Camellia oleifera

Details Top

Internal ID UUID64400f0a90dcf781394948
Scientific name Camellia oleifera
Authority C.Abel
First published in Narr. Journey China : 174 (1818)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

In southern China, leaves of Camellia oleifera have long been gathered for simple home teas, usually taken warm for daily cleansing and gentle appetite support. In parts of northern Vietnam, vendors set out fresh leaves for hot infusions alongside herbal mixes, often mixed with ginger and citrus zest to soften the bitterness. According to Van Pham’s Vietnamese medicinal plants (2013), local women also apply crushed young leaves as a poultice to clean minor wounds or soothe irritated skin after bathing. In northern Laos, informants reported drinking a mild leaf tea to aid digestion after heavy meals (Mühlbauer et al., 2012). Across these practices, the part of the plant is the young leaves and leaf buds; the seeds are pressed for oil, while the residual oil‑cake is a traditional soap and fertilizer. A practical mild tea uses about 4–6 g (roughly a small handful) of dried leaf tips steeped in 200–250 mL just‑off‑boiling water for 3–5 minutes, then strained. A stronger leaf decoction simmers 10–15 g of chopped fresh or dried leaves in 300–400 mL water for 15–20 minutes. In all cases, moderation is advised; the safety profile has not been fully established for long‑term internal use and there is no rigorous dose guideline, so pregnant and breastfeeding people should avoid Camellia oleifera leaf drinks (Van Pham, 2013; He & Xia, 2012).

Seed oil is the most widespread traditional product. In Hunan and Jiangxi, women rub a few drops into the scalp or massage it into dry hair to improve shine and manageability (Lee et al., 2012). The same oil is a common frying medium in Guangxi and Guizhou, prized for its high smoke point and mild flavor (Chen, 2008). If making a topical blend, combine one part Camellia oleifera oil with one part carrier oil such as almond or sesame, apply sparingly to hair or scalp, and leave on for 30–60 minutes before shampooing. In this type of topical use, a patch test on the inner wrist is wise, especially for those with sensitive skin (Lee et al., 2012).

What makes these applications plausible is the oil’s chemistry. The seeds contain high levels of monounsaturated oleic acid and the antioxidant α‑tocopherol, while the leaves provide catechins such as epicatechin and small amounts of caffeine, supported by HPLC analyses and fatty‑acid profiling (Jiang et al., 2007; Lee et al., 2012). These constituents align with the cooking, cosmetic, and mild bitter tonic roles recorded in ethnobotanical accounts.

Current research is active: recent studies explore anti‑inflammatory and skin‑barrier effects of the oil, while market interest in the plant continues to grow for culinary oil and hair‑care products. Although Camellia sinensis remains the world’s tea, Camellia oleifera retains its distinct niche as a household leaf tonic and a valued seed oil in southern China and northern Vietnam (He & Xia, 2012; Van Pham, 2013).

General Uses Top

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Common products:
The seed of Camellia oleifera yields a yellow, mildly nutty-flavored oil after cleaning, dehulling, pressing (cold or hot), and refining (degumming, neutralization, bleaching, deodorization). The solid press cake (seed meal) is a by‑product of oil extraction.

Food and beverages (non-medicinal):
Camellia oleifera seed oil is used as an edible cooking oil and frying fat in East and Southeast Asia. It is employed in salad dressings, marinades, and processed foods. It is distinct in composition and regulatory status from oil of Camellia sinensis (tea seed oil), which is sometimes marketed under a similar name. Typical edible uses reflect its high oleic content and absence of erucic acid, with refined oil suitable for high‑temperature cooking. The press cake is used as a protein‑rich animal feed and fertilizer.

Fragrance and cosmetics:
Refined Camellia oleifera oil is used in soaps, shampoos, and leave‑in hair products for emollient properties and mild odor. It is a carrier oil in fragrance and skin‑care formulations, including creams and lotions, and can be incorporated into makeup bases and cleansers. Cosmetic use reflects its fatty‑acid profile (high oleic), oxidative stability, and low irritation potential compared with more unsaturated oils.

Colorants and tanning:
Camellia oleifera seed cake contains saponins and phenolics and has historically been used as a washing agent (as a soap substitute for textiles and hair). It is a source of natural surfactants for non‑food applications.

Industrial and craft applications:
The oil is a feed‑stock for biodiesel production via transesterification, leveraging its high oleic acid content to yield stable esters with good cold‑flow properties. It also serves as a non‑drying oil in inks and as a component in textile finishes and other industrial formulations, though these uses are secondary to food and cosmetic applications.

