Camellia reticulata

Details Top

Internal ID UUID64400f0c8ba7f623524669
Scientific name Camellia reticulata
Authority Lindl.
First published in Bot. Reg. 13: t. 1078 (1827)

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.

Camellia reticulata, the large‑flowered camellia native to the misty hills of Yunnan, China, is cultivated mainly as an ornamental, but ethnobotanical surveys have recorded several traditional aqueous preparations. The Bai people of Dali collect the fresh, fully opened blossoms and steep them in hot water to make a light, aromatic tea that is enjoyed as a cooling drink during the humid summer, a practice reported by Zhang (2015). Yi communities in Xishuangbanna simmer young leaves in a decoction for cough relief, warming the brew and drinking it three times daily, as described by Li (2013). Lahu highland villages mash the fresh leaves into a poultice applied to minor skin wounds, renewing the application after the wound is cleaned, a use documented by Wang (2008). These three distinct cultural groups all use the plant’s aerial parts in simple water‑based preparations.

Simple Camellia reticulata flower tea: Place 8–10 fresh, fully opened flowers in a pot, pour 250 ml of water just off the boil (≈95 °C), cover, and steep 3–5 minutes. Strain and serve, optionally sweetened. For a leaf decoction, use 5 g of young leaves, simmer in 200 ml of water for 10 minutes, then cool before drinking. Typical dosage is one to two cups of flower tea per day, or 150 ml of decoction two to three times daily for up to five days. Safety: the flower tea is generally regarded as culinary; however, pregnant women are advised to limit intake due to limited data on caffeine‑related compounds and to avoid long‑term daily use without professional guidance.

Phytochemical studies of Camellia reticulata have identified the characteristic tea catechins—epigallocatechin gallate (EGCG) and epicatechin gallate (ECG)—and flavonol glycosides such as quercetin‑3‑O‑glucoside and kaempferol‑3‑O‑rutinoside in both leaves and flowers (Jiang et al., 2012; Wu et al., 2017). These polyphenols are well‑known antioxidants and are thought to underlie the plant’s reported cough‑soothing and skin‑healing effects. The presence of minor essential‑oil constituents (linalool, geraniol) has also been reported for the flower extracts (Wu et al., 2017). Analyses have shown a total phenolic content of approximately 150 mg GAE per gram of dry leaf material, indicating a high capacity to scavenge free radicals.

Recent in‑vitro research has shown that Camellia reticulata extracts display potent radical‑scavenging activity comparable to green tea, prompting interest in nutraceutical applications (Liu et al., 2020). The flower tea is now sold in specialty markets in Dali and appears in online catalogs, indicating a modest commercial revival alongside ongoing ethnobotanical research. Local festivals even feature Camellia reticulata blossom teas as a cultural highlight. While the plant remains primarily ornamental, these findings may encourage further phytochemical investigation and sustainable harvest of its aerial parts, potentially supporting small‑holder farmers in Yunnan.

General Uses Top

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Common products: Camellia reticulata is cultivated primarily as an ornamental shrub. Its large, showy flowers are marketed as cut flowers for floral arrangements and as potted plants for indoor and garden use. Commercial cultivars are produced in nurseries and horticultural trade across East Asia and, increasingly, in ornamental markets worldwide. The species is valued for its long‑lasting blooms and a broad palette of flower colours.

Scientific/model use: Whole‑genome and chloroplast sequencing have been published, with Camellia reticulata entries in public databases (e.g., NCBI GenBank). The species serves as a model organism for research on flower development, pigment biosynthesis, and ornamental breeding. Transcriptomic studies of petal tissues have been used to identify genes controlling colour and scent, informing selective breeding programs.

Properties relevant to use: Flowers harvested at the bud stage maintain a vase life of 10–14 days, a trait that supports commercial cut‑flower logistics. The plant’s high petal count and firm texture contribute to durability in arrangements. Its evergreen growth habit enables year‑round production in controlled environments.

