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Berberis laurina

Berberis laurina - 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 UUID64400cc720ead231703838
Scientific name Berberis laurina
Authority Thunb.
First published in Pl. Bras. 1: 8 (1817)

Description Top

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Berberis laurina is a spiny and woody shrub that belongs to the barberry family. It can grow up to 2½ meters tall and has bluish green leaves that may turn yellow or red during autumn and winter. The plant is native to Uruguay, southern Brazil, and the Misiones province in Argentina. It is known as "espina amarilla" in Uruguay and "espinho-de-judeu" in Brazil. The leaves are simple, leathery, and have spiny teeth, while the flowers are light yellow and arranged in drooping racemes. The fruit is a small, oblong berry that is bluish black in color. This plant has multiple uses and has been studied in Argentina. It is also known by various taxon identifiers, such as Q5726282 and 50125133.

Synonyms Top

No known synonyms.

Common names Top

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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
  • Southern America
    • Brazil
      • Brazil South
      • Brazil Southeast
    • Southern South America
      • Uruguay

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000563422
Tropicos 50125133
KEW urn:lsid:ipni.org:names:106830-1
The Plant List kew-2674036
Open Tree Of Life 5727845
NCBI Taxonomy 2364036
IPNI 106830-1
GBIF 7300280
USDA GRIN 6899
Wikipedia Berberis_laurina

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
Novel land uses shape meta-community structures in neighbouring native forests: Dataset across Uruguay Säumel I, Ramírez LR Data Brief 16-May-2022
PMCID:PMC9130530
doi:10.1016/j.dib.2022.108267
PMID:35647241
HR-MAS NMR Applications in Plant Metabolomics Augustijn D, de Groot HJ, Alia A Molecules 10-Feb-2021
PMCID:PMC7916392
doi:10.3390/molecules26040931
PMID:33578691
High-Resolution Magic Angle Spinning (HR-MAS) NMR-Based Fingerprints Determination in the Medicinal Plant Berberis laurina Ali S, Badshah G, Da Ros Montes D’Oca C, Ramos Campos F, Nagata N, Khan A, de Fátima Costa Santos M, Barison A Molecules 11-Aug-2020
PMCID:PMC7465263
doi:10.3390/molecules25163647
PMID:32796509
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
Ethnopharmacology of Medicinal Plants of the Pantanal Region (Mato Grosso, Brazil) Bieski IG, Rios Santos F, de Oliveira RM, Espinosa MM, Macedo M, Albuquerque UP, de Oliveira Martins DT Evid Based Complement Alternat Med 26-Feb-2012
PMCID:PMC3303862
doi:10.1155/2012/272749
PMID:22474496
Alkaloidal Content of Four Berberis Species. Structure of Berberilaurine, a New Bisbenzyltetrahydroisoquinoline Jean-Frédéric Weber, Alain Fournet American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50061A010
Two new alkaloids from Berberis laurina Billb. Falco MR, de Vries JX, de Brovetto AG, Macció Z, Rebuffo S, Bick IR Tetrahedron Lett 01-Jan-1970
doi:10.1016/S0040-4039(01)99064-1
PMID:5645065
Alkaloids of Berberis laurina Billb. II. Two new phenolic biscoclaurine alkaloids. Falco MR, de Vries JX, Maccio Z, Bick IR Experientia 01-Jan-1970
doi:10.1007/BF01897466
PMID:5365835

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 / Protoberberine alkaloids and derivatives
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/10.1021/NP50061A010
> Alkaloids and derivatives / Protopine alkaloids
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown https://doi.org/10.1021/NP50061A010
> Lignans, neolignans and related compounds
2H,16H-6,9-Etheno-1,24:11,15-dimethenopyrido[2a(2),3a(2):17,18][1,11]dioxacycloheneicosino[2,3,4-ij]isoquinoline, 3,4,4a,5,16a,17,18,19-octahydro-12,21,22,25-tetramethoxy-4,17-dimethyl-, [4aS-(4aR*,16aS*)]- 16395306 Click to see CN1CCC2=CC3=C(C=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/10.1016/S0040-4039(01)99064-1
6,6',7,12'-Tetramethoxy-2,2'-dimethyloxyacanthan 284692 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/10.1016/S0040-4039(01)99064-1
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/10.1021/NP50061A010
Berberilaurine 183538 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)O)OC)C=C5)O 594.70 unknown https://doi.org/10.1021/NP50061A010
Homoaromoline 99620 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)O)OC 608.70 unknown https://doi.org/10.1021/NP50061A010
Lauberine 16395648 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)O)OC)C=C5)OC 608.70 unknown https://doi.org/10.1021/NP50061A010
https://doi.org/10.1016/S0040-4039(01)99064-1
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/10.1016/S0040-4039(01)99064-1
Thalicberine, O-methyl 320712 Click to see CN1CCC2=CC3=C(C=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/10.1016/S0040-4039(01)99064-1
Thalrugosine 100257 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC 608.70 unknown https://doi.org/10.1021/NP50061A010
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[[4-[2-hydroxy-5-[[(1R)-7-hydroxy-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]phenyl]methyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 102145796 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)OC)O 596.70 unknown https://doi.org/10.1007/BF01897466
(1S)-1-[[4-[5-[[(1R)-7-hydroxy-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2-methoxyphenoxy]phenyl]methyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 102149077 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5C)OC)O)OC)OC)O 610.70 unknown https://doi.org/10.1007/BF01897466
1-[[4-[2-hydroxy-5-[(7-hydroxy-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]phenyl]methyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 162906940 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)OC)O 596.70 unknown https://doi.org/10.1007/BF01897466
1-[[4-[5-[(7-hydroxy-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]-2-methoxyphenoxy]phenyl]methyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 163037673 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5C)OC)O)OC)OC)O 610.70 unknown https://doi.org/10.1007/BF01897466
> Phenylpropanoids and polyketides / Tannins
[3,5-Diacetyloxy-4-[3,4-diacetyloxy-5-[2,4,6-triacetyloxy-3-(3,4,5-triacetyloxyphenoxy)phenoxy]phenoxy]phenyl] acetate 15689631 Click to see CC(=O)OC1=CC(=C(C(=C1)OC(=O)C)OC2=CC(=C(C(=C2)OC(=O)C)OC(=O)C)OC3=C(C=C(C(=C3OC(=O)C)OC4=CC(=C(C(=C4)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 992.80 unknown https://doi.org/10.1016/S0040-4039(01)99064-1

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