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Berberis nummularia

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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 UUID64400cd20d4c9066216821
Scientific name Berberis nummularia
Authority Bunge
First published in Linnaea 18: 149 (1844)

Description Top

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Synonyms Top

Scientific name Authority First published in
Berberis integerrima var. pyrocarpa Regel Trudy Imp. S.-Peterburgsk. Bot. Sada 5: 228 1877
Berberis nummularia var. pyrocarpa C.K.Schneid. Bull. Herb. Boissier II, 5: 460 1905

Common names Top

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Language Common/alternative name
Azerbaijani sikkəvari zirinc
Russian Барбарис монетовидный
Russian Барбарис монетный
Chinese 新疆小檗
Chinese 红果小檗

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
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000563601
Tropicos 3500318
KEW urn:lsid:ipni.org:names:106940-1
The Plant List kew-2674208
Open Tree Of Life 5727785
Observations.org 136003
NCBI Taxonomy 1439896
IPNI 106940-1
GBIF 3981055
EPPO BEBNU
EOL 2880085
Elurikkus 445064

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
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
Evaluation of Biochemical Properties, Antioxidant Activities and Phenolic Content of Two Wild-Grown Berberis Fruits: Berberis nummularia and Berberis atrocarpa Abudureheman B, Zhou X, Shu X, Chai Z, Xu Y, Li S, Tian J, Pan H, Ye X Foods 25-Aug-2022
PMCID:PMC9455689
doi:10.3390/foods11172569
PMID:36076754
The role of biocatalysis in the asymmetric synthesis of alkaloids – an update Cigan E, Eggbauer B, Schrittwieser JH, Kroutil W RSC Adv 20-Aug-2021
PMCID:PMC9038100
doi:10.1039/d1ra04181a
PMID:35480754
Berberine: Botanical Occurrence, Traditional Uses, Extraction Methods, and Relevance in Cardiovascular, Metabolic, Hepatic, and Renal Disorders Neag MA, Mocan A, Echeverría J, Pop RM, Bocsan CI, Crişan G, Buzoianu AD Front Pharmacol 21-Aug-2018
PMCID:PMC6111450
doi:10.3389/fphar.2018.00557
PMID:30186157
μ Opioid receptor: novel antagonists and structural modeling Kaserer T, Lantero A, Schmidhammer H, Spetea M, Schuster D Sci Rep 18-Feb-2016
PMCID:PMC4757823
doi:10.1038/srep21548
PMID:26888328
Berberis alkaloids XXXV. The structure of nummularine M. F. Faskhutdinov, A. Karimov, M. G. Levkovich, N. D. Abdullaev, R. Shakirov Springer Science and Business Media LLC 08-Dec-2005
doi:10.1007/BF02273928
Berberis alkaloids. XX. Investigation of the alkaloids of Berberis iliensis A. Karimov, R. Shakirov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00631020
Berberis alkaloids A. Karimov Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630564
Berberis alkaloids. XXIV. Structure of bernumine A. Karimov, M. G. Levkovich, N. D. Abdullaev, R. Shakirov Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630532
Berberis alkaloids. XXX. Dynamics of the accumulation of the alkaloids ofBerberis integerrima andB. nummularia A. Karimov, S. Meliboev, V. Olimov, R. Shakirov Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630556
Berberis alkaloids. XXV. Structures of bernumidine and bernumicine A. Karimov, R. Shakirov Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630533
Alkaloids of three species ofBerberis A. Karimov, M. V. Telezhenetskaya, K. L. Lutfullin, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00564845

