PlantaeDB Logo
Login Sign-up

Cirsium japonicum

Cirsium japonicum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Cirsium japonicum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Cirsium japonicum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID643fcc6d0ad16409757744
Scientific name Cirsium japonicum
Authority DC.
First published in Prodr. 6: 640 (1838)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Cirsium ibukiense Nakai Bot. Mag. (Tokyo) 46: 623 (1932)
Cirsium xanthacanthum Nakai Bot. Mag. (Tokyo) 46: 619 (1932)
Cnicus taquetii H.Lév. & Vaniot Repert. Spec. Nov. Regni Veg. 8: 168 (1910)
Cirsium maackii var. horridum (Nakai) Nakai Bot. Mag. (Tokyo) 26: 375 (1912)
Cirsium japonicum f. nakaianum (H.Lév. & Vaniot) W.Lee Lineamenta Florae Koreae 1130. 1996
Cirsium kawakamii Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(Art. 1): 159 (1911)
Cirsium japonicum f. albiflorum Akasawa Bull. Kochi Women's Coll. 25: 5 (1977)
Cnicus cerberus Vaniot Bull. Acad. Int. Géogr. Bot. 12: 120 (1903)
Cirsium kiusianum Nakai Bot. Mag. (Tokyo) 26: 366 (1912)
Cirsium belingshanicum Petr. ex Hand.-Mazz. Anzeiger der Akademie der Wissenschaften in Wien. Mathmematische-naturwissenschaftliche Klasse. Wien 63: 110 1926
Cnicus bodinieri Vaniot Bull. Acad. Int. Géogr. Bot. 12: 121 (1903)
Cirsium maackii var. kiusianum Nakai Bot. Mag. (Tokyo) 46: 624 (1932)
Cirsium taquetii Nakai Bot. Mag. (Tokyo) 26: 373 (1912)
Cirsium japonicum var. fukienense Kitam. Acta Phytotax. Geobot. 1: 149 (1932)
Cirsium lacinulatum Nakai Bot. Mag. (Tokyo) 46: 622 (1932)
Carduus japonicus Franch. Nouv. Arch. Mus. Hist. Nat. , sér. 2, 6: 571 (1883)
Cirsium smithianum Petr. Mitth. Thüring. Bot. Vereins , n.s., 1: 175 (1943)
Cirsium nakaianum (H.Lév. & Vaniot) Nakai Bot. Mag. 26: 378 (1912)
Cirsium bodinieri H.Lév. Repert. Spec. Nov. Regni Veg. 12: 189 (1913)
Alfredia japonica Miq. Ann. Mus. Bot. Lugduno-Batavi 2: 185 (1866)
Cirsium cerberus H.Lév. Repert. Spec. Nov. Regni Veg. 12: 189. 1913
Cirsium japonicum var. horridum Nakai Bot. Mag. (Tokyo) 25: 60 (1911)
Cirsium japonicum var. kiusianum (Nakai) Nemoto Fl. Jap. Suppl.: 761 (1936)
Cnicus japonicus var. intermedius Maxim. Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 9: 325 (1873)
Cirsium japonicum var. intermedium (Maxim.) Matsum. Index Pl. Jap. 2: 640 (1912)
Cirsium maackii var. intermedium (Maxim.) Nakai Bot. Mag. (Tokyo) 26: 376 (1912)
Cirsium maackii var. vulcani (Nakai) Nakai Bot. Mag. (Tokyo) 26: 372 (1912)
Cirsium japonicum var. ibukiense (Nakai) Nakai ex Kitam. Mem. Coll. Sci. Kyoto Imp. Univ., Ser. B, Biol. 13: 66 (1937)
Cirsium japonicum var. vulcani Nakai Bot. Mag. (Tokyo) 25: 60 (1911)
Cirsium japonicum f. fukienense (Kitam.) Kitam. Acta Phytotax. Geobot. 41: 179 (1990)
Cirsium kitagoense Nakai J. Jap. Bot. 25: 134 (1950)
Cnicus japonicus Maxim. Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 , 19(5): 503 (1874)
Cirsium hainanense Masam. Trans. Nat. Hist. Soc. Taiwan 33: 167 (1943)
Cirsium belingschanicum Petr. Anz. Akad. Wiss. Wien, Math.-Naturwiss. Kl. 63: 110 (1926)
Cnicus nakaianus H.Lév. & Vaniot Repert. Spec. Nov. Regni Veg. 8: 168 (1910)
Cirsium senile Nakai Bot. Mag. (Tokyo) 46: 623 (1932)
Cirsium japonicum var. villosum Kadota Fl. Jap. 3b: 135 (1995)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English japanese thistle
Japanese ノアザミ
Korean 개엉겅퀴
szy nipaluma-cicekaay sama
Vietnamese Ô rô cạn
Vietnamese Đại kế
Chinese 南國薊
Chinese 大薊
Chinese 雞角刺
Chinese 薊
Chinese 小薊
Chinese 山萝卜
Chinese 南國小薊
Chinese 刺薊
Chinese 地萝卜
Chinese 蓟（大蓟）
Chinese 罗平蓟
Chinese 白花小薊
Chinese 大蓟虫瘿
Chinese 蓟
Chinese 大蓟

