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Duboisia leichhardtii

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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
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Details Top

Internal ID UUID6440411c81284447941715
Scientific name Duboisia leichhardtii
Authority (F.Muell.) F.Muell.
First published in Syst. Census Austral. Pl.

Description Top

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Synonyms Top

Scientific name Authority First published in
Anthocercis leichhardtii F.Muell. Fragm. (Mueller) 6(45): 142. 1868

Common names Top

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Language Common/alternative name
English leichhardt's duboisia
Chinese 雷氏澳茄

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001021492
UNII U9EEQ29815
USDA Plants DULE
Tropicos 100327334
KEW urn:lsid:ipni.org:names:94818-3
The Plant List kew-2778802
Open Tree Of Life 810423
NCBI Taxonomy 195736
IUCN Red List 146114459
IPNI 815655-1
iNaturalist 698946
GBIF 5341763
EPPO DUBLE
EOL 486417
USDA GRIN 14733

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
Hairy root culture: a potent method for improved secondary metabolite production of Solanaceous plants Biswas D, Chakraborty A, Mukherjee S, Ghosh B Front Plant Sci 04-Sep-2023
PMCID:PMC10507345
doi:10.3389/fpls.2023.1197555
PMID:37731987
Emerging Issues on Tropane Alkaloid Contamination of Food in Europe de Nijs M, Crews C, Dorgelo F, MacDonald S, Mulder PP Toxins (Basel) 19-Jan-2023
PMCID:PMC9961018
doi:10.3390/toxins15020098
PMID:36828413
In vitro strategies for the enhancement of secondary metabolite production in plants: a review Fazili MA, Bashir I, Ahmad M, Yaqoob U, Geelani SN Bull Natl Res Cent 19-Feb-2022
PMCID:PMC8857880
doi:10.1186/s42269-022-00717-z
PMID:35221660
Application of metabolic engineering to enhance the content of alkaloids in medicinal plants Mora-Vásquez S, Wells-Abascal GG, Espinosa-Leal C, Cardineau GA, García-Lara S Metab Eng Commun 16-Feb-2022
PMCID:PMC8881666
doi:10.1016/j.mec.2022.e00194
PMID:35242556
A Stable Agrobacterium rhizogenes-Mediated Transformation of Cotton (Gossypium hirsutum L.) and Plant Regeneration From Transformed Hairy Root via Embryogenesis Cui ML, Liu C, Piao CL, Liu CL Front Plant Sci 14-Dec-2020
PMCID:PMC7767857
doi:10.3389/fpls.2020.604255
PMID:33381137
Effect of different Agrobacterium rhizogenes strains for in-vitro hairy root induction, total phenolic, flavonoids contents, antibacterial and antioxidant activity of (Cucumis anguria L.) Joseph Sahayarayan J, Udayakumar R, Arun M, Ganapathi A, Alwahibi MS, Aldosari NS, Morgan AM Saudi J Biol Sci 06-Sep-2020
PMCID:PMC7569140
doi:10.1016/j.sjbs.2020.08.050
PMID:33100855
Silencing of quinolinic acid phosphoribosyl transferase (QPT) gene for enhanced production of scopolamine in hairy root culture of Duboisia leichhardtii Singh P, Prasad R, Tewari R, Jaidi M, Kumar S, Rout PK, Rahman LU Sci Rep 17-Sep-2018
PMCID:PMC6141460
doi:10.1038/s41598-018-32396-0
PMID:30224763
Biotechnology, In Vitro Production of Natural Bioactive Compounds, Herbal Preparation, and Disease Management (Treatment and Prevention) Alamgir AN Therapeutic Use of Medicinal Plants and their Extracts: Volume 2 24-Jun-2018
PMCID:PMC7123938
doi:10.1007/978-3-319-92387-1_7
Studies on Duboisia Species. V. Alkaloids in Cultured Cells of Duboisia leichhardtii KENGO KAGEI, MAKOTO IKEDA, TADASHI SATO, YOSHITAKE OGATA, SHOJI TOYOSHIMA, SHIN MATSUURA Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1947.100.5_574
Studies on Duboisia Species. IV. Minor Alkaloids in Leaves of Duboisia leichhardtii KENGO KAGEI, MAKOTO IKEDA, TADASHI SATO, YOSHITAKE OGATA, TOSHINOBU KUNII, SHOJI TOYOSHIMA, SHIN MATSUURA Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1947.100.2_216
Diseases of the Nervous System N/A Veterinary Medicine 10-Feb-2017
PMCID:PMC7322266
doi:10.1016/B978-0-7020-5246-0.00014-0
Combination of Plant Metabolic Modules Yields Synthetic Synergies Rajabi F, Heene E, Maisch J, Nick P PLoS One 12-Jan-2017
PMCID:PMC5231347
doi:10.1371/journal.pone.0169778
PMID:28081182
The potential of selected Australian medicinal plants with anti-Proteus activity for the treatment and prevention of rheumatoid arthritis Cock IE, Winnett V, Sirdaarta J, Matthews B Pharmacogn Mag 01-May-2015
PMCID:PMC4461961
doi:10.4103/0973-1296.157734
PMID:26109767
The role of biocatalysis in the asymmetric synthesis of alkaloids Schrittwieser JH, Resch V RSC Adv 07-Aug-2013
PMCID:PMC4285126
doi:10.1039/c3ra42123f
PMID:25580241
Conversion of Phenylalanine and Tropic Acid into Tropane Alkaloids by Duboisia leichhardtii Root Cultures Yoshie Kitamura, Atsuko Taura, Yumi Kajiya, Hiroshi Miura Elsevier BV 23-Jan-2012
doi:10.1016/S0176-1617(11)80924-7

