Works matching DE "TETRAHYDROISOQUINOLINES"
Results: 346
Asymmetric synthesis of tetrahydroisoquinolines by enzymatic Pictet-Spengler reaction.
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- Bioscience, Biotechnology & Biochemistry, 2014, v. 78, n. 4, p. 701, doi. 10.1080/09168451.2014.890039
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- Article
In Vivo Bioconversion of Tetrahydroisoquinoline by Recombinant Coclaurine N-Methyltransferase.
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- Bioscience, Biotechnology & Biochemistry, 2004, v. 68, n. 4, p. 939, doi. 10.1271/bbb.68.939
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CBr<sub>4</sub> as a Mild Oxidant‐Enabled Oxidation of a sp<sup>3</sup> C−H Bond: A Facile Synthesis of the Persistent Iminium Salts of Tetrahydroisoquinolines.
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- Chemistry - A European Journal, 2024, v. 30, n. 14, p. 1, doi. 10.1002/chem.202303952
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Divergent and Nucleophile‐Assisted Rearrangement in the Construction of Pyrrolo[2,1‐b][3]benzazepine and Pyrido[2,1‐a]isoquinoline Scaffolds.
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- Chemistry - A European Journal, 2024, v. 30, n. 3, p. 1, doi. 10.1002/chem.202302919
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Selective Ring‐Opening Amination of Isochromans and Tetrahydroisoquinolines.
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- Angewandte Chemie, 2024, v. 136, n. 17, p. 1, doi. 10.1002/ange.202401318
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Intramolecular Carboamination of Aminodienes to N‐Heterocycles via C−N Bond Activation.
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- Angewandte Chemie, 2024, v. 136, n. 8, p. 1, doi. 10.1002/ange.202316563
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- Article
Boosting Hydrogen Production via Selective Two‐electron Mild Electrochemical Oxidation of Tetrahydroisoquinolines Completely to Dihydroisoquinolines.
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- Angewandte Chemie, 2023, v. 135, n. 11, p. 1, doi. 10.1002/ange.202216347
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A Modular Approach for Diversity‐Oriented Synthesis of 1,3‐trans‐Disubstituted Tetrahydroisoquinolines: Seven‐Step Asymmetric Synthesis of Michellamines B and C.
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- Angewandte Chemie, 2022, v. 134, n. 31, p. 1, doi. 10.1002/ange.202205245
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Iridium‐Catalyzed Asymmetric Hydrogenation of 2,3‐Diarylallyl Amines with a Threonine‐Derived P‐Stereogenic Ligand for the Synthesis of Tetrahydroquinolines and Tetrahydroisoquinolines.
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- Angewandte Chemie, 2022, v. 134, n. 29, p. 1, doi. 10.1002/ange.202204300
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Nickel‐Catalyzed Enantioselective Synthesis of 2,3,4‐Trisubstituted 3‐Pyrrolines.
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- Angewandte Chemie, 2022, v. 134, n. 29, p. 1, doi. 10.1002/ange.202203494
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- Article
Cu<sup>II</sup>/TEMPO‐Catalyzed Enantioselective C(sp<sup>3</sup>)–H Alkynylation of Tertiary Cyclic Amines through Shono‐Type Oxidation.
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- Angewandte Chemie, 2020, v. 132, n. 35, p. 15366, doi. 10.1002/ange.202005099
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Integrating Hydrogen Production with Aqueous Selective Semi‐Dehydrogenation of Tetrahydroisoquinolines over a Ni<sub>2</sub>P Bifunctional Electrode.
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- Angewandte Chemie, 2019, v. 131, n. 35, p. 12142, doi. 10.1002/ange.201903327
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Synthesis and Cardiotropic Activity of bis-(2,3,4-Trimethoxybenzyl)Alkanediamines.
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- Pharmaceutical Chemistry Journal, 2021, v. 55, n. 4, p. 331, doi. 10.1007/s11094-021-02422-z
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Synthesis and Comparative Inotropic Effects of Several Isoquinoline Alkaloids.
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- Pharmaceutical Chemistry Journal, 2020, v. 54, n. 1, p. 7, doi. 10.1007/s11094-020-02148-4
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Synthesis and antibacterial activity of N-amino-derivatives of condensed pyridines.
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- Pharmaceutical Chemistry Journal, 2013, v. 47, n. 5, p. 257, doi. 10.1007/s11094-013-0940-3
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SYNTHESIS AND STRUCTURE OF PALLADACYCLOPENTADIENYL COMPLEX WITH ACENAPHTHENE-1,2-DIIMINE LIGAND.
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- Journal of Structural Chemistry, 2022, v. 63, n. 8, p. 1304, doi. 10.1134/S002247662208011X
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Synthesis, Structural Commentary, Supramolecular Architecture and Molecular Docking Investigations of a Novel Thiophene-Fused 1,2,3,4-Tetrahydroisoquinoline Derivative as a Potent Anti-Cancer Agent.