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Cirsium japonicum var. diabolicum (Kitam.) Kadota Fl. Jap. 3b: 134 (1995)
Cirsium japonicum var. maackii (Maxim.) Matsum. Index Pl. Jap. 2(2): 641 (1912)
Cirsium japonicum var. maritimum Konta & Katsuy. Bull. Natl. Sci. Mus. Tokyo, B 31(4): 142 (147-148, 152; fig (2005)
Cirsium japonicum var. vestitum Kitam. Cirs. Nov. Or.-Asiat. 11. 1931

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Cirsium japonicum f. arakii (Kitam.) Kitam. Mem. Coll. Sci. Kyoto Imp. Univ., Ser. B, Biol. 13: 67 (1937)

Germination/Propagation Top

Suggest a correction or add new data!
Maintain seeds at a constant 10°C.

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
      • Inner Mongolia
      • Qinghai
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000062624
UNII WCA3C9S0OM
USDA Plants CIJA2
Tropicos 50001700
KEW urn:lsid:ipni.org:names:195527-1
The Plant List gcc-19621
Open Tree Of Life 365894
NCBI Taxonomy 516546
IPNI 195527-1
iNaturalist 354344
GBIF 3112887
Freebase /m/0v4gw1v
EPPO CIRJA
USDA GRIN 419814
CMAUP NPO20096

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
Cirsimaritin Alleviates Dextran Sodium Sulfate-Induced Acute Colitis in Experimental Animals: A Therapeutic Approach for Inflammatory Bowel Disease Alqudah A, Qnais E, Gammoh O, Bseiso Y, Wedyan M, Alqudah M, Hatahet T Prev Nutr Food Sci 31-Mar-2024
PMCID:PMC10987388
doi:10.3746/pnf.2024.29.1.31
PMID:38576881
Essential oil composition, morphological characterization, phenolic content and antioxidant activity of Iranian populations of Hymenocrater longiflorus Benth. (Lamiaceae) Fattahpour B, Fattahi M, Hassani A Sci Rep 27-Mar-2024
PMCID:PMC10973450
doi:10.1038/s41598-024-57826-0
PMID:38538705
Uncovering the Role of Hydroxycinnamoyl Transferase in Boosting Chlorogenic Acid Accumulation in Carthamus tinctorius Cells under Methyl Jasmonate Elicitation Liu Z, Zhu X, Mohsin A, Sun H, Du L, Yin Z, Zhuang Y, Guo M Int J Mol Sci 27-Feb-2024
PMCID:PMC10931740
doi:10.3390/ijms25052710
PMID:38473957
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Temperature‐sensitive hydrogel releasing pectolinarin facilitate scarless wound healing Chen X, Song H, Song K, Zhang Y, Wang J, Hong J, Xie Q, Zhao J, Liu M, Wang X J Cell Mol Med 08-Feb-2024
PMCID:PMC10853586
doi:10.1111/jcmm.18130
PMID:38332511
Moringa oleifera (drumstick tree)—nutraceutical, cosmetological and medicinal importance: a review Klimek-Szczykutowicz M, Gaweł-Bęben K, Rutka A, Blicharska E, Tatarczak-Michalewska M, Kulik-Siarek K, Kukula-Koch W, Malinowska MA, Szopa A Front Pharmacol 02-Feb-2024
PMCID:PMC10869624
doi:10.3389/fphar.2024.1288382
PMID:38370483
Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C J Ethnobiol Ethnomed 15-Jan-2024
PMCID:PMC10790445
doi:10.1186/s13002-023-00638-9
PMID:38225656
Potential Antioxidant and Anti-Inflammatory Properties of Polyphenolic Compounds from Cirsium japonicum Extract Kim HH, Jeong SH, Park MY, Bhosale PB, Abusaliya A, Kim HW, Seong JK, Kim DI, Lee SJ, Park KI, Kim GS Int J Mol Sci 08-Jan-2024
PMCID:PMC10815310
doi:10.3390/ijms25020785
PMID:38255858
Analysis of Genes Associated with Feeding Preference and Detoxification in Various Developmental Stages of Aglais urticae Xi O, Guo W, Hu H Insects 03-Jan-2024
PMCID:PMC10816842
doi:10.3390/insects15010030
PMID:38249036
The mechanism of Shenbing Decoction II against IgA nephropathy renal fibrosis revealed by UPLC-MS/MS, network pharmacology and experimental verification Liu H, Chen W, Tian C, Deng Y, Xu L, Ouyang W, Qiu R, You Y, Jiang P, Zhou L, Cheng J, Kwan HY, Zhao X, Sun X Heliyon 03-Nov-2023
