Hypericum erectum - Unknown
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Internal ID UUID64402151465fb822322156
Scientific name Hypericum erectum
Authority Thunb.
First published in Syst. Veg. ed. 14 : 702 (1784)

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Synonyms Top

Scientific name Authority First published in
Hypericum erectum f. wichurae R.Keller Bull. Herb. Boissier 5: 640 1897
Hypericum erectum var. wichurae (R.Keller) H.Lév. Bull. Soc. Bot. France 53: 500 1906
Hypericum erectum var. divaricatum Blume Mus. Bot. 2: 25. 1856
Hypericum erectum var. obtusifolium Blume Mus. Bot. 2: 25. 1856
Hypericum erectum f. montanum Nakai Chosen-shokubutsu 1: 160 1914
Hypericum erectum subsp. vaniotii H.Lév.
Hypericum sachalinense H.Lév. Repert. Spec. Nov. Regni Veg. 6: 330. 1909

Common names Top

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Language Common/alternative name
Azerbaijani dikduran dazı
Danish gemo
Danish smalbladet perikon
Japanese ショウレンギョウ
Japanese 小連翹
Japanese 弟切草
Japanese オトギリソウ
Korean 고추나물
Russian Зверобой прямостоящий
Chinese 千金子
Chinese 小对叶草
Chinese 小连翘
Chinese 小連翹
Chinese 小金雀
Chinese 旱莓草

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Varieties (abbr. var.) Top

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Name Authority First published in
Hypericum erectum var. caespitosum Makino Bot. Mag. (Tokyo) 18: 104 (1904)
Hypericum erectum var. erectum Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Name Authority First published in
Hypericum erectum f. angustifolium (Y.Kimura) Y.Kimura Nov. Fl. Jap. 10: 150 (1951)
Hypericum erectum f. debile R.Keller Bull. Herb. Boissier 5: 640 (1897)
Hypericum erectum f. lutchuense (Koidz.) Y.Kimura Nov. Fl. Jap. 10: 152 (1951)
Hypericum erectum f. papillosum (Y.Kimura) Y.Kimura Nov. Fl. Jap. 10: 150 (1951)
Hypericum erectum f. tateutianum (Koidz.) Y.Kimura Nov. Fl. Jap. 10: 150 (1951)
Hypericum erectum f. vaniotii (H.Lév.) Y.Kimura Nov. Fl. Jap. 10: 151 (1951)

Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan
    • Russian Far East
      • Kuril Islands
      • Sakhalin

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000727608
UNII 441M3DNK9R
Tropicos 7800881
KEW urn:lsid:ipni.org:names:927425-1
The Plant List kew-2858084
Open Tree Of Life 304180
Observations.org 124456
NCBI Taxonomy 282539
IPNI 927425-1
iNaturalist 502260
GBIF 7330122
Freebase /m/0nbgdyy
EPPO HYPER
EOL 2889769
Elurikkus 663030
USDA GRIN 19568

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
Hypericum Genus as a Natural Source for Biologically Active Compounds Caldeira GI, Gouveia LP, Serrano R, Silva OD Plants (Basel) 26-Sep-2022
PMCID:PMC9573133
doi:10.3390/plants11192509
PMID:36235373
Flavonoids-Rich Plant Extracts Against Helicobacter pylori Infection as Prevention to Gastric Cancer Ivyna de Araújo Rêgo R, Guedes Silvestre GF, Ferreira de Melo D, Albino SL, Pimentel MM, Silva Costa Cruz SB, Silva Wurzba SD, Rodrigues WF, Goulart de Lima Damasceno BP, Cançado Castellano LR Front Pharmacol 31-Aug-2022
PMCID:PMC9470917
