ALTERIO, VINCENZO
 Distribuzione geografica
Continente #
AS - Asia 1.742
NA - Nord America 1.037
EU - Europa 477
SA - Sud America 317
AF - Africa 27
Continente sconosciuto - Info sul continente non disponibili 3
OC - Oceania 1
Totale 3.604
Nazione #
US - Stati Uniti d'America 981
SG - Singapore 714
CN - Cina 432
BR - Brasile 245
IT - Italia 173
HK - Hong Kong 164
VN - Vietnam 140
FR - Francia 83
KR - Corea 81
NL - Olanda 50
JP - Giappone 43
BD - Bangladesh 40
GB - Regno Unito 37
IN - India 37
AR - Argentina 26
DE - Germania 26
FI - Finlandia 26
CA - Canada 23
MX - Messico 15
EC - Ecuador 12
PL - Polonia 12
ZA - Sudafrica 12
PE - Perù 11
ID - Indonesia 10
IQ - Iraq 10
RU - Federazione Russa 10
IL - Israele 9
PK - Pakistan 9
UA - Ucraina 9
SA - Arabia Saudita 8
ES - Italia 7
MA - Marocco 7
PY - Paraguay 7
SE - Svezia 7
IE - Irlanda 6
UZ - Uzbekistan 6
AT - Austria 5
AZ - Azerbaigian 5
CL - Cile 5
TR - Turchia 5
CO - Colombia 4
CR - Costa Rica 4
LB - Libano 4
VE - Venezuela 4
BY - Bielorussia 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
GR - Grecia 3
HN - Honduras 3
JM - Giamaica 3
JO - Giordania 3
KE - Kenya 3
LT - Lituania 3
PH - Filippine 3
SV - El Salvador 3
UY - Uruguay 3
HU - Ungheria 2
KZ - Kazakistan 2
MN - Mongolia 2
NP - Nepal 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
BG - Bulgaria 1
BH - Bahrain 1
CH - Svizzera 1
CW - ???statistics.table.value.countryCode.CW??? 1
CZ - Repubblica Ceca 1
EE - Estonia 1
EG - Egitto 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
TH - Thailandia 1
TJ - Tagikistan 1
TM - Turkmenistan 1
YT - Mayotte 1
Totale 3.604
Città #
Singapore 438
Santa Clara 280
Hefei 170
San Jose 159
Hong Kong 158
Ashburn 96
Seoul 81
Los Angeles 76
Beijing 74
Lauterbourg 71
Ho Chi Minh City 48
Naples 47
Dallas 32
Hanoi 30
Tokyo 30
São Paulo 28
New York 21
Milan 15
Casandrino 14
Helsinki 13
Buffalo 12
Lappeenranta 12
Amsterdam 11
Orem 11
Warsaw 11
Frankfurt am Main 10
London 10
Minamishinagawa 10
Montreal 9
Bengaluru 8
Johannesburg 8
Rome 8
Da Nang 7
Haiphong 7
Shanghai 7
Atlanta 6
Buenos Aires 6
Chennai 6
Chicago 6
Dublin 6
Fortaleza 6
Phoenix 6
Stockholm 6
Tashkent 6
Agra 5
Baku 5
Belo Horizonte 5
Düsseldorf 5
Florence 5
Guayaquil 5
Lima 5
Mexico City 5
Porto Alegre 5
Rio de Janeiro 5
Vienna 5
Afragola 4
Asunción 4
Baghdad 4
Boardman 4
Campinas 4
Casablanca 4
Charlotte 4
Curitiba 4
Houston 4
Mumbai 4
Portsmouth 4
Riyadh 4
Turin 4
Washington 4
Amman 3
Ankara 3
Aracaju 3
Ashland 3
Blumenau 3
Brooklyn 3
Council Bluffs 3
Dhaka 3
Figino 3
Guarulhos 3
Hải Dương 3
Katy 3
Kyiv 3
Manchester 3
Nairobi 3
Nha Trang 3
North Bergen 3
Ribeirão Preto 3
Salt Lake City 3
San Bernardo 3
San José 3
San Salvador 3
Seattle 3
Thái Bình 3
Venice 3
Aarhus 2
Athens 2
Bari 2
Belford Roxo 2
Bentonville 2
Birmingham 2
Totale 2.274
Nome #
Inhibition of carbonic anhydrases IX/XII by SLC-0111 boosts cisplatin effects in hampering head and neck squamous carcinoma cell growth and invasion 122
Z-Carbonic anhydrases 106
α-CAs from Photosynthetic Organisms 91
Discovery of a novel series of potent carbonic anhydrase inhibitors with selective affinity for μ Opioid receptor for Safer and long-lasting analgesia 83
2-Mercaptobenzoxazoles: a class of carbonic anhydrase inhibitors with a novel binding mode to the enzyme active site 81
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 78
Benzyl alcohol inhibits carbonic anhydrases by anchoring to the zinc coordinated water molecule 77
THE CRYSTAL STRUCTURE OF HCA I/TOPIRAMATE COMPLEX PROVIDES USEFUL INSIGHTS INTO RATIONAL DRUG DESIGN OF ANTI-OBESITY DRUGS 74
Thermostable carbonic anhydrases in biotechnological applications 69
6-Substituted Triazolyl Benzoxaboroles as Selective Carbonic Anhydrase Inhibitors: In Silico Design, Synthesis, and X-ray Crystallography 67
Recent advances in structural studies of the carbonic anhydrase family: the crystal structure of human CA IX and CA XIII. 66
Structure and inhibition insights into Carbonic anhydrase CDCA1 from marine diatom Thalassiosira Weissflogii. 66
Structural study of the Carbonic Anhydrase SazCA from the thermophilic bacterium Sulfurihydrogenibium Azorense 66
