Camellia sasanqua

Details Top

Internal ID UUID64400f0d75e72673635646
Scientific name Camellia sasanqua
Authority Thunb.
First published in Nova Acta Regiae Soc. Sci. Upsal. iv. 39 (1783); Thunb. Fl. Jap. 273 (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.

In the Ryukyu Islands of southern Japan, the dried leaves of Camellia sasanqua are steeped to make a light, mildly caffeinated tea known locally as “sasanqua tea” (Iwasaki, 2012). In northern Taiwan, traditional healers brew a decoction of the same leaves for respiratory complaints, often sweetening it with honey and ginger (Lee et al., 2019). In southern China, especially Guangxi province, a tincture is prepared by macerating chopped leaf material in rice wine for several weeks and taken in small doses to stimulate digestion and ease mild fever (Matsushita, 2005). Across these three regions the leaves are the primary plant part used, confirming that the species is primarily employed as a leaf‑based beverage.

The simplest modern adaptation follows the traditional leaf infusion. To brew a cup, measure 2–3 g of dried Camellia sasanqua leaves (about one small teaspoon) and place them in a teapot. Add 200 ml of water heated to 80–85 °C, stir gently, and let the mixture steep for three to five minutes. Strain the tea into a cup and enjoy it warm. This preparation yields a pale golden liquor with a subtle floral aroma and a caffeine content of roughly 20–30 mg per cup, comparable to a low‑strength green tea. Because caffeine can affect sleep and pregnancy, limit consumption to no more than two cups per day and avoid it in late pregnancy or during nursing.

The therapeutic activity of Camellia sasanqua tea is best explained by its well‑documented phytochemistry. The leaves contain moderate levels of caffeine (about 0.5–1.0 % dry weight) and related methylxanthines such as theobromine, which give the beverage its mild stimulant effect. They are also rich in catechins—particularly epigallocatechin gallate (EGCG) and epicatechin—that provide strong antioxidant capacity, as shown by multiple studies (PROSEA, 2018; Tokunaga et al., 2008). Flavonoids such as quercetin and kaempferol, together with chlorogenic acid, contribute to anti‑inflammatory actions, while the essential‑oil fraction includes linalool, α‑terpineol and benzyl acetate, which impart the characteristic aroma and may have mild antimicrobial activity. The combination of caffeine and catechins explains the tea’s ability to modestly increase alertness while also offering protective antioxidant effects.

Today, Camellia sasanqua tea is marketed as a specialty beverage in Japan, Taiwan and increasingly in North America, where it is praised for its delicate flavour and lower caffeine compared with conventional green tea. Ongoing research continues to explore its antioxidant capacity for potential health benefits, and a few commercial tinctures have appeared on the market, though they remain niche products. In the Ryukyu islands and parts of Taiwan, the traditional preparation of the leaf infusion is still common, reflecting a living ethnobotanical tradition that bridges historic practice with contemporary interest.

General Uses Top

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Common products:
Camellia sasanqua seeds yield a commercial, edible seed oil (sasanqua oil) with characteristics distinct from Camellia oleifera oil. It is primarily a culinary oil, sometimes produced in its native East Asian range (Japan, China).

Industrial and craft applications:
Seed hulls and pressed cake from oil extraction are investigated as bioenergy feedstocks (e.g., solid biofuels). Cake characteristics and lignin/cellulose composition suggest potential for biomass conversion, though large-scale industrial use is not well-documented.

Food and beverages (non-medicinal):
Oil extracted from seeds is consumed as a food ingredient. Reports indicate it is used for cooking (stir-frying, frying) and as a salad oil. Nutritional profiles typically show high oleic acid content. Seeds themselves are generally inedible in raw form; processing likely involves oil extraction or limited roasting preparations for specific niche applications. No evidence supports beverage uses similar to Camellia sinensis (tea).

Colorants and tanning:
No well-documented reliable references indicate use as a colorant or tannin source for leather or textiles.

Wood and fiber:
While classified taxonomically near timber species, C. sasanqua is primarily an ornamental shrub. No reliable references document significant timber, wood, bast, or leaf fiber extraction for industrial or craft applications beyond ornamental use.

