S. M. Monti

发表

Maleness-on-the-Y (MoY) orchestrates male sex determination in major agricultural fruit fly pests

J. Ragoussis, J. Nagaraju, M. Robinson, 2019, Science.

Maleness-on-the-Y (MoY) orchestrates male sex determination in major agricultural fruit fly pests

Mark D. Robinson, Jiannis Ragoussis, Marco Salvemini, 2019, Science.

Identification of non-specific Lipid Transfer Protein gene family members in Solanum lycopersicum and insights into the features of Sola l 3 protein

S. M. Monti, A. Barone, N. D’Agostino, 2019, Scientific Reports.

Carbonic anhydrase inhibitors: X-ray and molecular modeling study for the interaction of a fluorescent antitumor sulfonamide with isozyme II and IX.

C. Supuran, A. Scozzafava, Alessandro Cecchi, 2006, Journal of the American Chemical Society.

Carbonic anhydrase inhibitors: crystallographic and solution binding studies for the interaction of a boron-containing aromatic sulfamide with mammalian isoforms I-XV.

C. Supuran, J. Winum, A. Innocenti, 2010, Bioorganic & medicinal chemistry letters.

Carbonic Anhydrase VII

C. Supuran, S. M. Monti, G. Simone, 2015 .

Carbonic anhydrase VII is S-glutathionylated without loss of catalytic activity and affinity for sulfonamide inhibitors.

C. Supuran, A. Innocenti, D. Vullo, 2012, Bioorganic & medicinal chemistry letters.

An immunological approach to monitor protein lactosylation of heated food model systems

V. Fogliano, S. M. Monti, A. Ritieni, 1997 .

Exploring benzoxaborole derivatives as carbonic anhydrase inhibitors: a structural and computational analysis reveals their conformational variability as a tool to increase enzyme selectivity

E. Langella, C. Supuran, J. Winum, 2019, Journal of enzyme inhibition and medicinal chemistry.

Insights into the binding mode of sulphamates and sulphamides to hCA II: crystallographic studies and binding free energy calculations

E. Langella, C. Supuran, J. Winum, 2017, Journal of enzyme inhibition and medicinal chemistry.

Discovery of 1,1'-Biphenyl-4-sulfonamides as a New Class of Potent and Selective Carbonic Anhydrase XIV Inhibitors.

C. Supuran, A. Coluccia, D. Vullo, 2015, Journal of medicinal chemistry.

Biochemical, biophysical and molecular dynamics studies on the proteoglycan-like domain of carbonic anhydrase IX

E. Langella, C. Supuran, D. Vullo, 2018, Cellular and Molecular Life Sciences.

Occurrence of fusaproliferin, fumonisin B1, and beauvericin in maize from Italy

A. Logrieco, V. Fogliano, S. M. Monti, 1997 .

The Amazing World of IDPs in Human Diseases

E. Langella, S. M. Monti, G. De Simone, 2021, Biomolecules.

Cadmium-Containing Carbonic Anhydrase CDCA1 in Marine Diatom Thalassiosira weissflogii

E. Langella, S. M. Monti, V. Alterio, 2015, Marine drugs.

Recent advances in structural studies of the carbonic anhydrase family: the crystal structure of human CA IX and CA XIII.

C. Supuran, S. M. Monti, V. Alterio, 2010, Current pharmaceutical design.

Benzoxaborole as a new chemotype for carbonic anhydrase inhibition.

C. Supuran, J. Winum, D. Vullo, 2016, Chemical communications.

Simultaneous quantification of amino acids and Amadori products in foods through ion-pairing liquid chromatography–high-resolution mass spectrometry

V. Fogliano, S. M. Monti, G. Roviello, 2014, Amino Acids.

Polyclonal antibodies against fusaproliferin.

A. Logrieco, V. Fogliano, S. M. Monti, 1999, Canadian journal of microbiology.

A new FcεRI receptor‐mimetic peptide (PepE) that blocks IgE binding to its high affinity receptor and prevents mediator release from RBL 2H3 cells

S. M. Monti, R. Palumbo, M. Ruvo, 2011, Journal of peptide science : an official publication of the European Peptide Society.

IgE-binding properties and selectivity of peptide mimics of the FcvarepsilonRI binding site.

S. M. Monti, N. Dathan, M. Saviano, 2009, Molecular immunology.

Expression and purification of the D4 region of PLD1 and characterization of its interaction with PED-PEA15.

S. M. Monti, F. Beguinot, C. Miele, 2008, Protein expression and purification.

Generation and functional characterization of a BCL10-inhibitory peptide that represses NF-kappaB activation.

S. Formisano, S. M. Monti, B. Tizzano, 2009, The Biochemical journal.

Formation of coloured Maillard reaction products in a gluten- glucose model system

V. Fogliano, S. M. Monti, A. Ritieni, 1999 .

Protein–Protein Interactions: A Simple Strategy to Identify Binding Sites and Peptide Antagonists

S. M. Monti, N. Dathan, C. Pedone, 2009, Chemical biology & drug design.

Crystal structure of the C183S/C217S mutant of human CA VII in complex with acetazolamide.

C. Supuran, S. M. Monti, N. Dathan, 2010, Bioorganic & medicinal chemistry letters.

α-CAs from Photosynthetic Organisms

E. Langella, S. M. Monti, K. D'Ambrosio, 2022, International journal of molecular sciences.

Analysis of bacterial lipodepsipeptides by matrix-assisted laser desorption/ionisation time-of-flight and high-performance liquid chromatography with electrospray mass spectrometry.

