IRIS
CARBONARA, Giuseppe Gerardo
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 4.670
AS - Asia 1.919
EU - Europa 1.757
SA - Sud America 487
AF - Africa 61
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 2
Totale 8.905
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 4.588
SG - Singapore 757
IT - Italia 527
CN - Cina 484
BR - Brasile 397
SE - Svezia 255
HK - Hong Kong 244
UA - Ucraina 172
FR - Francia 166
DE - Germania 161
RU - Federazione Russa 155
FI - Finlandia 116
VN - Vietnam 104
GB - Regno Unito 96
IN - India 92
BD - Bangladesh 39
CA - Canada 39
AR - Argentina 26
IR - Iran 26
TR - Turchia 25
MX - Messico 24
CI - Costa d'Avorio 22
IQ - Iraq 22
ID - Indonesia 19
IE - Irlanda 18
CO - Colombia 17
BE - Belgio 15
SA - Arabia Saudita 15
EC - Ecuador 12
ES - Italia 12
JP - Giappone 12
ZA - Sudafrica 12
PH - Filippine 11
CZ - Repubblica Ceca 10
CL - Cile 9
NL - Olanda 9
PK - Pakistan 9
VE - Venezuela 9
AU - Australia 8
JM - Giamaica 8
CH - Svizzera 7
KR - Corea 7
LT - Lituania 7
MY - Malesia 7
UZ - Uzbekistan 7
PE - Perù 6
DZ - Algeria 5
JO - Giordania 5
RO - Romania 5
AT - Austria 4
IL - Israele 4
KE - Kenya 4
KG - Kirghizistan 4
MA - Marocco 4
NP - Nepal 4
PL - Polonia 4
RS - Serbia 4
UY - Uruguay 4
BO - Bolivia 3
EG - Egitto 3
HN - Honduras 3
PS - Palestinian Territory 3
PY - Paraguay 3
TT - Trinidad e Tobago 3
A1 - Anonimo 2
BA - Bosnia-Erzegovina 2
CR - Costa Rica 2
DK - Danimarca 2
GE - Georgia 2
KW - Kuwait 2
KZ - Kazakistan 2
MM - Myanmar 2
OM - Oman 2
SN - Senegal 2
TN - Tunisia 2
AD - Andorra 1
AE - Emirati Arabi Uniti 1
AL - Albania 1
AO - Angola 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BH - Bahrain 1
CY - Cipro 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GA - Gabon 1
GR - Grecia 1
GT - Guatemala 1
GY - Guiana 1
HU - Ungheria 1
LK - Sri Lanka 1
LV - Lettonia 1
LY - Libia 1
MD - Moldavia 1
MG - Madagascar 1
MK - Macedonia 1
NG - Nigeria 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
Totale 8.899
Salva come PNG Salva come JPEG
Città #
Ashburn 414
Jacksonville 395
Fairfield 378
Chandler 369
Woodbridge 362
Singapore 347
San Jose 248
Hong Kong 239
Houston 221
Milan 204
Cambridge 185
Nyköping 182
Ann Arbor 171
Seattle 143
Wilmington 130
Beijing 105
Dallas 94
Nanjing 93
Lawrence 88
Roxbury 88
Lauterbourg 75
Rome 73
Bari 67
Princeton 67
Boardman 66
Des Moines 59
Los Angeles 55
New York 50
Ho Chi Minh City 42
Inglewood 40
São Paulo 33
Marseille 32
Figino 30
Santa Clara 29
Brooklyn 27
Munich 25
Buffalo 24
Council Bluffs 24
Nanchang 24
Helsinki 23
Abidjan 22
Hanoi 21
Jiaxing 21
Hebei 20
Tianjin 19
Dublin 18
Chicago 17
Changsha 16
Orem 16
Brussels 15
London 15
San Diego 15
Toronto 15
Washington 15
Mumbai 14
Rio de Janeiro 14
Chennai 13
Shenyang 13
Paris 12
San Francisco 12
Tokyo 12
Turin 12
Frankfurt am Main 11
Guangzhou 11
Istanbul 11
Mexico City 11
Augusta 10
Brasília 10
Leawood 10
Belo Horizonte 9
Stockholm 9
Baghdad 8
Dearborn 8
Long Beach 8
Ardabil 7
Atlanta 7
Bologna 7
Dhaka 7
Jeddah 7
Johannesburg 7
Lausanne 7
Manchester 7
Medellín 7
North Bergen 7
San Mateo 7
Shanghai 7
Tashkent 7
Turku 7
Wuhan 7
Boydton 6
Delhi 6
Florence 6
Haikou 6
Jakarta 6
Poplar 6
Porto Alegre 6
Quito 6
Amman 5
Amsterdam 5
Auburn Hills 5
Totale 5.952
Salva come PNG Salva come JPEG
Nome #
Probiotic and Tea Tree Oil Treatments Improve Therapy of Vaginal Candidiasis: A Preliminary Clinical Study 248
