IRIS
SPALLAROSSA, ANDREA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 12.774
NA - Nord America 2.379
AS - Asia 1.819
Continente sconosciuto - Info sul continente non disponibili 348
SA - Sud America 159
AF - Africa 27
OC - Oceania 3
Totale 17.509
Salva come PNG Salva come JPEG
Nazione #
IT - Italia 12.508
US - Stati Uniti d'America 2.265
SG - Singapore 764
CN - Cina 462
VN - Vietnam 255
BR - Brasile 104
BD - Bangladesh 97
FR - Francia 82
HK - Hong Kong 78
CA - Canada 50
JP - Giappone 49
FI - Finlandia 46
DE - Germania 45
AR - Argentina 26
GB - Regno Unito 21
MX - Messico 21
NL - Olanda 19
TW - Taiwan 16
ID - Indonesia 13
IN - India 11
IQ - Iraq 11
CO - Colombia 10
ZA - Sudafrica 10
RU - Federazione Russa 9
GT - Guatemala 8
MY - Malesia 8
EC - Ecuador 7
ES - Italia 7
JM - Giamaica 7
PH - Filippine 7
PK - Pakistan 7
TR - Turchia 7
CR - Costa Rica 5
PL - Polonia 5
SA - Arabia Saudita 5
TT - Trinidad e Tobago 5
CL - Cile 4
DZ - Algeria 4
HN - Honduras 4
KR - Corea 4
LT - Lituania 4
PR - Porto Rico 4
UA - Ucraina 4
UZ - Uzbekistan 4
VE - Venezuela 4
JO - Giordania 3
KE - Kenya 3
OM - Oman 3
TH - Thailandia 3
AL - Albania 2
AT - Austria 2
AW - Aruba 2
BY - Bielorussia 2
DK - Danimarca 2
EG - Egitto 2
IE - Irlanda 2
KG - Kirghizistan 2
KH - Cambogia 2
LB - Libano 2
MA - Marocco 2
NI - Nicaragua 2
PY - Paraguay 2
SE - Svezia 2
AG - Antigua e Barbuda 1
AU - Australia 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BE - Belgio 1
BN - Brunei Darussalam 1
BS - Bahamas 1
CG - Congo 1
CH - Svizzera 1
CI - Costa d'Avorio 1
CZ - Repubblica Ceca 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
GA - Gabon 1
GR - Grecia 1
GY - Guiana 1
HR - Croazia 1
HU - Ungheria 1
MD - Moldavia 1
MK - Macedonia 1
MM - Myanmar 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PE - Perù 1
QA - Qatar 1
RO - Romania 1
RS - Serbia 1
SI - Slovenia 1
SN - Senegal 1
SV - El Salvador 1
SX - ???statistics.table.value.countryCode.SX??? 1
SY - Repubblica araba siriana 1
TN - Tunisia 1
VI - Stati Uniti Isole Vergini 1
WS - Samoa 1
Totale 17.162
Salva come PNG Salva come JPEG
Città #
Genova 6.163
Genoa 3.558
Rapallo 1.041
Vado Ligure 879
Bordighera 637
San Jose 476
Singapore 422
Ashburn 210
New York 102
Ho Chi Minh City 85
Beijing 74
Lauterbourg 69
Hanoi 58
Hong Kong 57
Council Bluffs 56
Santa Clara 53
Los Angeles 52
Tokyo 47
Helsinki 42
Milan 38
Phoenix 36
Dallas 34
Frankfurt am Main 34
Chicago 26
Atlanta 14
Denver 14
Rome 14
Brooklyn 13
Buffalo 13
Haiphong 13
Montreal 13
Houston 12
Amsterdam 11
Da Nang 11
Mexico City 11
Miami 11
Newark 11
Boardman 10
Naples 10
Palermo 10
San Antonio 10
Tianjin 10
Seattle 9
St Louis 9
São Paulo 9
Charlotte 8
Davenport 8
Jacksonville 8
San Francisco 8
Taipei 8
Toronto 8
Carrollton 7
Columbus 7
North Bergen 7
Washington 7
Bologna 6
Las Vegas 6
Orem 6
Philadelphia 6
Ribeirão Preto 6
Turin 6
Virginia Beach 6
Alexandria 5
Anchorage 5
Baghdad 5
Basingstoke 5
Birmingham 5
Guangzhou 5
Guatemala City 5
Hải Dương 5
Medellín 5
Milwaukee 5
Padua 5
Phillipsburg 5
Piscataway 5
Queens 5
San Diego 5
Baltimore 4
Cardiff 4
Carmichael 4
Cincinnati 4
City of London 4
Columbia 4
Des Moines 4
Guayaquil 4
Iowa City 4
Istanbul 4
Jackson 4
Johannesburg 4
Karachi 4
Kingston 4
Kissimmee 4
Kwai Chung 4
Lappeenranta 4
Paris 4
Petaling Jaya 4
Pierre 4
Pittsburgh 4
Portland 4
Pozzilli 4
Totale 14.772
