Works matching DE "ISOQUINOLINE alkaloids"
Results: 970
Urea‐Promoted Neat Synthesis of Fused Dihydroisoquinolines and Disubstituted Pyridines: A Mechanistic Observation with Molecular‐Sensing Studies.
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- Chemistry - A European Journal, 2024, v. 30, n. 13, p. 1, doi. 10.1002/chem.202303287
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Proteome profiling of methyl jasmonate elicitation of Maytenus ilicifolia in vitro roots reveals insights into sesquiterpene pyridine alkaloids.
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- Plant Cell, Tissue & Organ Culture, 2022, v. 151, n. 3, p. 551, doi. 10.1007/s11240-022-02371-9
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Analyses of diverse low alkaloid tobacco germplasm identify naturally occurring nucleotide variability contributing to reduced leaf nicotine accumulation.
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- Molecular Breeding, 2022, v. 42, n. 1, p. 1, doi. 10.1007/s11032-021-01274-5
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Alkaloids of Lindelofia macrostyla and a New Unsaturated Carboxylic Acid.
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- Chemistry of Natural Compounds, 2024, v. 60, n. 6, p. 1084, doi. 10.1007/s10600-024-04525-x
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A New Crown Ether of Mahonia fortunei.
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- Chemistry of Natural Compounds, 2024, v. 60, n. 3, p. 440, doi. 10.1007/s10600-024-04346-y
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Pinacol Rearrangement of Lappaconine.
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- Chemistry of Natural Compounds, 2023, v. 59, n. 6, p. 1212, doi. 10.1007/s10600-023-04234-x
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Antiviral Isoquinolines from the Cigar Tobacco Derived Endophytic Fungi Aspergillus fumigatus.
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- Chemistry of Natural Compounds, 2023, v. 59, n. 5, p. 876, doi. 10.1007/s10600-023-04139-9
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A New Acridone Alkaloid from the Leaves of Glycosmis lucida.
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- Chemistry of Natural Compounds, 2023, v. 59, n. 5, p. 872, doi. 10.1007/s10600-023-04138-w
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Alkaloids from Delphinium oreophilum and Biological Activity of 14-Acetylbrowniine.
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- Chemistry of Natural Compounds, 2023, v. 59, n. 2, p. 339, doi. 10.1007/s10600-023-03989-7
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Perfirine, a New Alkaloid from the Plant Haplophyllum perforatum.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 5, p. 892, doi. 10.1007/s10600-022-03823-6
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Synthesis of 1,2,3-Triazolyl-Substituted Derivatives of the Alkaloids Sinomenine and Tetrahydrothebaine on Ring A and Their Analgesic Activity.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 5, p. 895, doi. 10.1007/s10600-022-03824-5
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Alkaloid and Glycoside Compounds from the Fruits of Berberis atrocarpa and Their Anticomplementary Activities.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 4, p. 782, doi. 10.1007/s10600-022-03795-7
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A New C<sub>19</sub>-Diterpenoid Alkaloid from Salted Aconiti Lateralis Radix Praeparata.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 3, p. 516, doi. 10.1007/s10600-022-03721-x
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Antinociceptive Diterpenoid Alkaloids from the Roots of Aconitum pseudostapfianum.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 2, p. 312, doi. 10.1007/s10600-022-03666-1
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Secondary Metabolites of Mahonia bealei.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 1, p. 181, doi. 10.1007/s10600-022-03629-6
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Furan Analog of the Alkaloid Dubiamine Based on 5-Hydroxymethylfurfurol.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 1, p. 185, doi. 10.1007/s10600-022-03630-z
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Two New Anti-Tobacco Mosaic Virus Quinoline Alkaloids from the Stems of Nicotiana tabacum.
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- Chemistry of Natural Compounds, 2022, v. 58, n. 1, p. 78, doi. 10.1007/s10600-022-03600-5
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Isoquinoline Alkaloids of Ilex latifolia.
