IRIS - Res&Arch Institutional Research Information System - Research & Archive

CECCHETTI, Violetta
 Distribuzione geografica
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Continente #
NA - Nord America 4.964
EU - Europa 4.217
AS - Asia 1.586
AF - Africa 17
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 7
SA - Sud America 6
Totale 10.806
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Nazione #
US - Stati Uniti d'America 4.958
UA - Ucraina 882
IE - Irlanda 865
IT - Italia 773
SE - Svezia 638
VN - Vietnam 491
HK - Hong Kong 415
SG - Singapore 291
DE - Germania 241
CN - Cina 228
FI - Finlandia 194
RU - Federazione Russa 186
BE - Belgio 105
GB - Regno Unito 98
FR - Francia 60
TR - Turchia 45
RO - Romania 44
JP - Giappone 38
CH - Svizzera 33
KR - Corea 27
NL - Olanda 24
PL - Polonia 24
UZ - Uzbekistan 20
CZ - Repubblica Ceca 17
AT - Austria 15
CI - Costa d'Avorio 11
LB - Libano 9
AU - Australia 8
EU - Europa 7
GR - Grecia 7
IN - India 7
CA - Canada 5
EG - Egitto 5
IR - Iran 5
DK - Danimarca 4
BG - Bulgaria 3
BR - Brasile 3
CL - Cile 3
MY - Malesia 3
PK - Pakistan 2
AZ - Azerbaigian 1
ES - Italia 1
HU - Ungheria 1
ID - Indonesia 1
IQ - Iraq 1
KZ - Kazakistan 1
MX - Messico 1
NZ - Nuova Zelanda 1
PT - Portogallo 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
ZA - Sudafrica 1
Totale 10.806
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Città #
Chandler 1.091
Dublin 865
Dong Ket 487
Jacksonville 480
San Mateo 460
Hong Kong 403
Boardman 307
Perugia 280
Medford 205
Princeton 203
Singapore 202
Ann Arbor 167
Wilmington 159
Altamura 146
Andover 128
Lawrence 123
Brussels 105
Beijing 92
Fremont 75
Des Moines 65
Saint Petersburg 57
West Jordan 48
Ashburn 44
Izmir 43
Redmond 43
Norwalk 39
Dearborn 36
Woodbridge 35
Tokyo 33
Falls Church 27
Los Angeles 27
Bucharest 25
Spoleto 25
Seoul 24
San Giustino 23
Helsinki 22
San Paolo di Civitate 22
Redwood City 21
Dallas 19
Moscow 18
New York 18
San Diego 17
Den Haag 16
Rome 16
Auburn Hills 14
Shanghai 14
Hanover 13
Philadelphia 12
Abidjan 11
Timisoara 11
Houston 9
Santa Clara 9
Olomouc 8
Lausanne 7
Melbourne 7
Nanjing 7
Radomsko 7
Bologna 6
Frankfurt Am Main 6
Kunming 6
Mcallen 6
Munich 6
Napoli 6
San Jose 6
Seattle 6
Brno 5
Milan 5
Terni 5
Anguillara Sabazia 4
Arak 4
Cambridge 4
Fairfield 4
Hanoi 4
Ottawa 4
Simi Valley 4
Urbino 4
Wuhan 4
Xian 4
Zhengzhou 4
Alameda 3
Cerro Maggiore 3
Chengdu 3
Chicago 3
Edinburgh 3
Ferrara 3
Florence 3
Lanciano 3
Mit Ghamr 3
Nichelino 3
Serra 3
Shaoyang 3
Siena 3
Silver Spring 3
Tappahannock 3
Umbertide 3
Valmadrera 3
Albinea 2
Bastia 2
Berlin 2
Cairo 2
Totale 7.036
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Nome #
1,4-Benzothiazine-2-carboxylic Acids 1-Oxide as Analogue of Antibacterial Quinolones 241
1,4-Benzothiazine ATP-Sensitive Potassium Channel Openers: Modifications at the C-2 and C-6 Positions 225
(1,4-Benzothiazinyloxy)alkylpiperazine Derivatives as Potential Antihypertensive Agents 220
1,2,4-triazolo[1,5-α]pyrimidines as a novel class of inhibitors of the HIV-1 reverse transcriptase-αssociated ribonuclease h activity 191
Derivati benzotiazinici come inibitori della pompa estrudente MDR NorA dello Staphylococcus aureus 117
Engagement of Nuclear Coactivator 7 by 3-Hydroxyanthranilic Acid Enhances Activation of Aryl Hydrocarbon Receptor in Immunoregulatory Dendritic Cells 114
Sintesi di nuovi inibitori della pompa di efflusso NorA dello S. aureus: dalle 3-fenil-1,4-benzotiazine alle 2-fenilchinossaline 111
