IRIS
CARBONARA, Giuseppe Gerardo
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 5.449
AS - Asia 1.945
EU - Europa 1.826
SA - Sud America 500
Continente sconosciuto - Info sul continente non disponibili 156
AF - Africa 68
OC - Oceania 9
Totale 9.953
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 5.280
SG - Singapore 759
IT - Italia 570
CN - Cina 485
BR - Brasile 406
SE - Svezia 255
HK - Hong Kong 245
UA - Ucraina 174
FR - Francia 167
RU - Federazione Russa 167
DE - Germania 162
FI - Finlandia 116
VN - Vietnam 104
GB - Regno Unito 99
IN - India 92
CA - Canada 71
BD - Bangladesh 43
AR - Argentina 27
TR - Turchia 27
IR - Iran 26
MX - Messico 25
CI - Costa d'Avorio 22
IQ - Iraq 22
ID - Indonesia 21
CO - Colombia 19
IE - Irlanda 18
SA - Arabia Saudita 17
BE - Belgio 15
CR - Costa Rica 14
ES - Italia 14
PH - Filippine 14
EC - Ecuador 13
JP - Giappone 12
ZA - Sudafrica 12
CZ - Repubblica Ceca 10
IL - Israele 10
NI - Nicaragua 10
NL - Olanda 10
TT - Trinidad e Tobago 10
CL - Cile 9
JM - Giamaica 9
PK - Pakistan 9
VE - Venezuela 9
AU - Australia 8
KR - Corea 8
LT - Lituania 8
CH - Svizzera 7
GT - Guatemala 7
MY - Malesia 7
PR - Porto Rico 7
UZ - Uzbekistan 7
HN - Honduras 6
PE - Perù 6
SC - Seychelles 6
DZ - Algeria 5
JO - Giordania 5
NP - Nepal 5
PL - Polonia 5
RO - Romania 5
AT - Austria 4
CW - ???statistics.table.value.countryCode.CW??? 4
GP - Guadalupe 4
KE - Kenya 4
KG - Kirghizistan 4
MA - Marocco 4
RS - Serbia 4
SV - El Salvador 4
UY - Uruguay 4
BO - Bolivia 3
EG - Egitto 3
PS - Palestinian Territory 3
PY - Paraguay 3
A1 - Anonimo 2
AE - Emirati Arabi Uniti 2
BA - Bosnia-Erzegovina 2
DK - Danimarca 2
GE - Georgia 2
KW - Kuwait 2
KZ - Kazakistan 2
MD - Moldavia 2
MM - Myanmar 2
OM - Oman 2
SN - Senegal 2
TN - Tunisia 2
AD - Andorra 1
AG - Antigua e Barbuda 1
AL - Albania 1
AO - Angola 1
AZ - Azerbaigian 1
BF - Burkina Faso 1
BG - Bulgaria 1
BH - Bahrain 1
CY - Cipro 1
DO - Repubblica Dominicana 1
EE - Estonia 1
ET - Etiopia 1
GA - Gabon 1
GR - Grecia 1
GY - Guiana 1
HU - Ungheria 1
Totale 9.789
Salva come PNG Salva come JPEG
Città #
Ashburn 584
Jacksonville 395
Fairfield 378
Chandler 369
Woodbridge 362
San Jose 357
Singapore 349
Hong Kong 240
Houston 224
Milan 209
Cambridge 185
Nyköping 182
Ann Arbor 171
Seattle 144
Council Bluffs 134
Wilmington 130
Beijing 105
Dallas 101
Nanjing 93
Lawrence 88
Roxbury 88
Rome 80
Lauterbourg 75
Bari 67
Princeton 67
Boardman 66
Los Angeles 63
Des Moines 59
New York 58
Washington 46
Ho Chi Minh City 42
Inglewood 40
Santa Clara 40
São Paulo 39
Marseille 32
Figino 30
Brooklyn 27
Buffalo 26
Munich 25
Nanchang 24
Helsinki 23
Abidjan 22
Chicago 22
Hanoi 21
Jiaxing 21
Hebei 20
Tianjin 19
Dublin 18
Toronto 18
Changsha 16
Orem 16
San Diego 16
Brussels 15
London 15
Rio de Janeiro 15
Mumbai 14
Bologna 13
Chennai 13
Shenyang 13
Istanbul 12
Paris 12
San Francisco 12
Tokyo 12
Turin 12
Columbus 11
Frankfurt am Main 11
Guangzhou 11
Mexico City 11
San José 11
Augusta 10
Brasília 10
Leawood 10
Managua 10
Belo Horizonte 9
Dearborn 9
Long Beach 9
North Bergen 9
Phoenix 9
Stockholm 9
Baghdad 8
Manchester 8
Ardabil 7
Atlanta 7
Dhaka 7
Jeddah 7
Johannesburg 7
Lausanne 7
Medellín 7
San Mateo 7
Shanghai 7
Tashkent 7
Turku 7
Wuhan 7
Boston 6
Boydton 6
Buenos Aires 6
Delhi 6
Florence 6
Haikou 6
Jakarta 6
Totale 6.475
Salva come PNG Salva come JPEG
Nome #
Probiotic and Tea Tree Oil Treatments Improve Therapy of Vaginal Candidiasis: A Preliminary Clinical Study 270
An efficient synthesis of the optically active isomers of 2H-1,4-benzoxazine derivatives, novel KATP channel modulators 222
Convenient synthesis of some 3-phenyl-1-benzofuran-2-carboxylic acid derivatives as new potential inhibitors of CLC-Kb channels 202
Activation and inhibition of kidney CLC-K chloride channels by fenamates 195
