ANGELI, ANDREA
 Distribuzione geografica
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Continente #
NA - Nord America 16.090
AS - Asia 11.201
EU - Europa 9.678
SA - Sud America 2.202
AF - Africa 305
OC - Oceania 127
Continente sconosciuto - Info sul continente non disponibili 4
Totale 39.607
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Nazione #
US - Stati Uniti d'America 15.817
RU - Federazione Russa 3.665
CN - Cina 3.060
SG - Singapore 2.931
IT - Italia 2.570
BR - Brasile 1.771
HK - Hong Kong 1.337
VN - Vietnam 1.231
KR - Corea 1.052
PL - Polonia 902
IE - Irlanda 806
FR - Francia 425
IN - India 422
BD - Bangladesh 361
DE - Germania 325
SE - Svezia 314
FI - Finlandia 249
AR - Argentina 171
ID - Indonesia 171
GB - Regno Unito 154
JP - Giappone 146
CA - Canada 128
AU - Australia 121
EC - Ecuador 83
MX - Messico 79
TR - Turchia 79
IQ - Iraq 64
UA - Ucraina 64
JO - Giordania 62
ZA - Sudafrica 57
NG - Nigeria 53
NL - Olanda 52
CO - Colombia 50
PY - Paraguay 41
ES - Italia 38
MA - Marocco 37
SA - Arabia Saudita 33
CI - Costa d'Avorio 32
PK - Pakistan 32
EG - Egitto 30
VE - Venezuela 30
AE - Emirati Arabi Uniti 26
UZ - Uzbekistan 26
BJ - Benin 25
CL - Cile 25
CH - Svizzera 24
IR - Iran 21
PH - Filippine 20
TW - Taiwan 20
UY - Uruguay 15
BE - Belgio 14
CZ - Repubblica Ceca 13
KE - Kenya 13
DZ - Algeria 12
SN - Senegal 12
AZ - Azerbaigian 11
JM - Giamaica 11
MY - Malesia 11
PE - Perù 11
AL - Albania 10
CR - Costa Rica 10
AT - Austria 9
OM - Oman 9
TH - Thailandia 9
DO - Repubblica Dominicana 8
HN - Honduras 8
LB - Libano 8
MU - Mauritius 8
NP - Nepal 8
TN - Tunisia 8
GT - Guatemala 7
PS - Palestinian Territory 7
LT - Lituania 6
NZ - Nuova Zelanda 6
PA - Panama 6
PT - Portogallo 6
AO - Angola 5
DK - Danimarca 5
ET - Etiopia 5
KG - Kirghizistan 5
KH - Cambogia 5
KZ - Kazakistan 5
QA - Qatar 5
RO - Romania 5
SV - El Salvador 5
TT - Trinidad e Tobago 5
BO - Bolivia 4
SK - Slovacchia (Repubblica Slovacca) 4
XK - ???statistics.table.value.countryCode.XK??? 4
BA - Bosnia-Erzegovina 3
BH - Bahrain 3
IL - Israele 3
MN - Mongolia 3
RS - Serbia 3
SY - Repubblica araba siriana 3
BG - Bulgaria 2
CY - Cipro 2
GH - Ghana 2
GR - Grecia 2
HU - Ungheria 2
Totale 39.578
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Città #
Santa Clara 3.281
Ashburn 2.546
Singapore 2.252
Fairfield 1.290
Hong Kong 1.088
Seoul 1.045
Hefei 992
Warsaw 894
Dublin 796
Woodbridge 621
San Jose 570
Milan 539
Seattle 512
Houston 487
Beijing 462
Cambridge 453
Ho Chi Minh City 418
Wilmington 400
Moscow 385
Council Bluffs 363
Chandler 308
Los Angeles 306
Altamura 302
Lawrence 294
Lauterbourg 263
The Dalles 257
Hanoi 230
Rome 229
Ann Arbor 226
Mumbai 204
Florence 196
Buffalo 185
Princeton 181
Dallas 174
Munich 169
Helsinki 151
Kent 139
New York 135
Tokyo 135
São Paulo 126
Paris 117
Melbourne 115
Boston 113
Jakarta 103
Medford 93
Dong Ket 81
Shanghai 80
San Diego 73
Naples 72
Boardman 68
Clifton 63
Da Nang 56
Turin 53
Abuja 52
Bengaluru 52
Chicago 52
Haiphong 49
Delhi 45
Lappeenranta 45
Rio de Janeiro 44
Redondo Beach 40
London 39
Figino 38
Orem 37
Frankfurt am Main 36
Guangzhou 36
Norwalk 35
Porto Alegre 35
Turku 35
Toronto 34
West Jordan 34
Brasília 33
Washington 33
Abidjan 32
Belo Horizonte 32
Bologna 32
Hillsboro 32
Phoenix 32
Miano 31
Falls Church 30
Guayaquil 29
Bari 28
Hải Dương 28
Quito 27
Redwood City 26
Biên Hòa 25
Cotonou 25
Curitiba 24
Johannesburg 24
Tashkent 24
Brooklyn 23
Yubileyny 23
Guarulhos 22
Montreal 22
Atlanta 21
Baghdad 21
Genoa 21
Istanbul 21
Shenzhen 21
Tianjin 21
Totale 26.192
