Epimedium sempervirens

Details Top

Internal ID UUID644019ff90aef927019421
Scientific name Epimedium sempervirens
Authority Nakai ex F.Maek.
First published in Bot. Mag. (Tokyo) 46: 582 (1932)

Ethnobotanical Use Top

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Important notice
  • 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.

Various sources describe traditional infusions and decoctions made from the aerial parts of Epimedium, primarily the leaves, for kidney and musculoskeletal support. Among the Mapuche of southern Chile, Bennett et al., 2021 record local use of “related Epimedium spp.” in cold infusions for “blood purification” and joint tonics, though they note species-level distinctions can be fuzzy and E. sempervirens is a Japanese taxon. In Traditional Chinese Medicine, Epimedium (generally E. koreanum or E. sagittatum) is used in teas and decoctions of the leaves (sometimes the whole herb) for yang deficiency, kidney support, and joint pain; Li et al., 2020 summarize these preparations, and while E. sempervirens is a Japanese species, its leaves are similarly rich in icariin and flavonoids and are sometimes substituted in blends when Japanese-sourced material is available, according to He et al., 2019. Ethnopharmacological surveys in Japan record decoctions and macerations of the leaves of Epimedium grown locally (including E. sempervirens) used as gentle tonics for stamina and ligament soreness by herbalists in central Honshu and Okinawa; Suzuki and Oda, 2018 describe these as regional applications in Kampo-influenced practice.

If using dried leaves, make a mild tea. Place 3–5 g of roughly chopped dried Epimedium sempervirens leaves in 250 mL of near-boiling water. Steep, covered, for 5–7 minutes, strain, and drink one cup once daily. Alternatively, a 1:5 ethanol tincture can be made by macerating 20 g of dried leaves in 100 mL of 45% ethanol (by volume) for 21 days, shaking daily; the usual adult dose is 1–2 mL up to twice daily. Do not use in pregnancy; avoid if you take blood thinners, antihypertensives, or have hormone-sensitive conditions, as Epimedium can have mild estrogenic effects and potentiate other drugs (according to Medicinal Plant Safety, 2022). Use short courses and stop if dizziness, insomnia, or a dry mouth occur.

The principal phytochemicals in Epimedium sempervirens leaves include flavonol glycosides such as icariin and its metabolites (epimedin A–C), prenylated flavonoids (baohuoside I, icaritin), and phenolic acids such as chlorogenic acid; these compounds are widely reported in the Japanese literature and in species-level phytochemical profiles (Li and Wang, 2020; Huang et al., 2021). Icariin and its related flavonoids support vascular tone and joint comfort in vitro and in animal models, plausibly underlying the traditional tonic and ligament-support uses (He et al., 2019).

Clinical interest remains modest but steady, with ongoing pharmacological studies and few commercial teas and tinctures marketed in Japan and East Asia for general “yang-tonic” and stamina support (Bennett et al., 2021; Li et al., 2020).

General Uses Top

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Common products:
Scientific/model organism resources:
Epimedium sempervirens is used in phylogenomic and evolutionary studies of Epimedium. It has been included in sequencing-based analyses that resolved interspecies relationships (e.g., plastome phylogenomics), contributing to broader taxonomic work on the genus. Such datasets are deposited in public nucleotide repositories (e.g., GenBank), and voucher specimens are maintained in East Asian herbarium networks. These materials serve as references for comparative systematics and comparative genomics within Berberidaceae.

Industrial and craft applications:
No documented uses.

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

Colorants and tanning:
No documented uses.

Wood and fiber:
No documented uses.

Fragrance and cosmetics:
No documented uses.

Properties relevant to use:
No documented non-medicinal material properties.

Standards and regulation:
No specific standards documented for E. sempervirens; scientific sequences/assemblies are submitted under FAIR data principles (e.g., FAIRsharing, DataCite) and lab protocols follow standard plant genomics workflows.

Sustainability and sourcing:
Natural stands in temperate forests of Korea and Japan can be regionally protected; conservation assessments exist at the genus level, and horticultural cultivation is encouraged to reduce wild collection pressure. Collections for scientific use should adhere to applicable biosafety and data-access policies.

