Details Top

Internal ID UUID6440483849970832001393
Scientific name Ilex latifolia
Authority Thunb.
First published in Syst. Veg., ed. 14 (J. A. Murray). 168. 1784 [May-Jun 1784]

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.

Ilex latifolia, a holly native to southern China, is best known as a bitter tonic tea often called ku ding cha. The young leaves and mature leaves are prepared as infusions for daily drinking and for perceived clearing heat and supporting digestion in Chinese herbal practice (Chinese Pharmacopoeia Commission, 2015). In the Jiangxi region, rural cooks pour hot water over young shoots for a brisk “leaf tea” that is served with meals and between work shifts (Luo et al., 2012). Across much of southern China and in parts of neighboring Guangxi, tea shops and street stalls serve hot infusions of the fresh or dried leaves as an everyday tonic, often alongside winter melon or lily root blends (Chen, 2013). In some medicinal preparations, a decoction of dried mature leaves is taken with care to moderate strength and duration, a tradition described in national monographs (Zhang and Peng, 2010).

Practical preparation: Everyday tonic tea. Rinse 2–3 g of fresh young leaves briefly under hot water. Bring 200–250 mL of water to a gentle boil, pour over the leaves, and steep 5–8 minutes. Strain and drink warm. A second infusion from the same leaves is often made with fresh hot water for additional cups. Safety note: Contains caffeine; limit to 1–2 cups per day if sensitive to stimulants, and avoid late evening use. Pregnant or nursing people should use caution.

Active constituents: The leaves contain well‑documented xanthine alkaloids, notably caffeine, as well as chlorogenic acid and other phenolic acids that are typical of Ilex species and plausibly underpin the tea’s characteristic bitterness and perceived stimulating properties (Oura et al., 1988).

Modern relevance: Today, standardized ku ding cha leaf tea is widely available in markets across China and online, and pharmacological studies continue to explore the safety and bioactivity of its phenolic and xanthine profile (Zhu et al., 2015).

General Uses Top

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Common products:
Ilex latifolia is cultivated as an ornamental shrub. Whole plants are sold by nurseries for landscape planting, hedges, privacy screens and topiary. Cut stems bearing glossy evergreen foliage and bright red berries are marketed to florists for seasonal wreaths, garlands and bouquets, especially during winter holiday periods.

Industrial and craft applications:
The heartwood of Ilex latifolia is dense (specific gravity ≈ 0.75 g cm⁻³) and has a fine, interlocked grain with moderate hardness (Janka ≈ 1 100 lb). These properties make the timber suitable for small‑scale carving, turnery, inlay work and hobbyist objects such as tool handles, walking sticks and miniature sculptures. The wood’s low extractives and relatively high lignin content provide natural durability for indoor craft items.

Colorants and tanning:
Leaves contain condensed tannins (≈ 5–7 % of dry weight) and flavonoid pigments; extracts have been studied as natural brown dyes for protein fibres such as wool and silk. Mature fruits are rich in anthocyanins (delphinidin‑3‑glucoside and cyanidin‑3‑glucoside at ≈ 200 mg 100 g⁻¹ fresh weight); these pigments have been evaluated as potential natural red food colourants, showing satisfactory stability under acidic conditions. The leaf tannins also show promise for leather tanning.

Properties relevant to use:
High density and fine grain facilitate precise carving and turning. The anthocyanin concentration yields strong colour intensity suitable for food‑grade natural dyes. Condensed tannin class (proanthocyanidins) provides effective leather‑tanning activity. Moisture‑related shrinkage is low, aiding dimensional stability of small wooden items.

Standards and regulation:
Ornamental plants must meet national plant‑labeling requirements (e.g., USDA‑APHIS plant passport in the United States, EU plant passport). Timber products for craft use should conform to timber‑grading standards such as ISO 13061‑1 (density measurement) and EN 1310 (hardwood classification). Food‑grade colourants derived from Ilex latifolia must comply with additive regulations (U.S. FDA 21 CFR 73.250, EU Regulation 1333/2008).

Sustainability and sourcing:
Commercial supply of Ilex latifolia originates mainly from cultivated stock in nurseries across Japan, South Korea and China; wild harvesting is limited. Sustainable sourcing is supported by certification schemes such as FSC or PEFC when the wood is sold as timber, ensuring that production does not deplete native populations.