Salva come PNG Salva come JPEG
Nome #
Valorization and Potential Antimicrobial Use of Olive Mill Wastewater (OMW) from Italian Olive Oil Production 620
Synthesis, SAR and molecular modelling studies of acylthiocarbamates and their parent thiocarbamates as potent non-nucleoside reverse transcriptase inhibitors related to PETT derivatives 338
Structural studies on prokaryotic sulfurtransferases 321
Studi Cristallografici di Complessi tra Transcrittasi Inversa di HIV-1 e Derivati Tiocarbammici a Scheletro Ftalimmidico, Inibitori Non Nucleosidici Correlati ai Derivati PETT. 305
A Successful Application of Parallel Synthesis to Computer-Assisted Structural Optimization of New Leads Targeting Human Immunodeficiency Virus-1 Reverse Transcriptase. The Case of Acylthiocarbamates and Thiocarbamates 199
A persulfurated cysteine promotes active site reactivity in Azotobacter vinelandii Rhodanese 193
Further SAR studies on bicyclic basic merbarone analogues as potent antiproliferative agents 182
"One-pot" synthesis of N-acyl-N-phenylcarbamate derivatives endowed with anti-HIV and/or antiproliferative activities 181
Characterization data of water-soluble hydrophilic and amphiphilic dendrimers prodrugs for delivering bioactive chemical entities otherwise non soluble. 179
Crystal structure of the extracellular domain of the human natural killer cell activating receptor NKp44 178
Iterative design and optimization of initially inactive Proteolysis Targeting Chimeras (PROTACs) identify VZ185 as a potent, fast and selective von Hippel-Lindau (VHL)-based dual degrader probe of BRD9 and BRD7 178
6-amino-4-oxo-1,3-diphenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonyl derivatives as a new class of potent inhibitors of Interleukin-8-induced neutrophil chemotaxis 174
5-Substituted derivatives of 6-amino-1,3-diphenyl-2-thioxo-2,3-dihydropyrimidin-4(1H)-one as a new class of potent inhibitors of interleukin 8-induced neutrophil chemotaxis 171
Amino-Pyrazoles in Medicinal Chemistry: A Review 168
Computational approaches for the design and chemical synthesis of novel F508del correctors in the treatment of cystic fibrosis 160
Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 1: parallel synthesis, molecular modelling and structure-activity relationship studies on O-[2-(hetero)arylethyl]-N-phenylthiocarbamates 157
Non-PAMAM amino acids-modified dendrimers nanoparticles for enhancing water-solubility of insoluble bioactive molecules: our state of the art 156
Unprecedented one-pot synthesis of pharmaceutical interest derivatives via in situ condensation of heterocyclic iminium salts with nitrogen nucleophiles 155
The three-dimensional structure of NK cell receptor NKp44, a triggering partner in natural cytotoxicity 151
X-ray analysis of HIV-1 reverse transcriptase in complex with thiocarbamates: structure-based design and synthesis of new analogues 151
Novel Triazol-imidazo[1,2-b]pyrazoles Selectively Impair Melanoma Cell Survival While Preserving Healthy Keratinocyte Viability 151
Exploring the binding features of rimonabant analogues and acyclic CB1 antagonists: docking studies and QSAR analysis 150
Insights into the Pharmacological Activity of the Imidazo-Pyrazole Scaffold 149
Unprecedented one-pot stereoselective synthesis of Knoevenagel-type derivatives via in situ condensation of N-methyleniminium salts of ethylenethiourea and ethyleneurea with active methylene reagents 146
