BORDI, Fabrizio
 Distribuzione geografica
Continente #
NA - Nord America 3.205
AS - Asia 2.771
EU - Europa 2.301
SA - Sud America 356
AF - Africa 149
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 1
Totale 8.788
Nazione #
US - Stati Uniti d'America 3.111
SG - Singapore 980
CN - Cina 886
FI - Finlandia 581
VN - Vietnam 393
SE - Svezia 367
IE - Irlanda 328
DE - Germania 290
BR - Brasile 272
UA - Ucraina 215
HK - Hong Kong 188
IT - Italia 169
TR - Turchia 100
ZA - Sudafrica 94
NL - Olanda 80
GB - Regno Unito 79
FR - Francia 75
CA - Canada 65
BD - Bangladesh 55
IN - India 37
CI - Costa d'Avorio 33
BE - Belgio 29
AR - Argentina 28
RU - Federazione Russa 22
PL - Polonia 17
MX - Messico 16
EC - Ecuador 15
JP - Giappone 15
ES - Italia 14
IQ - Iraq 14
PH - Filippine 12
PK - Pakistan 11
TH - Thailandia 11
KR - Corea 9
CZ - Repubblica Ceca 8
ID - Indonesia 8
UZ - Uzbekistan 8
VE - Venezuela 8
BO - Bolivia 6
CO - Colombia 6
MA - Marocco 6
CL - Cile 5
JO - Giordania 5
LT - Lituania 5
PE - Perù 5
PY - Paraguay 5
UY - Uruguay 5
AT - Austria 4
AU - Australia 4
AZ - Azerbaigian 4
BY - Bielorussia 4
DZ - Algeria 4
IR - Iran 4
OM - Oman 4
SA - Arabia Saudita 4
EG - Egitto 3
HR - Croazia 3
KZ - Kazakistan 3
LB - Libano 3
NP - Nepal 3
TW - Taiwan 3
AE - Emirati Arabi Uniti 2
DO - Repubblica Dominicana 2
EE - Estonia 2
ET - Etiopia 2
GE - Georgia 2
HN - Honduras 2
IL - Israele 2
LY - Libia 2
MD - Moldavia 2
NI - Nicaragua 2
PA - Panama 2
TN - Tunisia 2
TT - Trinidad e Tobago 2
AL - Albania 1
AM - Armenia 1
AO - Angola 1
BB - Barbados 1
BW - Botswana 1
CH - Svizzera 1
EU - Europa 1
GA - Gabon 1
GR - Grecia 1
GY - Guiana 1
JM - Giamaica 1
LV - Lettonia 1
MN - Mongolia 1
MY - Malesia 1
PR - Porto Rico 1
RO - Romania 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
SY - Repubblica araba siriana 1
TJ - Tagikistan 1
TV - Tuvalu 1
Totale 8.788
Città #
Singapore 480
Ashburn 371
Chandler 337
Dublin 328
Jacksonville 284
San Jose 266
Beijing 212
Santa Clara 194
Hong Kong 182
Ann Arbor 159
Dearborn 129
Dallas 127
Ho Chi Minh City 118
Nanjing 105
Boardman 97
Izmir 90
New York 90
Johannesburg 88
Hanoi 78
Los Angeles 72
Munich 68
Princeton 63
Shanghai 63
San Mateo 56
Lauterbourg 54
Toronto 45
Parma 43
Helsinki 41
Wilmington 38
Shenyang 36
Abidjan 33
Hefei 33
Bremen 32
Nanchang 32
Turku 31
Brussels 29
Kunming 29
Hebei 27
Jinan 26
Buffalo 25
Haiphong 25
Des Moines 22
Grafing 22
São Paulo 22
Frankfurt am Main 21
Columbus 20
Da Nang 18
Tianjin 18
London 17
Guangzhou 16
Changsha 13
Moscow 13
Tokyo 13
Brooklyn 11
The Dalles 11
Warsaw 11
Atlanta 9
Montreal 9
Woodbridge 9
Zhengzhou 9
Can Tho 8
Denver 8
Phoenix 8
Seattle 8
Augusta 7
Council Bluffs 7
Jiaxing 7
Milan 7
Norwalk 7
Orem 7
Pune 7
Rio de Janeiro 7
San Francisco 7
Stockholm 7
Taiyuan 7
Wuhan 7
Bexley 6
Biên Hòa 6
Falkenstein 6
Fuzhou 6
Genoa 6
Haikou 6
Lahore 6
Mordano 6
Redondo Beach 6
Tashkent 6
Tân Tiến 6
Amman 5
Amsterdam 5
Baghdad 5
Belo Horizonte 5
Charlotte 5
Chengdu 5
Chicago 5
Curitiba 5
Düsseldorf 5
Guayaquil 5
Houston 5
Manchester 5
Mexico City 5
Totale 5.167
Nome #
Irreversible Inhibition of Epidermal Growth Factor Receptor Activity by 3-Aminopropanamides. 214
Dibasic biphenyl H(3) receptor antagonists: Steric tolerance for a lipophilic side chain. 208
