ALTERIO, VINCENZO
 Distribuzione geografica
Continente #
AS - Asia 1.732
NA - Nord America 890
EU - Europa 448
SA - Sud America 308
AF - Africa 27
Continente sconosciuto - Info sul continente non disponibili 2
OC - Oceania 1
Totale 3.408
Nazione #
US - Stati Uniti d'America 841
SG - Singapore 714
CN - Cina 432
BR - Brasile 241
HK - Hong Kong 163
IT - Italia 151
VN - Vietnam 140
FR - Francia 83
KR - Corea 81
NL - Olanda 50
JP - Giappone 43
IN - India 37
GB - Regno Unito 36
BD - Bangladesh 31
DE - Germania 26
AR - Argentina 25
FI - Finlandia 25
CA - Canada 19
MX - Messico 15
PL - Polonia 12
ZA - Sudafrica 12
PE - Perù 11
EC - Ecuador 10
ID - Indonesia 10
IQ - Iraq 10
RU - Federazione Russa 10
IL - Israele 9
PK - Pakistan 9
UA - Ucraina 9
SA - Arabia Saudita 8
MA - Marocco 7
SE - Svezia 7
ES - Italia 6
IE - Irlanda 6
PY - Paraguay 6
UZ - Uzbekistan 6
AT - Austria 5
AZ - Azerbaigian 5
CL - Cile 5
TR - Turchia 5
LB - Libano 4
VE - Venezuela 4
BY - Bielorussia 3
CO - Colombia 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
KZ - Kazakistan 2
MN - Mongolia 2
NP - Nepal 2
TN - Tunisia 2
TW - Taiwan 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
AM - Armenia 1
BG - Bulgaria 1
BH - Bahrain 1
CH - Svizzera 1
CR - Costa Rica 1
CW - ???statistics.table.value.countryCode.CW??? 1
CZ - Repubblica Ceca 1
DK - Danimarca 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
XK - ???statistics.table.value.countryCode.XK??? 1
YT - Mayotte 1
Totale 3.408
Città #
Singapore 438
Santa Clara 279
Hefei 170
Hong Kong 157
San Jose 133
Seoul 81
Los Angeles 75
Beijing 74
Lauterbourg 71
Ashburn 63
Ho Chi Minh City 48
Naples 44
Hanoi 30
Tokyo 30
Dallas 29
São Paulo 28
New York 19
Casandrino 14
Helsinki 12
Lappeenranta 12
Amsterdam 11
Orem 11
Warsaw 11
Frankfurt am Main 10
London 10
Minamishinagawa 10
Buffalo 9
Montreal 9
Bengaluru 8
Johannesburg 8
Milan 8
Da Nang 7
Haiphong 7
Shanghai 7
Buenos Aires 6
Chennai 6
Chicago 6
Dublin 6
Phoenix 6
Rome 6
Stockholm 6
Tashkent 6
Agra 5
Baku 5
Belo Horizonte 5
Düsseldorf 5
Florence 5
Fortaleza 5
Lima 5
Mexico City 5
Porto Alegre 5
Rio de Janeiro 5
Vienna 5
Afragola 4
Atlanta 4
Baghdad 4
Campinas 4
Casablanca 4
Houston 4
Mumbai 4
Portsmouth 4
Riyadh 4
Turin 4
Amman 3
Ankara 3
Aracaju 3
Asunción 3
Blumenau 3
Boardman 3
Brooklyn 3
Charlotte 3
Council Bluffs 3
Curitiba 3
Dhaka 3
Guarulhos 3
Guayaquil 3
Hải Dương 3
Kyiv 3
Manchester 3
Nairobi 3
Nha Trang 3
North Bergen 3
Ribeirão Preto 3
San Bernardo 3
San Salvador 3
Thái Bình 3
Venice 3
Athens 2
Bari 2
Belford Roxo 2
Birmingham 2
Biên Hòa 2
Bologna 2
Boscotrecase 2
Brasília 2
Bắc Ninh 2
Caracas 2
Carney 2
Cercola 2
Ciudad del Este 2
Totale 2.174
Nome #
Inhibition of carbonic anhydrases IX/XII by SLC-0111 boosts cisplatin effects in hampering head and neck squamous carcinoma cell growth and invasion 118
Z-Carbonic anhydrases 105
α-CAs from Photosynthetic Organisms 90
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 80
THE CRYSTAL STRUCTURE OF HCA I/TOPIRAMATE COMPLEX PROVIDES USEFUL INSIGHTS INTO RATIONAL DRUG DESIGN OF ANTI-OBESITY DRUGS 72
Benzyl alcohol inhibits carbonic anhydrases by anchoring to the zinc coordinated water molecule 72
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 69
6-Substituted Triazolyl Benzoxaboroles as Selective Carbonic Anhydrase Inhibitors: In Silico Design, Synthesis, and X-ray Crystallography 67
Structure and inhibition insights into Carbonic anhydrase CDCA1 from marine diatom Thalassiosira Weissflogii. 66
Thermostable carbonic anhydrases in biotechnological applications 66
Recent advances in structural studies of the carbonic anhydrase family: the crystal structure of human CA IX and CA XIII. 64
A Combined in Silico and Structural Study Opens New Perspectives on Aliphatic Sulfonamides, a Still Poorly Investigated Class of CA Inhibitors 62
A Novel Inhibitor of Carbonic Anhydrases Prevents Hypoxia-Induced TNBC Cell Plasticity 62