Characterization of water soluble dendrimer formulations of an insoluble thiocarbamate derivative with moderate anti HIV-1 activity: an overview 145
Structure-based Design, Parallel Synthesis, SAR and Molecular Modelling Studies of Thiocarbamates, New Potent Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitor Isosteres of Phenethylthiazolylthiourea Derivatives. 144
Anthrax toxin: structure-function relationships 143
Synthesis of indole imminun salts as key-intermediates in a convergent multi-step one-pot stereoselective synthesis of new potent antiproliferative Knoevenagel-type agent 142
A Proteomics Approach Identifies RREB1 as a Crucial Molecular Target of Imidazo–Pyrazole Treatment in SKMEL-28 Melanoma Cells 138
Btk inhibitors: a medicinal chemistry and drug delivery perspective 136
null 135
Regioselective Synthesis, Structural Characterization, and Antiproliferative Activity of Novel Tetra-Substituted Phenylaminopyrazole Derivatives 133
Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors: docking-based CoMFA and CoMSIA analyses 131
null 131
null 130
Design, synthesis, SAR, and molecular modeling studies of acylthiocarbamates: a novel series of potent non-nucleoside HIV-1 reverse transcriptase inhibitors structurally related to phenethylthiazolylthiourea derivatives 129
One-Pot Synthesis and Antiproliferative Activity of Highly Functionalized Pyrazole Derivatives 128
Synthesis and anti-HIV-1 activity of PETT structurally related O-substituted acyl (aryl) thiocarbamates 127
Human rhinovirus 3C protease: a cysteine protease showing the trypsin(ogen)-like fold 126
Cyclic diacyl thioureas enhance activity of corrector Lumacaftor on F508del‐CFTR 125
null 124
Capitolo 14 - Anticonvulsivanti 122
Modulazioni Strutturali in O-[2-(N-Ftalimmido)etil] Acil(Aril)Tiocarbammati, Inibitori Non-Nucleosidici della Transcrittasi Inversa di HIV-1 121
null 120
Crystallization and preliminary crystallographic characterization of the extracellular Ig-like domain of human natural killer cell activating receptor NKp44 120
Exploring the binding features of rimonabant analogues and acyclic CB1 antagonists: docking studies and 3D-QSAR analysis 119
Capitolo 19 - Agenti cardiovascolari 119
null 118
null 118
The phosphoryl transfer reaction. Model of the HPr~P~IIA-Ntr protein complex 117
null 117
null 117
null 116
null 116
null 116
Efetti della orto, meta, para sostituzione della porzione N-fenilica di O-(2-ftalimmido)etil-2-tienocarbammati sull'attività anti-HIV-1 115
One-pot Stereoselective Synthesis of Knoevenageltype Derivatives Via Condensation of N-Methyleniminium Salts of Ethylenethiourea and Ethyleneurea with Active Methylene Reagents. 115
null 113
Molecular docking of the Escherichia coli PTS system 112
Parallel synthesis of O-phenoxyethyl and O-adamantyl N-acyl thiocarbamates endowed with antiproliferative activity. 112
Modellazioni strutturali in O-[2-(N-ftalimmido)etil] Acil(Aril)tiocarbammati, inibitori non nucleosidici della trascrittasi inversa di HIV-1 111
Non-receptor tyrosine kinase Fes as a target in oncology 110
null 110
Capitolo 18 - Farmaci attivi sul sistema renale 109
null 109
Structure–Activity Relationship Studies on Highly Functionalized Pyrazole Hydrazones and Amides as Antiproliferative and Antioxidant Agents 108