5-Benzylidene-hydantoins as new EGFR inhibitors with antiproliferative activity 206
5-Benzylidene-hydantoins: synthesis and antiproliferative activity on A549 lung cancer cell line 203
Synthesis, biological activity, QSAR and QSPR study of 2/aminobenzimidazole derivatives as potent H3-antagonists 198
Application of 3D-QSAR in the Rational Design of Receptor Ligands and Enzyme Inhibitors 194
Novel Irreversible Epidermal Growth Factor Receptor Inhibitors by Chemical Modulation of the Cysteine-Trap Portion 191
Azionifarmacologiche di composti alchilaminoalchilfenilbenzisotiazolici sul trattogastrointestinale 191
The Role of HB-Donor Groups in the Heterocyclic Polar Fragment of H3-Antagonists. I. Synthesis and Biological Assays 183
Validation of a histamine H3 receptor model through structure–activity relationships for classical H3 antagonists 177
4-(1,2-benzisothiazol-3-)alkanoic and phenylalkanoic acids: synthesis and anti-inflammatory, analgesic and antipyretic activities 175
Action of histamine and ofdifferent synthetic P^ receptor stimulants on the isolated gastric fundus of theguinea pig 173
4-(3-Oxo-1,2-benzisothiazolin-2-yl)alkanoic, phenyl and phenoxyalkanoic acids: synthesis and anti-inflammatory, analgesic, and antipyretic properties 173
A New Potent and Selective Histamine H3-Receptor Antagonist, 4(5)-{2-[4(5)-cyclohexylimidazol-2-ylthio]ethyl}imidazole 165
Dibasic non-imidazole histamine H3 receptor antagonists with a rigid byphenyl scaffold. 162
Meccanismo d’azione di UPR 1024: un nuovo farmaco con attività antiproliferativa in cellule di carcinoma polmonare umano 158
A Short and Efficient Synthesis of the Selective H4 Receptor Agonist 4-Methylhistamine 157
H3-antagonists: synthesis and activity of 2-amino-5-thiazolyl derivatives 151
Development and validation of a LC-MS method with electrospray ionization for the determination of the imidazole H(3) antagonist ROS203 in rat plasma. 151
Effects of antimuscarinic agents, H2-blockers and omeprazole on rat chronic gastric ulcer after long-a and short-term administration 150
Synthesis and 3D-QSAR Analysis of H3 Receptor Antagonists Containing a Neutral Heterocyclic Polar Group 149
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 149
Dual mechanisms of action of the 5-benzylidene-hydantoin UPR1024 on lung cancer cell lines 147
Structural researcheson H^-agonists: the structures of the dipicrates of 2-(2-amino-4-imidazolyl)ethylamine, its 5-methyl derivative and N^f-dimeihyl-2-(2-am'mo-l,3-thiazol-5-yl)ethylamine 145
Functional Studies of New Imidazole H3-Antagonists on Guinea-Pig Isolated Preparations 144
Are histamine receptors involved in the stimulant activities of thiazolylethylamines supposed as cyclic models of dimaprit? 143
A possible physiological role ofhistamine H^-receptors in rat mesenteric circulation 140
A possible physiological role of histamine H2-receptors in rat mesenteric circulation 138
Synthesis and biological evaluation of new non-imidazole H(3)-receptor antagonists of the 2-aminobenzimidazole series 138
Hz-agonistiimidazolici: importanza della 2-amino sostituzione per 1'attivita farmacologica 138
Synthesis and biological assays of new H3-antagonists with imidazole and imidazoline polar groups 137
