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Berberis fortunei

Berberis fortunei - 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 UUID64400cb6dea3f565364347
Scientific name Berberis fortunei
Authority Lindl.
First published in J. Hort. Soc. London 1: 231 (1846)

Description Top

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Synonyms Top

Scientific name Authority First published in
Mahonia fortunei Fedde Bot. Jahrb. Syst. 31: 130 (1901)
Berberis fortunei var. szechuanica (Ahrendt) Laferr. Bot. Zhurn. (Moscow & Leningrad) 82(9): 97. 1997 [19 Nov 1997]
Mahonia fortunei var. szechuanica Ahrendt J. Linn. Soc., Bot. 57: 328 1961
Mahonia tikushiensis Hayata Icon. Pl. Formosan. 5: 5 (1915)

Common names Top

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Language Common/alternative name
Indonesian kayu ni
Japanese ホソバヒイラギナンテン
Chinese 狭叶十大功劳
Chinese 细叶十大功劳
Chinese 十大功劳

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 South-central
      • China Southeast
    • Eastern Asia
      • Korea
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000563161
UNII XM51FFR4ES
Tropicos 50193470
KEW urn:lsid:ipni.org:names:106663-1
Open Tree Of Life 854430
NCBI Taxonomy 258162
IPNI 106663-1
GBIF 7300364
Freebase /m/0gmg887
Elurikkus 585099
USDA GRIN 6860
CMAUP NPO11640
Wikipedia Berberis_fortunei

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
Potential usage of biosynthesized zinc oxide nanoparticles from mangosteen peel ethanol extract to inhibit Xanthomonas oryzae and promote rice growth Jaithon T, Atichakaro T, Phonphoem W, T-Thienprasert J, Sreewongchai T, T-Thienprasert NP Heliyon 07-Jan-2024
PMCID:PMC10792570
doi:10.1016/j.heliyon.2024.e24076
PMID:38234900
Recent Advances in Chemistry and Bioactivities of Secondary Metabolites from the Genus Acremonium Qin Y, Lu H, Qi X, Lin M, Gao C, Liu Y, Luo X J Fungi (Basel) 03-Jan-2024
PMCID:PMC10820033
doi:10.3390/jof10010037
PMID:38248947
Preliminary exploration of herbal tea products based on traditional knowledge and hypotheses concerning herbal tea selection: a case study in Southwest Guizhou, China Long X, Ranjitkar S, Waldstein A, Wu H, Li Q, Geng Y J Ethnobiol Ethnomed 02-Jan-2024
PMCID:PMC10763305
doi:10.1186/s13002-023-00645-w
PMID:38169414
Biological Activity and Structural Diversity of Steroids Containing Aromatic Rings, Phosphate Groups, or Halogen Atoms Dembitsky VM Molecules 20-Jul-2023
PMCID:PMC10384810
doi:10.3390/molecules28145549
PMID:37513423
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Editorial: Nanomaterials to combat pathogenic microorganisms Alavi M, Kahrizi D, Martinez F, Rai M Front Microbiol 13-Apr-2023
PMCID:PMC10135854
doi:10.3389/fmicb.2023.1160196
PMID:37125191
Determination of Selected Isoquinoline Alkaloids from Chelidonium majus, Mahonia aquifolium and Sanguinaria canadensis Extracts by Liquid Chromatography and Their In Vitro and In Vivo Cytotoxic Activity against Human Cancer Cells Tuzimski T, Petruczynik A, Plech T, Kaproń B, Makuch-Kocka A, Szultka-Młyńska M, Misiurek J, Buszewski B, Waksmundzka-Hajnos M Int J Mol Sci 28-Mar-2023
PMCID:PMC10093986
doi:10.3390/ijms24076360
PMID:37047332
Secondary metabolites from the Endophytic fungi Fusarium decemcellulare F25 and their antifungal activities Song Z, Sun YJ, Xu S, Li G, Yuan C, Zhou K Front Microbiol 01-Feb-2023
PMCID:PMC9929939
doi:10.3389/fmicb.2023.1127971
PMID:36819056
Natural Inhibitors of Cholinesterases: Chemistry, Structure–Activity and Methods of Their Analysis Smyrska-Wieleba N, Mroczek T Int J Mol Sci 01-Feb-2023
PMCID:PMC9916849
doi:10.3390/ijms24032722
PMID:36769043
Key insights into secondary metabolites from various Chaetomium species Dwibedi V, Rath SK, Jain S, Martínez-Argueta N, Prakash R, Saxena S, Rios-Solis L Appl Microbiol Biotechnol 17-Jan-2023
PMCID:PMC9843691
doi:10.1007/s00253-023-12365-y
PMID:36648526
Visual preference of plant features in different living environments using eye tracking and EEG Ding N, Zhong Y, Li J, Xiao Q, Zhang S, Xia H PLoS One 30-Dec-2022
PMCID:PMC9803246
doi:10.1371/journal.pone.0279596
PMID:36584138
A novel ambigrammatic mycovirus, PsV5, works hand in glove with wheat stripe rust fungus to facilitate infection Zhang Y, Liang X, Zhao M, Qi T, Guo H, Zhao J, Zhao J, Zhan G, Kang Z, Zheng L Plant Commun 15-Dec-2022
PMCID:PMC10203264
doi:10.1016/j.xplc.2022.100505
PMID:36527233
Metabolic Profiling for the Discovery of Structurally Diverse Gibberellins and Their Precursors from the Endophytic Fungus Fusarium sp. NJ-F5 Wang K, Peng XP, Feng D, Tian C, Wan WL, Lou HX, Li G ACS Omega 03-Dec-2022
PMCID:PMC9753110
doi:10.1021/acsomega.2c06454
PMID:36530227
Phylogenomics, plastome structure and species identification in Mahonia (Berberidaceae) Tong R, Gui C, Zhang Y, Su N, Hou X, Liu M, Yang Z, Kang B, Chang Z, Jabbour F, Zhao L BMC Genomics 23-Nov-2022
PMCID:PMC9682747
doi:10.1186/s12864-022-08964-0
PMID:36418947
Green synthesis of silver nanoparticles from Mahonia fortunei extracts and characterization of its inhibitory effect on Chinese cabbage soft rot pathogen Wei Z, Xu S, Jia H, Zhang H Front Microbiol 21-Oct-2022
PMCID:PMC9635054
doi:10.3389/fmicb.2022.1030261
PMID:36338072