PMCID:PMC10654229
doi:10.1016/j.heliyon.2023.e21997
PMID:38027651
Complete Chloroplast Genomes of Saussurea katochaete, Saussurea superba, and Saussurea stella: Genome Structures and Comparative and Phylogenetic Analyses He H, Wang T, Tang C, Cao Z, Pu X, Li Y, Li X Genes (Basel) 26-Oct-2023
PMCID:PMC10670953
doi:10.3390/genes14112002
PMID:38002945
Effects of natural products on polycystic ovary syndrome: From traditional medicine to modern drug discovery Jung W, Choi H, Kim J, Kim J, Kim W, Nurkolis F, Kim B Heliyon 11-Oct-2023
PMCID:PMC10589870
doi:10.1016/j.heliyon.2023.e20889
PMID:37867816
Mid-to-late Holocene climate variability in coastal East Asia and its impact on ancient Korean societies Park J, Bahk J, Park J, Kim H, Choi J Sci Rep 16-Sep-2023
PMCID:PMC10505234
doi:10.1038/s41598-023-42551-x
PMID:37717094
Targeting SARS-CoV-2 Non-Structural Proteins Tam D, Lorenzo-Leal AC, Hernández LR, Bach H Int J Mol Sci 20-Aug-2023
PMCID:PMC10455537
doi:10.3390/ijms241613002
PMID:37629182
Protective Effects and Mechanisms of Pectolinarin against H2O2-Induced Oxidative Stress in SH-SY5Y Neuronal Cells Pang QQ, Kim JH, Kim HY, Kim JH, Cho EJ Molecules 02-Aug-2023
PMCID:PMC10420989
doi:10.3390/molecules28155826
PMID:37570795

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives
3-[Hydroxy(phenyl)methyl]-4-[(3-methylimidazol-4-yl)methyl]oxolan-2-one 114553 Click to see CN1C=NC=C1CC2COC(=O)C2C(C3=CC=CC=C3)O 286.33 unknown https://doi.org/10.1007/S10600-011-9904-6
Pilosine 442869 Click to see CN1C=NC=C1CC2COC(=O)C2C(C3=CC=CC=C3)O 286.33 unknown https://doi.org/10.1007/S10600-011-9904-6
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
6-O-(3,4,5-Trihydroxybenzoyl)-alpha-D-glucopyranose 11968480 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)O 332.26 unknown via CMAUP database
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Hydroquinones
N-(2,5-Dihydroxyphenyl)pyridinium(1+) 411955 Click to see C1=CC=[N+](C=C1)C2=C(C=CC(=C2)O)O 188.20 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
1-Tridecene-3,5,7,9,11-pentayne 441552 Click to see CC#CC#CC#CC#CC#CC=C 162.19 unknown https://doi.org/10.1271/BBB1961.44.903
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkadienes
8-Heptadecenylene 529542 Click to see CCCCCCCCC=CCCCCCC=C 236.40 unknown https://doi.org/10.1016/S0031-9422(00)86798-9
Tetrahydroaplotaxene 11413696 Click to see CCCCCCCCC=CCCCCCC=C 236.40 unknown https://doi.org/10.1016/S0031-9422(00)86798-9
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Acyclic olefins / Alkatrienes
(Z,Z)-Heptadeca-1,8,11-triene 5352709 Click to see CCCCCC=CCC=CCCCCCC=C 234.40 unknown https://doi.org/10.1016/S0031-9422(00)86798-9
Heptadeca-1,8,11-triene 92017 Click to see CCCCCC=CCC=CCCCCCC=C 234.40 unknown https://doi.org/10.1016/S0031-9422(00)86798-9
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Heptadecene 23217 Click to see CCCCCCCCCCCCCCCC=C 238.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Sesamin 382073 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Coniferyl 9-O-(6-O-beta-D-apiofuranosyl-beta-D-glucopyranoside) 11408873 Click to see COC1=C(C=CC(=C1)C=CCOC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O)O 474.50 unknown via CMAUP database
Sinapyl 9-O-(6-O-beta-D-apiofuranosyl-beta-D-glucopyranoside) 11386564 Click to see COC1=CC(=CC(=C1O)OC)C=CCOC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 504.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
(10-Acetyloxy-9-hydroxyheptadec-1-en-11,13-diyn-8-yl) acetate 14863183 Click to see CCCC#CC#CC(C(C(CCCCCC=C)OC(=O)C)O)OC(=O)C 362.50 unknown https://doi.org/10.1016/0031-9422(91)83640-7