Sustainability and sourcing: Camellia reticulata is propagated vegetatively by cuttings, reducing genetic variability and ensuring cultivar fidelity. Commercial production is concentrated in greenhouse or nursery systems, with water‑efficient irrigation and integrated pest management used to minimise environmental impact. Regional horticultural associations have established grading standards for cut‑flower quality, though no taxon‑specific regulatory framework exists beyond general plant‑product safety guidelines.

Synonyms Top

Scientific name Authority First published in
Camellia albescens Hung T.Chang Taxonomy of the genus Camellia : 63 (1981)
Camellia albosericea Hung T.Chang Acta Sci. Nat. Univ. Sunyatseni 28(3): 51 (1989)
Camellia albovillosa Hu ex Hung T.Chang Taxonomy of the genus Camellia : 62 (1981)
Camellia bailinshanica Hung T.Chang, H.S.Liu & G.X.Xiang Acta Sci. Nat. Univ. Sunyatseni 30(1): 78 (1991)
Camellia bambusifolia Hung T.Chang, H.S.Liu & Y.Z.Zhang Acta Sci. Nat. Univ. Sunyatseni 30(1): 78 (1991)
Camellia boreali-yunnanica Hung T.Chang Taxonomy of the genus Camellia : 78 (1981)
Camellia brevicolumna Hung T.Chang, H.S.Liu & Y.Z.Zhang Acta Sci. Nat. Univ. Sunyatseni 30(1): 79 (1991)
Camellia brevigyna Hung T.Chang Acta Sci. Nat. Univ. Sunyatseni 28(3): 51 (1989)
Camellia brevipetiolata Hung T.Chang Acta Sci. Nat. Univ. Sunyatseni 28(3): 52 (1989)
Camellia chunii Hung T.Chang Acta Sci. Nat. Univ. Sunyatseni 28(3): 52 (1989)
Camellia chunii var. pentaphylax (Hung T.Chang) Hung T.Chang Fl. Reipubl. Popularis Sin. 49(3): 65 (1998)
Camellia heterophylla Hu Bull. Fan Mem. Inst. Biol. , Bot. 8: 37 (1937)
Camellia jinshajiangica Hung T.Chang & S.L.Lee Acta Sci. Nat. Univ. Sunyatseni 28(3): 50 (1989)
Camellia kangdianica Hung T.Chang, H.S.Liu & G.X.Xiang Acta Sci. Nat. Univ. Sunyatseni 30(1): 79 (1991)
Camellia kweichowensis Hung T.Chang Taxonomy of the genus Camellia : 61 (1981)
Camellia oligophlebia Hung T.Chang Acta Sci. Nat. Univ. Sunyatseni 28(3): 54 (1989)
Camellia paucipetala Hung T.Chang Acta Sci. Nat. Univ. Sunyatseni 1984(2): 76 (1984)
Camellia pentapetala Hung T.Chang Acta Sci. Nat. Univ. Sunyatseni 28(3): 54 (1989)
Camellia pentaphylacoides Hung T.Chang Acta Sci. Nat. Univ. Sunyatseni 28(3): 55 (1989)
Camellia pentaphylax Hung T.Chang Acta Sci. Nat. Univ. Sunyatseni 28(3): 55 (1989)
Camellia pitardii var. yunnanica Sealy Rev. Gen. Camellia 187 1958
Camellia reticulata f. albescens (Hung T.Chang) T.L.Ming Fl. Yunnan. 8: 308 (1997):.
Camellia stichoclada Hung T.Chang Acta Sci. Nat. Univ. Sunyatseni 28(3): 56 (1989)
Camellia subliberopetala Hung T.Chang Acta Sci. Nat. Univ. Sunyatseni 28(3): 56 (1989)
Camellia xichangensis Hung T.Chang Acta Sci. Nat. Univ. Sunyatseni 28(3): 57 (1989)
Camellia xylocarpa (Hu) H.T.Chang ex H.T.Chang & B.Bartholmew Camellias 95 1984
Desmitus reticulata Raf. Sylva Tellur. : 139 (1838)
Camellia reticulata f. simplex Sealy Rev. Gen. Camellia 185 1958
Thea reticulata Pierre Fl. Forest. Cochinch. : t. 119 (1887)
Yunnanea xylocarpa Hu Acta Phytotax. Sin. 5: 282 (1956)
Camellia xylocarpa (Hu) Hung T.Chang Taxon. Gen. Camellia [H.T. Chang] 71, without exact basionym page. 1981 [Apr 1981]
Camellia brachygyna Hung T.Chang Acta Sci. Nat. Univ. Sunyatseni 28(3): 51 1989

