CERUSO, MARIANGELA
 Distribuzione geografica
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Continente #
NA - Nord America 5.761
EU - Europa 1.849
AS - Asia 1.362
SA - Sud America 272
AF - Africa 29
OC - Oceania 23
Continente sconosciuto - Info sul continente non disponibili 1
Totale 9.297
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Nazione #
US - Stati Uniti d'America 5.723
RU - Federazione Russa 722
IT - Italia 534
SG - Singapore 364
CN - Cina 284
HK - Hong Kong 248
BR - Brasile 220
VN - Vietnam 202
IE - Irlanda 196
KR - Corea 125
SE - Svezia 89
FI - Finlandia 67
FR - Francia 60
DE - Germania 52
IN - India 47
PL - Polonia 34
ES - Italia 32
GB - Regno Unito 24
AU - Australia 23
CA - Canada 21
IQ - Iraq 21
AR - Argentina 15
EC - Ecuador 14
BD - Bangladesh 13
CI - Costa d'Avorio 10
ID - Indonesia 9
TR - Turchia 9
UA - Ucraina 9
MX - Messico 8
PK - Pakistan 8
CO - Colombia 7
JO - Giordania 7
NL - Olanda 7
JP - Giappone 6
PY - Paraguay 6
CL - Cile 5
PT - Portogallo 5
CH - Svizzera 4
DZ - Algeria 4
EG - Egitto 4
SA - Arabia Saudita 4
UZ - Uzbekistan 4
AL - Albania 3
JM - Giamaica 3
KE - Kenya 3
PA - Panama 3
ZA - Sudafrica 3
AE - Emirati Arabi Uniti 2
BE - Belgio 2
LT - Lituania 2
LV - Lettonia 2
MY - Malesia 2
PH - Filippine 2
VE - Venezuela 2
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EE - Estonia 1
EU - Europa 1
GA - Gabon 1
KZ - Kazakistan 1
MA - Marocco 1
NG - Nigeria 1
NI - Nicaragua 1
NP - Nepal 1
OM - Oman 1
PE - Perù 1
SN - Senegal 1
TN - Tunisia 1
TW - Taiwan 1
UY - Uruguay 1
Totale 9.297
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Città #
Santa Clara 1.348
Fairfield 766
Ashburn 666
Woodbridge 349
Seattle 318
Houston 294
Cambridge 277
Singapore 259
Wilmington 212
Dublin 196
Hong Kong 196
Chandler 153
Milan 133
Princeton 122
Seoul 122
Altamura 110
San Jose 105
Lawrence 97
Ann Arbor 95
Ho Chi Minh City 76
The Dalles 61
Clifton 52
Beijing 50
Lauterbourg 50
Hanoi 46
Los Angeles 40
Rome 40
Boston 38
Warsaw 34
Florence 32
Barcelona 30
Medford 29
Kent 27
Shanghai 27
Moscow 26
Council Bluffs 24
Mumbai 24
San Diego 23
Melbourne 22
Redondo Beach 22
Buffalo 19
São Paulo 19
Munich 18
New York 17
Boardman 16
Dallas 16
Falls Church 16
Bologna 12
Hefei 12
Miano 12
Abidjan 10
Brooklyn 10
Chicago 10
Falkenstein 10
Figino 10
Gavirate 10
Guangzhou 10
Frankfurt am Main 9
London 9
Naples 9
Norwalk 9
Da Nang 8
Montreal 8
Turku 8
Guayaquil 7
Hillsboro 7
Turin 7
Helsinki 6
Laurel 6
New Delhi 6
Rio de Janeiro 6
San Francisco 6
Tokyo 6
Toronto 6
Venice 6
Amsterdam 5
Andover 5
Bari 5
Haiphong 5
Hải Dương 5
Jakarta 5
Lahore 5
Monza 5
Paris 5
Quito 5
Shenzhen 5
Belo Horizonte 4
Bern 4
Biên Hòa 4
Cairo 4
Goiânia 4
Padua 4
Phoenix 4
Tashkent 4
Verona 4
Acton 3
Americana 3
Asunción 3
Baghdad 3
Betim 3
Totale 7.053
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Nome #
4-Arylbenzenesulfonamides as Human Carbonic Anhydrase Inhibitors (hCAIs): Synthesis by Pd Nanocatalyst-Mediated Suzuki-Miyaura Reaction, Enzyme Inhibition, and X-ray Crystallographic Studies 239
Geographical characterization by MAE-HPLC and NIR methodologies and carbonic anhydrase inhibition of Saffron components 224
Discovery of β-Adrenergic Receptors Blocker-Carbonic Anhydrase Inhibitor Hybrids for Multitargeted Antiglaucoma Therapy 219
Carbonic anhydrase inhibitors: Synthesis, molecular docking, cytotoxic and inhibition of the human carbonic anhydrase isoforms I, II, IX, XII with novel benzenesulfonamides incorporating pyrrole, pyrrolopyrimidine and fused pyrrolopyrimidine moieties 217
7-Aryl-triazolyl-substituted sulfocoumarins are potent, selective inhibitors of the tumor-associated carbonic anhydrase IX and XII 205