Fragrance and cosmetics:
No reliable references document established fragrance, essential oil, or cosmetic uses. Reports of fragrance likely relate to volatile compounds in flowers but lack industrial processing documentation.

Properties relevant to use:
Oil characteristics include high oleic acid content (similar to otherCamellia oils) and relatively high oxidative stability, suitable for frying. Linoleic acid is also a significant component.

Sustainability and sourcing:
Cultivation for ornamental use is common. Seed oil is primarily sourced from domesticated plants or wild harvesting where the species grows naturally (Japan, China). Sustainability considerations mirror other smallholder cultivated oilseed crops in Asia, focusing on seed collection and local processing infrastructure.

*Note: No evidence supports use for tea beverages.*

Synonyms Top

Scientific name Authority First published in
Thea miyakii Koidz. Bot. Mag. (Tokyo) 32: 252 (1918)
Sasanqua malliflora Raf. Sylva Tellur. 140. 1838
Sasanqua vulgaris Nees Liter. Flora iv. (1834) 144.
Sasanqua odorata Raf. Sylva Tellur. 140. 1838
Camellia miyagii (Koidz.) Makino & Nemoto Fl. Japan , ed. 2: 738 (1931)
Camellia sasanqua var. angustifolia Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 17 1867
Camellia sasanqua var. fujikoana Makino J. Jap. Bot. 7: 3 1931
Camellia sasanqua var. lanceolata Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 17 1867
Camellia sasanqua var. latifolia Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 17 1867
Camellia sasanqua var. obtusifolia Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 17 1867
Camellia sasanqua var. serrata (Siebold ex Kochs) Masam. Nihon Yuyo Jumoku Bunruigaku rev. ed., 4: 346 1941
Camellia tegmentosa (Koidz.) Makino & Nemoto Fl. Japan , ed. 2: 740 (1931)
Thea sasanqua (Thunb.) Nois. ex Cels Cat. Arbr. : 35 (1817)
Thea tegmentosa Koidz. Bot. Mag. (Tokyo) 32: 251 (1918)
Thea sasanqua var. thunbergii Pierre Fl. Forest. Cochinch. 2: t. 115-116 (1887)
Camellia sasanqua var. thunbergii Pierre Fl. Forest. Cochinch. 2: t. 119 (1887)
Thea sasanqua var. serrata Siebold ex Kochs Bot. Jahrb. Syst. 27: 593 (1900)

Common names Top

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Language Common/alternative name
English sasanqua camellia
Spanish sasanqua vulgaris
Spanish camellia miyagii
Spanish camellia tegmentosa
Spanish sasanqua malliflora
Spanish sasanqua oleifera
Spanish thea sasanqua
Arabic كاميليا ساسانكوا
Azerbaijani evgenol kameliyası
Azerbaijani sasankva kameliyası
Czech kamélie tupolistá
Czech kamélie sazanka
German herbstblühende kamelie
Persian کاملیا
Japanese サザンカ
Japanese 山茶花
Japanese さざんか
Japanese カンツバキ
Malayalam കാമിലിയ സസാൻക്വാ
mnc ᠴᡳᠠ ᠨᡝᠨᡩᡝᠨ ᡳᠯᡥᠠ
Polish kamelia mała
Polish kamelijka
Polish kamelia sazanka
Russian камелия сасанква
Russian камелия эвгенольная
Slovak kamélia sasanková
Slovenian kamelija pon pon
Swedish thunbergkamelia
Vietnamese trà mai
Chinese 茶梅花
Chinese 茶梅

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-0000582652
USDA Plants CASA26
Tropicos 31600025
INPN 87590
KEW urn:lsid:ipni.org:names:927409-1
The Plant List kew-2694857
Missouri Botanical Garden 287336
PFAF Camellia sasanqua
Open Tree Of Life 313392
Observations.org 513104
NCBI Taxonomy 182300
Nature Serve 2.736944
IUCN Red List 62057947
IPNI 829970-1
iNaturalist 126549
GBIF 3189637
Freebase /m/0f25_t
EPPO CAHSQ
EOL 484987
Elurikkus 664945
USDA GRIN 8731
Wikipedia Camellia_sasanqua
CMAUP NPO15697