doi:10.3389/fphar.2022.951125
PMID:36120379
Bioinspired Total Synthesis of Erectones A and B, and the Revised Structure of Hyperelodione D Franov LJ, Hart JD, Pullella GA, Sumby CJ, George JH Angew Chem Int Ed Engl 14-Mar-2022
PMCID:PMC9314102
doi:10.1002/anie.202200420
PMID:35225410
A prospective, single-arm trial of fluorescent ureteroscopy-assisted thulium-holmium:YAG dual laser ablation for upper urinary tract cancer: Study protocol of the FLUAM trial Miyake M, Yoshida T, Nishimura N, Oda Y, Shimizu T, Nakahama T, Hori S, Morizawa Y, Gotoh D, Nakai Y, Anai S, Torimoto K, Fujii T, Tanaka N, Fujimoto K Contemp Clin Trials Commun 02-Mar-2022
PMCID:PMC8897668
doi:10.1016/j.conctc.2022.100902
PMID:35257033
Naturally Occurring Chromone Glycosides: Sources, Bioactivities, and Spectroscopic Features Amen Y, Elsbaey M, Othman A, Sallam M, Shimizu K Molecules 16-Dec-2021
PMCID:PMC8704703
doi:10.3390/molecules26247646
PMID:34946728
Evaluation of sampling effort required to assess pollen species richness on pollinators using rarefaction Nikkeshi A, Hiraiwa MK, Ushimaru A, Hoshizaki K, Makita A, Mizuki I Appl Plant Sci 27-Feb-2021
PMCID:PMC7910805
doi:10.1002/aps3.11411
PMID:33680582
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
Antiprotozoal and Antitumor Activity of Natural Polycyclic Endoperoxides: Origin, Structures and Biological Activity Dembitsky VM, Ermolenko E, Savidov N, Gloriozova TA, Poroikov VV Molecules 28-Jan-2021
PMCID:PMC7865715
doi:10.3390/molecules26030686
PMID:33525706
Ovule and seed production patterns in relation to flower size variations in actinomorphic and zygomorphic flower species Mochizuki J, Itagaki T, Aoyagi Blue Y, Ito M, Sakai S AoB Plants 23-Sep-2019
PMCID:PMC6804480
doi:10.1093/aobpla/plz061
PMID:31656557
The aetiology, prevalence and morbidity of outbreaks of photosensitisation in livestock: A review Chen Y, Quinn JC, Weston LA, Loukopoulos P PLoS One 27-Feb-2019
PMCID:PMC6392228
doi:10.1371/journal.pone.0211625
PMID:30811417
Development and Validation of an Ultra-Performance Liquid Chromatography Method for the Determination of Wedelolactone in Rat Plasma and its Application in a Pharmacokinetic Study Chen Q, Wu X, Gao X, Song H, Zhu X Molecules 20-Feb-2019
PMCID:PMC6413069
doi:10.3390/molecules24040762
PMID:30791539
Rhamnus davurica leaf extract inhibits Fyn activation by antigen in mast cells for anti-allergic activity Kim JH, Kim AR, Kim HS, Kim HW, Park YH, You JS, Park YM, Her E, Kim HS, Kim YM, Choi WS BMC Complement Altern Med 25-Mar-2015
PMCID:PMC4379541
doi:10.1186/s12906-015-0607-6
PMID:25887889
Noneczematous Contact Dermatitis Bonamonte D, Foti C, Vestita M, Angelini G ISRN Allergy 15-Sep-2013
PMCID:PMC3787648
doi:10.1155/2013/361746
PMID:24109520
Antiplasmodial and cytotoxic activity of phloroglucinol derivatives from Hypericum erectum Thunb. Moon HI Phytother Res 01-Jun-2010
doi:10.1002/PTR.3104
PMID:20127665
Polyprenylated benzoylphloroglucinol-type derivatives including novel cage compounds from Hypericum erectum. Ishida Y, Shirota O, Sekita S, Someya K, Tokita F, Nakane T, Kuroyanagi M Chem Pharm Bull (Tokyo) 01-Mar-2010
