CNR Institutional Research Information System

DI FIORE, ANNA
 Distribuzione geografica
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Continente #
NA - Nord America 311
AS - Asia 134
EU - Europa 42
Totale 487
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Nazione #
US - Stati Uniti d'America 311
SG - Singapore 118
IT - Italia 24
KR - Corea 12
FI - Finlandia 8
NL - Olanda 6
CN - Cina 4
AT - Austria 2
BE - Belgio 1
DE - Germania 1
Totale 487
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Città #
Santa Clara 284
Singapore 94
Naples 13
Seoul 12
Helsinki 8
Amsterdam 2
Boardman 2
Cercola 2
Dongguan 2
Prineville 2
Vienna 2
Ashburn 1
Boscotrecase 1
Brussels 1
Cascina 1
Falkenstein 1
Forest City 1
Fort Worth 1
Phoenix 1
Sorrento 1
Springfield 1
Totale 433
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Nome #
α-CAs from Photosynthetic Organisms 18
Biochemical and Structural Insights into the Winged Helix Domain of P150, the Largest Subunit of the Chromatin Assembly Factor 1 15
Discovery of a novel series of potent carbonic anhydrase inhibitors with selective affinity for μ Opioid receptor for Safer and long-lasting analgesia 15
The crystal structures of 2-(4-benzhydrylpiperazin-1-yl)-N-(4-sulfamoylphenyl)acetamide in complex with human carbonic anhydrase II and VII provide insights into selective CA inhibitor development 14
Biochemical and structural characterisation of a protozoan beta-carbonic anhydrase fromTrichomonas vaginalis 13
X-Ray Crystallography of Carbonic Anhydrase Inhibitors and Its Importance in Drug Design 12
Crystal structure of the most catalytically effective carbonic anhydrase enzyme known, SazCA from the thermophilic bacterium Sulfurihydrogenibium azorense 11
The anticonvulsant sulfamide JNJ-26990990 and its S,S-dioxide analog strongly inhibit carbonic anhydrases: solution and X-ray crystallographic studies 11
Recent advances in structural studies of the carbonic anhydrase family: the crystal structure of human CA IX and CA XIII. 10
Biochemical, structural, and computational studies of a ?-carbonic anhydrase from the pathogenic bacterium Burkholderia pseudomallei 10
ALPHA-CARBONIC ANHYDRASES 10
Exploration of the residues modulating the catalytic features of human carbonic anhydrase XIII by a site-specific mutagenesis approach 9
Carbonic anhydrase inhibitors: X-ray crystal structure of a benzenesulfonamide strong CA II and CA IX inhibitor bearing a pentafluorophenylaminothioureido tail in complex with isozyme II 9
Looking toward the Rim of the Active Site Cavity of Druggable Human Carbonic Anhydrase Isoforms 9
Insights into the role of reactive sulfhydryl groups of Carbonic Anhydrase III and VII during oxidative damage 9
Inhibition of the β-carbonic anhydrase from the protozoan pathogen Trichomonas vaginalis with sulphonamides 9
Carbonic anhydrase inhibitors: Valdecoxib binds to a different active site region of the human isoform II as compared to the structurally related cyclooxygenase II "selective" inhibitor celecoxib. 8
The Crystal Structure of a hCA VII Variant Provides Insights into the Molecular Determinants Responsible for Its Catalytic Behavior 8
X-ray structure of the first 'extremo-alfa-carbonic anhydrase', a dimeric enzyme from the thermophilic bacterium Sulfurihydrogenibium yellowstonense YO3AOP1 8
CARBONIC ANHYDRASE INHIBITORS: X-RAY CRYSTALLOGRAPHIC STUDIES FOR THE BINDING OF 5-AMINO-1,3,4-THIADIZOLE-2-SULFONAMIDE AND 5-(4-AMINO-3-CHLORO-5-FLUOROPHENYLSULFONAMIDO)-1,3,4-THIADIAZOLE-2-SULFONAMIDE TO HUMAN ISOFORM II 8
Crystal structure of the C183S/C217S mutant of human CA VII in complex with acetazolamide. 8
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. 8
Faox enzymes inhibited Maillard reaction development during storage both in protein glucose model system and low lactose UHT milk. 7
Are carbonic anhydrase inhibitors suitable for obtaining antiobesity drugs? 7
Inhibition of carbonic anhydrase IX targets primary tumors, metastases, and cancer stem cells: Three for the price of one 7
Post-translational modifications in tumor-associated carbonic anhydrases 7
Structural study of the Carbonic Anhydrase SazCA from the thermophilic bacterium Sulfurihydrogenibium Azorense 7
Protective Role of Carbonic Anhydrases III and VII in Cellular Defense Mechanisms upon Redox Unbalance 7
Exploring structural properties of potent human carbonic anhydrase inhibitors bearing a 4-(cycloalkylamino-1-carbonyl) benzenesulfonamide moiety 7
Probing Molecular Interactions between Human Carbonic Anhydrases (hCAs) and a Novel Class of Benzenesulfonamides 7
Eta- and teta-carbonic anhydrase 7
Biochemical characterization of CA IX, one of the most active Carbonic Anhydrase isozymes. 7
Benzoxaborole as a new chemotype for carbonic anhydrase inhibition 7
Human Carbonic Anhydrases and Post-Translational Modifications: A Hidden World Possibly Affecting Protein Properties and Functions 7
Disclosing the interaction of carbonic anhydrase ix with cullin-associated nedd8-dissociated protein 1 by molecular modeling and integrated binding measurements. 7