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 / Tropane alkaloids
(1R,2S,3R,4S,5R,6R)-8-azabicyclo[3.2.1]octane-1,2,3,4,6-pentol 10081256 Click to see C1C(C2C(C(C(C1(N2)O)O)O)O)O 191.18 unknown https://doi.org/10.1016/S0031-9422(96)00865-5
(1R,3R,5S,6R)-8-azabicyclo[3.2.1]octane-3,6-diol 637042 Click to see C1C2CC(C(N2)CC1O)O 143.18 unknown https://doi.org/10.1016/S0031-9422(96)00865-5
(1R,3S,5R,6RS)-6-Hydroxy-8-methyl-8-azabicyclo(3.2.1)oct-3-YL (2S)-3-hydroxy-2-phenylpropanoate 139033153 Click to see CN1C2CC(CC1C(C2)O)OC(=O)C(CO)C3=CC=CC=C3 305.40 unknown https://doi.org/10.1016/0031-9422(92)80431-D
(8-Methyl-8-azabicyclo[3.2.1]octan-3-yl) 2-methylpropanoate 12302177 Click to see CC(C)C(=O)OC1CC2CCC(C1)N2C 211.30 unknown https://doi.org/10.1111/J.2042-7158.1954.TB10963.X
https://doi.org/10.1002/CBER.19530861110
(R)-(-)-Littorine 12311316 Click to see CN1C2CCC1CC(C2)OC(=O)C(CC3=CC=CC=C3)O 289.40 unknown https://doi.org/10.1016/0031-9422(92)80431-D
(S)-((1R,3r,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 3-hydroxy-2-phenylpropanoate 6931560 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1021/NP50023A006
https://doi.org/10.1016/0031-9422(92)80431-D
https://doi.org/10.1007/BF00270196
https://doi.org/10.1016/S0176-1617(11)80924-7
3beta,6beta-Dihydroxynortropane 22297531 Click to see C1C2CC(C(N2)CC1O)O 143.18 unknown https://doi.org/10.1016/S0031-9422(96)00865-5
8-Azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-phenylpropanoate 64701 Click to see C1CC2CC(CC1N2)OC(=O)C(CO)C3=CC=CC=C3 275.34 unknown https://doi.org/10.1039/JR9440000480
8-Azabicyclo[3.2.1]octane-1,2,3,4-tetraol 3693124 Click to see C1CC2(C(C(C(C1N2)O)O)O)O 175.18 unknown https://doi.org/10.1016/S0031-9422(96)00865-5
8-Azabicyclo[3.2.1]octane-1,2,3,4,6-pentol 3851514 Click to see C1C(C2C(C(C(C1(N2)O)O)O)O)O 191.18 unknown https://doi.org/10.1016/S0031-9422(96)00865-5
8-Azabicyclo[3.2.1]octane-1,2,3,6-tetraol 3804328 Click to see C1C2C(CC(N2)(C(C1O)O)O)O 175.18 unknown https://doi.org/10.1016/S0031-9422(96)00865-5
8-Azabicyclo[3.2.1]octane-1,3,4-triol 75093330 Click to see C1CC2(CC(C(C1N2)O)O)O 159.18 unknown https://doi.org/10.1016/S0031-9422(96)00865-5
Apoatropine 64695 Click to see CN1C2CCC1CC(C2)OC(=O)C(=C)C3=CC=CC=C3 271.35 unknown https://doi.org/10.1248/CPB.39.1263
Atropine 174174 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1016/0031-9422(96)00090-8
Atropine sulfate 3661 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1248/CPB.39.1263
https://doi.org/10.1039/JR9440000480