doi:10.1248/CPB.58.336
PMID:20190438

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Corynanthean-type alkaloids
Methyl 15-ethyl-13-(hydroxymethyl)-3,17-diazapentacyclo[12.3.1.02,10.04,9.012,17]octadeca-2,4,6,8-tetraene-13-carboxylate 163006423 Click to see CCC1CN2C3CC1C(C2CC4C3=NC5=CC=CC=C45)(CO)C(=O)OC 354.40 unknown https://doi.org/10.1002/PTR.3104
https://doi.org/10.1016/S0031-9422(01)00408-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3-Hydroxy-4-methoxybenzoic acid 12575 Click to see COC1=C(C=C(C=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1007/S11418-008-0256-X
> Benzenoids / Benzene and substituted derivatives / Benzophenones
[(3R)-6-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,5,7-trihydroxy-2,2-dimethyl-3,4-dihydrochromen-8-yl]-phenylmethanone 163187466 Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)CC(C(O2)(C)C)O)C(=O)C3=CC=CC=C3)O)C)C 450.60 unknown https://doi.org/10.1248/CPB.58.336
[6-(3,7-Dimethylocta-2,6-dienyl)-3,5,7-trihydroxy-2,2-dimethyl-3,4-dihydrochromen-8-yl]-phenylmethanone 75104407 Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)CC(C(O2)(C)C)O)C(=O)C3=CC=CC=C3)O)C)C 450.60 unknown https://doi.org/10.1248/CPB.58.336
phenyl-[(2R,3S)-3,5,7-trihydroxy-2-methyl-6-(3-methylbut-2-enyl)-2-(4-methylpent-3-enyl)-3,4-dihydrochromen-8-yl]methanone 163033352 Click to see CC(=CCCC1(C(CC2=C(C(=C(C(=C2O1)C(=O)C3=CC=CC=C3)O)CC=C(C)C)O)O)C)C 450.60 unknown https://doi.org/10.1248/CPB.58.336
Phenyl-[3,5,7-trihydroxy-2-methyl-6-(3-methylbut-2-enyl)-2-(4-methylpent-3-enyl)-3,4-dihydrochromen-8-yl]methanone 75104406 Click to see CC(=CCCC1(C(CC2=C(C(=C(C(=C2O1)C(=O)C3=CC=CC=C3)O)CC=C(C)C)O)O)C)C 450.60 unknown https://doi.org/10.1248/CPB.58.336
> Hydrocarbons / Unsaturated hydrocarbons / Olefins / Cyclic olefins
trans-1-[(1z)-Hexenyl]-2-vinylcyclopropane 16752617 Click to see CCCCC=CC1CC1C=C 150.26 unknown https://doi.org/10.1248/CPB.58.336
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octacosanol 68406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCO 410.80 unknown https://doi.org/10.1007/S11418-008-0256-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Effusanin D 44585547 Click to see CC(=O)OCC1(CCC(C23C1C(C(C45C2CCC(C4)C(=C)C5=O)(OC3)O)O)OC(=O)C)C 448.50 unknown https://doi.org/10.1016/0031-9422(91)85100-E
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
4-(3,7-Dimethylocta-2,6-dienyl)-3,5-dihydroxy-6-(3-methylbut-2-enyl)cyclohexa-3,5-diene-1,2-dione 78200671 Click to see CC(=CCCC(=CCC1=C(C(=O)C(=O)C(=C1O)CC=C(C)C)O)C)C 344.40 unknown https://doi.org/10.1002/PTR.3104
Erectquione A 636511 Click to see CC(=CCCC(=CCC1=C(C(=O)C(=O)C(=C1O)CC=C(C)C)O)C)C 344.40 unknown https://doi.org/10.1016/S0031-9422(01)00408-3
https://doi.org/10.1002/PTR.3104
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Prenylquinones
