IRIS
SILVA, Claudia
 Distribuzione geografica
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Continente #
NA - Nord America 3.792
AS - Asia 2.750
EU - Europa 2.494
SA - Sud America 345
AF - Africa 135
Continente sconosciuto - Info sul continente non disponibili 48
OC - Oceania 7
Totale 9.571
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Nazione #
US - Stati Uniti d'America 3.659
SG - Singapore 913
CN - Cina 861
FI - Finlandia 494
VN - Vietnam 400
SE - Svezia 384
IT - Italia 352
IE - Irlanda 331
DE - Germania 280
BR - Brasile 255
UA - Ucraina 221
HK - Hong Kong 208
ZA - Sudafrica 92
FR - Francia 89
GB - Regno Unito 88
BD - Bangladesh 81
NL - Olanda 78
CA - Canada 75
TR - Turchia 73
IN - India 52
RU - Federazione Russa 52
AR - Argentina 32
BE - Belgio 29
MX - Messico 28
KR - Corea 23
CI - Costa d'Avorio 21
PL - Polonia 21
EC - Ecuador 20
JP - Giappone 20
PH - Filippine 17
IQ - Iraq 15
AT - Austria 14
PK - Pakistan 14
ES - Italia 12
CO - Colombia 10
ID - Indonesia 10
CZ - Repubblica Ceca 9
TH - Thailandia 9
OM - Oman 8
LT - Lituania 7
VE - Venezuela 7
AU - Australia 6
CL - Cile 6
EE - Estonia 6
MA - Marocco 6
MY - Malesia 6
PY - Paraguay 6
RO - Romania 6
TW - Taiwan 6
BY - Bielorussia 5
HN - Honduras 5
JM - Giamaica 5
CR - Costa Rica 4
PA - Panama 4
PE - Perù 4
UZ - Uzbekistan 4
AE - Emirati Arabi Uniti 3
CH - Svizzera 3
GE - Georgia 3
IL - Israele 3
LB - Libano 3
NI - Nicaragua 3
NP - Nepal 3
PR - Porto Rico 3
SA - Arabia Saudita 3
AO - Angola 2
AZ - Azerbaigian 2
BG - Bulgaria 2
BO - Bolivia 2
DZ - Algeria 2
EG - Egitto 2
HR - Croazia 2
KZ - Kazakistan 2
QA - Qatar 2
SI - Slovenia 2
UY - Uruguay 2
AM - Armenia 1
BS - Bahamas 1
BW - Botswana 1
DO - Repubblica Dominicana 1
EU - Europa 1
GA - Gabon 1
GD - Grenada 1
GL - Groenlandia 1
GY - Guiana 1
HU - Ungheria 1
IS - Islanda 1
KE - Kenya 1
KG - Kirghizistan 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
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 9.516
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Città #
Singapore 450
Ashburn 385
Dublin 329
San Jose 308
Chandler 284
Jacksonville 253
Santa Clara 230
Dallas 201
Hong Kong 201
Ann Arbor 199
Beijing 191
Ho Chi Minh City 131
Dearborn 127
Council Bluffs 118
Boardman 101
Los Angeles 94
Johannesburg 85
New York 85
Nanjing 84
Hanoi 75
Parma 68
Munich 66
Hefei 65
Washington 62
Izmir 59
Princeton 57
Shanghai 53
Lauterbourg 52
Bremen 48
Helsinki 45
San Mateo 44
Toronto 43
Wilmington 37
Shenyang 35
Hebei 31
Jinan 31
Buffalo 30
Kunming 28
Moscow 28
Nanchang 26
Brussels 25
Da Nang 25
São Paulo 24
Abidjan 21
Columbus 19
Turku 19
Grafing 18
Phoenix 17
Tokyo 17
Chicago 16
Des Moines 16
Haiphong 16
London 16
Modena 16
Seoul 15
Changsha 14
Milan 14
Seattle 14
Tianjin 14
Warsaw 14
Woodbridge 13
Brooklyn 12
Denver 12
Guangzhou 12
Jiaxing 12
Mexico City 12
Orem 12
The Dalles 12
Vienna 12
Rome 11
Chennai 10
Montreal 10
Atlanta 9
Bologna 9
Zhengzhou 9
Baghdad 8
Boston 8
Düsseldorf 8
Frankfurt am Main 8
North Bergen 8
Pune 8
Quito 8
Stockholm 8
Wuhan 8
Can Tho 7
Fuzhou 7
Guayaquil 7
Houston 7
Lahore 7
Norwalk 7
Nuremberg 7
San Francisco 7
Brno 6
Chengdu 6
Follonica 6
Fremont 6
Mordano 6
Muscat 6
Poplar 6
Redondo Beach 6
Totale 5.532
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Nome #
Balancing reactivity and antitumor activity: heteroarylthioacetamide derivatives as potent and time-dependent inhibitors of EGFR 370
2-Aminobenzimidazoles as new potent H3-antagonists 238
Amino acid derivatives as palmitoylethanolamide prodrugs: Synthesis, in vitro metabolism and in vivo plasma profile in rats 227
Creatine as a compatible osmolyte in muscle cells exposed to hypertonic stress 219
