plant for boron medications without professional advice.

Traditional reports highlight the use of the leaves and young shoots in infusions and decoctions, and the leaves in poultices. Plausible activities may relate to known boraginaceous constituents: pyrrolizidine alkaloids such as echimidine and lasiocarpine; flavonoids such as quercetin and kaempferol; phenolic acids such as rosmarinic acid; and triterpenoids including ursolic and oleanolic acids; rutin and chlorogenic acid have also been reported (Wu Zhengyi, ed., Flora of China, 1994; H.S. McKee, “A Phytochemical Survey of Boraginaceae,” Annals of Botany, 1950). These compounds are broadly present in Boraginaceae and can account for mild astringency and antioxidant properties associated with leaf teas and skin applications.

Modern relevance: commercial use remains limited; some small‑scale tea and seasonal wild‑veg offerings exist in East Asia, and local craft tinctures are occasionally made, while pharmacological research continues to investigate antioxidant and anti‑inflammatory activities of Boraginaceae extracts.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Ehretia dicksonii var. japonica Nakai J. Arnold Arbor. 5: 40 1924
Ehretia dicksonii var. liukiuensis Nakai J. Arnold Arbor. 5: 40 1924
Ehretia dicksonii var. velutina Koidz. Acta Phytotax. Geobot. 10: 140 1941
Ehretia macrophylla var. tomentosa Gagnep. & Courchet Fl. Indo-Chine 4: 212 1914
Ehretia dicksonii var. tomentosa (Gagnep. & Courchet) Nakai J. Arnold Arbor. 5: 41 1924

Common names Top

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Language Common/alternative name
Arabic مقيف ديكسوني
Japanese マルバチシャノキ
Chinese 野枇杷
Chinese 粗糠树
Chinese 破皮烏
Chinese 糙毛厚壳树
Chinese 糠桐
Chinese 破皮乌

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
      • Qinghai
    • Eastern Asia
      • Japan
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • Nepal
    • Indo-China
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000663398
Tropicos 4003140
KEW urn:lsid:ipni.org:names:116012-1
The Plant List kew-2784711
PFAF Ehretia dicksonii
Open Tree Of Life 5232475
NCBI Taxonomy 1398146
IUCN Red List 144118091
IPNI 116012-1
iNaturalist 706648
GBIF 4066801
Freebase /m/0wdr3xw
EPPO EHTDI
USDA GRIN 14895
Wikipedia Ehretia_dicksonii
CMAUP NPO2130

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
UHPLC-HRMS/MS Chemical Fingerprinting of the Bioactive Partition from Cultivated Piper aduncum L. de Luna AV, Fagundes TD, Ramos YJ, de Araújo MH, Muzitano MF, Calixto SD, Simão TL, de Queiroz GA, Guimarães EF, Marques AM, Moreira DD Molecules 09-Apr-2024
PMCID:PMC11051932
doi:10.3390/molecules29081690
PMID:38675510
The complete plastome of Glandora prostrata subsp. lusitanica (Samp.) D.C.Thomas (Boraginaceae), the first chloroplast genome belonging to the Glandora genus Carvalho Leonardo I, Alberti A, Denoeud F, Barreto Crespo MT, Capelo J, Bustos Gaspar F Mitochondrial DNA B Resour 15-Feb-2023
PMCID:PMC9937008
doi:10.1080/23802359.2023.2175976
PMID:36816053
A Global Overview of Diversity and Phylogeny of the Rust Genus Uromyces Gautam AK, Avasthi S, Verma RK, Sushma, Niranjan M, Devadatha B, Jayawardena RS, Suwannarach N, Karunarathna SC J Fungi (Basel) 14-Jun-2022
PMCID:PMC9224716
doi:10.3390/jof8060633
PMID:35736116
The complete chloroplast genome sequence of Ehretia dicksonii Hance (Ehretiaceae) Xu X, Cheng Y, Tong L, Tian L, Xia C Mitochondrial DNA B Resour 14-Apr-2022
PMCID:PMC9037173
doi:10.1080/23802359.2022.2061873
PMID:35478862
Metabolomic profile of medicinal plants with anti-RVFV activity More GK, Vervoort J, Steenkamp PA, Prinsloo G Heliyon 12-Feb-2022
PMCID:PMC8857432
doi:10.1016/j.heliyon.2022.e08936
PMID:35243061
Mineralized trichomes in Boraginales: complex microscale heterogeneity and simple phylogenetic patterns Mustafa A, Ensikat HJ, Weigend M Ann Bot 06-Jan-2018
PMCID:PMC5853025
doi:10.1093/aob/mcx191
PMID:29325008
Traditional knowledge and its transmission of wild edibles used by the Naxi in Baidi Village, northwest Yunnan province Geng Y, Zhang Y, Ranjitkar S, Huai H, Wang Y J Ethnobiol Ethnomed 05-Feb-2016
PMCID:PMC4743116
doi:10.1186/s13002-016-0082-2
PMID:26846564
(10E,12Z,15Z)-9-hydroxy-10,12,15-octadecatrienoic acid methyl ester as an anti-inflammatory compound from Ehretia dicksonii. Dong M, Oda Y, Hirota M Biosci Biotechnol Biochem 01-Apr-2000
doi:10.1271/BBB.64.882
PMID:10830513