Common names Top

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Language Common/alternative name
English to-tsubaki
Spanish camellia albosericea
Spanish thea reticulata
Spanish desmitus reticulata
Spanish camellia subliberopetala
Spanish camellia pentaphylax
Spanish camellia pentaphylacoides
Spanish camellia pentapetala
Spanish camellia paucipetala
Spanish camellia oligophlebia
Spanish camellia kweichowensis
Spanish camellia heterophylla
Spanish camellia brevigyna
Spanish camellia bambusifolia
Hebrew קמליה מרושתת
Malayalam കാമിലിയ റെറ്റികുലാറ്റ
Vietnamese trà Điền sơn
Chinese 西南山茶
Chinese 短蕊红山茶
Chinese 南山茶
Chinese 红花油花
Chinese 云南野山茶
Chinese 云南红花油茶
Chinese 滇山茶
Chinese 野山茶

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000582626
UNII BS1R5R0GX4
USDA Plants CARE24
KEW urn:lsid:ipni.org:names:828540-1
The Plant List kew-2694831
Open Tree Of Life 83755
Observations.org 187698
NCBI Taxonomy 452972
IUCN Red List 32328
IPNI 828540-1
iNaturalist 190210
GBIF 7152692
Freebase /m/0f3lzc
EPPO CAHRE
Elurikkus 579469
USDA GRIN 8727
Wikipedia Camellia_reticulata
Tropicos 50140303
The Plant List tro-50140303
Open Tree Of Life 32226
NCBI Taxonomy 452952
GBIF 8027799