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 219
A Rapid and Specific HPLC Method to Determine Chemical and Radiochemical Purity of [68Ga] Ga-DOTA-Pentixafor (PET) Tracer: Development and Validation 209
Synthesis, biological activity, QSAR and QSPR study of 2/aminobenzimidazole derivatives as potent H3-antagonists 208
A Specific HPLC Method to Determine Residual HEPES in [68Ga]Ga-Radiopharmaceuticals: Development and Validation 207
Aminobenzimidazoles as new potent H3-antagonists 207
Analysis of illicit dietary supplements sold in the Italian market: Identification of a sildenafil thioderivative as adulterant using UPLC-TOF/MS and GC/MS. 204
Novel Irreversible Epidermal Growth Factor Receptor Inhibitors by Chemical Modulation of the Cysteine-Trap Portion 202
Biphenyl-3-yl alkylcarbamates as fatty acid amide hydrolase (FAAH) inhibitors: steric effects of N-alkyl chain on rat plasma and liver stability 199
The Role of HB-Donor Groups in the Heterocyclic Polar Fragment of H3-Antagonists. I. Synthesis and Biological Assays 195
4-(1,2-benzisothiazol-3-)alkanoic and phenylalkanoic acids: synthesis and anti-inflammatory, analgesic and antipyretic activities 189
A second generation of carbamate-based fatty acid amide hydrolase inhibitors with improved activity in vivo 187
4-(3-Oxo-1,2-benzisothiazolin-2-yl)alkanoic, phenyl and phenoxyalkanoic acids: synthesis and anti-inflammatory, analgesic, and antipyretic properties 186
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 178
Anomalous responses to histamine stimulation of guinea-pig oesophageal muscularis mucosae. 170
Brain Pharmacokinetics of Non-Imidazole Biphenyl H3 Receptor Antagonists: a Liquid Chromatography/Electrospray-Mass Spectrometry and ex vivo Binding Study in Rats 167
Anomalous responses to histamine stimulation of guinea-pig oesophageal muscularis mucosae 165
Development and validation of a LC-MS method with electrospray ionization for the determination of the imidazole H(3) antagonist ROS203 in rat plasma. 165
N-(Anilinoethyl)amides: design and synthesis of metabolically stable, selective melatonin receptor ligands 163
H3-antagonists: synthesis and activity of 2-amino-5-thiazolyl derivatives 163
Synthesis and 3D-QSAR Analysis of H3 Receptor Antagonists Containing a Neutral Heterocyclic Polar Group 162
2,4(5)-Diarylimidazoles as Inhibitors of hNaV1.2 Sodium Channels: Pharmacological Evaluationand Structure-Property Relationships 160
Antioxidant and cytoprotective activity of indole derivatives related to melatonin 160
N-(2-Oxo-3-oxetanyl)carbamic Acid Esters as N-Acylethanolamine Acid Amidase Inhibitors: Synthesis, Structure–Activity and Structure–Property Relationships. 160
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 157
Synthesis and biological assays of new H3-antagonists with imidazole and imidazoline polar groups 152
Heteroarylaminoethyl and heteroarylthioethylimidazoles. Synthesis and H3-receptor affinity 145
Indole-based analogs of melatonin: in vitro antioxidant and cytoprotective activities 144
Long-lasting inhibition of EGFR autophosphorylation in A549 tumor cells by intracellular accumulation of non-covalent inhibitors 143
HPLC detection ofthioperamide from biological samples and its determination in rat blood and brainafter systemic administration 142
Predicting the reactivity of nitrile-carrying compounds with cysteine: a combined computational and experimental study. 141
Histamine H3-antagonists: the basicity of the polar group in quantitative structure-activity and structure-property relationship 139
Three-Dimensional Quantitative Structure-Activity Relationship Studies on Selected MT1 and MT2 Melatonin Receptor Ligands: Requirements for Subtype Selectivity and Intrinsic Activity Modulation 137
