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Berberis amurensis

Berberis amurensis - 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 UUID64400ca18dea8933707686
Scientific name Berberis amurensis
Authority Rupr.
First published in Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 15: 260 (1857)

Description Top

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Synonyms Top

Scientific name Authority First published in
Berberis amurensis f. bretschneideri (Rehder) Ohwi Bull. Natl. Sci. Mus. Tokyo 33: 72 1953
Berberis amurensis var. brevifolia Nakai Bot. Mag. (Tokyo) 43: 441 1929
Berberis amurensis f. brevifolia (Nakai) Ohwi Bull. Natl. Sci. Mus. Tokyo 33: 72 1953
Berberis amurensis var. japonica (Regel) Rehder Stand. Cycl. Hort. 1: 154 (1914)
Berberis amurensis var. latifolia Nakai J. Coll. Sci. Imp. Univ. Tokyo 26(1): 41 1909
Berberis amurensis f. latifolia (Nakai) W.Lee Lineamenta Florae Koreae 350. 1996
Berberis amurensis var. licentii Ahrendt J. Linn. Soc., Bot. 57: 194 1961
Berberis bretschneideri Rehder Trees & Shrubs 2: 21 (1907)
Berberis japonica Schneider Bull. Herb. Boissier Ser. II. v. 667.
Berberis quelpaertensis Nakai Bot. Mag. (Tokyo) 27: 31 (1913)
Berberis regeliana Koehne ex C.K.Schneid. Mitt. Deutsch. Dendrol. Ges. 14: 119 (1905)
Berberis vulgaris var. japonica Regel Trudy Imp. S.-Peterburgsk. Bot. Sada 2: 415 (1873)
Berberis vulgaris var. amurensis (Rupr.) Regel Tent. Fl. Ussur. 46 1861
Berberis amurensis var. quelpaertensis (Nakai) Nakai Fl. Sylv. Kor. 21: 71 (1936)

Common names Top

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Language Common/alternative name
English amur barberry
Azerbaijani amur zirinci
Belarusian барбарыс амурскі
Bulgarian амурски кисел трън
German amur-berberitze
Estonian amuuri kukerpuu
Persian زرشک آمور
Armenian Կծոխուր ամուրյան
Icelandic drekabroddur
Japanese ヒロハヘビノボラズ
Korean 매발톱나무
Dutch siberische zuurbes
Russian Барбарис амурский
Chinese 黄芦木（大叶小檗、小檗）
Chinese 大叶小檗
Chinese 黄芦木
Chinese 小檗

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 Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
      • Sakhalin

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000562758
UNII 5T3GDO3TJX
Tropicos 3500198
KEW urn:lsid:ipni.org:names:106405-1
The Plant List kew-2673404
PFAF Berberis amurensis
Open Tree Of Life 803512
Observations.org 115501
NCBI Taxonomy 258140
IPNI 106405-1
iNaturalist 543766
GBIF 7300239
Freebase /m/0105lk4y
EPPO BEBAM
EOL 5514484
Elurikkus 3070
USDA GRIN 6810
Wikipedia Berberis_amurensis
CMAUP NPO18295

