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Internal ID UUID64404839df05c623516974
Scientific name Ilex hainanensis
Authority Merr.
First published in Lingnan Sci. J. 13: 60 (1934)

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 山绿茶
Chinese 海南冬青

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 South-central
      • China Southeast
      • Hainan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001078611
Tropicos 2000489
KEW urn:lsid:ipni.org:names:83351-1
The Plant List tro-2000489
Open Tree Of Life 172476
NCBI Taxonomy 1043421
IUCN Red List 151277276
IPNI 83351-1
GBIF 5534541
EOL 2907110
CMAUP NPO3619

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
Chinese patent medicine combined with calcium channel blockers in the treatment of essential hypertension:a Bayes network meta-analysis and systematic review Cui L, Liu X, Li Y, Jing T, Liu D, Ren C, Yin T, Wang Y, Zhao Z, Wang J, Han X, Wang L Front Pharmacol 15-Mar-2024
PMCID:PMC10978809
doi:10.3389/fphar.2024.1321405
PMID:38560355
Comparison of pharmacokinetic profiles of seven major bioactive components in normal and non-alcoholic fatty liver disease (NAFLD) rats after oral administration of Ling-Gui-Zhu-Gan decoction by UPLC-MS/MS Nie W, Yang Y, Li L, Ding Y, Chen X, Li M, He N, Ji G, Zhang Y, Kang P, Zhang T Front Pharmacol 04-May-2023
PMCID:PMC10192568
doi:10.3389/fphar.2023.1174742
PMID:37214449
Ethnobotanical study on herbal tea drinks in Guangxi, China Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C J Ethnobiol Ethnomed 31-Mar-2023
PMCID:PMC10064729
doi:10.1186/s13002-023-00579-3
PMID:37004116
Natural Products as Anticancer Agents: Current Status and Future Perspectives Naeem A, Hu P, Yang M, Zhang J, Liu Y, Zhu W, Zheng Q Molecules 30-Nov-2022
PMCID:PMC9737905
doi:10.3390/molecules27238367
PMID:36500466
Advances in the Bioactivities of Phytochemical Saponins in the Prevention and Treatment of Atherosclerosis Luo H, Chen J, Su C, Zha L Nutrients 24-Nov-2022
PMCID:PMC9735883
doi:10.3390/nu14234998
PMID:36501028
Targeting SREBP-1-Mediated Lipogenesis as Potential Strategies for Cancer Zhao Q, Lin X, Wang G Front Oncol 14-Jul-2022
PMCID:PMC9330218
doi:10.3389/fonc.2022.952371
PMID:35912181
Medicinal Plants for the Treatment of Gastrointestinal Cancers From the Metabolomics Perspective Guo W, Cao P, Wang X, Hu M, Feng Y Front Pharmacol 27-Jun-2022
PMCID:PMC9271783
doi:10.3389/fphar.2022.909755
PMID:35833022
The Role of Cyclodextrins in the Design and Development of Triterpene-Based Therapeutic Agents Prodea A, Mioc A, Banciu C, Trandafirescu C, Milan A, Racoviceanu R, Ghiulai R, Mioc M, Soica C Int J Mol Sci 10-Jan-2022
PMCID:PMC8775686
doi:10.3390/ijms23020736
PMID:35054925
Naturally Occurring Chromone Glycosides: Sources, Bioactivities, and Spectroscopic Features Amen Y, Elsbaey M, Othman A, Sallam M, Shimizu K Molecules 16-Dec-2021
PMCID:PMC8704703
doi:10.3390/molecules26247646
PMID:34946728
Anti-Hepatocellular Carcinoma Biomolecules: Molecular Targets Insights Juaid N, Amin A, Abdalla A, Reese K, Alamri Z, Moulay M, Abdu S, Miled N Int J Mol Sci 06-Oct-2021
PMCID:PMC8509806
doi:10.3390/ijms221910774
PMID:34639131
Comprehensive Utilization of Immature Honey Pomelo Fruit for the Production of Value-Added Compounds Using Novel Continuous Phase Transition Extraction Technology Liu G, Hou T, Guo S, Lin H, Chen M, Miao J, Liu X, Huang Y, Cao Y, Lan Y, Song M Biology (Basel) 23-Aug-2021
PMCID:PMC8389540
doi:10.3390/biology10080815
PMID:34440047
Novel Insights and Current Evidence for Mechanisms of Atherosclerosis: Mitochondrial Dynamics as a Potential Therapeutic Target Li D, Yang S, Xing Y, Pan L, Zhao R, Zhao Y, Liu L, Wu M Front Cell Dev Biol 07-Jul-2021
PMCID:PMC8293691
doi:10.3389/fcell.2021.673839
PMID:34307357
Mechanisms of Atherosclerosis Induced by Postprandial Lipemia Zhao Y, Liu L, Yang S, Liu G, Pan L, Gu C, Wang Y, Li D, Zhao R, Wu M Front Cardiovasc Med 29-Apr-2021
PMCID:PMC8116525
doi:10.3389/fcvm.2021.636947
PMID:33996937
Nutraceutical Compounds Targeting Inflammasomes in Human Diseases Castejón-Vega B, Giampieri F, Alvarez-Suarez JM Int J Mol Sci 08-Jul-2020
PMCID:PMC7402342
doi:10.3390/ijms21144829
PMID:32650482
Ursolic Acid and Its Derivatives as Bioactive Agents Mlala S, Oyedeji AO, Gondwe M, Oyedeji OO Molecules 29-Jul-2019
PMCID:PMC6695944
doi:10.3390/molecules24152751
PMID:31362424

