Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

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General Uses Top

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Common products:
Dye material from the whole herb.

Industrial and craft applications:
None established beyond dye use.

Food and beverages (non-medicinal):
No documented non-medicinal food uses.

Colorants and tanning:
The flowering herb is reported as a source of brown–yellow textile dyes in Japanese dyeing literature; dye is obtained by boiling plant material in water. While H. erectum is not a major commercial dye plant, small-scale craft dyers in East Asia have used it for protein fibers. Tannins are present across Hypericum and may contribute to washfastness, but the absolute dye performance and compounds are not standardized. No separate industrial tanning use is documented.

Wood and fiber:
No documented timber or fiber applications.

Fragrance and cosmetics:
No documented fragrance, flavor, or cosmetic uses.

Properties relevant to use:
Water-soluble pigments and tannins can bind to fibers and improve washfastness; the exact chromophores and tannin content in H. erectum have not been quantified in industrial contexts.

Standards and regulation:
No specific ISO/ASTM/EN standards for this species as a dye; commercial dye use follows general textile-colorant regulations.

Sustainability and sourcing:
Wild-harvested plant material is local to parts of East Asia; no cultivated supply chains for dye production are documented.

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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Filter by language:

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

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
Hypericum erectum var. deviatum	Y.Kimura	Bot. Mag. (Tokyo) 52: 403 (1938)

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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)
Hypericum erectum f. perforatum	Y.Kimura	Nov. Fl. Jap. 10: 151 (1951)

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan
- Russian Far East
  - Kuril Islands
  - Sakhalin

Links to other databases Top

Suggest others/fix!

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

Exploring the Therapeutic Potential of Traditional Antimalarial and Antidengue Plants: A Mechanistic Perspective

Kamaraj C, Ragavendran C, Prem P, Naveen Kumar S, Ali A, Kazmi A, Ullah A, Chandra Satish Kumar R, Khan SU, Luna-Arias JP, Mashwani ZU, Balasubramani G, Rehman SU

Can J Infect Dis Med Microbiol

28-Oct-2023

PMCID:	PMC10625492
doi:	10.1155/2023/1860084
PMID:	37927532

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

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 / 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	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
Isovanillic Acid	12575	Click to see	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	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	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	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	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	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	484.60	unknown	https://doi.org/10.1002/PTR.3104 https://doi.org/10.1016/S0031-9422(01)00408-3
> 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	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	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	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	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	262.30	unknown	https://doi.org/10.1016/S0031-9422(01)00408-3 https://doi.org/10.1002/PTR.3104
> 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
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
Stigmast-5-en-3-ol	22012	Click to see	414.70	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	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	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	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	430.50	unknown	https://doi.org/10.1016/S0031-9422(01)00408-3 https://doi.org/10.1002/PTR.3104
Erectquione C	5317158	Click to see	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	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	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	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	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	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	346.50	unknown	https://doi.org/10.1016/0031-9422(91)85100-E https://doi.org/10.1002/PTR.3104
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	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	602.80	unknown	https://doi.org/10.1248/CPB.58.336
Adotogirin	15694257	Click to see	346.50	unknown	https://doi.org/10.1002/PTR.3104 https://doi.org/10.1016/0031-9422(91)85100-E
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
3-Hydroxy-2-methoxyxanthen-9-one	5386264	Click to see	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	228.20	unknown	https://doi.org/10.1007/S11418-008-0256-X
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
Hyperxanthone	14757909	Click to see	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	480.70	unknown	https://doi.org/10.1016/S0040-4039(01)02118-9
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Proanthocyanidin B2	5320711	Click to see	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	866.80	unknown	https://doi.org/10.1055/S-2006-961020
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Epicatechin	72276	Click to see	290.27	unknown	https://doi.org/10.1055/S-2006-961020
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	286.24	unknown	https://doi.org/10.1007/S11418-008-0256-X
Quercetin	5280343	Click to see	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	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	452.40	unknown	https://doi.org/10.1007/S11418-008-0256-X
Luteolin 3'-glucoside	12309350	Click to see	448.40	unknown	https://doi.org/10.1007/S11418-008-0256-X
Luteolin 4'-glucoside	51521836	Click to see	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	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	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	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	314.25	unknown	https://doi.org/10.1248/CPB.33.202

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Hypericum erectum

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