Attivatori dei canali KATP a struttura 1,4-benzotiazinica. Modificazioni in N-4 103
1,2,4-Triazolo[1,5-a]pyrimidines: Efficient One-step Synthesis and Functionalization as Influenza Polymerase PA-PB1 Interaction Disruptors 100
6-Aminoquinolones, their Synthesis and their Use as Antibacterial Agents. 96
4H-1,4-Benzothiopyran-4-one-3-carboxylic Acids and 3,4-Dihydro-2H-isothiazolo[5,4-b][1]benzothiopyran-3,4-diones as Quinolone Antibacterial Analogs 95
Attivatori dei canali K-ATP a struttura 1,4-benzotiazinica: modificazioni in C-2 e C-6 93
SINTESI DI NUOVI INIBITORI DELLA POMPA DI EFFLUSSO NorA DELLO S. aureus: DALLE 3-FENIL-1,4-BENZOTIAZINE ALLE 2-FENILCHINOLINE 87
6-Aminoquinolones: a New Class of Quinolone Antibacterials? 87
Structure-activity relationship study on anti-HIV 6-desfluoroquinolones. 86
Syhtesis and Biological Evaluation of 2-Phenylquinolones Targeted at Tat/TAR Recognition 85
Chemometric Rationalization of the Structural and Physicochemical Basis for Selective Cyclooxygenase-2 Inhibition: Toward More Specific Ligands 83
Process for the Preparation of 9-Fluoro-10-(4-methyl-1-piperazinyl)-7-oxo-2,3-dihydro-7H-pyrido[1,2,3-de][1,4]benzothiazine-6-carboxylic Acid Hydrochloride 81
Functionalized 2,1-benzothiazine 2,2-dioxides as new inhibitors of Dengue NS5 RNA-dependent RNA polymerase 79
Targeting CDKs to inhibit the HIV-1 TAT-mediated transcription 76
2-Phenylquinoline S. aureus NorA Efflux Pump Inhibitors: Evaluation of the Importance of Methoxy Group Introduction 76
A Comprehensive Structural Overview of p38α MAPK in Complex with Type I Inhibitors 75
A 1,8-Naphthyridone Derivative Targets the HIV-1 Tat-Mediated Transcription and Potently Inhibits the HIV-1 Replication. 74
Chinoloni anti-HIV: studi volti all’identificazione del target molecolare 73
Studies on 6-Aminoquinolones: Synthesis and Antibacterial Evaluation of 6-Amino-8-ethyl- and 6-Amino-8-methoxyquinolones 73
Cell-dependent Interference with viral transactivation by 6-aminoquinolone derivatives. 72
Inhibition of Subgenomic Hepatitis C Virus RNA Replication by Acridone Derivatives: Identification of an NS3 Helicase Inhibitor. 72
Allosteric inhibition of the hepatitis C virus NS5B polymerase: in silico strategies for drug discovery and development 72
Disegno e Sintesi di Nuovi Inibitori Allosterici della NS5B Polimerasi dell'HCV 71
Chemometric Rationalization of the Structural Features Affecting the Antibacterial Activity of Quinolones Against Staphylococcus aureus 69
6-Desfluoroquinolones as promising HIV transcription inhibitors 69
The antibacterial activity of quinolones against E.coli: a chemometric study 69
Antitubercular polyhalogenated phenothiazines and phenoselenazine with reduced binding to CNS receptors 69
Accounting for target flexibility and water molecules by docking to ensembles of target structures: The HCV NS5B Palm Site I inhibitors case study. 69
Synthesis of 2-(Arylamino)ethanethiols via Lewis Acid catalyzed Aminolysis of 2,2-Dimethylthiirane as Precursors of the 1,4-Benzothiazine Nucleus 68
2-Phenylquinolones as Inhibitors of the HIV-1 Tat/TAR Interaction. 68
Discovery of potent p38α MAPK inhibitors through a funnel like workflow combining in silico screening and in vitro validation 68
Small Molecules as HIV-1 Tat-TAR Complex Inhibitors 67