Synthesis, in vitro evaluation, and molecular modeling investigation of benzenesulfonimide peroxisome proliferator-activated receptors α antagonists 193
Kidney CLC-K Chloride Channels Show Differential Pharmacological Profiles Depending on the Heterologous Expression System 180
ChemInform Abstract: Convenient Synthesis of Some 3-Phenyl-1-benzofuran-2-carboxylic Acid Derivatives as New Potential Inhibitors of CLC-Kb Channels. 173
2-(9-Antryl)alcanoic acids as chloride channel modulators 168
Synthesis, biological evaluation, and molecular modeling investigation of chiral 2-(4-chloro-phenoxy)-3-phenyl-propanoic acid derivatives with PPARα and PPARγ agonist activity 166
Carboxylic acids and skeletal muscle chloride channel conductance: Effects on the biological activity induced by the introduction of an aryloxyalkyl group α to the carboxylic function of 4-chloro-phenoxyacetic acid 165
Comparative LC Enantioseparation of Novel PPAR Agonists on Cellulose- and Amylose-Based Chiral Stationary Phases 158
Repositioning of Endonuclear Receptors Binders as Potential Antibacterial and Antifungal Agents. Eptyloxìm: A Potential and Novel Gyrase B and Cytochrome Cyp51 Inhibitor 155
Carbonic anhydrase inhibitors are specific openers of skeletal muscle BK channel of K+ - deficient rats 152
AGONISTI DEI RECETTORI NUCLEARI PPARs COME POTENZIALI NUOVI AGENTI TERAPEUTICI PER IL TRATTAMENTO DELLA SINDROME METABOLICA. 145
Elucidation of the synergistic action of Mentha Piperita essential oil with common antimicrobials 138
Molecular determinants for the activating/blocking actions of the 2H-1,4-benzoxazine derivatives, a class of potassium channel modulators targeting the skeletal muscle KATP channels 137
Design, synthesis and biological evaluation of a class of bioisosteric oximes of the novel dual peroxisome proliferator-activated receptor alpha/gamma ligand LT175 136
Agonisti dei Recettori Nucleari PPARs come Potenziali Nuovi Agenti Terapeutici per il Trattamento della Sindrome Metabolica 134
(contributo in convegno) MOLECULAR DETERMINANTS FOR NUCLEAR RECEPTORS SELECTIVITY; CHEMOMETRIC ANALYSIS, DOCKINGS AND SITE-DIRECTED MUTAGENESIS OF DUAL PEROXISOME PROLIFERATOR-ACTIVATED RECEPTORS α/γ AGONISTS 134
Kidney CLC-K Chloride Channels Inhibitors: Definition of Novel Structural Requirements and Efficacy in CLC-K Polymorphism Associated with Hypertension 129
Synthesis, Biological Evaluation, and Molecular Modeling Investigation of Chiral Phenoxyacetic Acid Analogues with PPARalpha and PPARgamma Agonist Activity 129
Kidney CLC-K chloride channels inhibitors: structure-based studies and efficacy in hypertension and associated CLC-K polymorphisms. 129
Allyphenyline Analogues Potentially Useful in the Management of Chronic Pain and Opioid Addiction 127
Chemical studies on Drug Metabolism (part II): N-demethylation and N-oxidation of some alicyclic amines by RuO4 126
Calcium activated K+ channel as a target of prompt-to-use drugs in neuromuscular disorders 126
MOLECULAR DETERMINANTS FOR NUCLEAR RECEPTORS SELECTIVITY: CHEMOMETRIC ANALYSIS, DOCKINGS AND SITE-DIRECTED MUTAGENESIS OF DUAL PEROXISOME PROLIFERATOR-ACTIVATED RECEPTORS α/γ AGONISTS 124
Analisi Farmaceutica 123
Comparative analysis of enantioselective separation of novel PPAR agonists by HPLC on cellulose- and amylose-based chiral stationary phases 121
Block of renal CLC-K channels by phenoxy-alkyl derivatives of clofibric acid 118
Studio delle proprietà enentioselettive di una fase stazionaria chirale a base di PGA 115
Enantiomeric separation of 2-aryloxyalkyl- and 2-arylalkyl-2-aryloxyacetic acids on a Penicillin G Acylase-based chiral stationary phase: influence of the chemical structure on retention and enantioselectivity 115