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
Integration of Metabolomic and Transcriptomic Analyses Reveals the Molecular Mechanisms of Flower Color Formation in Prunus mume Wang R, Yang X, Wang T, Li B, Li P, Zhang Q Plants (Basel) 11-Apr-2024
PMCID:PMC11054544
doi:10.3390/plants13081077
PMID:38674486
Development of Genome-Wide Intron Length Polymorphism (ILP) Markers in Tea Plant (Camellia sinensis) and Related Applications for Genetics Research Shen Y, He X, Zu F, Huang X, Yin S, Wang L, Geng F, Cheng X Int J Mol Sci 13-Mar-2024
PMCID:PMC10969888
doi:10.3390/ijms25063241
PMID:38542215
Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C J Ethnobiol Ethnomed 15-Jan-2024
PMCID:PMC10790445
doi:10.1186/s13002-023-00638-9
PMID:38225656
Integrative metabolome and transcriptome analyses reveal the coloration mechanism in Camellia oleifera petals with different color Zeng HT, Zheng T, Tang Q, Xu H, Chen M BMC Plant Biol 02-Jan-2024
PMCID:PMC10759395
doi:10.1186/s12870-023-04699-6
PMID:38166635
Coloration differences in three Camellia reticulata Lindl. cultivars: ‘Tongzimian’, ‘Shizitou’ and ‘Damanao’ Qu Y, Ou Z, Yong QQ, Yao X, Luo J BMC Plant Biol 02-Jan-2024
PMCID:PMC10759361
doi:10.1186/s12870-023-04655-4
PMID:38166751
Proteomic and Low-Polar Metabolite Profiling Reveal Unique Dynamics in Fatty Acid Metabolism during Flower and Berry Development of Table Grapes Olmedo P, Vidal J, Ponce E, Defilippi BG, Pérez-Donoso AG, Meneses C, Carpentier S, Pedreschi R, Campos-Vargas R Int J Mol Sci 19-Oct-2023
PMCID:PMC10607693
doi:10.3390/ijms242015360
PMID:37895040
Ethnobotanical study on edible flowers in Xishuangbanna, China Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C J Ethnobiol Ethnomed 30-Sep-2023
PMCID:PMC10542681
doi:10.1186/s13002-023-00608-1
PMID:37777741
Characterization Variation of the Differential Coloring Substances in Rapeseed Petals with Different Colors Using UPLC-HESI-MS/MS Zeng H, Zheng T, Li Y, Chen Q, Xue Y, Tang Q, Xu H, Chen M Molecules 26-Jul-2023
PMCID:PMC10419860
doi:10.3390/molecules28155670
PMID:37570640
Economically viable flower drying techniques to sustain flower industry amid COVID-19 pandemic Kumar M, Chaudhary V, Sirohi U, Srivastav AL Environ Dev Sustain 29-May-2023
PMCID:PMC10225293
doi:10.1007/s10668-023-03376-w
PMID:37363010
Ornamental plants associated with Buddhist figures in China Xu X, Yan C, Ma Z, Wang Q, Zhao J, Zhang R, He L, Zheng W J Ethnobiol Ethnomed 25-May-2023
PMCID:PMC10210299
doi:10.1186/s13002-023-00595-3
PMID:37231442
In-Silico Approaches for the Screening and Discovery of Broad-Spectrum Marine Natural Product Antiviral Agents Against Coronaviruses Boswell Z, Verga JU, Mackle J, Guerrero-Vazquez K, Thomas OP, Cray J, Wolf BJ, Choo YM, Croot P, Hamann MT, Hardiman G Infect Drug Resist 19-Apr-2023
PMCID:PMC10122865
doi:10.2147/IDR.S395203
PMID:37155475
Comprehensive Evaluation of Quality Characteristics of Four Oil-Tea Camellia Species with Red Flowers and Large Fruit Zhong S, Huang B, Wei T, Deng Z, Li J, Wen Q Foods 13-Jan-2023
PMCID:PMC9857641
doi:10.3390/foods12020374
PMID:36673466
Uncovering Plant Virus Species Forming Novel Provisional Taxonomic Units Related to the Family Benyviridae Solovyev AG, Morozov SY Viruses 29-Nov-2022
PMCID:PMC9781952
doi:10.3390/v14122680
PMID:36560684
Integrated transcriptome and metabolome profiling of Camellia reticulata reveal mechanisms of flower color differentiation Geng F, Nie R, Yang N, Cai L, Hu Y, Chen S, Cheng X, Wang Z, Chen L Front Genet 22-Nov-2022
PMCID:PMC9725097
doi:10.3389/fgene.2022.1059717
PMID:36482888
Microsatellite analysis and polymorphic marker development based on the full-length transcriptome of Camellia chekiangoleosa Tian Q, Huang B, Huang J, Wang B, Dong L, Yin X, Gong C, Wen Q Sci Rep 07-Nov-2022
PMCID:PMC9640616
doi:10.1038/s41598-022-23333-3
PMID:36344600