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 C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C 342.40 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
16,17-Dimethoxy-6-tritio-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaene 10246509 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 338.40 unknown via CMAUP database
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown via CMAUP database
Jatrorrhizine 72323 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)O)OC)OC 338.40 unknown via CMAUP database
Palmatine 19009 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)OC)OC 352.40 unknown via CMAUP database
> Benzenoids / Anthracenes
Palmidin A 5320384 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2C4C5=C(C(=CC=C5)O)C(=O)C6=C4C=C(C=C6O)CO)C=C(C=C3O)O 510.50 unknown via CMAUP database
> Lignans, neolignans and related compounds
(-)-Repandine 10031631 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC 608.70 unknown via CMAUP database
(1S,14R)-20,21,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),18,20,22(33),24,26,31-dodecaen-6-ol 5320345 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC 608.70 unknown via CMAUP database
Berbamine 275182 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown via CMAUP database
Oxyacanthine 442333 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC 608.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3As,6r,6ar,9r,9as,9bs)-6,9-dihydroxy-6,9-dimethyl-3-methylidene-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[5,4-d]furan-2-one 5319198 Click to see CC1(CCC2C(C3C1CCC3(C)O)OC(=O)C2=C)O 266.33 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
21,22,26-Trimethoxy-16,31-dimethyl-8,24-dioxa-16,31-diazaheptacyclo[23.6.2.13,7.19,13.115,19.028,32.023,34]hexatriaconta-3(36),4,6,9,11,13(35),19,21,23(34),25,27,32-dodecaen-10-ol 45356938 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=CC=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 10065647 Click to see COC1=C(C2=CN3CCC4=CC(=O)C(=CC4=C3C=C2C=C1)OC)OC 337.40 unknown https://doi.org/10.1016/S0031-6865(99)00061-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Oxyayanin A 5281676 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3O)OC)O)O 360.30 unknown via CMAUP database

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