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Berberis brandisiana

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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 UUID64400ca7559b3616705222
Scientific name Berberis brandisiana
Authority Ahrendt
First published in J. Roy. Asiat. Soc. Bengal 11: 2 (1945)

Description Top

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Synonyms Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000562867
Tropicos 100297438
KEW urn:lsid:ipni.org:names:106475-1
The Plant List kew-2673508
Open Tree Of Life 6129465
IPNI 106475-1
GBIF 3981304
EOL 2877653
CMAUP NPO16041

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)!
Title Authors Publication Released IDs
(-)-Natalamine, an Aporphinoid Alkaloid from Berberis empetrifolia S. Fazal Hussain, Victor Fajardo, Maurice Shamma American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50063A029
Berbidine: A Simple Isoquinoline-Isoquinolone Dimer S. Fazal Hussain, M. Tariq Siddiqui, Maurice Shamma American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50062A016
Berbamine 2'-β-N-oxide, a New Bisbenzylisoquinoline from Berberis brandisiana S. Fazal Hussain, M. Tariq Siddiqui, Lajber Khan, Alan J. Freyer, Hélène Guinaudeau, Maurice Shamma American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50045A032

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
Isoboldine 133323 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1021/NP50045A032
> 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/10.1021/NP50045A032
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/NP50045A032
> Lignans, neolignans and related compounds
(+)-Berbamine 2'-beta-N-oxide 102153975 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=CC(=C(C=C7CC[N+]6(C)[O-])OC)O3)C=C5)OC)OC 624.70 unknown https://doi.org/10.1021/NP50045A032
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/10.1021/NP50045A032
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/10.1021/NP50045A032
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/10.1021/NP50045A032
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
19Alpha-Hydroxyasiatic Acid 490367 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)O 504.70 unknown via CMAUP database
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Asiatic Acid 119034 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O 488.70 unknown via CMAUP database
Betulinaldehyde 99615 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C=O 440.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Tormentic acid 73193 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> 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/10.1021/NP50045A032
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
2-[4-[[(1S)-7-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-8-yl)oxy]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]-4-(methoxymethyl)phenol 162861977 Click to see CN1CCC2=CC(=C(C(=C2C1)OC3=C(C=C4CCN(C(C4=C3)CC5=CC=C(C=C5)OC6=C(C=CC(=C6)COC)O)C)OC)OC)OC 640.80 unknown https://doi.org/10.1021/NP50063A029
Reticuline 439653 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC 329.40 unknown https://doi.org/10.1021/NP50045A032
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
7-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-8-yl)oxy]-6-methoxy-2-methyl-3,4-dihydroisoquinolin-1-one 155510763 Click to see CN1CCC2=CC(=C(C(=C2C1)OC3=C(C=C4CCN(C(=O)C4=C3)C)OC)OC)OC 412.50 unknown https://doi.org/10.1021/NP50062A016
8-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-8-yl)oxy]-6-methoxy-2-methyl-3,4-dihydroisoquinolin-1-one 163104756 Click to see CN1CCC2=CC(=C(C(=C2C1)OC3=CC(=CC4=C3C(=O)N(CC4)C)OC)OC)OC 412.50 unknown https://doi.org/10.1021/NP50063A029
Thalifoline 89048 Click to see CN1CCC2=CC(=C(C=C2C1=O)O)OC 207.23 unknown https://doi.org/10.1021/NP50045A032
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database

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