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- Chemistry of Natural Compounds, 2021, v. 57, n. 6, p. 1175, doi. 10.1007/s10600-021-03580-y
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Angustifoline A, A New Alkaloid from Epilobium angustifolium.
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- Chemistry of Natural Compounds, 2021, v. 57, n. 5, p. 903, doi. 10.1007/s10600-021-03507-7
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A New Tyramine Derivative from the Branches and Leaves of Glycosmis craibii.
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- Chemistry of Natural Compounds, 2021, v. 57, n. 5, p. 894, doi. 10.1007/s10600-021-03505-9
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Biological Activity of Protein Constituents and Alkaloids from the Plant Phragmites communis.
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- Chemistry of Natural Compounds, 2021, v. 57, n. 3, p. 597, doi. 10.1007/s10600-021-03429-4
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Antinociceptive C19-Diterpenoid Alkaloids from Aconitum episcopale.
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- Chemistry of Natural Compounds, 2021, v. 57, n. 3, p. 503, doi. 10.1007/s10600-021-03397-9
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Secondary Metabolites of the Leaves of Mahonia fortunei.
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- Chemistry of Natural Compounds, 2020, v. 56, n. 6, p. 1178, doi. 10.1007/s10600-020-03261-2
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Alkaloids and Terpenoids from Trigonostemon lutescens and their Potential Antiproliferative Activity.
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- Chemistry of Natural Compounds, 2020, v. 56, n. 4, p. 763, doi. 10.1007/s10600-020-03144-6
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Indole Alkaloids from Hosta plantaginea and Inhibition of Steroid 5α-Reductase Activities In Vitro.
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- Chemistry of Natural Compounds, 2020, v. 56, n. 5, p. 888, doi. 10.1007/s10600-020-03176-y
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Alkaloids from the Plant Delphinium naviculare var. lasiocarpum.
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- Chemistry of Natural Compounds, 2020, v. 56, n. 4, p. 771, doi. 10.1007/s10600-020-03146-4
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Alkaloids and Flavonoids from Illigera aromatica.
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- Chemistry of Natural Compounds, 2020, v. 56, n. 3, p. 580, doi. 10.1007/s10600-020-03099-8
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Bioactive Alkaloids of Stephania sinica Showing Anti-Drug-Resistance Activity.
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- Chemistry of Natural Compounds, 2020, v. 56, n. 3, p. 572, doi. 10.1007/s10600-020-03096-x
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Synthesis of Derivatives of the 2-Arylquinoline Alkaloid Dubamine and their Cytotoxicity.
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- Chemistry of Natural Compounds, 2020, v. 56, n. 3, p. 511, doi. 10.1007/s10600-020-03074-3
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Isoquinoline Alkaloids from Whole Plants of Thalictrum cirrhosum and Their Antirotavirus Activity.
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- Chemistry of Natural Compounds, 2020, v. 56, n. 3, p. 504, doi. 10.1007/s10600-020-03072-5
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Two New Isoquinoline Alkaloids from Whole Plants of Thalictrum glandulosissimum and their Anti-TMV Activity.
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- Chemistry of Natural Compounds, 2020, v. 56, n. 3, p. 500, doi. 10.1007/s10600-020-03071-6
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Diterpenoid Alkaloids from the Roots of Aconitum iochanicum.
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- Chemistry of Natural Compounds, 2020, v. 56, n. 3, p. 492, doi. 10.1007/s10600-020-03069-0
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Synthesis of Phenanthrene Alkaloids in Subcritical Water Using Secoboldine as an Example.
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- Chemistry of Natural Compounds, 2020, v. 56, n. 1, p. 183, doi. 10.1007/s10600-020-02981-9
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Isoquinoline Alkaloids from Corydalis pallida.
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- Chemistry of Natural Compounds, 2018, v. 54, n. 5, p. 1020, doi. 10.1007/s10600-018-2541-6
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A New Aporphine Alkaloid from Aconitum carmichaelii.