(9-Acetyloxy-10-hydroxyheptadec-1-en-11,13-diyn-8-yl) acetate 14863181 Click to see CCCC#CC#CC(C(C(CCCCCC=C)OC(=O)C)OC(=O)C)O 362.50 unknown https://doi.org/10.1016/0031-9422(91)83640-7
[(8S,9R,10S)-10-acetyloxy-9-hydroxyheptadec-1-en-11,13-diyn-8-yl] acetate 14863184 Click to see CCCC#CC#CC(C(C(CCCCCC=C)OC(=O)C)O)OC(=O)C 362.50 unknown https://doi.org/10.1016/0031-9422(91)83640-7
[(8S,9R,10S)-9-acetyloxy-10-hydroxyheptadec-1-en-11,13-diyn-8-yl] acetate 162877578 Click to see CCCC#CC#CC(C(C(CCCCCC=C)OC(=O)C)OC(=O)C)O 362.50 unknown https://doi.org/10.1016/0031-9422(91)83640-7
[(8S,9S,10R)-9,10-dihydroxyheptadec-1-en-11,13-diyn-8-yl] acetate 163057510 Click to see CCCC#CC#CC(C(C(CCCCCC=C)OC(=O)C)O)O 320.40 unknown https://doi.org/10.1016/0031-9422(90)85345-G
Ciryneol A 15730329 Click to see CCCC#CC#CC(C(C(CCCCCC=C)OC(=O)C)O)O 320.40 unknown https://doi.org/10.1016/0031-9422(90)85345-G
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(1R)-1-[(2S,3R)-3-hept-6-enyloxiran-2-yl]octa-2,4-diyn-1-ol 162866456 Click to see CCCC#CC#CC(C1C(O1)CCCCCC=C)O 260.40 unknown https://doi.org/10.1016/S0031-9422(00)83837-6
https://doi.org/10.1271/BBB1961.44.903
(8R,9R,10R)-heptadec-1-en-11,13-diyne-8,9,10-triol 162905802 Click to see CCCC#CC#CC(C(C(CCCCCC=C)O)O)O 278.40 unknown https://doi.org/10.1016/0031-9422(90)85345-G
(8R,9S,10S)-10-methoxyheptadec-16-en-4,6-diyne-8,9-diol 163054613 Click to see CCCC#CC#CC(C(C(CCCCCC=C)OC)O)O 292.40 unknown https://doi.org/10.1016/0031-9422(90)85345-G
10-Methoxyheptadec-16-en-4,6-diyne-8,9-diol 15730330 Click to see CCCC#CC#CC(C(C(CCCCCC=C)OC)O)O 292.40 unknown https://doi.org/10.1016/0031-9422(90)85345-G
Dotriacontanol 96117 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 466.90 unknown https://doi.org/10.1055/S-0036-1596440
Heptadec-1-en-11,13-diyne-8,9,10-triol 10423696 Click to see CCCC#CC#CC(C(C(CCCCCC=C)O)O)O 278.40 unknown https://doi.org/10.1016/0031-9422(90)85345-G
Oxiranemethanol, alpha-1,3-heptadiynyl-3-(6-heptenyl)- 156010 Click to see CCCC#CC#CC(C1C(O1)CCCCCC=C)O 260.40 unknown https://doi.org/10.1016/S0031-9422(00)83837-6
https://doi.org/10.1271/BBB1961.44.903
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Punicic Acid 5281126 Click to see CCCCC=CC=CC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Borneol 6552009 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 51531959 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O 488.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,10S,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 7048528 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
[(3S,4aR,6aR,6bR,8aR,12R,12aS,14aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-yl] acetate 10742933 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown via CMAUP database
24-Hydroxyursolic acid 44568920 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
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 via CMAUP database
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 via CMAUP database
beta-Sitosterol acetate 5354503 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C 456.70 unknown via CMAUP database
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
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
CID 3003153 3003153 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C46CCC(C5(C)C)(OC6)O)C)C2C1)C)C(=O)O)C 470.70 unknown via CMAUP database
Epifriedelin 15559350 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
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
Lupeol 259846 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
