Works matching DE "THIOL derivatives"
Results: 82
Visible‐Light‐Driven Germyl Radical Generation via EDA‐Catalyzed ET–HAT Process.
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- Chemistry - A European Journal, 2024, v. 30, n. 41, p. 1, doi. 10.1002/chem.202401546
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Synthesis of New Sesquiterpenoid Thio-Derivatives Based on Betulenone.
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- Chemistry of Natural Compounds, 2017, v. 53, n. 1, p. 66, doi. 10.1007/s10600-017-1913-7
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Thiol‐Ene Photopolymerization under Blue, Green and Red LED Irradiation.
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- ChemPhotoChem, 2021, v. 5, n. 6, p. 571, doi. 10.1002/cptc.202100028
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New DNA Methylation Inhibitors Based on 1,2,4-Triazole Thioether Derivatives.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 7, p. 1390, doi. 10.1134/S1070363218070071
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Effects of erdosteine on hemostasis: An experimental study.
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- Human & Experimental Toxicology, 2012, v. 31, n. 6, p. 574, doi. 10.1177/0960327111426588
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Synthesis and Antioxidant Activity of 2-Amino-5-methylthiazol Derivatives Containing 1,3,4-Oxadiazole-2-thiol Moiety.
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- ISRN Organic Chemistry, 2013, p. 1, doi. 10.1155/2013/620718
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Decomposition of 2-Mercaptoethyl O-Ester: S<sub>N</sub>2 Displacement or Acyl Transfer? A Theoretical Study.
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- Chinese Journal of Chemistry, 2014, v. 32, n. 4, p. 335, doi. 10.1002/cjoc.201300874
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Preparation of Diosgenin-Functionalized Gold Nanoparticles: From Synthesis to Antitumor Activities.
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- International Journal of Molecular Sciences, 2025, v. 26, n. 3, p. 1088, doi. 10.3390/ijms26031088
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Multifunctionalized Sequence-Defined Oligomers from a Single Building Block.
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- Angewandte Chemie, 2013, v. 125, n. 50, p. 13503, doi. 10.1002/ange.201307439
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Catalytic Enantioselective Synthesis of Tertiary Thiols From 5 H-Thiazol-4-ones and Nitroolefins: Bifunctional Ureidopeptide-Based Brønsted Base Catalysis.
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- Angewandte Chemie, 2013, v. 125, n. 45, p. 12062, doi. 10.1002/ange.201305644
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Planning, Synthesis, and Pharmacological Activity of Alkyl Derivatives of 3-Mercapto-4-Phenyl-5-Arylaminomethyl-1,2,4-Triazole-(4H).
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- Pharmaceutical Chemistry Journal, 2014, v. 47, n. 11, p. 581, doi. 10.1007/s11094-014-1011-0
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Problems of the Synthesis of Mercapto Derivatives from the Corresponding Hydroxy Polyphenylene Derivatives.
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- Russian Journal of Organic Chemistry, 2023, v. 59, n. 5, p. 826, doi. 10.1134/S1070428023050135
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NOVEL SYNTHESIS OF (E)-4-(BENZYLIDENEAMINO)-5-(3-METHOXY-2-METHYLPHENYL) -4H-1, 2, 4-TRIAZOLE-3-THIOL DERIVATIVES AND THEIR BIOLOGICAL SIGNIFICANCE.
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- Journal of Advanced Scientific Research, 2021, v. 11, p. 125
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Synthesis, characterization, and antitumor activity of some novel S-functionalized benzo[d]thiazole-2-thiol derivatives; regioselective coupling to the -SH group.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2018, v. 73, n. 9, p. 647, doi. 10.1515/znb-2018-0078
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Expression, purification and initial characterization of human serum albumin domain I and its cysteine 34.
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- PLoS ONE, 2020, v. 15, n. 10, p. 1, doi. 10.1371/journal.pone.0240580
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N-Acetyl cysteine and erdosteine treatment in acetaminophen-induced liver damage.
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- Toxicology & Industrial Health, 2014, v. 30, n. 7, p. 670, doi. 10.1177/0748233712463780
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S-Alkylated/aralkylated 2-(1H-indol-3-yl-methyl)-1,3,4- oxadiazole-5-thiol derivatives. 2. Anti-bacterial, enzymeinhibitory and hemolytic activities.
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- Tropical Journal of Pharmaceutical Research, 2016, v. 15, n. 7, p. 1525, doi. 10.4314/tjpr.v15i7.24
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Methylthio-Aspochalasins from a Marine-Derived Fungus Aspergillus sp.