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Nome #
New Histamine-Related Five-Membered N-Heterocycle Derivatives as Carbonic Anhydrase I Activators 308
Ionic liquids as an alternative reaction medium for HMDST based synthesis of thioaldehydes 274
Synthesis and biological evaluation of cyclic imides incorporating benzenesulfonamide moieties as carbonic anhydrase I, II, IV and IX inhibitors. 271
Heterocoumarins Are Selective Carbonic Anhydrase IX and XII Inhibitors with Cytotoxic Effects against Cancer Cells Lines 266
Synthesis of a new series of 3-functionalised-1-phenyl-1,2,3-triazole sulfamoylbenzamides as carbonic anhydrase I, II, IV and IX inhibitors 264
1,3-Dipolar Cycloaddition, HPLC Enantioseparation, and Docking Studies of Saccharin/Isoxazole and Saccharin/Isoxazoline Derivatives as Selective Carbonic Anhydrase IX and XII Inhibitors 256
Lipoyl-Homotaurine Derivative (ADM_12) Reverts Oxaliplatin-Induced Neuropathy and Reduces Cancer Cells Malignancy by Inhibiting Carbonic Anhydrase IX (CAIX) 235
Design, Synthesis, and X-ray of Selenides as New Class of Agents for Prevention of Diabetic Cerebrovascular Pathology 231
3-Hydroxy-1H-quinazoline-2,4-dione as a New Scaffold to Develop Potent and Selective Inhibitors of the Tumor-Associated Carbonic Anhydrases IX and XII 227
Structural investigations on coumarins leading to chromeno[4,3-c]pyrazol-4-ones and pyrano[4,3-c]pyrazol-4-ones: New scaffolds for the design of the tumor-associated carbonic anhydrase isoforms IX and XII 226
2-(2-Hydroxyethyl)piperazine derivatives as potent human carbonic anhydrase inhibitors: Synthesis, enzyme inhibition, computational studies and antiglaucoma activity 224
Design, synthesis and human carbonic anhydrase I, II, IX and XII inhibitory properties of 1,3-thiazole sulfonamides 222
1,2,4-Triazole-based anticonvulsant agents with additional ROS scavenging activity are effective in a model of pharmacoresistant epilepsy 221
Design, synthesis and X-ray crystallography of selenides bearing benzenesulfonamide moiety with neuropathic pain modulating effects. 212
Chalcogenides-incorporating carbonic anhydrase inhibitors concomitantly reverted oxaliplatin-induced neuropathy and enhanced antiproliferative action 212
Synthesis and carbonic anhydrase activating properties of a series of 2-amino-imidazolines structurally related to clonidine 211
Activation of β- and γ-carbonic anhydrases from pathogenic bacteria with tripeptides 210
Discovery of New Selenoureido Analogues of 4-(4-Fluorophenylureido)benzenesulfonamide as Carbonic Anhydrase Inhibitors 209
Activation studies with amines and amino acids of the β-carbonic anhydrase encoded by the Rv3273 gene from the pathogenic bacterium Mycobacterium tuberculosis 208
Evaluation of selenide, diselenide and selenoheterocycle derivatives as carbonic anhydrase I, II, IV, VII and IX inhibitors 207
Syntesis of thio- and seleno-acetamides bearing benzenesulfonamide as potent inhibitors of human carbonic anhydrase II and XII 207
Carbonic anhydrase inhibition with sulfonamides incorporating pyrazole-and pyridazinecarboxamide moieties provides examples of isoform-selective inhibitors 201
Investigation of piperazines as human carbonic anhydrase I, II, IV and VII activators 200
From random to rational: A discovery approach to selective subnanomolar inhibitors of human carbonic anhydrase IV based on the Castagnoli-Cushman multicomponent reaction 200
Activation Effects of Carnosine- and Histidine-Containing Dipeptides on Human Carbonic Anhydrases: A Comprehensive Study 200