Growth hormone secretagogues exert differential effects on skeletal muscle calcium homeostasis in male rats depending on the peptidyl/non-peptidyl structure 113
BIOLOGICAL ACTIVITY OF NEW POTENT 2H-1,4-BENZOXAZINE DERIVATIVES ON THE NATIVE SKELETAL MUSCLE KATP CHANNEL 112
Elucidation of the enantioselective recognition mechanism of a penicillin G acylase-based chiral stationary phase towards a series of 2-aryloxy-2-arylacetic acids 112
Attività biologica sui canali KATP del muscolo scheletrico nativo di nuovi e potenti derivati delle 2H-1,4-Benzossazine 111
Might the observed a2A-adrenoreceptor agonism or antagonism of allyphenyline analogues be ascribed to different molecular conformations? 111
Ossidazione di ammine policicliche terziarie con RuO4 110
KIDNEY CLC-K CHLORIDE CHANNELS SHOW DIFFERENTIAL PHARMACOLOGICAL PROFILES DEPENDING ON THE HETEROLOGOUS EXPRESSION SYSTEM 110
Exploring the molecular basis of the enantioselective binding of penicillin G acylase towards a series of 2 aryloxyalkanoic acids: A docking and molecular dynamics study 110
Structural nucleotide analogs are potent activators/inhibitors of pancreatic beta-cell KATP channels: an emerging mechanism supporting their use as anti-diabetic drugs. 108
Molecular determinants for nuclear receptors selectivity: chemometric analysis, dockings and site-directed mutagenesis of dual peroxisome proliferator-activated receptors alpha/gamma agonists 101
Chemical studies on Drug Metabolism: Oxidation with ruthenium tetroxide of some medicinal alicyclic N-metylamines 100
Molecular requisites for drug binding to muscle CLC-1 and renal CLC-K channel revealed by the use of phenoxy-alkyl derivatives of 2-(p-chlorophenoxy)propionic acid 99
Synthesis, biological evaluation and molecular investigation of fluorinated peroxisome proliferator-activated receptors alpha/gamma dual agonists 98
Sintesi di una nuova serie di acidi 2-benzofuran-carbossilici a potenziale attività bloccante dei canali al cloro voltaggio-dipendenti CLC-K 97
INNOVATIVE METHODOLOGIES IN NANOTECHNOLOGY FOR THE PREVENTION OF BACTERIAL DISEASES 95
H-1-NMR determination of the enantiomeric excess of the antiarrhythmic drug Mexiletine by using mandelic acid analogues as chiral solvating agents 95
Molecular switch for CLC-K Cl– channel block/activation: Optimal pharmacophoric requirements towards high-affinity ligands 92
Dimeric analogs of the dual PPARα/γ agonist LT-175: design, synthesis and biological evaluation. 91
Synthesis and biological screening of new chiral a-aryloxy-alkanoic acids as PPARs agonists 91
MOLECULAR SPATIAL GEOMETRY OF CLC-K LIGANDS: OPTIMAL REQUIREMENTS TOWARDS HIGH AFFINITY CHANNEL BLOCK. 88
Selective oxidation of nitrogen organic compounds 87
Selective oxidation of Nitrogen organic compounds by Ruthenium tetroxide 87
SINTESI E VALUTAZIONE BIOLOGICA DI DERIVATI SEMI-RIGIDI DELL'ACIDO 2-(4-CLOROFENOSSI)-3-FENIL-PROPANOICO COME BLOCCANTI DEI CANALI AL CLORO VOLTAGGIO-DIPENDENTI CLC-K 86
Enantioselective properties of Penicillin G Acylase: Liquid Crhomatographic studies end docking simulations 85
Molecular spatial geometry of CLC-K ligands: optimal requirements towards high affinity channel block 85
DESIGN, SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW ANALOGS OF THE DUAL PPARα/γ AGONIST LT175. 83
Tissue specific action of the 2-(propyl)-1,4-benzoxazine on pancreatic beta cell ATP-sensitive potassium channels 83
Molecular spatial geometry of CLC-K ligands: optimal requirements towards high affinity channel block 80
Determinanti Molecolari della Selettività di Recettori Nucleari: Analisi Chemiometrica e Docking di Agonisti Selettivi di Recettori PPARs 79
Design, synthesis and biological evaluation of a dimeric analog of the dual PPARα/γ agonist 2-(4-phenyl-phenoxy)-3-phenyl-propanoic acid. 78