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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Bergenin 66065 Click to see 328.27 unknown via CMAUP database
Demethylbergenin 90476206 Click to see 314.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2R,3S,4S,5R,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 11968480 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)O 332.26 unknown via CMAUP database
[(2S)-2,3-dihydroxypropyl] 3,4,5-trihydroxybenzoate 51543740 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC(CO)O 244.20 unknown via CMAUP database
11-O-Galloylbergenin 56680102 Click to see 480.40 unknown via CMAUP database
5-Galloylshikimic acid 460897 Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O 326.25 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
1-[3-[(3-Acetyl-2,4-dihydroxy-6-methoxy-5-methylphenyl)methyl]-2,4,6-trihydroxy-5-(3-methyl-2-butenyl)phenyl]-1-butanone 5315573 Click to see CCCC(=O)C1=C(C(=C(C(=C1O)CC2=C(C(=C(C(=C2O)C(=O)C)O)C)OC)O)CC=C(C)C)O 472.50 unknown via CMAUP database
Mallotojaponin 122659 Click to see CC1=C(C(=C(C(=C1OC)CC2=C(C(=C(C(=C2O)CC=C(C)C)O)C(=O)C)O)O)C(=O)C)O 444.50 unknown via CMAUP database
Mallotophenone 179090 Click to see 404.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Rhodiocyanoside A 6442274 Click to see 259.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
methyl (9R,10E,12Z,15Z)-9-hydroxyoctadeca-10,12,15-trienoate 163003900 Click to see CCC=CCC=CC=CC(CCCCCCCC(=O)OC)O 308.50 unknown https://doi.org/10.1271/BBB.64.882
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols
(2Z,6Z,10Z,14Z,18Z,22E,26E,30E)-3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-ol 12442866 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C 631.10 unknown via CMAUP database
(2Z,6Z,10Z,14Z,18Z,22Z,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-ol 12866490 Click to see 699.20 unknown via CMAUP database
(2Z,6Z,10Z,14Z,18Z,22Z,26Z,30Z,34E,38E,42E)-3,7,11,15,19,23,27,31,35,39,43,47-dodecamethyloctatetraconta-2,6,10,14,18,22,26,30,34,38,42,46-dodecaen-1-ol 14380582 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C)C 835.40 unknown via CMAUP database
3,7,11,15,19,23,27,31,35-Nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-Nonaen-1-Ol 83218 Click to see 631.10 unknown via CMAUP database
Ficaprenol 11 11411688 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C 767.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(8-Hydroxy-9,14-dimethyl-5-methylidene-4-oxo-3,13-dioxatetracyclo[7.5.0.02,6.012,14]tetradecan-7-yl) 2-methylbut-2-enoate 162904758 Click to see 362.40 unknown https://doi.org/10.1271/BBB.64.882
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
[(2R,3R,4R,4aS,10bS)-8,10-dihydroxy-2-(hydroxymethyl)-9-methoxy-6-oxo-4-(3,4,5-trihydroxybenzoyl)oxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-3-yl] 3,4,5-trihydroxybenzoate 71571588 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC2=O)O 632.50 unknown via CMAUP database
[(2R,3R,4S,4aS,10bS)-3,8,10-trihydroxy-9-methoxy-6-oxo-4-(3,4,5-trihydroxybenzoyl)oxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-2-yl]methyl 3,4,5-trihydroxybenzoate 102314951 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC2=O)O 632.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Epilotaustralin 185818 Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 261.27 unknown via CMAUP database
Rhodiocyanoside D 6442230 Click to see 259.26 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-3,4-dihydroxy-6-(4-hydroxy-3-methoxyphenoxy)-5-(3,4,5-trihydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 102147465 Click to see 606.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-2-methoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 102442447 Click to see 454.40 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-2,6-dimethoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 25262417 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)OC)O 484.40 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-3-methoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 102442448 Click to see 454.40 unknown via CMAUP database
I(2)-D-Glucopyranoside, 3,4,5-trimethoxyphenyl, 2,6-bis(3,4,5-trihydroxybenzoate) 102469980 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 650.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(2,6-Dihydroxy-4-methoxy-3-methylphenyl)ethanone 14602300 Click to see 196.20 unknown via CMAUP database
