CNR Institutional Research Information System

ALTERIO, VINCENZO
 Distribuzione geografica
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Continente #
AS - Asia 1.792
NA - Nord America 1.410
EU - Europa 514
SA - Sud America 339
Continente sconosciuto - Info sul continente non disponibili 97
AF - Africa 27
OC - Oceania 1
Totale 4.180
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Nazione #
US - Stati Uniti d'America 1.330
SG - Singapore 726
CN - Cina 434
BR - Brasile 253
IT - Italia 197
HK - Hong Kong 168
VN - Vietnam 145
FR - Francia 85
KR - Corea 81
NL - Olanda 51
BD - Bangladesh 50
JP - Giappone 43
GB - Regno Unito 42
IN - India 37
CA - Canada 31
AR - Argentina 28
DE - Germania 26
FI - Finlandia 26
ID - Indonesia 17
MX - Messico 15
PL - Polonia 13
CO - Colombia 12
EC - Ecuador 12
ZA - Sudafrica 12
CR - Costa Rica 11
PE - Perù 11
IQ - Iraq 10
PK - Pakistan 10
RU - Federazione Russa 10
UA - Ucraina 10
IL - Israele 9
ES - Italia 8
SA - Arabia Saudita 8
JM - Giamaica 7
MA - Marocco 7
PH - Filippine 7
PY - Paraguay 7
SE - Svezia 7
VE - Venezuela 7
IE - Irlanda 6
UZ - Uzbekistan 6
AT - Austria 5
AZ - Azerbaigian 5
CL - Cile 5
TR - Turchia 5
LB - Libano 4
SV - El Salvador 4
BY - Bielorussia 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
GR - Grecia 3
HN - Honduras 3
JO - Giordania 3
KE - Kenya 3
KZ - Kazakistan 3
LT - Lituania 3
MY - Malesia 3
UY - Uruguay 3
BB - Barbados 2
CH - Svizzera 2
HU - Ungheria 2
MN - Mongolia 2
NP - Nepal 2
TH - Thailandia 2
TN - Tunisia 2
TW - Taiwan 2
XK - ???statistics.table.value.countryCode.XK??? 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
AM - Armenia 1
BE - Belgio 1
BG - Bulgaria 1
BH - Bahrain 1
BM - Bermuda 1
BO - Bolivia 1
CW - ???statistics.table.value.countryCode.CW??? 1
CZ - Repubblica Ceca 1
EE - Estonia 1
EG - Egitto 1
GP - Guadalupe 1
GT - Guatemala 1
HR - Croazia 1
HT - Haiti 1
KG - Kirghizistan 1
LK - Sri Lanka 1
LV - Lettonia 1
MM - Myanmar 1
MT - Malta 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PT - Portogallo 1
QA - Qatar 1
RO - Romania 1
SI - Slovenia 1
SN - Senegal 1
TJ - Tagikistan 1
TM - Turkmenistan 1
YT - Mayotte 1
Totale 4.086
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Città #
Singapore 445
Santa Clara 301
San Jose 200
Hefei 170
Hong Kong 161
Ashburn 116
Seoul 81
Los Angeles 78
Beijing 75
Lauterbourg 72
Ho Chi Minh City 48
Naples 48
New York 46
Dallas 34
Hanoi 34
Tokyo 30
São Paulo 29
Milan 20
Council Bluffs 15
Casandrino 14
Buffalo 13
Helsinki 13
Lappeenranta 12
Amsterdam 11
London 11
Orem 11
Rome 11
Warsaw 11
Frankfurt am Main 10
Minamishinagawa 10
Montreal 9
Phoenix 9
Atlanta 8
Bengaluru 8
Johannesburg 8
Chicago 7
Da Nang 7
Haiphong 7
San José 7
Shanghai 7
Brooklyn 6
Buenos Aires 6
Chennai 6
Dublin 6
Fortaleza 6
Houston 6
Philadelphia 6
Stockholm 6
Tashkent 6
Agra 5
Baku 5
Belo Horizonte 5
Charlotte 5
Columbus 5
Düsseldorf 5
Florence 5
Guayaquil 5
Lima 5
Mexico City 5
Miami 5
Porto Alegre 5
Rio de Janeiro 5
Salt Lake City 5
Turin 5
Vienna 5
Afragola 4
Asunción 4
Baghdad 4
Boardman 4
Bogotá 4
Campinas 4
Casablanca 4
Curitiba 4
Katy 4
Meridian 4
Mumbai 4
Portsmouth 4
Riyadh 4
San Salvador 4
The Bronx 4
Virginia Beach 4
Washington 4
Akron 3
Amman 3
Anaheim 3
Ankara 3
Aracaju 3
Ashland 3
Blumenau 3
Brasília 3
Caracas 3
Dayton 3
Denver 3
Dhaka 3
Figino 3
Guarulhos 3
Hải Dương 3
Kyiv 3
Lahore 3
Manchester 3
Totale 2.463
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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 131
Z-Carbonic anhydrases 112
α-CAs from Photosynthetic Organisms 98
Discovery of a novel series of potent carbonic anhydrase inhibitors with selective affinity for μ Opioid receptor for Safer and long-lasting analgesia 90
2-Mercaptobenzoxazoles: a class of carbonic anhydrase inhibitors with a novel binding mode to the enzyme active site 89
Benzyl alcohol inhibits carbonic anhydrases by anchoring to the zinc coordinated water molecule 84
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 79
THE CRYSTAL STRUCTURE OF HCA I/TOPIRAMATE COMPLEX PROVIDES USEFUL INSIGHTS INTO RATIONAL DRUG DESIGN OF ANTI-OBESITY DRUGS 77
A Novel Inhibitor of Carbonic Anhydrases Prevents Hypoxia-Induced TNBC Cell Plasticity 76
Thermostable carbonic anhydrases in biotechnological applications 74