Thermostable carbonic anhydrases in biotechnological applications 6
Hydroxamate represents a versatile zinc binding group for the development of new carbonic anhydrase inhibitors 6
Multiple binding modes of inhibitors to carbonic anhydrases: How to design specific drugs targeting 15 different isoforms? 6
STRUCTURAL AND INHIBITION STUDIES OF CARBONIC ANHYDRASE INHIBITORS CONTAINING THE SULFAMIDE ZINC BINDING GROUP 6
Exploring benzoxaborole derivatives as carbonic anhydrase inhibitors: a structural and computational analysis reveals their conformational variability as a tool to increase enzyme selectivity 6
A new role of Human Carbonic Anhydrase VII in the protection of the cells from oxidative damage 6
FAOX enzymes from Aspergillus sp as enzymatic tools for preventing AGE formation . In: 11th Maillard Reaction 6
2-Substituted Estradiol Bis-sulfamates, Multitargeted Antitumor Agents: Synthesis, In Vitro SAR, Protein Crystallography, and In Vivo Activity 6
Human carbonic Anydrase VII protects cells from oxidative damage 5
Design, synthesis and biochemical evaluation of novel carbonic anhydrase inhibitors triggered by structural knowledge on hCA VII 5
Inhibition of the newly discovered ?-carbonic anhydrase from the protozoan pathogen Trichomonas vaginalis with inorganic anions and small molecules 5
STRUCTURAL CHARACTERIZATION OF CARBONIC ANHYDRASE INHIBITORS INCORPORATING NEW METAL BINDING FUNCTIONALITIES 5
Crystal structure of the catalytic domain of the tumor-associated human carbonic anhydrase IX. 5
The zinc coordination pattern in the eta-carbonic anhydrase from Plasmodium falciparum is different from all other carbonic anhydrase genetic families 5
Carbonic anhydrase inhibitors as emerging drugs for the treatment of obesity 5
Anticancer steroid sulfatase inhibitors: Synthesis of a potent fluorinated second-generation agent, in vitro and in vivo activities, molecular modeling, and protein crystallography. 5
CARBONIC ANHYDRASE INHIBITORS: X-RAY CRYSTALLOGRAPHIC STUDIES FOR THE BINDING OF MOLECULES CONTAINING A SULFAMIDE MOIETY 5
Biochemical and Structural Analysis of a New Carbonic Anhydrase from the Thermophilic Bacterium Sulfurihydrogenibium sp. YO3AOP1 5
Insights into the catalytic mechanism of the carbonic anhydrase family from the crystal structure of human isoform 5
Insights into the carbonic anhydrase family: biochemical characterization of the human isozyme VII 5
Structure-activity relationships of C-17 cyano-substituted estratrienes as anticancer agents 5
X-ray crystallographic and kinetic investigations of 6-sulfamoyl-saccharin as a carbonic anhydrase inhibitor 5
Biochemical and Structural Analysis of a New Carbonic Anhydrase from the Thermophilic Bacterium Sulfurihydrogenibium sp. YO3AOP1 5
Structural analysis of BldR from Sulfolobus solfataricus provides insights into the molecular basis of transcriptional activation in Archaea by MarR family proteins 5
Carbonic anhydrase inhibitors: crystallographic and solution binding studies for the interaction of a boron-containing aromatic sulfamide with mammalian isoforms I-XV. 5
Hydroxylamine-O-sulfonamide is a versatile lead compound for the development of carbonic anhydrase inhibitors 5
Peptides mimicking IC tail of hCA IX tumor enzyme interact with nuclear transport factors 5
Hydrophobic Substituents of the Phenylmethylsulfamide Moiety Can Be Used for the Development of New Selective Carbonic Anhydrase Inhibitors 5
Carbonic anhydrase inhibitors: the X-ray crystal structure of ethoxzolamide complexed to human isoform II reveals the importance of Thr200 and Gln92 for obtaining tight-binding inhibitors. 5
Structural characterization of human carbonic anhydrase VII. 5
Insights into the catalytic mechanism of the carbonic anhydrase family from the crystal structure of human isoform XIII 5
A NEW LEAD COMPOUND FOR THE DEVELOPMENT OF CARBONIC ANHYDRASE INHIBITORS 5
Crystal structure of the catalytic domain of the tumor-associated hCA IX 5
Design, synthesis and characterization of peptides mimicking hCA IX IC tail able to interact with nuclear transport factors 5
Recent developments of carbonic anhydrase inhibitors as potential drugs 4
Carbonic anhydrase inhibitors: hypoxia-activatable sulfonamides incorporating disulfide bonds that target the tumor-associated isoform IX 4
Human Carbonic Anhydrase VII protects cells from oxidative damage 4
Insights into Carbonic Anhydrase VII functional role 4
Carbonic anhydraseinhibitors: X-ray crystallographic studies for the binding of N-substitutedbenzenesulfonamides to human isoform II 4
Carbonic anhydrase VII is S-glutathionylated without loss of catalytic activity and affinity for sulfonamide inhibitors 4
Carbonic Anhydrase VII 4
Totale 529
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Categoria #
all - tutte 2.347
article - articoli 1.707
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 136
Totale 4.190
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202428 0 0 0 0 0 0 0 0 7 3 13 5
2024/2025501 7 11 118 44 276 45 0 0 0 0 0 0
Totale 529