Properties relevant to use:
The seed oil has a high oleic acid proportion (typically about 80–85%), with linoleic and saturated fatty acids present in smaller amounts. It is low in erucic acid. Refined oil exhibits favorable oxidative stability and a smoke point suitable for culinary frying. The press cake provides protein and nitrogen; its saponin content supports surfactant applications.

Standards and regulation:
Edible Camellia oleifera oil in China is covered by national specifications and grading rules that specify quality indices for the oil type (e.g., peroxide value, moisture and volatiles, impurity limits, fatty‑acid limits). Cosmetic formulations are subject to general safety and labeling requirements for cosmetic products in their respective markets.

Sustainability and sourcing:
Camellia oleifera is cultivated in mixed agroforestry systems and on degraded or marginal lands, supporting rural income. Oil mills report yields per hectare that depend on orchard age and agronomy. Sustainability concerns center on supply‑chain traceability, quality control in oil processing, and waste utilization (press cake for feed/fertilizer), with regional initiatives promoting certification and bonnes pratiques to support long‑term orchard productivity.

Synonyms Top

Scientific name Authority First published in
Theaphylla oleifera Raf. Sylva Tellur. : 139 (1838)
Theopsis banksiana (Lindl. ex Tutcher) Nakai J. Jap. Bot. 16: 705 (1940)
Sasanqua oleifera Raf. Sylva Tellur. 140. 1838
Camellia banksiana Lindl. ex Tutcher J. Linn. Soc., Bot. 37: 63 (1905)
Camellia drupifera f. biflora (Hayata) S.S.Ying Mem. Coll. Agric. Natl. Taiwan Univ. 29(1): 93 (1989):.
Camellia obscura Nakai J. Jap. Bot. 16: 696 (1940)
Camellia podogyna Melch. Nat. Pflanzenfam. ed. 2 , 21: 131 (1925)
Camellia sasanqua Blanco Fl. Filip. [F.M. Blanco] 530. 1837
Camellia biflora Cohen-Stuart Meded. Proefstat. Thee 11: 67 (1916)
Thea biflora Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 44 (1911)
Thea podogyna H.Lév. Sert. Yunnan. : 2 (1916)
Thea oleifera Rehder & E.H.Wilson Pl. Wilson. 2: 393 (1915)
Thea sasanqua var. loureiroi Pierre
Camellia caudata Griff. Not. Pl. Asiat. 4: 559 (1854)
Camellia oleifera var. monosperma Hung T.Chang Acta Sci. Nat. Univ. Sunyatseni 31(1): 75 (1992)
Camellia banksiana Lindl. ex Champ. Hooker's J. Bot. Kew Gard. Misc. 3: 310 (1851)

Common names Top

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Language Common/alternative name
Spanish thea sasanqua var. loureiroi
Spanish thea podogyna
Spanish thea oleifera
Spanish thea biflora
Arabic كاميليا أوليفيرا
Bulgarian маслинова камелия
Japanese 油茶
Japanese ユチャ
Lithuanian aliejinė kamelija
Malayalam കാമിലിയ ഒലിഫെറ
Polish thea oleifera
Polish kamelia olejodajna
Russian Камелия масличная
za youzcaz
Chinese 小叶油茶
Chinese 苦茶
Chinese 茶油粑
Chinese 茶枯
Chinese 油茶花
Chinese 油茶油
Chinese 油茶根
Chinese 油茶子
Chinese 油茶叶
Chinese 油茶(小叶油茶)
Chinese 茶油
Chinese 油茶

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.
store seed cold and moist

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
    • Indo-China
      • Laos
      • Myanmar
      • Vietnam

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000582552
UNII 1C0QTA61GT
Tropicos 31600017
KEW urn:lsid:ipni.org:names:828535-1
The Plant List kew-2694757
Missouri Botanical Garden 287333
Open Tree Of Life 140993
NCBI Taxonomy 385388
IUCN Red List 62056210
IPNI 828535-1
iNaturalist 487657
GBIF 7314015
Freebase /m/0f613v
EPPO CAHOL
EOL 2889646
USDA GRIN 8721
Wikipedia Camellia_oleifera

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_022316695.1 ASM2231669v1 Chromosome Research Institute of Subtropical Forestry 2022-02-24 100 2.69 Gb

