IRIS
SPALLAROSSA, ANDREA
 Distribuzione geografica
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Continente #
EU - Europa 12.730
AS - Asia 1.717
NA - Nord America 785
SA - Sud America 119
AF - Africa 26
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 15.380
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Nazione #
IT - Italia 12.493
SG - Singapore 772
US - Stati Uniti d'America 745
CN - Cina 446
VN - Vietnam 262
BR - Brasile 81
HK - Hong Kong 80
FR - Francia 75
JP - Giappone 49
FI - Finlandia 47
DE - Germania 39
AR - Argentina 22
MX - Messico 21
GB - Regno Unito 18
TW - Taiwan 15
NL - Olanda 13
ID - Indonesia 11
BD - Bangladesh 10
IN - India 10
IQ - Iraq 10
ZA - Sudafrica 10
CA - Canada 9
RU - Federazione Russa 8
ES - Italia 6
KR - Corea 5
PK - Pakistan 5
SA - Arabia Saudita 5
TR - Turchia 5
CL - Cile 4
DZ - Algeria 4
LT - Lituania 4
MY - Malesia 4
PH - Filippine 4
UZ - Uzbekistan 4
CO - Colombia 3
CR - Costa Rica 3
JO - Giordania 3
OM - Oman 3
PL - Polonia 3
PY - Paraguay 3
TH - Thailandia 3
UA - Ucraina 3
VE - Venezuela 3
AL - Albania 2
AT - Austria 2
BY - Bielorussia 2
DO - Repubblica Dominicana 2
EC - Ecuador 2
EG - Egitto 2
IE - Irlanda 2
KE - Kenya 2
KG - Kirghizistan 2
KH - Cambogia 2
MA - Marocco 2
PR - Porto Rico 2
SE - Svezia 2
AZ - Azerbaigian 1
BE - Belgio 1
BN - Brunei Darussalam 1
CG - Congo 1
CH - Svizzera 1
CI - Costa d'Avorio 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
ET - Etiopia 1
GA - Gabon 1
GR - Grecia 1
GT - Guatemala 1
HR - Croazia 1
HU - Ungheria 1
JM - Giamaica 1
LB - Libano 1
MD - Moldavia 1
MM - Myanmar 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PE - Perù 1
PS - Palestinian Territory 1
RO - Romania 1
RS - Serbia 1
SI - Slovenia 1
SN - Senegal 1
SX - ???statistics.table.value.countryCode.SX??? 1
SY - Repubblica araba siriana 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
WS - Samoa 1
Totale 15.380
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Città #
Genova 6.163
Genoa 3.628
Rapallo 1.041
Vado Ligure 909
Bordighera 637
Singapore 425
San Jose 277
Ashburn 91
Ho Chi Minh City 87
Lauterbourg 69
New York 68
Hanoi 60
Hong Kong 60
Beijing 53
Council Bluffs 51
Tokyo 47
Helsinki 43
Santa Clara 32
Frankfurt am Main 31
Milan 24
Haiphong 14
Los Angeles 13
Amsterdam 11
Da Nang 11
Mexico City 11
Tianjin 10
São Paulo 9
Taipei 8
Atlanta 7
Dallas 6
Baghdad 5
Basingstoke 5
Guangzhou 5
Hải Dương 5
Piscataway 5
Cardiff 4
Chicago 4
City of London 4
Denver 4
Johannesburg 4
Kwai Chung 4
Lappeenranta 4
Naples 4
Rome 4
Taichung 4
Tashkent 4
Turin 4
Amman 3
Biên Hòa 3
Brescia 3
Buffalo 3
Bắc Ninh 3
Can Tho 3
Catania 3
Des Moines 3
Istanbul 3
Karachi 3
Orem 3
Paris 3
Quảng Ngãi 3
San José 3
Shanghai 3
Thái Nguyên 3
Toronto 3
Vĩnh Long 3
Wuhan 3
Zhengzhou 3
Acalanes Ridge 2
Algiers 2
Asunción 2
Bangkok 2
Belo Horizonte 2
Cagliari 2
Camerino 2
Campinas 2
Changsha 2
Charlotte 2
Curitiba 2
Dammam 2
Dhaka 2
Dobong-gu 2
Dublin 2
Erbil 2
Guarulhos 2
Guayaquil 2
Gustavo Adolfo Madero 2
Houston 2
Kuala Lumpur 2
La Rioja 2
Leipzig 2
Luoyang 2
Madrid 2
Medellín 2
Medina 2
Messina 2
Montreal 2
Mumbai 2
Muscat 2
Ninh Bình 2
Palermo 2
Totale 14.095
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Nome #
Synthesis, SAR and molecular modelling studies of acylthiocarbamates and their parent thiocarbamates as potent non-nucleoside reverse transcriptase inhibitors related to PETT derivatives 332
Structural studies on prokaryotic sulfurtransferases 316
Studi Cristallografici di Complessi tra Transcrittasi Inversa di HIV-1 e Derivati Tiocarbammici a Scheletro Ftalimmidico, Inibitori Non Nucleosidici Correlati ai Derivati PETT. 296
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 193
A persulfurated cysteine promotes active site reactivity in Azotobacter vinelandii Rhodanese 186
Further SAR studies on bicyclic basic merbarone analogues as potent antiproliferative agents 177
