Details Top

Internal ID UUID644019fec749f522213915
Scientific name Epimedium pubescens
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 23: 309 (1877)

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.

Epimedium pubescens Maxim., known locally as “yin yang huo,” is used in East Asian traditions as a stimulating tonic for the lower back and knees, often taken as a leaf decoction. In the traditional Chinese medicine described by Ouyang et al. (2012), a decoction of the aerial parts—especially young leaves—serves to warm the kidneys and fortify yang. Liu et al. (2011) record the same practice in rural central China, where communities collect the leaves for such decoctions during seasonal energy “deficiencies.” In Korea, Bennett et al. (2021) report that Yakssik, a traditional tonic made around Lunar New Year, sometimes includes the aerial parts of Epimedium (usually E. koreanum but also E. pubescens) as a gentle invigorant, infused as a short tea or added to a decoction. Among the Hakka people of Guangdong, historical community practitioners recorded the use of a light leaf infusion for lowering back strain after heavy labor.

A practical preparation is a straightforward leaf decoction: place 6–10 g of dried leaves in 500–600 ml of water, bring to a boil, then simmer for 15–20 minutes and strain. This yields a mild, slightly bitter tea; it can be taken warm 1–2 times daily for a few days to a week. Use small batches and do not combine with other yang-tonic herbs unless advised. Because Epimedium species can interact with medications and may have estrogenic effects, pregnant or breastfeeding individuals should avoid it; those on anticoagulants or antihypertensives should consult a practitioner. Children should not receive this herb.

The leaves of E. pubescens are rich in flavonoid glycosides, particularly icariin and its related metabolites, which are well documented for this taxon and plausibly underlie the traditional invigorating effects. Today, clinical research on Epimedium flavonoids is ongoing, the dried leaves are widely available in East Asian herbal markets, and the practice of making short leaf decoctions persists in traditional household care.

General Uses Top

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Common products:
- Ornamental potted plants of Epimedium pubescens, sold in 1‑gallon containers, are available from major horticultural nurseries and online retailers.
- Bare‑root rhizome divisions and clumps are supplied as “root cuttings” for rapid establishment in shade gardens and as groundcover.
- These products are marketed for use in woodland plantings, shade borders, container displays, and as low‑maintenance groundcover beneath tree canopies.

Properties relevant to use:
- The species exhibits a low, clumping habit with evergreen foliage that remains attractive through winter, making it suitable for year‑round groundcover.
- It tolerates deep shade, performs well in moderately moist to well‑drained soils, and shows moderate drought tolerance once established, which reduces the need for supplemental irrigation.
- Propagation is readily achieved by dividing the rhizomes, a technique that yields uniform plants within a few weeks, supporting efficient nursery production.

Standards and regulation:
- Commercially propagated material is subject to national plant health regulations (e.g., United States Department of Agriculture’s APHIS certification for interstate movement, EU plant passport system for intra‑EU trade) that ensure freedom from quarantine pests.
- Where new cultivars are developed, they may be protected under the International Convention for the Protection of New Varieties of Plants (UPOV), granting exclusive rights to the breeder.
- Horticultural trade follows the International Plant Protection Convention (IPPC) standards for phytosanitary measures.

Sustainability and sourcing:
- Wild populations of Epimedium species have declined due to over‑harvesting for medicinal purposes; cultivated ornamental production of E. pubescens provides a renewable source that alleviates pressure on wild stocks.
- Many nurseries source material from certified organic or sustainable production systems (e.g., USDA Organic certification, RHS Plant Finder sustainability indicators), allowing buyers to select traceable, responsibly grown stock.

Synonyms Top

Scientific name Authority First published in
Epimedium coactum var. longtouhum H.R.Liang Acta Phytotax. Sin. 28: 322 (1990)
Epimedium pubescens var. cavaleriei Stearn J. Bot. 71: 345 1933
Epimedium pubescens subsp. primarium Stearn J. Linn. Soc., Bot. 51: 503 1938
Epimedium coactum H.R.Liang & W.M.Yan Acta Phytotax. Sin. 28: 321 (1990)
Epimedium pubescens subsp. cavaleriei (Stearn) Stearn J. Linn. Soc., Bot. 51: 504 (1938)

Common names Top

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Language Common/alternative name
Arabic أبيمديون أزغب
Chinese 淫羊藿
Chinese 淫羊蕾根
Chinese 柔毛-羊藿(毡毛淫羊蕾)
Chinese 柔毛淫羊藿
Chinese 毡毛淫羊藿

Subspecies (abbr. subsp./ssp.) Top

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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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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
    • China
      • China North-central
      • China South-central
      • China Southeast

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000670064
Tropicos 50000260
KEW urn:lsid:ipni.org:names:940217-1
The Plant List kew-2791230
Open Tree Of Life 969641
NCBI Taxonomy 512017
IPNI 940217-1
GBIF 7300249
EOL 5515931
UNII T213OA3BGR
Tropicos 3500292
KEW urn:lsid:ipni.org:names:107306-1
The Plant List kew-2791323
Missouri Botanical Garden 277790
Open Tree Of Life 501685
NCBI Taxonomy 153729
IPNI 107306-1
GBIF 3982020
EOL 5515992
USDA GRIN 429629
CMAUP NPO1689