[4-(3,7-Dimethylocta-2,6-dienyl)-2-(3-methylbut-2-enyl)-5-(2-methylpropanoyloxy)-3,6-dioxocyclohexa-1,4-dien-1-yl] 2-methylpropanoate 78384868 Click to see CC(C)C(=O)OC1=C(C(=O)C(=C(C1=O)OC(=O)C(C)C)CC=C(C)CCC=C(C)C)CC=C(C)C 484.60 unknown https://doi.org/10.1002/PTR.3104
https://doi.org/10.1016/S0031-9422(01)00408-3
[4-[(2E)-3,7-dimethylocta-2,6-dienyl]-2-(3-methylbut-2-enyl)-5-(2-methylpropanoyloxy)-3,6-dioxocyclohexa-1,4-dien-1-yl] 2-methylpropanoate 5317014 Click to see CC(C)C(=O)OC1=C(C(=O)C(=C(C1=O)OC(=O)C(C)C)CC=C(C)CCC=C(C)C)CC=C(C)C 484.60 unknown https://doi.org/10.1016/S0031-9422(01)00408-3
https://doi.org/10.1002/PTR.3104
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,3R,4R,6S,8R)-8-benzoyl-1-[(2E)-3,7-dimethylocta-2,6-dienyl]-4-(2-hydroxypropan-2-yl)-7,7-dimethyl-3-(3-methylbut-2-enyl)tricyclo[4.3.1.13,8]undecane-2,9,11-trione 163190219 Click to see CC(=CCCC(=CCC12CC3CC(C(C1=O)(C(=O)C(C2=O)(C3(C)C)C(=O)C4=CC=CC=C4)CC=C(C)C)C(C)(C)O)C)C 586.80 unknown https://doi.org/10.1248/CPB.58.336
(1S,7R,11S,12R,13R)-7-[(2E)-3,7-dimethylocta-2,6-dienyl]-12,13-dihydroxy-2,2,10-trimethyl-5-(3-methylbut-2-enyl)-3-oxatetracyclo[9.2.1.04,13.07,12]tetradeca-4,9-dien-6-one 10322920 Click to see CC1=CCC2(C(=O)C(=C3C4(C2(C1CC4C(O3)(C)C)O)O)CC=C(C)C)CC=C(C)CCC=C(C)C 480.70 unknown https://doi.org/10.1016/S0040-4039(01)02118-9
7-(3,7-Dimethylocta-2,6-dienyl)-12,13-dihydroxy-2,2,10-trimethyl-5-(3-methylbut-2-enyl)-3-oxatetracyclo[9.2.1.04,13.07,12]tetradeca-4,9-dien-6-one 85110018 Click to see CC1=CCC2(C(=O)C(=C3C4(C2(C1CC4C(O3)(C)C)O)O)CC=C(C)C)CC=C(C)CCC=C(C)C 480.70 unknown https://doi.org/10.1016/S0040-4039(01)02118-9
8-Benzoyl-1-(3,7-dimethylocta-2,6-dienyl)-4-(2-hydroxypropan-2-yl)-7,7-dimethyl-3-(3-methylbut-2-enyl)tricyclo[4.3.1.13,8]undecane-2,9,11-trione 75104365 Click to see CC(=CCCC(=CCC12CC3CC(C(C1=O)(C(=O)C(C2=O)(C3(C)C)C(=O)C4=CC=CC=C4)CC=C(C)C)C(C)(C)O)C)C 586.80 unknown https://doi.org/10.1248/CPB.58.336
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aR,11S,12aS,14aR,14bR)-8a-carboxy-11-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,4,6a,6b,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 162931394 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)C(=O)O)O)O)O)C)CC=C5C3(CCC6(C5CC(CC6)(C)COC7C(C(C(C(O7)CO)O)O)OC8C(C(C(CO8)O)O)O)C(=O)O)C)C)C 943.10 unknown https://doi.org/10.1016/0031-9422(91)85100-E
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
9a-Hydroxy-3,4a,5-trimethyl-4,5,8a,9-tetrahydrobenzo[f][1]benzofuran-2,6-dione 162985867 Click to see CC1C(=O)C=CC2C1(CC3=C(C(=O)OC3(C2)O)C)C 262.30 unknown https://doi.org/10.1002/PTR.3104
https://doi.org/10.1016/S0031-9422(01)00408-3
> 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/10.1007/S11418-008-0256-X
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/S11418-008-0256-X
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1007/S11418-008-0256-X
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 https://doi.org/10.1007/S11418-008-0256-X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
