Nano Letters, ISSN 1530-6984, 07/2007, Volume 7, Issue 7, pp. 2112 - 2115
We report a new strategy for preparing silver nanoparticle−oligonucleotide conjugates that are based upon DNA with cyclic disulfide-anchoring groups. These...
AQUEOUS DISPERSIONS | MATERIALS SCIENCE, MULTIDISCIPLINARY | NANOSCIENCE & NANOTECHNOLOGY | ULTRASENSITIVE DETECTION | HYBRIDIZATION | COLORIMETRIC DETECTION | CHEMISTRY, MULTIDISCIPLINARY | PROBES | FILMS | SPECTROSCOPY | ASSEMBLIES | MODIFIED GOLD NANOPARTICLES | AGGREGATION | Silver | DNA | Disulfides | Oligonucleotides | Metal Nanoparticles | Organophosphates
AQUEOUS DISPERSIONS | MATERIALS SCIENCE, MULTIDISCIPLINARY | NANOSCIENCE & NANOTECHNOLOGY | ULTRASENSITIVE DETECTION | HYBRIDIZATION | COLORIMETRIC DETECTION | CHEMISTRY, MULTIDISCIPLINARY | PROBES | FILMS | SPECTROSCOPY | ASSEMBLIES | MODIFIED GOLD NANOPARTICLES | AGGREGATION | Silver | DNA | Disulfides | Oligonucleotides | Metal Nanoparticles | Organophosphates
Journal Article
Analytical Chemistry, ISSN 0003-2700, 03/2017, Volume 89, Issue 5, pp. 3015 - 3020
We present a feasible paradigm of developing original fluorescent probes for target biomolecules via combinatorial chemistry. In this developmental program,...
THIOLS | CHEMISTRY, ANALYTICAL | AROMATIC DISULFIDES | CARBON-MONOXIDE | GLUTATHIONE | OXYGEN SPECIES GENERATION | RECENT PROGRESS | CYSTEINE | HYDROGEN-PEROXIDE | TOXICITY | WATER SAMPLES | Fluorescent Dyes - chemistry | Optical Imaging | Cysteine - analysis | Humans | Pyrimidines - chemistry | Hep G2 Cells | Sulfhydryl Compounds - analysis | Phenols - analysis | Animals | Glutathione - analysis | Homocysteine - analysis | Phenols - chemistry | Sulfhydryl Compounds - chemistry | Mice | HeLa Cells | Microscopy, Fluorescence
THIOLS | CHEMISTRY, ANALYTICAL | AROMATIC DISULFIDES | CARBON-MONOXIDE | GLUTATHIONE | OXYGEN SPECIES GENERATION | RECENT PROGRESS | CYSTEINE | HYDROGEN-PEROXIDE | TOXICITY | WATER SAMPLES | Fluorescent Dyes - chemistry | Optical Imaging | Cysteine - analysis | Humans | Pyrimidines - chemistry | Hep G2 Cells | Sulfhydryl Compounds - analysis | Phenols - analysis | Animals | Glutathione - analysis | Homocysteine - analysis | Phenols - chemistry | Sulfhydryl Compounds - chemistry | Mice | HeLa Cells | Microscopy, Fluorescence
Journal Article
Journal of Controlled Release, ISSN 0168-3659, 03/2018, Volume 274, pp. 93 - 101
Cell impurities are an emerging nucleating molecular barriers having the capability in disordering the metabolic chain reactions of proteolysis, glycolysis and...