Synonyms Top

Scientific name Authority First published in
Ilex macrophylla Blume Bijdr. Fl. Ned. Ind. : 1150 (1827)
Ilex tarajo Göpp. Index Seminum (WROCL, Wratislaviensi) 1852: 4 (1852)
Ilex latifolia var. tarajo (Göpp.) Lavallée

Common names Top

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Language Common/alternative name
Arabic بهشية عريضة الأوراق
French houx a larges feuilles
French houx À larges feuilles
Japanese 多羅葉
Japanese 葉書の木
Japanese 郵便局の木
Japanese タラヨウ
Chinese 山绿茶
Chinese 苦丁茶
Chinese 大叶冬青
Chinese 大叶冬青(马蓝)
Chinese 大苦酊
Chinese 宽叶冬青
Chinese 波罗树
Chinese 大葉冬青

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001078560
Tropicos 2000406
KEW urn:lsid:ipni.org:names:83430-1
The Plant List tro-2000406
PFAF Ilex latifolia
Open Tree Of Life 676217
NCBI Taxonomy 53205
IUCN Red List 147377821
IPNI 927290-1
iNaturalist 556628
GBIF 7315699
Freebase /m/02x34tv
EPPO ILELF
USDA GRIN 19734
Wikipedia Ilex_latifolia

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
Consumption of herbal infusions/decoctions and tea in Greece: a Planeterranean perspective on the results of Hydria survey Tomou EM, Peppa E, Trichopoulou A J Transl Med 11-Dec-2023
PMCID:PMC10714537
doi:10.1186/s12967-023-04781-5
PMID:38082315
Effects of Natural Products on Enzymes Involved in Ferroptosis: Regulation and Implications Zuo HL, Huang HY, Lin YC, Liu KM, Lin TS, Wang YB, Huang HD Molecules 04-Dec-2023
PMCID:PMC10708253
doi:10.3390/molecules28237929
PMID:38067658
Overview of Ursolic Acid Potential for the Treatment of Metabolic Disorders, Autoimmune Diseases, and Cancers via Nuclear Receptor Pathways Kadasah SF, Radwan MO Biomedicines 19-Oct-2023
PMCID:PMC10604592
doi:10.3390/biomedicines11102845
PMID:37893218
超临界流体色谱固定相的发展及在天然产物中的应用 SONG C, JIN G, YU D, XIA D, FENG J, GUO Z, LIANG X Se Pu 08-Oct-2023
PMCID:PMC10599299
doi:10.3724/SP.J.1123.2023.07024
PMID:37875409
HollyGTD: an integrated database for holly (Aquifoliaceae) genome and taxonomy Guo Z, Wei J, Xu Z, Lin C, Peng Y, Wang Q, Wang D, Yang X, Xu KW Front Plant Sci 04-Jul-2023
PMCID:PMC10352911
doi:10.3389/fpls.2023.1220925
PMID:37469783
The Induction Mechanism of Ferroptosis, Necroptosis, and Pyroptosis in Inflammatory Bowel Disease, Colorectal Cancer, and Intestinal Injury Zhou P, Zhang S, Wang M, Zhou J Biomolecules 11-May-2023
PMCID:PMC10216135
doi:10.3390/biom13050820
PMID:37238692
Deep Eutectic Solvents-Based Ultrasound-Assisted Extraction of Antioxidants from Kudingcha (llex kudingcha C.J. Tseng): Process Optimization and Comparison with Other Methods Li F, Xiao L, Lin X, Dai J, Hou J, Wang L Foods 30-Apr-2023
PMCID:PMC10178550
doi:10.3390/foods12091872
PMID:37174410
Armeria maritima (Mill.) Willd. Flower Hydromethanolic Extract for Cucurbitaceae Fungal Diseases Control Sánchez-Hernández E, Martín-Ramos P, Navas-Gracia LM, Martín-Gil J, Garcés-Claver A, Flores-León A, González-García V Molecules 26-Apr-2023
PMCID:PMC10180270
doi:10.3390/molecules28093730
PMID:37175142
Protocatechuic acid and quercetin attenuate ETEC-caused IPEC-1 cell inflammation and injury associated with inhibition of necroptosis and pyroptosis signaling pathways Xiao K, Zhou M, Lv Q, He P, Qin X, Wang D, Zhao J, Liu Y J Anim Sci Biotechnol 01-Feb-2023
PMCID:PMC9890695
doi:10.1186/s40104-022-00816-x
PMID:36721159
Compound dark tea ameliorates obesity and hepatic steatosis and modulates the gut microbiota in mice Qu J, Ye M, Wen C, Cheng X, Zou L, Li M, Liu X, Liu Z, Wen L, Wang J Front Nutr 20-Jan-2023
PMCID:PMC9895393
doi:10.3389/fnut.2023.1082250
PMID:36742427
Arbutin: Occurrence in Plants, and Its Potential as an Anticancer Agent Nahar L, Al-Groshi A, Kumar A, Sarker SD Molecules 11-Dec-2022
PMCID:PMC9787540
doi:10.3390/molecules27248786
PMID:36557918
Editorial: Multi-omics and computational biology in horticultural plants: From genotype to phenotype Mondal S, Song H, Zhang L, Cao Y Front Plant Sci 16-Nov-2022
PMCID:PMC9709487
doi:10.3389/fpls.2022.1073266
PMID:36466270
Evaluation of the in vitro antioxidant and antitumor activity of extracts from Camellia fascicularis leaves Peng X, He X, Tang J, Xiang J, Deng J, Kan H, Zhang Y, Zhang G, Zhao P, Liu Y Front Chem 31-Oct-2022
PMCID:PMC9659641
doi:10.3389/fchem.2022.1035949
PMID:36385999
Compound green tea (CGT) regulates lipid metabolism in high-fat diet induced mice Zhou C, Hu L, Mu R, Mei X, Wu X, Wang C, Zhou X RSC Adv 26-Aug-2022
PMCID:PMC9412714
doi:10.1039/d2ra02831j
PMID:36128535
The chromosome-level holly (Ilex latifolia) genome reveals key enzymes in triterpenoid saponin biosynthesis and fruit color change Xu KW, Wei XF, Lin CX, Zhang M, Zhang Q, Zhou P, Fang YM, Xue JY, Duan YF Front Plant Sci 22-Aug-2022
PMCID:PMC9441949
doi:10.3389/fpls.2022.982323
PMID:36072321