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Oleanolic Acid 10494 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
psi-Taraxasteryl acetate 13970053 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC=C1C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown via CMAUP database
Punicanolic acid 25132490 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1(C)O)C(=O)O)C)C)(C)C)O)C 474.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
(8S,9S,13S,14R)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one 670995 Click to see CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O 270.40 unknown via CMAUP database
Estrone 5870 Click to see CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O 270.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone 8955 Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 316.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 6432744 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
(3R,8R,9R,10S,13R,14R,17R)-17-[(E,2R,5R)-5-ethyl-6-methylhept-3-en-2-yl]-3,10,13-trimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene 50930798 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)C)C)C)C(C)C 410.70 unknown via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-0036-1596440
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1055/S-0036-1596440
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-Phenylethyl D-rutinoside 11166301 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=CC=C3)O)O)O)O)O)O 430.40 unknown via CMAUP database
Icariside D1 13893575 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=CC=C3)O)O)O)O)(CO)O 416.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(Z)-Syringin 9799599 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol 11850 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown via CMAUP database
Glycerin 753 Click to see C(C(CO)O)O 92.09 unknown via CMAUP database
Mannitol 6251 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown via CMAUP database
> Organohalogen compounds / Halohydrins / Chlorohydrins
(8R,9S,10R)-10-chloroheptadec-16-en-4,6-diyne-8,9-diol 162982361 Click to see CCCC#CC#CC(C(C(CCCCCC=C)Cl)O)O 296.80 unknown https://doi.org/10.1016/0031-9422(90)85345-G
Ciryneol C 15730331 Click to see CCCC#CC#CC(C(C(CCCCCC=C)Cl)O)O 296.80 unknown https://doi.org/10.1016/0031-9422(90)85345-G
> Organoheterocyclic compounds / Piperidines
1-[(2R)-piperidin-2-yl]propan-2-one 3034881 Click to see CC(=O)CC1CCCCN1 141.21 unknown via CMAUP database
1-[(2S)-1-methylpiperidin-2-yl]propan-2-one 820378 Click to see CC(=O)CC1CCCCN1C 155.24 unknown via CMAUP database
N-Methylpelletierine 1548928 Click to see CC(=O)CC1CCCCN1C 155.24 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines / Piperidinones
Granatonine 6602484 Click to see CN1C2CCCC1CC(=O)C2 153.22 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
2-(1-Propenyl)-3,4,5,6-tetrahydropyridine 15937508 Click to see CC=CC1=NCCCC1 123.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Ethyl caffeate 5317238 Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O 208.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
cis-p-Coumaric acid 1549106 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Isofraxidin 5318565 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)O 222.19 unknown via CMAUP database
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.3746/JFN.2003.8.4.330
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.3746/JFN.2003.8.4.330
Tricetin 5281701 Click to see C1=C(C=C(C(=C1O)O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1007/S10600-011-9904-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