Scaffold biomaterials | Crystal growth | Ester | Mesosphere vesicles | Polar groups | Non-polar groups | Methionine | Disulfide moieties | Histone | Lipopeptides | CRYSTALLIZATION | BIOACTIVE PEPTIDES | FOOD PROTEINS | STABILITY | DIFFERENTIAL SCANNING CALORIMETRY | CHEMISTRY, MULTIDISCIPLINARY | OPIOID RECEPTOR LIGANDS | MILK-PROTEINS | DISEASE | PHARMACOLOGY & PHARMACY | NUTRITION | FUNCTIONALITIES
Scaffold biomaterials | Crystal growth | Ester | Mesosphere vesicles | Polar groups | Non-polar groups | Methionine | Disulfide moieties | Histone | Lipopeptides | CRYSTALLIZATION | BIOACTIVE PEPTIDES | FOOD PROTEINS | STABILITY | DIFFERENTIAL SCANNING CALORIMETRY | CHEMISTRY, MULTIDISCIPLINARY | OPIOID RECEPTOR LIGANDS | MILK-PROTEINS | DISEASE | PHARMACOLOGY & PHARMACY | NUTRITION | FUNCTIONALITIES
Journal Article
Express Polymer Letters, ISSN 1788-618X, 04/2017, Volume 11, Issue 4, pp. 266 - 277
Aromatic disulfide dynamic structures were incorporated as chain extenders in waterborne organic-inorganic polyurethane hybrids in order to provide autonomic...
Smart polymers | Healing | Disulfide bonds | Waterborne polyurethanes | Metathesis | POLYMER SCIENCE | RESOLUTION | LINKS | SELF-HEALING MATERIALS | COMPOSITES | COPOLYMERS | RUBBER | POLYMER NETWORKS | disulfide bonds | healing | SILICATES | metathesis | waterborne polyurethanes | smart polymers | Physical properties | Acetone
Smart polymers | Healing | Disulfide bonds | Waterborne polyurethanes | Metathesis | POLYMER SCIENCE | RESOLUTION | LINKS | SELF-HEALING MATERIALS | COMPOSITES | COPOLYMERS | RUBBER | POLYMER NETWORKS | disulfide bonds | healing | SILICATES | metathesis | waterborne polyurethanes | smart polymers | Physical properties | Acetone
Journal Article
Journal of Controlled Release, ISSN 0168-3659, 2011, Volume 155, Issue 2, pp. 331 - 340
The effects of the presence of two different types of phenylboronic acids as side groups in disulfide-containing poly(amido amine)s (SS-PAA) were investigated...
Phenylboronic acid | Gene delivery | Polyplex | Bioreducible polymer | Poly(amido amine) | CELLS | PARTICLES | PHYSIOLOGICAL PH | NUCLEOTIDE ADSORPTION | SUGARS | CHEMISTRY, MULTIDISCIPLINARY | SIDE-CHAINS | CONTAINING COPOLYMERS | PHARMACOLOGY & PHARMACY | BINDING | DISULFIDE LINKAGES | Hemolysis - drug effects | Gene Transfer Techniques | Cricetinae | Polyamines - chemistry | Cell Survival | Humans | Cercopithecus aethiops | DNA - administration & dosage | Nylons - chemistry | Nylons - chemical synthesis | Boronic Acids - chemistry | Drug Carriers - chemical synthesis | Nylons - pharmacology | Drug Carriers - chemistry | Erythrocytes - drug effects | DNA - genetics | Animals | Transfection | Molecular Structure | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | COS Cells | Boronic Acids - chemical synthesis | Boronic Acids - pharmacology
Phenylboronic acid | Gene delivery | Polyplex | Bioreducible polymer | Poly(amido amine) | CELLS | PARTICLES | PHYSIOLOGICAL PH | NUCLEOTIDE ADSORPTION | SUGARS | CHEMISTRY, MULTIDISCIPLINARY | SIDE-CHAINS | CONTAINING COPOLYMERS | PHARMACOLOGY & PHARMACY | BINDING | DISULFIDE LINKAGES | Hemolysis - drug effects | Gene Transfer Techniques | Cricetinae | Polyamines - chemistry | Cell Survival | Humans | Cercopithecus aethiops | DNA - administration & dosage | Nylons - chemistry | Nylons - chemical synthesis | Boronic Acids - chemistry | Drug Carriers - chemical synthesis | Nylons - pharmacology | Drug Carriers - chemistry | Erythrocytes - drug effects | DNA - genetics | Animals | Transfection | Molecular Structure | Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | COS Cells | Boronic Acids - chemical synthesis | Boronic Acids - pharmacology
Journal Article
European Journal of Medicinal Chemistry, ISSN 0223-5234, 2008, Volume 43, Issue 4, pp. 808 - 815
The reaction of 2,3,5-trichlorobenzoic acid hydrazide with carbon disulfide and potassium hydroxide followed by treatment with hydrazine hydrate afforded...