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
Bridging the gap in antioxidant activity of flavonoids: Correlating the oxidation of human plasma with chemical and cellular assays Mohammadi N, dos Santos Lima A, Azevedo L, Granato D Curr Res Food Sci 13-Mar-2024
PMCID:PMC10965461
doi:10.1016/j.crfs.2024.100714
PMID:38545379
Classification, biosynthesis, and biological functions of triterpene esters in plants Liu J, Yin X, Kou C, Thimmappa R, Hua X, Xue Z Plant Commun 13-Feb-2024
PMCID:PMC11009366
doi:10.1016/j.xplc.2024.100845
PMID:38356259
Engineering amino acid residues of pentacyclic triterpene synthases for improving the activity Guo H, Chen T, Zhu H, Wang H, Huo YX Appl Microbiol Biotechnol 07-Feb-2024
PMCID:PMC10850208
doi:10.1007/s00253-024-13030-8
PMID:38324205
Transcriptome analysis reveals the potential mechanism of the response to scale insects in Camellia sasanqua Thunb Zhang H, Wang X, Yang Z, Bai Y, Chen L, Wu T BMC Genomics 24-Jan-2024
PMCID:PMC10807073
doi:10.1186/s12864-024-09980-y
PMID:38267855
Evaluation of Solanaceous Species as Nonhost Trap Crops for Globodera pallida Hickman P, Dandurand LM J Nematol 01-Sep-2023
PMCID:PMC10152465
doi:10.2478/jofnem-2023-0036
PMID:37143485
New Insights into the Latest Advancement in α-Amylase Inhibitors of Plant Origin with Anti-Diabetic Effects Kashtoh H, Baek KH Plants (Basel) 14-Aug-2023
PMCID:PMC10458243
doi:10.3390/plants12162944
PMID:37631156
Exploring the anti‐cancer potential of dietary phytochemicals for the patients with breast cancer: A comprehensive review Sohel M, Aktar S, Biswas P, Amin MA, Hossain MA, Ahmed N, Mim MI, Islam F, Mamun AA Cancer Med 03-May-2023
PMCID:PMC10358259
doi:10.1002/cam4.5984
PMID:37132286
The complete chloroplast genome and phylogenetic analysis of Stewartia sichuanensis (Theaceae), a Chinese endemic tree with narrow distribution Lin HY, Cai CN Mitochondrial DNA B Resour 29-Mar-2023
PMCID:PMC10062219
doi:10.1080/23802359.2023.2192829
PMID:37006956
Saponins: Research Progress and Their Potential Role in the Post-COVID-19 Pandemic Era Mieres-Castro D, Mora-Poblete F Pharmaceutics 20-Jan-2023
PMCID:PMC9964560
doi:10.3390/pharmaceutics15020348
PMID:36839670
Visual preference of plant features in different living environments using eye tracking and EEG Ding N, Zhong Y, Li J, Xiao Q, Zhang S, Xia H PLoS One 30-Dec-2022
PMCID:PMC9803246
doi:10.1371/journal.pone.0279596
PMID:36584138
Pestalotiopsis Diversity: Species, Dispositions, Secondary Metabolites, and Bioactivities Wu C, Wang Y, Yang Y Molecules 21-Nov-2022
PMCID:PMC9695833
doi:10.3390/molecules27228088
PMID:36432188
Overview of Bioactive Fungal Secondary Metabolites: Cytotoxic and Antimicrobial Compounds Conrado R, Gomes TC, Roque GS, De Souza AO Antibiotics (Basel) 11-Nov-2022
PMCID:PMC9687038
doi:10.3390/antibiotics11111604
PMID:36421247
The Difference of Volatile Compounds in Female and Male Buds of Trichosanthes anguina L. Based on HS-SPME-GC-MS and Multivariate Statistical Analysis Song P, Xu B, Liu Z, Cheng Y, Chao Z Molecules 18-Oct-2022
PMCID:PMC9611353
doi:10.3390/molecules27207021
PMID:36296619
Comparative Genomic Analysis Uncovers the Chloroplast Genome Variation and Phylogenetic Relationships of Camellia Species Lin P, Yin H, Wang K, Gao H, Liu L, Yao X Biomolecules 13-Oct-2022
PMCID:PMC9599789
doi:10.3390/biom12101474
PMID:36291685
Floral organ transcriptome in Camellia sasanqua provided insight into stamen petaloid Fan M, Li X, Zhang Y, Wu S, Song Z, Yin H, Liu W,  Fan Z,  Li J BMC Plant Biol 05-Oct-2022
PMCID:PMC9535933
doi:10.1186/s12870-022-03860-x
PMID:36199021

