CNR Institutional Research Information System

ALTERIO, VINCENZO
 Distribuzione geografica
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Continente #
NA - Nord America 334
AS - Asia 187
EU - Europa 136
SA - Sud America 3
AF - Africa 2
OC - Oceania 1
Totale 663
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Nazione #
US - Stati Uniti d'America 333
SG - Singapore 155
IT - Italia 67
NL - Olanda 34
KR - Corea 13
FI - Finlandia 11
DE - Germania 5
AT - Austria 4
CN - Cina 4
HK - Hong Kong 3
IE - Irlanda 3
LT - Lituania 3
IN - India 2
MA - Marocco 2
UZ - Uzbekistan 2
AL - Albania 1
AR - Argentina 1
AZ - Azerbaigian 1
BR - Brasile 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
EE - Estonia 1
GB - Regno Unito 1
HR - Croazia 1
IL - Israele 1
KG - Kirghizistan 1
LK - Sri Lanka 1
LV - Lettonia 1
MX - Messico 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PE - Perù 1
PK - Pakistan 1
SA - Arabia Saudita 1
SE - Svezia 1
TJ - Tagikistan 1
TM - Turkmenistan 1
Totale 663
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Città #
Santa Clara 269
Singapore 112
Naples 25
Casandrino 14
Seoul 13
Helsinki 11
Los Angeles 7
Vienna 4
Amsterdam 3
Hong Kong 3
Afragola 2
Boardman 2
Boscotrecase 2
Cercola 2
Dublin 2
Marigliano 2
Phoenix 2
Rome 2
San Vito di Fagagna 2
Shenzhen 2
Soccavo 2
Tashkent 2
Trieste 2
Turin 2
Vilnius 2
Ashburn 1
Ashgabat 1
Baku 1
Bansha 1
Bishkek 1
Buenos Aires 1
Cascina 1
Colombo 1
Dushanbe 1
Falkenstein 1
Formigine 1
Fort Worth 1
Haifa 1
Islamabad 1
Lima 1
Ludhiana 1
Mexico City 1
Mumbai 1
New Plymouth 1
Newark 1
Prague 1
Prineville 1
Rabat 1
Riga 1
Riyadh 1
Sandefjord 1
Sorrento 1
Springfield 1
São Paulo 1
Tallinn 1
Tirana 1
Zagreb 1
Zurich 1
Totale 524
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Nome #
Inhibition of carbonic anhydrases IX/XII by SLC-0111 boosts cisplatin effects in hampering head and neck squamous carcinoma cell growth and invasion 30
α-CAs from Photosynthetic Organisms 23
6-Substituted Triazolyl Benzoxaboroles as Selective Carbonic Anhydrase Inhibitors: In Silico Design, Synthesis, and X-ray Crystallography 23
Discovery of a novel series of potent carbonic anhydrase inhibitors with selective affinity for μ Opioid receptor for Safer and long-lasting analgesia 22
null 21
A Novel Inhibitor of Carbonic Anhydrases Prevents Hypoxia-Induced TNBC Cell Plasticity 21
Zeta-carbonic anhydrases show CS2 hydrolase activity: A new metabolic carbon acquisition pathway in diatoms? 20
A Combined in Silico and Structural Study Opens New Perspectives on Aliphatic Sulfonamides, a Still Poorly Investigated Class of CA Inhibitors 19
2-Mercaptobenzoxazoles: a class of carbonic anhydrase inhibitors with a novel binding mode to the enzyme active site 16
Z-Carbonic anhydrases 16
Functional and structural features of the oxyanion hole in a thermophilic esterase from Alicyclobacillus acidocaldarius 16
Benzyl alcohol inhibits carbonic anhydrases by anchoring to the zinc coordinated water molecule 15
Exploring the binding mode of phenyl and vinyl boronic acids to human carbonic anhydrases 15
X-Ray Crystallography of Carbonic Anhydrase Inhibitors and Its Importance in Drug Design 14
Structural study of the Carbonic Anhydrase SazCA from the thermophilic bacterium Sulfurihydrogenibium Azorense 14
ALPHA-CARBONIC ANHYDRASES 14
Recent advances in structural studies of the carbonic anhydrase family: the crystal structure of human CA IX and CA XIII. 12
Crystal structure of the most catalytically effective carbonic anhydrase enzyme known, SazCA from the thermophilic bacterium Sulfurihydrogenibium azorense 12
Carbonic Anhydrases as new targets against the bacterial pathogen Brucella suis 12
Cadmium-containing carbonic anhydrase CDCA1 in marine diatom Thalassiosira weissflogii 12