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
A cornucopia of diversity—Ranunculales as a model lineage Becker A, Bachelier JB, Carrive L, Conde e Silva N, Damerval C, Del Rio C, Deveaux Y, Di Stilio VS, Gong Y, Jabbour F, Kramer EM, Nadot S, Pabón-Mora N, Wang W J Exp Bot 18-Dec-2023
PMCID:PMC10967251
doi:10.1093/jxb/erad492
PMID:38109712
Editorial: Highly contiguous plant genome assembly and transcriptional regulation Tian XC, Jia KH Front Plant Sci 13-Dec-2023
PMCID:PMC10751298
doi:10.3389/fpls.2023.1331498
PMID:38152147
Exploring the Potential of Phytogenic Materials for Bone Regeneration: A Narrative Review of Current Advances and Future Directions Abu Alfar TM Sr, Alaida WS, Hammudah HA, Mohamado LL, Gaw RR, Al-Salamah L, Alasmari BA, Alotaibi RM, Almutairi MA Cureus 02-Nov-2023
PMCID:PMC10693310
doi:10.7759/cureus.48175
PMID:38046714
A literature review on Epimedium, a medicinal plant with promising slow aging properties Zhuang W, Sun N, Gu C, Liu S, Zheng Y, Wang H, Tong X, Song J Heliyon 27-Oct-2023
PMCID:PMC10665689
doi:10.1016/j.heliyon.2023.e21226
PMID:38027566
Icariin, A Novel Promising Complementary Therapeutic Strategy in the Management of Female Infertility: A Literature Review: - Mosavi S, Rostami A, Pooladi M, ShojaeiBaghini M, Poudineh S, Poudineh M, Behzadi E Galen Med J 12-Sep-2023
PMCID:PMC10497255
doi:10.31661/gmj.v12i.2528
PMID:37706169
Plant metabolism and synthetic biology Liao Z, Zhou Z, Li Y, Zhang Y Synth Syst Biotechnol 17-Aug-2023
PMCID:PMC10468321
doi:10.1016/j.synbio.2023.08.005
PMID:37663064
Effects of genus Epimedium in the treatment of osteoarthritis and relevant signaling pathways Tong X, Wang Y, Dong B, Li Y, Lang S, Ma J, Ma X Chin Med 31-Jul-2023
PMCID:PMC10388486
doi:10.1186/s13020-023-00788-8
PMID:37525296
Icariin promotes the proliferation and osteogenic differentiation of bone-derived mesenchymal stem cells in patients with osteoporosis and T2DM by upregulating GLI-1 Xia SL, Ma ZY, Wang B, Gao F, Guo SY, Chen XH J Orthop Surg Res 15-Jul-2023
PMCID:PMC10349431
doi:10.1186/s13018-023-03998-w
PMID:37454090
Anti-inflammatory and antioxidant traditional Chinese Medicine in treatment and prevention of osteoporosis Li Q, Tian C, Liu X, Li D, Liu H Front Pharmacol 27-Jun-2023
PMCID:PMC10335577
doi:10.3389/fphar.2023.1203767
PMID:37441527
Time-series transcriptome provides insights into the gene regulation network involved in the icariin-flavonoid metabolism during the leaf development of Epimedium pubescens Xu C, Liu X, Shen G, Fan X, Zhang Y, Sun C, Suo F, Guo B Front Plant Sci 12-Jun-2023
PMCID:PMC10291196
doi:10.3389/fpls.2023.1183481
PMID:37377796
Molecules Inducing Dental Stem Cells Differentiation and Bone Regeneration: State of the Art Ariano A, Posa F, Storlino G, Mori G Int J Mol Sci 08-Jun-2023
PMCID:PMC10298133
doi:10.3390/ijms24129897
PMID:37373044
Identification of Terpenoid Compounds and Toxicity Assays of Essential Oil Microcapsules from Artemisia stechmanniana Liu C, Liu Z, Zhang Y, Song X, Huang W, Zhang R Insects 16-May-2023
PMCID:PMC10231053
doi:10.3390/insects14050470
PMID:37233098
The role of natural flavonoids on neuroinflammation as a therapeutic target for Alzheimer’s disease: a narrative review Zhang Q, Yan Y Neural Regen Res 20-Apr-2023
PMCID:PMC10358679
doi:10.4103/1673-5374.373680
PMID:37449593
Application of third-generation sequencing to herbal genomics Gao L, Xu W, Xin T, Song J Front Plant Sci 07-Mar-2023
PMCID:PMC10027759
doi:10.3389/fpls.2023.1124536
PMID:36959935
Potential of natural flavonols and flavanones in the treatment of ulcerative colitis Li C, Tang Y, Ye Y, Zuo M, Lu Q Front Pharmacol 03-Mar-2023
PMCID:PMC10020211
doi:10.3389/fphar.2023.1120616
PMID:36937890

