IRIS
CARBONARA, Giuseppe Gerardo
 Distribuzione geografica
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Continente #
NA - Nord America 3.685
EU - Europa 1.125
AS - Asia 626
SA - Sud America 62
OC - Oceania 7
AF - Africa 6
Continente sconosciuto - Info sul continente non disponibili 2
Totale 5.513
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Nazione #
US - Stati Uniti d'America 3.662
CN - Cina 339
SE - Svezia 246
SG - Singapore 188
UA - Ucraina 169
RU - Federazione Russa 143
IT - Italia 135
DE - Germania 127
FI - Finlandia 94
FR - Francia 80
GB - Regno Unito 61
BR - Brasile 56
IN - India 29
IR - Iran 20
IE - Irlanda 17
CA - Canada 16
BE - Belgio 14
TR - Turchia 11
CZ - Repubblica Ceca 9
HK - Hong Kong 8
CH - Svizzera 7
AU - Australia 6
ID - Indonesia 5
KR - Corea 5
LT - Lituania 5
VN - Vietnam 5
DZ - Algeria 4
IQ - Iraq 4
JM - Giamaica 4
NL - Olanda 4
AT - Austria 3
ES - Italia 3
A1 - Anonimo 2
BD - Bangladesh 2
CL - Cile 2
EC - Ecuador 2
IL - Israele 2
JP - Giappone 2
MX - Messico 2
RS - Serbia 2
AR - Argentina 1
BG - Bulgaria 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
GE - Georgia 1
KE - Kenya 1
LV - Lettonia 1
MA - Marocco 1
MD - Moldavia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PK - Pakistan 1
PL - Polonia 1
PT - Portogallo 1
SY - Repubblica araba siriana 1
TW - Taiwan 1
UZ - Uzbekistan 1
VE - Venezuela 1
Totale 5.513
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Città #
Jacksonville 393
Fairfield 378
Chandler 369
Woodbridge 362
Ashburn 252
Houston 221
Cambridge 185
Nyköping 182
Ann Arbor 171
Seattle 140
Wilmington 129
Singapore 101
Nanjing 93
Lawrence 88
Roxbury 88
Princeton 67
Boardman 64
Bari 60
Des Moines 59
Beijing 45
Inglewood 40
New York 36
Marseille 32
Nanchang 24
Jiaxing 21
Los Angeles 21
Brooklyn 20
Hebei 20
Tianjin 18
Dublin 17
Changsha 16
San Diego 15
Santa Clara 15
Brussels 14
Shenyang 13
Toronto 12
Washington 12
Paris 11
Augusta 10
Guangzhou 10
Leawood 10
London 9
Dearborn 8
Helsinki 8
Long Beach 8
Ardabil 7
Lausanne 7
Mumbai 7
North Bergen 7
Rome 7
San Mateo 7
Wuhan 7
Boydton 6
Haikou 6
Munich 6
San Francisco 6
Shanghai 6
Auburn Hills 5
Formello 5
Genova 5
Hong Kong 5
Moscow 5
Pune 5
São Paulo 5
Bologna 4
Dong Ket 4
Gilbert 4
Guys Hill 4
Istanbul 4
Napoli 4
Norwalk 4
Prague 4
Sydney 4
Zhengzhou 4
Belo Horizonte 3
Brahmapur 3
Cleveland 3
Jinan 3
Kunming 3
Redwood City 3
Ústí nad Labem 3
Alfafar 2
Algiers 2
Americana 2
Belgrade 2
Brasília 2
Camden 2
Cassano Magnago 2
Chennai 2
Chicago 2
Council Bluffs 2
Delhi 2
East Hartford 2
Frankfurt am Main 2
Hefei 2
Heze 2
Indiana 2
Jakarta 2
Karbala 2
Kenmore 2
Totale 4.080
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Nome #
An efficient synthesis of the optically active isomers of 2H-1,4-benzoxazine derivatives, novel KATP channel modulators 145
Probiotic and Tea Tree Oil Treatments Improve Therapy of Vaginal Candidiasis: A Preliminary Clinical Study 137
Kidney CLC-K Chloride Channels Show Differential Pharmacological Profiles Depending on the Heterologous Expression System 132
Synthesis, biological evaluation, and molecular modeling investigation of chiral 2-(4-chloro-phenoxy)-3-phenyl-propanoic acid derivatives with PPARα and PPARγ agonist activity 130
Activation and inhibition of kidney CLC-K chloride channels by fenamates 128
Synthesis, in vitro evaluation, and molecular modeling investigation of benzenesulfonimide peroxisome proliferator-activated receptors α antagonists 126
Convenient synthesis of some 3-phenyl-1-benzofuran-2-carboxylic acid derivatives as new potential inhibitors of CLC-Kb channels 124
Comparative LC Enantioseparation of Novel PPAR Agonists on Cellulose- and Amylose-Based Chiral Stationary Phases 121
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 109
ChemInform Abstract: Convenient Synthesis of Some 3-Phenyl-1-benzofuran-2-carboxylic Acid Derivatives as New Potential Inhibitors of CLC-Kb Channels. 102
Repositioning of Endonuclear Receptors Binders as Potential Antibacterial and Antifungal Agents. Eptyloxìm: A Potential and Novel Gyrase B and Cytochrome Cyp51 Inhibitor 101
Kidney CLC-K Chloride Channels Inhibitors: Definition of Novel Structural Requirements and Efficacy in CLC-K Polymorphism Associated with Hypertension 100