M. Gallo, V. Fogliano, S. M. Monti, 2001, Rapid communications in mass spectrometry : RCM.

ζ-Carbonic anhydrases

E. Langella, S. M. Monti, V. Alterio, 2019, Carbonic Anhydrases.

CDCA1 From Thalassiosira weissflogii as Representative Member of ζ-Class CAs: General Features and Biotechnological Applications

C. Supuran, S. M. Monti, V. Alterio, 2015 .

Teratogenic Effects of Fusaproliferin on Chicken Embryos

A. Logrieco, V. Fogliano, S. M. Monti, 1997 .

STABILITY OF FUSAPROLIFERIN, A MYCOTOXIN FROM FUSARIUM SPP.

A. Logrieco, V. Fogliano, S. M. Monti, 1999 .

Not Only Systemin: Prosystemin Harbors Other Active Regions Able to Protect Tomato Plants

E. Langella, A. Aprile, S. M. Monti, 2022, Frontiers in Plant Science.

A Virulence Factor Encoded by a Polydnavirus Confers Tolerance to Transgenic Tobacco Plants against Lepidopteran Larvae, by Impairing Nutrient Absorption

S. M. Monti, F. Pennacchio, M. Casartelli, 2014, PloS one.

Biochemical characterization of the chloroplastic β-carbonic anhydrase from Flaveria bidentis (L.) “Kuntze”

C. Supuran, D. Vullo, S. M. Monti, 2014, Journal of enzyme inhibition and medicinal chemistry.

Anticancer carbonic anhydrase inhibitors: a patent review (2008 – 2013)

C. Supuran, S. M. Monti, G. De Simone, 2013, Expert opinion on therapeutic patents.

Dithiocarbamates are strong inhibitors of the beta-class fungal carbonic anhydrases from Cryptococcus neoformans, Candida albicans and Candida glabrata.

C. Supuran, A. Scozzafava, S. M. Monti, 2012, Bioorganic & medicinal chemistry letters.

Carotenoids from tomatoes inhibit heterocyclic amine formation

V. Fogliano, S. M. Monti, P. Vitaglione, 2002 .

Targeting of PED/PEA-15 Molecular Interaction with Phospholipase D1 Enhances Insulin Sensitivity in Skeletal Muscle Cells*

S. M. Monti, P. Formisano, F. Beguinot, 2008, Journal of Biological Chemistry.

Characterization of phenolic compounds in virgin olive oil and their effect on the formation of carcinogenic/mutagenic heterocyclic amines in a model system.

V. Fogliano, S. M. Monti, R. Sacchi, 2001, Journal of agricultural and food chemistry.

Kinetic and anion inhibition studies of a β-carbonic anhydrase (FbiCA 1) from the C4 plant Flaveria bidentis.

C. Supuran, A. Scozzafava, D. Vullo, 2013, Bioorganic & medicinal chemistry letters.

The chemical synthesis of the GstI protein by NCL on a X-Met site.

A. Chambery, S. M. Monti, P. Botti, 2006, Biopolymers.

Antioxidant activity of virgin olive oil phenolic compounds in a micellar system

M. Gallo, V. Fogliano, S. M. Monti, 1999 .

Discovery of 4-sulfamoyl-phenyl-β-lactams as a new class of potent carbonic anhydrase isoforms I, II, IV and VII inhibitors: The first example of subnanomolar CA IV inhibitors.

S. M. Monti, A. Angeli, Mallika Alvala, 2017, Bioorganic & medicinal chemistry.

Carbonic Anhydrase Inhibitors Targeting Metabolism and Tumor Microenvironment

S. Carradori, C. Supuran, S. Dedhar, 2020, Metabolites.

Synthesis of isoxazole-containing sulfonamides with potent carbonic anhydrase II and VII inhibitory properties.

C. Supuran, S. M. Monti, M. Buonanno, 2017, Bioorganic & medicinal chemistry.

Inhibition of carbonic anhydrase IX targets primary tumors, metastases, and cancer stem cells: Three for the price of one

C. Supuran, S. M. Monti, F. Carta, 2018, Medicinal research reviews.

Crystal structure of the catalytic domain of the tumor-associated human carbonic anhydrase IX

A. Scaloni, C. Supuran, A. Scozzafava, 2009, Proceedings of the National Academy of Sciences.

Microwave-assisted extraction, HPLC analysis, and inhibitory effects on carbonic anhydrase I, II, VA, and VII isoforms of 14 blueberry Italian cultivars

S. Carradori, A. Mollica, C. Supuran, 2016, Journal of enzyme inhibition and medicinal chemistry.

Discovery of Benzenesulfonamides with Potent Human Carbonic Anhydrase Inhibitory and Effective Anticonvulsant Action: Design, Synthesis, and Pharmacological Assessment.

C. B. Mishra, C. Supuran, S. M. Monti, 2017, Journal of medicinal chemistry.

Structural basis for the rational design of new anti-Brucella agents: the crystal structure of the C366S mutant of L-histidinol dehydrogenase from Brucella suis.

J. Winum, S. M. Monti, N. Dathan, 2014, Biochimie.

The influence of pH on the non-volatile reaction products of aqueous Maillard model systems by HPLC with diode array detection

S. M. Monti, J. Ames, R. G. Bailey, 1998 .

Identification of a β-lactoglobulin lactosylation site

V. Fogliano, A. Facchiano, S. M. Monti, 1998 .