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
Effect of Oregon grape root extracts on P-glycoprotein mediated transport in in vitro cell lines Fan Y, Zhou Z, Zhang L J Pharm Pharm Sci 18-Jan-2024
PMCID:PMC10830684
doi:10.3389/jpps.2023.11927
PMID:38304488
Pharmacological profiling of a berbamine derivative for lymphoma treatment Xu S, Wu S, Zhang M, Xie J, Lin M, Jin L, Zhang J, Wang Y, Fan M, Fang Z, Li W, Ouyang C, Kwon D, Que N, Li Z, Mao J, Chen H, Harris J, Wu X, Wu J, Yin H, Chan WC, Horne D, Huang W Blood Adv 17-Nov-2023
PMCID:PMC10824694
doi:10.1182/bloodadvances.2023010873
PMID:37967356
Mid-to-late Holocene climate variability in coastal East Asia and its impact on ancient Korean societies Park J, Bahk J, Park J, Kim H, Choi J Sci Rep 16-Sep-2023
PMCID:PMC10505234
doi:10.1038/s41598-023-42551-x
PMID:37717094
Potential factors promoting the natural regeneration of Larix principis-rupprechtii in North China Zhao W, Sun Y, Gao Y PeerJ 08-Aug-2023
PMCID:PMC10416772
doi:10.7717/peerj.15809
PMID:37576508
The Anticancer Effect of Napabucasin (BBI608), a Natural Naphthoquinone Shao Z, Wang H, Ren H, Sun Y, Chen X Molecules 27-Jul-2023
PMCID:PMC10420168
doi:10.3390/molecules28155678
PMID:37570646
Complete chloroplast genome data of Ranunculus membranaceus (Ranunculaceae), an important medicinal plant species Ren Y, Wang M, Wang Z, Wu L, Wan JZ, Zhou H, Ma Z, Zhang C Data Brief 16-Jul-2023
PMCID:PMC10369386
doi:10.1016/j.dib.2023.109416
PMID:37501731
Berbamine, a bioactive alkaloid, suppresses equine herpesvirus type 1 in vitro and in vivo Li Z, He Y, Ge L, Quan R, Chen J, Hu Y, Sa R, Liu J, Ran D, Fu Q, Shi H Front Vet Sci 25-May-2023
PMCID:PMC10247970
doi:10.3389/fvets.2023.1163780
PMID:37303732
Antidiabetic activity of Berberis brandisiana is possibly mediated through modulation of insulin signaling pathway, inflammatory cytokines and adipocytokines in high fat diet and streptozotocin-administered rats Mehdi S, Mehmood MH, Ahmed MG, Ashfaq UA Front Pharmacol 06-Apr-2023
PMCID:PMC10117783
doi:10.3389/fphar.2023.1085013
PMID:37089941
A systematic review on impact of SARS-CoV-2 infection Thirumugam G, Radhakrishnan Y, Ramamurthi S, Bhaskar JP, Krishnaswamy B Microbiol Res 15-Mar-2023
PMCID:PMC10015779
doi:10.1016/j.micres.2023.127364
PMID:36989761
The Role of Natural and Semi-Synthetic Compounds in Ovarian Cancer: Updates on Mechanisms of Action, Current Trends and Perspectives Islam MR, Rahman MM, Dhar PS, Nowrin FT, Sultana N, Akter M, Rauf A, Khalil AA, Gianoncelli A, Ribaudo G Molecules 22-Feb-2023
PMCID:PMC10004182
doi:10.3390/molecules28052070
PMID:36903316
Modulation of AKT Pathway-Targeting miRNAs for Cancer Cell Treatment with Natural Products Shiau JP, Chuang YT, Yen CY, Chang FR, Yang KH, Hou MF, Tang JY, Chang HW Int J Mol Sci 12-Feb-2023
PMCID:PMC9961959
doi:10.3390/ijms24043688
PMID:36835100
DNA barcode sequencing discovered the aecial host of Puccinia chunjiei Hambleton S, Liu M Mycoscience 26-Dec-2022
PMCID:PMC10025072
doi:10.47371/mycosci.2022.11.001
PMID:37089896
Berbamine Hydrochloride Inhibits African Swine Fever Virus Infection In Vitro Zhu J, Huang L, Gao F, Jian W, Chen H, Liao M, Qi W Molecules 25-Dec-2022
PMCID:PMC9822360
doi:10.3390/molecules28010170
PMID:36615369
Bioactivity and In Silico Studies of Isoquinoline and Related Alkaloids as Promising Antiviral Agents: An Insight Sharma D, Sharma N, Manchanda N, Prasad SK, Sharma PC, Thakur VK, Rahman MM, Dhobi M Biomolecules 21-Dec-2022
PMCID:PMC9856122
doi:10.3390/biom13010017
PMID:36671402
Natural Products as Anticancer Agents: Current Status and Future Perspectives Naeem A, Hu P, Yang M, Zhang J, Liu Y, Zhu W, Zheng Q Molecules 30-Nov-2022
PMCID:PMC9737905
doi:10.3390/molecules27238367
PMID:36500466

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
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
Magnoflorine iodide, (+)-(RG) 131664584 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)[O-])OC)C.I 469.30 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
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-3-ol;iodide 5459338 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)O)OC)OC.[I-] 465.30 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 https://doi.org/10.1007/BF00630534
Columbamine 72310 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)O)OC 338.40 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
Pseudopalmatine 644002 Click to see COC1=C(C=C2C(=C1)CC[N+]3=CC4=CC(=C(C=C4C=C23)OC)OC)OC 352.40 unknown https://doi.org/10.1007/BF00630534
> 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
> Benzenoids / Naphthalenes / Naphthoquinones
Javanicin 10149 Click to see CC1=C(C(=C2C(=C1O)C(=O)C=C(C2=O)OC)O)CC(=O)C 290.27 unknown via CMAUP database
> Lignans, neolignans and related compounds
6,6',7-Trimethoxy-2,2'-dimethylberbaman-12-ol 10170 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 https://doi.org/10.1248/CPB1953.4.121
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 https://doi.org/10.1248/CPB1953.4.121
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 https://doi.org/10.1007/BF00630534
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
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Magnograndiolide 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
793JX7VC6J 457914 Click to see COC1=CC=C2C=C3C4=CC5=C(C=C4CCN3C=C2C1=O)OCO5 321.30 unknown https://doi.org/10.1007/BF00630534
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Berbamunine 440585 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5C)OC)O)O)O)OC 596.70 unknown https://doi.org/10.1007/BF00630534
Berbamuninium(2+) 46931116 Click to see C[NH+]1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CC[NH+]5C)OC)O)O)O)OC 598.70 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/10.1007/BF00630534
Oxyberberine 11066 Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2=O)OCO5)OC 351.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
2-[(8S)-2-oxo-8,9-dihydrofuro[2,3-h]chromen-8-yl]propan-2-yl (Z)-2-methylbut-2-enoate 53399217 Click to see CC=C(C)C(=O)OC(C)(C)C1CC2=C(O1)C=CC3=C2OC(=O)C=C3 328.40 unknown via CMAUP database
> 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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