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
Epiphytic and endophytic bacteria on Camellia oleifera phyllosphere: exploring region and cultivar effect Chen X, Li L, He Y BMC Ecol Evol 13-May-2024
PMCID:PMC11089727
doi:10.1186/s12862-024-02240-3
PMID:38735962
YOLOv8-RMDA: Lightweight YOLOv8 Network for Early Detection of Small Target Diseases in Tea Ye R, Shao G, He Y, Gao Q, Li T Sensors (Basel) 01-May-2024
PMCID:PMC11086262
doi:10.3390/s24092896
PMID:38733002
Three undescribed dihydrostilbene glycosides from leaves of Camellia oleifera Abel. And their anti-inflammatory activity Xu Y, Tang SQ, Suo ZW, Wei KX, Luyten W, Huang H, Li XJ Heliyon 30-Apr-2024
PMCID:PMC11088326
doi:10.1016/j.heliyon.2024.e30507
PMID:38737284
Artemisia annua L. polysaccharide improves the growth performance and intestinal barrier function of broilers challenged with Escherichia coli Guo S, Shi B, Xing Y, Xu Y, Jin X, Hong L, Zhang S, Qiao M, Yan S Front Microbiol 30-Apr-2024
PMCID:PMC11091311
doi:10.3389/fmicb.2024.1390815
PMID:38746748
Genome-wide investigation of the LARP gene family: focus on functional identification and transcriptome profiling of ZmLARP6c1 in maize pollen Xiang X, Deng Q, Zheng Y, He Y, Ji D, Vejlupkova Z, Fowler JE, Zhou L BMC Plant Biol 29-Apr-2024
PMCID:PMC11057080
doi:10.1186/s12870-024-05054-z
PMID:38684961
A critical review of the bioactive ingredients and biological functions of camellia oleifera oil Qin P, Shen J, Wei J, Chen Y Curr Res Food Sci 25-Apr-2024
PMCID:PMC11081779
doi:10.1016/j.crfs.2024.100753
PMID:38725963
The Expression and Function of Notch Involved in Ovarian Development and Fecundity in Basilepta melanopus Xie Y, Tan Y, Wen X, Deng W, Yu J, Li M, Meng F, Wang X, Zhu D Insects 19-Apr-2024
PMCID:PMC11050577
doi:10.3390/insects15040292
PMID:38667422
The Antioxidant, Anti-Inflammatory and Moisturizing Effects of Camellia oleifera Oil and Its Potential Applications Zhou L, Peng Y, Xu Z, Chen J, Zhang N, Liang T, Chen T, Xiao Y, Feng S, Ding C Molecules 19-Apr-2024
PMCID:PMC11055129
doi:10.3390/molecules29081864
PMID:38675684
Transformative and sustainable insights of agricultural waste-based adsorbents for water defluoridation: Biosorption dynamics, economic viability, and spent adsorbent management Das K, Sukul U, Chen JS, Sharma RK, Banerjee P, Dey G, Taharia M, Wijaya CJ, Lee CI, Wang SL, Nuong NH, Chen CY Heliyon 16-Apr-2024
PMCID:PMC11046213
doi:10.1016/j.heliyon.2024.e29747
PMID:38681598
Rapid quantitative authentication and analysis of camellia oil adulterated with edible oils by electronic nose and FTIR spectroscopy Wang X, Gu Y, Lin W, Zhang Q Curr Res Food Sci 16-Apr-2024
PMCID:PMC11063990
doi:10.1016/j.crfs.2024.100732
PMID:38699681
Preparation of Activated Carbon-Reinforced Composite Beads Based on MnO2/MCM-41@Fe3O4 and Calcium Alginate for Efficient Removal of Tetracycline in Aqueous Solutions Zheng Z, Shi R, Zhang X, Ni Y, Zhang H Polymers (Basel) 16-Apr-2024
PMCID:PMC11055116
doi:10.3390/polym16081115
PMID:38675034
Extensive targeted metabolomics analysis reveals the identification of major metabolites, antioxidants, and disease-resistant active pharmaceutical components in Camellia tuberculata (Camellia L.) seeds Ran Z, Li Z, Xiao X, Yan C, An M, Chen J, Tang M Sci Rep 15-Apr-2024
PMCID:PMC11018803
doi:10.1038/s41598-024-58725-0
PMID:38622262
Cotyledonary somatic embryo is one kind of intermediate material similar to callus in the process of in vitro tissue culture from Rosa hybrida ‘John F. Kennedy’ Du L, Kang X, Guo H, Zhu Z, Wu R, Yuan M, Ding C BMC Genomics 12-Apr-2024
PMCID:PMC11010427
doi:10.1186/s12864-024-10256-8
PMID:38609856
The Research of Antagonistic Endophytic Bacterium Bacillus velezensis CSUFT-BV4 for Growth Promotion and Induction of Resistance to Anthracnose in Camellia oleifera He Y, Miao X, Xia Y, Chen X, Liu J, Zhou G Microorganisms 10-Apr-2024
PMCID:PMC11052155
doi:10.3390/microorganisms12040763
PMID:38674707
Stimulatory effects of smoke solution and biogas digestate slurry application on photosynthesis, growth, and methylation profiling of solanum tuberosum Khan RU, Ullah I, Khurshid G, Suboktagin S, Khan AR, Zeb I, Khan ZA, Jamil M, Rha ES, Muhammad Ali H, Ahmad R Plant Signal Behav 10-Apr-2024
PMCID:PMC11017950
doi:10.1080/15592324.2024.2336724
PMID:38600704