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- Journal of Structural Chemistry, 2019, v. 60, n. 7, p. 1143, doi. 10.1134/S0022476619070163
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Synthesis, Structural, Spectral Studies and Activity Studies of 6-Methyl-4-(3-Nitro-Phenyl)-2-Oxo-1,2,3,4 Tetrahydropyrimidine-5-Carboxylic Acid Ethyl Ester Catalyzed Using BF<sub>3</sub>-OEt<sub>2</sub>.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 6, p. 4137, doi. 10.1080/10406638.2023.2247116
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6,7-Dimethoxy-2-phenethyl-1,2,3,4-tetrahydroisoquinoline amides and corresponding ester isosteres as multidrug resistance reversers.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2020, v. 35, n. 1, p. 974, doi. 10.1080/14756366.2020.1747449
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Design and Synthesis of Indole and Tetrahydroisoquinoline Hydantoin Derivatives as Human Chymase Inhibitors.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2004, v. 19, n. 2, p. 137, doi. 10.1080/14756360310001650200
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Determination of Endogenous Neurotoxin 1-Acetyl-6,7-Dihydroxyl-1,2,3,4-Tetrahydroisoquinoline in Rat Substantia Nigra by High Performance Liquid Chromatography-Electrospray Ionization-Tandem Mass Spectrometry.
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- Analytical Letters, 2013, v. 46, n. 18, p. 2828, doi. 10.1080/00032719.2013.814057
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Chemoenzymatic One-Pot Process for the Synthesis of Tetrahydroisoquinolines.
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- Catalysts (2073-4344), 2021, v. 11, n. 11, p. 1389, doi. 10.3390/catal11111389
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- Article
AETIQ: A Novel Synthetic Compound with Anti-inflammatory Properties in Activated Microglia.
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- Inflammation, 2014, v. 37, n. 3, p. 766, doi. 10.1007/s10753-013-9795-8
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Synergistic dopaminergic neurotoxicity of MPTP and inflammogen lipopolysaccharide: relevance to the etiology of Parkinson's disease.
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- FASEB Journal, 2003, v. 17, n. 13, p. 1957, doi. 10.1096/fj.03-0203fje
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The mechanism of 1,2,3,4-tetrahydroisoquinolines neuroprotection: the importance of free radicals scavenging properties and inhibition of glutamate-induced excitotoxicity.
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- Journal of Neurochemistry, 2006, v. 97, n. 3, p. 846, doi. 10.1111/j.1471-4159.2006.03756.x
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Evaluation of neurotoxicity of TIQ and MPTP and of parkinsonism-preventing effect of 1-MeTIQ by in vivo measurement of pre-synaptic dopamine transporters and post-synaptic dopamine D[sub 2] receptors in the mouse striatum.
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- Journal of Neurochemistry, 2001, v. 79, n. 4, p. 868, doi. 10.1046/j.1471-4159.2001.00619.x
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Different action on dopamine catabolic pathways of two endogenous 1,2,3,4-tetrahydroisoquinolines with similar antidopaminergic properties.
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- Journal of Neurochemistry, 2001, v. 78, n. 1, p. 100, doi. 10.1046/j.1471-4159.2001.00391.x
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The Endogenous Amine 1-Methyl-1,2,3,4- Tetrahydroisoquinoline Prevents the Inhibition of Complex I of the Respiratory Chain Produced by MPP<sup>+</sup>.
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- Journal of Neurochemistry, 2000, v. 75, n. 1, p. 65, doi. 10.1046/j.1471-4159.2000.0750065.x
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Synthesis of 2,2'-bithiophene-5,5'-tetrahydroisoquinoline as michellamine analogs.
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- Journal of Sulfur Chemistry, 2004, v. 25, n. 4, p. 275, doi. 10.1080/1741599042000272593
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Occurrence of.
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- Chirality, 2016, v. 28, n. 3, p. 169, doi. 10.1002/chir.22566
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Amphiphilic Fluorescein Triazoles: Synthesis and Visible-Light Catalysis in Water.
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- Organics, 2024, v. 5, n. 3, p. 346, doi. 10.3390/org5030018
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Erratum: Synthetic chloroinconazide compound exhibits highly efficient antiviral activity against tobacco mosaic virus.
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- 2021
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- Correction Notice
Two novel alkaloids from Corydalis curviflora Maxim. and their insecticidal activity.
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- Pest Management Science, 2020, v. 76, n. 7, p. 2360, doi. 10.1002/ps.5772
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Synthesis, crystal structures and biological activity of palladium(II) complexes with 1-methyl-1H-1,2,3,4-tetrazole-5-thiol and substituted 2,20-bipyridines.
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- Journal of Coordination Chemistry, 2020, v. 73, n. 23, p. 3249, doi. 10.1080/00958972.2020.1844883
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Fragmentation of RGD-peptidomimetics, derivatives of 7-amino-1,2,3,4-tetrahydroisoquinoline and isophthalic acid, by fast atom bombardment mass spectrometry in positive and negative ion modes.