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- Marine Drugs, 2014, v. 12, n. 10, p. 5124, doi. 10.3390/md12105124
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Hemi-synthesis of Thione and Thiol Derivatives from Artemisia judaica L. Essential Oil, and Antimicrobial Tests.
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- Kemija u Industriji, 2022, v. 71, n. 5/6, p. 287, doi. 10.15255/KUI.2021.062
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Synthesis and Biological Activity of 2-Mercapto-7,10-Dimethyl-3H-Spiro[Benzo[H]Quinazoline-5,1′-Cyclopentane]-4(6H)-One from Ethyl 4′-Amino-5′,8′-Dimethyl-1′H-Spiro[Cyclopentane-1,2′-Naphthalene]-3′-Carboxylate.
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- Pharmaceutical Chemistry Journal, 2018, v. 51, n. 12, p. 1057, doi. 10.1007/s11094-018-1740-6
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Synthesis of new transition metal complexes of 1 H-perimidine derivatives having antimicrobial and anti-inflammatory activities.
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- Research on Chemical Intermediates, 2012, v. 38, n. 7, p. 1527, doi. 10.1007/s11164-011-0482-9
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AlCl<sub>3</sub>-Catalyzed Intermolecular Annulation of Thiol Derivatives and Alkynes by 1,2-Sulfur Migration: Construction of 6-Substituted Benzo[b]thiophenes.
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- European Journal of Organic Chemistry, 2017, v. 2017, n. 30, p. 4405, doi. 10.1002/ejoc.201700607
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Enantiomeric Catalytic Formal Thiolation of 2,5-Dimethyl-3-[1-(arylsulfonyl)alkyl]pyrroles in an Oil/Water Biphasic System.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 35, p. 5826, doi. 10.1002/ejoc.201601180
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Enantioselective Catalytic Domino Aza-Michael-Henry Reactions: One-Pot Asymmetric Synthesis of 3-Nitro-1,2-dihydroquinolines via Iminium Activation.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 9, p. 1702, doi. 10.1002/ejoc.201501618
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Synthesis, Cytotoxicity Assessment and Molecular Docking of N-(5-(substituted-benzylthio)-1,3,4-thiadiazole-2-yl)-2-p-fluorophenylacetamide Derivatives as Tyrosine Kinase Inhibitors.
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- Indian Journal of Pharmaceutical Sciences, 2019, v. 81, n. 1, p. 63, doi. 10.4172/pharmaceutical-sciences.1000480
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Effects of erdosteine on alpha amanitin-induced hepatotoxicity in mice.
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- Toxin Reviews, 2016, v. 35, n. 1/2, p. 4, doi. 10.1080/15569543.2016.1178146
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Ion‐Selective Electrodes Based on Hydrophilic Ionophore‐Modified Nanopores.
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- Angewandte Chemie, 2018, v. 130, n. 17, p. 4842, doi. 10.1002/ange.201800954
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Site-Specific N-Terminal Labeling of Peptides and Proteins using Butelase 1 and Thiodepsipeptide.
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- Angewandte Chemie, 2015, v. 127, n. 52, p. 15920, doi. 10.1002/ange.201506810
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Linear Dendritic Block Copolymers as Promising Biomaterials for the Manufacturing of Soft Tissue Adhesive Patches Using Visible Light Initiated Thiol-Ene Coupling Chemistry.
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- Advanced Functional Materials, 2015, p. 6596, doi. 10.1002/adfm.201503235
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Role of PbSe Structural Stabilization in Photovoltaic Cells.
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- Advanced Functional Materials, 2015, v. 25, n. 6, p. 928, doi. 10.1002/adfm.201401816
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Effect of loading 5-phenyl-4H-1,2,4-triazole-3-thiol onto polypyrrole chitosan core shell nanoparticles on release rate, antimicrobial, and antitumor activities.
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- Journal of Bioactive & Compatible Polymers, 2017, v. 32, n. 2, p. 111, doi. 10.1177/0883911516658781
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TFA/DMSO‐Promoted Cross‐Dehydrogenative Coupling of Hetaryl Thiols with Indoles: Access to 3‐(Hetarylsulfenyl)indole under Mild Conditions.
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- Asian Journal of Organic Chemistry, 2022, v. 11, n. 2, p. 1, doi. 10.1002/ajoc.202100751
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Catalytic Asymmetric Conjugate Addition of Tritylthiol to Azadienes with a Bifunctional Organocatalyst.