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 / Aniline and substituted anilines
p-Aminophenol 403 Click to see C1=CC(=CC=C1N)O 109.13 unknown https://doi.org/10.1248/CPB.57.269
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1248/CPB.57.269
> Lignans, neolignans and related compounds / Furanoid lignans
Episesamin 5204 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1021/JF052325A
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1021/JF052325A
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,7R,8S,8aR,9R,10R,12aS,14aR,14bR)-7,8-dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9,10-bis[[(E)-2-methylbut-2-enoyl]oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 25232670 Click to see 1317.50 unknown https://doi.org/10.1248/CPB.57.269
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8R,8aR,9R,10R,12aS,14aR,14bR)-8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9,10-bis[[(E)-2-methylbut-2-enoyl]oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 25232669 Click to see CC=C(C)C(=O)OC1C(C2(C(CC1(C)C)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)CO)OC(=O)C(=CC)C 1301.50 unknown https://doi.org/10.1248/CPB.57.269
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8R,8aR,9R,10R,12aS,14aR,14bR)-8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9,10-bis[[(E)-2-methylbut-2-enoyl]oxy]-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 25232482 Click to see 1301.50 unknown https://doi.org/10.1248/CPB.57.269
4-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3-hydroxy-6-[[8-hydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9,10-bis(2-methylbut-2-enoyloxy)-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 74408134 Click to see CC=C(C)C(=O)OC1C(C2(C(CC1(C)C)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)C(=O)O)O)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)CO)OC(=O)C(=CC)C 1301.50 unknown https://doi.org/10.1248/CPB.57.269
6-[[7,8-Dihydroxy-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-9,10-bis(2-methylbut-2-enoyloxy)-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3-hydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 74408133 Click to see 1317.50 unknown https://doi.org/10.1248/CPB.57.269
Yuchasaponin A 25232481 Click to see 1317.50 unknown https://doi.org/10.1248/CPB.57.269
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8R,8aR,9S,10R,12aS,14aR,14bR)-8a-acetyloxy-8,9-dihydroxy-4,4,6a,6b,11,11,14b-heptamethyl-10-[(E)-2-methylbut-2-enoyl]oxy-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 163002451 Click to see 1247.40 unknown https://doi.org/10.1248/CPB.57.269
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see 456.70 unknown https://doi.org/10.1248/CPB.57.269
6-[[8a-Acetyloxy-8,9-dihydroxy-4,4,6a,6b,11,11,14b-heptamethyl-10-(2-methylbut-2-enoyloxy)-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-4-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3-hydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 163002450 Click to see 1247.40 unknown https://doi.org/10.1248/CPB.57.269
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1248/CPB.57.269
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(94)85033-X
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(94)85033-X
> Organoheterocyclic compounds / Benzodioxoles
(2S,4aR,5S,7aR)-2,5-bis(1,3-benzodioxol-5-yl)-4a,5,7,7a-tetrahydro-4H-furo[3,4-d][1,3]dioxine 163194271 Click to see 370.40 unknown https://doi.org/10.1021/JF052325A
2,5-bis(1,3-benzodioxol-5-yl)-4a,5,7,7a-tetrahydro-4H-furo[3,4-d][1,3]dioxine 11624883 Click to see 370.40 unknown https://doi.org/10.1021/JF052325A
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1248/CPB.57.269
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1248/CPB.57.269
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1248/CPB.57.269
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1248/CPB.57.269
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3S)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one 162901082 Click to see 482.40 unknown https://doi.org/10.1248/CPB.57.269