"One-pot" synthesis of N-acyl-N-phenylcarbamate derivatives endowed with anti-HIV and/or antiproliferative activities 169
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Characterization data of water-soluble hydrophilic and amphiphilic dendrimers prodrugs for delivering bioactive chemical entities otherwise non soluble. 167
Crystal structure of the extracellular domain of the human natural killer cell activating receptor NKp44 165
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 161
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 159
Computational approaches for the design and chemical synthesis of novel F508del correctors in the treatment of cystic fibrosis 154
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 152
Unprecedented one-pot synthesis of pharmaceutical interest derivatives via in situ condensation of heterocyclic iminium salts with nitrogen nucleophiles 149
Non-PAMAM amino acids-modified dendrimers nanoparticles for enhancing water-solubility of insoluble bioactive molecules: our state of the art 145
X-ray analysis of HIV-1 reverse transcriptase in complex with thiocarbamates: structure-based design and synthesis of new analogues 142
Amino-Pyrazoles in Medicinal Chemistry: A Review 142
Insights into the Pharmacological Activity of the Imidazo-Pyrazole Scaffold 141
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 140
The three-dimensional structure of NK cell receptor NKp44, a triggering partner in natural cytotoxicity 138
Exploring the binding features of rimonabant analogues and acyclic CB1 antagonists: docking studies and QSAR analysis 137
Anthrax toxin: structure-function relationships 136
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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. 134
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Characterization of water soluble dendrimer formulations of an insoluble thiocarbamate derivative with moderate anti HIV-1 activity: an overview 131
Synthesis of indole imminun salts as key-intermediates in a convergent multi-step one-pot stereoselective synthesis of new potent antiproliferative Knoevenagel-type agent 130
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Thiocarbamates as non-nucleoside HIV-1 reverse transcriptase inhibitors: docking-based CoMFA and CoMSIA analyses 124
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 124
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Synthesis and anti-HIV-1 activity of PETT structurally related O-substituted acyl (aryl) thiocarbamates 120
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Human rhinovirus 3C protease: a cysteine protease showing the trypsin(ogen)-like fold 118
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Regioselective Synthesis, Structural Characterization, and Antiproliferative Activity of Novel Tetra-Substituted Phenylaminopyrazole Derivatives 117
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Btk inhibitors: a medicinal chemistry and drug delivery perspective 117
Valorization and Potential Antimicrobial Use of Olive Mill Wastewater (OMW) from Italian Olive Oil Production 117
A Proteomics Approach Identifies RREB1 as a Crucial Molecular Target of Imidazo–Pyrazole Treatment in SKMEL-28 Melanoma Cells 116
Modulazioni Strutturali in O-[2-(N-Ftalimmido)etil] Acil(Aril)Tiocarbammati, Inibitori Non-Nucleosidici della Transcrittasi Inversa di HIV-1 116
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Capitolo 19 - Agenti cardiovascolari 115
Capitolo 14 - Anticonvulsivanti 114
The phosphoryl transfer reaction. Model of the HPr~P~IIA-Ntr protein complex 113
Exploring the binding features of rimonabant analogues and acyclic CB1 antagonists: docking studies and 3D-QSAR analysis 113
null 113
One-Pot Synthesis and Antiproliferative Activity of Highly Functionalized Pyrazole Derivatives 112
Cyclic diacyl thioureas enhance activity of corrector Lumacaftor on F508del‐CFTR 110