Interactions of new and conventional H3-blockers with non-histaminergic receptors involved in neurogenic and myogenic contractile responses of guinea-pig ileum 131
Antipyretic activity of new compounds "4-(3-OXO-1,2-BENZISOTHIAZOLIN-2-YL) PHENYLALKANOIC acids, their esters, amides and 1,1-dioxide derivatives 130
Synthesis, antioxidant activity and structure-activity relationships for a new series of 2-(N-acylaminoethyl)indoles with melatonin-like cytoprotective activity 129
QSAR study on H3-receptor affinity of benzothiazole derivatives of thioperamide 129
H3-receptor antagonists: Synthesis and structure relationships of para- and meta-substituted 4(5)-phenyl-2-((2-(4(5)-imidazolyl)ethyl)thio)imidazoles 127
Relationship between structure and ex-vivo binding of imidazole H3 antagonists to rat brain H3 receptors 124
Plasma concentration and brain penetration of the H3-receptor antagonist Thioperamide in rats 124
Structure-property relationships of a class of carbamate-based fatty acid amide hydrolase (FAAH) inhibitors: chemical and biological stability 124
In vitro characterization of potency, affinity and selectivity of H3-antagonists: from thioperamide to thioperamide unrelated derivatives 124
Structure-Property Relationships on Histamine H3-Antagonists: Binding of Phenyl-substituted Alkylthioimidazole Derivatives to Rat Plasma Proteins 118
Ligands for the histamine H3-receptor: new potent antagonists of the 2-thioimidazole type 116
Imidazole H3-antagonists: Relationship between Structure and Ex-vivo binding to Rat Brain H3-Receptors 115
Antipyreticactivity of new compounds 4-(3-oxo-l,2-benzisothiazolin-2-yl)puenyialkanoicacids, their esters, amides and 1,1 dioxide derivatives 114
Liquid chromatography-mass spectrometric method for determination of the non-imidazole H(3) -receptor antagonist UPR1056 in rat plasma. 114
Sviluppo e caratterizzazione farmacologica di un nuovo potente e selettivo H3-bloccante istaminico non-tioureico 112
Synthesis and binding assays of H3-receptor ligands. 112
Pharmacological profile of new thioperamide derivatives at histamine peripheral H1-, H2-, H3-receptors in guinea-pig 108
Qualitative structure-metabolism relationships in the hydrolysis of carbamates 108
Quantitative structure-property relationships of a class of carbamate-based fatty acid amide hydrolase (FAAH) inhibitors. 107
Rat protein binding and cerebral phospholipid affinity of the H3-receptor antagonist thioperamide 106
Synthesis and stability in biological media of 1H-imidazole-1-carboxylates of ROS203, an antagonist of the histamine H3 receptor. 105
Pharmacological profile of new thioperamide derivatives at histamine peripheral H1-, H2, H3-receptors in guinea-pig 98
Structural analogues of thioperamide: pharmacological evaluation of new benzothiazole derivatives at peripheral histamine receptor subtypes 95
Recent advances in the discovery of ALKBH 1–8 inhibitors. 85
Melatonin Receptor Ligands: Synthesis of New Melatonin Derivatives and Comprehensive Comparative Molecular Field Analysis (CoMFA) Study. 84
pH-partition profiles of 4-(3-oxo-1,2-benzisothiazolin-2-yl)phenyl and phenoxyalkanoic acids 80
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Totale 9.571
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Categoria #
all - tutte 33.476
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 33.476
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022285 0 0 0 0 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
2025/20263.298 258 349 375 341 465 219 322 106 433 231 121 78
2026/2027691 69 157 213 239 13 0 0 0 0 0 0 0
Totale 9.571