Details Top

Internal ID UUID644019fa901ee958615625
Scientific name Epimedium diphyllum
Authority G.Lodd.
First published in Bot. Mag. 62: t. 3448. 1835 [1 Nov 1835]

Ethnobotanical Use Top

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General Uses Top

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Common products:
Live ornamental potted plants of Epimedium diphyllum are sold by specialist nurseries for garden planting in shade and woodland settings. The whole plant, propagated by division of mature clumps or by seed that requires cold stratification, serves as a low‑maintenance groundcover, in mixed borders, and in containers for seasonal display. Nurseries also offer selected clones with uniform foliage or flower color for commercial sale. Fresh or dried stems and foliage are marketed to the floristry trade for use in fresh and dried floral arrangements.

Industrial and craft applications:
Dried stems and foliage of E. diphyllum are incorporated into floral craft, dried‑flower compositions, wreath making, and potpourri; the fine‑textured, glossy leaves and persistent pinkish‑white flower color after drying enable these craft uses. No further industrial processing beyond horticultural propagation is documented.

Food and beverages (non‑medicinal):
No documented culinary use.

Colorants and tanning:
No documented use as a dye or tannin source.

Wood and fiber:
No timber or fiber product is recorded.

Fragrance and cosmetics:
No fragrance or cosmetic application is reported.

Properties relevant to use:
The species forms a compact, semi‑evergreen mound 10–30 cm tall with heart‑shaped, glossy leaves 2–5 cm long that retain ornamental value throughout the growing season. Stems are slender and maintain their shape when dried, facilitating craft use. Flowers are small, pinkish‑white to pale yellow, appearing in early spring, and retain color after drying. Shade tolerance and winter hardiness (USDA zones 5–9) make it suitable for low‑light garden positions, while the plant’s rhizomatous growth habit enables rapid propagation by division.

Standards and regulation:
Trade of live Epimedium diphyllum plants is regulated under the International Plant Protection Convention (IPPC) and national phytosanitary frameworks such as the EU Plant Health Directive (2000/29/EC) and the United States Animal and Plant Health Inspection Service (APHIS). Nursery production follows national ornamental plant standards for labeling, quarantine, and disease certification.

Sustainability and sourcing:
Commercial material originates almost exclusively from controlled nursery propagation; wild collection is discouraged to protect native populations. Sustainable practices include propagation by division or tissue culture, avoidance of synthetic chemical inputs, and use of locally sourced, peat‑free substrates. The species is not listed as threatened, but its commercial production is managed to prevent any impact on wild stands.

Synonyms Top

Scientific name Authority First published in
Aceranthus diphyllus C.Morren & Decne. Ann. Sci. Nat., Bot. , sér. 2, 2: 350 (1834)
Epimedium japonicum Siebold ex Miq. Ann. Mus. Bot. Lugduno-Batavi 2: 71 (1865)

Common names Top

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Language Common/alternative name
Arabic أبيمديون ثنائي الورق
Japanese バイカイカリソウ

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Epimedium diphyllum subsp. kitamuranum (Yamanaka) K.Suzuki J. Jap. Bot. 57: 68 (1982)
Epimedium diphyllum subsp. diphyllum Unknown

Varieties (abbr. var.) Top

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No variety added yet.

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000669977
KEW urn:lsid:ipni.org:names:107274-1
The Plant List kew-2791240
Missouri Botanical Garden 277795
Open Tree Of Life 749541
NCBI Taxonomy 253601
IPNI 107274-1
GBIF 7300237
EOL 5515939
Elurikkus 658366
USDA GRIN 435108