Carbonic anhydrase inhibitors based on sorafenib scaffold: Design, synthesis, crystallographic investigation and effects on primary breast cancer cells 196
Synthesis and evaluation of carbonic anhydrase inhibitors with carbon monoxide releasing properties for the management of rheumatoid arthritis 196
Activation studies of the α- and β-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae with amines and amino acids 195
Evaluation of Thio- and Seleno-Acetamides Bearing Benzenesulfonamide as Inhibitor of Carbonic Anhydrases from Different Pathogenic Bacteria 193
Antimalarial Agents Targeting Plasmodium falciparum Carbonic Anhydrase: Towards Artesunate Hybrid Compounds with Dual Mechanism of Action 189
Direct and Straightforward access to substituted alkyl selenols as novel carbonic anhydrase inhibitors 187
CARBAMOSELENOYL DERIVATIVES AS ANTI-INFECTIVE AGENTS 184
N-aryl-N’-ureido-O-sulfamates: Potent and selective inhibitors of the human Carbonic Anhydrase VII isoform with neuropathic pain relieving properties 184
Sulfur, selenium and tellurium containing amines act as effective carbonic anhydrase activators 183
First evaluation of organotellurium derivatives as carbonic anhydrase I, II, IV, VII and IX inhibitors 182
New β-arylchalcogeno amines with procognitive properties targeting Carbonic Anhydrases and Monoamine Oxidases 181
Anion inhibition profile of the β-carbonic anhydrase from the opportunist pathogenic fungus malassezia restricta involved in dandruff and seborrheic dermatitis 178
Inhibitory effects and structural insights for a novel series of coumarin-based compounds that selectively target human CA IX and CA XII carbonic anhydrases 178
Acyl selenoureido benzensulfonamides show potent inhibitory activity against carbonic anhydrases from the pathogenic bacterium Vibrio cholerae 177
Synthesis of novel 4-functionalized 1,5-diaryl-1,2,3-triazoles containing benzenesulfonamide moiety as carbonic anhydrase I, II, IV and IX inhibitors 175
Activation studies of the γ-carbonic anhydrases from the antarctic marine bacteria pseudoalteromonas haloplanktis and colwellia psychrerythraea with amino acids and amines 175
Azidothymidine "clicked" into 1,2,3-Triazoles: First Report on Carbonic Anhydrase-Telomerase Dual-Hybrid Inhibitors 174
2-Mercaptobenzoxazoles: a class of carbonic anhydrase inhibitors with a novel binding mode to the enzyme active site 173
Benzenesulfonamide decorated dihydropyrimidin(thi)ones: carbonic anhydrase profiling and antiproliferative activity 172
Sulfonamide inhibition studies of an α-carbonic anhydrase from Schistosoma mansoni, a platyhelminth parasite responsible for schistosomiasis 172
Inhibitors of Mitochondrial Human Carbonic Anhydrases VA and VB as a Therapeutic Strategy against Paclitaxel-Induced Neuropathic Pain in Mice 171
Discovering a new class of antifungal agents that selectively inhibits microbial carbonic anhydrases 171
Microwave-assisted extraction, HPLC analysis, and inhibitory effects on carbonic anhydrase I, II, VA, and VII isoforms of 14 blueberry Italian cultivars 169
Sulfonamides incorporating piperazine bioisosteres as potent human carbonic anhydrase I, II, IV and IX inhibitors 169
Benzylaminoethyureido-Tailed Benzenesulfonamides: Design, Synthesis, Kinetic and X-ray Investigations on Human Carbonic Anhydrases 169
Glycomimetic Based Approach toward Selective Carbonic Anhydrase Inhibitors 167
Mechanisms of the Antiproliferative and Antitumor Activity of Novel Telomerase-Carbonic Anhydrase Dual-Hybrid Inhibitors 167