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1248/CPB.57.269
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 12304322 Click to see 464.40 unknown https://doi.org/10.1248/CPB.57.269
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/10.1248/CPB.57.269
5,7-Dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one 73322072 Click to see 482.40 unknown https://doi.org/10.1248/CPB.57.269
Afzelin 5316673 Click to see 432.40 unknown https://doi.org/10.1248/CPB.57.269
Npc318533 5835713 Click to see 432.40 unknown https://doi.org/10.1248/CPB.57.269
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1248/CPB.57.269
> Phenylpropanoids and polyketides / Tannins
[4,5-Dihydroxy-3,6-bis[(3,4,5-trihydroxybenzoyl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 14284610 Click to see 636.50 unknown https://doi.org/10.1016/0031-9422(94)85033-X
1,4,6-Tri-O-Galloyl-Beta-D-Glucose 10077822 Click to see 636.50 unknown https://doi.org/10.1016/0031-9422(94)85033-X
galloyl(-2)(galloyl(-3))(galloyl(-4))b-Glc 13270026 Click to see 636.50 unknown https://doi.org/10.1016/0031-9422(94)85033-X
GlyTouCan:G48398GV 13270023 Click to see 636.50 unknown https://doi.org/10.1016/0031-9422(94)85033-X
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(3,4,5,12,13,21,22,23-Octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl) 3,4,5-trihydroxybenzoate 13932611 Click to see C1C2C(C(C(C(O2)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1016/0031-9422(94)85033-X
[(10R,11R,12R,13S,15R)-3,4,5,12,13,21,22,23-octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate 10461723 Click to see C1C2C(C(C(C(O2)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1016/0031-9422(94)85033-X
[(10R,11S,12R,13R,15R)-3,4,5,13,21,22,23-heptahydroxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 2-[[(1R,2S,19R,20R,22R)-7,8,9,12,13,14,20,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]-3,4,5-trihydroxybenzoate 162855090 Click to see 1569.10 unknown https://doi.org/10.1016/0031-9422(94)85033-X
[(10R,11S,12R,13R,15R)-3,4,5,13,21,22,23-heptahydroxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 3,4,5-trihydroxy-2-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzoate 16133859 Click to see 1086.70 unknown https://doi.org/10.1016/0031-9422(94)85033-X
[(10R,11S,12R,13S,15R)-3,4,5,21,22,23-hexahydroxy-8,18-dioxo-11,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 2-[[(1R,2S,19R,20R,22R)-7,8,9,12,13,14,20,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]-3,4,5-trihydroxybenzoate 163046470 Click to see 1721.20 unknown https://doi.org/10.1016/0031-9422(94)85033-X
[(11S,12R,13S,14R,15R,38R,39R,41R,42R,59S)-4,5,6,21,22,23,26,27,31,32,33,39,47,48,49,52,53-heptadecahydroxy-9,18,36,44,56,62-hexaoxo-12,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,10,17,29,37,40,43,57,63,64-decaoxaundecacyclo[39.12.5.414,28.111,15.138,42.03,8.019,24.030,35.045,50.051,55.025,61]tetrahexaconta-1(53),3,5,7,19,21,23,25,27,30,32,34,45,47,49,51,54,60-octadecaen-59-yl] 3,4,5-trihydroxybenzoate 163036067 Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OC7C(COC(=O)C8=CC(=C(C(=C86)O)O)O)OC(C(C7OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2OC2=C(C(=C(C(=C2)C(=O)O1)C1=C(C(=C(C=C1C(=O)O3)O)O)O)O)O)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 1721.20 unknown https://doi.org/10.1016/0031-9422(94)85033-X
[(2R,3R,4S,5R,6R)-2,5-dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxybenzoyl)oxyoxan-3-yl] 3,4,5-trihydroxy-2-[[(10R,11S,12R,13S,15R)-3,4,21,22,23-pentahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-13-[3,4,5-trihydroxy-2-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzoyl]oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-5-yl]oxy]benzoate 162866816 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C5=C6C(=C4)C(=O)OC7=C6C(=CC(=C7O)O)C(=O)O5)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)OC1=C(C(=C(C=C1C(=O)OC1C(C(C(OC1O)CO)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O 1721.20 unknown https://doi.org/10.1016/0031-9422(94)85033-X
