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Hypericum ascyron

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644021470ddfa552991266
Scientific name Hypericum ascyron
Authority L.
First published in Sp. Pl. 2: 783. 1753 [1 May 1753]

Ethnobotanical Use Top

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General Uses Top

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Scientific and model-organism uses:
• Hypericum ascyron is listed in major plant genome and sequencing resources, including the National Center for Biotechnology Information (NCBI) Taxonomy Browser and the CoL (Catalogue of Life), indicating availability for genomic and transcriptomic studies (e.g., for phylogenetic and secondary-metabolite research). Such listings enable use as a research organism in genetics, molecular biology, and natural-products investigations.

Synonyms Top

Scientific name Authority First published in
Roscyna gmelinii Spach Ann. Sci. Nat., Bot. , sér. 2, 5: 364 (1836)
Ascyrum sibiricum Poir. Tabl. Encycl. 3: 200 (1823)
Ascyrum tetragonum Moench Methodus : 130 (1794)
Hypericum baldaccii R.Keller ex Bald. Malpighia 9: 68 (1895)
Hypericum yabei H.Lév. & Vaniot Repert. Spec. Nov. Regni Veg. 5: 279. 1908
Hypericum ascyron var. giraldii R.Keller Bot. Jahrb. Syst. 33: 550. 1904
Hypericum ascyron var. hupehense Pamp. Nuovo Giorn. Bot. Ital. n.s., 17: 669. 1910
Hypericum ascyron var. longistylum Maxim. Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 65. 1859
Hypericum ascyron var. micropetalum R.Keller Bull. Herb. Boissier 5: 638. 1897
Hypericum ascyron var. umbellatum R.Keller Bot. Jahrb. Syst. 33: 550. 1904
Hypericum ascyron var. macrosepalum Ledeb. Fl. Altaic. 3: 364. 1831
Hypericum ascyron var. vilmorinii Rehder Mitt. Deutsch. Dendrol. Ges. 24: 235. 1916
Hypericum ascyron var. adamii R.Keller Bot. Jahrb. Syst. 58: 191. 1923
Hypericum ascyron f. vilmorinii (Rehder) Rehder Bibl. Cult. Trees 462 1949
Hypericum ascyron f. angustifolium Y.Kimura Nov. Fl. Jap. 10: 125 1951
Hypericum ascyron var. genuinum Maxim. Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 65 (1859)

Common names Top

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Language Common/alternative name
English great st. johnswort
Azerbaijani İri dazı
Bulgarian голяма звъника
Japanese トモエソウ
Korean 물레나물
Russian Зверобой большой
Ukrainian Звіробій великий
Chinese 六安茶
Chinese 金丝蝴蝶
Chinese 禁宫花
Chinese 牛心菜
Chinese 湖南连翘
Chinese 救牛草
Chinese 大金雀
Chinese 大叶牛心菜
Chinese 降龙草
Chinese 黄海棠（湖南连翘、红旱莲）
Chinese 黄海棠
Chinese 黃海棠
Chinese 红旱莲
Chinese 湖南連翹
Chinese 水黄花
Chinese 连翘
Chinese 連翹
Chinese 八宝茶
Chinese 对月草
Chinese 山辣椒
Chinese 大叶金丝桃
Chinese 鸡蛋花

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Hypericum ascyron subsp. ascyron
Hypericum ascyron subsp. gebleri (Ledeb.) N.Robson Bull. Nat. Hist. Mus. (London), Bot. 31: 57 (2001)
Hypericum ascyron subsp. pyramidatum (Aiton) N.Robson Bull. Nat. Hist. Mus. (London), Bot. 31: 58 (2001)

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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Begin at 20°C for 6 weeks, cool to 4°C for 6 weeks, then gradually increase to 10°C over 6 weeks. If no germination, the cycle is repeated.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

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-0000727365
Canadensys 6151
USDA Plants HYAS80
Tropicos 7800027
KEW urn:lsid:ipni.org:names:30453546-2
The Plant List kew-2857746
Open Tree Of Life 215651
NCBI Taxonomy 210378
Nature Serve 2.138496
IPNI 433206-1
iNaturalist 163955
GBIF 3189479
Freebase /m/0nbcrvx
WisFlora 13088
EPPO HYPAS
EOL 487116
USDA GRIN 19559
Wikipedia Hypericum_ascyron
CMAUP NPO14089
Plantarium 20468