Benzenesulfonamides Incorporating Flexible Triazole Moieties Are Highly Effective Carbonic Anhydrase Inhibitors: Synthesis and Kinetic, Crystallographic, Computational, and Intraocular Pressure Lowering Investigations 203
Aryl-4,5-dihydro-1H-pyrazole-1-carboxamide derivatives bearing a sulfonamide moiety show single-digit nanomolar-to-subnanomolar inhibition constants against the tumor-associated human carbonic anhydrases IX and XII 201
Amido/ureidosubstituted benzenesulfonamides-isatin conjugates as low nanomolar/subnanomolar inhibitors of the tumor-associated carbonic anhydrase isoform XII 200
Overexpression of the transmembrane carbonic anhydrase isoforms IX and XII in the inflamed synovium 198
Click-tailed coumarins with potent and selective inhibitory action against the tumor-associated carbonic anhydrases IX and XII 192
Design, synthesis and evaluation of N-substituted saccharin derivatives as selective inhibitors of tumor-associated carbonic anhydrase XII 189
Design and validation of FRESH, a drug discovery paradigm resting on robust chemical synthesis 187
New series of sulfonamides containing amino acid moiety act as effective and selective inhibitors of tumor-associated carbonic anhydrase XII 185
Carbonic anhydrase inhibitors: Design, synthesis and structural characterization of new heteroaryl-N-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms 178
Cyclic tertiary sulfamates: Selective inhibition of the tumor-associated carbonic anhydrases IX and XII by N- and O-substituted acesulfame derivatives 175
Carbonic anhydrase inhibitory activity of sulfonamides and carboxylic acids incorporating cyclic imide scaffolds 173
Synthesis 4-[2-(2-mercapto-4-oxo-4H-quinazolin-3-yl)-ethyl]-benzenesulfonamides with subnanomolar carbonic anhydrase II and XII inhibitory properties 171
Development of 3-(4-aminosulphonyl)-phenyl-2-mercapto-3H-quinazolin-4-ones as inhibitors of carbonic anhydrase isoforms involved in tumorigenesis and glaucoma 170
Design and synthesis of benzothiazole-6-sulfonamides acting as highly potent inhibitors of carbonic anhydrase isoforms I, II, IX and XII 168
Pyrazolylbenzo[d]imidazoles as new potent and selective inhibitors of carbonic anhydrase isoforms hCA IX and XII 166
A novel library of saccharin and acesulfame derivatives as potent and selective inhibitors of carbonic anhydrase IX and XII isoforms 166
New natural product carbonic anhydrase inhibitors incorporating phenol moieties 165
Pyrazolo[4,3-e][1,2,4]triazine sulfonamides as carbonic anhydrase inhibitors with antitumor activity 163
Arylamino bisphosphonates: Potent and selective inhibitors of the tumor-associated carbonic anhydrase XII 163
Carbonic anhydrase inhibitors: Design, synthesis, and biological evaluation of novel sulfonyl semicarbazide derivatives 163
Inhibition of carbonic anhydrase isoforms I, II, IX and XII with novel Schiff bases: Identification of selective inhibitors for the tumor-associated isoforms over the cytosolic ones 162
Inhibition studies of new ureido-substituted sulfonamides incorporating a GABA moiety against human carbonic anhydrase isoforms I-XIV. 161
Synthesis of Schiff base derivatives of 4-(2-aminoethyl)-benzenesulfonamide with inhibitory activity against carbonic anhydrase isoforms I, II, IX and XII 161
4-Functionalized 1,3-diarylpyrazoles bearing 6-aminosulfonylbenzothiazole moiety as potent inhibitors of carbonic anhydrase isoforms hCA I, II, IX and XII 160
A new class of quinazoline-sulfonamides acting as efficient inhibitors against the α-carbonic anhydrase from Trypanosoma cruzi 159
New approaches to the synthesis of sildenafil analogues and their enzyme inhibitory activity 158
Open saccharin-based secondary sulfonamides as potent and selective inhibitors of cancer-related carbonic anhydrase IX and XII isoforms 158
