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Camellia sasanqua

Camellia sasanqua - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

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).

Description Top

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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)

Common names Top

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Language Common/alternative name
English sasanqua camellia
Spanish sasanqua oleifera
Arabic كاميليا ساسانكوا
Azerbaijani sasankva kameliyası
Azerbaijani evgenol kameliyası
Czech kamélie tupolistá
Czech kamélie sazanka
German herbstblühende kamelie
Persian کاملیا
Japanese さざんか
Japanese 山茶花
Japanese サザンカ
Japanese カンツバキ
Malayalam കാമിലിയ സസാൻക്വാ
Polish kamelia sazanka
Polish kamelijka
Polish kamelia mała
Russian камелия эвгенольная
Russian камелия сасанква
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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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

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

Links to other databases Top

Suggest others/fix!
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 CC1=CC2=C(C(=C1)O)C(=O)C3=CC(=C(C(=C3C2=O)O)C4=C(C=C5C(=C4O)C(=O)C6=C(C5=O)C(=CC(=C6)C)O)O)O 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 COC1=C(C=CC(=C1)CC=C)O 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 COC1=C(C=CC(=C1)CC(COC(=O)C=CC2=CC(=C(C=C2)O)OC)C(CC3=CC(=C(C=C3)O)OC)COC(=O)C=CC4=CC(=C(C=C4)O)OC)O 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 CC1=C(C2CC(CCC2(CC1)C)(C)C)CCC=C(C)CCC(=C(C)C)C(C)CCCO 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 CC1=C(C2CC(CCC2(CC1)C)(C)C)CCC=C(C)CCC(=C(C)C)C(C)CCCOC(=O)C 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 CC1=C(C2CC(CCC2(CC1)C)(C)C)CCC=C(C)CCC(=C(C)C)C(C)CCCOC(=O)C 470.80 unknown https://doi.org/10.1021/NP980336A
Camelliol B 6476389 Click to see CC1=C(C2CC(CCC2(CC1)C)(C)C)CCC=C(C)CCC(=C(C)C)C(C)CCCO 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 CC(=CCCC1(CCC2(C3CCC(=C(C)C)C(C3(CCC2(C1)C)C)CCCO)C)C)C 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
(21R)-Hopa-22(29)-ene-3beta,30-diol 102032092 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CCC4C3(CCC5C4(CCC5C(=C)CO)C)C)C)C 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 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
[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 CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 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 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
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 CC1=CC(CC(C1C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC23C(CC(CC2(O3)C)O)(C)C)C)C)(C)C)O 584.90 unknown https://doi.org/10.1007/BF00607557
Violaxanthin 448438 Click to see CC(=CC=CC=C(C)C=CC=C(C)C=CC12C(CC(CC1(O2)C)O)(C)C)C=CC=C(C)C=CC34C(CC(CC3(O4)C)O)(C)C 600.90 unknown https://doi.org/10.1007/BF00607557
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(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
(3I(2),4I+/-,16I+/-,22I+/-)-Olean-12-ene-3,16,22,23,28-pentol 10051276 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1)O)CO)O)C)C)(C)CO)O)C)C 490.70 unknown https://doi.org/10.1016/S0040-4039(00)90650-6
(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 CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 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 CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1O)O)CO)O)C)C)(C)C=O)O)C)C 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 CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 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 CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 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 CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC=C1C)C)C)C)(C)C)O)C 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 CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)CO 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 CC(=O)OC1CCC2(C3CCC4C(CCC4(C3(CCC2C1(C)C)C)C)C(=C)CCC5C(O5)(C)C)C 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 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
[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 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
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 CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C)C)C2C1)C)C(=O)O)C 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 CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 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 CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 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 CC1=CCC(C(C1CCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)(C)C)O 426.70 unknown https://doi.org/10.1021/NP980336A
Dammaradienol 13893946 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1021/NP970490H
delta-Amyrin 12358447 Click to see CC1(CCC2(CCC3(C(=C2C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.45.2016
Euphol 441678 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
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 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 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
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 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
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
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 CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=O)C)C)C 430.70 unknown https://doi.org/10.1007/BF00607557
Theasapogenol E 12302288 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CC(C2(C(C1O)O)CO)O)C)C)(C)C=O)O)C)C 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 CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 426.70 unknown https://doi.org/10.1248/CPB.45.2016
CID 9547213 9547213 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 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 CC1(C=C2C(=O)C(C(=O)C(C2(OO1)O)(C)C)(C)C)C 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 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
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 CC(C)CC1C2=C(C(=C3C(=C2OC4=C1C(=O)C(C(=O)C4(C)C)(C)C)C5C6=C(C(C(=O)C(C6=O)(C)C)(C)C)OC5(O3)C(C)C)C(=O)CC(C)C)O 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 CC(C)CC1C2=C(C(=C(C=C2O)O)C(=O)CC(C)C)OC3=C1C(=O)C(C(=O)C3(C)C)(C)C 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 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
Tomentosone A 56929124 Click to see CC(C)CC1C2=C(C(=C3C(=C2OC4=C1C(=O)C(C(=O)C4(C)C)(C)C)C5C6=C(C(C(=O)C(C6=O)(C)C)(C)C)OC5(O3)C(C)C)C(=O)CC(C)C)O 688.80 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
Ascorbic Acid 54670067 Click to see C(C(C1C(=C(C(=O)O1)O)O)O)O 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 COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)OC)OC)OC)O 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 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 via CMAUP database
Gemin D 471119 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)C(C(C=O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O 634.50 unknown https://doi.org/10.1248/CPB.38.2681

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