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
Potential Implications of Hyperoside on Oxidative Stress-Induced Human Diseases: A Comprehensive Review Wang K, Zhang H, Yuan L, Li X, Cai Y J Inflamm Res 13-Oct-2023
PMCID:PMC10581022
doi:10.2147/JIR.S418222
PMID:37854313
Endophytic fungus Biscogniauxia petrensis produces antibacterial substances Han L, Zheng W, He Z, Qian S, Ma X, Kang J PeerJ 07-Jun-2023
PMCID:PMC10257390
doi:10.7717/peerj.15461
PMID:37304871
The complete chloroplast genome of Calophyllum soulattri Burm. f. (Calophyllaceae) Pahayo DG, Cadorna CA, Quimado MO, Rey JD Mitochondrial DNA B Resour 25-May-2023
PMCID:PMC10215020
doi:10.1080/23802359.2023.2215350
PMID:37250208
Recent advances in the discovery, biosynthesis, and therapeutic potential of isocoumarins derived from fungi: a comprehensive update Tammam MA, Gamal El-Din MI, Abood A, El-Demerdash A RSC Adv 10-Mar-2023
PMCID:PMC9999372
doi:10.1039/d2ra08245d
PMID:36909763
Carascynol A, a hybrid of caryophyllane-type terpenoid and a C6 unit degraded by polyprenylated acylphloroglucinols from Hypericum ascyron Hu YL, Li XR, Xu G Nat Prod Bioprospect 07-Nov-2022
PMCID:PMC9640506
doi:10.1007/s13659-022-00362-z
PMID:36342546
Exploring the potential of endophytes and their metabolites for bio-control activity Sharma A, Kaushik N, Sharma A, Marzouk T, Djébali N 3 Biotech 13-Sep-2022
PMCID:PMC9470801
doi:10.1007/s13205-022-03321-0
PMID:36275362
Prospects of ultrasonically extracted food bioactives in the field of non-invasive biomedical applications – A review Mounika A, Ilangovan B, Mandal S, Shraddha Yashwant W, Priya Gali S, Shanmugam A Ultrason Sonochem 12-Aug-2022
PMCID:PMC9403563
doi:10.1016/j.ultsonch.2022.106121
PMID:35987106
Gene loss, genome rearrangement, and accelerated substitution rates in plastid genome of Hypericum ascyron (Hypericaceae) Claude SJ, Park S, Park S BMC Plant Biol 23-Mar-2022
PMCID:PMC8941745
doi:10.1186/s12870-022-03515-x
PMID:35321651
Endophytic Fungal Terpenoids: Natural Role and Bioactivities Galindo-Solís JM, Fernández FJ Microorganisms 01-Feb-2022
PMCID:PMC8875210
doi:10.3390/microorganisms10020339
PMID:35208794
Section 1: 5th IUPHAR WCP-NP, 2019 INDIA N/A Indian J Pharmacol 01-Dec-2021
PMCID:PMC9045588
Herbal Medicine, Gut Microbiota, and COVID-19 Chen Z, Lv Y, Xu H, Deng L Front Pharmacol 07-Jul-2021
PMCID:PMC8293616
doi:10.3389/fphar.2021.646560
PMID:34305582
Characteristic metabolites of Hypericum plants: their chemical structures and biological activities Tanaka N, Kashiwada Y J Nat Med 08-Feb-2021
PMCID:PMC8159811
doi:10.1007/s11418-021-01489-y
PMID:33555487
Smart Responsive Nanoformulation for Targeted Delivery of Active Compounds From Traditional Chinese Medicine Jiang X, Lin M, Huang J, Mo M, Liu H, Jiang Y, Cai X, Leung W, Xu C Front Chem 10-Dec-2020
PMCID:PMC7758496
doi:10.3389/fchem.2020.559159
PMID:33363102
In Vitro Evaluation of Chemically Analyzed Hypericum Triquetrifolium Extract Efficacy in Apoptosis Induction and Cell Cycle Arrest of the HCT-116 Colon Cancer Cell Line Mahajna S, Kadan S, Tietel Z, Saad B, Khasib S, Tumeh A, Ginsberg D, Zaid H Molecules 15-Nov-2019
PMCID:PMC6891740
doi:10.3390/molecules24224139
PMID:31731693
Traditional Chinese medicine-combination therapies utilizing nanotechnology-based targeted delivery systems: a new strategy for antitumor treatment Ma Z, Fan Y, Wu Y, Kebebe D, Zhang B, Lu P, Pi J, Liu Z Int J Nanomedicine 22-Mar-2019
PMCID:PMC6435121
doi:10.2147/IJN.S197889
PMID:30962686