6-Substituted Triazolyl Benzoxaboroles as Selective Carbonic Anhydrase Inhibitors: In Silico Design, Synthesis, and X-ray Crystallography 74
Structural study of the Carbonic Anhydrase SazCA from the thermophilic bacterium Sulfurihydrogenibium Azorense 72
Structure and inhibition insights into Carbonic anhydrase CDCA1 from marine diatom Thalassiosira Weissflogii. 70
Zeta-carbonic anhydrases show CS2 hydrolase activity: A new metabolic carbon acquisition pathway in diatoms? 70
Recent advances in structural studies of the carbonic anhydrase family: the crystal structure of human CA IX and CA XIII. 69
A Combined in Silico and Structural Study Opens New Perspectives on Aliphatic Sulfonamides, a Still Poorly Investigated Class of CA Inhibitors 68
ALPHA-CARBONIC ANHYDRASES 67
X-Ray Crystallography of Carbonic Anhydrase Inhibitors and Its Importance in Drug Design 63
Saccharomyces cerevesiae, Candida spp. and Cryptococcus neoformans β-CAs 63
Discovery of 1,1'-Biphenyl-4-sulfonamides as a New Class of Potent and Selective Carbonic Anhydrase XIV Inhibitors 62
A NEW LEAD COMPOUND FOR THE DEVELOPMENT OF CARBONIC ANHYDRASE INHIBITORS 62
Inhibition of carbonic anhydrase IX targets primary tumors, metastases, and cancer stem cells: Three for the price of one 59
Crystal structure of the most catalytically effective carbonic anhydrase enzyme known, SazCA from the thermophilic bacterium Sulfurihydrogenibium azorense 58
Exploring the binding mode of phenyl and vinyl boronic acids to human carbonic anhydrases 58
Exploring benzoxaborole derivatives as carbonic anhydrase inhibitors: a structural and computational analysis reveals their conformational variability as a tool to increase enzyme selectivity 58
Editorial: Emerging advancements in the carbonic anhydrase field 57
Biochemical and Structural Insights into Carbonic Anhydrase XII/Fab6A10 Complex 56
Crystal structure of an S-formylglutathione hydrolase from pseudoalteromonas haloplanktis TAC125. 56
The anticonvulsant sulfamide JNJ-26990990 and its S,S-dioxide analog strongly inhibit carbonic anhydrases: solution and X-ray crystallographic studies 53
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 51
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 51
Structural and inhibition insights into carbonic anhydrase CDCA1 from the marine diatom Thalassiosira weissflogii 50
Molecular organization of the cullin E3 ligase adaptor KCTD11 50
Functional and structural features of the oxyanion hole in a thermophilic esterase from Alicyclobacillus acidocaldarius 49
Disclosing the interaction of carbonic anhydrase ix with cullin-associated nedd8-dissociated protein 1 by molecular modeling and integrated binding measurements. 49
Biochemical characterization of the chloroplastic beta-carbonic anhydrase from Flaveria bidentis (L.) "Kuntze" 48
Multiple Binding Modes of Inhibitors to Human Carbonic Anhydrases: An Update on the Design of Isoform-Specific Modulators of Activity 47
Inhibition of carbonic anhydrases by a substrate analog: benzyl carbamate directly coordinates the catalytic zinc ion mimicking bicarbonate binding 47
Fungal α-carbonic anhydrases 47
Carbonic Anhydrases as new targets against the bacterial pathogen Brucella suis 46
Benzoxaborole as a new chemotype for carbonic anhydrase inhibition 46
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 45
Cadmium-containing carbonic anhydrase CDCA1 in marine diatom Thalassiosira weissflogii 45
Depsides from Origanum dictamnus and Satureja pilosa as selective inhibitors of carbonic anhydrases: Isolation, structure elucidation, X‐ray crystallography 44
STRUCTURAL AND INHIBITION STUDIES OF CARBONIC ANHYDRASE INHIBITORS CONTAINING THE SULFAMIDE ZINC BINDING GROUP 43
The crystal structure of an EST2 mutant unveils structural insights on the H group of the carboxylesterase/lipase family. 42
Insights into the binding mode of sulphamates and sulphamides to hCA II: crystallographic studies and binding free energy calculations 41
Multiple binding modes of inhibitors to carbonic anhydrases: How to design specific drugs targeting 15 different isoforms? 40
A new role of Human Carbonic Anhydrase VII in the protection of the cells from oxidative damage 40
Design, synthesis and characterization of peptides mimicking hCA IX IC tail able to interact with nuclear transport factors 40
Crystal structure of the C183S/C217S mutant of human CA VII in complex with acetazolamide. 39