https://doi.org/10.1016/0031-9422(96)00090-8
Calystegine A5 12110705 Click to see C1CC2(CC(C(C1N2)O)O)O 159.18 unknown https://doi.org/10.1016/S0031-9422(96)00865-5
Calystegine B1 164245 Click to see C1C2C(CC(N2)(C(C1O)O)O)O 175.18 unknown https://doi.org/10.1016/S0031-9422(96)00865-5
Calystegine B2 124434 Click to see C1CC2(C(C(C(C1N2)O)O)O)O 175.18 unknown https://doi.org/10.1016/S0031-9422(96)00865-5
Calystegine B4 10559162 Click to see C1CC2(C(C(C(C1N2)O)O)O)O 175.18 unknown https://doi.org/10.1016/S0031-9422(96)00865-5
Calystegine C2 101700059 Click to see C1C(C2C(C(C(C1(N2)O)O)O)O)O 191.18 unknown https://doi.org/10.1016/S0031-9422(96)00865-5
L-Hyoscyamine 64692 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1021/NP50023A006
https://doi.org/10.1016/0031-9422(92)80431-D
https://doi.org/10.1016/S0031-9422(00)81107-3
https://doi.org/10.1007/BF00270196
https://doi.org/10.1016/S0176-1617(11)80924-7
Littorine 443005 Click to see CN1C2CCC1CC(C2)OC(=O)C(CC3=CC=CC=C3)O 289.40 unknown https://doi.org/10.1016/0031-9422(92)80431-D
Valtropine 12444666 Click to see CCC(C)C(=O)OC1CC2CCC(C1)N2C 225.33 unknown https://doi.org/10.1111/J.2042-7158.1954.TB10963.X
https://doi.org/10.1002/CBER.19530861110
> Benzenoids / Benzene and substituted derivatives
Phenylacetic Acid 999 Click to see C1=CC=C(C=C1)CC(=O)O 136.15 unknown https://doi.org/10.1016/0031-9422(93)80022-K
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Methyl 2-hexa-2,4-diynyl-6-methoxybenzoate 15559375 Click to see CC#CC#CCC1=C(C(=CC=C1)OC)C(=O)OC 242.27 unknown https://doi.org/10.1111/J.2042-7158.1954.TB10963.X
https://doi.org/10.1248/YAKUSHI1947.100.2_216
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1111/J.2042-7158.1954.TB10963.X
https://doi.org/10.1002/CBER.19530861110
> Lipids and lipid-like molecules / Saccharolipids / Acyltrehaloses
stearoyl(-2)Hex6Ac(?1-1?)Hex 85149698 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1C(C(C(OC1OC2C(C(C(C(O2)CO)O)O)O)COC(=O)C)O)O 650.80 unknown https://doi.org/10.1111/J.2042-7158.1954.TB10963.X
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[5-acetyloxy-4a-(acetyloxymethyl)-7,8-dimethyl-8-[2-(2-methylbutanoyloxy)-2-(5-oxo-2H-furan-3-yl)ethyl]spiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-1-yl] 2-methylbutanoate 76394383 Click to see CCC(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)CC(C4=CC(=O)OC4)OC(=O)C(C)CC)COC(=O)C 634.80 unknown https://doi.org/10.1111/J.2042-7158.1954.TB10963.X
https://doi.org/10.1002/CBER.19530861110