MOLECULAR DETERMINANTS FOR NUCLEAR RECEPTORS SELECTIVITY: CHEMOMETRIC ANALYSIS, DOCKINGS AND SITE-DIRECTED MUTAGENESIS OF DUAL PEROXISOME PROLIFERATOR-ACTIVATED RECEPTORS α/γ AGONISTS 93
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 93
Elucidation of the synergistic action of Mentha Piperita essential oil with common antimicrobials 91
Carbonic anhydrase inhibitors are specific openers of skeletal muscle BK channel of K+ - deficient rats 85
Synthesis, Biological Evaluation, and Molecular Modeling Investigation of Chiral Phenoxyacetic Acid Analogues with PPARalpha and PPARgamma Agonist Activity 82
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 81
Comparative analysis of enantioselective separation of novel PPAR agonists by HPLC on cellulose- and amylose-based chiral stationary phases 79
2-(9-Antryl)alcanoic acids as chloride channel modulators 77
Might the observed a2A-adrenoreceptor agonism or antagonism of allyphenyline analogues be ascribed to different molecular conformations? 76
Chemical studies on Drug Metabolism (part II): N-demethylation and N-oxidation of some alicyclic amines by RuO4 75
Kidney CLC-K chloride channels inhibitors: structure-based studies and efficacy in hypertension and associated CLC-K polymorphisms. 75
Attività biologica sui canali KATP del muscolo scheletrico nativo di nuovi e potenti derivati delle 2H-1,4-Benzossazine 74
Analisi Farmaceutica 72
Elucidation of the enantioselective recognition mechanism of a penicillin G acylase-based chiral stationary phase towards a series of 2-aryloxy-2-arylacetic acids 71
KIDNEY CLC-K CHLORIDE CHANNELS SHOW DIFFERENTIAL PHARMACOLOGICAL PROFILES DEPENDING ON THE HETEROLOGOUS EXPRESSION SYSTEM 70
Design, synthesis and biological evaluation of a class of bioisosteric oximes of the novel dual peroxisome proliferator-activated receptor alpha/gamma ligand LT175 69
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 68
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Molecular switch for CLC-K Cl– channel block/activation: Optimal pharmacophoric requirements towards high-affinity ligands 66
Sintesi di una nuova serie di acidi 2-benzofuran-carbossilici a potenziale attività bloccante dei canali al cloro voltaggio-dipendenti CLC-K 64
Allyphenyline Analogues Potentially Useful in the Management of Chronic Pain and Opioid Addiction 63
Agonisti dei Recettori Nucleari PPARs come Potenziali Nuovi Agenti Terapeutici per il Trattamento della Sindrome Metabolica 63
Growth hormone secretagogues exert differential effects on skeletal muscle calcium homeostasis in male rats depending on the peptidyl/non-peptidyl structure 63
Studio delle proprietà enentioselettive di una fase stazionaria chirale a base di PGA 61
BIOLOGICAL ACTIVITY OF NEW POTENT 2H-1,4-BENZOXAZINE DERIVATIVES ON THE NATIVE SKELETAL MUSCLE KATP CHANNEL 60
Ossidazione di ammine policicliche terziarie con RuO4 59
Calcium activated K+ channel as a target of prompt-to-use drugs in neuromuscular disorders 59
Block of renal CLC-K channels by phenoxy-alkyl derivatives of clofibric acid 59
Molecular determinants for nuclear receptors selectivity: chemometric analysis, dockings and site-directed mutagenesis of dual peroxisome proliferator-activated receptors alpha/gamma agonists 59
AGONISTI DEI RECETTORI NUCLEARI PPARs COME POTENZIALI NUOVI AGENTI TERAPEUTICI PER IL TRATTAMENTO DELLA SINDROME METABOLICA. 59
INNOVATIVE METHODOLOGIES IN NANOTECHNOLOGY FOR THE PREVENTION OF BACTERIAL DISEASES 57
(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 57
Selective oxidation of nitrogen organic compounds 56
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 56
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Chemical studies on Drug Metabolism: Oxidation with ruthenium tetroxide of some medicinal alicyclic N-metylamines 55
Dimeric analogs of the dual PPARα/γ agonist LT-175: design, synthesis and biological evaluation. 54
Tissue specific action of the 2-(propyl)-1,4-benzoxazine on pancreatic beta cell ATP-sensitive potassium channels 52
Structural nucleotide analogs are potent activators/inhibitors of pancreatic beta-cell KATP channels: an emerging mechanism supporting their use as anti-diabetic drugs. 52