A Novel Inhibitor of Carbonic Anhydrases Prevents Hypoxia-Induced TNBC Cell Plasticity 66
A Combined in Silico and Structural Study Opens New Perspectives on Aliphatic Sulfonamides, a Still Poorly Investigated Class of CA Inhibitors 64
ALPHA-CARBONIC ANHYDRASES 62
X-Ray Crystallography of Carbonic Anhydrase Inhibitors and Its Importance in Drug Design 60
Zeta-carbonic anhydrases show CS2 hydrolase activity: A new metabolic carbon acquisition pathway in diatoms? 60
Saccharomyces cerevesiae, Candida spp. and Cryptococcus neoformans β-CAs 59
Discovery of 1,1'-Biphenyl-4-sulfonamides as a New Class of Potent and Selective Carbonic Anhydrase XIV Inhibitors 57
A NEW LEAD COMPOUND FOR THE DEVELOPMENT OF CARBONIC ANHYDRASE INHIBITORS 56
Exploring the binding mode of phenyl and vinyl boronic acids to human carbonic anhydrases 55
Crystal structure of an S-formylglutathione hydrolase from pseudoalteromonas haloplanktis TAC125. 55
Editorial: Emerging advancements in the carbonic anhydrase field 54
Crystal structure of the most catalytically effective carbonic anhydrase enzyme known, SazCA from the thermophilic bacterium Sulfurihydrogenibium azorense 52
Inhibition of carbonic anhydrase IX targets primary tumors, metastases, and cancer stem cells: Three for the price of one 50
The anticonvulsant sulfamide JNJ-26990990 and its S,S-dioxide analog strongly inhibit carbonic anhydrases: solution and X-ray crystallographic studies 50
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 49
Exploring benzoxaborole derivatives as carbonic anhydrase inhibitors: a structural and computational analysis reveals their conformational variability as a tool to increase enzyme selectivity 48
Biochemical and Structural Insights into Carbonic Anhydrase XII/Fab6A10 Complex 48
Structural and inhibition insights into carbonic anhydrase CDCA1 from the marine diatom Thalassiosira weissflogii 45
Functional and structural features of the oxyanion hole in a thermophilic esterase from Alicyclobacillus acidocaldarius 45
Disclosing the interaction of carbonic anhydrase ix with cullin-associated nedd8-dissociated protein 1 by molecular modeling and integrated binding measurements. 43
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 42
Multiple Binding Modes of Inhibitors to Human Carbonic Anhydrases: An Update on the Design of Isoform-Specific Modulators of Activity 41
Carbonic Anhydrases as new targets against the bacterial pathogen Brucella suis 40
Fungal α-carbonic anhydrases 40
Depsides from Origanum dictamnus and Satureja pilosa as selective inhibitors of carbonic anhydrases: Isolation, structure elucidation, X‐ray crystallography 40
Inhibition of carbonic anhydrases by a substrate analog: benzyl carbamate directly coordinates the catalytic zinc ion mimicking bicarbonate binding 39
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 39
Cadmium-containing carbonic anhydrase CDCA1 in marine diatom Thalassiosira weissflogii 39
Biochemical characterization of the chloroplastic beta-carbonic anhydrase from Flaveria bidentis (L.) "Kuntze" 39
The crystal structure of an EST2 mutant unveils structural insights on the H group of the carboxylesterase/lipase family. 38
Benzoxaborole as a new chemotype for carbonic anhydrase inhibition 38
A new role of Human Carbonic Anhydrase VII in the protection of the cells from oxidative damage 37
Insights into the binding mode of sulphamates and sulphamides to hCA II: crystallographic studies and binding free energy calculations 36
STRUCTURAL AND INHIBITION STUDIES OF CARBONIC ANHYDRASE INHIBITORS CONTAINING THE SULFAMIDE ZINC BINDING GROUP 36
Design, synthesis and characterization of peptides mimicking hCA IX IC tail able to interact with nuclear transport factors 36
Structural insights into Carbonic anhydrase CDCA1 from marine diatom Thalassiosira Weissflogii 35
Multi-faceted exploration of the novel active γ-carbonic anhydrase PaCAγ1 in the human pathogen Pseudomonas aeruginosa 35
Multiple binding modes of inhibitors to carbonic anhydrases: How to design specific drugs targeting 15 different isoforms? 34