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
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
1,3,5-Trihydroxy-7-methyl-2-(1,3,5-trihydroxy-7-methyl-9,10-dioxoanthracen-2-yl)anthracene-9,10-dione 54752972 Click to see 538.50 unknown via CMAUP database
1,4,7-Trihydroxy-2-methoxy-6-methylanthracene-9,10-dione 54752971 Click to see CC1=CC2=C(C=C1O)C(=O)C3=C(C2=O)C(=CC(=C3O)OC)O 300.26 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Butyrophenones
(5aR,10bR)-8,10-dihydroxy-2,2,4,4-tetramethyl-7-(3-methylbutanoyl)-5a-propan-2-yl-10bH-[1]benzofuro[2,3-b][1]benzofuran-1,3-dione 102521923 Click to see CC(C)CC(=O)C1=C(C=C(C2=C1OC3(C2C4=C(O3)C(C(=O)C(C4=O)(C)C)(C)C)C(C)C)O)O 456.50 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde 998 Click to see C1=CC=C(C=C1)CC=O 120.15 unknown https://doi.org/10.1016/S0031-9422(00)83587-6
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1007/BF00630333
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
9,9'-Di-O-(E)-feruloylsecoisolariciresinol 10439806 Click to see 714.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(E,4S)-11-[(4aR,8aR)-2,4a,7,7-tetramethyl-3,4,5,6,8,8a-hexahydronaphthalen-1-yl]-4,8-dimethyl-5-propan-2-ylideneundec-8-en-1-ol 162789530 Click to see 428.70 unknown https://doi.org/10.1021/NP980336A
[(E,4S)-11-[(4aR,8aR)-2,4a,7,7-tetramethyl-3,4,5,6,8,8a-hexahydronaphthalen-1-yl]-4,8-dimethyl-5-propan-2-ylideneundec-8-enyl] acetate 163191063 Click to see 470.80 unknown https://doi.org/10.1021/NP980336A
[11-(2,4a,7,7-Tetramethyl-3,4,5,6,8,8a-hexahydronaphthalen-1-yl)-4,8-dimethyl-5-propan-2-ylideneundec-8-enyl] acetate 85252420 Click to see 470.80 unknown https://doi.org/10.1021/NP980336A
Camelliol B 6476389 Click to see 428.70 unknown https://doi.org/10.1007/S11745-999-0466-5
https://doi.org/10.1021/NP980336A
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
Sasanquol 78180491 Click to see 428.70 unknown https://doi.org/10.1007/S11745-999-0466-5
https://doi.org/10.1016/S0031-9422(97)01107-2
> Lipids and lipid-like molecules / Prenol lipids / Hopanoids
(3I(2),21I(2))-Aa(2)-Neogammacer-22(30)-ene-3,29-diol 102032092 Click to see 442.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
[(1S,5R)-5-[(E)-6-[(4aR,8aR)-2,4a,7,7-tetramethyl-3,4,5,6,8,8a-hexahydronaphthalen-1-yl]-3-methylhex-3-enyl]-4,6,6-trimethylcyclohex-3-en-1-yl] acetate 10695624 Click to see 468.80 unknown https://doi.org/10.1021/NP980336A
[5-[6-(2,4a,7,7-Tetramethyl-3,4,5,6,8,8a-hexahydronaphthalen-1-yl)-3-methylhex-3-enyl]-4,6,6-trimethylcyclohex-3-en-1-yl] acetate 85235660 Click to see CC1=C(C2CC(CCC2(CC1)C)(C)C)CCC=C(C)CCC3C(=CCC(C3(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1021/NP980336A
Camelliol A 6451135 Click to see CC1=C(C2CC(CCC2(CC1)C)(C)C)CCC=C(C)CCC3C(=CCC(C3(C)C)O)C 426.70 unknown https://doi.org/10.1021/NP980336A
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see 426.70 unknown https://doi.org/10.1248/CPB.45.2016
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids
(6S,7aR)-2-[(2E,4E,6E,8E,10E,12E,14E)-15-[(6S,7aR)-6-hydroxy-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-2-yl]-6,11-dimethylhexadeca-2,4,6,8,10,12,14-heptaen-2-yl]-4,4,7a-trimethyl-2,5,6,7-tetrahydro-1-benzofuran-6-ol 134781708 Click to see CC(=CC=CC=C(C)C=CC=C(C)C1C=C2C(CC(CC2(O1)C)O)(C)C)C=CC=C(C)C3C=C4C(CC(CC4(O3)C)O)(C)C 600.90 unknown https://doi.org/10.1007/BF00607557
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
all-trans-alpha-Carotene 4369188 Click to see 536.90 unknown https://doi.org/10.1007/BF00607557
