IRIS
CARBONARA, Giuseppe Gerardo
 Distribuzione geografica
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Continente #
NA - Nord America 4.166
AS - Asia 1.612
EU - Europa 1.243
SA - Sud America 408
AF - Africa 46
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 2
Totale 7.485
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Nazione #
US - Stati Uniti d'America 4.111
SG - Singapore 680
CN - Cina 440
BR - Brasile 359
SE - Svezia 254
HK - Hong Kong 236
UA - Ucraina 171
DE - Germania 154
RU - Federazione Russa 148
IT - Italia 144
FI - Finlandia 101
FR - Francia 90
GB - Regno Unito 85
VN - Vietnam 78
IN - India 50
CA - Canada 28
IR - Iran 26
CI - Costa d'Avorio 22
AR - Argentina 18
IE - Irlanda 18
TR - Turchia 17
MX - Messico 16
BE - Belgio 15
BD - Bangladesh 14
ID - Indonesia 14
CZ - Repubblica Ceca 10
EC - Ecuador 10
ES - Italia 10
IQ - Iraq 9
JP - Giappone 9
AU - Australia 7
CH - Svizzera 7
KR - Corea 7
NL - Olanda 7
SA - Arabia Saudita 7
ZA - Sudafrica 7
CO - Colombia 6
LT - Lituania 6
CL - Cile 5
DZ - Algeria 5
JM - Giamaica 5
AT - Austria 4
PE - Perù 4
PK - Pakistan 4
VE - Venezuela 4
IL - Israele 3
JO - Giordania 3
KE - Kenya 3
PL - Polonia 3
RO - Romania 3
A1 - Anonimo 2
BA - Bosnia-Erzegovina 2
DK - Danimarca 2
EG - Egitto 2
HN - Honduras 2
MA - Marocco 2
NP - Nepal 2
RS - Serbia 2
TT - Trinidad e Tobago 2
UZ - Uzbekistan 2
AD - Andorra 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BH - Bahrain 1
DO - Repubblica Dominicana 1
GA - Gabon 1
GE - Georgia 1
GR - Grecia 1
GT - Guatemala 1
GY - Guiana 1
KW - Kuwait 1
KZ - Kazakistan 1
LV - Lettonia 1
MD - Moldavia 1
MM - Myanmar 1
NG - Nigeria 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PH - Filippine 1
PS - Palestinian Territory 1
PT - Portogallo 1
PY - Paraguay 1
SD - Sudan 1
SN - Senegal 1
SY - Repubblica araba siriana 1
TN - Tunisia 1
TW - Taiwan 1
Totale 7.485
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Città #
Jacksonville 393
Fairfield 378
Chandler 369
Woodbridge 362
Ashburn 351
Singapore 296
Hong Kong 232
Houston 221
Cambridge 185
Nyköping 182
Ann Arbor 171
Seattle 143
Wilmington 130
Beijing 101
Nanjing 93
Dallas 90
Lawrence 88
Roxbury 88
Princeton 67
Boardman 64
Bari 60
Des Moines 59
Los Angeles 49
New York 41
Inglewood 40
Ho Chi Minh City 35
Marseille 32
São Paulo 30
Munich 25
Brooklyn 24
Nanchang 24
Buffalo 23
Abidjan 22
Jiaxing 21
Council Bluffs 20
Hebei 20
Santa Clara 20
Tianjin 19
Dublin 18
Chicago 17
Changsha 16
Hanoi 16
Brussels 15
San Diego 15
London 13
Shenyang 13
Toronto 13
Rio de Janeiro 12
Washington 12
Guangzhou 11
Paris 11
Augusta 10
Leawood 10
Rome 10
San Francisco 10
Belo Horizonte 9
Mumbai 9
Tokyo 9
Brasília 8
Dearborn 8
Helsinki 8
Long Beach 8
Stockholm 8
Ardabil 7
Frankfurt am Main 7
Istanbul 7
Lausanne 7
North Bergen 7
San Mateo 7
Shanghai 7
Turku 7
Wuhan 7
Boydton 6
Haikou 6
Mexico City 6
Quito 6
Auburn Hills 5
Caxias do Sul 5
Chennai 5
Formello 5
Genova 5
Jeddah 5
Johannesburg 5
Moscow 5
Norwalk 5
Porto Alegre 5
Pune 5
Sydney 5
Zhengzhou 5
Amsterdam 4
Atlanta 4
Baghdad 4
Bologna 4
Campinas 4
Cleveland 4
Dhaka 4
Dong Ket 4
Florence 4
Gilbert 4
Goiânia 4
Totale 5.053
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Nome #
An efficient synthesis of the optically active isomers of 2H-1,4-benzoxazine derivatives, novel KATP channel modulators 190
Probiotic and Tea Tree Oil Treatments Improve Therapy of Vaginal Candidiasis: A Preliminary Clinical Study 189