Delphinidin 3,5-diglucoside 10100906 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 627.50 unknown via CMAUP database
Pelargonin 441772 Click to see C1=CC(=CC=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 595.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Apigenin-4'-glucoside 5491384 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 432.40 unknown via CMAUP database
Cirsimarin 159460 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)OC 476.40 unknown https://doi.org/10.1016/S0031-9422(00)80123-5
Luteolin 3'-glucoside 12309350 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Luteolin 3'-xylopyranoside 101675298 Click to see C1C(C(C(C(O1)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)O 418.30 unknown via CMAUP database
Luteolin-4'-o-glucoside 5319116 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown via CMAUP database
Luteolin-5-O-b-D-glucopyranoside 15559460 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-(4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 5480901 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O 592.50 unknown https://doi.org/10.1007/S10600-011-9904-6
5-hydroxy-6-methoxy-2-(4-methoxyphenyl)-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 134728117 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)OC)O)O)O)O)O)O 622.60 unknown https://doi.org/10.1248/CPB.35.861
5-hydroxy-6-methoxy-2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 163024879 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)OC)O)O)O)O)O)O 622.60 unknown https://doi.org/10.1248/CPB.35.861
5-hydroxy-6-methoxy-2-(4-methoxyphenyl)-7-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 90470831 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)OC)O)O)O)O)O)O 622.60 unknown via CMAUP database
5-hydroxy-6-methoxy-2-(4-methoxyphenyl)-7-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-2-oxanyl]oxymethyl]-2-oxanyl]oxy]-1-benzopyran-4-one 6708644 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)OC)O)O)O)O)O)O 622.60 unknown via CMAUP database
5-Hydroxy-6-methoxy-2-(4-methoxyphenyl)-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 3818047 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)OC)O)O)O)O)O)O 622.60 unknown https://doi.org/10.1016/J.INTIMP.2006.02.002
https://doi.org/10.1080/14786410701494686
https://doi.org/10.1007/S10600-011-9904-6
https://doi.org/10.1248/CPB.35.861
7-[(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]oxy-5-hydroxy-2-(4-hydroxyphenyl)-6-methoxychromen-4-one 101926086 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)OC)CO)O)O)O)O)O 608.50 unknown https://doi.org/10.1016/0031-9422(94)00897-3
Hispidulin 7-neohesperidoside 44258449 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)OC)CO)O)O)O)O)O 608.50 unknown via CMAUP database
Hispidulin 7-O-neohesperidoside 102004832 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)O)O)OC)O)O)O)O)O)O 608.50 unknown https://doi.org/10.1002/PTR.1299
Linarin 5317025 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O 592.50 unknown https://doi.org/10.1007/S10600-011-9904-6
https://doi.org/10.1016/0031-9422(94)00897-3
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
Pectolinaroside 168849 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(C(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)OC)O)O)O)O)O)O 622.60 unknown https://doi.org/10.1016/J.INTIMP.2006.02.002
https://doi.org/10.1080/14786410701494686
https://doi.org/10.1007/S10600-011-9904-6
https://doi.org/10.1248/CPB.35.861
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