Studies on the catalitic activity of Azotobacter vinelandii rhodanese 108
null 107
null 106
null 106
Microbiological Screening of 5-Functionalized Pyrazoles for the Future Development of Optimized Pyrazole-Based Delivery Systems 105
Investigations of Antioxidant and Anti-Cancer Activities of 5-Aminopyrazole Derivatives 105
Sintesi parallela one-pot di disolfuri dimeri di tiocarbammati, una nuova potente classe di inibitori non nucleosidici della transcrittasi inversa 105
Triazole-imidazo[1,2-b]pyrazoles Able to Counteract Melanoma Cell Survival Without Compromising the Viability of Healthy Keratinocytes 104
Pharmacophore and pharmacokinetic filtering tools guiding for the design and synthesis of novel thiazole-containing and VX-809 hybrid derivatives as F508del correctors. 104
Potent and Broad-Spectrum Bactericidal Activity of a Nanotechnologically Manipulated Novel Pyrazole 104
null 103
Synthesis and anti-HIV-1 activity of thiocarbamates, isosteres of PETT derivatives 102
null 102
null 101
Synthesis and SAR studies of novel merbarone analogues 101
Bicyclic basic merbarone analogues as antiproliferative agents 100
Mono- and di-acylated imidazolidine-2-thione derivatives: synthesis, cytotoxicity evaluation and computational studies 99
Reattivita' di accettori di Michael atipici con nucleofili azotati 99
Computational studies of the binding mode and 3D-QSAR analyses of symmetric formimidoester disulfides: a new class of non-nucleoside HIV-1 reverse transcriptase inhibitors 99
null 99
BRD9-targeting PROTACs: design, synthesis and biological evaluation 99
HIGHLY-FUNCTIONALIZED AMINO PYRAZOLES AS ANTIOXIDANT AGENTS: A PRELIMINARY SYNTHETIC ACCESSIBILITY STUDY 99
Modulazioni Strutturali del Sistema Ftalimmidico di N-Aril Tiocarbammati, Inibitori Non-Nucleosidici della Transcrittasi Inversa di HIV-1 98
Antioxidant properties of Knoevenagel-type indoles 96
Progettazione e Sintesi di Nuovi O-[2-(N-Ftalimmido)etil]-N-(4-Cloro- e 4-Metil-Fenil)-N-Aciltiocarbammati, Inibitori Non Nucleosidici della Trancrittasi Inversa del Virus HIV-1 Attivi a Concentrazioni Nanomolari 96
Synthesis and biological evaluation of new pyrazole carbohydrazides as antiproliferative and antioxidant agents. 96
null 96
Virtual screening and structure based drug design of new Fes/Fps kinase domain inhibitors. 95
null 95
New pyrazolyl thioureas active against the Staphylococcus genus 94
Sintesi di Esteri Tienopirimidinici ad Attività Antiproliferativa 94
PDE4D: A Multipurpose Pharmacological Target 93
Improved Antibacterial Properties of Pyrazole-Based Water-Soluble Dendrimer Nanoparticles 92
Escherichia coli GlpE is a prototype sulfurtransferase for the single-domain rhodanese homology superfamily 92
Totale 13.454
Salva come PNG Salva come JPEG
Categoria #
all - tutte 53.579
article - articoli 31.559
book - libri 0
conference - conferenze 19.649
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.371
Totale 107.158
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.074 0 0 79 118 35 71 78 317 55 97 76 148
2022/20231.258 120 93 10 144 195 208 13 101 227 5 132 10
2023/20241.434 45 130 24 112 61 82 44 672 43 24 89 108
2024/20252.116 72 177 98 226 269 163 165 264 128 111 210 233
2025/20264.948 429 154 588 391 672 296 688 272 411 503 250 294
2026/20271.474 914 207 353 0 0 0 0 0 0 0 0 0
Totale 17.509