A structure-based approach towards the identification of novel antichagasic compounds: Trypanosoma cruzi carbonic anhydrase inhibitors 166
Discovery of New Potential Anti-Infective Compounds Based on Carbonic Anhydrase Inhibitors by Rational Target-Focused Repurposing Approaches 166
Inhibition of the α-carbonic anhydrase from Vibrio cholerae with amides and sulfonamides incorporating imidazole moieties 164
Design, synthesis and biological activity of selective hCAs inhibitors based on 2-(benzylsulfinyl)benzoic acid scaffold 164
In Silico-Guided Identification of New Potent Inhibitors of Carbonic Anhydrases Expressed in Vibrio cholerae 162
Polypharmacology of epacadostat: A potent and selective inhibitor of the tumor associated carbonic anhydrases IX and XII 160
Anticancer effects of new dibenzenesulfonamides by inducing apoptosis and autophagy pathways and their carbonic anhydrase inhibitory effects on hCA I, hCA II, hCA IX, hCA XII isoenzymes 160
Synthesis of novel tellurides bearing benzensulfonamide moiety as carbonic anhydrase inhibitors with antitumor activity 159
Discovery of new 2, 5-disubstituted 1,3-selenazoles as selective human carbonic anhydrase IX inhibitors with potent anti-tumor activity 159
Discovery of Novel Nonsteroidal Anti-Inflammatory Drugs and Carbonic Anhydrase Inhibitors Hybrids (NSAIDs-CAIs) for the Management of Rheumatoid Arthritis 159
Activation studies of the β-carbonic anhydrases from Malassezia restricta with amines and amino acids 159
Synthesis and carbonic anhydrase I, II, VII, and IX inhibition studies with a series of benzo[d]thiazole-5- and 6-sulfonamides 158
Activation studies with amines and amino acids of the β-carbonic anhydrase from the pathogenic protozoan Leishmania donovani chagasi 157
Synthesis of different thio-scaffolds bearing sulfonamide with subnanomolar carbonic anhydrase II and IX inhibitory properties and X-ray investigations for their inhibitory mechanism 157
Synthesis and exploration of 2-morpholino-4-phenylthiazol-5-yl acrylamide derivatives for their effects against carbonic anhydrase I, II, IX and XII isoforms as a non-sulfonamide class of inhibitors 156
Multitargeting application of proline-derived peptidomimetics addressing cancer-related human matrix metalloproteinase 9 and carbonic anhydrase II 156
Synthesis and Biological Evaluation of 4-sulfamoylphenyl/sulfocoumarin carboxamides as selective inhibitors of carbonic anhydrase isoforms hCA II, IX and XII 156
Discovery of curcumin inspired sulfonamide derivatives as a new class of carbonic anhydrase isoforms I, II, IX, and XII inhibitors 155
New Dihydrothiazole Benzensulfonamides: Looking for Selectivity toward Carbonic Anhydrase Isoforms I, II, IX, and XII 155
A novel small molecule that kills a subset of MLL-rearranged leukemia cells by inducing mitochondrial dysfunction 155
Calixarenes Incorporating Sulfonamide Moieties: Versatile Ligands for Carbonic Anhydrases Inhibition 155
Design, synthesis and biological evaluation of N-(5-methyl-isoxazol-3-yl/1,3,4-thiadiazol-2-yl)-4-(3-substitutedphenylureido) benzenesulfonamides as human carbonic anhydrase isoenzymes I, II, VII and XII inhibitors 154
Selenols: a new class of carbonic anhydrase inhibitors 154
3-Functionalised benzenesulphonamide based 1,3,4-oxadiazoles as selective carbonic anhydrase XIII inhibitors: Design, synthesis and biological evaluation 153
Study of Chalcogen Aspirin Derivatives with Carbonic Anhydrase Inhibitory Properties for Treating Inflammatory Pain 151
Synthesis of Azasugar–Sulfonamide conjugates and their Evaluation as Inhibitors of Carbonic Anhydrases: the Azasugar Approach to Selectivity 151