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 / Galloyl esters
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(3S,4R,4aR,6aR,6bS,8aR,11R,12aS,14aR,14bR)-3-hydroxy-11-(hydroxymethyl)-4,6a,6b,11,14b-pentamethyl-8a-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 162979267 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)CO 664.80 unknown https://doi.org/10.1002/MRC.2355
(3S,4R,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-3-hydroxy-4,6a,6b,11,11,14b-hexamethyl-8a-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 162976175 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 648.80 unknown https://doi.org/10.1002/MRC.2355
3-Hydroxy-11-(hydroxymethyl)-4,6a,6b,11,14b-pentamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 73157029 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)CO 664.80 unknown https://doi.org/10.1002/MRC.2355
3-Hydroxy-4,6a,6b,11,11,14b-hexamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 73157030 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 648.80 unknown https://doi.org/10.1002/MRC.2355
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2R,3R,4S,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-2,3,12-trihydroxy-4,6a,6b,11,12,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid 21606530 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1(C)O)C)C(=O)O 518.70 unknown https://doi.org/10.1002/HLCA.200790005
(3S,4R,4aR,6aR,6bS,8aR,11R,12aS,14aR,14bR)-3-hydroxy-11-(hydroxymethyl)-4,6a,6b,11,14b-pentamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid 102588660 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1)C)C(=O)O)CO 502.70 unknown https://doi.org/10.1002/HLCA.200790005
(3S,4R,4aR,6aR,6bS,8aR,12S,12aS,14aR,14bR)-3,12-dihydroxy-4,6a,6b,11,11,14b-hexamethyl-8a-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 162976017 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 664.80 unknown https://doi.org/10.1002/MRC.2355
(3S,4R,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-3-hydroxy-11-(hydroxymethyl)-4,6a,6b,12,14b-pentamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-4,8a-dicarboxylic acid 102588659 Click to see CC1C(CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C(=O)O)O)C)C(=O)O)CO 502.70 unknown https://doi.org/10.1002/HLCA.200790005
(3S,4S,4aR,6aR,6bS,8aR,12S,12aS,14aR,14bR)-3,12-dihydroxy-4-(hydroxymethyl)-6a,6b,11,11,14b-pentamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid 102588662 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(CO)C(=O)O)O)C)C)C2C1O)C)C(=O)O)C 518.70 unknown https://doi.org/10.1002/HLCA.200790005
(3S,4S,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-3,12-dihydroxy-4-(hydroxymethyl)-6a,6b,11,12,14b-pentamethyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid 102588661 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(CO)C(=O)O)O)C)C)C2C1(C)O)C)C(=O)O 518.70 unknown https://doi.org/10.1002/HLCA.200790005
2alpha,3beta,19alpha-Trihydroxyoleana-12-ene-23,28-dioic acid 14805211 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1O)C)C(=O)O)C 518.70 unknown https://doi.org/10.1002/HLCA.200790005
3-Hydroxy-11-(hydroxymethyl)-4,6a,6b,11,14b-pentamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid 73022111 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1)C)C(=O)O)CO 502.70 unknown https://doi.org/10.1002/HLCA.200790005
3-hydroxy-11-(hydroxymethyl)-4,6a,6b,12,14b-pentamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-4,8a-dicarboxylic acid 163007098 Click to see CC1C(CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C(=O)O)O)C)C(=O)O)CO 502.70 unknown https://doi.org/10.1002/HLCA.200790005
3,12-Dihydroxy-4-(hydroxymethyl)-6a,6b,11,11,14b-pentamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid 162845956 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(CO)C(=O)O)O)C)C)C2C1O)C)C(=O)O)C 518.70 unknown https://doi.org/10.1002/HLCA.200790005