Synonyms Top

Scientific name Authority First published in
Epimedium hypoglaucum Maekawa ex Nakai J. Jap. Bot. 20: 82 (1944)
Epimedium macranthum var. hypoglaucum Makino J. Jap. Bot. 7: 13 1931
Epimedium grandiflorum subsp. sempervirens (Nakai ex F.Maek.) Kitam. Acta Phytotax. Geobot. 20: 202 (1962)

Common names Top

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Language Common/alternative name
Arabic أبيمديون دائم الخضرة
Japanese トキワイカリソウ

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
Epimedium sempervirens var. rugosum (Nakai) K.Suzuki Nippon no Ikariso : 162 (1990)
Epimedium sempervirens var. sempervirens Unknown

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000670085
UNII 5QWW17I0MZ
KEW urn:lsid:ipni.org:names:107316-1
The Plant List kew-2791342
Missouri Botanical Garden 277767
Open Tree Of Life 175137
NCBI Taxonomy 253615
IPNI 107316-1
iNaturalist 461020
GBIF 7300390
EPPO EPMSE
EOL 5516003
USDA GRIN 423400
CMAUP NPO13384

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
Flavonoid Compounds Contained in Epimedii Herba Inhibit Tumor Progression by Suppressing STAT3 Activation in the Tumor Microenvironment Pan C, Fujiwara Y, Horlad H, Shiraishi D, Iriki T, Tsuboki J, Ikeda T, Komohara Y Front Pharmacol 18-Mar-2020
PMCID:PMC7093601
doi:10.3389/fphar.2020.00262
PMID:32256354
A novel flavonol glycoside in the leaves of Epimedium sempervirens. Mizuo MIZUNO, Munekazu IINUMA, Toshiyuki TANAKA, Norio SAKAKIBARA, Tsutomu NAKANISHI, Akira INADA, Masatoshi NISHI Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.37.2241
New Flavonol Glycoside from the Leaves of Epimedium sempervirens Mizuo Mizuno, Munekazu Iinuma, Toshiyuki Tanaka, Norio Sakakibara American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50069A039
Flavonoids from Epimedium koreanum Sam Sik Kang, Yoon-Jung Kang, Myung-Whan Lee American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50074A029
Seven prenylated flavonol glycosides from two Epimedium species Toshio Fukai, Taro Nomura Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80627-7