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
Characterization of Four New Compounds from Protea cynaroides Leaves and Their Tyrosinase Inhibitory Potential Yalo M, Makhaba M, Hussein AA, Sharma R, Koki M, Nako N, Mabusela WT Plants (Basel) 30-Jun-2022
PMCID:PMC9269349
doi:10.3390/plants11131751
PMID:35807702
LaPT2 Gene Encodes a Flavonoid Prenyltransferase in White Lupin Liu J, Xia Y, Jiang W, Shen G, Pang Y Front Plant Sci 11-Jun-2021
PMCID:PMC8226212
doi:10.3389/fpls.2021.673337
PMID:34177989
Natural drug sources for respiratory diseases from Fritillaria: chemical and biological analyses Wang Y, Hou H, Ren Q, Hu H, Yang T, Li X Chin Med 31-May-2021
PMCID:PMC8165352
doi:10.1186/s13020-021-00450-1
PMID:34059098
Metabolic engineering Escherichia coli for efficient production of icariside D2 Liu X, Li L, Liu J, Qiao J, Zhao GR Biotechnol Biofuels 06-Nov-2019
PMCID:PMC6833136
doi:10.1186/s13068-019-1601-x
PMID:31709010
Flavonol glycosides in Epimedium species. MIZUO MIZUNO, MUNEKAZU IINUMA, TOSHIYUKI TANAKA, NORIO SAKAKIBARA, SAKURA HANIOKA, XIN-SHUN LIU Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.36.3487
Flavonol glycoside production in callus cultures of Epimedium diphyllum H Yamamoto Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80170-J
Flavonol glycosides in the roots of Epimedium diphyllum Mizuo Mizuno, Munekazu Iinuma, Toshiyuki Tanaka, Norio Sakakibara, Takudai Fujikawa, Sakura Hanioka, Yuka Ishida, Xin-Shun Liu, Hiroko Murata Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80784-2
Ionone and lignan glycosides from Epimedium diphyllum Toshio Miyase, Akira Ueno, Nobuo Takizawa, Hiromi Kobayashi, Hiroko Oguchi Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80369-3
A flavonol glycoside from Epimedium diphyllum Mizuo Mizuno, Munekazu Iinuma, Toshiyuki Tanaka, Norio Sakakibara, Masatoshi Nishi, Akira Iinada, Tsutomu Nakanishi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)98026-9

