Berberis sibirica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Berberis sibirica - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID64400cdf6ac73592269330
Scientific name Berberis sibirica
Authority Pall.
First published in Fl. Ross. 2: 42 (1815)

Description Top

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Synonyms Top

Scientific name Authority First published in
Berberis altaica Pall. Fl. Ross. 2: 41 (1815)
Berberis sibirica f. subintegerrima Krasnob. Sist. Zametki Mater. Gerb. Krylova Tomsk. Gosud. Univ. Kuybysheva 85(27): 2. 1975 [1974 publ. 1975]

Common names Top

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Language Common/alternative name
Azerbaijani sibir zirinci
Bulgarian сибирски кисел трън
Estonian siberi kukerpuu
Armenian Սիբիրյան ծորենի
Russian Барбарис сибирский
Chinese 大黄连刺
Chinese 刺叶小檗
Chinese 西伯利亚小檗

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
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Xinjiang
    • Middle Asia
      • Kazakhstan
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000563832
Tropicos 3500323
KEW urn:lsid:ipni.org:names:107079-1
The Plant List kew-2674429
PFAF Berberis sibirica
Open Tree Of Life 5727781
Observations.org 144625
NCBI Taxonomy 1433329
IPNI 107079-1
iNaturalist 850962
GBIF 7300402
EPPO BEBSB
Elurikkus 3077
USDA GRIN 6958

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
Zebrafish as a robust preclinical platform for screening plant-derived drugs with anticonvulsant properties—a review Knap B, Nieoczym D, Kundap U, Kusio-Targonska K, Kukula-Koch W, Turski WA, Gawel K Front Mol Neurosci 28-Aug-2023
PMCID:PMC10493295
doi:10.3389/fnmol.2023.1221665
PMID:37701853
Evaluation of the Antioxidant and Anti-Lipoxygenase Activity of Berberis vulgaris L. Leaves, Fruits, and Stem and Their LC MS/MS Polyphenolic Profile Och A, Olech M, Bąk K, Kanak S, Cwener A, Cieśla M, Nowak R Antioxidants (Basel) 21-Jul-2023
PMCID:PMC10376855
doi:10.3390/antiox12071467
PMID:37508005
Technologies for Solubility, Dissolution and Permeation Enhancement of Natural Compounds Alshamrani M, Khan MK, Khan BA, Salawi A, Almoshari Y Pharmaceuticals (Basel) 25-May-2022
PMCID:PMC9227247
doi:10.3390/ph15060653
PMID:35745572
Current Evidence and Future Directions of Berberine Intervention in Depression Zhu WQ, Wu HY, Sun ZH, Guo Y, Ge TT, Li BJ, Li X, Cui RJ Front Pharmacol 23-May-2022
PMCID:PMC9168319
doi:10.3389/fphar.2022.824420
PMID:35677435
Current state of populations of Rhodiola rosea L. (Crassulaceae) in East Kazakhstan Kubentayev SA, Zhumagul MZ, Kurmanbayeva MS, Alibekov DT, Kotukhov JA, Sitpayeva GT, Mukhtubayeva SK, Izbastina KS Bot Stud 07-Nov-2021
PMCID:PMC8572951
doi:10.1186/s40529-021-00327-4
PMID:34746988
8-, 9-, and 11-Aryloxy Dimeric Aporphines and Their Pharmacological Activities Ali G, Cuny GD Molecules 27-Jul-2021
PMCID:PMC8347945
doi:10.3390/molecules26154521
PMID:34361671
6-Gingerol, a Major Constituent of Zingiber officinale Rhizoma, Exerts Anticonvulsant Activity in the Pentylenetetrazole-Induced Seizure Model in Larval Zebrafish Gawel K, Kukula-Koch W, Banono NS, Nieoczym D, Targowska-Duda KM, Czernicka L, Parada-Turska J, Esguerra CV Int J Mol Sci 20-Jul-2021
PMCID:PMC8305044
doi:10.3390/ijms22147745
PMID:34299361
Effect of Berberine Isolated from Barberry Species by Centrifugal Partition Chromatography on Memory and the Expression of Parvalbumin in the Mouse Hippocampus Proper Szalak R, Kukula-Koch W, Matysek M, Kruk-Słomka M, Koch W, Czernicka L, Khurelbat D, Biała G, Arciszewski MB Int J Mol Sci 26-Apr-2021
PMCID:PMC8123463
doi:10.3390/ijms22094487
PMID:33925781
Superior Antioxidant Capacity of Berberis iliensis—HPLC-Q-TOF-MS Based Phytochemical Studies and Spectrophotometric Determinations Abdykerimova S, Sakipova Z, Nakonieczna S, Koch W, Biernasiuk A, Grabarska A, Malm A, Kozhanova K, Kukula-Koch W Antioxidants (Basel) 09-Jun-2020
PMCID:PMC7346193
doi:10.3390/antiox9060504
PMID:32526940
The Influence of Palmatine Isolated from Berberis sibirica Radix on Pentylenetetrazole-Induced Seizures in Zebrafish Gawel K, Kukula-Koch W, Nieoczym D, Stepnik K, van der Ent W, Banono NS, Tarabasz D, Turski WA, Esguerra CV Cells 16-May-2020
PMCID:PMC7290958
doi:10.3390/cells9051233
PMID:32429356
Synergistic or Additive Pharmacological Interactions between Magnoflorine and Cisplatin in Human Cancer Cells of Different Histological Origin Okon E, Luszczki JJ, Kukula-Koch W, Halasa M, Jarzab A, Khurelbat D, Stepulak A, Wawruszak A Int J Mol Sci 19-Apr-2020
PMCID:PMC7215826
doi:10.3390/ijms21082848
PMID:32325867
“A herder’s duty is to think”: landscape partitioning and folk habitats of Mongolian herders in a mountain forest steppe (Khuvsugul-Murun region) Gantuya B, Avar Á, Babai D, Molnár Á, Molnár Z J Ethnobiol Ethnomed 20-Nov-2019
PMCID:PMC6868869
doi:10.1186/s13002-019-0328-x
PMID:31747913
Berberis alkaloids A. Karimov Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630564
Berberis alkaloids. XXIX. An investigation of the alkaloids ofBerberis sibirica A. Karimov, M. G. Levkovich, N. D. Abdullaev, R. Shakirov Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630540

