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

IRACI, NUNZIO
 Distribuzione geografica
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Continente #
NA - Nord America 1.701
EU - Europa 1.483
AS - Asia 499
Continente sconosciuto - Info sul continente non disponibili 4
AF - Africa 3
SA - Sud America 2
OC - Oceania 1
Totale 3.693
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Nazione #
US - Stati Uniti d'America 1.691
UA - Ucraina 356
IE - Irlanda 289
SE - Svezia 226
VN - Vietnam 211
IT - Italia 201
HK - Hong Kong 136
CN - Cina 94
DE - Germania 90
FI - Finlandia 86
GB - Regno Unito 83
RU - Federazione Russa 68
TR - Turchia 42
BE - Belgio 33
FR - Francia 11
CH - Svizzera 10
AT - Austria 9
CA - Canada 9
NL - Olanda 8
UZ - Uzbekistan 7
RO - Romania 5
EU - Europa 4
IN - India 4
BG - Bulgaria 2
BR - Brasile 2
CI - Costa d'Avorio 2
KR - Corea 2
BZ - Belize 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
GR - Grecia 1
HU - Ungheria 1
JP - Giappone 1
LB - Libano 1
NZ - Nuova Zelanda 1
PL - Polonia 1
SG - Singapore 1
SK - Slovacchia (Repubblica Slovacca) 1
ZA - Sudafrica 1
Totale 3.693
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Città #
Chandler 349
Dublin 288
Dong Ket 211
Jacksonville 190
San Mateo 180
Hong Kong 130
Perugia 103
Medford 77
Princeton 76
Andover 65
Fremont 64
Wilmington 54
Dearborn 52
Ann Arbor 48
Beijing 44
Izmir 40
Ashburn 37
Altamura 35
Brussels 32
Lawrence 30
Norwalk 23
Saint Petersburg 23
West Jordan 20
Des Moines 15
San Giustino 13
Boardman 11
Helsinki 10
Redmond 10
Falls Church 9
Nanjing 9
Moscow 8
Auburn Hills 7
Philadelphia 7
Simi Valley 7
Redwood City 6
San Diego 6
Toronto 6
Den Haag 5
Hefei 5
Lappeenranta 5
San Paolo di Civitate 5
Spoleto 5
Woodbridge 5
Zhengzhou 5
Houston 4
Los Angeles 4
Mcallen 4
New York 4
Rome 4
Chengdu 3
Hebei 3
Kunming 3
Nanchang 3
Ottawa 3
Shanghai 3
Abidjan 2
Alameda 2
Camerino 2
Fairfield 2
Frankfurt Am Main 2
Guangdong 2
Guangzhou 2
Jinan 2
Laredo 2
Nürnberg 2
San Jose 2
Seoul 2
Sovicille 2
Timisoara 2
Wuhan 2
Xian 2
Atlanta 1
Baotou 1
Belize City 1
Bratislava 1
Budapest 1
Buffalo 1
Chicago 1
Dunedin 1
Edinburgh 1
Fuzhou 1
Gettysburg 1
Harbin 1
Huizingen 1
Kiev 1
Kocaeli 1
Las Vegas 1
Limbiate 1
London 1
Ludwigshafen 1
Mazzano Romano 1
Milan 1
Modena 1
Monmouth Junction 1
Muizenberg 1
Nanning 1
Napoli 1
Odesa 1
Pitesti 1
Reggio Nell'emilia 1
Totale 2.429
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Nome #
1,3-DIIDRO-BENZIMIDAZOLONI ANALOGHI: PROGETTAZIONE, SINTESI E SAR DI NUOVI INIBITORI NON-NUCLEOSIDICI DELL’RT 225
1,3-Diidro-benzimidazoloni analoghi: progettazione, sintesi e SAR di nuovi inibitori non-nucleosidici dell'RT 223
beta-CYCLODEXTRIN HINDERS PLGA PLASTICIZATION DURING MICROPARTICLE MANUFACTURING 124
Prion protein ligands as therapeutic agents for neurodegenerative disorders 101
Targeting CDKs to inhibit the HIV-1 TAT-mediated transcription 74
A Comprehensive Structural Overview of p38α MAPK in Complex with Type I Inhibitors 69
Allosteric inhibition of the hepatitis C virus NS5B polymerase: in silico strategies for drug discovery and development 68
Structure-Based Pharmacophore Identification of New Chemical Scaffolds as Non–Nucleoside reverse Transcriptase Inhibitors 65
From 3D-pharmacophore models to synthetic route towards anti-HIV agents 65
Accounting for target flexibility and water molecules by docking to ensembles of target structures: The HCV NS5B Palm Site I inhibitors case study. 65
Pharmacophore Identification of New Chemical Scaffolds as Non-Nucleoside Reverse Transcriptase Inhibitors. 64
Design and Synthesis of DiselenoBisBenzamides (DISeBAs) as Nucleocapsid Protein 7 (NCp7) Inhibitors with anti-HIV Activity 64
A New 3D Pharmacophore Model for HIV-1 Integrase Strand Transfer Inhibitors 63
3D pharmacophore model and the synthesis of NMDA receptor subunit NR2B antagonists 61