Triazolothiadiazines | Antimicrobial screening | Trichlorophenyl moiety | Triazolothiadiazoles | Anti-inflammatory | CHEMISTRY, MEDICINAL | antimicrobial screening | trichlorophenyl moiety | ANTIBACTERIAL | HETEROCYCLES | anti-inflammatory | triazolothiadiazoles | AGENTS | ANTIFUNGAL ACTIVITIES | triazolothiadiazines | CIPROFLOXACIN | DERIVATIVES | THIOSEMICARBAZIDES | Fungi - drug effects | Magnetic Resonance Spectroscopy | Anti-Inflammatory Agents - pharmacology | Anti-Infective Agents - pharmacology | Bacteria - drug effects | Rats | Edema - drug therapy | Structure-Activity Relationship | Anti-Infective Agents - chemical synthesis | Microbial Sensitivity Tests | Animals | Anti-Inflammatory Agents - chemistry | Thiadiazoles - chemical synthesis | Thiadiazoles - chemistry | Anti-Infective Agents - chemistry | Anti-Inflammatory Agents - chemical synthesis | Molecular Structure | Carrageenan | Edema - chemically induced | Thiadiazoles - pharmacology | Carbon disulfide | Anti-inflammatory drugs
Triazolothiadiazines | Antimicrobial screening | Trichlorophenyl moiety | Triazolothiadiazoles | Anti-inflammatory | CHEMISTRY, MEDICINAL | antimicrobial screening | trichlorophenyl moiety | ANTIBACTERIAL | HETEROCYCLES | anti-inflammatory | triazolothiadiazoles | AGENTS | ANTIFUNGAL ACTIVITIES | triazolothiadiazines | CIPROFLOXACIN | DERIVATIVES | THIOSEMICARBAZIDES | Fungi - drug effects | Magnetic Resonance Spectroscopy | Anti-Inflammatory Agents - pharmacology | Anti-Infective Agents - pharmacology | Bacteria - drug effects | Rats | Edema - drug therapy | Structure-Activity Relationship | Anti-Infective Agents - chemical synthesis | Microbial Sensitivity Tests | Animals | Anti-Inflammatory Agents - chemistry | Thiadiazoles - chemical synthesis | Thiadiazoles - chemistry | Anti-Infective Agents - chemistry | Anti-Inflammatory Agents - chemical synthesis | Molecular Structure | Carrageenan | Edema - chemically induced | Thiadiazoles - pharmacology | Carbon disulfide | Anti-inflammatory drugs
Journal Article
Journal of Molecular Structure, ISSN 0022-2860, 07/2018, Volume 1164, pp. 137 - 154
A series of new dimer complexes of copper (II) and nickel (II) were designed and synthesized using the Schiff base ligands which was formed by the condensation...