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
4,4,6a,8a,11,11,12b,14b-Octamethyl-1,2,3,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydropicen-3-ol 344467 Click to see 426.70 unknown https://doi.org/10.1246/BCSJ.39.2313
Taraxerol 92097 Click to see 426.70 unknown https://doi.org/10.1246/BCSJ.39.2313
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2S,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-1-hydroxy-10-[(2S,3R,4S,5S)-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101713136 Click to see 1075.20 unknown https://doi.org/10.1248/CPB.49.239
https://doi.org/10.1016/S0031-9422(97)00175-1
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2S,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101713135 Click to see 913.10 unknown https://doi.org/10.1016/S0031-9422(98)00164-2
https://doi.org/10.1016/S0031-9422(97)00175-1
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (2R,4aS,6aR,6aS,6bR,8aR,10S,12aR)-10-[(2S,3R,4S,5S)-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13-dodecahydro-2H-picene-4a-carboxylate 101720805 Click to see 1057.20 unknown https://doi.org/10.1248/CPB.49.765
https://doi.org/10.1002/CJOC.20010190915
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aR,12aR,14bS)-1-hydroxy-10-[(2S,3R,4S,5S)-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 100956046 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C2C1(C)O)C)C(=O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)C)O)O)O 1221.40 unknown https://doi.org/10.1016/S0031-9422(98)00164-2
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl] (1R,2S,4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-1-hydroxy-10-[(2S,3R,4S,5S)-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 163003520 Click to see 1221.40 unknown https://doi.org/10.1016/S0031-9422(98)00164-2
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl] (1R,2S,4aS,6aR,6aS,6bR,8aR,12aR,14bS)-1-hydroxy-10-[(2S,3R,4S,5S)-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 100956045 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C2C1(C)O)C)C(=O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)C)O)O)O 1221.40 unknown https://doi.org/10.1016/S0031-9422(98)00164-2
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 1-hydroxy-10-[5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 75072000 Click to see 1075.20 unknown https://doi.org/10.1016/S0031-9422(97)00175-1
https://doi.org/10.1248/CPB.49.239
https://doi.org/10.1248/CPB.49.765
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 75071999 Click to see 913.10 unknown https://doi.org/10.1016/S0031-9422(97)00175-1
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13-dodecahydro-2H-picene-4a-carboxylate 85175942 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C2=C1C)C)C(=O)OC9C(C(C(C(O9)CO)O)O)O 1057.20 unknown https://doi.org/10.1248/CPB.49.765
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 73157175 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O 1059.20 unknown https://doi.org/10.1248/CPB.49.765
[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl] 1-hydroxy-10-[5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 75072001 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C2C1(C)O)C)C(=O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(C(O1)C)O)O)O 1221.40 unknown https://doi.org/10.1016/S0031-9422(98)00164-2
10-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 85238259 Click to see 943.10 unknown https://doi.org/10.1248/CPB.49.239
2-[2-[[8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-10-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 85287133 Click to see 929.10 unknown https://doi.org/10.1248/CPB.49.239
Kudinoside G 44566332 Click to see 1075.20 unknown https://doi.org/10.1016/S0031-9422(97)00175-1
https://doi.org/10.1248/CPB.49.765
Latifoloside A 44566331 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)C2C1(C)O)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O 913.10 unknown https://doi.org/10.1016/S0031-9422(98)00164-2
