2020 - Fellow, National Academy of Inventors
George Barany spends much of his time researching Stereochemistry, Peptide synthesis, Solid-phase synthesis, Biochemistry and Peptide. In the field of Stereochemistry, his study on Related derivatives overlaps with subjects such as Elaboration. His work carried out in the field of Peptide synthesis brings together such families of science as Nanotechnology, Phase, Methylene, Chromatography and Racemization.
His Solid-phase synthesis research is multidisciplinary, incorporating elements of Cyclic peptide, Proteolytic enzymes, Amide, Alkoxy group and Combinatorial chemistry. His research in Biochemistry intersects with topics in Organosulfur compounds and Biophysics. His Peptide research integrates issues from Proteolysis, Peptide sequence and Solvent.
George Barany mainly focuses on Stereochemistry, Combinatorial chemistry, Solid-phase synthesis, Peptide and Peptide synthesis. His work focuses on many connections between Stereochemistry and other disciplines, such as Alkoxy group, that overlap with his field of interest in Tris. George Barany has researched Combinatorial chemistry in several fields, including Disulfide bond and Organic chemistry, Phase.
His work in Solid-phase synthesis is not limited to one particular discipline; it also encompasses Cyclic peptide. To a larger extent, George Barany studies Biochemistry with the aim of understanding Peptide. His Peptide synthesis research is multidisciplinary, incorporating perspectives in Protecting group and Racemization.
His primary areas of study are Stereochemistry, Peptide, Biochemistry, Peptide synthesis and Solid-phase synthesis. The study incorporates disciplines such as Amino acid, Disulfide bond, Amide, Molecule and Alkoxy group in addition to Stereochemistry. His research integrates issues of Residue, Cysteine and Monomer in his study of Peptide.
His study in the fields of Prenylation, Glycoprotein, DNA ligase and Polymerase chain reaction under the domain of Biochemistry overlaps with other disciplines such as Sequencing by ligation. His work deals with themes such as Cleavage, Protecting group, Chromatography, Combinatorial chemistry and Organic chemistry, which intersect with Peptide synthesis. George Barany interconnects High-performance liquid chromatography, Sodium cyanoborohydride and Circular dichroism in the investigation of issues within Solid-phase synthesis.
His scientific interests lie mostly in Stereochemistry, Peptide synthesis, Peptide, Solid-phase synthesis and Amino acid. His Stereochemistry research includes elements of Methylene, Propionate and Amide. George Barany focuses mostly in the field of Peptide synthesis, narrowing it down to matters related to Chromatography and, in some cases, Nanotechnology, Dimethyl sulfoxide, Trypsin and Protein folding.
His Peptide study is related to the wider topic of Biochemistry. His Solid-phase synthesis research is multidisciplinary, relying on both Tertiary amine, Tris and Alkoxy group. His study in Amino acid is interdisciplinary in nature, drawing from both Valeric acid and Organic chemistry, Polyethylene glycol, Xanthate.
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Detection of nucleic acid sequence differences using coupled ligase detection and polymerase chain reactions
Francis Barany;Matthew Lubin;George Barany;Robert P. Hammer.
(1997)
Effects of organosulfur compounds from garlic and onions on benzo[a]pyrene-induced neoplasia and glutathione S-transferase activity in the mouse
Velta L. Sparnins;George Barany;Lee W. Wattenberg.
Carcinogenesis (1988)
Universal DNA microarray method for multiplex detection of low abundance point mutations.
Norman P Gerry;Nancy E Witowski;Joseph Day;Robert P Hammer.
Journal of Molecular Biology (1999)
Backbone Amide Linker (BAL) Strategy for Solid-Phase Synthesis of C-Terminal-Modified and Cyclic Peptides1,2,3
Knud J. Jensen;Jordi Alsina;Michael F. Songster;Josef Vágner.
Journal of the American Chemical Society (1998)
Inhibition of N-Nitrosodiethylamine Carcinogenesis in Mice by Naturally Occurring Organosulfur Compounds and Monoterpenes
Lee W. Wattenberg;Velta L. Sparnins;George Barany.
Cancer Research (1989)
Preparation and application of the 5-(4-(9-fluorenylmethyloxycarbonyl)aminomethyl-3,5-dimethoxyphenoxy)-valeric acid (PAL) handle for the solid-phase synthesis of C-terminal peptide amides under mild conditions
Fernando Albericio;Nancy Kneib-Cordonier;Sara Biancalana;Lajos Gera.
Journal of Organic Chemistry (1990)
A new amino protecting group removable by reduction. Chemistry of the dithiasuccinoyl (Dts) function.
G. Barany;R. B. Merrifield.
Journal of the American Chemical Society (1977)
A novel, convenient, three-dimensional orthogonal strategy for solid-phase synthesis of cyclic peptides
Steven A. Kates;Nuria A. Solé;Charles R. Johnson;Derek Hudson.
Tetrahedron Letters (1993)
Optimization of solid-phase synthesis of [Ala8]-dynorphin A
Nuria A. Sole;George Barany.
Journal of Organic Chemistry (1992)
Solid-phase peptide synthesis: a silver anniversary report
George Barany;Nancy Kneib‐Cordonier;Daniel G. Mullen.
International Journal of Peptide and Protein Research (2009)
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