Novel sulfonamide bearing coumarin scaffolds as selective inhibitors of tumor associated carbonic anhydrase isoforms IX and XII 158
Flow synthesis and biological activity of aryl sulfonamides as selective carbonic anhydrase IX and XII inhibitors 157
Inhibition studies of quinazoline-sulfonamide derivatives against the γ-CA (PgiCA) from the pathogenic bacterium, Porphyromonas gingivalis 157
Quinazoline-sulfonamides with potent inhibitory activity against the α-carbonic anhydrase from Vibrio cholerae 155
Synthesis of 4-sulfamoylphenyl-benzylamine derivatives with inhibitory activity against human carbonic anhydrase isoforms I, II, IX and XII 155
Selective inhibition of human carbonic anhydrases by novel amide derivatives of probenecid: Synthesis, biological evaluation and molecular modelling studies 150
Synthesis, carbonic anhydrase inhibition and cytotoxic activity of novel chromone-based sulfonamide derivatives 150
Inhibition studies of bacterial, fungal and protozoan β-class carbonic anhydrases with Schiff bases incorporating sulfonamide moieties 149
New 4-[(3-cyclohexyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzene-1-sulfonamides, synthesis and inhibitory activity toward carbonic anhydrase I, II, IX, XII 149
Dual carbonic anhydrase/matrix metalloproteinase inhibitors incorporating bisphosphonic acid moieties targeting bone tumors 147
Sulfonamide bearing pyrazolylpyrazolines as potent inhibitors of carbonic anhydrase isoforms I, II, IX and XII 147
Inhibition of carbonic anhydrase isoforms I, II, IV, VII and XII with carboxylates and sulfonamides incorporating phthalimide/phthalic anhydride scaffolds 147
Inhibition studies of Brucella suis β-carbonic anhydrases with a series of 4-substituted pyridine-3-sulphonamides 146
Novel sulfonamides bearing pyrrole and pyrrolopyrimidine moieties as carbonic anhydrase inhibitors: Synthesis, cytotoxic activity and molecular modeling 145
New pyrazolo[4,3-e][1,2,4]triazine sulfonamides as carbonic anhydrase inhibitors 143
Structure–Activity Relationships of Benzenesulfonamide-Based Inhibitors towards Carbonic Anhydrase Isoform Specificity 142
Sulfonamides incorporating fluorine and 1,3,5-triazine moieties are effective inhibitors of three β-class carbonic anhydrases from Mycobacterium tuberculosis. 141
Sulfamide derivatives with selective carbonic anhydrase VII inhibitory action 139
Exploring new Probenecid-based carbonic anhydrase inhibitors: Synthesis, biological evaluation and docking studies 136
Synthesis and carbonic anhydrase I, II, IX and XII inhibitory activity of sulfamates incorporating piperazinyl-ureido moieties 133
Synthesis of sulfonamides with effective inhibitory action against Porphyromonas gingivalis γ-carbonic anhydrase. 131
New amide derivatives of Probenecid as selective inhibitors of carbonic anhydrase IX and XII: Biological evaluation and molecular modelling studies 130
Sulfonamides with potent inhibitory action and selectivity against the α-carbonic anhydrase from Vibrio cholerae 130
5-Arylisothiazol-3(2H)-one-1,(1)-(di)oxides: A new class of selective tumor-associated carbonic anhydrases (hCA IX and XII) inhibitors 122
Inhibition of carbonic anhydrase isoforms I, II, IX and XII with Schiff’s bases incorporating iminoureido moieties 116
Totale 9.374
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Categoria #
all - tutte 25.721
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 25.721
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022343 14 4 43 10 6 24 9 35 16 23 34 125
2022/2023876 153 241 47 48 40 127 118 30 44 3 18 7
2023/2024212 9 24 61 9 19 11 4 29 2 8 28 8
2024/20252.646 112 227 108 284 1.099 401 63 154 39 46 60 53
2025/20262.566 172 322 160 229 257 107 297 166 162 193 72 429
2026/20277 7 0 0 0 0 0 0 0 0 0 0 0
Totale 9.374