[(1R,9R,12S)-12-(2-hydroxypropan-2-yl)-9-methyl-4-(3-methylbut-2-enyl)-3,6-dioxo-8-oxatricyclo[7.3.1.02,7]trideca-2(7),4-dien-5-yl] 2-methylpropanoate 6325147 Click to see CC(C)C(=O)OC1=C(C(=O)C2=C(C1=O)OC3(CCC(C2C3)C(C)(C)O)C)CC=C(C)C 430.50 unknown https://doi.org/10.1002/PTR.3104
https://doi.org/10.1016/S0031-9422(01)00408-3
[(1R,9S,12S)-12-(2-hydroxypropan-2-yl)-9-methyl-4-(3-methylbut-2-enyl)-3,6-dioxo-8-oxatricyclo[7.3.1.02,7]trideca-2(7),4-dien-5-yl] 2-methylpropanoate 162972916 Click to see CC(C)C(=O)OC1=C(C(=O)C2=C(C1=O)OC3(CCC(C2C3)C(C)(C)O)C)CC=C(C)C 430.50 unknown https://doi.org/10.1016/S0031-9422(01)00408-3
[(1S,9S,12R)-12-(2-hydroxypropan-2-yl)-9-methyl-4-(3-methylbut-2-enyl)-3,6-dioxo-8-oxatricyclo[7.3.1.02,7]trideca-2(7),4-dien-5-yl] 2-methylpropanoate 162972917 Click to see CC(C)C(=O)OC1=C(C(=O)C2=C(C1=O)OC3(CCC(C2C3)C(C)(C)O)C)CC=C(C)C 430.50 unknown https://doi.org/10.1002/PTR.3104
[12-(2-Hydroxypropan-2-yl)-9-methyl-4-(3-methylbut-2-enyl)-3,6-dioxo-8-oxatricyclo[7.3.1.02,7]trideca-2(7),4-dien-5-yl] 2-methylpropanoate 636512 Click to see CC(C)C(=O)OC1=C(C(=O)C2=C(C1=O)OC3(CCC(C2C3)C(C)(C)O)C)CC=C(C)C 430.50 unknown https://doi.org/10.1002/PTR.3104
https://doi.org/10.1016/S0031-9422(01)00408-3
Erectquione C 5317158 Click to see CC(C)C(=O)OC1=C(C(=O)C2=C(C1=O)OC3(CCC(C2C3)C(C)(C)O)C)CC=C(C)C 430.50 unknown https://doi.org/10.1016/S0031-9422(01)00408-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Salidroside 159278 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown https://doi.org/10.1007/S11418-008-0256-X
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5R,6R)-2-(4-hydroxy-2-methoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 154496802 Click to see COC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O 302.28 unknown https://doi.org/10.1007/S11418-008-0256-X
(2S,3S,4S,5R,6R)-2-(4-hydroxy-3-methoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 159263713 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)O 302.28 unknown https://doi.org/10.1007/S11418-008-0256-X
3-Hydroxytyrosol 3-O-glucoside 5315870 Click to see C1=CC(=C(C=C1CCO)OC2C(C(C(C(O2)CO)O)O)O)O 316.30 unknown https://doi.org/10.1007/S11418-008-0256-X
Vanilloloside 44577222 Click to see COC1=C(C=CC(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 316.30 unknown https://doi.org/10.1007/S11418-008-0256-X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(1R,3S,7S,9S,11R,13S)-11-benzoyl-13-[(2E)-3,7-dimethylocta-2,6-dienyl]-3-(2-hydroxypropan-2-yl)-6,6,10,10-tetramethyl-4,5-dioxatetracyclo[9.3.1.19,13.01,7]hexadecane-12,14,15-trione 163188825 Click to see CC(=CCCC(=CCC12CC3CC4C(OOC(CC4(C1=O)C(=O)C(C2=O)(C3(C)C)C(=O)C5=CC=CC=C5)C(C)(C)O)(C)C)C)C 618.80 unknown https://doi.org/10.1248/CPB.58.336
(1S,3R,4S,7R,9R,11S)-1-benzoyl-11-[(2E)-3,7-dimethylocta-2,6-dienyl]-4-hydroxy-6,6,13,13-tetramethyl-3-(3-methylbut-2-enyl)-5-oxatetracyclo[7.3.1.03,7.04,11]tridecane-2,12-dione 163194389 Click to see CC(=CCCC(=CCC12CC3CC4C(OC1(C4(C(=O)C(C2=O)(C3(C)C)C(=O)C5=CC=CC=C5)CC=C(C)C)O)(C)C)C)C 586.80 unknown https://doi.org/10.1248/CPB.58.336