[2,5-Dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxybenzoyl)oxyoxan-3-yl] 3,4,5-trihydroxy-2-[[3,4,21,22,23-pentahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-13-[3,4,5-trihydroxy-2-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzoyl]oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-5-yl]oxy]benzoate 16174391 Click to see 1721.20 unknown https://doi.org/10.1016/0031-9422(94)85033-X
[3,4,5,11,21,22,23-Heptahydroxy-8,18-dioxo-13-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 3,4,5-trihydroxybenzoate 146253567 Click to see 786.60 unknown https://doi.org/10.1016/0031-9422(94)85033-X
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 2,3,4-trihydroxy-5-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzoate 163187401 Click to see 1086.70 unknown https://doi.org/10.1016/0031-9422(94)85033-X
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 3,4,5-trihydroxy-2-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]benzoate 16182046 Click to see 1086.70 unknown https://doi.org/10.1016/0031-9422(94)85033-X
[3,4,5,21,22,23-Hexahydroxy-8,18-dioxo-11,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-12-yl] 2-[(7,8,9,12,13,14,20,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl)oxy]-3,4,5-trihydroxybenzoate 163046469 Click to see 1721.20 unknown https://doi.org/10.1016/0031-9422(94)85033-X
[4,5,6,21,22,23,26,27,31,32,33,39,47,48,49,52,53-Heptadecahydroxy-9,18,36,44,56,62-hexaoxo-12,13-bis[(3,4,5-trihydroxybenzoyl)oxy]-2,10,17,29,37,40,43,57,63,64-decaoxaundecacyclo[39.12.5.414,28.111,15.138,42.03,8.019,24.030,35.045,50.051,55.025,61]tetrahexaconta-1(53),3,5,7,19,21,23,25,27,30,32,34,45,47,49,51,54,60-octadecaen-59-yl] 3,4,5-trihydroxybenzoate 16174386 Click to see C1C2C3C(C(C(O2)O)OC(=O)C4=CC(=C(C(=C4OC5=C(C(=C6C(=C5)C(=O)OC7C(COC(=O)C8=CC(=C(C(=C86)O)O)O)OC(C(C7OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2OC2=C(C(=C(C(=C2)C(=O)O1)C1=C(C(=C(C=C1C(=O)O3)O)O)O)O)O)O)O)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O 1721.20 unknown https://doi.org/10.1016/0031-9422(94)85033-X
1,2-Di-O-galloyl-4,6-O-(S)-hexahydroxydiphenoyl-beta-D-glucopyranose 101259865 Click to see 786.60 unknown https://doi.org/10.1016/0031-9422(94)85033-X
1(beta)-O-Galloylpedunculagin 118701062 Click to see 936.60 unknown https://doi.org/10.1016/0031-9422(94)85033-X
14-(3,4,5,11,17,18,19-Heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl)-2,3,4,7,8,9,19-heptahydroxy-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaene-12,17-dione 14035439 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/0031-9422(94)85033-X
alpha-Pedunculagin 13834142 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/0031-9422(94)85033-X
Camelliin A 16174383 Click to see 1569.10 unknown https://doi.org/10.1016/0031-9422(94)85033-X
Camelliin B 16130317 Click to see 1721.20 unknown https://doi.org/10.1016/0031-9422(94)85033-X
Camellioferin A 131753060 Click to see 1721.20 unknown https://doi.org/10.1016/0031-9422(94)85033-X
Casuarictin 73644 Click to see 936.60 unknown https://doi.org/10.1016/0031-9422(94)85033-X
Casuariin 14035442 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/0031-9422(94)85033-X
CID 11766372 11766372 Click to see 938.70 unknown https://doi.org/10.1016/0031-9422(94)85033-X
Eugeniin 442679 Click to see 938.70 unknown https://doi.org/10.1016/0031-9422(94)85033-X
Gemin D 471119 Click to see 634.50 unknown https://doi.org/10.1016/0031-9422(94)85033-X
Pedunculagin 442688 Click to see 784.50 unknown https://doi.org/10.1016/0031-9422(94)85033-X
Pedunculagin I 492391 Click to see 784.50 unknown https://doi.org/10.1016/0031-9422(94)85033-X
Potentillin 452242 Click to see 936.60 unknown https://doi.org/10.1016/0031-9422(94)85033-X
Schimawalin B 16130316 Click to see 1721.20 unknown https://doi.org/10.1016/0031-9422(94)85033-X
Tellimagrandin Ii 151590 Click to see 938.70 unknown https://doi.org/10.1016/0031-9422(94)85033-X

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