Dimer copper (II) and nickel (II) complexes | Crystal structures of disulfide Schiff bases | Antibacterial screening activities | 2-Aminothiophenol moiety | Catalytic SOD-Like properties | TRANSITION-METAL-COMPLEXES | CHEMISTRY, PHYSICAL | SEMICARBAZONE LIGANDS | ZINC(II) COMPLEXES | COORDINATION-COMPOUNDS | PALLADIUM(II) COMPLEXES | SUPEROXIDE-DISMUTASE ACTIVITY | ANTIMICROBIAL ACTIVITIES | BIOLOGICAL-ACTIVITY | COBALT(II) COMPLEXES | COPPER(II)-DISULFIDE INTERACTION | Schiff bases | Diffraction | Analysis | X-rays | Crystals | Copper compounds | Nickel | Chemical properties | Structure | Antibacterial agents
Dimer copper (II) and nickel (II) complexes | Crystal structures of disulfide Schiff bases | Antibacterial screening activities | 2-Aminothiophenol moiety | Catalytic SOD-Like properties | TRANSITION-METAL-COMPLEXES | CHEMISTRY, PHYSICAL | SEMICARBAZONE LIGANDS | ZINC(II) COMPLEXES | COORDINATION-COMPOUNDS | PALLADIUM(II) COMPLEXES | SUPEROXIDE-DISMUTASE ACTIVITY | ANTIMICROBIAL ACTIVITIES | BIOLOGICAL-ACTIVITY | COBALT(II) COMPLEXES | COPPER(II)-DISULFIDE INTERACTION | Schiff bases | Diffraction | Analysis | X-rays | Crystals | Copper compounds | Nickel | Chemical properties | Structure | Antibacterial agents
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 05/2014, Volume 52, Issue 10, pp. 1448 - 1457
ABSTRACT We describe a new strategy for preparation of benzoxazine monomers based on in situ preparation of a thiol‐functionalized benzoxazine and successive...
thiol | benzoxazine | differential scanning calorimetry (DSC) | thermogravimetric analysis (TGA) | monomers | thermosets | MAIN-CHAIN | POLYMER SCIENCE | POLYBENZOXAZINES | CROSS-LINKING BEHAVIOR | CLICK CHEMISTRY | RING-OPENING POLYMERIZATION | Acrylates | Sulfides | Usage | Thermoplastics | Thiols | Analysis | Polymerization | Precursors | Disulfides | Benzoxazines | Monomers | Bearing
thiol | benzoxazine | differential scanning calorimetry (DSC) | thermogravimetric analysis (TGA) | monomers | thermosets | MAIN-CHAIN | POLYMER SCIENCE | POLYBENZOXAZINES | CROSS-LINKING BEHAVIOR | CLICK CHEMISTRY | RING-OPENING POLYMERIZATION | Acrylates | Sulfides | Usage | Thermoplastics | Thiols | Analysis | Polymerization | Precursors | Disulfides | Benzoxazines | Monomers | Bearing
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 06/2013, Volume 78, Issue 11, pp. 5463 - 5469
Water-soluble cationic cyclophane having diphenyl disulfide moieties (1a) was synthesized as a reduction-responsive degradable host. The stoichiometry for the...
HOSTS | BIS-ANS | GENE DELIVERY | MOLECULAR RECOGNITION | INTRACELLULAR DRUG-DELIVERY | AQUEOUS-MEDIA | CHEMISTRY, ORGANIC | SURFACE-PLASMON RESONANCE | SENSITIVE DISULFIDE | IMMOBILIZED GUESTS | BLOCK-COPOLYMER | Macrocyclic Compounds - chemistry | Oxidation-Reduction | Disulfides - chemistry | Aza Compounds - chemical synthesis | Solubility | Water - chemistry | Aza Compounds - chemistry | Molecular Structure | Binding Sites | Macrocyclic Compounds - chemical synthesis | Thermal properties | Fluorescence spectroscopy | Usage | Water chemistry | Cyclophanes | Chemical reaction, Rate of | Analysis | Chemical properties
HOSTS | BIS-ANS | GENE DELIVERY | MOLECULAR RECOGNITION | INTRACELLULAR DRUG-DELIVERY | AQUEOUS-MEDIA | CHEMISTRY, ORGANIC | SURFACE-PLASMON RESONANCE | SENSITIVE DISULFIDE | IMMOBILIZED GUESTS | BLOCK-COPOLYMER | Macrocyclic Compounds - chemistry | Oxidation-Reduction | Disulfides - chemistry | Aza Compounds - chemical synthesis | Solubility | Water - chemistry | Aza Compounds - chemistry | Molecular Structure | Binding Sites | Macrocyclic Compounds - chemical synthesis | Thermal properties | Fluorescence spectroscopy | Usage | Water chemistry | Cyclophanes | Chemical reaction, Rate of | Analysis | Chemical properties
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 04/2018, Volume 59, Issue 17, pp. 1674 - 1678
Various spirooxindoles bearing 2,3-(or 2,5-)dihydrothiophene-2-thione moiety have been synthesized via [3+2] annulation reaction of carbon disulfide and the...