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
> Alkaloids and derivatives / Protopine alkaloids
8-[(2S,4R,5R,6S)-4,5-dihydroxy-6-methyloxan-2-yl]oxy-1-hydroxy-5-methoxy-3-methyl-6-[(3S)-2-oxopiperidin-3-yl]-5H-benzo[b]phenanthridine-7,12-dione 139589544 Click to see CC1C(C(CC(O1)OC2=CC=CC3=C2C(=O)C4=C(C3=O)C5=C(C=C(C=C5O)C)C(N4C6CCCNC6=O)OC)O)O 564.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Alkaloids and derivatives / Strychnos alkaloids
[(1S,9S,10R,11R,17S)-12-[(E)-2-[(4S,12S,13R,16S,17S,18S,20S,21S)-16-methyl-15-oxa-1,11-diazahexacyclo[15.3.1.04,12.04,20.05,10.013,18]henicosa-5,7,9-trien-21-yl]ethenyl]-8,14-diazapentacyclo[9.5.2.01,9.02,7.014,17]octadeca-2,4,6,12-tetraen-10-yl]methanol 162913727 Click to see 588.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Benzenoids / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Methyl 1-hydroxy-9,10-dioxoanthracene-2-carboxylate 2870897 Click to see 282.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Bergenin 66065 Click to see 328.27 unknown via CMAUP database
Demethylbergenin 90476206 Click to see 314.24 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2R,3S,4S,5R,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 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
[(2S)-2,3-dihydroxypropyl] 3,4,5-trihydroxybenzoate 51543740 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC(CO)O 244.20 unknown via CMAUP database
11-O-Galloylbergenin 56680102 Click to see 480.40 unknown via CMAUP database
5-Galloylshikimic acid 460897 Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O 326.25 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
1-[3-[(3-Acetyl-2,4-dihydroxy-6-methoxy-5-methylphenyl)methyl]-2,4,6-trihydroxy-5-(3-methyl-2-butenyl)phenyl]-1-butanone 5315573 Click to see CCCC(=O)C1=C(C(=C(C(=C1O)CC2=C(C(=C(C(=C2O)C(=O)C)O)C)OC)O)CC=C(C)C)O 472.50 unknown via CMAUP database
Mallotojaponin 122659 Click to see CC1=C(C(=C(C(=C1OC)CC2=C(C(=C(C(=C2O)CC=C(C)C)O)C(=O)C)O)O)C(=O)C)O 444.50 unknown via CMAUP database
Mallotophenone 179090 Click to see 404.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
(2,4-Dihydroxyphenyl)-[5-(2,4-dihydroxyphenyl)-2-(4-hydroxyphenyl)-4-[(4-hydroxyphenyl)methyl]oxolan-3-yl]methanone 14162794 Click to see 514.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Rhodiocyanoside A 6442274 Click to see 259.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
[(1S,2S,4aS,8aS)-2-acetyloxy-4-[(E)-5-hydroxy-3-methylpent-3-enyl]-3,4a,8,8-tetramethyl-1,2,5,6,7,8a-hexahydronaphthalen-1-yl] acetate 44448158 Click to see 406.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Hypercalin B 5281562 Click to see 518.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
4-Hydroxy-6-methyl-3,7-bis(3-methylbut-2-enyl)-6-(4-methylpent-3-enyl)-5-(2-methylpropanoyl)bicyclo[3.3.1]non-3-ene-2,9-dione 53394331 Click to see 468.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1R,4S)-1-(hydroxymethyl)-4-propan-2-ylcyclohex-2-en-1-ol 162946780 Click to see 170.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
3,5-Dihydroxy-4-[(2-hydroxy-2-methyl-5-prop-1-en-2-ylcyclopentyl)methyl]-2-(3-methylbutanoyl)-6,6-bis(3-methylbut-2-enyl)cyclohexa-2,4-dien-1-one 14502643 Click to see CC(C)CC(=O)C1=C(C(=C(C(C1=O)(CC=C(C)C)CC=C(C)C)O)CC2C(CCC2(C)O)C(=C)C)O 498.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
3,5-Dihydroxy-4-[(2-hydroxy-2-methyl-5-prop-1-en-2-ylcyclopentyl)methyl]-6,6-bis(3-methylbut-2-enyl)-2-(2-methylpropanoyl)cyclohexa-2,4-dien-1-one 14502639 Click to see 484.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
3,5-dihydroxy-4-[[(1R,2S,5S)-2-hydroxy-2-methyl-5-prop-1-en-2-ylcyclopentyl]methyl]-2-(3-methylbutanoyl)-6,6-bis(3-methylbut-2-enyl)cyclohexa-2,4-dien-1-one 163049149 Click to see CC(C)CC(=O)C1=C(C(=C(C(C1=O)(CC=C(C)C)CC=C(C)C)O)CC2C(CCC2(C)O)C(=C)C)O 498.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
3,5-dihydroxy-4-[[(1R,2S,5S)-2-hydroxy-2-methyl-5-prop-1-en-2-ylcyclopentyl]methyl]-6,6-bis(3-methylbut-2-enyl)-2-(2-methylpropanoyl)cyclohexa-2,4-dien-1-one 72944684 Click to see CC(C)C(=O)C1=C(C(=C(C(C1=O)(CC=C(C)C)CC=C(C)C)O)CC2C(CCC2(C)O)C(=C)C)O 484.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
Hypercalin C 14502640 Click to see 484.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols
(2Z,6Z,10Z,14Z,18Z,22E,26E,30E)-3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-ol 12442866 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C 631.10 unknown via CMAUP database
(2Z,6Z,10Z,14Z,18Z,22Z,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-ol 12866490 Click to see 699.20 unknown via CMAUP database
(2Z,6Z,10Z,14Z,18Z,22Z,26Z,30Z,34E,38E,42E)-3,7,11,15,19,23,27,31,35,39,43,47-dodecamethyloctatetraconta-2,6,10,14,18,22,26,30,34,38,42,46-dodecaen-1-ol 14380582 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C)C 835.40 unknown via CMAUP database
3,7,11,15,19,23,27,31,35-Nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-Nonaen-1-Ol 83218 Click to see 631.10 unknown via CMAUP database
Ficaprenol 11 11411688 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C 767.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(8-acetyloxy-8a-hydroxy-3,4a,5-trimethyl-9-oxo-5,6,7,8-tetrahydro-4H-benzo[f][1]benzofuran-4-yl) 2-methylprop-2-enoate 163028731 Click to see 390.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Escin Ivd 6476035 Click to see 1131.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4R,4aS,6aS,6aR,6bS,8aR,12aS,14aR,14bS)-4,4a,6b,8a,11,11,14a-heptamethyl-1,2,4,5,6,6a,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-one 163193143 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
4,4a,6b,8a,11,11,14a-Heptamethyl-1,2,4,5,6,6a,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-one 76578925 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
Friedelinol 101341 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
[(2R,3R,4R,4aS,10bS)-8,10-dihydroxy-2-(hydroxymethyl)-9-methoxy-6-oxo-4-(3,4,5-trihydroxybenzoyl)oxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-3-yl] 3,4,5-trihydroxybenzoate 71571588 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC2=O)O 632.50 unknown via CMAUP database
[(2R,3R,4S,4aS,10bS)-3,8,10-trihydroxy-9-methoxy-6-oxo-4-(3,4,5-trihydroxybenzoyl)oxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-2-yl]methyl 3,4,5-trihydroxybenzoate 102314951 Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC2=O)O 632.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
14-hydroxy-13-methyl-17-(5-oxo-2H-furan-3-yl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-10-carbaldehyde 14859015 Click to see 550.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
3-[(5R,10R,14S)-3-[(2R,3S,4R,5S,6S)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-14-hydroxy-10-(hydroxymethyl)-13-methyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one 6325934 Click to see 550.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1016/S0031-9422(99)00412-4
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
[(1aR,3R,3aR,4R,5R,6R,7aS)-5-acetyloxy-3-[(2S)-2-hydroxy-5-oxo-2H-furan-3-yl]-6-[(1S,6R)-6-(2-methoxy-2-oxoethyl)-1,5,5-trimethyl-4-oxocyclohex-2-en-1-yl]-3a-methyl-7-methylidene-1a,2,3,4,5,6-hexahydroindeno[1,7a-b]oxiren-4-yl] 2-methylpropanoate 162963836 Click to see CC(C)C(=O)OC1C(C(C(=C)C23C1(C(CC2O3)C4=CC(=O)OC4O)C)C5(C=CC(=O)C(C5CC(=O)OC)(C)C)C)OC(=O)C 614.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
2-[6,9-Dimethyl-4-(2-methylbut-2-enoyloxy)-3-methylidene-2,8-dioxo-3a,4,5,10a-tetrahydrofuro[2,3-e]oxonin-6-yl]acetic acid 73799030 Click to see 392.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Epilotaustralin 185818 Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 261.27 unknown via CMAUP database
Rhodiocyanoside D 6442230 Click to see 259.26 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3R,4S,5S,6R)-2-[[(1R,2S,4R,5R,6S,7S)-5-hydroxy-3,8-dioxatricyclo[4.4.0.02,4]dec-9-en-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162950848 Click to see 332.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-3,4-dihydroxy-6-(4-hydroxy-3-methoxyphenoxy)-5-(3,4,5-trihydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 102147465 Click to see 606.50 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-2-methoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 102442447 Click to see 454.40 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-2,6-dimethoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 25262417 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)OC)O 484.40 unknown via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-3-methoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 102442448 Click to see 454.40 unknown via CMAUP database