ALPHA-CARBONIC ANHYDRASES 59
Zeta-carbonic anhydrases show CS2 hydrolase activity: A new metabolic carbon acquisition pathway in diatoms? 59
X-Ray Crystallography of Carbonic Anhydrase Inhibitors and Its Importance in Drug Design 58
Discovery of 1,1'-Biphenyl-4-sulfonamides as a New Class of Potent and Selective Carbonic Anhydrase XIV Inhibitors 56
Crystal structure of an S-formylglutathione hydrolase from pseudoalteromonas haloplanktis TAC125. 54
Exploring the binding mode of phenyl and vinyl boronic acids to human carbonic anhydrases 53
Structural study of the Carbonic Anhydrase SazCA from the thermophilic bacterium Sulfurihydrogenibium Azorense 52
Crystal structure of the most catalytically effective carbonic anhydrase enzyme known, SazCA from the thermophilic bacterium Sulfurihydrogenibium azorense 50
A NEW LEAD COMPOUND FOR THE DEVELOPMENT OF CARBONIC ANHYDRASE INHIBITORS 50
Saccharomyces cerevesiae, Candida spp. and Cryptococcus neoformans β-CAs 50
Editorial: Emerging advancements in the carbonic anhydrase field 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
The anticonvulsant sulfamide JNJ-26990990 and its S,S-dioxide analog strongly inhibit carbonic anhydrases: solution and X-ray crystallographic studies 48
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 47
Biochemical and Structural Insights into Carbonic Anhydrase XII/Fab6A10 Complex 46
Inhibition of carbonic anhydrase IX targets primary tumors, metastases, and cancer stem cells: Three for the price of one 45
Functional and structural features of the oxyanion hole in a thermophilic esterase from Alicyclobacillus acidocaldarius 44
Structural and inhibition insights into carbonic anhydrase CDCA1 from the marine diatom Thalassiosira weissflogii 42
Disclosing the interaction of carbonic anhydrase ix with cullin-associated nedd8-dissociated protein 1 by molecular modeling and integrated binding measurements. 42
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 41
Carbonic Anhydrases as new targets against the bacterial pathogen Brucella suis 39
Depsides from Origanum dictamnus and Satureja pilosa as selective inhibitors of carbonic anhydrases: Isolation, structure elucidation, X‐ray crystallography 39
Inhibition of carbonic anhydrases by a substrate analog: benzyl carbamate directly coordinates the catalytic zinc ion mimicking bicarbonate binding 38
Multiple Binding Modes of Inhibitors to Human Carbonic Anhydrases: An Update on the Design of Isoform-Specific Modulators of Activity 37
Fungal α-carbonic anhydrases 37
Cadmium-containing carbonic anhydrase CDCA1 in marine diatom Thalassiosira weissflogii 37
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 36
A new role of Human Carbonic Anhydrase VII in the protection of the cells from oxidative damage 36
Structural insights into Carbonic anhydrase CDCA1 from marine diatom Thalassiosira Weissflogii 35
Benzoxaborole as a new chemotype for carbonic anhydrase inhibition 35
Insights into the binding mode of sulphamates and sulphamides to hCA II: crystallographic studies and binding free energy calculations 34
The crystal structure of an EST2 mutant unveils structural insights on the H group of the carboxylesterase/lipase family. 34
Biochemical characterization of the chloroplastic beta-carbonic anhydrase from Flaveria bidentis (L.) "Kuntze" 34
Design, synthesis and characterization of peptides mimicking hCA IX IC tail able to interact with nuclear transport factors 34
Thermal-stable carbonic anhydrases: a structural overview. 32
Crystal structure of the C183S/C217S mutant of human CA VII in complex with acetazolamide. 32
Insights into plant beta- carbonic anhydrase isolated from Flaveria Bidentis 32
Multiple binding modes of inhibitors to carbonic anhydrases: How to design specific drugs targeting 15 different isoforms? 31