Nuovi antagonisti non-competitivi del recettore NMDA/NR2B:design and sintesi 61
Pharmacophore-Based Repositioning of Approved Drugs as Novel Staphylococcus aureus NorA Efflux Pump Inhibitors 61
A refined pharmacophore model and optimization of 1H-benzylindole HIV-1 integrase inhibitors 59
Structure-based insights into p38α MAPK: from crystal structures analysis to hit optimization 59
Improvement of water solubility of non-competitive AMPA receptor antagonists by complexation with beta-cyclodextrin. 58
Pyridobenzothiazole derivatives as new chemotype targeting the HCV NS5B polymerase 58
Design, synthesis and structure-activity relationships of 1,3-dihydrobenzimidazol-2-one analogues as anti-HIV agents 55
A structure-based approach to ligand discovery for inhibition of HIV-1 IN-LEDGF/p75 interaction: a new target for anti-AIDS therapy 53
2-Phenylquinazolinone fragment imparts anti-CDKs and anti-HIV activities 53
p38 alpha MAPK and Type I Inhibitors: Binding Site Analysis and Use of Target Ensembles in Virtual Screening 53
Exploration of the binding mode of HIV-1 integrase strand transfer inhibitors through different computational approaches. 52
Design and synthesis of NR2B Subtype-Selective Antagonist 52
RE-EVOLUTION OF THE 2-PHENYL-4-HYDROXYQUINOLINES: OPTIMIZATION OF A POTENT NEW CLASS OF S. AUREUS NorA EFFLUX PUMP INHIBITORS 51
Binding Mode Prediction of Strand Transfer HIV-1 Integrase Inhibitors Using Tn5 Transposase as a Plausible Surrogate Model for HIV-1 Integrase 50
Diselenides and benzisoselenazolones as antiproliferative agents and glutathione-S-transferase inhibitors 50
Computational Strategies for Discovering novel HIV-1 RT Inhibitors 49
A highly intensified ART regimen induces long-term viral suppression and restriction of the viral reservoir in a simian AIDS model. 49
Computer-Aided Identification of Fragments as CDK9 Inhibitors with Anti-HIV-1 Tat-Mediated Transcription Activity 49
Novel targets for HIV therapy: small molecules blocking IN-LEDGF/p75 interaction 47
New Pyrazolobenzothiazine Derivatives As Hepatitis C Virus NS5B Polymerase Palm Site I Inhibitors 47
DECODING THE FUNCTION OF THE N-TERMINAL TAIL OF THE CELLULAR PRION PROTEIN TO INSPIRE NOVEL THERAPEUTIC AVENUES FOR NEURODEGENERATIVE DISEASES 46
Computer-Aided Design, Synthesis and Validation of 2-Phenylquinazolinone Fragments as CDK9 Inhibitors with Anti-HIV-1 Tat-Mediated Transcription Activity 45
Sviluppo di modello farmacoforico predittivo per gli NR2B antagonisti del recettore NMDA 44
Designed Multiple Ligands (DLMs) as innovative anti-HIV agents 44
Re-evolution of the 2-phenylquinolines: Ligand-Based Design, Synthesis, and Biological Evaluation of a Potent New Class of Staphylococcus aureus NorA Efflux Pump Inhibitors to Combat Antimicrobial Resistance 44
MOLECULAR MODELING STUDIES AND SYNTHESIS FOR THE DISCOVERY OF HIV-1 IN-LEDGF/P75 INTERACTION INHIBITORS 43
Tn5 Transposase as a useful platform to simulate HIV-1 Integrase inhibitor binding mode 43
Structure-Based Discovery of Pyrazolobenzothiazine Derivatives As Inhibitors of Hepatitis C Virus Replication 43
Nuovo modello farmacoforico per inibitori dell’Integrasi dell’HIV-1: ottimizzazione della potenza di composti a struttura 1H-benzilindolica 42
HIV-1-IN Strand-Transfer Inhibitors: phenyl ring exploration and synthesis of 1H-benzylindole derivative through fluorine substitutions 42
Molecular Modeling Studies: Discovery of Novel Potent Non-Nucleoside RT Inhibitors 41
Exploiting the anti-HIV 6-desfluoroquinolones to design multiple ligands 40
Synthesis and SAR of new 1,3-dihydro-benzimidazolone analogues as non-nucleoside reverse transcriptase inhibitors (NNRTIs) 39
Identificazione di Nuovi Inibitori Non-Nucleosidici della Trascrittasi Inversa dell’ HIV-1 Mediante Tecniche di Virtual screening. 39