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- Asian Journal of Organic Chemistry, 2018, v. 7, n. 8, p. 1561, doi. 10.1002/ajoc.201800299
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A Combined Synthetic and DFT Study on the Catalyst-Free and Solvent-Assisted Synthesis of 1,3,4-Oxadiazole-2-thiol Derivatives.
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- Journal of Chemistry, 2013, p. 1, doi. 10.1155/2013/476358
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Evaluation of thiol-disulphide homeostasis in radiation workers.
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- International Journal of Radiation Biology, 2017, v. 93, n. 7, p. 705, doi. 10.1080/09553002.2017.1304668
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Synthesis of Electro-active Compounds Suitable for Adsorption on Metal Surfaces.
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- Organic Preparations & Procedures International, 2017, v. 49, n. 5, p. 389, doi. 10.1080/00304948.2017.1374065
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DNA sequence-dependent fluorescence of doxorubicin for turn-on detection of biothiols in human serum.
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- Analytical & Bioanalytical Chemistry, 2016, v. 408, n. 3, p. 683, doi. 10.1007/s00216-015-9168-2
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p-Tolyl isocyanate derivatization for analysis of CWC-related polar degradation products by mass spectrometry.
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- Analytical & Bioanalytical Chemistry, 2014, v. 406, n. 21, p. 5093, doi. 10.1007/s00216-014-7624-z
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Hydrogels from norbornene-functionalized carboxymethyl cellulose using a UV-initiated thiol-ene click reaction.
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- Cellulose, 2018, v. 25, n. 11, p. 6531, doi. 10.1007/s10570-018-2015-9
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Dynamic thiol-disulfide balance in patients with chronic sinusitis with and without nasal polyposis.
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- Annals of Medical of Research, 2020, v. 27, n. 11, p. 3076, doi. 10.5455/annalsmedres.2020.04.313
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Biological evaluation and synthesis of new pyrimidine-2(1H)-ol/-thiol derivatives derived from chalcones using the solid phase microwave method.
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- Turkish Journal of Chemistry, 2018, v. 42, n. 2, p. 520, doi. 10.3906/kim-1711-9
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Theoretical Study on Design and Feasibility of Novel Circumtrindene Derivatives to Remove Ionic Contaminants.
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- Polycyclic Aromatic Compounds, 2024, v. 44, n. 2, p. 1037, doi. 10.1080/10406638.2023.2185642
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The new H<sub>2</sub>S-releasing compound ACS94 exerts protective effects through the modulation of thiol homoeostasis.
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- Journal of Enzyme Inhibition & Medicinal Chemistry, 2018, v. 33, n. 1, p. 1392, doi. 10.1080/14756366.2018.1509211
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Linkage Isomerization in Nitrosothiols (RSNOs): The X-ray Crystal Structure of an S -nitrosocysteine and DFT Analysis of its Metastable MS 1 and MS 2 Isomers.
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- Comments on Inorganic Chemistry, 2016, v. 36, n. 2, p. 81, doi. 10.1080/02603594.2015.1095185
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Simple, Rapid, and Sensitive Determination of Thiols by Liquid Chromatography with Fluorescence Detection.
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- Analytical Letters, 2019, v. 52, n. 9, p. 1487, doi. 10.1080/00032719.2018.1548020
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Synergistic stabilization by nitrosoglutathione-induced thiol modifications in the stromal interaction molecule-2 luminal domain suppresses basal and store operated calcium entry.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-66961-3
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Novel bismaleimide/diallylbisphenol A resin modified with multifunctional thiol containing isocyanuric ring and long-chain aliphatic unit.
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- High Performance Polymers, 2016, v. 28, n. 5, p. 591, doi. 10.1177/0954008315591191
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Continuous flow as a benign strategy for the synthesis of Thioesters via selective C-N bond cleavage.
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- Journal of Flow Chemistry, 2020, v. 10, n. 3, p. 507, doi. 10.1007/s41981-020-00090-w
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Synergistic Antioxidant Effects of Cysteine Derivative and Sm-Cluster for Food Applications.
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- Antioxidants, 2024, v. 13, n. 8, p. 910, doi. 10.3390/antiox13080910
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Tribology and oxidation studies of fatty acid sulfide derivatives synthesized via thiol-ene 'Click' additions.
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- European Journal of Lipid Science & Technology, 2016, v. 118, n. 3, p. 495, doi. 10.1002/ejlt.201500119
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