Effetti sulla conduttanza dei canali al cloro della muscolatura scheletrica indotti dall’introduzione di un sostituente arilossialchilico in a alla funzione carbossilica dell’acido 4-cloro-fenossiacetico 78
Oxidation of tertiary polycyclic amines by RuO4 77
PROGETTAZIONE, SINTESI E VALUTAZIONE BIOLOGICA DI DERIVATI OSSIMMINICI AD ATTIVITA’ AGONISTA DUALE PPARα/γ. 77
NEW CHIRAL CLOFIBRIC ACID ANALOGS AS LIGANDS OF PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR (PPAR) alpha AND gamma 76
Progettazione e sintesi di nuovi agenti antimicrobici e studio dell'attività biologica in associazione con differenti olii essenziali 75
Traduzione Capitoli 1-9 75
EFFETTI DERIVANTI DALL'INTRODUZIONE DI SOSTITUENTI SUL NUCLEO DIFENILICO DEL COMPOSTO LT175, AGONISTA DUALE DEI RECETTORI NUCLEARI PPARalfa E PPARgamma 74
Evaluation of biophysical and pharmacological properties of chloride channels belonging to ClC family by the use of chiral clofibric acid derivatives 70
Novel dual PPARalpha/gamma Agonists, as hypoglycemic and antidiabetic agents 69
Synthesis and biological evaluation of new fluorinated analogues with PPARα and PPARγ agonist activity 68
Dal brodo primordiale alla farmacogenomica 67
Synthesis and biological screening of new chiral 2-(4-chloro-phenoxy)-3-phenylpropanoic acid analogs as potential PPAR alpha/gamma dual agonists 67
null 66
sintesi di una nuova serie di acidi 2-benzofuran-carbossilici e valutazione della loro attività bloccante dei canali al cloro voltaggio-dipendenti CLC-K 66
Design, synthesis and biological evaluation of a dimeric analog of the dual PPARα/γ agonist 2-(4-phenyl-phenoxy)-3-phenyl-propanoic acid 65
NEW CHIRAL DERIVATIVES OF 2-(4-PHENYL-PHENOXY)-3-PHENYLPROPANOIC ACID WITH PPARalpha/gamma DUAL ACTIVITY. 64
Effects on skeletal muscle chloride channel conductance of a-aryloxyalkyl-4-chlorophenoxyacetic acids 62
Molecular spatial geometry of CLC-K ligands: optimal requirements towards high affinity channel block 62
Synthesis and biological screening of new chiral fibrates as potential PPAR α/γ dual agonists 61
Ureidofibrate-like analogs as PPARgamma Agonists endowed with anti-proliferative activity 60
Synthesis, biological evaluation and molecular modeling investigation of fibrates analogues with PPARalpha945; and PPARgamma47; agonist activity 58
Dimeric analogs of the dual PPARα/γ agonist LT-175: design, synthesis and biological evaluation 57
null 56
EVALUATION OF BIOPHYSICAL AND PHARMACOLOGICAL PROPERTIES OF CHLORIDE CHANNELS BELONGING TO CLC FAMILY BY THE USE OF CHIRAL CLOFIBRIC ACID DERIVATIVES. 54
DESIGN, SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW ANALOGS OF THE DUAL PPARalpha/gamma AGONIST LT175 54
Novel imidazoline compounds as partial or full agonists of D2-like dopamine receptors inspired by I2-imidazoline binding sites ligand 2-BFI 54
MOLECULAR DETERMINANTS FOR NUCLEAR RECEPTORS SELECTIVITY: CHEMIOMETRIC ANALYSIS AND DOCKING OF DUAL PPAR AGONISTS. 50
Synthesis and preliminary biological evaluation on PPARs of new ureidofibrate-like analogs 47
Sintesi e valutazione dell’attivita' agonista sui Peroxisome Proliferator-Activated Receptors (PPARs) di una nuova serie di derivati dell’acido 2-fenossi-3-fenil-propanoico 44
null 38
null 37
null 37
null 32
null 30
null 30
null 29
null 27
null 25
null 25
Totale 9.745
Salva come PNG Salva come JPEG
Categoria #
all - tutte 40.228
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 40.228
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022466 0 0 0 0 25 23 29 28 24 27 119 191
2022/20231.064 185 68 60 93 140 146 10 110 214 4 14 20
2023/2024404 26 66 21 25 50 103 23 24 11 11 12 32
2024/20251.257 52 32 124 54 33 82 79 107 61 52 168 413
2025/20262.732 389 178 187 296 233 143 307 81 221 255 71 371
2026/2027937 56 157 271 395 58 0 0 0 0 0 0 0
Totale 9.953