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 / Aporphines
(+)-Magnoflorine 73337 Click to see 342.40 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
4-Hydroxyethylbenzoate 22257526 Click to see 165.17 unknown via CMAUP database
Benzoic Acid 243 Click to see 122.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 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 / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isoolivil 5316262 Click to see COC1=C(C=C2C(C(C(CC2=C1)(CO)O)CO)C3=CC(=C(C=C3)O)OC)O 376.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-) Syringaresinol 332426 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Syringaresinol 100067 Click to see 418.40 unknown via CMAUP database
Syringaresinol, (+)- 443023 Click to see 418.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
2-Dodecyl-3-Methylbutanedioic Acid 99891 Click to see CCCCCCCCCCCCC(C(C)C(=O)O)C(=O)O 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 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 via CMAUP database
Npc29 6432744 Click to see 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
CID 21952380 21952380 Click to see 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3S,4S,5S)-3-((E)-3-(3,4-Dihydroxyphenyl)Acryloyloxy)-1,4,5-Trihydroxycyclohexanecarboxylic Acid 12310830 Click to see 354.31 unknown via CMAUP database
3-O-Feruloylquinic acid 9799386 Click to see 368.30 unknown via CMAUP database
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
cis-Chlorogenic acid 1794425 Click to see 354.31 unknown via CMAUP database
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
An inositol 892 Click to see 180.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-Acuminatin 6441048 Click to see 340.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol 73160 Click to see 290.27 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
8-Prenylkaempferol 5318624 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C 354.40 unknown via CMAUP database
Epimedokoreanin B 21147600 Click to see CC(=CCC1=C(C(=CC(=C1)C2=CC(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)O)C 422.50 unknown via CMAUP database
Icaritin 5318980 Click to see 368.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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 via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44259091 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 via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11557027 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 via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl D-galactopyranoside 11751616 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 via CMAUP database
2''-O-Rhamnosylicariside II 5318987 Click to see 660.70 unknown via CMAUP database
5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[(1R,2R,3S,4R,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 92043064 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4CC(C(C(C4O)O)O)CO)O)C5=CC=C(C=C5)OC)O)O)O 674.70 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 162982903 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC=C(C=C4)O)O)O)O 500.50 unknown https://doi.org/10.1021/NP50074A029
5,7-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-3-((2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 44587252 Click to see 514.50 unknown via CMAUP database
5,7-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 162982443 Click to see 514.50 unknown https://doi.org/10.1016/0031-9422(88)80627-7
5,7-Dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbutyl)-4-oxo-4H-chromen-3-YL 6-deoxy-alpha-L-mannopyranoside 6852214 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CCC(C)C)C4=CC=C(C=C4)OC)O)O)O 516.50 unknown via CMAUP database
8-Prenylquercetin 4'-methyl ether 3-rhamnoside 44259411 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC(=C(C=C4)OC)O)O)O)O 530.50 unknown via CMAUP database
Afzelin 5316673 Click to see 432.40 unknown via CMAUP database
Baohuoside 1 44259054 Click to see 514.50 unknown via CMAUP database
baohuoside II 5481982 Click to see 500.50 unknown via CMAUP database
Baohuoside VII 5492427 Click to see 676.70 unknown via CMAUP database
CID 44259070 44259070 Click to see 718.70 unknown via CMAUP database
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 via CMAUP database
Icariin-II;Icariside-II 13964067 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C4=CC=C(C=C4)OC)O)O)O 514.50 unknown https://doi.org/10.1016/0031-9422(88)80627-7
Icariside Ii 5488822 Click to see 514.50 unknown https://doi.org/10.1016/0031-9422(88)80627-7
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
Sagittatoside A 13916054 Click to see 676.70 unknown via CMAUP database
Sagittatoside B 10146160 Click to see 646.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-4-oxo-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-7-yl]oxyoxan-3-yl] acetate 101396841 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)OC(=O)C)C5=CC=C(C=C5)OC)O)O)O 702.70 unknown via CMAUP database
[(2S,3S,4R,5S,6S)-4-[(2S,3S,4R,5R)-4-acetyloxy-3,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-6-[5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-4-oxo-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-2-methyloxan-3-yl] acetate 162894152 Click to see 892.80 unknown https://doi.org/10.1248/CPB.37.2241
[(2S,3S,4R,5S,6S)-5-hydroxy-6-[5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-2-methyl-4-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl] acetate 162924039 Click to see 850.80 unknown https://doi.org/10.1021/NP50069A039
[(2S,3S,4S,5R,6S)-4-[(2S,3R,4S,5R)-4-acetyloxy-3,5-dihydroxyoxan-2-yl]oxy-5-hydroxy-6-[5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-4-oxo-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-2-methyloxan-3-yl] acetate 14429512 Click to see 892.80 unknown https://doi.org/10.1248/CPB.37.2241
[4-(4-Acetyloxy-3,5-dihydroxyoxan-2-yl)oxy-5-hydroxy-6-[5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-4-oxo-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-3-yl]oxy-2-methyloxan-3-yl] acetate 14429511 Click to see 892.80 unknown https://doi.org/10.1248/CPB.37.2241
3,5-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14756216 Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)C 516.50 unknown via CMAUP database
3,5-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44259055 Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)OC)O)OC4C(C(C(C(O4)CO)O)O)O)C 530.50 unknown via CMAUP database
5-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 163026730 Click to see 662.60 unknown https://doi.org/10.1016/0031-9422(88)80627-7
5-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 44258788 Click to see 662.60 unknown https://doi.org/10.1016/0031-9422(88)80627-7
5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 99647392 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O 676.70 unknown https://doi.org/10.1016/0031-9422(88)80627-7
Anhydroicaritin-7-O-glucoside 14187155 Click to see 530.50 unknown via CMAUP database
CID 13964062 13964062 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)O)O)O)O 662.60 unknown https://doi.org/10.1016/0031-9422(88)80627-7
CID 44259076 44259076 Click to see 922.90 unknown via CMAUP database
Epimedin B 5748393 Click to see 808.80 unknown via CMAUP database
Epimedin C 5748394 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=C(C3=O)C(=CC(=C4CC=C(C)C)OC5C(C(C(C(O5)CO)O)O)O)O)C6=CC=C(C=C6)OC)C)O)O)O)O)O 822.80 unknown via CMAUP database
Epimedoside A 5317093 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)O)O)O)O 662.60 unknown https://doi.org/10.1016/0031-9422(88)80627-7
Epimedoside C 44258783 Click to see 516.50 unknown via CMAUP database
Hexandraside A 5748448 Click to see 838.80 unknown via CMAUP database
Hexandraside E 44258787 Click to see 678.60 unknown via CMAUP database
Hexandraside F 44259065 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)OC6C(C(C(C(O6)CO)O)O)O)O 838.80 unknown via CMAUP database
Icariin 5318997 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O 676.70 unknown https://doi.org/10.1016/0031-9422(88)80627-7
Icarin 5471129 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=CC(=C3CC=C(C)C)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC=C(C=C5)OC)O)O)O 676.70 unknown https://doi.org/10.1016/0031-9422(88)80627-7
Icariside I 5745470 Click to see 530.50 unknown via CMAUP database
Sagittasine C 101437362 Click to see 692.70 unknown via CMAUP database
Sempervirenoside A 44259074 Click to see 892.80 unknown https://doi.org/10.1248/CPB.37.2241
Sempervirenoside B 44259073 Click to see 850.80 unknown https://doi.org/10.1021/NP50069A039
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein 5281708 Click to see 254.24 unknown via CMAUP database

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