7-(Disubstituted thiazolyl)-3,5-dihydroxy-6-heptenoic/heptanoic acid derivatives as HMG-COa reductase inhibitors 67
Synthesis and chromatographic enantioresolution of anti-HIVquinolone derivatives 67
From cycloheptathiophene-3-carboxamide to oxazinone-based derivatives as allosteric HIV-1 ribonuclease H inhibitors 67
Chemometric Methodologies in a Quantitative Structure-Activity Relationship Study: the Antibacterial Activity of 6-Aminoquinolones 66
QSAR study and VolSurf characterization of anti-HIV quinolone library 65
Studies on Anti-HIV Quinolones: New Insights on the C-6 Position 65
A Broad Anti-influenza Hybrid Small Molecule that Potently Disrupts the Polymerase Acidic Protein-Basic Protein 1 (PA-PB1) Subunits Interaction 64
The Pyrazolobenzothiazine Core as a New Chemotype of p38 Alpha Mitogen-Activated Protein Kinase Inhibitors 64
Pharmacophore-Based Repositioning of Approved Drugs as Novel Staphylococcus aureus NorA Efflux Pump Inhibitors 64
Synthesis and Antibacterial Evaluation of [1,3]Benzothiazino[3,2-a]quinoline and [3,1]Benzothiazino[1,2-a]quinoline-6-carboxylic Acid Derivatives 63
6-Aminoquinolones as New Potential Anti-HIV Agents 63
8-Methyl-7-substituted-1,6-naphthyridine-3-carboxylic Acids as New 6-Desfluoroquinolone Antibacterials 63
Structure-based insights into p38α MAPK: from crystal structures analysis to hit optimization 63
Advantageous Use of Ionic Liquids for the Synthesis of Pharmaceutically Relevant Quinolones 63
Deciphering the molecular recognition mechanism of multidrug resistance staphylococcus aureus nora efflux pump using a supervised molecular dynamics approach 63
Pyridobenzothiazolones Exert Potent Anti-Dengue Activity by Hampering Multiple Functions of NS5 Polymerase 63
In Vitro Activities of New Quinolones Against Helicobacter pylori 62
2-Phenylquinazolinone fragment imparts anti-CDKs and anti-HIV activities 62
New Insights on KCa3.1 Channel Modulation 62
A New Derivative with Ultra-Potent Anti-HIV Activity 61
A new 6-aminoquinolone compound with anti-HCMV activity 60
A New Promising Class of pyrazolobenzothiazine inhibitors of S. aureus NorA Efflux Pump 60
Bicyclic octahydrocyclohepta[b]pyrrol-4(1H)one derivatives as novel selective anti-hepatitis C virus agents 60
Studies on 2-phenylquinoline Staphylococcus aureus NorA efflux pump inhibitors: New insights on the C-6 position 60
Proceedings of the X National Biotechnology Congress. 59
Pyridobenzothiazole derivatives as new chemotype targeting the HCV NS5B polymerase 59
A Journey around the Medicinal Chemistry of Hepatitis C Virus Inhibitors Targeting NS4B: From Target to Preclinical Drug Candidates 59
S. aureus NorA efflux pump: the discovery of new potent inhibitors 58
Evolution from a natural flavones nucleus to obtain 2-(4-Propoxyphenyl)quinoline derivatives as potent inhibitors of the S. aureus NorA efflux pump. 58
One-Pot Synthesis of Rufloxacin 57
The 6-aminoquinolone WC5 inhibits human cytomegalovirus replication at an early stage by interfering with the transactivating activity of viral immediate-early 2 protein 57
Synthesis of Novel Inhibitors of the S. aureus Efflux pumps: from the 4-hydroxy-2-phenylquinolines to the 4-hydroxy-2-phenylquinazolines 57
p38 alpha MAPK and Type I Inhibitors: Binding Site Analysis and Use of Target Ensembles in Virtual Screening 57
Broad spectrum anti-flavivirus pyridobenzothiazolones leading to less infective virions 57
Structural Modifications of the Quinolin-4-yloxy Core to Obtain New Staphylococcus aureus NorA Inhibitors 57