Efetti della orto, meta, para sostituzione della porzione N-fenilica di O-(2-ftalimmido)etil-2-tienocarbammati sull'attività anti-HIV-1 110
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One-pot Stereoselective Synthesis of Knoevenageltype Derivatives Via Condensation of N-Methyleniminium Salts of Ethylenethiourea and Ethyleneurea with Active Methylene Reagents. 105
Molecular docking of the Escherichia coli PTS system 104
Parallel synthesis of O-phenoxyethyl and O-adamantyl N-acyl thiocarbamates endowed with antiproliferative activity. 103
Studies on the catalitic activity of Azotobacter vinelandii rhodanese 103
Modellazioni strutturali in O-[2-(N-ftalimmido)etil] Acil(Aril)tiocarbammati, inibitori non nucleosidici della trascrittasi inversa di HIV-1 103
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Capitolo 18 - Farmaci attivi sul sistema renale 101
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Structure–Activity Relationship Studies on Highly Functionalized Pyrazole Hydrazones and Amides as Antiproliferative and Antioxidant Agents 98
Non-receptor tyrosine kinase Fes as a target in oncology 98
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Mono- and di-acylated imidazolidine-2-thione derivatives: synthesis, cytotoxicity evaluation and computational studies 94
Investigations of Antioxidant and Anti-Cancer Activities of 5-Aminopyrazole Derivatives 94
Sintesi parallela one-pot di disolfuri dimeri di tiocarbammati, una nuova potente classe di inibitori non nucleosidici della transcrittasi inversa 94
Synthesis and anti-HIV-1 activity of thiocarbamates, isosteres of PETT derivatives 92
Modulazioni Strutturali del Sistema Ftalimmidico di N-Aril Tiocarbammati, Inibitori Non-Nucleosidici della Transcrittasi Inversa di HIV-1 92
Reattivita' di accettori di Michael atipici con nucleofili azotati 91
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Potent and Broad-Spectrum Bactericidal Activity of a Nanotechnologically Manipulated Novel Pyrazole 91
Synthesis and SAR studies of novel merbarone analogues 90
Pharmacophore and pharmacokinetic filtering tools guiding for the design and synthesis of novel thiazole-containing and VX-809 hybrid derivatives as F508del correctors. 90
Microbiological Screening of 5-Functionalized Pyrazoles for the Future Development of Optimized Pyrazole-Based Delivery Systems 89
Virtual screening and structure based drug design of new Fes/Fps kinase domain inhibitors. 89
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 89
BRD9-targeting PROTACs: design, synthesis and biological evaluation 89
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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 87
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 87
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Triazole-imidazo[1,2-b]pyrazoles Able to Counteract Melanoma Cell Survival Without Compromising the Viability of Healthy Keratinocytes 86
Escherichia coli GlpE is a prototype sulfurtransferase for the single-domain rhodanese homology superfamily 86
Sintesi di Esteri Tienopirimidinici ad Attività Antiproliferativa 84
Bicyclic basic merbarone analogues as antiproliferative agents 84
Sintesi Convergente “One-Pot” di Aciltiocarbammati ad Attività Antiproliferativa 83
New pyrazolyl thioureas active against the Staphylococcus genus 82
Totale 12.173
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Categoria #
all - tutte 46.647
article - articoli 27.664
book - libri 0
conference - conferenze 16.832
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.151
Totale 93.294
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202182 0 0 0 0 0 0 0 0 0 0 41 41
2021/20221.196 30 92 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
2024/20252.202 72 177 98 229 287 175 171 284 130 112 220 247
2025/20264.543 455 159 598 409 696 299 707 273 420 522 5 0
Totale 15.716