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
> 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 https://doi.org/10.1016/0031-9422(89)80369-3
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5R)-2-[[(1S,2R,3R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-3-(hydroxymethyl)-6,8-dimethoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 14521039 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)COC4C(C(C(CO4)O)O)O 552.60 unknown https://doi.org/10.1016/0031-9422(89)80369-3
Nudiposide 14521040 Click to see 552.60 unknown https://doi.org/10.1016/0031-9422(89)80369-3
> 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/10.1016/0031-9422(89)80369-3
> 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/10.1016/0031-9422(89)80369-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
Icaritin 5318980 Click to see 368.40 unknown https://doi.org/10.1016/0031-9422(88)80784-2
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4R,5S,6S)-2-[5,7-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-4-oxochromen-3-yl]oxy-5-hydroxy-6-methyl-3-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl] acetate 133562578 Click to see 718.70 unknown https://doi.org/10.1248/CPB.36.3487
3-((3R,4R,5R,6S)-4,5-Dihydroxy-6-methyl-3-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yloxy)-5,7-dihydroxy-2-(4-hydroxy-phenyl)-8-(3-methyl-but-2-enyl)-1-benzopyran-4-one 5481981 Click to see 662.60 unknown https://doi.org/10.1248/CPB.36.3487
3-[(2S,3R,4S,5R)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one 5318413 Click to see 632.60 unknown https://doi.org/10.1248/CPB.36.3487
3-[(2S,3S,5R)-4,5-dihydroxy-6-methyl-3-[(2S,3R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one 44258785 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(C(O5)CO)O)O)O)O)O 662.60 unknown https://doi.org/10.1248/CPB.36.3487
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 14185727 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)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/S0031-9422(00)98026-9
3-[4,5-dihydroxy-6-methyl-3-[(2R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one 137705382 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 https://doi.org/10.1248/CPB.36.3487
3-[4,5-dihydroxy-6-methyl-3-[(2R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one 138114684 Click to see 646.60 unknown https://doi.org/10.1248/CPB.36.3487
baohuoside II 5481982 Click to see 500.50 unknown https://doi.org/10.1248/CPB.36.3487
Icariside Ii 5488822 Click to see 514.50 unknown https://doi.org/10.1248/CPB.36.3487
ikarisoside D 44258796 Click to see 542.50 unknown https://doi.org/10.1248/CPB.36.3487
Sagittatoside A 13916054 Click to see 676.70 unknown https://doi.org/10.1248/CPB.36.3487
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3-((2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl)oxy-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 11972345 Click to see 822.80 unknown https://doi.org/10.1248/CPB.36.3487
https://doi.org/10.1016/0031-9422(92)80170-J
3-[(2R,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-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 162918290 Click to see 808.80 unknown https://doi.org/10.1016/0031-9422(88)80784-2
3-[(2R,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2R,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 122173198 Click to see 822.80 unknown https://doi.org/10.1016/0031-9422(88)80784-2
3-[(2R,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-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 162990306 Click to see 794.70 unknown https://doi.org/10.1016/0031-9422(88)80784-2
3-[(2R,3R,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(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 162944697 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)OC6C(C(C(C(O6)CO)O)O)O)O)O 824.80 unknown https://doi.org/10.1016/0031-9422(88)80784-2
3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-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 5318412 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)O)CO)O)O)O)O)O 824.80 unknown https://doi.org/10.1016/0031-9422(92)80170-J
3-[(2S,3S,5R)-4,5-dihydroxy-6-methyl-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44258792 Click to see 808.80 unknown https://doi.org/10.1016/0031-9422(92)80170-J
https://doi.org/10.1248/CPB.36.3487
https://doi.org/10.1016/0031-9422(88)80784-2
3-[(2S,4S,5R)-4,5-dihydroxy-6-methyl-3-[(2S,5S)-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,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44258791 Click to see 824.80 unknown https://doi.org/10.1016/0031-9422(92)80170-J
3-[4,5-Dihydroxy-6-methyl-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14187151 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)O)C)O)O)O)O)O 808.80 unknown https://doi.org/10.1016/0031-9422(88)80784-2
3-[4,5-Dihydroxy-6-methyl-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 10350361 Click to see 794.70 unknown https://doi.org/10.1016/0031-9422(88)80784-2
3-[4,5-dihydroxy-6-methyl-3-[(2S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 137705275 Click to see 822.80 unknown https://doi.org/10.1016/0031-9422(88)80784-2
https://doi.org/10.1016/S0031-9422(00)98026-9
https://doi.org/10.1016/0031-9422(92)80170-J
https://doi.org/10.1248/CPB.36.3487
3-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11765972 Click to see 824.80 unknown https://doi.org/10.1016/0031-9422(88)80784-2
3-[4,5-Dihydroxy-6-methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13916050 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)OC6C(C(C(C(O6)CO)O)O)O)O)O 838.80 unknown https://doi.org/10.1248/CPB.36.3487
https://doi.org/10.1016/0031-9422(92)80170-J
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)80784-2
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/10.1248/CPB.36.3487
https://doi.org/10.1016/0031-9422(92)80170-J
https://doi.org/10.1016/0031-9422(88)80784-2
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)80784-2
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)80784-2
Diphylloside C 44258794 Click to see 986.90 unknown https://doi.org/10.1016/S0031-9422(00)98026-9
Epimedin B 5748393 Click to see 808.80 unknown https://doi.org/10.1248/CPB.36.3487
https://doi.org/10.1016/0031-9422(92)80170-J
https://doi.org/10.1016/S0031-9422(00)98026-9
Epimedin-C;Baohuoside-VI 13916066 Click to see 822.80 unknown https://doi.org/10.1016/0031-9422(88)80784-2
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/10.1248/CPB.36.3487
https://doi.org/10.1016/0031-9422(92)80170-J
https://doi.org/10.1016/0031-9422(88)80784-2
Epimedoside E 44258790 Click to see 794.70 unknown https://doi.org/10.1016/0031-9422(92)80170-J
https://doi.org/10.1016/0031-9422(88)80784-2
https://doi.org/10.1248/CPB.36.3487
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(92)80170-J
https://doi.org/10.1016/S0031-9422(00)98026-9
https://doi.org/10.1248/CPB.36.3487
https://doi.org/10.1016/0031-9422(88)80784-2
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)80784-2
Icariside I 5745470 Click to see 530.50 unknown https://doi.org/10.1248/CPB.36.3487

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