An efficient synthesis of the optically active isomers of 2H-1,4-benzoxazine derivatives, novel KATP channel modulators 208
Convenient synthesis of some 3-phenyl-1-benzofuran-2-carboxylic acid derivatives as new potential inhibitors of CLC-Kb channels 192
Activation and inhibition of kidney CLC-K chloride channels by fenamates 186
Synthesis, in vitro evaluation, and molecular modeling investigation of benzenesulfonimide peroxisome proliferator-activated receptors α antagonists 183
Kidney CLC-K Chloride Channels Show Differential Pharmacological Profiles Depending on the Heterologous Expression System 173
ChemInform Abstract: Convenient Synthesis of Some 3-Phenyl-1-benzofuran-2-carboxylic Acid Derivatives as New Potential Inhibitors of CLC-Kb Channels. 162
2-(9-Antryl)alcanoic acids as chloride channel modulators 159
Synthesis, biological evaluation, and molecular modeling investigation of chiral 2-(4-chloro-phenoxy)-3-phenyl-propanoic acid derivatives with PPARα and PPARγ agonist activity 158
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 156
Comparative LC Enantioseparation of Novel PPAR Agonists on Cellulose- and Amylose-Based Chiral Stationary Phases 154
Repositioning of Endonuclear Receptors Binders as Potential Antibacterial and Antifungal Agents. Eptyloxìm: A Potential and Novel Gyrase B and Cytochrome Cyp51 Inhibitor 142
Carbonic anhydrase inhibitors are specific openers of skeletal muscle BK channel of K+ - deficient rats 140
Elucidation of the synergistic action of Mentha Piperita essential oil with common antimicrobials 131
AGONISTI DEI RECETTORI NUCLEARI PPARs COME POTENZIALI NUOVI AGENTI TERAPEUTICI PER IL TRATTAMENTO DELLA SINDROME METABOLICA. 130
Agonisti dei Recettori Nucleari PPARs come Potenziali Nuovi Agenti Terapeutici per il Trattamento della Sindrome Metabolica 128
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 128
Kidney CLC-K Chloride Channels Inhibitors: Definition of Novel Structural Requirements and Efficacy in CLC-K Polymorphism Associated with Hypertension 125
(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 122
Allyphenyline Analogues Potentially Useful in the Management of Chronic Pain and Opioid Addiction 120
Analisi Farmaceutica 119
MOLECULAR DETERMINANTS FOR NUCLEAR RECEPTORS SELECTIVITY: CHEMOMETRIC ANALYSIS, DOCKINGS AND SITE-DIRECTED MUTAGENESIS OF DUAL PEROXISOME PROLIFERATOR-ACTIVATED RECEPTORS α/γ AGONISTS 119
Design, synthesis and biological evaluation of a class of bioisosteric oximes of the novel dual peroxisome proliferator-activated receptor alpha/gamma ligand LT175 119
Synthesis, Biological Evaluation, and Molecular Modeling Investigation of Chiral Phenoxyacetic Acid Analogues with PPARalpha and PPARgamma Agonist Activity 117
Kidney CLC-K chloride channels inhibitors: structure-based studies and efficacy in hypertension and associated CLC-K polymorphisms. 117
Comparative analysis of enantioselective separation of novel PPAR agonists by HPLC on cellulose- and amylose-based chiral stationary phases 115
Chemical studies on Drug Metabolism (part II): N-demethylation and N-oxidation of some alicyclic amines by RuO4 114
Block of renal CLC-K channels by phenoxy-alkyl derivatives of clofibric acid 114
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 111
Might the observed a2A-adrenoreceptor agonism or antagonism of allyphenyline analogues be ascribed to different molecular conformations? 106