(1S,3R,5S,7S,8R)-5-benzoyl-3-[(2E)-3,7-dimethylocta-2,6-dienyl]-6,6-dimethyl-1-(3-methylbut-2-enyl)-8-(2-methylprop-1-enyl)adamantane-2,4,9-trione 45258324 Click to see CC(=CCCC(=CCC12CC3C(C(C1=O)(C(=O)C(C2=O)(C3(C)C)C(=O)C4=CC=CC=C4)CC=C(C)C)C=C(C)C)C)C 568.80 unknown https://doi.org/10.1248/CPB.58.336
(1S,3S,8R,10R)-8-benzoyl-3-[(2R,5S)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,9-dimethyl-6,10-bis(3-methylbut-2-enyl)-4-oxatricyclo[6.3.1.01,5]dodec-5-ene-7,12-dione 162922945 Click to see CC(=CCC1CC23CC(OC2=C(C(=O)C(C3=O)(C1(C)C)C(=O)C4=CC=CC=C4)CC=C(C)C)C5(CCC(O5)C(C)(C)O)C)C 602.80 unknown https://doi.org/10.1248/CPB.58.336
1-[4-[(3,7-Dimethyl-2,6-octadienyl)oxy]-2,6-dihydroxy-3-methylphenyl]-2-methyl-1-propanone 54359303 Click to see CC1=C(C=C(C(=C1O)C(=O)C(C)C)O)OCC=C(C)CCC=C(C)C 346.50 unknown https://doi.org/10.1002/PTR.3104
https://doi.org/10.1016/0031-9422(91)85100-E
11-Benzoyl-13-(3,7-dimethylocta-2,6-dienyl)-3-(2-hydroxypropan-2-yl)-6,6,10,10-tetramethyl-4,5-dioxatetracyclo[9.3.1.19,13.01,7]hexadecane-12,14,15-trione 75104364 Click to see CC(=CCCC(=CCC12CC3CC4C(OOC(CC4(C1=O)C(=O)C(C2=O)(C3(C)C)C(=O)C5=CC=CC=C5)C(C)(C)O)(C)C)C)C 618.80 unknown https://doi.org/10.1248/CPB.58.336
5-Benzoyl-3-(3,7-dimethylocta-2,6-dienyl)-6,6-dimethyl-1-(3-methylbut-2-enyl)-8-(2-methylprop-1-enyl)adamantane-2,4,9-trione 75104363 Click to see CC(=CCCC(=CCC12CC3C(C(C1=O)(C(=O)C(C2=O)(C3(C)C)C(=O)C4=CC=CC=C4)CC=C(C)C)C=C(C)C)C)C 568.80 unknown https://doi.org/10.1248/CPB.58.336
8-Benzoyl-3-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-9,9-dimethyl-6,10-bis(3-methylbut-2-enyl)-4-oxatricyclo[6.3.1.01,5]dodec-5-ene-7,12-dione 75104405 Click to see CC(=CCC1CC23CC(OC2=C(C(=O)C(C3=O)(C1(C)C)C(=O)C4=CC=CC=C4)CC=C(C)C)C5(CCC(O5)C(C)(C)O)C)C 602.80 unknown https://doi.org/10.1248/CPB.58.336
Adotogirin 15694257 Click to see CC1=C(C=C(C(=C1O)C(=O)C(C)C)O)OCC=C(C)CCC=C(C)C 346.50 unknown https://doi.org/10.1016/0031-9422(91)85100-E
https://doi.org/10.1002/PTR.3104
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
3-Hydroxy-2-methoxyxanthen-9-one 5386264 Click to see COC1=C(C=C2C(=C1)C(=O)C3=CC=CC=C3O2)O 242.23 unknown https://doi.org/10.1007/S11418-008-0256-X
9H-Xanthen-9-one, 3-hydroxy-2,4-dimethoxy- 12214333 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=CC=CC=C3O2)OC)O 272.25 unknown https://doi.org/10.1007/S11418-008-0256-X
Euxanthone 5281631 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=C(C=C3)O)O 228.20 unknown https://doi.org/10.1007/S11418-008-0256-X
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
Hyperxanthone 14757909 Click to see CC1(C=CC2=C(O1)C(=CC3=C2C(=O)C4=C(O3)C=C(C=C4)O)O)C 310.30 unknown https://doi.org/10.1007/S11418-008-0256-X
> Organoheterocyclic compounds / Naphthofurans
(1S,7R,11S,12R,13R)-5-[(2E)-3,7-dimethylocta-2,6-dienyl]-12,13-dihydroxy-2,2,10-trimethyl-7-(3-methylbut-2-enyl)-3-oxatetracyclo[9.2.1.04,13.07,12]tetradeca-4,9-dien-6-one 10917814 Click to see CC1=CCC2(C(=O)C(=C3C4(C2(C1CC4C(O3)(C)C)O)O)CC=C(C)CCC=C(C)C)CC=C(C)C 480.70 unknown https://doi.org/10.1016/S0040-4039(01)02118-9
