SILVA, Claudia
 Distribuzione geografica
Continente #
NA - Nord America 3.098
AS - Asia 2.649
EU - Europa 2.379
SA - Sud America 330
AF - Africa 134
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 2
Totale 8.599
Nazione #
US - Stati Uniti d'America 3.009
SG - Singapore 904
CN - Cina 850
FI - Finlandia 494
VN - Vietnam 395
SE - Svezia 367
IE - Irlanda 330
IT - Italia 290
DE - Germania 279
BR - Brasile 253
UA - Ucraina 220
HK - Hong Kong 204
ZA - Sudafrica 92
FR - Francia 83
NL - Olanda 77
GB - Regno Unito 74
TR - Turchia 73
CA - Canada 56
IN - India 49
RU - Federazione Russa 48
AR - Argentina 29
BE - Belgio 29
BD - Bangladesh 26
MX - Messico 24
KR - Corea 22
CI - Costa d'Avorio 21
JP - Giappone 20
EC - Ecuador 18
PL - Polonia 18
IQ - Iraq 15
AT - Austria 14
PH - Filippine 13
ES - Italia 11
PK - Pakistan 11
CZ - Repubblica Ceca 9
ID - Indonesia 9
TH - Thailandia 9
OM - Oman 8
LT - Lituania 7
AU - Australia 6
CL - Cile 6
MA - Marocco 6
PY - Paraguay 6
RO - Romania 6
TW - Taiwan 6
BY - Bielorussia 5
VE - Venezuela 5
CO - Colombia 4
PE - Perù 4
UZ - Uzbekistan 4
AE - Emirati Arabi Uniti 3
CH - Svizzera 3
GE - Georgia 3
LB - Libano 3
MY - Malesia 3
NP - Nepal 3
PA - Panama 3
SA - Arabia Saudita 3
AO - Angola 2
AZ - Azerbaigian 2
BG - Bulgaria 2
BO - Bolivia 2
DZ - Algeria 2
EE - Estonia 2
EG - Egitto 2
HR - Croazia 2
IL - Israele 2
KZ - Kazakistan 2
NI - Nicaragua 2
QA - Qatar 2
SI - Slovenia 2
UY - Uruguay 2
AM - Armenia 1
BW - Botswana 1
DO - Repubblica Dominicana 1
EU - Europa 1
GA - Gabon 1
GL - Groenlandia 1
GY - Guiana 1
HN - Honduras 1
HU - Ungheria 1
IS - Islanda 1
JM - Giamaica 1
KE - Kenya 1
LA - Repubblica Popolare Democratica del Laos 1
LU - Lussemburgo 1
LY - Libia 1
MD - Moldavia 1
MU - Mauritius 1
NG - Nigeria 1
PS - Palestinian Territory 1
PT - Portogallo 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
SY - Repubblica araba siriana 1
TG - Togo 1
TJ - Tagikistan 1
TN - Tunisia 1
TV - Tuvalu 1
XK - ???statistics.table.value.countryCode.XK??? 1
Totale 8.598
Città #
Singapore 444
Dublin 329
Ashburn 314
Chandler 284
Jacksonville 252
San Jose 234
Ann Arbor 199
Dallas 197
Hong Kong 197
Beijing 185
Santa Clara 182
Ho Chi Minh City 130
Dearborn 127
Boardman 98
Johannesburg 85
Los Angeles 84
Nanjing 84
Hanoi 74
New York 67
Parma 67
Munich 66
Hefei 65
Izmir 59
Princeton 57
Lauterbourg 52
Shanghai 52
Bremen 48
Helsinki 45
San Mateo 44
Toronto 41
Wilmington 37
Shenyang 35
Hebei 31
Jinan 31
Kunming 28
Moscow 28
Buffalo 26
Nanchang 26
Brussels 25
Da Nang 25
São Paulo 24
Abidjan 21
Columbus 19
Turku 19
Grafing 18
Tokyo 17
Council Bluffs 16
Des Moines 16
Haiphong 16
London 15
Changsha 14
Seoul 14
Tianjin 14
Woodbridge 13
Guangzhou 12
Jiaxing 12
Phoenix 12
Seattle 12
The Dalles 12
Vienna 12
Warsaw 12
Modena 11
Brooklyn 10
Chennai 10
Chicago 10
Denver 10
Mexico City 10
Orem 10
Milan 9
Zhengzhou 9
Atlanta 8
Baghdad 8
Düsseldorf 8
Frankfurt am Main 8
Montreal 8
Pune 8
Quito 8
Stockholm 8
Wuhan 8
Boston 7
Can Tho 7
Fuzhou 7
Houston 7
Norwalk 7
Nuremberg 7
Brno 6
Chengdu 6
Follonica 6
Fremont 6
Guayaquil 6
Lahore 6
Mordano 6
Muscat 6
Poplar 6
Redondo Beach 6
San Francisco 6
Bengaluru 5
Biên Hòa 5
Campinas 5
Genoa 5
Totale 5.063
Nome #
Balancing reactivity and antitumor activity: heteroarylthioacetamide derivatives as potent and time-dependent inhibitors of EGFR 350
2-Aminobenzimidazoles as new potent H3-antagonists 222
Amino acid derivatives as palmitoylethanolamide prodrugs: Synthesis, in vitro metabolism and in vivo plasma profile in rats 198
A Rapid and Specific HPLC Method to Determine Chemical and Radiochemical Purity of [68Ga] Ga-DOTA-Pentixafor (PET) Tracer: Development and Validation 198
Analysis of illicit dietary supplements sold in the Italian market: Identification of a sildenafil thioderivative as adulterant using UPLC-TOF/MS and GC/MS. 197