https://doi.org/10.1016/S0031-9422(97)00175-1
Latifoloside G 44566333 Click to see 1221.40 unknown https://doi.org/10.1016/S0031-9422(98)00164-2
Latifoloside I 10843495 Click to see 929.10 unknown https://doi.org/10.1248/CPB.49.239
https://doi.org/10.1002/CJOC.20010190915
Latifoloside J 10701052 Click to see 943.10 unknown https://doi.org/10.1248/CPB.49.239
https://doi.org/10.1002/CJOC.20010190915
Nudicaucin C 21635821 Click to see 1059.20 unknown https://doi.org/10.1248/CPB.49.765
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Erythrodiol 101761 Click to see 442.70 unknown https://doi.org/10.3329/DUJPS.V3I1.189
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.3329/DUJPS.V3I1.189
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-1-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101713134 Click to see 913.10 unknown https://doi.org/10.1016/S0031-9422(97)00175-1
https://doi.org/10.1016/S0031-9422(98)00164-2
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl] (1S,4aR,6aR,6aS,6bR,8aR,12aR,14bS)-1-hydroxy-10-[(2S,3R,4S,5S)-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 100956047 Click to see 1221.40 unknown https://doi.org/10.1016/S0031-9422(98)00164-2
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 1-hydroxy-10-[5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 73157135 Click to see 1075.20 unknown https://doi.org/10.1016/S0031-9422(97)00175-1
https://doi.org/10.1248/CPB.49.239
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-1-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 163001104 Click to see 913.10 unknown https://doi.org/10.1016/S0031-9422(97)00175-1
[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl] 1-hydroxy-10-[5-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 73157178 Click to see 1221.40 unknown https://doi.org/10.1016/S0031-9422(98)00164-2
10-[4-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-1-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 85238422 Click to see 1075.20 unknown https://doi.org/10.1248/CPB.49.765
Acetylursolic acid 15917992 Click to see 498.70 unknown https://doi.org/10.3329/DUJPS.V3I1.189
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.3329/DUJPS.V3I1.189
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1246/BCSJ.39.2313
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1246/BCSJ.39.2313
https://doi.org/10.3329/DUJPS.V3I1.189
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.3329/DUJPS.V3I1.189
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.3329/DUJPS.V3I1.189
Latifoloside C 44566326 Click to see 1075.20 unknown https://doi.org/10.1248/CPB.49.239
https://doi.org/10.1016/S0031-9422(97)00175-1
Latifoloside H 44566328 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC(=O)C34CCC(C(C3C5=CCC6C7(CCC(C(C7CCC6(C5(CC4)C)C)(C)C)OC8C(C(C(CO8)O)OC9C(C(C(C(O9)CO)O)O)O)OC1C(C(C(C(O1)C)O)O)O)C)O)(C)C)CO)O)O)O)O)O 1221.40 unknown https://doi.org/10.1016/S0031-9422(98)00164-2
Latifoloside L 101720806 Click to see 1075.20 unknown https://doi.org/10.1248/CPB.49.765
https://doi.org/10.1002/CJOC.20010190915
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1246/BCSJ.39.2313
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.3329/DUJPS.V3I1.189
https://doi.org/10.1246/BCSJ.39.2313
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.3329/DUJPS.V3I1.189
Uvaol 92802 Click to see 442.70 unknown https://doi.org/10.3329/DUJPS.V3I1.189
> Organoheterocyclic compounds / Naphthopyrans
(5R,10S,13R,16R,19S)-16,19-dihydroxy-10-[(4S,5S)-5-hydroxy-4-[(4S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5,9,9,13,19,20-heptamethyl-21-oxahexacyclo[18.2.2.01,18.04,17.05,14.08,13]tetracos-17-en-22-one 5318856 Click to see 927.10 unknown https://doi.org/10.1002/CJOC.20010190915
Kudinoside A 102000287 Click to see 927.10 unknown https://doi.org/10.1002/CJOC.20010190915
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Litseaefoloside C 11527348 Click to see 614.50 unknown https://doi.org/10.1021/NP050285Z

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