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Dillenia indica

Dillenia indica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Dillenia indica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Dillenia indica - 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 UUID64401711dfce4323315069
Scientific name Dillenia indica
Authority L.
First published in Sp. Pl. : 535 (1753)

Description Top

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Dillenia indica, also known as elephant apple or ou tenga, is a species of evergreen shrub or tree native to China and tropical Asia. It was first described by Linnaeus in 1759. The plant can grow up to 30 meters tall and has large, corrugated leaves and white flowers with two sets of stamens. Its fruit is large, round, and greenish yellow, with a fibrous and glutinous pulp containing edible seeds. The name elephant apple comes from the fact that the fruit is only accessible to large animals like elephants, making them important seed dispersers. However, the tree has also developed a backup system where the fruits soften on the forest floor, allowing access to smaller animals. The fruit pulp is used in Indian cuisine and the tree is also a source of firewood. Due to its importance in the forest ecosystem, collection and sale of the fruit is prohibited.

Synonyms Top

Scientific name Authority First published in
Dillenia elongata Miq. Fl. Ned. Ind. 1(2): 12 (1858)
Dillenia indica f. elongata (Miq.) Miq. Ann. Mus. Bot. Lugduno-Batavi 4: 79 1868

Common names Top

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Language Common/alternative name
English elephant apple
English hondapara tree
English indian catmon
English chulta
Arabic ديلنيا هندية
Assamese ঔ টেঙা
Bengali চাইলতে
Bengali চালিতা
Bengali চালতা
German indischer rosenapfel
Persian سیب فیلی
Finnish intiandillenia
Hungarian pompás dillénia
Indonesian jongi
Japanese ビワモドキ
jv apel gajah
Kannada ಬೆಟ್ಟಕಣಿಗಲು
Korean 딜레니아
Malayalam മലമ്പുന്ന
mnw သပြု၊ တၞံ
Burmese သပြုပင်
Oriya ଓଉ
Polish ukęśl indyjska
Polish ukęśla indyjska
Portuguese maçã de elefante
Portuguese Árvore da pataca
Portuguese Árvore do dinheiro
Portuguese Árvore-da-pataca
Portuguese Árvore-do-dinheiro
Portuguese dilênia
Portuguese flor de abril
Portuguese flor-de-abril
Portuguese maça de elefante
Portuguese maçã-de-elefante
Russian Слоновое яблоко
Slovenian slonje jabolko
Tamil உவா மரம்
Tamil யானை ஆப்பிள்
Tamil பாங்கர்
Tamil ஓமை
Telugu రేవడిచెట్టు
Telugu పెద్దకళింగ
Thai มะตาด
Urdu سیب فیلی
Chinese 第倫桃
Chinese 五桠果

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • West-central Tropical Africa
      • Gulf Of Guinea Islands
    • Western Indian Ocean
      • Comoros
      • Mauritius
      • Réunion
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines
      • Sumatera
  • Southern America
    • Caribbean
      • Cuba
      • Trinidad-Tobago
      • Windward Islands
    • Western South America
      • Ecuador

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000647564
USDA Plants DIIN6
Tropicos 10900002
INPN 447112
KEW urn:lsid:ipni.org:names:316684-1
The Plant List kew-2768269
Open Tree Of Life 244320
NCBI Taxonomy 4378
IUCN Red List 61994577
IPNI 316684-1
iNaturalist 327691
GBIF 5383898
Freebase /m/02x8lf0
EPPO DLNIN
EOL 396514
USDA GRIN 14122
Wikipedia Dillenia_indica
CMAUP NPO21691