Convenient synthesis of some 3-phenyl-1-benzofuran-2-carboxylic acid derivatives as new potential inhibitors of CLC-Kb channels 171
Activation and inhibition of kidney CLC-K chloride channels by fenamates 166
Kidney CLC-K Chloride Channels Show Differential Pharmacological Profiles Depending on the Heterologous Expression System 157
Synthesis, in vitro evaluation, and molecular modeling investigation of benzenesulfonimide peroxisome proliferator-activated receptors α antagonists 157
Synthesis, biological evaluation, and molecular modeling investigation of chiral 2-(4-chloro-phenoxy)-3-phenyl-propanoic acid derivatives with PPARα and PPARγ agonist activity 144
ChemInform Abstract: Convenient Synthesis of Some 3-Phenyl-1-benzofuran-2-carboxylic Acid Derivatives as New Potential Inhibitors of CLC-Kb Channels. 143
Comparative LC Enantioseparation of Novel PPAR Agonists on Cellulose- and Amylose-Based Chiral Stationary Phases 140
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 137
Repositioning of Endonuclear Receptors Binders as Potential Antibacterial and Antifungal Agents. Eptyloxìm: A Potential and Novel Gyrase B and Cytochrome Cyp51 Inhibitor 127
2-(9-Antryl)alcanoic acids as chloride channel modulators 124
Carbonic anhydrase inhibitors are specific openers of skeletal muscle BK channel of K+ - deficient rats 119
Kidney CLC-K Chloride Channels Inhibitors: Definition of Novel Structural Requirements and Efficacy in CLC-K Polymorphism Associated with Hypertension 115
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 112
Elucidation of the synergistic action of Mentha Piperita essential oil with common antimicrobials 111
AGONISTI DEI RECETTORI NUCLEARI PPARs COME POTENZIALI NUOVI AGENTI TERAPEUTICI PER IL TRATTAMENTO DELLA SINDROME METABOLICA. 105
MOLECULAR DETERMINANTS FOR NUCLEAR RECEPTORS SELECTIVITY: CHEMOMETRIC ANALYSIS, DOCKINGS AND SITE-DIRECTED MUTAGENESIS OF DUAL PEROXISOME PROLIFERATOR-ACTIVATED RECEPTORS α/γ AGONISTS 104
Chemical studies on Drug Metabolism (part II): N-demethylation and N-oxidation of some alicyclic amines by RuO4 102
Comparative analysis of enantioselective separation of novel PPAR agonists by HPLC on cellulose- and amylose-based chiral stationary phases 101
Design, synthesis and biological evaluation of a class of bioisosteric oximes of the novel dual peroxisome proliferator-activated receptor alpha/gamma ligand LT175 99
(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 99
Analisi Farmaceutica 98
Agonisti dei Recettori Nucleari PPARs come Potenziali Nuovi Agenti Terapeutici per il Trattamento della Sindrome Metabolica 98
Growth hormone secretagogues exert differential effects on skeletal muscle calcium homeostasis in male rats depending on the peptidyl/non-peptidyl structure 98
Synthesis, Biological Evaluation, and Molecular Modeling Investigation of Chiral Phenoxyacetic Acid Analogues with PPARalpha and PPARgamma Agonist Activity 97
Allyphenyline Analogues Potentially Useful in the Management of Chronic Pain and Opioid Addiction 96
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 96
Attività biologica sui canali KATP del muscolo scheletrico nativo di nuovi e potenti derivati delle 2H-1,4-Benzossazine 96
Kidney CLC-K chloride channels inhibitors: structure-based studies and efficacy in hypertension and associated CLC-K polymorphisms. 96