[3+2] Annulation | Spirooxindoles | Dihydrothiophene-2-thione | Carbon disulfide | Morita-Baylis-Hillman carbonates | ISOTHIOCYANATES | OXIDE | 1,3-DIPOLAR CYCLOADDITION | 1,4,2-OXATHIAZOLES | CHEMISTRY, ORGANIC | FRAGMENTATION
[3+2] Annulation | Spirooxindoles | Dihydrothiophene-2-thione | Carbon disulfide | Morita-Baylis-Hillman carbonates | ISOTHIOCYANATES | OXIDE | 1,3-DIPOLAR CYCLOADDITION | 1,4,2-OXATHIAZOLES | CHEMISTRY, ORGANIC | FRAGMENTATION
Journal Article
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 09/2016, Volume 26, Issue 18, pp. 4414 - 4416
A series of novel nonsymmetrical disulfides bearing 1,3,4-oxadiazole moiety were synthesized and evaluated for their in vitro antiproliferative activities...
1,3,4-Oxadiazole | Antiproliferative activity | Nonsymmetrical disulfides | ACETOHYDROXYACID SYNTHASE | DESIGN | CHEMISTRY, MEDICINAL | SERIES | ANTICANCER AGENTS | 3D-QSAR | CHEMISTRY, ORGANIC | ANTITUMOR-ACTIVITY | BIOLOGICAL EVALUATION | INHIBITORS | DERIVATIVES | Disulfides - chemistry | Antineoplastic Agents - chemical synthesis | Humans | Cell Line, Tumor | Inhibitory Concentration 50 | Antineoplastic Agents - pharmacology | Fluorouracil - pharmacology | Oxadiazoles - chemistry
1,3,4-Oxadiazole | Antiproliferative activity | Nonsymmetrical disulfides | ACETOHYDROXYACID SYNTHASE | DESIGN | CHEMISTRY, MEDICINAL | SERIES | ANTICANCER AGENTS | 3D-QSAR | CHEMISTRY, ORGANIC | ANTITUMOR-ACTIVITY | BIOLOGICAL EVALUATION | INHIBITORS | DERIVATIVES | Disulfides - chemistry | Antineoplastic Agents - chemical synthesis | Humans | Cell Line, Tumor | Inhibitory Concentration 50 | Antineoplastic Agents - pharmacology | Fluorouracil - pharmacology | Oxadiazoles - chemistry
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 05/2017, Volume 23, Issue 30, pp. 7278 - 7286
Honeycomb‐structured films represent an intriguing class of two‐dimensional porous materials. Specifically, polyoxometalate (POM) macroanions can be introduced...
ionic liquid | honeycomb structure | photoluminescence | polyoxometalates | phase transfer
ionic liquid | honeycomb structure | photoluminescence | polyoxometalates | phase transfer
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 7/2001, Volume 98, Issue 15, pp. 8513 - 8518
A covalently linked protein-protein conjugate between ThiF and ThiS thiocarboxylate was found in a partially purified coexpressed ThiF/ThiS protein mixture by...