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
Ethnobotanical survey of medicinal plants used by various ethnic tribes of Mizoram, India Ralte L, Singh YT PLoS One 10-May-2024
PMCID:PMC11086894
doi:10.1371/journal.pone.0302792
PMID:38728345
Electrospun nanofibers synthesized from polymers incorporated with bioactive compounds for wound healing Palani N, Vijayakumar P, Monisha P, Ayyadurai S, Rajadesingu S J Nanobiotechnology 27-Apr-2024
PMCID:PMC11056076
doi:10.1186/s12951-024-02491-8
PMID:38678271
Development and Performance Analysis of an Automatic Core Cutter for Elephant Apple (Dillenia indica L.) Processing Saikia D, Kesavan R, Sharma M, Inbaraj BS, Nayak PK, Sridhar K Foods 11-Mar-2024
PMCID:PMC10969683
doi:10.3390/foods13060848
PMID:38540838
Effects of Thermosonication on the Antioxidant Capacity and Physicochemical, Bioactive, Microbiological, and Sensory Qualities of Blackcurrant Juice Qiu X, Su J, Nie J, Zhang Z, Ren J, Wang S, Pei Y, Li X Foods 06-Mar-2024
PMCID:PMC10931099
doi:10.3390/foods13050809
PMID:38472922
Biosynthesis of silver nanoparticles by banana pulp extract: Characterizations, antibacterial activity, and bioelectricity generation Ohiduzzaman M, Khan MN, Khan KA, Paul B Heliyon 01-Feb-2024
PMCID:PMC10848009
doi:10.1016/j.heliyon.2024.e25520
PMID:38327438
Tailoring the Structural and Optical Properties of Cerium Oxide Nanoparticles Prepared by an Ecofriendly Green Route Using Plant Extracts Fifere N, Ardeleanu R, Doroftei F, Dobromir M, Airinei A Int J Mol Sci 04-Jan-2024
PMCID:PMC10779659
doi:10.3390/ijms25010681
PMID:38203851
Selenium Nanoparticles: Green Synthesis and Biomedical Application Mikhailova EO Molecules 15-Dec-2023
PMCID:PMC10745377
doi:10.3390/molecules28248125
PMID:38138613
Dynamics of Endophytic Fungal Communities Associated with Cultivated Medicinal Plants in Farmland Ecosystem He C, Meng D, Li W, Li X, He X J Fungi (Basel) 04-Dec-2023
PMCID:PMC10744690
doi:10.3390/jof9121165
PMID:38132766
The presence of wild edible plants and determinants influencing their harvest, consumption, and conservation in south eastern Bhutan Bajgai RC, Bajgai Y, Johnson SB PLoS One 10-Oct-2023
PMCID:PMC10564141
doi:10.1371/journal.pone.0285936
PMID:37816046
Comparative transcriptomics reveals divergence in pathogen response gene families amongst 20 forest tree species Lu M, Cao M, Yang J, Swenson NG G3 (Bethesda) 09-Oct-2023
PMCID:PMC10700026
doi:10.1093/g3journal/jkad233
PMID:37812763
Current Overview of Metal Nanoparticles’ Synthesis, Characterization, and Biomedical Applications, with a Focus on Silver and Gold Nanoparticles Burlec AF, Corciova A, Boev M, Batir-Marin D, Mircea C, Cioanca O, Danila G, Danila M, Bucur AF, Hancianu M Pharmaceuticals (Basel) 04-Oct-2023
PMCID:PMC10610223
doi:10.3390/ph16101410
PMID:37895881
Molecular Identification of Juglans Regia Endophyte LTL-G3, Its Antifungal Potential and Bioactive Substances Hao Y, Hui J, Du T, Ge X, Zhai M Iran J Biotechnol 01-Oct-2023
PMCID:PMC10804068
doi:10.30498/ijb.2023.352005.3450
PMID:38269197
Interactions of naturally occurring compounds with antimicrobials Malczak I, Gajda A J Pharm Anal 23-Sep-2023
PMCID:PMC10785267
doi:10.1016/j.jpha.2023.09.014
PMID:38223447
Application of thermosonication for guava juice processing: Impacts on bioactive, microbial, enzymatic and quality attributes Kalsi BS, Singh S, Alam MS, Bhatia S Ultrason Sonochem 07-Sep-2023
PMCID:PMC10506052
doi:10.1016/j.ultsonch.2023.106595
PMID:37699293
Hippophae rhamnoides L. (sea buckthorn) mediated green synthesis of copper nanoparticles and their application in anticancer activity Dadhwal P, Dhingra HK, Dwivedi V, Alarifi S, Kalasariya H, Yadav VK, Patel A Front Mol Biosci 24-Aug-2023
PMCID:PMC10484619
doi:10.3389/fmolb.2023.1246728
PMID:37692067