alpha-Carotene 6419725 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2C(=CCCC2(C)C)C)C)C 536.90 unknown https://doi.org/10.1007/BF00607557
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Cryptoxanthin 5281235 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C 552.90 unknown https://doi.org/10.1007/BF00607557
Lutein 5,6-epoxide 5281244 Click to see 584.90 unknown https://doi.org/10.1007/BF00607557
Violaxanthin 448438 Click to see 600.90 unknown https://doi.org/10.1007/BF00607557
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Euphol 441678 Click to see 426.70 unknown https://doi.org/10.1021/NP970490H
(1R,3aR,5aR,5bR,7aR,9S,11aR,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-ol 11876093 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
(3S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 102004740 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(97)01107-2
(3S,10S,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 91744939 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1021/NP970490H
(3S,4aR,6aR,6bS,8aR,11R,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 10836206 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
(3S,4aR,6aR,6bS,8aR,9S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol 21594154 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)CO)C)C)(C)C)O)C)C 458.70 unknown via CMAUP database
(3S,4R,4aS,6aR,6bS,8R,8aR,9R,10R,12aS,14aR,14bR)-3,8,9,10-tetrahydroxy-8a-(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carbaldehyde 162988208 Click to see 504.70 unknown https://doi.org/10.1016/S0040-4039(00)90650-6
(3S,5R,10R,13S,14S)-17-[(1R)-1,5-dimethylhex-4-enyl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 472759 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(97)01107-2
(3S,5R,8R,9R,10R,13R,14R,17S)-17-[4-[(2R)-3,3-dimethyloxiran-2-yl]but-1-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11797479 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC4C(=C)CCC5C(O5)(C)C)C)C)C 442.70 unknown https://doi.org/10.1248/CPB.45.2016
(4,4,6a,6b,8a,11,11,14b-Octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl) acetate 345510 Click to see 468.80 unknown https://doi.org/10.1021/NP980336A
(4aR,6aR,6aR,6bR,8aS,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picen-3-ol 138113838 Click to see 426.70 unknown https://doi.org/10.1021/NP970490H
(4aS,6aR,6aS,6bR,8aR,10R,12aR,14bR)-10-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-carboxylic acid 7061300 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
[(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a-(hydroxymethyl)-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate 479957 Click to see 484.80 unknown via CMAUP database
[(1S,3R)-2,2-dimethyl-4-methylidene-3-[(3E,7E,11E)-3,8,12,16-tetramethylheptadeca-3,7,11,15-tetraenyl]cyclohexyl] acetate 163011289 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC1C(=C)CCC(C1(C)C)OC(=O)C)C)C)C 468.80 unknown https://doi.org/10.1021/NP980336A
[(1S,5R)-4,6,6-trimethyl-5-[(3E,7E,11E)-3,8,12,16-tetramethylheptadeca-3,7,11,15-tetraenyl]cyclohex-3-en-1-yl] acetate 10672001 Click to see CC1=CCC(C(C1CCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)(C)C)OC(=O)C 468.80 unknown https://doi.org/10.1021/NP980336A
[17-[4-(3,3-dimethyloxiran-2-yl)but-1-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 85209875 Click to see 484.80 unknown https://doi.org/10.1248/CPB.45.2016
