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Epimedium hunanense

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644019fc2d3e8071919448
Scientific name Epimedium hunanense
Authority (Hand.-Mazz.) Hand.-Mazz.
First published in Symb. Sin. 7: 324 (1931)

Description Top

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Synonyms Top

Scientific name Authority First published in
Epimedium davidii var. hunanense Hand.-Mazz. Anz. Akad. Wiss. Wien, Math.-Naturwiss. Kl. 62: 131 1925
Epimedium kunawarense S.Clay Present-Day Rock Garden : 209 (1937)

Common names Top

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Language Common/alternative name
Chinese 湖南淫羊藿

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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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-0000670002
Tropicos 50064799
KEW urn:lsid:ipni.org:names:107281-1
The Plant List kew-2791264
Open Tree Of Life 301958
NCBI Taxonomy 471939
IPNI 107281-1
GBIF 3982313
EOL 5515957

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
Comparative analysis of codon usage patterns in chloroplast genomes of ten Epimedium species Wang Y, Jiang D, Guo K, Zhao L, Meng F, Xiao J, Niu Y, Sun Y BMC Genom Data 09-Jan-2023
PMCID:PMC9830715
doi:10.1186/s12863-023-01104-x
PMID:36624369
Isolation and immunomodulatory effect of flavonol glycosides from Epimedium hunanense. Liang HR, Vuorela P, Vuorela H, Hiltunen R Planta Med 01-Aug-1997
doi:10.1055/S-2006-957690
PMID:9270375
Characterization of flavonoids in extracts from four species of Epimedium by micellar electrokinetic capillary chromatography with diode-array detection. Liang HR, Sirén H, Jyske P, Reikkola ML J Chromatogr Sci 01-Mar-1997
doi:10.1093/CHROMSCI/35.3.117
PMID:9182124

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Thalictoside 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/10.1055/S-2006-957690
> 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 https://doi.org/10.1055/S-2006-957690
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Baohuoside I 5488822 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/10.1055/S-2006-957690
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/10.1093/CHROMSCI/35.3.117
https://doi.org/10.1055/S-2006-957690
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
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 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 https://doi.org/10.1055/S-2006-957690
https://doi.org/10.1093/CHROMSCI/35.3.117
Epimedin B 5748393 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(CO6)O)O)O)O)O 808.80 unknown https://doi.org/10.1055/S-2006-957690
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/10.1055/S-2006-957690
https://doi.org/10.1093/CHROMSCI/35.3.117
> 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 https://doi.org/10.1055/S-2006-957690

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