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 / Anthracenes
(10S)-10-[(9R)-4,5-dihydroxy-2-methyl-10-oxo-9H-anthracen-9-yl]-1,3,8-trihydroxy-6-methyl-10H-anthracen-9-one 44567184 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C5=C(C(=CC(=C5)C)O)C(=O)C6=C4C=C(C=C6O)O)C=CC=C3O 494.50 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
4-hydroxy-9,10-dioxo-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(oxalooxymethyl)oxan-2-yl]oxyanthracene-2-carboxylic acid 11972451 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC(=O)C(=O)O)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)C(=O)O 518.40 unknown via CMAUP database
Rhein 10168 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)C(=O)O 284.22 unknown via CMAUP database
Rhein-8-glucoside 5320961 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)C(=O)O 446.40 unknown via CMAUP database
Sennidin A 92826 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C5=C(C(=CC=C5)O)C(=O)C6=C4C=C(C=C6O)C(=O)O)C=C(C=C3O)C(=O)O 538.50 unknown via CMAUP database
Sennoside A 73111 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2C5C6=C(C(=CC=C6)OC7C(C(C(C(O7)CO)O)O)O)C(=O)C8=C5C=C(C=C8O)C(=O)O)C=C(C=C4O)C(=O)O 862.70 unknown via CMAUP database
Sennoside C 46173829 Click to see C1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2C5C6=C(C(=CC=C6)OC7C(C(C(C(O7)CO)O)O)O)C(=O)C8=C5C=C(C=C8O)C(=O)O)C=C(C=C4O)CO 848.80 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
1-hydroxy-3-methoxy-6-methyl-8-[(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]oxyanthracene-9,10-dione 5320543 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)C(=O)C5=C(C2=O)C=C(C=C5O)OC 608.50 unknown via CMAUP database
Aloe emodin 10207 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)CO 270.24 unknown via CMAUP database
Aloe-emodin-glucoside 147295 Click to see C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)COC4C(C(C(C(O4)CO)O)O)O 432.40 unknown via CMAUP database
Chrysophanein 6324923 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=CC=C4O 416.40 unknown via CMAUP database
Chrysophanic acid 10208 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O 254.24 unknown via CMAUP database
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown via CMAUP database
Pulmatin 442731 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown via CMAUP database
Rheochrysin 168938 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)OC 446.40 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown via CMAUP database
Emodin 1-O-beta-D-glucoside 5319333 Click to see CC1=CC2=C(C(=C1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C4=C(C2=O)C=C(C=C4O)O 432.40 unknown via CMAUP database
Emodin-8-glucoside 99649 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O 432.40 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 C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(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
6-O-galloyl-beta-D-glucose 5317463 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
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carbaldehyde 317607 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O 440.70 unknown via CMAUP database
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/J.PHYMED.2009.07.010
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/J.PHYMED.2009.07.010
> 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
(2S)-5-amino-2-ammonio-5-oxopentanoate 6992086 Click to see C(CC(=O)N)C(C(=O)[O-])[NH3+] 146.14 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[1-hydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 5319972 Click to see CC1=CC2=C(C(=CC=C2)OC3C(C(C(C(O3)CO)O)O)O)C(=C1C(=O)C)O 378.40 unknown via CMAUP database
1-[1,6-dihydroxy-3-methyl-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxynaphthalen-2-yl]ethanone 100753 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)O 394.40 unknown via CMAUP database
2-[[(2R,3S,4S,5R,6S)-6-(7-acetyl-8-hydroxy-3-methoxy-6-methylnaphthalen-1-yl)oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-2-oxoacetic acid 5321979 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)COC(=O)C(=O)O)O)O)O)OC 480.40 unknown via CMAUP database
