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Epimedium acuminatum

Epimedium acuminatum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID644019f9917e9464848191
Scientific name Epimedium acuminatum
Authority Franch.
First published in Bull. Soc. Bot. France 33: 109 (1886)

Description Top

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Epimedium acuminatum, also known as the acuminate barrenwort, is a type of flowering plant found in southern and southeastern China. It is part of the Epimedium genus and has been recognized by the Royal Horticultural Society with the Award of Garden Merit.

Synonyms Top

Scientific name Authority First published in
Epimedium chlorandrum Stearn Kew Bull. 52: 660 (1997)
Epimedium komarovii H.Lév. Repert. Spec. Nov. Regni Veg. 7: 259 (1909)
Epimedium simplicifolium T.S.Ying Acta Phytotax. Sin. 13(2): 51 (1975)

Common names Top

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Language Common/alternative name
Arabic أبيمديون مستدق
Chinese 大花柳叶菜
Chinese 粗毛淫羊藿

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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-0000669946
Tropicos 3500294
KEW urn:lsid:ipni.org:names:107259-1
The Plant List kew-2791211
Missouri Botanical Garden 277792
Open Tree Of Life 175152
NCBI Taxonomy 253612
IPNI 107259-1
GBIF 3981102
EOL 5515918
USDA GRIN 405334
Wikipedia Epimedium_acuminatum

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
Dietary Supplements for Erectile Dysfunction: Analysis of Marketed Products, Systematic Review, Meta-Analysis and Rational Use Petre GC, Francini-Pesenti F, Vitagliano A, Grande G, Ferlin A, Garolla A Nutrients 22-Aug-2023
PMCID:PMC10490034
doi:10.3390/nu15173677
PMID:37686709
Functional and chemical properties of Phoenix dactylifera l. Polysaccharides and the effect of date flesh and seed intervention on some blood biomarkers: A contrastive analysis Noorbakhsh H, Rabbani Khorasgani M Food Chem X 09-Aug-2023
PMCID:PMC10534174
doi:10.1016/j.fochx.2023.100834
PMID:37780309
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
Network pharmacology implicates traditional Chinese medicine in regulating systemic homeostasis to benefit Alzheimer’s disease Tsai ST, Huang HY Tzu Chi Med J 13-Feb-2023
PMCID:PMC10227678
doi:10.4103/tcmj.tcmj_125_22
PMID:37261294
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
Untargeted metabolomics analysis of the hippocampus and cerebral cortex identified the neuroprotective mechanisms of Bushen Tiansui formula in an aβ25-35-induced rat model of Alzheimer’s disease Li H, Tan Y, Cheng X, Zhang Z, Huang J, Hui S, Zhu L, Liu Y, Zhao D, Liu Z, Peng W Front Pharmacol 20-Oct-2022
PMCID:PMC9630565
doi:10.3389/fphar.2022.990307
PMID:36339577
New 8-prenylated quercetin glycosides from the flowers of Epimedium acuminatum and their testosterone production-promoting activities Zhang Y, Zhang C, Li Z, Zeng C, Xue Z, Li E, Li G, Li J, Shen G, Xu C, Wang Y, Ma B, Zhang H, Guo B Front Chem 10-Oct-2022
PMCID:PMC9588921
doi:10.3389/fchem.2022.1014110
PMID:36300020
Two Polysaccharides from Liupao Tea Exert Beneficial Effects in Simulated Digestion and Fermentation Model In Vitro Qiu S, Huang L, Xia N, Teng J, Wei B, Lin X, Khan MR Foods 21-Sep-2022
PMCID:PMC9564304
doi:10.3390/foods11192958
PMID:36230033
Distribution of Therapeutic Efficacy of Ranunculales Plants Used by Ethnic Minorities on the Phylogenetic Tree of Chinese Species Hao DC, Zhang Y, He CN, Xiao PG Evid Based Complement Alternat Med 12-Jan-2022
PMCID:PMC8769838
doi:10.1155/2022/9027727
PMID:35069772
Cellular and Molecular Mechanism of Traditional Chinese Medicine on Ventricular Remodeling Zhu YC, Liang B, Gu N Front Cardiovasc Med 01-Dec-2021
PMCID:PMC8671630
doi:10.3389/fcvm.2021.753095
PMID:34926607
Herbal plants traded at the Kaili medicinal market, Guizhou, China Liu S, Zhang B, Zhou J, Lei Q, Fang Q, Kennelly EJ, Long C J Ethnobiol Ethnomed 29-Nov-2021
PMCID:PMC8628420
doi:10.1186/s13002-021-00495-4
PMID:34844607
The Anti-Inflammatory Effect of a Combination of Five Compounds From Five Chinese Herbal Medicines Used in the Treatment of COPD Li J, Zhao P, Tian Y, Li K, Zhang L, Guan Q, Mei X, Qin Y Front Pharmacol 27-Oct-2021
PMCID:PMC8578279
doi:10.3389/fphar.2021.709702
PMID:34776947
Prebiotic, Antioxidant, and Immunomodulatory Properties of Acidic Exopolysaccharide From Marine Rhodotorula RY1801 Wang Z, Zhao Y, Jiang Y, Chu W Front Nutr 23-Aug-2021
PMCID:PMC8419279
doi:10.3389/fnut.2021.710668
PMID:34497821
Ethnobotanical study on herbal market at the Dragon Boat Festival of Chuanqing people in China Wang Q, Zhao L, Gao C, Zhao J, Ren Z, Shen Y, Yao R, Yin H J Ethnobiol Ethnomed 23-Mar-2021
PMCID:PMC7985747
doi:10.1186/s13002-021-00447-y
PMID:33757555
The complete chloroplast genome of Stephania tetrandra (Menispermaceae) Cao L, Mu Z, Sheng S, Chen Y, Zhong G, Du X Mitochondrial DNA B Resour 24-Dec-2020
PMCID:PMC7759292
doi:10.1080/23802359.2020.1840935
PMID:33426289