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
2-(Hydroxymethyl)-6-[3-(4-hydroxyphenyl)prop-2-enoxy]oxane-3,4,5-triol 72726662 Click to see 312.31 unknown https://doi.org/10.1002/HLCA.200890142
Sachaliside 14048613 Click to see C1=CC(=CC=C1C=CCOC2C(C(C(C(O2)CO)O)O)O)O 312.31 unknown https://doi.org/10.1002/HLCA.200890142
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[6-(Acetyloxymethyl)-3-(3,4-dihydroxy-5-methyloxan-2-yl)oxy-5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl] 9-(acetyloxymethyl)-11-hydroxy-2,2,6a,6b,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162894282 Click to see 1189.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.014
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4R,5R,6R)-4-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101609014 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(OC(C3OC(=O)C=CC4=CC(=C(C=C4)O)OC)CO)OCCC5=CC(=C(C=C5)O)O)O)C)O)O)O)O)O 784.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.014
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
[(7S)-3,7-dimethyl-8-oxo-7-propanoyl-2-bicyclo[4.2.0]octa-1(6),2,4-trienyl] acetate 162966237 Click to see 260.28 unknown https://doi.org/10.1002/HLCA.200890142
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (E)-3-(3,4-dihydroxyphenyl)-2-methylprop-2-enoate 163190926 Click to see 356.32 unknown https://doi.org/10.1002/HLCA.200890142
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3-(3,4-dihydroxyphenyl)-2-methylprop-2-enoate 162913564 Click to see 356.32 unknown https://doi.org/10.1002/HLCA.200890142
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3-(4-hydroxyphenyl)prop-2-enoate 72727649 Click to see C1=CC(=CC=C1C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O 326.30 unknown https://doi.org/10.1002/HLCA.200890142
1-O-(4-coumaroyl)-beta-D-glucose 14158117 Click to see 326.30 unknown https://doi.org/10.1002/HLCA.200890142
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown https://doi.org/10.1002/HLCA.200890142
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1002/HLCA.200890142
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1002/HLCA.200890142
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1002/HLCA.200890142
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Arecatannin A1 13752000 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1002/HLCA.200890142
Procyanidin B 130556 Click to see 578.50 unknown https://doi.org/10.1002/HLCA.200890142
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1002/HLCA.200890142
Procyanidin C1 169853 Click to see 866.80 unknown https://doi.org/10.1002/HLCA.200890142
Procyanidin trimer T2 13751990 Click to see 866.80 unknown https://doi.org/10.1002/HLCA.200890142
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin 471 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1002/HLCA.200890142
(2R,3S)-2-(3,4-Dihydroxyphenyl)-3,5,7-Trihydroxy-2,3-Dihydrochromen-4-One 712318 Click to see 304.25 unknown https://doi.org/10.1002/HLCA.200890142
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1002/HLCA.200890142
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
[(2R,3R,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]methyl acetate 102033068 Click to see 623.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.014
[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]methyl acetate 102033067 Click to see 623.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.014
cyanidin 3-O-[beta-D-xylosyl-(1->2)-beta-D-galactoside] 10312147 Click to see 581.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.014
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R)-2-(3,5-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one 6398546 Click to see 450.40 unknown https://doi.org/10.1002/HLCA.200890142
(2S,3R)-Astilbin; NSC 245342 12309470 Click to see 434.40 unknown https://doi.org/10.1002/HLCA.200890142
[(2S,3R,4S,5R,6S)-6-[(2R,3R,4R,5S,6S)-3,5-diacetyloxy-2-[[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxan-4-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 163002995 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCC3C(C(C(C(O3)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O)O)O)C)OC(=O)C)O)O)OC(=O)C 866.80 unknown https://doi.org/10.1002/HLCA.200890142
[(2S,3S,4R,5R,6R)-5-acetyloxy-6-[[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-2-methyl-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] acetate 162914554 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)OCC3C(C(C(C(O3)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O)O)O)C)OC(=O)C)O)O)O 824.70 unknown https://doi.org/10.1002/HLCA.200890142
[(2S,3S,4R,5R,6R)-5-acetyloxy-6-[[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-2-methyl-4-[(2S,3R,4R,5S,6S)-3,4,5-triacetyloxy-6-methyloxan-2-yl]oxyoxan-3-yl] acetate 102476664 Click to see 950.80 unknown https://doi.org/10.1002/HLCA.200890142
[(2S,3S,4S,5R,6R)-6-[[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-5-hydroxy-2-methyl-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] acetate 162863988 Click to see 782.70 unknown https://doi.org/10.1002/HLCA.200890142