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- Chemistry of Natural Compounds, 2017, v. 53, n. 3, p. 501, doi. 10.1007/s10600-017-2031-2
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(+)-(6a R,7 R)-7-Hydroxy- N-Butyrylcaaverine, a New Aporphine Alkaloid from the Roots of Illigera luzonensis with Cytotoxic Activity.
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- Chemistry of Natural Compounds, 2015, v. 51, n. 4, p. 739, doi. 10.1007/s10600-015-1397-2
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Synthesis and Antitubercular Activity of Berberine Derivatives.
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- Chemistry of Natural Compounds, 2014, v. 50, n. 2, p. 321, doi. 10.1007/s10600-014-0942-8
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Synthesis of Hydroxyethyl Derivatives of 1-Aryltetrahydroisoquinoline Alkaloids.
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- Chemistry of Natural Compounds, 2014, v. 49, n. 6, p. 1095, doi. 10.1007/s10600-014-0828-9
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Synthesis of bis-tetrahydroisoquinolines based on homoveratrylamine and a series of dibasic acids. 1.
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- Chemistry of Natural Compounds, 2013, v. 49, n. 2, p. 302, doi. 10.1007/s10600-013-0586-0
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Isoquinoline Alkaloids from Corydalis impatiens.
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- Chemistry of Natural Compounds, 2013, v. 49, n. 1, p. 187, doi. 10.1007/s10600-013-0554-8
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Synthesis of berberine bromide analogs containing tertiary amides of acetic acid in the 9- O-position.
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- Chemistry of Natural Compounds, 2013, v. 48, n. 6, p. 1047, doi. 10.1007/s10600-013-0461-z
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Synthesis of isoquinoline alkaloid derivatives from eugenol.
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- Chemistry of Natural Compounds, 2012, v. 48, n. 2, p. 285, doi. 10.1007/s10600-012-0222-4
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An improved micropropagation protocol for the ex situ conservation of Mitragyna parvifolia (Roxb.) Korth. (Rubiaceae): an endangered tree of pharmaceutical importance.
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- In Vitro Cellular & Developmental Biology Plant, 2020, v. 56, n. 6, p. 817, doi. 10.1007/s11627-020-10089-6
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Back to the plant: overcoming roadblocks to the microbial production of pharmaceutically important plant natural products.
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- Journal of Industrial Microbiology & Biotechnology, 2020, v. 47, n. 9/10, p. 815, doi. 10.1007/s10295-020-02300-9
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药食同源代代花药理作用及应用研究进展.
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- Modern Food Science & Technology, 2023, v. 39, n. 10, p. 349, doi. 10.13982/j.mfst.1673-9078.2023.10.1307
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Jatrorrhizine Suppresses Murine-Norovirus-Triggered N-GSDMD-Dependent Pyroptosis in RAW264.7 Macrophages.
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- Vaccines, 2023, v. 11, n. 1, p. 164, doi. 10.3390/vaccines11010164
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Peroxo Complexes of Th(IV) and Zr(IV) Ions Containing Aspartic Acid and Amine Bases as Potential Biological Agents.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 8, p. 1553, doi. 10.1134/S1070363220080253
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X-Ray Diffraction Structural Studies of a Series of 4-Aryl-1-di- and 4-Aryl-1-trichloromethylisoquinolines and Their 1,2,4-Triazine Precursors.
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- Russian Journal of General Chemistry, 2020, v. 90, n. 7, p. 1192, doi. 10.1134/S1070363220070038
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Synthesis of isoindolo[2,1- b]isoquinoline-5,7-dione via the wittig intramolecular cyclization.
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- Russian Journal of General Chemistry, 2015, v. 85, n. 11, p. 2665, doi. 10.1134/S1070363215110274
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Gold-Catalyzed Synthetic Strategies towards Four-Carbon Ring Systems.
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- Catalysts (2073-4344), 2020, v. 10, n. 10, p. 1178, doi. 10.3390/catal10101178
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