Her primary scientific interests are in Carbonic anhydrase, Enzyme, Biochemistry, Active site and Stereochemistry. Her Carbonic anhydrase study integrates concerns from other disciplines, such as Protein structure, Lyase and Mechanism of action. Her Enzyme research incorporates themes from Dithiocarbamate, Small molecule and Cancer research.
Her Active site research includes elements of Cell membrane, Binding site and Sulfonamide. Her Stereochemistry study combines topics in areas such as Nucleic acid and Heteroduplex. Her research investigates the connection between Isozyme and topics such as Acetazolamide that intersect with problems in Gene isoform.
Carbonic anhydrase, Biochemistry, Enzyme, Stereochemistry and Active site are her primary areas of study. Her work carried out in the field of Carbonic anhydrase brings together such families of science as Lyase, Sulfonamide, Isozyme, Enzyme inhibitor and Gene isoform. Her Gene isoform research incorporates elements of Catalysis and Cytosol.
Her work on Esterase as part of general Enzyme research is frequently linked to Zonisamide, thereby connecting diverse disciplines of science. Her Stereochemistry research is multidisciplinary, incorporating perspectives in Adduct, Molecule, Carbonic anhydrase II and Crystal structure. Her Active site study combines topics from a wide range of disciplines, such as Zinc and Binding site.
Her scientific interests lie mostly in Carbonic anhydrase, Enzyme, Stereochemistry, Biochemistry and Active site. Her Carbonic anhydrase research is multidisciplinary, relying on both Proteoglycan, Drug target and Thiocyanate. Her work on Enzyme family as part of general Enzyme research is often related to Plasmodium species, thus linking different fields of science.
Her research in Stereochemistry intersects with topics in Catalysis, Carbonic anhydrase II and Gene isoform. Giuseppina De Simone combines subjects such as Marine diatom, Phaeodactylum tricornutum and Bacteria with her study of Biochemistry. Her studies deal with areas such as Molecule and Moiety as well as Active site.
Her primary areas of investigation include Carbonic anhydrase, Enzyme, Biochemistry, Trichomonas vaginalis and Gene isoform. She has included themes like Tumor microenvironment, Carbohydrate metabolism, Transcription factor, Active site and Metabolism in her Carbonic anhydrase study. In her study, which falls under the umbrella issue of Enzyme, Leishmaniasis and Trypanosoma is strongly linked to Microbiology.
As part of her studies on Biochemistry, Giuseppina De Simone frequently links adjacent subjects like Sulfamide. Her Gene isoform research integrates issues from Racemic mixture, Stereochemistry and Carbonic anhydrase II. The various areas that Giuseppina De Simone examines in her Stereochemistry study include Bicarbonate, Mutagenesis, Site-directed mutagenesis and Cytosol.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Multiple Binding Modes of Inhibitors to Carbonic Anhydrases: How to Design Specific Drugs Targeting 15 Different Isoforms?
Vincenzo Alterio;Anna Di Fiore;Katia D’Ambrosio;Claudiu T. Supuran.
Chemical Reviews (2012)
Crystal structure of the catalytic domain of the tumor-associated human carbonic anhydrase IX
Vincenzo Alterio;Mika Hilvo;Anna Di Fiore;Claudiu T. Supuran.
Proceedings of the National Academy of Sciences of the United States of America (2009)
Histone deacetylase and Cullin3-REN(KCTD11) ubiquitin ligase interplay regulates Hedgehog signalling through Gli acetylation
Gianluca Canettieri;Lucia Di Marcotullio;Azzura Greco;Sonia Coni.
Nature Cell Biology (2010)
Biochemical characterization of CA IX, one of the most active carbonic anhydrase isozymes.
Mika Hilvo;Lina Baranauskiene;Anna Maria Salzano;Andrea Scaloni.
Journal of Biological Chemistry (2008)
Anticancer carbonic anhydrase inhibitors: a patent review (2008 – 2013)
Simona Maria Monti;Claudiu T Supuran;Giuseppina De Simone.
Expert Opinion on Therapeutic Patents (2013)
Exploiting the hydrophobic and hydrophilic binding sites for designing carbonic anhydrase inhibitors.
Giuseppina De Simone;Vincenzo Alterio;Claudiu T Supuran.
Expert Opinion on Drug Discovery (2013)
In)organic anions as carbonic anhydrase inhibitors.
Giuseppina De Simone;Claudiu T. Supuran.
Journal of Inorganic Biochemistry (2012)
Carbonic anhydrase inhibitors: X-ray and molecular modeling study for the interaction of a fluorescent antitumor sulfonamide with isozyme II and IX.
Vincenzo Alterio;Rosa Maria Vitale;Simona Maria Monti;Carlo Pedone.
Journal of the American Chemical Society (2006)
Carbonic anhydrase IX: Biochemical and crystallographic characterization of a novel antitumor target.
Giuseppina De Simone;Claudiu T. Supuran.
Biochimica et Biophysica Acta (2010)
Carbonic anhydrase inhibitors: stacking with Phe131 determines active site binding region of inhibitors as exemplified by the X-ray crystal structure of a membrane-impermeant antitumor sulfonamide complexed with isozyme II.
Valeria Menchise;Giuseppina De Simone;Vincenzo Alterio;Anna Di Fiore.
Journal of Medicinal Chemistry (2005)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
University of Florence
University of Naples Federico II
University of Florence
University of Montpellier
Tampere University
University of Florence
National Research Council (CNR)
National Academies of Sciences, Engineering, and Medicine
University of Florence
University of Florence
Hohai University
University of Greenwich
University of California, Irvine
Hokkaido University
Arizona State University
University of Jinan
Scripps Research Institute
University of Glasgow
Arizona State University
Collège de France
University of Puerto Rico
University of Oregon
Syracuse University
University College London
University of Oxford
Concordia University