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(-)-Scopolamine 5184 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown https://doi.org/10.1039/JR9440000480
[(2R,4S)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl] (2R)-3-hydroxy-2-phenylpropanoate 134767951 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown https://doi.org/10.1016/S0176-1617(11)80924-7
https://doi.org/10.1021/NP50023A006
https://doi.org/10.1016/0031-9422(92)80431-D
https://doi.org/10.1007/BF00240724
https://doi.org/10.1016/S0031-9422(00)81107-3
https://doi.org/10.1016/0031-9422(96)00090-8
https://doi.org/10.1007/BF00270196
https://doi.org/10.1016/0031-9422(90)85026-C
Tropic acid ester with scopine 153311 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown https://doi.org/10.1007/BF00270196
https://doi.org/10.1016/0031-9422(90)85026-C
https://doi.org/10.1016/0031-9422(96)00090-8
https://doi.org/10.1007/BF00240724
https://doi.org/10.1039/JR9440000480
https://doi.org/10.1016/0031-9422(92)80431-D
https://doi.org/10.1021/NP50023A006
https://doi.org/10.1248/CPB.39.1263
https://doi.org/10.1016/S0176-1617(11)80924-7
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
Nigericin 34230 Click to see CC1CCC(OC1C(C)C(=O)O)CC2CC(C(C3(O2)C(CC(O3)(C)C4CCC(O4)(C)C5C(CC(O5)C6C(CC(C(O6)(CO)O)C)C)C)C)C)OC 725.00 unknown https://doi.org/10.1039/JR9440000480
> Organoheterocyclic compounds / Oxepanes
(1R,2S,3S,5R,6R,9R,10R,12S,16R,18S,20R,22R,23S,25R)-3,9,23-trihydroxy-22-methoxy-1,5,20-trimethyl-6-(5-oxo-2H-furan-3-yl)-11,17,19,24-tetraoxaheptacyclo[12.12.0.02,10.05,9.010,12.016,25.018,23]hexacos-14-en-4-one 21632918 Click to see CC1CC(C2(C(O1)OC3C=C4CC5C6(O5)C(C4(CC3O2)C)C(C(=O)C7(C6(CCC7C8=CC(=O)OC8)O)C)O)O)OC 574.60 unknown https://doi.org/10.1111/J.2042-7158.1954.TB10963.X
https://doi.org/10.1248/YAKUSHI1947.100.5_574
> Organoheterocyclic compounds / Pyridines and derivatives / Pyrrolidinylpyridines
3-(1-Methylpyrrolidin-2-yl)pyridine 942 Click to see CN1CCCC1C2=CN=CC=C2 162.23 unknown https://doi.org/10.1016/0031-9422(90)85026-C
https://doi.org/10.1007/BF00270196
Nicotine 89594 Click to see CN1CCCC1C2=CN=CC=C2 162.23 unknown https://doi.org/10.1007/BF00270196
https://doi.org/10.1016/0031-9422(90)85026-C
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
9-[2-Hydroxy-3-(3-hydroxyheptadeca-1,9-dien-4,6-diyn-8-yloxy)-3-methylbutoxy]-4-methoxyfuro[3,2-g]chromen-7-one 85130530 Click to see CCCCCCCC=CC(C#CC#CC(C=C)O)OC(C)(C)C(COC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)O 576.70 unknown https://doi.org/10.1039/JR9440000480

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