3,12-Dihydroxy-4-(hydroxymethyl)-6a,6b,11,12,14b-pentamethyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid 162881010 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(CO)C(=O)O)O)C)C)C2C1(C)O)C)C(=O)O 518.70 unknown https://doi.org/10.1002/HLCA.200790005
3,12-Dihydroxy-4,6a,6b,11,11,14b-hexamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 45783098 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C 664.80 unknown https://doi.org/10.1002/MRC.2355
3beta-[[2-O-(alpha-L-Rhamnopyranosyl)-3-O-(2-O,3-O-diacetyl-alpha-L-arabinofuranosyl)-beta-L-arabinopyranosyl]oxy]-23-hydroxyoleana-12-ene-28-oic acid 53483549 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)OC8C(C(C(O8)CO)OC(=O)C)OC(=O)C)O)O)O 967.10 unknown via CMAUP database
3beta-[[2-O-(alpha-L-Rhamnopyranosyl)-3-O-(3-O-acetyl-alpha-L-arabinofuranosyl)-beta-L-arabinopyranosyl]oxy]-23-hydroxyoleana-12-ene-28-oic acid 53483550 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)OC8C(C(C(O8)CO)OC(=O)C)O)O)O)O 925.10 unknown via CMAUP database
3beta-[2-O-(3-O-alpha-L-Arabinopyranosyl-alpha-L-rhamnopyranosyl)-alpha-L-arabinopyranosyloxy]-23-hydroxyoleana-12-ene-28-oic acid 21637697 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O 883.10 unknown via CMAUP database
3beta-[2-O-(alpha-L-Rhamnopyranosyl)-3-O-(alpha-L-arabinofuranosyl)-beta-L-arabinopyranosyloxy]-23-hydroxyolean-12-en-28-oic acid 101682282 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)OC8C(C(C(O8)CO)O)O)O)O)O 883.10 unknown via CMAUP database
Bartogenic acid 45272347 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1O)C)C(=O)O)C 518.70 unknown https://doi.org/10.1002/HLCA.200790005
Corosin 286498 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1(C)O)C)C(=O)O 518.70 unknown https://doi.org/10.1002/HLCA.200790005
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Rarasaponin III 24866792 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)O)O)O 925.10 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
2(5H)-Furanone, 4-(hydroxymethyl)- 157706 Click to see C1C(=CC(=O)O1)CO 114.10 unknown via CMAUP database
> Organoheterocyclic compounds / Furofurans
lappaceolide B 11572139 Click to see C1C(=O)OCC12COC3(C2OC(=O)C3)CO 228.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1080/14786410802044885
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1080/14786410802044885
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1080/14786410802044885
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
Tiliroside 5320686 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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/10.1080/14786410802044885
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown via CMAUP database
Isoquercetin 5280804 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/10.1080/14786410802044885
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 https://doi.org/10.1080/14786410802044885
Vitamin P 5293655 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 https://doi.org/10.1080/14786410802044885
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-5,7,3',5'-tetrahydroxyflavanone-7-O-beta-D-glucopyranoside 16215147 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=CC(=C4)O)O 450.40 unknown https://doi.org/10.1080/14786410802044885
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 14484601 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)O)O)O)O 610.50 unknown https://doi.org/10.1080/14786410802044885
2-(3,5-Dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 162907511 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=CC(=C4)O)O 450.40 unknown https://doi.org/10.1080/14786410802044885
kaempferol 3-O-beta-D-glucopyranosyl-7-O-alpha-L-rhamnopyranoside 21606527 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown via CMAUP database
Quercetin 3-rhamnoside-7-glucoside 6325870 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC(=C(C=C5)O)O)O)O)O 610.50 unknown https://doi.org/10.1080/14786410802044885
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
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

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