Growth hormone secretagogues exert differential effects on skeletal muscle calcium homeostasis in male rats depending on the peptidyl/non-peptidyl structure 105
KIDNEY CLC-K CHLORIDE CHANNELS SHOW DIFFERENTIAL PHARMACOLOGICAL PROFILES DEPENDING ON THE HETEROLOGOUS EXPRESSION SYSTEM 104
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 104
Attività biologica sui canali KATP del muscolo scheletrico nativo di nuovi e potenti derivati delle 2H-1,4-Benzossazine 104
Elucidation of the enantioselective recognition mechanism of a penicillin G acylase-based chiral stationary phase towards a series of 2-aryloxy-2-arylacetic acids 102
BIOLOGICAL ACTIVITY OF NEW POTENT 2H-1,4-BENZOXAZINE DERIVATIVES ON THE NATIVE SKELETAL MUSCLE KATP CHANNEL 101
Structural nucleotide analogs are potent activators/inhibitors of pancreatic beta-cell KATP channels: an emerging mechanism supporting their use as anti-diabetic drugs. 100
Calcium activated K+ channel as a target of prompt-to-use drugs in neuromuscular disorders 99
Molecular determinants for nuclear receptors selectivity: chemometric analysis, dockings and site-directed mutagenesis of dual peroxisome proliferator-activated receptors alpha/gamma agonists 94
Studio delle proprietà enentioselettive di una fase stazionaria chirale a base di PGA 93
Synthesis, biological evaluation and molecular investigation of fluorinated peroxisome proliferator-activated receptors alpha/gamma dual agonists 92
Sintesi di una nuova serie di acidi 2-benzofuran-carbossilici a potenziale attività bloccante dei canali al cloro voltaggio-dipendenti CLC-K 91
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 89
Chemical studies on Drug Metabolism: Oxidation with ruthenium tetroxide of some medicinal alicyclic N-metylamines 88
INNOVATIVE METHODOLOGIES IN NANOTECHNOLOGY FOR THE PREVENTION OF BACTERIAL DISEASES 88
Molecular switch for CLC-K Cl– channel block/activation: Optimal pharmacophoric requirements towards high-affinity ligands 86
Ossidazione di ammine policicliche terziarie con RuO4 84
Selective oxidation of nitrogen organic compounds 82
Dimeric analogs of the dual PPARα/γ agonist LT-175: design, synthesis and biological evaluation. 81
MOLECULAR SPATIAL GEOMETRY OF CLC-K LIGANDS: OPTIMAL REQUIREMENTS TOWARDS HIGH AFFINITY CHANNEL BLOCK. 80
Enantioselective properties of Penicillin G Acylase: Liquid Crhomatographic studies end docking simulations 80
Selective oxidation of Nitrogen organic compounds by Ruthenium tetroxide 79
H-1-NMR determination of the enantiomeric excess of the antiarrhythmic drug Mexiletine by using mandelic acid analogues as chiral solvating agents 79
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 79
Tissue specific action of the 2-(propyl)-1,4-benzoxazine on pancreatic beta cell ATP-sensitive potassium channels 77
DESIGN, SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW ANALOGS OF THE DUAL PPARα/γ AGONIST LT175. 75
NEW CHIRAL CLOFIBRIC ACID ANALOGS AS LIGANDS OF PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR (PPAR) alpha AND gamma 71
Design, synthesis and biological evaluation of a dimeric analog of the dual PPARα/γ agonist 2-(4-phenyl-phenoxy)-3-phenyl-propanoic acid. 70
Determinanti Molecolari della Selettività di Recettori Nucleari: Analisi Chemiometrica e Docking di Agonisti Selettivi di Recettori PPARs 70
Oxidation of tertiary polycyclic amines by RuO4 69
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 68