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 49
Synthesis, biological evaluation and molecular investigation of fluorinated peroxisome proliferator-activated receptors alpha/gamma dual agonists 48
Oxidation of tertiary polycyclic amines by RuO4 46
MOLECULAR SPATIAL GEOMETRY OF CLC-K LIGANDS: OPTIMAL REQUIREMENTS TOWARDS HIGH AFFINITY CHANNEL BLOCK. 45
Selective oxidation of Nitrogen organic compounds by Ruthenium tetroxide 43
DESIGN, SYNTHESIS AND BIOLOGICAL EVALUATION OF NEW ANALOGS OF THE DUAL PPARα/γ AGONIST LT175. 42
Enantioselective properties of Penicillin G Acylase: Liquid Crhomatographic studies end docking simulations 42
Progettazione e sintesi di nuovi agenti antimicrobici e studio dell'attività biologica in associazione con differenti olii essenziali 40
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Dal brodo primordiale alla farmacogenomica 38
H-1-NMR determination of the enantiomeric excess of the antiarrhythmic drug Mexiletine by using mandelic acid analogues as chiral solvating agents 38
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Design, synthesis and biological evaluation of a dimeric analog of the dual PPARα/γ agonist 2-(4-phenyl-phenoxy)-3-phenyl-propanoic acid. 36
EFFETTI DERIVANTI DALL'INTRODUZIONE DI SOSTITUENTI SUL NUCLEO DIFENILICO DEL COMPOSTO LT175, AGONISTA DUALE DEI RECETTORI NUCLEARI PPARalfa E PPARgamma 36
Effects on skeletal muscle chloride channel conductance of a-aryloxyalkyl-4-chlorophenoxyacetic acids 34
Traduzione Capitoli 1-9 33
Determinanti Molecolari della Selettività di Recettori Nucleari: Analisi Chemiometrica e Docking di Agonisti Selettivi di Recettori PPARs 33
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NEW CHIRAL CLOFIBRIC ACID ANALOGS AS LIGANDS OF PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR (PPAR) alpha AND gamma 27
Evaluation of biophysical and pharmacological properties of chloride channels belonging to ClC family by the use of chiral clofibric acid derivatives 26
Novel dual PPARalpha/gamma Agonists, as hypoglycemic and antidiabetic agents 26
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Molecular spatial geometry of CLC-K ligands: optimal requirements towards high affinity channel block 25
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 25
Synthesis and biological screening of new chiral a-aryloxy-alkanoic acids as PPARs agonists 25
Molecular spatial geometry of CLC-K ligands: optimal requirements towards high affinity channel block 24
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Dimeric analogs of the dual PPARα/γ agonist LT-175: design, synthesis and biological evaluation 23
Synthesis and biological screening of new chiral 2-(4-chloro-phenoxy)-3-phenylpropanoic acid analogs as potential PPAR alpha/gamma dual agonists 23
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NEW CHIRAL DERIVATIVES OF 2-(4-PHENYL-PHENOXY)-3-PHENYLPROPANOIC ACID WITH PPARalpha/gamma DUAL ACTIVITY. 22
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EVALUATION OF BIOPHYSICAL AND PHARMACOLOGICAL PROPERTIES OF CHLORIDE CHANNELS BELONGING TO CLC FAMILY BY THE USE OF CHIRAL CLOFIBRIC ACID DERIVATIVES. 21
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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 21
PROGETTAZIONE, SINTESI E VALUTAZIONE BIOLOGICA DI DERIVATI OSSIMMINICI AD ATTIVITA’ AGONISTA DUALE PPARα/γ. 21
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Synthesis and biological evaluation of new fluorinated analogues with PPARα and PPARγ agonist activity 20
Design, synthesis and biological evaluation of a dimeric analog of the dual PPARα/γ agonist 2-(4-phenyl-phenoxy)-3-phenyl-propanoic acid 20
MOLECULAR DETERMINANTS FOR NUCLEAR RECEPTORS SELECTIVITY: CHEMIOMETRIC ANALYSIS AND DOCKING OF DUAL PPAR AGONISTS. 20
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Totale 5.537
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Categoria #
all - tutte 24.051
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 24.051
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020209 0 0 0 0 0 0 0 0 0 52 127 30
2020/2021779 138 27 59 40 80 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
2024/2025635 52 32 124 54 33 82 79 107 61 11 0 0
Totale 5.662