Camellia reticulata, also known as C. heterophylla, is a flowering plant in the tea family native to southwestern China. It is a shrub or small tree that can reach up to 15 meters in height. The leaves are elliptic to oblong-elliptic and the flowers are soft-pink to deep-pink, with 5-7 petals. It is susceptible to cold weather and blooms late in the season. This plant has a significant cultural and economic importance, being the floral emblem of Yunnan and cultivated for tea oil and ornamental purposes. It was first imported to England in 1820 and remained the only known cultivar in Europe for over a century.

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)

Common names Top

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Filter by language:

Language	Common/alternative name
English	to-tsubaki
Hebrew	קמליה מרושתת
Malayalam	കാമിലിയ റെറ്റികുലാറ്റ
Vietnamese	trà Điền sơn
Chinese	西南山茶
Chinese	野山茶
Chinese	滇山茶
Chinese	云南红花油茶
Chinese	云南野山茶
Chinese	红花油花
Chinese	南山茶

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

Asia-temperate click to expand
- China
  - China South-central

Links to other databases Top

Suggest others/fix!

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

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

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
> 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 C1=CC(=CC=C1C=CCOC2C(C(C(C(O2)CO)O)O)O)O	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 CC1COC(C(C1O)O)OC2C(C(C(OC2OC(=O)C34CCC(CC3C5=CCC6C(C5(CC4)C)(CCC7C6(CC(C(C7(C)COC(=O)C)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)(C)C)COC(=O)C)O)OC9C(C(C(C(O9)CO)O)O)O	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 CCC(=O)C1(C2=C(C1=O)C(=C(C=C2)C)OC(=O)C)C	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 CC(=CC1=CC(=C(C=C1)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O	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 CC(=CC1=CC(=C(C=C1)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O	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 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
> 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 COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1002/HLCA.200890142
4-Hydroxycinnamic acid	322	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1002/HLCA.200890142
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	https://doi.org/10.1002/HLCA.200890142
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	https://doi.org/10.1002/HLCA.200890142
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	130556	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
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 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 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 trimer T2	13751990	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
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Epitaxifolin	712318	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
(+/-)-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
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 CC(=O)OCC1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C=C4)O)O)O)O)OC5C(C(C(CO5)O)O)O)O)O	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 CC(=O)OCC1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C=C4)O)O)O)O)OC5C(C(C(CO5)O)O)O)O)O	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 C1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)CO)O)O)O)O)O	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 CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=CC(=C4)O)O)O)O)O	450.40	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 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)OC(=O)C)OC6C(C(C(C(O6)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C	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 CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C)C)OCC3C(C(C(C(O3)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O)O)O)O)O)O)O	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 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
[(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 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)OC(=O)C)OC(=O)C	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 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)OC(=O)C)OC(=O)C	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 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)OC(=O)C)OC6C(C(C(C(O6)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C	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 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
[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 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
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 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)OC6C(C(C(CO6)O)O)O)O)O)O)O	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 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)OC6C(C(C(CO6)O)O)O)O)O)O)O	742.60	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 CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=CC(=C4)O)O)O)O)O	450.40	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
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 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	594.50	unknown	https://doi.org/10.1002/HLCA.200890142
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	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
Isoengelitin	12309470	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 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-rhamnoside	5835713	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	https://doi.org/10.1002/HLCA.200890142
Kaempferol-3-O-rutinoside	5318767	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	594.50	unknown	https://doi.org/10.1002/HLCA.200890142
Quercetin 3-O-rhamnoside	5353915	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)O	448.40	unknown	https://doi.org/10.1002/HLCA.200890142
Quercitrin	5280459	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)O	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 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
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 C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)O	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 C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)O	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 C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)O	786.60	unknown	https://doi.org/10.1002/HLCA.200890142
Isostrictinin	13917513	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1002/HLCA.200890142
Sanguiin H1	14429413	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)O	786.60	unknown	https://doi.org/10.1002/HLCA.200890142
Sanguiin H4	13917512	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1002/HLCA.200890142

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Camellia reticulata

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