3,3',4',5,5',7-Hexahydroxyflavylium 128853 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O 303.24 unknown via CMAUP database
Cyanidin 128861 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O)O 287.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown https://doi.org/10.1007/S10600-011-9904-6
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1007/S10600-011-9904-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.3746/JFN.2003.8.4.330
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown https://doi.org/10.1016/J.INTIMP.2006.02.002
https://doi.org/10.1080/14786410701494686
https://doi.org/10.1007/S10600-011-9904-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1016/S0031-9422(00)80123-5
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
(1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylic acid 102004656 Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)O 292.20 unknown via CMAUP database
Brevifolin[Geranium] 10131135 Click to see C1CC(=O)C2=C1C3=C(C(=C(C=C3C(=O)O2)O)O)O 248.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,2,3-Tri-O-galloyl-beta-D-glucose 5322038 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)CO)O 636.50 unknown via CMAUP database
1,2,4-tri-O-galloyl-beta-glucopyranose 88204715 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(OC(C(C2O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)CO 636.50 unknown via CMAUP database
1,2,4,6-Tetragalloylglucose 11297287 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 788.60 unknown via CMAUP database
1,2,6-Trigalloylglucose 440308 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 636.50 unknown via CMAUP database
1,3,4-tri-O-galloyl-beta-glucopyranose 16066749 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(OC(C(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)CO 636.50 unknown via CMAUP database
1,4,6-tri-O-galloyl-beta-D-glucose 10077822 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 636.50 unknown via CMAUP database
Pentagalloylglucose 65238 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(10R,11R)-10-[(14S,15R,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,11,17,18,19,22,23,34,35-undecahydroxy-9,13,25,32-tetraoxaheptacyclo[25.8.0.02,7.015,20.021,30.024,29.028,33]pentatriaconta-1(35),2,4,6,15,17,19,21,23,27,29,33-dodecaene-8,14,26,31-tetrone 44567110 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C4C5=C3C(=O)OC6=C(C(=C(C7=C(C(=C(C=C7C(=O)O1)O)O)O)C(=C56)C(=O)O4)O)O)O)O)O)O)O)C8C9C(C1=C(C(=C(C(=C1C(=O)O9)C1=C(C(=C(C=C1C(=O)O8)O)O)O)O)O)O)O)O 1084.70 unknown via CMAUP database
(1R,35R,37R,38R,55S)-6,7,8,11,12,23,24,27,28,29,37,43,44,45,48,49,50-heptadecahydroxy-2,14,21,33,36,39,54-heptaoxaundecacyclo[33.20.0.04,9.010,19.013,18.016,25.017,22.026,31.038,55.041,46.047,52]pentapentaconta-4,6,8,10,12,16,18,22,24,26,28,30,41,43,45,47,49,51-octadecaene-3,15,20,32,40,53-hexone 16148440 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(=C8C9=C7C(=O)OC2=C(C(=C(C3=C(C(=C(C=C3C(=O)O1)O)O)O)C(=C92)C(=O)O8)O)O)O)O)O)O)O 1084.70 unknown via CMAUP database
[(10R,11S)-10-[(14R,15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 17999934 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)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown via CMAUP database
[(1R,19R,21S,22R,23R)-6,7,8,11,12,13,22-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl] 3,4,5-trihydroxybenzoate 14411426 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 786.60 unknown via CMAUP database
1-Desgalloyleugeniin 9918701 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown via CMAUP database