Might the observed a2A-adrenoreceptor agonism or antagonism of allyphenyline analogues be ascribed to different molecular conformations? 92
KIDNEY CLC-K CHLORIDE CHANNELS SHOW DIFFERENTIAL PHARMACOLOGICAL PROFILES DEPENDING ON THE HETEROLOGOUS EXPRESSION SYSTEM 91
Block of renal CLC-K channels by phenoxy-alkyl derivatives of clofibric acid 90
BIOLOGICAL ACTIVITY OF NEW POTENT 2H-1,4-BENZOXAZINE DERIVATIVES ON THE NATIVE SKELETAL MUSCLE KATP CHANNEL 84
Elucidation of the enantioselective recognition mechanism of a penicillin G acylase-based chiral stationary phase towards a series of 2-aryloxy-2-arylacetic acids 84
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 84
Sintesi di una nuova serie di acidi 2-benzofuran-carbossilici a potenziale attività bloccante dei canali al cloro voltaggio-dipendenti CLC-K 82
Molecular switch for CLC-K Cl– channel block/activation: Optimal pharmacophoric requirements towards high-affinity ligands 82
Calcium activated K+ channel as a target of prompt-to-use drugs in neuromuscular disorders 79
Structural nucleotide analogs are potent activators/inhibitors of pancreatic beta-cell KATP channels: an emerging mechanism supporting their use as anti-diabetic drugs. 79
Synthesis, biological evaluation and molecular investigation of fluorinated peroxisome proliferator-activated receptors alpha/gamma dual agonists 79
Studio delle proprietà enentioselettive di una fase stazionaria chirale a base di PGA 77
Molecular determinants for nuclear receptors selectivity: chemometric analysis, dockings and site-directed mutagenesis of dual peroxisome proliferator-activated receptors alpha/gamma agonists 77
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 74
INNOVATIVE METHODOLOGIES IN NANOTECHNOLOGY FOR THE PREVENTION OF BACTERIAL DISEASES 73
Chemical studies on Drug Metabolism: Oxidation with ruthenium tetroxide of some medicinal alicyclic N-metylamines 72
Ossidazione di ammine policicliche terziarie con RuO4 72
Dimeric analogs of the dual PPARα/γ agonist LT-175: design, synthesis and biological evaluation. 71
Tissue specific action of the 2-(propyl)-1,4-benzoxazine on pancreatic beta cell ATP-sensitive potassium channels 70
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 67
Selective oxidation of nitrogen organic compounds 66
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MOLECULAR SPATIAL GEOMETRY OF CLC-K LIGANDS: OPTIMAL REQUIREMENTS TOWARDS HIGH AFFINITY CHANNEL BLOCK. 64
Selective oxidation of Nitrogen organic compounds by Ruthenium tetroxide 61
H-1-NMR determination of the enantiomeric excess of the antiarrhythmic drug Mexiletine by using mandelic acid analogues as chiral solvating agents 61
Oxidation of tertiary polycyclic amines by RuO4 60
NEW CHIRAL CLOFIBRIC ACID ANALOGS AS LIGANDS OF PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR (PPAR) alpha AND gamma 60
Enantioselective properties of Penicillin G Acylase: Liquid Crhomatographic studies end docking simulations 59
DESIGN, SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW ANALOGS OF THE DUAL PPARα/γ AGONIST LT175. 58
Molecular spatial geometry of CLC-K ligands: optimal requirements towards high affinity channel block 56
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Progettazione e sintesi di nuovi agenti antimicrobici e studio dell'attività biologica in associazione con differenti olii essenziali 54
Design, synthesis and biological evaluation of a dimeric analog of the dual PPARα/γ agonist 2-(4-phenyl-phenoxy)-3-phenyl-propanoic acid. 54