Crystal structure of the C183S/C217S mutant of human CA VII in complex with acetazolamide. 34
Thermal-stable carbonic anhydrases: a structural overview. 33
Insights into plant beta- carbonic anhydrase isolated from Flaveria Bidentis 33
Kinetic and X-ray crystallographic investigations of substituted 2-thio-6-oxo-1,6-dihydropyrimidine-benzenesulfonamides acting as carbonic anhydrase inhibitors 31
CDCA1 FROM THALASSIOSIRA WEISSFLOGII AS REPRESENTATIVE MEMBER OF ZETA-CLASS CAs: GENERAL FEATURES AND BIOTECHNOLOGICAL APPLICATIONS 30
Crystal structure of the catalytic domain of the tumor-associated human carbonic anhydrase IX. 29
CARBONIC ANHYDRASE INHIBITORS: X-RAY CRYSTALLOGRAPHIC STUDIES FOR THE BINDING OF MOLECULES CONTAINING A SULFAMIDE MOIETY 29
Peptides mimicking IC tail of hCA IX tumor enzyme interact with nuclear transport factors 29
X-ray crystallographic and kinetic investigations of 6-sulfamoyl-saccharin as a carbonic anhydrase inhibitor 28
Carbonic anhydrase inhibitors: Inhibition of human, bacterial, and archaeal isozymes with benzene-1,3-disulfonamides - Solution and crystallographic studies 28
Probing Molecular Interactions between Human Carbonic Anhydrases (hCAs) and a Novel Class of Benzenesulfonamides 27
Metal ion substitution in catalytic site greatly affects the binding of sulfhydryl-containing compounds to bovine leucyl aminopeptidase 27
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. 27
Hypoxia-targeting carbonic anhydrase IX inhibitors by a new series of nitroimidazole-sulfonamides/sulfamides/sulfamates 26
Carbonic anhydraseinhibitors: X-ray crystallographic studies for the binding of N-substitutedbenzenesulfonamides to human isoform II 26
Exploiting the hydrophobic and hydrophilic binding sites for designing carbonic anhydrase inhibitors 26
Hydroxylamine-O-sulfonamide is a versatile lead compound for the development of carbonic anhydrase inhibitors 26
Hydrophobic Substituents of the Phenylmethylsulfamide Moiety Can Be Used for the Development of New Selective Carbonic Anhydrase Inhibitors 26
Recent developments of carbonic anhydrase inhibitors as potential drugs 25
The first example of a significant active site conformational rearrangement in a carbonic anhydrase-inhibitor adduct: the carbonic anhydrase I-topiramate complex. 25
The crystal structure of CA I/Topiramate complex provides useful insights into rational drug design of anti-obesity drug 24
Insights into the carbonic anhydrase family: biochemical characterization of the human isozyme VII 24
The structural comparison between membrane-associated human carbonic anhydrases provides insights into drug design of selective inhibitors 24
Crystal structure of the catalytic domain of the tumor-associated hCA IX 24
Carbonic Anhydrase Inhibitors: X-ray and Molecular Modeling Study for the Interaction of a Fluorescent Antitumor Sulfonamide with Isozyme II and IX 24
Identification and characterization of a new form of oncosuppressor KCTD11 23
NUCLEAR TRANSPORT FACTORS IMPORTIN KAPbeta2 AND EXPORTIN CRM1 INTERACT WITH THE TUMOR ENZYME hCA IX 22
The crystal structure of the (Zn/Zn)bLAP/zofenoprilat complex. 22
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 22
Carbonic anhydrase VII is S-glutathionylated without loss of catalytic activity and affinity for sulfonamide inhibitors 21
Structural characterization of human carbonic anhydrase VII. 21
Human Carbonic Anhydrase VII protects cells from oxidative damage 20
Carbonic anhydrase inhibitors: comparison of aliphatic sulfamate/bis-sulfamate adducts with isozimes II and IX 18
Insights into Carbonic Anhydrase VII functional role 17
STRUCTURAL CHARACTERIZATION OF HUMAN CARBONIC ANHYDRASE 16
Totale 3.695
Categoria #
all - tutte 12.371
article - articoli 8.696
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.020
Totale 22.087


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
2024/20251.240 26 11 134 47 275 39 12 71 63 55 250 257
2025/20262.338 112 198 187 327 355 189 327 115 141 138 149 100
2026/202786 86 0 0 0 0 0 0 0 0 0 0 0
Totale 3.695