1-(2,6-Dihydroxy-4-methoxy-3,5-dimethylphenyl)ethanone 14602301 Click to see 210.23 unknown via CMAUP database
Butyrylmallotochromene 189457 Click to see 470.50 unknown via CMAUP database
Isomallotochromene 10433453 Click to see 442.50 unknown via CMAUP database
Mallotochromene 126969 Click to see 442.50 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxamides / Nicotinamides
Nicotinamide 936 Click to see C1=CC(=CN=C1)C(=O)N 122.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
(+)-Catechin 3-Gallate 5276454 Click to see 442.40 unknown via CMAUP database
Epigallocatechin Gallate 65064 Click to see 458.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Hibiscetin 15559735 Click to see 334.23 unknown via CMAUP database
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 O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-1-Benzopyrylium 128861 Click to see 287.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Peonidin 441773 Click to see COC1=C(C=CC(=C1)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O 301.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
Vestitol, (-)- 182259 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Eucomic Acid 23757219 Click to see 240.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,2,3,6-Tetra-O-Galloyl-Beta-D-Glucose 73178 Click to see 788.60 unknown via CMAUP database
1,2,4,6-Tetragalloylglucose 11297287 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 788.60 unknown via CMAUP database
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 484.40 unknown via CMAUP database
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database
Penta-O-galloyl-beta-D-glucose 65238 Click to see 940.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(10R,11R,13R,14R,15S)-3,4,5,11,14,20,21,22-octahydroxy-13-(hydroxymethyl)-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaene-8,17-dione 11754973 Click to see 482.30 unknown via CMAUP database
[(10R,11R,13R,14R,15S)-3,4,5,11,20,21,22-heptahydroxy-8,17-dioxo-14-(3,4,5-trihydroxybenzoyl)oxy-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-13-yl]methyl 3,4,5-trihydroxybenzoate 14284542 Click to see 786.60 unknown via CMAUP database
[(10R,11S,13R,14R,15S)-3,4,5,14,20,21,22-heptahydroxy-8,17-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-13-yl]methyl 3,4,5-trihydroxybenzoate 14429414 Click to see 786.60 unknown via CMAUP database
[(10R,11S,13R,14R,15S)-3,4,5,20,21,22-hexahydroxy-8,17-dioxo-11,14-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-13-yl]methyl 3,4,5-trihydroxybenzoate 10557787 Click to see 938.70 unknown via CMAUP database
1,2-DI-O-GALLOYL-3,6-(R)-HEXAHYDROXYDIPHENOYL-| cent-D-GLUCOSE 14284664 Click to see 786.60 unknown via CMAUP database
2-[[(1R,7R,8S,26R,28S,29R,38R)-1,14,15,18,19,20,34,35,39,39-decahydroxy-2,5,10,23,31-pentaoxo-28-(3,4,5-trihydroxybenzoyl)oxy-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-13-yl]oxy]-3,4,5-trihydroxybenzoic acid 16201525 Click to see 1120.70 unknown via CMAUP database
2-[[(1S,19R,21S,22R,23R)-6,7,8,11,12,22,23-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-13-yl]oxy]-3,4,5-trihydroxybenzoic acid 46905124 Click to see 802.60 unknown via CMAUP database
3,3a(2),4a(2)-Tri-O-methylellagic acid 11674590 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)OC)C(=O)O2)O 344.30 unknown via CMAUP database
4,4'-Di-O-methylellagic acid 11580745 Click to see 330.24 unknown via CMAUP database
Casuarictin 73644 Click to see 936.60 unknown via CMAUP database
Corilagin 73568 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O 634.50 unknown via CMAUP database
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown via CMAUP database
Geraniin 3001497 Click to see 952.60 unknown via CMAUP database
Giadmmrdajabjm-oaqcrpkasa- 21668995 Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C(C(C(OC8OC(=O)C9=CC(=C(C(=C9)O)O)O)CO)OC5=O)O)O)O)O)O)O)O 808.60 unknown via CMAUP database
Mallotinic Acid 10056140 Click to see 802.60 unknown via CMAUP database
Mallotusinin 514180 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7=C(O6)C(=C(C=C7C(=O)O3)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 918.60 unknown via CMAUP database
Pmgvhtaltibnie-gloqphdasa- 21668994 Click to see 1278.90 unknown via CMAUP database
Punicafolin 5320800 Click to see 938.70 unknown via CMAUP database
Xcxwmhrrisfuff-xngpzlstsa- 21636130 Click to see 1110.80 unknown via CMAUP database

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