Aminobenzimidazoles as new potent H3-antagonists 194
Synthesis, biological activity, QSAR and QSPR study of 2/aminobenzimidazole derivatives as potent H3-antagonists 190
Development and validation of an analytical hplc method to assess chemical and radiochemical purity of [68ga]ga-nodaga-exendin-4 produced by a fully automated method 178
Creatine as a compatible osmolyte in muscle cells exposed to hypertonic stress 177
Novel Irreversible Epidermal Growth Factor Receptor Inhibitors by Chemical Modulation of the Cysteine-Trap Portion 177
A second generation of carbamate-based fatty acid amide hydrolase inhibitors with improved activity in vivo 176
4-(1,2-benzisothiazol-3-)alkanoic and phenylalkanoic acids: synthesis and anti-inflammatory, analgesic and antipyretic activities 173
Biphenyl-3-yl alkylcarbamates as fatty acid amide hydrolase (FAAH) inhibitors: steric effects of N-alkyl chain on rat plasma and liver stability 173
4-(3-Oxo-1,2-benzisothiazolin-2-yl)alkanoic, phenyl and phenoxyalkanoic acids: synthesis and anti-inflammatory, analgesic, and antipyretic properties 171
The Role of HB-Donor Groups in the Heterocyclic Polar Fragment of H3-Antagonists. I. Synthesis and Biological Assays 169
Investigations on the 4-Quinolone-3-carboxylic Acid Motif. 7. Synthesis and Pharmacological Evaluation of 4-Quinolone-3-carboxamides and 4-Hydroxy-2-quinolone-3-carboxamides as High Affinity Cannabinoid Receptor 2 (CB2R) Ligands with Improved Aqueous Solubility 161
A Specific HPLC Method to Determine Residual HEPES in [68Ga]Ga-Radiopharmaceuticals: Development and Validation 159
Anomalous responses to histamine stimulation of guinea-pig oesophageal muscularis mucosae. 157
Anomalous responses to histamine stimulation of guinea-pig oesophageal muscularis mucosae 152
Synthesis and 3D-QSAR Analysis of H3 Receptor Antagonists Containing a Neutral Heterocyclic Polar Group 148
H3-antagonists: synthesis and activity of 2-amino-5-thiazolyl derivatives 148
Antioxidant and cytoprotective activity of indole derivatives related to melatonin 148
Biological studies on 1,2-benzisothiazole derivatives. V. Antimicrobial properties of N-alkanoic, N-arylalkanoic and N-aryloxyalkanoic derivatives of 1,2-benzisothiazolin-3-one: QSAR study and genotoxicity evaluation 148
Development and validation of a LC-MS method with electrospray ionization for the determination of the imidazole H(3) antagonist ROS203 in rat plasma. 146
2,4(5)-Diarylimidazoles as Inhibitors of hNaV1.2 Sodium Channels: Pharmacological Evaluationand Structure-Property Relationships 144
N-(Anilinoethyl)amides: design and synthesis of metabolically stable, selective melatonin receptor ligands 139
Brain Pharmacokinetics of Non-Imidazole Biphenyl H3 Receptor Antagonists: a Liquid Chromatography/Electrospray-Mass Spectrometry and ex vivo Binding Study in Rats 137
N-(2-Oxo-3-oxetanyl)carbamic Acid Esters as N-Acylethanolamine Acid Amidase Inhibitors: Synthesis, Structure–Activity and Structure–Property Relationships. 137
HPLC detection ofthioperamide from biological samples and its determination in rat blood and brainafter systemic administration 135
Synthesis and biological assays of new H3-antagonists with imidazole and imidazoline polar groups 135
Heteroarylaminoethyl and heteroarylthioethylimidazoles. Synthesis and H3-receptor affinity 133
Indole-based analogs of melatonin: in vitro antioxidant and cytoprotective activities 132
Long-lasting inhibition of EGFR autophosphorylation in A549 tumor cells by intracellular accumulation of non-covalent inhibitors 132
Histamine H3-antagonists: the basicity of the polar group in quantitative structure-activity and structure-property relationship 129
Predicting the reactivity of nitrile-carrying compounds with cysteine: a combined computational and experimental study. 129