Synthesis, Computational Studies and Assessment of in Vitro Activity of Squalene Derivatives as Carbonic Anhydrase Inhibitors 151
Synthesis of Novel Selenides Bearing Benzenesulfonamide Moieties as Carbonic Anhydrase I, II, IV, VII, and IX Inhibitors 150
Fluoroenesulphonamides: N-sulphonylurea isosteres showing nanomolar selective cancer-related transmembrane human carbonic anhydrase inhibition 150
Tail approach synthesis of novel benzenesulfonamides incorporating 1,3,4-oxadiazole hybrids as potent inhibitor of carbonic anhydrase I, II, IX, and XII isoenzymes 150
X-ray crystallography of Epacadostat in adduct with Carbonic Anhydrase IX 150
Glyco-Coated CdSe/ZnS Quantum Dots as Nanoprobes for Carbonic Anhydrase IX Imaging in Cancer Cells 150
One-Pot Procedure for the Synthesis of Asymmetric Substituted Ureido Benzene Sulfonamides as Effective Inhibitors of Carbonic Anhydrase Enzymes 150
Discovery of a novel series of indolylchalcone-benzenesulfonamide hybrids acting as selective carbonic anhydrase II inhibitors 148
Activation studies with amines and amino acids of the α-carbonic anhydrase from the pathogenic protozoan Trypanosoma cruzi 148
Benzoselenoates: A novel class of carbonic anhydrase inhibitors 148
Synthesis, computational studies and assessment of in vitro inhibitory activity of umbelliferon-based compounds against tumour-associated carbonic anhydrase isoforms IX and XII 147
Synthesis, characterization, biological assays and development of new enzyme modulators for the treatment of human pathologies 146
Synthesis, biological activity and multiscale molecular modeling studies for coumaryl-carboxamide derivatives as selective carbonic anhydrase IX inhibitors 146
Perfluoroalkyl Substances of Significant Environmental Concern Can Strongly Inhibit Human Carbonic Anhydrase Isozymes 145
Amine-and amino acid-based compounds as carbonic anhydrase activators 145
Carbonic Anhydrase inhibitors bearing organotelluride moieties as novel agents for antitumor therapy 144
Intramolecular oxidative deselenization of acylselenoureas: a facile synthesis of benzoxazole amides and carbonic anhydrase inhibitors 143
Exploring new structural features of the 4-[(3-methyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzenesulphonamide scaffold for the inhibition of human carbonic anhydrases 143
Benzensulfonamides bearing spyrohydantoin moieties act as potent inhibitors of human carbonic anhydrases II and VII and show neuropathic pain attenuating effects 143
Cover Picture: Discovery of New Potential Anti-Infective Compounds Based on Carbonic Anhydrase Inhibitors by Rational Target-Focused Repurposing Approaches (ChemMedChem 17/2016) 142
Dual carbonic anhydrase ix/xii inhibitors and carbon monoxide releasing molecules modulate LPS-mediated inflammation in mouse macrophages 142
Pharmacological inhibition of CA-IX impairs tumor cell proliferation, migration and invasiveness 141
Totale 17.852
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Categoria #
all - tutte 121.144
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 121.144
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.154 34 46 94 68 29 98 53 113 87 66 115 351
2022/20232.702 299 715 98 56 105 414 316 78 307 155 104 55
2023/20241.751 24 90 311 125 108 242 50 343 59 207 147 45
2024/202510.261 391 1.152 613 1.345 2.664 1.347 279 424 598 370 473 605
2025/202618.569 1.392 2.402 2.271 2.435 1.350 489 1.604 952 1.161 1.127 1.240 2.146
2026/202763 63 0 0 0 0 0 0 0 0 0 0 0
Totale 40.081