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
(6aS)-9-[4-[[(1R)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]-2-methoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,10-diol 163058336 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown https://doi.org/10.1007/BF00630540
9-[4-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]-2-methoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,10-diol 21769997 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown https://doi.org/10.1007/BF00630540
Pakistanine 193239 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)O)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)OC)O)OC 608.70 unknown https://doi.org/10.1007/BF00630540
> Alkaloids and derivatives / Proaporphines
(R)-Pronuciferine 628376 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC 311.40 unknown https://doi.org/10.1007/BF00630540
Pronuciferine 200480 Click to see CN1CCC2=CC(=C(C3=C2C1CC34C=CC(=O)C=C4)OC)OC 311.40 unknown https://doi.org/10.1007/BF00630540
https://doi.org/10.1007/BF00630564
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
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/BF00630540
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 https://doi.org/10.1007/BF00630540
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 https://doi.org/10.1007/BF00630540
> Lignans, neolignans and related compounds
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/10.1007/BF00630540
CID 12300053 12300053 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/10.1007/BF00630540
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/BF00630540
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid amides / Acetamides / N-acetyl-2-arylethylamines
N-Acetylhomoveratrylamine 80465 Click to see CC(=O)NCCC1=CC(=C(C=C1)OC)OC 223.27 unknown https://doi.org/10.1007/BF00630540
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
(1S,15R)-10,21,22,26-tetramethoxy-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-dodecaene 161604992 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=CC=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown https://doi.org/10.1007/BF00630564
> 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/BF00630540

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