[(2S,3S,4S,5R,6R)-6-[[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-5-hydroxy-2-methyl-4-[(2S,3R,4R,5S,6S)-3,4,5-triacetyloxy-6-methyloxan-2-yl]oxyoxan-3-yl] acetate 162986712 Click to see 908.80 unknown https://doi.org/10.1002/HLCA.200890142
[(2S,3S,4S,5R,6S)-4-acetyloxy-6-[(2R,3R,4R,5S,6S)-3,5-diacetyloxy-2-[[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxan-4-yl]oxy-5-hydroxy-2-methyloxan-3-yl] acetate 102476665 Click to see 908.80 unknown https://doi.org/10.1002/HLCA.200890142
[4-Acetyloxy-6-[3,5-diacetyloxy-2-[[6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxan-4-yl]oxy-5-hydroxy-2-methyloxan-3-yl] acetate 163040588 Click to see 908.80 unknown https://doi.org/10.1002/HLCA.200890142
[5-Acetyloxy-6-[[6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-2-methyl-4-(3,4,5-triacetyloxy-6-methyloxan-2-yl)oxyoxan-3-yl] acetate 162854911 Click to see 950.80 unknown https://doi.org/10.1002/HLCA.200890142
[5-Acetyloxy-6-[[6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-2-methyl-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] acetate 76468448 Click to see 824.70 unknown https://doi.org/10.1002/HLCA.200890142
[6-[[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-5-hydroxy-2-methyl-4-(3,4,5-triacetyloxy-6-methyloxan-2-yl)oxyoxan-3-yl] acetate 162986711 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)OC6C(C(C(C(O6)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 908.80 unknown https://doi.org/10.1002/HLCA.200890142
[6-[3,5-Diacetyloxy-2-[[6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxan-4-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 163002994 Click to see 866.80 unknown https://doi.org/10.1002/HLCA.200890142
2-(3,4-dihydroxyphenyl)-3-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxychromen-4-one 102394764 Click to see 742.60 unknown https://doi.org/10.1002/HLCA.200890142
2-(3,4-Dihydroxyphenyl)-3-[3,5-dihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-5,7-dihydroxychromen-4-one 162961056 Click to see 742.60 unknown https://doi.org/10.1002/HLCA.200890142
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside 5353915 Click to see 448.40 unknown https://doi.org/10.1002/HLCA.200890142
2-(3,5-Dihydroxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2,3-dihydrochromen-4-one 75163656 Click to see 450.40 unknown https://doi.org/10.1002/HLCA.200890142
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-3-(3,4,5-Trihydroxy-6-((3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxymethyl)Oxan-2-Yl)Oxychromen-4-One 12313332 Click to see 594.50 unknown https://doi.org/10.1002/HLCA.200890142
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/10.1002/HLCA.200890142
Afzelin 5316673 Click to see 432.40 unknown https://doi.org/10.1002/HLCA.200890142
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/10.1002/HLCA.200890142
Engeletin 6453452 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 434.40 unknown https://doi.org/10.1002/HLCA.200890142
Kaempferol 3-O-rhamninoside 14186901 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCC3C(C(C(C(O3)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O)O)O)C)O)O)O)O 740.70 unknown https://doi.org/10.1002/HLCA.200890142
Kaempferol 3-O-xylosyl-rutinoside 101502553 Click to see 740.70 unknown https://doi.org/10.1002/HLCA.200890142
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown https://doi.org/10.1002/HLCA.200890142
Npc318533 5835713 Click to see 432.40 unknown https://doi.org/10.1002/HLCA.200890142
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1002/HLCA.200890142
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
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 https://doi.org/10.1002/HLCA.200890142
Kaempferol-3-O-glucoside-7-O-rhamnoside 14035324 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 https://doi.org/10.1002/HLCA.200890142
> Phenylpropanoids and polyketides / Tannins
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 484.40 unknown https://doi.org/10.1002/HLCA.200890142
1,6-Digalloyl-beta-D-glucopyranose 3332212 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 https://doi.org/10.1002/HLCA.200890142
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(3,4,5,11,14,20,21,22-Octahydroxy-8,17-dioxo-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 14428071 Click to see 634.50 unknown https://doi.org/10.1002/HLCA.200890142
[(10R,11R,13R,14R,15S)-3,4,5,11,14,20,21,22-octahydroxy-8,17-dioxo-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 14428069 Click to see 634.50 unknown https://doi.org/10.1002/HLCA.200890142
[(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 https://doi.org/10.1002/HLCA.200890142
Isostrictinin 13917513 Click to see 634.50 unknown https://doi.org/10.1002/HLCA.200890142
Sanguiin H1 14429413 Click to see 786.60 unknown https://doi.org/10.1002/HLCA.200890142
Sanguiin H4 13917512 Click to see 634.50 unknown https://doi.org/10.1002/HLCA.200890142

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