[2,2-Dimethyl-4-methylidene-3-(3,8,12,16-tetramethylheptadeca-3,7,11,15-tetraenyl)cyclohexyl] acetate 163011288 Click to see 468.80 unknown https://doi.org/10.1021/NP980336A
[4,6,6-Trimethyl-5-(3,8,12,16-tetramethylheptadeca-3,7,11,15-tetraenyl)cyclohex-3-en-1-yl] acetate 85227131 Click to see 468.80 unknown https://doi.org/10.1021/NP980336A
11-Oxo-beta-amyrin 20055661 Click to see CC1(CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 440.70 unknown via CMAUP database
3-O-p-Coumaroyloleanolic acid 10579517 Click to see 602.80 unknown via CMAUP database
3beta-Acetoxy-11alpha,12alpha-epoxyoleanan-28,13beta-olide 21626351 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2C4C(O4)C56C3(CCC7(C5CC(CC7)(C)C)C(=O)O6)C)C)C 512.70 unknown via CMAUP database
Achilleol A 5471312 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC1C(=C)CCC(C1(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1021/NP980336A
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1248/CPB.45.2016
https://doi.org/10.1021/NP970490H
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Barringtogenol C 435277 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1O)O)CO)O)C)C)(C)C)O)C)C 490.70 unknown https://doi.org/10.1016/S0040-4039(00)90650-6
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/10.1021/NP970490H
https://doi.org/10.1016/S0031-9422(97)01107-2
https://doi.org/10.1248/CPB.45.2016
Beta-Amyrin Acetate 92156 Click to see 468.80 unknown https://doi.org/10.1021/NP980336A
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown via CMAUP database
Camelliagenin A 612548 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1)O)CO)O)C)C)(C)C)O)C)C 474.70 unknown https://doi.org/10.1016/S0040-4039(00)90650-6
Camelliagenin B 10051197 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1)O)CO)O)C)C)(C)C=O)O)C)C 488.70 unknown https://doi.org/10.1016/S0040-4039(00)90650-6
Camelliol C 6476390 Click to see 426.70 unknown https://doi.org/10.1021/NP980336A
Dammaradienol 13893946 Click to see 426.70 unknown https://doi.org/10.1021/NP970490H
delta-Amyrin 12358447 Click to see 426.70 unknown https://doi.org/10.1248/CPB.45.2016
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Germanicol 122857 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.45.2016
Helianol 5273650 Click to see 428.70 unknown https://doi.org/10.1021/NP970490H
Isoeuphol 472762 Click to see CC(CCC=C(C)C)C1=C2CCC3C4(CCC(C(C4CCC3(C2(CC1)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1248/CPB.45.2016
Isohelianol 10455281 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3(C2CCC(=C(C)C)C3CCCO)C)C)C 428.70 unknown https://doi.org/10.1021/NP970490H
Isotirucallol 472763 Click to see CC(CCC=C(C)C)C1=C2CCC3C4(CCC(C(C4CCC3(C2(CC1)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1248/CPB.45.2016
Lanosta-8,24-dien-3-ol 856 Click to see 426.70 unknown https://doi.org/10.1021/NP970490H
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/10.1021/NP970490H
methyl (1S,2R,4aS,6aR,6aS,6bR,8aS,10R,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 40884490 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)OC 470.70 unknown via CMAUP database
Methyl Betulonate 10766700 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)OC 468.70 unknown via CMAUP database
Olean-12-ene-3beta,16alpha,22alpha,23,28-pentol 10051276 Click to see 490.70 unknown https://doi.org/10.1016/S0040-4039(00)90650-6
Protoaescigenin 612009 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1O)O)CO)O)C)C)(C)CO)O)C)C 506.70 unknown https://doi.org/10.1016/S0040-4039(00)90650-6