New chemotypes to fight HCV infection: discovery of selective inhibitors of HCV replication with pyrazolobenzothiazine scaffold 39
Pyrazolo[4,3-c][1,2]benzothiazines 5,5-Dioxide: A Promising New Class of Staphylococcus aureus NorA Efflux Pump Inhibitors 38
Docking studies on a new HIV integrase–Mg-DNA complex: phenyl ring exploration and synthesis of 1H-benzylindole derivatives through fluorine substitutions 38
Induced-fit docking approach provides insight into the binding mode and mechanism of action of HIV-1 integrase inhibitors. ChemMedChem 37
Discovery of novel benzimidazolones as potent non-nucleoside reverse transcriptase inhibitors active against wild-type and mutant HIV-1 strains 37
Studi Computazionali per l’Identificazione di Nuovi Inibitori Non-Nucleosidici della Trascrittasi Inversa dell’HIV- 36
Design, Synthesis and SAR of New Potent HIV-1 RT Inhibitors”. Antiviral Research 35
Structural optimization of the 2-Phenyl-4-hydroxyquinoline Class of S. aureus NorA Efflux Pump Inhibitors 35
Structure-Based Pharmacophore Identification of New Chemical Scaffolds as Non-Nucleoside Reverse Transcriptase Inhibitors. 34
Targeting the HIV Tat-mediated transcriptional machinery: P-TEFb complex inhibitors 34
The versatile nature of the 6-aminoquinolone scaffold: identification of submicromolar hepatitis C virus NS5B inhibitors 34
Novel N1-substituted 1,3-dihydro-2H-benzimidazol-2-ones as potent non-nucleoside reverse transcriptase inhibitors. 34
Nuovi chemotipi di inibitori dell'HCV NS5B polimerasi 33
INTEGRASE STRAND TRANSFER INHIBITORS (INSTIs): SYNTHESIS AND ANTIVIRAL EFFETCS OF CHLORO-FLUORO SUBSTITUTIONS 32
Novel 1,3-dihydro-benzimidazol-2-ones and their analogues as potent non-nucleoside HIV-1 reverse transcriptase inhibitors. 31
Progettazione, sintesi e SAR di analoghi 1,3-diidro-benzimidazoloni come nuovi agenti anti-HIV 30
Pharmacophore Modeling, Docking Experiments And Discovery Of New HIV-1 NNRTIs. 30
Response of a simian immunodeficiency virus (SIVmac251) to raltegravir: a basis for a new treatment for simian AIDS and an animal model for studying lentiviral persistence during antiretroviral therapy. 30
A refined pharmacophore model for HIV-1 integrase inhibitors: Optimization of potency in the 1H-benzylindole series. 30
Rational design, synthesis and SAR of 1,3-dihydro- benzimidazolone analogues as new anti-HIV agents 29
Design, synthesis, and structure-activity relationships of 1,3-dihydrobenzimidazol-2-one analogues as anti-HIV agents. 28
Pharmacological agents targeting the cellular prion protein 28
NCp7: targeting a multitasking protein for next-generation anti-HIV drug development part 1: covalent inhibitors 26
Pharmacophore-based discovery of small-molecule inhibitors of protein-protein interactions between HIV-1 integrase and cellular cofactor LEDGF/p75. 26
TARGETING CDKs TO INHIBIT THE HIV-1 TAT-MEDIATED TRANSCRIPTION 24
NCp7: Targeting a multitask protein for next-generation anti-HIV drug development part 2. Noncovalent inhibitors and nucleic acid binders 24
Identification of Anti-Influenza A Compounds Inhibiting the Viral Non-Structural Protein 1 (NS1) Using a Type I Interferon-Driven Screening Strategy 22
From Small to Powerful: The Fragments Universe and its "Chem-Appeal" 21
L-arginine improves solubility and anti sars-cov-2 mpro activity of rutin but not the antiviral activity in cells 11
Totale 3.878
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Categoria #
all - tutte 12.749
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 12.749
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019101 0 0 0 0 0 0 0 0 0 0 91 10
2019/2020462 3 7 59 3 59 51 119 15 71 27 7 41
2020/2021882 10 57 25 49 201 77 59 5 94 26 56 223
2021/2022708 16 135 12 37 47 7 5 231 27 15 88 88
2022/2023989 82 141 15 91 82 109 0 56 356 2 33 22
2023/2024348 36 62 23 11 5 8 73 35 63 29 3 0
Totale 3.878