EFFETTI DERIVANTI DALL'INTRODUZIONE DI SOSTITUENTI SUL NUCLEO DIFENILICO DEL COMPOSTO LT175, AGONISTA DUALE DEI RECETTORI NUCLEARI PPARalfa E PPARgamma 53
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 51
Traduzione Capitoli 1-9 49
Determinanti Molecolari della Selettività di Recettori Nucleari: Analisi Chemiometrica e Docking di Agonisti Selettivi di Recettori PPARs 49
Evaluation of biophysical and pharmacological properties of chloride channels belonging to ClC family by the use of chiral clofibric acid derivatives 48
Dal brodo primordiale alla farmacogenomica 47
Effects on skeletal muscle chloride channel conductance of a-aryloxyalkyl-4-chlorophenoxyacetic acids 45
Novel dual PPARalpha/gamma Agonists, as hypoglycemic and antidiabetic agents 45
Synthesis and biological screening of new chiral a-aryloxy-alkanoic acids as PPARs agonists 45
NEW CHIRAL DERIVATIVES OF 2-(4-PHENYL-PHENOXY)-3-PHENYLPROPANOIC ACID WITH PPARalpha/gamma DUAL ACTIVITY. 43
Design, synthesis and biological evaluation of a dimeric analog of the dual PPARα/γ agonist 2-(4-phenyl-phenoxy)-3-phenyl-propanoic acid 43
Synthesis and biological evaluation of new fluorinated analogues with PPARα and PPARγ agonist activity 42
Molecular spatial geometry of CLC-K ligands: optimal requirements towards high affinity channel block 41
Synthesis and biological screening of new chiral 2-(4-chloro-phenoxy)-3-phenylpropanoic acid analogs as potential PPAR alpha/gamma dual agonists 41
Novel imidazoline compounds as partial or full agonists of D2-like dopamine receptors inspired by I2-imidazoline binding sites ligand 2-BFI 41
Molecular spatial geometry of CLC-K ligands: optimal requirements towards high affinity channel block 40
Synthesis and biological screening of new chiral fibrates as potential PPAR α/γ dual agonists 39
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sintesi di una nuova serie di acidi 2-benzofuran-carbossilici e valutazione della loro attività bloccante dei canali al cloro voltaggio-dipendenti CLC-K 37
Dimeric analogs of the dual PPARα/γ agonist LT-175: design, synthesis and biological evaluation 35
PROGETTAZIONE, SINTESI E VALUTAZIONE BIOLOGICA DI DERIVATI OSSIMMINICI AD ATTIVITA’ AGONISTA DUALE PPARα/γ. 35
EVALUATION OF BIOPHYSICAL AND PHARMACOLOGICAL PROPERTIES OF CHLORIDE CHANNELS BELONGING TO CLC FAMILY BY THE USE OF CHIRAL CLOFIBRIC ACID DERIVATIVES. 34
DESIGN, SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW ANALOGS OF THE DUAL PPARalpha/gamma AGONIST LT175 34
MOLECULAR DETERMINANTS FOR NUCLEAR RECEPTORS SELECTIVITY: CHEMIOMETRIC ANALYSIS AND DOCKING OF DUAL PPAR AGONISTS. 33
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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 29
Synthesis, biological evaluation and molecular modeling investigation of fibrates analogues with PPARalpha945; and PPARgamma47; agonist activity 28
Ureidofibrate-like analogs as PPARgamma Agonists endowed with anti-proliferative activity 28
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Totale 7.429
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Categoria #
all - tutte 31.856
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 31.856
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021435 0 0 0 0 0 13 59 33 73 110 93 54
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
2025/20261.350 389 178 187 296 233 67 0 0 0 0 0 0
Totale 7.634