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R,3R,3'R)-2,2'-Bis(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-2H,2'H-4,8'-bichromene-3,3',5,5',7,7'-hexol 5320711 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1055/S-2006-961020
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1055/S-2006-961020
Procyanidin C1 169853 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1055/S-2006-961020
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1055/S-2006-961020
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/S11418-008-0256-X
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/S11418-008-0256-X
https://doi.org/10.1248/CPB.58.336
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2S,3R,4S,5S,6S)-2-[[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-5-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496323 Click to see C1C(C(OC2=C1C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown https://doi.org/10.1007/S11418-008-0256-X
(2S,3S,4S,5S,6S)-2-[[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-5-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162936878 Click to see C1C(C(OC2=C1C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O)O 452.40 unknown https://doi.org/10.1007/S11418-008-0256-X
5,7-dihydroxy-2-[3-hydroxy-4-[(2S,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 51521836 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 https://doi.org/10.1007/S11418-008-0256-X
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 https://doi.org/10.1007/S11418-008-0256-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 51652818 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1007/S11418-008-0256-X
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one 5317364 Click to see C1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 436.40 unknown https://doi.org/10.1007/S11418-008-0256-X
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxychromen-4-one 14749097 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 418.30 unknown https://doi.org/10.1007/S11418-008-0256-X
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 12358426 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1007/S11418-008-0256-X
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1007/S11418-008-0256-X
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/10.1055/S-2006-961020
Quercitrin 5280459 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2006-961020
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S,3R)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 163008247 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 466.40 unknown https://doi.org/10.1007/S11418-008-0256-X
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Demethylwedelolactone 5489605 Click to see C1=C(C=C2C(=C1O)C3=C(C4=CC(=C(C=C4O3)O)O)C(=O)O2)O 300.22 unknown https://doi.org/10.1248/CPB.33.202
Wedelolactone 5281813 Click to see COC1=CC(=C2C(=C1)OC(=O)C3=C2OC4=CC(=C(C=C43)O)O)O 314.25 unknown https://doi.org/10.1248/CPB.33.202

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