Biochemical and Structural Insights into Carbonic Anhydrase XII/Fab6A10 Complex 12
Exploring benzoxaborole derivatives as carbonic anhydrase inhibitors: a structural and computational analysis reveals their conformational variability as a tool to increase enzyme selectivity 11
The anticonvulsant sulfamide JNJ-26990990 and its S,S-dioxide analog strongly inhibit carbonic anhydrases: solution and X-ray crystallographic studies 11
Crystal structure of an S-formylglutathione hydrolase from pseudoalteromonas haloplanktis TAC125. 11
Insights into the binding mode of sulphamates and sulphamides to hCA II: crystallographic studies and binding free energy calculations 10
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. 10
Disclosing the interaction of carbonic anhydrase ix with cullin-associated nedd8-dissociated protein 1 by molecular modeling and integrated binding measurements. 10
THE CRYSTAL STRUCTURE OF HCA I/TOPIRAMATE COMPLEX PROVIDES USEFUL INSIGHTS INTO RATIONAL DRUG DESIGN OF ANTI-OBESITY DRUGS 9
Inhibition of carbonic anhydrase IX targets primary tumors, metastases, and cancer stem cells: Three for the price of one 9
A new role of Human Carbonic Anhydrase VII in the protection of the cells from oxidative damage 9
Crystal structure of the C183S/C217S mutant of human CA VII in complex with acetazolamide. 9
Benzoxaborole as a new chemotype for carbonic anhydrase inhibition 9
Thermal-stable carbonic anhydrases: a structural overview. 8
Phenyl(thio)phosphon(amid)ate Benzenesulfonamides as Potent and Selective Inhibitors of Human Carbonic Anhydrases II and VII Counteract Allodynia in a Mouse Model of Oxaliplatin-Induced Neuropathy 8
CDCA1 FROM THALASSIOSIRA WEISSFLOGII AS REPRESENTATIVE MEMBER OF ZETA-CLASS CAs: GENERAL FEATURES AND BIOTECHNOLOGICAL APPLICATIONS 8
Inhibition of carbonic anhydrases by a substrate analog: benzyl carbamate directly coordinates the catalytic zinc ion mimicking bicarbonate binding 8
Crystal structure of the human carbonic anhydrase II adduct with 1-(4-sulfamoylphenyl-ethyl)-2,4,6-triphenylpyridinium perchlorate, a membrane-impermeant, isoform selective inhibitor 8
Biochemical characterization of the chloroplastic beta-carbonic anhydrase from Flaveria bidentis (L.) "Kuntze" 8
Carbonic Anhydrase Inhibitors. Comparison of Aliphatic Sulfamate/Bis-sulfamate Adducts with Isozymes II and IX as a Platform for Designing Tight-Binding, More Isoform-Selective Inhibitors 7
Thermostable carbonic anhydrases in biotechnological applications 7
The first example of a significant active site conformational rearrangement in a carbonic anhydrase-inhibitor adduct: the carbonic anhydrase I-topiramate complex. 7
Multiple binding modes of inhibitors to carbonic anhydrases: How to design specific drugs targeting 15 different isoforms? 7
Probing Molecular Interactions between Human Carbonic Anhydrases (hCAs) and a Novel Class of Benzenesulfonamides 7
The crystal structure of an EST2 mutant unveils structural insights on the H group of the carboxylesterase/lipase family. 7
Depsides from Origanum dictamnus and Satureja pilosa as selective inhibitors of carbonic anhydrases: Isolation, structure elucidation, X‐ray crystallography 7
Structure and inhibition insights into Carbonic anhydrase CDCA1 from marine diatom Thalassiosira Weissflogii. 6
Hypoxia-targeting carbonic anhydrase IX inhibitors by a new series of nitroimidazole-sulfonamides/sulfamides/sulfamates 6
CARBONIC ANHYDRASE INHIBITORS: X-RAY CRYSTALLOGRAPHIC STUDIES FOR THE BINDING OF MOLECULES CONTAINING A SULFAMIDE MOIETY 6
Insights into the carbonic anhydrase family: biochemical characterization of the human isozyme VII 6