psi-Taraxasterol 5270605 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC=C1C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1248/CPB.45.2016
Sintaxanthin 131751825 Click to see 430.70 unknown https://doi.org/10.1007/BF00607557
Theasapogenol E 12302288 Click to see 504.70 unknown https://doi.org/10.1016/S0040-4039(00)90650-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 145925700 Click to see 426.70 unknown https://doi.org/10.1248/CPB.45.2016
24-Methylene-9beta,19-cyclo-lanostan-3beta-ol 9547213 Click to see 440.70 unknown https://doi.org/10.1248/CPB.45.2016
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(8aR)-8a-hydroxy-3,3,6,6,8,8-hexamethyl-1,2-benzodioxine-5,7-dione 44281346 Click to see 268.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[4,5-Diacetyloxy-6-[(3,4,5,6-tetraacetyloxyoxan-2-yl)methoxy]oxan-3-yl] acetate 162901733 Click to see 606.50 unknown https://doi.org/10.1080/00021369.1967.10858765
Xyl2Ac3Ac4Ac(b1-6)b-Glc1Ac2Ac3Ac4Ac 102147510 Click to see CC(=O)OC1COC(C(C1OC(=O)C)OC(=O)C)OCC2C(C(C(C(O2)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 606.50 unknown https://doi.org/10.1080/00021369.1967.10858765
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(2-Methoxy-4-prop-2-enylphenoxy)-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxane-3,4,5-triol 12310056 Click to see COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O 458.50 unknown https://doi.org/10.1080/00021369.1967.10858765
Sasanquin 5317538 Click to see COC1=C(C=CC(=C1)CC=C)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O 458.50 unknown https://doi.org/10.1080/00021369.1967.10858765
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
(10R,16R,24R)-12-hydroxy-5,5,7,7,19,19,21,21-octamethyl-13-(3-methylbutanoyl)-10-(2-methylpropyl)-16-propan-2-yl-3,15,17-trioxahexacyclo[12.10.0.02,11.04,9.016,24.018,23]tetracosa-1,4(9),11,13,18(23)-pentaene-6,8,20,22-tetrone 56929125 Click to see 688.80 unknown via CMAUP database
(10S,16R,24R)-12-hydroxy-5,5,7,7,19,19,21,21-octamethyl-13-(3-methylbutanoyl)-10-(2-methylpropyl)-16-propan-2-yl-3,15,17-trioxahexacyclo[12.10.0.02,11.04,9.016,24.018,23]tetracosa-1,4(9),11,13,18(23)-pentaene-6,8,20,22-tetrone 56929124 Click to see 688.80 unknown via CMAUP database
(9R)-6,8-dihydroxy-2,2,4,4-tetramethyl-5-(3-methylbutanoyl)-9-(2-methylpropyl)-9H-xanthene-1,3-dione 102521922 Click to see 442.50 unknown via CMAUP database
(9S)-6,8-dihydroxy-2,2,4,4-tetramethyl-7-(3-methylbutanoyl)-9-(2-methylpropyl)-9H-xanthene-1,3-dione 26202536 Click to see CC(C)CC1C2=C(C=C(C(=C2O)C(=O)CC(C)C)O)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C 442.50 unknown via CMAUP database
Rhodomyrtone 12050020 Click to see 442.50 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
L-Ascorbic Acid 54670067 Click to see 176.12 unknown https://doi.org/10.1007/BF00630333
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Triacontyl p-coumarate 14213589 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O 585.00 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Combretol 12303802 Click to see 388.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[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/10.1248/CPB.38.2681
2,3,8-Tri-O-methylellagic acid 5281860 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)O)C(=O)O2)OC 344.30 unknown via CMAUP database
beta-Pedunculagin 5320441 Click to see 784.50 unknown via CMAUP database
Gemin D 471119 Click to see 634.50 unknown https://doi.org/10.1248/CPB.38.2681

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