Nuovi 6-DFQ come inibitori della Transattivazione dell’HIV-1 56
6-Aminoquinolones: photostability, cellular distribution and phototoxicity. 56
6-Desfluoroquinolones as HIV-1 Tat-mediated Transcription Inhibitors 56
Cinnamoyl compounds as small-molecules inhibitors of histone acetyltransferase enzymes 56
6-Hydrogen-8-Methylquinolones Active Against Replicating and Non-replicating Mycobacterium tuberculosis 56
Efficient and regioselective one-step synthesis of 7-aryl-5-methyl- and 5-aryl-7-methyl-2-amino-[1,2,4]triazolo[1,5-a] pyrimidine derivatives 56
Synthesis and Characterization of 1,2,4-Triazolo[1,5-a]pyrimidine-2-carboxamide-based Compounds Targeting the PA-PB1 Interface of Influenza A Virus Polymerase. 56
Quinolones as potential anti HIV-1 agents targeted at Tat/TAR recognition 55
Binding studies and GRIND/ALMOND-based 3D QSAR analysis of benzothiazine type K-ATP channel openers 55
Disegno e sintesi di agenti anti-HIV a duplice attività 55
N-Benzoyl-N-methylsulfonyl anthranilates: unexpected cyclization reaction to 4-alkoxy-2,1-benzothiazines 55
Computer-Aided Identification of Fragments as CDK9 Inhibitors with Anti-HIV-1 Tat-Mediated Transcription Activity 55
Searching for Novel Inhibitors of the S. aureus NorA Efflux Pump: Synthesis and Biological Evaluation of the 3-Phenyl-1,4-benzothiazine Analogues 55
Chemometric rationalization of the structural features affecting the antibacterial activity of quinolones 55
C-2 phenyl replacements to obtain potent quinoline-based Staphylococcus aureus NorA inhibitors 55
Symbiotic approach to drug design: N-[(4-chloro-3-sulfamoylbenzamido)-ethyl]propanolamine derivatives as β-adrenergic blocking agents with diuretic activity 54
RE-EVOLUTION OF THE 2-PHENYL-4-HYDROXYQUINOLINES: OPTIMIZATION OF A POTENT NEW CLASS OF S. AUREUS NorA EFFLUX PUMP INHIBITORS 54
Sali Quaternari di Aminoetil-p-aminobenzoati e Aminoetil-p-aminobenzamidi. Sintesi ed Attività Farmacologica 54
Pyrazolobenzothiazines as potent TNF-alpha production inhibitors. 54
Enantiomers of 8-(3-tert-Butylamino-2-hydroxypropoxy)-3,4-dihydro-3-oxo-2H-(1,4)benzothiazine: Racemic Resolution, Chiral Synthesis and Biological Activity. 54
New Heterocyclic Ring Systems. XIII.7,11-Dithiaazasteroid Analogues 53
Structure modifications of 6-aminoquinolones with potent anti-HIV activity 53
A 6-Aminoquinolone Compound, WC5, with Potent and Selective Anti-Human Cytomegalovirus Activity. 53
Chemometric Studies on the Bactericidal Activity of Quinolones via an Extended VolSurf Approach 53
A New 6-Aminoquinolone compound, WC5, with Specific Anti-HCMV Activity 51
Sintesi del 2,2-dimetil-2,3-diidro-4H-1,4-benzotiazine via 2,2-dimetiltiirano catalizzata da acidi di Lewis. 51
Synthesis and Evaluation of Benzothiazine Derivatives as Inhibitors of NorA Efflux Pump of Staphylococcus aureus 50
Totale 7.262
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Categoria #
all - tutte 45.230
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 45.230
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020899 0 0 146 5 132 48 177 19 158 121 16 77
2020/20212.280 17 151 65 162 539 152 209 14 233 68 147 523
2021/20222.004 58 337 42 129 145 17 48 570 88 58 241 271
2022/20233.237 227 527 49 304 282 338 3 164 1.156 24 119 44
2023/20241.396 83 192 68 32 24 39 292 34 171 93 169 199
2024/2025414 51 287 76 0 0 0 0 0 0 0 0 0
Totale 11.342