2-Hydroxy-3-methoxy-7,8-methylenedioxy-4,9-dioxapyrene-5,10-dione 10336592 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC5=C(C(=C43)OC2=O)OCO5)O 328.23 unknown via CMAUP database
2-O,3-O-[4,4',5,5',6,6'-Hexahydroxy-1,1'-biphenyl-2,2'-diylbis(carbonyl)]-beta-D-glucopyranose 11754973 Click to see C1=C2C(=C(C(=C1O)O)O)C3=C(C(=C(C=C3C(=O)OC4C(C(C(OC4O)CO)O)OC2=O)O)O)O 482.30 unknown via CMAUP database
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
3-O-methylellagic acid 13915428 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O)O 316.22 unknown via CMAUP database
3-O-Methylellagic acid 4-O-rhamnoside 16720461 Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)OC)O)O)O 462.40 unknown via CMAUP database
3,3'-Di-O-methylellagic acid 5488919 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)OC)O)O 330.24 unknown via CMAUP database
3,4,4'-Tri-O-methylellagic acid 11674590 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)OC)C(=O)O2)O 344.30 unknown via CMAUP database
3,4,8,9,10-Pentahydroxybenzo[c]chromen-6-one 18504424 Click to see C1=CC(=C(C2=C1C3=C(C(=C(C=C3C(=O)O2)O)O)O)O)O 276.20 unknown via CMAUP database
4,4'-Di-O-methylellagic acid 11580745 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4O)OC)C(=O)O2)O 330.24 unknown via CMAUP database
5-Desgalloylstachyurin 10417809 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 via CMAUP database
8-O-[(1R,19R,21R,22R,23R)-6,7,8,11,12,13,22-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl] 1-O-methyl (1R,3aR,8bR)-5,6-dihydroxy-3a-(2-methoxy-2-oxoethyl)-3-oxo-1,8b-dihydrofuro[3,4-b][1]benzofuran-1,8-dicarboxylate 71475292 Click to see COC(=O)CC12C(C(OC1=O)C(=O)OC)C3=C(O2)C(=C(C=C3C(=O)OC4C5COC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)OC4C(C(O5)OC(=O)C8=CC(=C(C(=C8)O)O)O)O)O)O)O)O)O)O)O)O 998.70 unknown via CMAUP database
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 via CMAUP database
CID 5464368 5464368 Click to see C1C2C(C(C(C(O2)O)O)O)OC(=O)C3=CC(=C(C(=C3C4=C(C(=C5C6=C4C(=O)OC7=C(C(=C(C8=C(C(=C(C=C8C(=O)O1)O)O)O)C(=C67)C(=O)O5)O)O)O)O)O)O)O 782.50 unknown via CMAUP database
Corilagin 73568 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O 634.50 unknown via CMAUP database
Diellagic acid 4-rhamnosylglucopyranoside 11968423 Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)O)O)O)OC6C(C(C(C(O6)COC7=C(C8=C9C(=C7)C(=O)OC1=C9C(=CC(=C1O)O)C(=O)O8)O)O)O)O 894.60 unknown via CMAUP database
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown via CMAUP database
Eschweilenol C 10026656 Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)O)O)O)O 448.30 unknown via CMAUP database
Flavogallonic acid 14503023 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=C3C(=C(C(=C4C5=C(C(=C(C=C5C(=O)O)O)O)O)O)O)OC2=O 470.30 unknown via CMAUP database
Gallagic acid 14754405 Click to see C1=C(C(=C(C(=C1O)O)O)C2=C(C(=C3C4=C2C(=O)OC5=C(C(=C(C(=C45)C(=O)O3)C6=C(C(=C(C=C6C(=O)O)O)O)O)O)O)O)O)C(=O)O 638.40 unknown via CMAUP database
Punicafolin 5320800 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 938.70 unknown via CMAUP database
Punigluconin 21637585 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 802.60 unknown via CMAUP database
Strictinin 73330 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)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 via CMAUP database
Terminalin 5281711 Click to see C1=C2C(=C(C(=C1O)O)O)C3=C4C5=C(C(=C3OC2=O)O)OC(=O)C6=C7C8=C(C(=C(C=C8C(=O)OC7=C(C(=C65)OC4=O)O)O)O)O 602.40 unknown via CMAUP database

Biological Material Top ebay Auctions

Please wait .. loading items ..

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.