Antipyretic activity of new compounds "4-(3-OXO-1,2-BENZISOTHIAZOLIN-2-YL) PHENYLALKANOIC acids, their esters, amides and 1,1-dioxide derivatives 123
Interactions of new and conventional H3-blockers with non-histaminergic receptors involved in neurogenic and myogenic contractile responses of guinea-pig ileum 120
Synthesis, antioxidant activity and structure-activity relationships for a new series of 2-(N-acylaminoethyl)indoles with melatonin-like cytoprotective activity 119
In vitro characterization of potency, affinity and selectivity of H3-antagonists: from thioperamide to thioperamide unrelated derivatives 119
Plasma concentration and brain penetration of the H3-receptor antagonist Thioperamide in rats 115
Three-Dimensional Quantitative Structure-Activity Relationship Studies on Selected MT1 and MT2 Melatonin Receptor Ligands: Requirements for Subtype Selectivity and Intrinsic Activity Modulation 115
Structure-property relationships of a class of carbamate-based fatty acid amide hydrolase (FAAH) inhibitors: chemical and biological stability 114
Relationship between structure and ex-vivo binding of imidazole H3 antagonists to rat brain H3 receptors 113
H3-receptor antagonists: Synthesis and structure relationships of para- and meta-substituted 4(5)-phenyl-2-((2-(4(5)-imidazolyl)ethyl)thio)imidazoles 113
QSAR study on H3-receptor affinity of benzothiazole derivatives of thioperamide 112
Liquid chromatography-mass spectrometric method for determination of the non-imidazole H(3) -receptor antagonist UPR1056 in rat plasma. 108
Sviluppo e caratterizzazione farmacologica di un nuovo potente e selettivo H3-bloccante istaminico non-tioureico 107
Imidazole H3-antagonists: Relationship between Structure and Ex-vivo binding to Rat Brain H3-Receptors 107
Structure-Property Relationships on Histamine H3-Antagonists: Binding of Phenyl-substituted Alkylthioimidazole Derivatives to Rat Plasma Proteins 106
Ligands for the histamine H3-receptor: new potent antagonists of the 2-thioimidazole type 106
Antipyreticactivity of new compounds 4-(3-oxo-l,2-benzisothiazolin-2-yl)puenyialkanoicacids, their esters, amides and 1,1 dioxide derivatives 105
Pharmacological profile of new thioperamide derivatives at histamine peripheral H1-, H2-, H3-receptors in guinea-pig 100
Rat protein binding and cerebral phospholipid affinity of the H3-receptor antagonist thioperamide 100
Quantitative structure-property relationships of a class of carbamate-based fatty acid amide hydrolase (FAAH) inhibitors. 99
Synthesis and stability in biological media of 1H-imidazole-1-carboxylates of ROS203, an antagonist of the histamine H3 receptor. 98
Synthesis and binding assays of H3-receptor ligands. 95
Pharmacological profile of new thioperamide derivatives at histamine peripheral H1-, H2, H3-receptors in guinea-pig 93
Qualitative structure-metabolism relationships in the hydrolysis of carbamates 93
Structural analogues of thioperamide: pharmacological evaluation of new benzothiazole derivatives at peripheral histamine receptor subtypes 89
Melatonin Receptor Ligands: Synthesis of New Melatonin Derivatives and Comprehensive Comparative Molecular Field Analysis (CoMFA) Study. 75
pH-partition profiles of 4-(3-oxo-1,2-benzisothiazolin-2-yl)phenyl and phenoxyalkanoic acids 74
Recent advances in the discovery of ALKBH 1–8 inhibitors. 61
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Totale 8.644
Categoria #
all - tutte 28.764
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 28.764


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202190 0 0 0 0 0 0 0 0 0 9 73 8
2021/2022342 10 7 4 36 18 29 44 41 20 24 28 81
2022/20231.281 156 115 86 80 144 142 23 62 402 19 39 13
2023/2024404 21 42 4 13 36 111 32 19 10 21 34 61
2024/20251.402 39 69 105 87 102 156 57 73 166 136 129 283
2025/20263.062 258 349 375 341 465 219 322 106 433 194 0 0
Totale 8.644