Biological Sciences | Gels | Plasmids | Ubiquitins | DNA | Thiazoles | Mass spectroscopy | Biosynthesis | Biochemistry | Sulfur | Alkylation | IN-VITRO BIOSYNTHESIS | THII | LIPOIC ACID | SULFURTRANSFERASE | MULTIDISCIPLINARY SCIENCES | ISCS | SULFUR | TRANSFER-RNA | 4-THIOURIDINE BIOSYNTHESIS | LARGE MOLECULES | MASS-SPECTROMETRY | Cross-Linking Reagents | Thiazoles - metabolism | Nucleotidyltransferases - chemistry | Thiamine Pyrophosphate - chemistry | Bacterial Proteins - chemistry | Disulfides | Ligases - metabolism | Ubiquitin-Protein Ligases | Escherichia coli Proteins | Escherichia coli - metabolism | Bacterial Proteins - metabolism | Thiamine Pyrophosphate - biosynthesis | Molecular Structure | Nucleotidyltransferases - metabolism | Ubiquitins - metabolism | Acylation | Carrier Proteins | Ubiquitin | Physiological aspects | Evolution | Genetic aspects | Escherichia coli | thiamine | ThiS protein | ThiF protein
Biological Sciences | Gels | Plasmids | Ubiquitins | DNA | Thiazoles | Mass spectroscopy | Biosynthesis | Biochemistry | Sulfur | Alkylation | IN-VITRO BIOSYNTHESIS | THII | LIPOIC ACID | SULFURTRANSFERASE | MULTIDISCIPLINARY SCIENCES | ISCS | SULFUR | TRANSFER-RNA | 4-THIOURIDINE BIOSYNTHESIS | LARGE MOLECULES | MASS-SPECTROMETRY | Cross-Linking Reagents | Thiazoles - metabolism | Nucleotidyltransferases - chemistry | Thiamine Pyrophosphate - chemistry | Bacterial Proteins - chemistry | Disulfides | Ligases - metabolism | Ubiquitin-Protein Ligases | Escherichia coli Proteins | Escherichia coli - metabolism | Bacterial Proteins - metabolism | Thiamine Pyrophosphate - biosynthesis | Molecular Structure | Nucleotidyltransferases - metabolism | Ubiquitins - metabolism | Acylation | Carrier Proteins | Ubiquitin | Physiological aspects | Evolution | Genetic aspects | Escherichia coli | thiamine | ThiS protein | ThiF protein
Journal Article
Synthetic Communications, ISSN 0039-7911, 02/2019, Volume 49, Issue 3, pp. 456 - 462
Alkyl (E)-2-(3-Alkyl-5-oxo-1-phenyl-1,5-dihydro-4H-pyrazol-4-ylidene)-5-(alkylamino)-1,3-dithiole-4-carboxylates have been obtained by condensation of...
carbon disulfide | Nef-isocyanide-Perkow reaction | cyclic ketene dithioacetal | Pyrazolone | polarized double bond | CONVENIENT SYNTHESIS | ASYMMETRIC-SYNTHESIS | CONSTRUCTION | CHEMISTRY, ORGANIC | BEARING
carbon disulfide | Nef-isocyanide-Perkow reaction | cyclic ketene dithioacetal | Pyrazolone | polarized double bond | CONVENIENT SYNTHESIS | ASYMMETRIC-SYNTHESIS | CONSTRUCTION | CHEMISTRY, ORGANIC | BEARING
Journal Article
Microsystem Technologies, ISSN 0946-7076, 1/2018, Volume 24, Issue 1, pp. 683 - 690
This paper describes selective recovery of Au(III), Pd(II), and Ag(I) from waste printed circuit boards (WPCBs) by CFP-g-PHCTMA, an adsorbent based on...
Electronics and Microelectronics, Instrumentation | Engineering | Mechanical Engineering | Nanotechnology | GOLD | PHYSICS, APPLIED | COTTON FIBERS | ELECTRONIC WASTE | MATERIALS SCIENCE, MULTIDISCIPLINARY | MOBILE PHONES | NANOSCIENCE & NANOTECHNOLOGY | CARBON-DISULFIDE | ADSORPTION | PRECIOUS METALS | ENGINEERING, ELECTRICAL & ELECTRONIC | CHELATING RESIN | 3-COMPONENT POLYADDITION | CYANIDE
Electronics and Microelectronics, Instrumentation | Engineering | Mechanical Engineering | Nanotechnology | GOLD | PHYSICS, APPLIED | COTTON FIBERS | ELECTRONIC WASTE | MATERIALS SCIENCE, MULTIDISCIPLINARY | MOBILE PHONES | NANOSCIENCE & NANOTECHNOLOGY | CARBON-DISULFIDE | ADSORPTION | PRECIOUS METALS | ENGINEERING, ELECTRICAL & ELECTRONIC | CHELATING RESIN | 3-COMPONENT POLYADDITION | CYANIDE
Journal Article
Applied Organometallic Chemistry, ISSN 0268-2605, 11/2013, Volume 27, Issue 11, pp. 639 - 643
The formation of ArSY (Y: C(= S)NMe2, Ph, P(= O)(OEt)2) by reductive elimination from σ‐aryl complexes (M(PPh3)2PhBr, M = Ni, Pd), associated with disulfides...