[(2S,3S,4R,5R,6S)-6-[4-[2-[3-(4-methoxyphenyl)prop-2-enoylamino]ethyl]phenoxy]-2-methyl-4,5-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-3-yl] acetate 162991180 Click to see 809.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
I(2)-D-Glucopyranoside, 3,4,5-trimethoxyphenyl, 2,6-bis(3,4,5-trihydroxybenzoate) 102469980 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 650.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(2,6-Dihydroxy-4-methoxy-3-methylphenyl)ethanone 14602300 Click to see 196.20 unknown via CMAUP database
1-(2,6-Dihydroxy-4-methoxy-3,5-dimethylphenyl)ethanone 14602301 Click to see 210.23 unknown via CMAUP database
Butyrylmallotochromene 189457 Click to see 470.50 unknown via CMAUP database
Isomallotochromene 10433453 Click to see 442.50 unknown via CMAUP database
Mallotochromene 126969 Click to see 442.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1-Hydroxy-7-methoxyxanthone 12214329 Click to see COC1=CC2=C(C=C1)OC3=CC=CC(=C3C2=O)O 242.23 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
1,5,6-Trihydroxy-7-methoxyxanthone 129685345 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=C(C=CC=C3O2)O)O)O 274.22 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
1,6-Dihydroxy-2,8-dimethoxy-9H-xanthen-9-one 5465786 Click to see 288.25 unknown via CMAUP database
2-Methoxy-9H-xanthen-9-one 71034 Click to see COC1=CC2=C(C=C1)OC3=CC=CC=C3C2=O 226.23 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
3,6-Dihydroxy-1,7-dimethoxyxanthone 101010505 Click to see 288.25 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
Euxanthone 5281631 Click to see 228.20 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
Vinetorin 5384285 Click to see 306.70 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
1,3,6,7-Tetrahydroxy-8-prenylxanthone 15307924 Click to see CC(=CCC1=C(C(=CC2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)O)C 328.30 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
Toxyloxanthone B 14886044 Click to see 326.30 unknown https://doi.org/10.1016/S0031-9422(99)00412-4
> Organoheterocyclic compounds / Furans / Furoic acid and derivatives / Furoic acid esters
CID 101485559 101485559 Click to see 757.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxamides / Nicotinamides
Nicotinamide 936 Click to see C1=CC(=CN=C1)C(=O)N 122.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Methyl Caffeate 689075 Click to see 194.18 unknown https://doi.org/10.1007/S11418-007-0152-9
> Phenylpropanoids and polyketides / Diarylheptanoids / Cyclic diarylheptanoids / Meta,meta-bridged biphenyls
(9S,11S)-tricyclo[12.3.1.12,6]nonadeca-1(17),2,4,6(19),14(18),15-hexaene-3,9,11,17-tetrol 91886681 Click to see 314.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown via CMAUP database
(+)-Catechin 3-Gallate 5276454 Click to see 442.40 unknown via CMAUP database
Epigallocatechin Gallate 65064 Click to see 458.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one 57339948 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(OC4O)CO)O)O)O)O 464.40 unknown via CMAUP database
Kaempferol oxoanion 25202062 Click to see 285.23 unknown via CMAUP database
Quercetin-7-olate 46906036 Click to see 301.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Hibiscetin 15559735 Click to see 334.23 unknown via CMAUP database
Isorhamnetin 5281654 Click to see 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1007/S11418-007-0152-9
https://doi.org/10.1016/S0031-9422(99)00412-4
https://doi.org/10.1007/BF00630668
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 302.23 unknown https://doi.org/10.1007/BF00630668
https://doi.org/10.1016/S0031-9422(99)00412-4
https://doi.org/10.1007/S11418-007-0152-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(2,3-Dihydroxyphenyl)-5,7-dihydroxy-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 53399169 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=C(C(=CC=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1007/BF00630668
4-[5,7-dihydroxy-4-oxo-3-[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-yl]-2-hydroxyphenolate 54758589 Click to see 463.40 unknown via CMAUP database