Multi-faceted exploration of the novel active γ-carbonic anhydrase PaCAγ1 in the human pathogen Pseudomonas aeruginosa 29
CARBONIC ANHYDRASE INHIBITORS: X-RAY CRYSTALLOGRAPHIC STUDIES FOR THE BINDING OF MOLECULES CONTAINING A SULFAMIDE MOIETY 28
CDCA1 FROM THALASSIOSIRA WEISSFLOGII AS REPRESENTATIVE MEMBER OF ZETA-CLASS CAs: GENERAL FEATURES AND BIOTECHNOLOGICAL APPLICATIONS 28
Kinetic and X-ray crystallographic investigations of substituted 2-thio-6-oxo-1,6-dihydropyrimidine-benzenesulfonamides acting as carbonic anhydrase inhibitors 28
Metal ion substitution in catalytic site greatly affects the binding of sulfhydryl-containing compounds to bovine leucyl aminopeptidase 27
Peptides mimicking IC tail of hCA IX tumor enzyme interact with nuclear transport factors 27
Crystal structure of the catalytic domain of the tumor-associated human carbonic anhydrase IX. 26
Probing Molecular Interactions between Human Carbonic Anhydrases (hCAs) and a Novel Class of Benzenesulfonamides 26
STRUCTURAL AND INHIBITION STUDIES OF CARBONIC ANHYDRASE INHIBITORS CONTAINING THE SULFAMIDE ZINC BINDING GROUP 26
X-ray crystallographic and kinetic investigations of 6-sulfamoyl-saccharin as a carbonic anhydrase inhibitor 26
Carbonic anhydrase inhibitors: Inhibition of human, bacterial, and archaeal isozymes with benzene-1,3-disulfonamides - Solution and crystallographic studies 26
The first example of a significant active site conformational rearrangement in a carbonic anhydrase-inhibitor adduct: the carbonic anhydrase I-topiramate complex. 25
Carbonic anhydraseinhibitors: X-ray crystallographic studies for the binding of N-substitutedbenzenesulfonamides to human isoform II 25
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. 25
Hydrophobic Substituents of the Phenylmethylsulfamide Moiety Can Be Used for the Development of New Selective Carbonic Anhydrase Inhibitors 25
Hypoxia-targeting carbonic anhydrase IX inhibitors by a new series of nitroimidazole-sulfonamides/sulfamides/sulfamates 24
The crystal structure of CA I/Topiramate complex provides useful insights into rational drug design of anti-obesity drug 24
The structural comparison between membrane-associated human carbonic anhydrases provides insights into drug design of selective inhibitors 24
Exploiting the hydrophobic and hydrophilic binding sites for designing carbonic anhydrase inhibitors 24
Hydroxylamine-O-sulfonamide is a versatile lead compound for the development of carbonic anhydrase inhibitors 24
Carbonic Anhydrase Inhibitors: X-ray and Molecular Modeling Study for the Interaction of a Fluorescent Antitumor Sulfonamide with Isozyme II and IX 24
Crystal structure of the catalytic domain of the tumor-associated hCA IX 23
Recent developments of carbonic anhydrase inhibitors as potential drugs 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
NUCLEAR TRANSPORT FACTORS IMPORTIN KAPbeta2 AND EXPORTIN CRM1 INTERACT WITH THE TUMOR ENZYME hCA IX 21
Insights into the carbonic anhydrase family: biochemical characterization of the human isozyme VII 21
Identification and characterization of a new form of oncosuppressor KCTD11 21
Carbonic anhydrase VII is S-glutathionylated without loss of catalytic activity and affinity for sulfonamide inhibitors 20
The crystal structure of the (Zn/Zn)bLAP/zofenoprilat complex. 20
Human Carbonic Anhydrase VII protects cells from oxidative damage 19
Structural characterization of human carbonic anhydrase VII. 19
Carbonic anhydrase inhibitors: comparison of aliphatic sulfamate/bis-sulfamate adducts with isozimes II and IX 17
Insights into Carbonic Anhydrase VII functional role 16
STRUCTURAL CHARACTERIZATION OF HUMAN CARBONIC ANHYDRASE 16
Totale 3.499
Categoria #
all - tutte 11.259
article - articoli 7.924
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 931
Totale 20.114


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
2025/20262.228 112 198 187 327 355 189 327 115 141 138 139 0
Totale 3.499