Metal ion substitution in catalytic site greatly affects the binding of sulfhydryl-containing compounds to bovine leucyl aminopeptidase 6
STRUCTURAL AND INHIBITION STUDIES OF CARBONIC ANHYDRASE INHIBITORS CONTAINING THE SULFAMIDE ZINC BINDING GROUP 6
Structural and inhibition insights into carbonic anhydrase CDCA1 from the marine diatom Thalassiosira weissflogii 6
Peptides mimicking IC tail of hCA IX tumor enzyme interact with nuclear transport factors 6
Insights into plant beta- carbonic anhydrase isolated from Flaveria Bidentis 6
Design, synthesis and characterization of peptides mimicking hCA IX IC tail able to interact with nuclear transport factors 6
Discovery of 1,1'-Biphenyl-4-sulfonamides as a New Class of Potent and Selective Carbonic Anhydrase XIV Inhibitors 5
Crystal structure of the catalytic domain of the tumor-associated human carbonic anhydrase IX. 5
Human Carbonic Anhydrase VII protects cells from oxidative damage 5
Structural insights into Carbonic anhydrase CDCA1 from marine diatom Thalassiosira Weissflogii 5
X-ray crystallographic and kinetic investigations of 6-sulfamoyl-saccharin as a carbonic anhydrase inhibitor 5
Hydroxylamine-O-sulfonamide is a versatile lead compound for the development of carbonic anhydrase inhibitors 5
Hydrophobic Substituents of the Phenylmethylsulfamide Moiety Can Be Used for the Development of New Selective Carbonic Anhydrase Inhibitors 5
Structural characterization of human carbonic anhydrase VII. 5
STRUCTURAL CHARACTERIZATION OF HUMAN CARBONIC ANHYDRASE 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
Carbonic Anhydrase Inhibitors: X-ray and Molecular Modeling Study for the Interaction of a Fluorescent Antitumor Sulfonamide with Isozyme II and IX 5
Recent developments of carbonic anhydrase inhibitors as potential drugs 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
The crystal structure of CA I/Topiramate complex provides useful insights into rational drug design of anti-obesity drug 4
The structural comparison between membrane-associated human carbonic anhydrases provides insights into drug design of selective inhibitors 4
Carbonic anhydrase VII is S-glutathionylated without loss of catalytic activity and affinity for sulfonamide inhibitors 4
Exploiting the hydrophobic and hydrophilic binding sites for designing carbonic anhydrase inhibitors 4
Kinetic and X-ray crystallographic investigations of substituted 2-thio-6-oxo-1,6-dihydropyrimidine-benzenesulfonamides acting as carbonic anhydrase inhibitors 4
Carbonic anhydrase inhibitors: Inhibition of human, bacterial, and archaeal isozymes with benzene-1,3-disulfonamides - Solution and crystallographic studies 4
Identification and characterization of a new form of oncosuppressor KCTD11 4
Carbonic anhydrase inhibitors: comparison of aliphatic sulfamate/bis-sulfamate adducts with isozimes II and IX 4
The crystal structure of the (Zn/Zn)bLAP/zofenoprilat complex. 4
Carbonic anhydrase inhibitors. Comparison of aliphatic sulfamate/bis-sulfamate adducts with isozymes II and IX as a platform for designing tight-binding, more isoform-selective inhibitors 4
NUCLEAR TRANSPORT FACTORS IMPORTIN KAPbeta2 AND EXPORTIN CRM1 INTERACT WITH THE TUMOR ENZYME hCA IX 1
Phenyl(thio)phosphon(amid)ate Benzenesulfonamides as Potent and Selective Inhibitors of Human Carbonic Anhydrases II and VII Counteract Allodynia in a Mouse Model of Oxaliplatin-Induced Neuropathy 1
Totale 738
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Categoria #
all - tutte 3.382
article - articoli 2.400
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 234
Totale 6.016
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2023/202431 0 0 0 0 0 0 0 0 12 0 16 3
2024/2025707 26 11 134 47 275 39 12 71 64 28 0 0
Totale 738