2-methyl-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromene-5-carboxylic acid 5315687 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)OC3C(C(C(C(O3)CO)O)O)O)C(=O)O 382.30 unknown via CMAUP database
3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-2-yl]oxybenzoic acid 11972354 Click to see C1=C(C=C(C(=C1O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)C(=O)O 484.40 unknown via CMAUP database
Raspberryketone glucoside 5320521 Click to see CC(=O)CCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 326.34 unknown via CMAUP database
Torachrysone 8-O-Glucoside 11972479 Click to see CC1=CC2=CC(=CC(=C2C(=C1C(=O)C)O)OC3C(C(C(C(O3)CO)O)O)O)OC 408.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl] (E)-3-phenylprop-2-enoate 11972309 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(OC2O)CO)O)O 310.30 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
2H-1-Benzopyran-5-acetic acid, 3,4-dihydro-7-hydroxy-2-methyl-4-oxo-, (S)- 5319543 Click to see CC1CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)O 236.22 unknown via CMAUP database
4H-1-Benzopyran-4-one, 5-acetyl-7-hydroxy-2-methyl- 5315891 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)C(=O)C 218.20 unknown via CMAUP database
7-Hydroxy-2-[(2S)-2-hydroxypropyl]-5-methyl-4H-1-benzopyran-4-one 45272307 Click to see CC1=CC(=CC2=C1C(=O)C=C(O2)CC(C)O)O 234.25 unknown via CMAUP database
7-Hydroxy-2-methyl-4-oxo-4H-1-benzopyran-5-acetic acid 14429402 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)O 234.20 unknown via CMAUP database
7-Hydroxy-2-methyl-4-oxo-4H-1-benzopyran-5-carboxylic acid 5315688 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)C(=O)O 220.18 unknown via CMAUP database
Cassiachromone 5319500 Click to see CC1=CC(=O)C2=C(C=C(C=C2O1)O)CC(=O)C 232.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
3,3'-Digalloylprocyanidin B2 124016 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 882.70 unknown via CMAUP database
procyanidin B1 3-O-gallate 12795888 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)O 730.60 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
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Dillenetin 5487855 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)OC 330.29 unknown https://doi.org/10.1039/P19750000612
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(+)-Catechin-5-O-I(2)-D-glucopyranoside 6324898 Click to see C1C(C(OC2=C1C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Rhapontigenin 5320954 Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)O)O)O 258.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
[(2R,3S,4S,5R,6S)-6-[4-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 5322088 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O 542.50 unknown via CMAUP database
Resveratrol 4'-O-beta-D-(2''-O-galloyl)-glucopyranoside 10325054 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 542.50 unknown via CMAUP database
Resveratroloside 5322089 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 390.40 unknown via CMAUP database
Rhapontin 637213 Click to see COC1=C(C=C(C=C1)C=CC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 420.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,2,6-Trigalloylglucose 440308 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)O 636.50 unknown via CMAUP database
1,6-bis-O-galloyl-beta-D-glucose 440221 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)O)O)O 484.40 unknown via CMAUP database
2-Cinnamoyl-1-galloylglucose 5315898 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(OC2OC(=O)C3=CC(=C(C(=C3)O)O)O)CO)O)O 462.40 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
I(2)-D-Glucopyranose, 2-[(2E)-3-phenyl-2-propenoate] 1,6-bis(3,4,5-trihydroxybenzoate) 6325082 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(OC2OC(=O)C3=CC(=C(C(=C3)O)O)O)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 614.50 unknown via CMAUP database

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