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- Journal of Analytical Chemistry, 2011, v. 66, n. 13, p. 1262, doi. 10.1134/S1061934811130041
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Anti-dryable, anti-freezable, and self-healable conductive hydrogel for adhesive electrodes.
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- Composite Interfaces, 2022, v. 29, n. 13, p. 1561, doi. 10.1080/09276440.2022.2068246
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- Article
SYNTHESIS, ANTIMICROBIAL AND ANTICANCER EVALUATION OF N-(2-(PHENYL)-4-OXOTHIAZOLIDIN-3- YL)-6-METHYL-4-(PHENYL)-2-OXO-1,2,3,4-TETRAHYDRO PYRIMIDINE-5-CARBOXAMIDE DERIVATIVES.
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- Rasayan Journal of Chemistry, 2022, v. 15, n. 4, p. 2782, doi. 10.31788/RJC.2022.1546994
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A facile approach for synthesis of thiazines-, thiazoles- and triazoles-annulated 6-styryl-2-thiouracil derivative.
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- Journal of the Iranian Chemical Society, 2020, v. 17, n. 1, p. 119, doi. 10.1007/s13738-019-01760-w
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Highly regio- and diastereoselective synthesis of oxo-1,2,3,4-tetrahydropyrazino[1,2-a]indoles, based on a post-Ugi condensation: joint experimental and computational study.
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- Journal of the Iranian Chemical Society, 2019, v. 16, n. 7, p. 1517, doi. 10.1007/s13738-019-01632-3
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Increased Levels of Monoamine-Derived Potential Neurotoxins in Fetal Rat Brain Exposed to Ethanol.
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- Neurochemical Research, 2013, v. 38, n. 2, p. 356, doi. 10.1007/s11064-012-0926-7
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Effects of single and repeated administration of 1,2,3,4-tetrahydroisoquinoline analogs on the binding of [<sup>11</sup>C]raclopride to dopamine D<sub>2</sub> receptors in the mouse brain.
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- Journal of Neural Transmission, 2001, v. 108, n. 10, p. 1111, doi. 10.1007/s007020170001
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Opposite effect of simple tetrahydroisoquinolines on amphetamine- and morphine-stimulated locomotor activity in mice.
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- Journal of Neural Transmission, 2001, v. 108, n. 5, p. 513, doi. 10.1007/s007020170053
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Antidopaminergic effects of 1,2,3,4-tetrahydroisoquinoline and salsolinol.
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- Journal of Neural Transmission, 2000, v. 107, n. 8/9, p. 1009, doi. 10.1007/s007020070049
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Analysis of tetrahydroisoquinolines formed after simultaneous consumption of ethanol and amphetamine or its derivatives by LC–MS/MS in human blood, brain, and liver tissue.
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- Analytical & Bioanalytical Chemistry, 2024, v. 416, n. 28, p. 6497, doi. 10.1007/s00216-024-05540-1
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Substituted tetrahydroisoquinoline compound B3 inhibited P-glycoprotein-mediated multidrug resistance in-vitro and in-vivo.
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- Journal of Pharmacy & Pharmacology, 2007, v. 59, n. 12, p. 1649, doi. 10.1211/jpp.59.12.0006
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Tetrahydroisoquinolines affect the whole-cell phenotype of Mycobacterium tuberculosis by inhibiting the ATP-dependent MurE ligase.
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- Journal of Antimicrobial Chemotherapy (JAC), 2015, v. 70, n. 6, p. 1691, doi. 10.1093/jac/dkv010
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Novel tetrahydroisoquinolines as DHFR and CDK2 inhibitors: synthesis, characterization, anticancer activity and antioxidant properties.
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- BMC Chemistry, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s13065-024-01139-w
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- Article
Antidepressant-Like Effect of the Endogenous Neuroprotective Amine, 1MeTIQ in Clonidine-Induced Depression: Behavioral and Neurochemical Studies in Rats.
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- Neurotoxicity Research, 2017, v. 32, n. 1, p. 94, doi. 10.1007/s12640-017-9715-z
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Comparison of the Effects of Acute and Chronic Administration of Tetrahydroisoquinoline Amines on the In Vivo Dopamine Release: A Microdialysis Study in the Rat Striatum.
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- Neurotoxicity Research, 2016, v. 30, n. 4, p. 648, doi. 10.1007/s12640-016-9661-1
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1-Benzyl-1,2,3,4-tetrahydroisoquinoline, an Endogenous Neurotoxic Compound, Disturbs the Behavioral and Biochemical Effects of l-DOPA: In Vivo and Ex Vivo Studies in the Rat.
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- Neurotoxicity Research, 2014, v. 26, n. 3, p. 240, doi. 10.1007/s12640-014-9476-x
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