Kinetic and X-ray crystallographic investigations of substituted 2-thio-6-oxo-1,6-dihydropyrimidine-benzenesulfonamides acting as carbonic anhydrase inhibitors 38
Thermal-stable carbonic anhydrases: a structural overview. 37
Structural insights into Carbonic anhydrase CDCA1 from marine diatom Thalassiosira Weissflogii 37
Multi-faceted exploration of the novel active γ-carbonic anhydrase PaCAγ1 in the human pathogen Pseudomonas aeruginosa 37
CDCA1 FROM THALASSIOSIRA WEISSFLOGII AS REPRESENTATIVE MEMBER OF ZETA-CLASS CAs: GENERAL FEATURES AND BIOTECHNOLOGICAL APPLICATIONS 36
X-ray crystallographic and kinetic investigations of 6-sulfamoyl-saccharin as a carbonic anhydrase inhibitor 35
Insights into plant beta- carbonic anhydrase isolated from Flaveria Bidentis 35
Recent developments of carbonic anhydrase inhibitors as potential drugs 34
Metal ion substitution in catalytic site greatly affects the binding of sulfhydryl-containing compounds to bovine leucyl aminopeptidase 34
Carbonic anhydrase inhibitors: Inhibition of human, bacterial, and archaeal isozymes with benzene-1,3-disulfonamides - Solution and crystallographic studies 34
Peptides mimicking IC tail of hCA IX tumor enzyme interact with nuclear transport factors 33
Carbonic anhydraseinhibitors: X-ray crystallographic studies for the binding of N-substitutedbenzenesulfonamides to human isoform II 32
CARBONIC ANHYDRASE INHIBITORS: X-RAY CRYSTALLOGRAPHIC STUDIES FOR THE BINDING OF MOLECULES CONTAINING A SULFAMIDE MOIETY 32
Probing Molecular Interactions between Human Carbonic Anhydrases (hCAs) and a Novel Class of Benzenesulfonamides 32
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. 32
Crystal structure of the catalytic domain of the tumor-associated human carbonic anhydrase IX. 31
Hydrophobic Substituents of the Phenylmethylsulfamide Moiety Can Be Used for the Development of New Selective Carbonic Anhydrase Inhibitors 31
Hypoxia-targeting carbonic anhydrase IX inhibitors by a new series of nitroimidazole-sulfonamides/sulfamides/sulfamates 30
The structural comparison between membrane-associated human carbonic anhydrases provides insights into drug design of selective inhibitors 30
Hydroxylamine-O-sulfonamide is a versatile lead compound for the development of carbonic anhydrase inhibitors 30
The first example of a significant active site conformational rearrangement in a carbonic anhydrase-inhibitor adduct: the carbonic anhydrase I-topiramate complex. 29
Exploiting the hydrophobic and hydrophilic binding sites for designing carbonic anhydrase inhibitors 29
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 29
The crystal structure of CA I/Topiramate complex provides useful insights into rational drug design of anti-obesity drug 28
NUCLEAR TRANSPORT FACTORS IMPORTIN KAPbeta2 AND EXPORTIN CRM1 INTERACT WITH THE TUMOR ENZYME hCA IX 27
Identification and characterization of a new form of oncosuppressor KCTD11 27
Crystal structure of the catalytic domain of the tumor-associated hCA IX 27
Insights into the carbonic anhydrase family: biochemical characterization of the human isozyme VII 26
Structural characterization of human carbonic anhydrase VII. 26
Carbonic Anhydrase Inhibitors: X-ray and Molecular Modeling Study for the Interaction of a Fluorescent Antitumor Sulfonamide with Isozyme II and IX 26
The crystal structure of the (Zn/Zn)bLAP/zofenoprilat complex. 25
Human Carbonic Anhydrase VII protects cells from oxidative damage 24
Carbonic anhydrase VII is S-glutathionylated without loss of catalytic activity and affinity for sulfonamide inhibitors 24
Carbonic anhydrase inhibitors: comparison of aliphatic sulfamate/bis-sulfamate adducts with isozimes II and IX 20
STRUCTURAL CHARACTERIZATION OF HUMAN CARBONIC ANHYDRASE 20
Insights into Carbonic Anhydrase VII functional role 18
Totale 4.180
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Categoria #
all - tutte 14.206
article - articoli 10.032
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.186
Totale 25.424
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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
2024/20251.247 26 11 135 48 277 39 12 71 63 55 252 258
2025/20262.370 112 199 188 333 360 190 330 116 142 140 150 110
2026/2027532 147 135 250 0 0 0 0 0 0 0 0 0
Totale 4.180