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
(r)-2,10-Dimethoxy-11-hydroxyaporphine 15627809 Click to see CN1CCC2=C3C1CC4=C(C3=CC(=C2)OC)C(=C(C=C4)OC)O 311.40 unknown https://doi.org/10.1007/BF00564845
1,2,10-Trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-11-ol 48704 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown https://doi.org/10.1007/BF02273928
2,9,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol 100020 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)O)OC 341.40 unknown https://doi.org/10.1007/BF00630533
https://doi.org/10.1007/BF00630532
https://doi.org/10.1007/BF00630556
Glaucine 16754 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC 355.40 unknown https://doi.org/10.1007/BF00630533
https://doi.org/10.1007/BF00630532
https://doi.org/10.1007/BF02273928
https://doi.org/10.1007/BF00630564
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1007/BF02273928
Isocorydine 10143 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC 341.40 unknown https://doi.org/10.1007/BF02273928
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 https://doi.org/10.1007/BF00630533
> 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/BF00630533
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/BF00630533
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/BF00630533
> Lignans, neolignans and related compounds
6,6'-Dimethoxy-2,2'-dimethyloxyacanthan-7,12'-diol 122728 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)O)OC 594.70 unknown https://doi.org/10.1007/BF02273928
https://doi.org/10.1007/BF00630533
Aromoline 362574 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)O)OC 594.70 unknown https://doi.org/10.1007/BF00630533
https://doi.org/10.1007/BF02273928
O-Methylberbamine 5351212 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)OC)OC 622.70 unknown https://doi.org/10.1007/BF00630533
https://doi.org/10.1007/BF00630532
Obaberine 100231 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)OC)OC 622.70 unknown https://doi.org/10.1007/BF02273928
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/BF00630533
https://doi.org/10.1007/BF02273928
https://doi.org/10.1007/BF00630532
https://doi.org/10.1007/BF00630564
Oxycanthine 371257 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/BF02273928
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Excisanin H 10066342 Click to see CC1(CCC(C23C1CC(C45C2CCC(C4(OC3)O)C(=C)C5=O)O)O)C 348.40 unknown https://doi.org/10.1007/BF00630532
https://doi.org/10.1007/BF02273928
https://doi.org/10.1007/BF00630533
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
[1-[2-Hydroxy-6-(3-hydroxypropyl)-1,2-dimethyl-5-(1-oxopropan-2-ylidene)cyclohexyl]-4,8,12-trimethyltrideca-3,6,11-trien-5-yl] acetate 162986646 Click to see CC(CCC=C(C)C)C=CC(C(=CCCC1(C(C(=C(C)C=O)CCC1(C)O)CCCO)C)C)OC(=O)C 516.80 unknown https://doi.org/10.1007/BF00564845
> 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/BF00631020
https://doi.org/10.1007/BF00630564
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1R)-2-[(3,4-dimethoxyphenyl)methyl]-7-methoxy-1-methyl-3,4-dihydro-1H-isoquinolin-6-ol 11256403 Click to see CC1C2=CC(=C(C=C2CCN1CC3=CC(=C(C=C3)OC)OC)O)OC 343.40 unknown https://doi.org/10.1007/BF00630533
(1S)-2-[(3-hydroxy-4-methoxyphenyl)methyl]-7-methoxy-1-methyl-3,4-dihydro-1H-isoquinolin-6-ol 163040189 Click to see CC1C2=CC(=C(C=C2CCN1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1007/BF02273928
(R)-laudanosine 978314 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)OC 357.40 unknown https://doi.org/10.1007/BF00630532
(R)-Reticuline 440586 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1007/BF00630533
(S)-Laudanosine 73397 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)OC 357.40 unknown https://doi.org/10.1007/BF00630532
2-[(3-hydroxy-4-methoxyphenyl)methyl]-7-methoxy-1-methyl-3,4-dihydro-1H-isoquinolin-6-ol 15859740 Click to see CC1C2=CC(=C(C=C2CCN1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1007/BF02273928
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/BF00631020
https://doi.org/10.1007/BF00630533
https://doi.org/10.1007/BF02273928
Laudanosine 15548 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)OC 357.40 unknown https://doi.org/10.1007/BF00630532
N-Methylcoclaurine 2752274 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 299.40 unknown https://doi.org/10.1007/BF00630533
Reticulin 10233 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1007/BF00630533
Reticuline 439653 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1007/BF00630533
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(1R)-2-(1,3-benzodioxol-5-yl)-7-methoxy-1-methyl-3,4-dihydro-1H-isoquinolin-6-ol 101102562 Click to see CC1C2=CC(=C(C=C2CCN1C3=CC4=C(C=C3)OCO4)O)OC 313.30 unknown https://doi.org/10.1007/BF00630533
(1R)-2-(1,3-benzodioxol-5-ylmethyl)-6,7-dimethoxy-1-methyl-3,4-dihydro-1H-isoquinoline 7097507 Click to see CC1C2=CC(=C(C=C2CCN1CC3=CC4=C(C=C3)OCO4)OC)OC 341.40 unknown https://doi.org/10.1007/BF00630533
(1S)-2-(1,3-benzodioxol-5-ylmethyl)-7-methoxy-1-methyl-3,4-dihydro-1H-isoquinolin-6-ol 163032540 Click to see CC1C2=CC(=C(C=C2CCN1CC3=CC4=C(C=C3)OCO4)O)OC 327.40 unknown https://doi.org/10.1007/BF00630532
2-(1,3-benzodioxol-5-ylmethyl)-6,7-dimethoxy-1-methyl-3,4-dihydro-1H-isoquinoline 16195645 Click to see CC1C2=CC(=C(C=C2CCN1CC3=CC4=C(C=C3)OCO4)OC)OC 341.40 unknown https://doi.org/10.1007/BF00630533
2-(1,3-benzodioxol-5-ylmethyl)-7-methoxy-1-methyl-3,4-dihydro-1H-isoquinolin-6-ol 21627930 Click to see CC1C2=CC(=C(C=C2CCN1CC3=CC4=C(C=C3)OCO4)O)OC 327.40 unknown https://doi.org/10.1007/BF00630532
Corypalline 280225 Click to see CN1CCC2=CC(=C(C=C2C1)O)OC 193.24 unknown https://doi.org/10.1007/BF02273928

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