null 66
Traduzione Capitoli 1-9 66
EFFETTI DERIVANTI DALL'INTRODUZIONE DI SOSTITUENTI SUL NUCLEO DIFENILICO DEL COMPOSTO LT175, AGONISTA DUALE DEI RECETTORI NUCLEARI PPARalfa E PPARgamma 66
Progettazione e sintesi di nuovi agenti antimicrobici e studio dell'attività biologica in associazione con differenti olii essenziali 65
Molecular spatial geometry of CLC-K ligands: optimal requirements towards high affinity channel block 63
Evaluation of biophysical and pharmacological properties of chloride channels belonging to ClC family by the use of chiral clofibric acid derivatives 63
Novel dual PPARalpha/gamma Agonists, as hypoglycemic and antidiabetic agents 62
Synthesis and biological evaluation of new fluorinated analogues with PPARα and PPARγ agonist activity 60
Synthesis and biological screening of new chiral a-aryloxy-alkanoic acids as PPARs agonists 60
Synthesis and biological screening of new chiral 2-(4-chloro-phenoxy)-3-phenylpropanoic acid analogs as potential PPAR alpha/gamma dual agonists 59
Dal brodo primordiale alla farmacogenomica 58
Design, synthesis and biological evaluation of a dimeric analog of the dual PPARα/γ agonist 2-(4-phenyl-phenoxy)-3-phenyl-propanoic acid 58
NEW CHIRAL DERIVATIVES OF 2-(4-PHENYL-PHENOXY)-3-PHENYLPROPANOIC ACID WITH PPARalpha/gamma DUAL ACTIVITY. 57
Effects on skeletal muscle chloride channel conductance of a-aryloxyalkyl-4-chlorophenoxyacetic acids 56
null 56
Molecular spatial geometry of CLC-K ligands: optimal requirements towards high affinity channel block 55
Synthesis and biological screening of new chiral fibrates as potential PPAR α/γ dual agonists 53
Molecular spatial geometry of CLC-K ligands: optimal requirements towards high affinity channel block 50
sintesi di una nuova serie di acidi 2-benzofuran-carbossilici e valutazione della loro attività bloccante dei canali al cloro voltaggio-dipendenti CLC-K 50
EVALUATION OF BIOPHYSICAL AND PHARMACOLOGICAL PROPERTIES OF CHLORIDE CHANNELS BELONGING TO CLC FAMILY BY THE USE OF CHIRAL CLOFIBRIC ACID DERIVATIVES. 48
Novel imidazoline compounds as partial or full agonists of D2-like dopamine receptors inspired by I2-imidazoline binding sites ligand 2-BFI 48
Dimeric analogs of the dual PPARα/γ agonist LT-175: design, synthesis and biological evaluation 46
PROGETTAZIONE, SINTESI E VALUTAZIONE BIOLOGICA DI DERIVATI OSSIMMINICI AD ATTIVITA’ AGONISTA DUALE PPARα/γ. 45
Ureidofibrate-like analogs as PPARgamma Agonists endowed with anti-proliferative activity 45
DESIGN, SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW ANALOGS OF THE DUAL PPARalpha/gamma AGONIST LT175 43
Synthesis, biological evaluation and molecular modeling investigation of fibrates analogues with PPARalpha945; and PPARgamma47; agonist activity 42
MOLECULAR DETERMINANTS FOR NUCLEAR RECEPTORS SELECTIVITY: CHEMIOMETRIC ANALYSIS AND DOCKING OF DUAL PPAR AGONISTS. 40
Synthesis and preliminary biological evaluation on PPARs of new ureidofibrate-like analogs 39
null 38
null 37
null 37
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 37
null 32
null 30
null 30
null 29
null 27
null 25
null 25
Totale 8.846
Salva come PNG Salva come JPEG
Categoria #
all - tutte 36.546
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 36.546
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022601 23 89 1 22 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
2026/202738 38 0 0 0 0 0 0 0 0 0 0 0
Totale 9.054