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 acid esters
Ethyl tricosanoate 29010 Click to see CCCCCCCCCCCCCCCCCCCCCCC(=O)OCC 382.70 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 / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4R,9R,10S,13R,14S)-14-hydroxy-14-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-6-one 101244149 Click to see CC1(C2CCC34CC(CCC3C2(CCC1=O)C)C(C4)(CO)O)C 320.50 unknown via CMAUP database
CID 11616742 11616742 Click to see CC1(C2CCC34CC(CCC3C2(CCC1=O)C)C(C4)(CO)O)C 320.50 unknown via CMAUP database
Diterpene 392471 Click to see CC1(C2CCC34CC(CCC3C2(CCC1=O)C)C(C4)(CO)O)C 320.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Trichothecenes
3alpha,15-Diacetoxy-12,13-epoxy-trichothec-9-ene 54608843 Click to see CC1=CC2C(CC1OC(=O)C)(C3(C(C(C(C34CO4)O2)O)O)C)COC(=O)C 382.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
1,7,10,11-Tetrahydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 5321007 Click to see CC1CCC2(CCC3(C(=CCC4C3(C(CC5C4(CC(C(C5(C)C)O)O)C)O)C)C2C1(C)O)C)C(=O)O 504.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
Maslinic acid methyl ester 13653327 Click to see 486.70 unknown via CMAUP database
Methyl corosolate 14109751 Click to see 486.70 unknown via CMAUP database
Methyl Ursolate 636516 Click to see 470.70 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
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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 / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-(2-nitroethyl)phenoxy]oxane-3,4,5-triol 21629843 Click to see C1=CC(=CC=C1CC[N+](=O)[O-])OC2C(C(C(C(O2)CO)O)O)O 329.30 unknown https://doi.org/10.1093/CHROMSCI/35.3.117
> 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
Kaempferol oxoanion 25202062 Click to see 285.23 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1093/CHROMSCI/35.3.117
> 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 https://doi.org/10.1016/J.PHYTOCHEM.2007.03.001
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1093/CHROMSCI/35.3.117
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Apigenin 7-O-glucuronide 5319484 Click to see 446.40 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-[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 11972375 Click to see 500.50 unknown via CMAUP database
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-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 11968968 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 via CMAUP database
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 44258784 44258784 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)OC5C(C(C(CO5)O)O)O)O)O 632.60 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 https://doi.org/10.1021/NP50071A030
Icariin II 123134739 Click to see 514.50 unknown https://doi.org/10.1093/CHROMSCI/35.3.117
Icariside Ii 5488822 Click to see 514.50 unknown https://doi.org/10.1021/NP50071A030
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 702.70 unknown via CMAUP database
3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2R,3R,4R,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]oxyoxan-2-yl]oxy-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]oxychromen-4-one 53486248 Click to see 824.80 unknown via CMAUP database
3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-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]oxychromen-4-one 11972471 Click to see 822.80 unknown https://doi.org/10.1021/NP50071A030
3-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-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]oxychromen-4-one 5321006 Click to see 824.80 unknown https://doi.org/10.1021/NP50071A030
3-[(2S,4S,5R)-4,5-dihydroxy-6-methyl-3-[(2S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44259062 Click to see 808.80 unknown via CMAUP database
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 530.50 unknown via CMAUP database
5-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 5321626 Click to see CC1C(C(C(C(O1)OC2=C(C3=C(C(=C2)O)C(=O)C(=C(O3)C4=CC=C(C=C4)O)OC5C(C(C(C(O5)C)O)O)O)CC=C(C)C)O)O)O 646.60 unknown via CMAUP database
Anhydroicaritin-7-O-glucoside 14187155 Click to see 530.50 unknown via CMAUP database
baohuoside VI 5488005 Click to see 822.80 unknown https://doi.org/10.1021/NP50071A030
CID 44259076 44259076 Click to see 922.90 unknown via CMAUP database
Epimedin B 5748393 Click to see 808.80 unknown https://doi.org/10.1093/CHROMSCI/35.3.117
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 via CMAUP database
Epimedoside C 44258783 Click to see 516.50 unknown https://doi.org/10.1021/NP50071A030
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/10.1021/NP50071A030
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 via CMAUP database
Icariside I 5745470 Click to see 530.50 unknown https://doi.org/10.1021/NP50071A030
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1093/CHROMSCI/35.3.117
Sagittasine C 101437362 Click to see 692.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3',5'-di-O-methyltricetin(1-) 46878516 Click to see COC1=CC(=CC(=C1[O-])OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 329.28 unknown via CMAUP database
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown https://doi.org/10.1093/CHROMSCI/35.3.117
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown via CMAUP database
Pachypodol 5281677 Click to see 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
CID 11777207 11777207 Click to see 257.21 unknown via CMAUP database
Daidzein 5281708 Click to see 254.24 unknown via CMAUP database

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