room temperature reaction | nickel complex | C−S cross‐coupling | disulfide | C-S cross-coupling
room temperature reaction | nickel complex | C−S cross‐coupling | disulfide | C-S cross-coupling
Journal Article
Tetrahedron, ISSN 0040-4020, 2012, Volume 68, Issue 6, pp. 1810 - 1818
Grundmann's ketone ( ) was used as a common building block for introduction of the C+D ring motif of steroids to prepare series of novel secosteroids...
Secosteroid | Nitrile | Cross-coupling reaction | Disulfide | DESIGN | CHEMISTRY, ORGANIC | WITHANOLIDES | ADDUCT | CYTOTOXIC ACTIVITY | Heterocyclic compounds | Analysis | Synthesis (chemistry) | Ketones | Disulfides | Tetrahedrons | Nitriles | Chemical reactions | Nuclear magnetic resonance | Steroids
Secosteroid | Nitrile | Cross-coupling reaction | Disulfide | DESIGN | CHEMISTRY, ORGANIC | WITHANOLIDES | ADDUCT | CYTOTOXIC ACTIVITY | Heterocyclic compounds | Analysis | Synthesis (chemistry) | Ketones | Disulfides | Tetrahedrons | Nitriles | Chemical reactions | Nuclear magnetic resonance | Steroids
Journal Article
Chemical and Pharmaceutical Bulletin, ISSN 0009-2363, 2017, Volume 65, Issue 10, pp. 950 - 958
A series of novel disulfides containing 1,3,4-thiadiazole moiety were designed, synthesized, and the structures of all products were identified by spectral...
disulfide | 1,3,4-thiadiazole | antiproliferative activity | 1-3-4-thiadiazole | ACETOHYDROXYACID SYNTHASE | CHEMISTRY, MEDICINAL | ANTITUMOR-EVALUATION | CHEMISTRY, MULTIDISCIPLINARY | 1,2,4-TRIAZOLE | ANTIOXIDANT | BIOLOGICAL EVALUATION | PHARMACOLOGY & PHARMACY | AGENTS | INHIBITORS | DERIVATIVES | A549 Cells | Antineoplastic Agents - chemical synthesis | Humans | Structure-Activity Relationship | Disulfides - chemistry | Thiadiazoles - chemistry | Drug Design | Cell Line, Tumor | Antineoplastic Agents - pharmacology | Cell Proliferation - drug effects | HeLa Cells | Drug Screening Assays, Antitumor | Thiadiazoles - pharmacology
disulfide | 1,3,4-thiadiazole | antiproliferative activity | 1-3-4-thiadiazole | ACETOHYDROXYACID SYNTHASE | CHEMISTRY, MEDICINAL | ANTITUMOR-EVALUATION | CHEMISTRY, MULTIDISCIPLINARY | 1,2,4-TRIAZOLE | ANTIOXIDANT | BIOLOGICAL EVALUATION | PHARMACOLOGY & PHARMACY | AGENTS | INHIBITORS | DERIVATIVES | A549 Cells | Antineoplastic Agents - chemical synthesis | Humans | Structure-Activity Relationship | Disulfides - chemistry | Thiadiazoles - chemistry | Drug Design | Cell Line, Tumor | Antineoplastic Agents - pharmacology | Cell Proliferation - drug effects | HeLa Cells | Drug Screening Assays, Antitumor | Thiadiazoles - pharmacology
Journal Article