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one 5320020 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1007/BF00630668
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00630668
Narcissin 5481663 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1007/BF00630668
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 7-O-beta-D-galactopyranoside 72551439 Click to see 448.40 unknown https://doi.org/10.1007/BF00630668
Kaempferol-7-o-glucoside 5480982 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00630668
scutellarein-7-O-gentiobioside 162897126 Click to see 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-1-Benzopyrylium 128861 Click to see 287.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Peonidin 441773 Click to see COC1=C(C=CC(=C1)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O 301.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
Vestitol, (-)- 182259 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
6-Hydroperoxy-2-hydroxy-2,6,10-trimethyl-15-methylidene-13,18-dioxatricyclo[9.6.1.012,16]octadec-4-en-14-one 73837280 Click to see 366.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.04.026
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Eucomic Acid 23757219 Click to see 240.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,2,3,6-Tetra-O-Galloyl-Beta-D-Glucose 73178 Click to see 788.60 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
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 484.40 unknown via CMAUP database
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database
Penta-O-galloyl-beta-D-glucose 65238 Click to see 940.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(10R,11R,13R,14R,15S)-3,4,5,11,14,20,21,22-octahydroxy-13-(hydroxymethyl)-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaene-8,17-dione 11754973 Click to see 482.30 unknown via CMAUP database
[(10R,11R,13R,14R,15S)-3,4,5,11,20,21,22-heptahydroxy-8,17-dioxo-14-(3,4,5-trihydroxybenzoyl)oxy-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-13-yl]methyl 3,4,5-trihydroxybenzoate 14284542 Click to see 786.60 unknown via CMAUP database
[(10R,11S,13R,14R,15S)-3,4,5,14,20,21,22-heptahydroxy-8,17-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-13-yl]methyl 3,4,5-trihydroxybenzoate 14429414 Click to see 786.60 unknown via CMAUP database
[(10R,11S,13R,14R,15S)-3,4,5,20,21,22-hexahydroxy-8,17-dioxo-11,14-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-13-yl]methyl 3,4,5-trihydroxybenzoate 10557787 Click to see 938.70 unknown via CMAUP database
1,2-DI-O-GALLOYL-3,6-(R)-HEXAHYDROXYDIPHENOYL-| cent-D-GLUCOSE 14284664 Click to see 786.60 unknown via CMAUP database
2-[[(1R,7R,8S,26R,28S,29R,38R)-1,14,15,18,19,20,34,35,39,39-decahydroxy-2,5,10,23,31-pentaoxo-28-(3,4,5-trihydroxybenzoyl)oxy-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-13-yl]oxy]-3,4,5-trihydroxybenzoic acid 16201525 Click to see 1120.70 unknown via CMAUP database
2-[[(1S,19R,21S,22R,23R)-6,7,8,11,12,22,23-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-13-yl]oxy]-3,4,5-trihydroxybenzoic acid 46905124 Click to see 802.60 unknown via CMAUP database
3,3a(2),4a(2)-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
4,4'-Di-O-methylellagic acid 11580745 Click to see 330.24 unknown via CMAUP database
Casuarictin 73644 Click to see 936.60 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
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database
Geraniin 3001497 Click to see 952.60 unknown via CMAUP database
Giadmmrdajabjm-oaqcrpkasa- 21668995 Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C(C(C(OC8OC(=O)C9=CC(=C(C(=C9)O)O)O)CO)OC5=O)O)O)O)O)O)O)O 808.60 unknown via CMAUP database
Mallotinic Acid 10056140 Click to see 802.60 unknown via CMAUP database
Mallotusinin 514180 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7=C(O6)C(=C(C=C7C(=O)O3)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 918.60 unknown via CMAUP database
Pmgvhtaltibnie-gloqphdasa- 21668994 Click to see 1278.90 unknown via CMAUP database
Punicafolin 5320800 Click to see 938.70 unknown via CMAUP database
Xcxwmhrrisfuff-xngpzlstsa- 21636130 Click to see 1110.80 unknown via CMAUP database

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