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
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
Icaritin 5318980 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=CC=C(C=C3)OC)O)C 368.40 unknown https://doi.org/10.1021/NP50096A021
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.03.001
> 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/10.1021/NP50096A021
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
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 CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3=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 822.80 unknown https://doi.org/10.1021/NP50096A021
5-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 44258935 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 578.50 unknown https://doi.org/10.1021/NP50083A019
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 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/10.1021/NP50083A019
7-[(2S,3R,4S,5S,6S)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one 163077257 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)OC5C(C(C(C(O5)CO)O)O)O)O)O)C 692.70 unknown https://doi.org/10.1021/NP50096A021
7-[(2S,3R,4S,5S,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3-[(2S,3S,4R,5R,6S)-4,5-dihydroxy-6-methyl-3-[(2S,3S,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)chromen-4-one 163105309 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)OC6C(C(C(C(O6)CO)O)O)O)O)C7=CC=C(C=C7)OC)C)O)O)O)O)O 984.90 unknown https://doi.org/10.1021/NP50083A019
7-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3-[4,5-dihydroxy-6-methyl-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)chromen-4-one 5748502 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)OC6C(C(C(C(O6)CO)O)O)O)O)C7=CC=C(C=C7)OC)C)O)O)O)O)O 984.90 unknown https://doi.org/10.1021/NP50083A019
Acuminatoside 44259068 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)OC6C(C(C(C(O6)CO)O)O)O)O)C7=CC=C(C=C7)OC)C)O)O)O)O)O 984.90 unknown https://doi.org/10.1021/NP50083A019
Baohuoside VI 5488005 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/10.1021/NP50096A021
Cuhuoside 44259061 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)OC5C(C(C(C(O5)CO)O)O)O)O)O)C 692.70 unknown https://doi.org/10.1021/NP50096A021
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/10.1021/NP50083A019
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/NP50083A019
https://doi.org/10.1021/NP50096A021
Icariside I 5745470 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 https://doi.org/10.1021/NP50096A021
> 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/10.1021/NP50096A021

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