HPLC detection ofthioperamide from biological samples and its determination in rat blood and brainafter systemic administration 135
Heteroarylaminoethyl and heteroarylthioethylimidazoles. Synthesis and H3-receptor affinity 134
Tricyclic Alkylamides as Melatonin Receptor Ligands with Antagonist or Inverse Agonist Activity 131
Irreversible EGFR inhibitor compounds with antiproliferative activity 130
Histamine H3-antagonists: the basicity of the polar group in quantitative structure-activity and structure-property relationship 130
Action of histamine and of different synthetic H2 receptor stimulants on the isolated gastric fundus of the guinea pig 130
Synthesis and structure-activity relationships for biphenyl H3 receptor antagonists with moderate anti-cholinesterase activity. 129
Antipyretic activity of new compounds "4-(3-OXO-1,2-BENZISOTHIAZOLIN-2-YL) PHENYLALKANOIC acids, their esters, amides and 1,1-dioxide derivatives 124
Auxin-like activity of 1,2-benzisothiazole derivatives 121
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
Pharmacological activities of two new histamine analogs 115
QSAR study on H3-receptor affinity of benzothiazole derivatives of thioperamide 115
H3-receptor antagonists: Synthesis and structure relationships of para- and meta-substituted 4(5)-phenyl-2-((2-(4(5)-imidazolyl)ethyl)thio)imidazoles 114
Influence of urea-equivalent groups in position 5 of 2-amino, 2-(1-aminoethylidenamino) and 2-guanidino thiazole derivatives on H3-receptor antagonist activity in gastric fistula cat 113
Sviluppo e caratterizzazione farmacologica di un nuovo potente e selettivo H3-bloccante istaminico non-tioureico 110
Structure-Property Relationships on Histamine H3-Antagonists: Binding of Phenyl-substituted Alkylthioimidazole Derivatives to Rat Plasma Proteins 108
Pharmacological profile of original potent H3 receptor antagonists 108
Imidazole H3-antagonists: Relationship between Structure and Ex-vivo binding to Rat Brain H3-Receptors 108
Liquid chromatography-mass spectrometric method for determination of the non-imidazole H(3) -receptor antagonist UPR1056 in rat plasma. 108
Ligands for the histamine H3-receptor: new potent antagonists of the 2-thioimidazole type 107
Antipyreticactivity of new compounds 4-(3-oxo-l,2-benzisothiazolin-2-yl)puenyialkanoicacids, their esters, amides and 1,1 dioxide derivatives 105
Rat protein binding and cerebral phospholipid affinity of the H3-receptor antagonist thioperamide 101
Studio di sostanze analoghe alDimaprit sulla secrezione gastrica "in vitro" 101
Pharmacological characterization of H3 receptor antagonists with imidazole, thioimidazole and thioimidazoline polar groups in the side chain 100
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. 96
Pharmacological profile of new thioperamide derivatives at histamine peripheral H1-, H2, H3-receptors in guinea-pig 93
Are histamine receptors involved in the stimulant activities ofthiazolylethylamines supposed as cyclic models of dimaprit? 91
Melatonin Receptor Ligands: Synthesis of New Melatonin Derivatives and Comprehensive Comparative Molecular Field Analysis (CoMFA) Study. 75
THIAZOLYLALKYLAMINES - SYNTHESIS OF ANALOGS OF IMIDAZOLYLETHYLAMINES AND THEIR INFLUENCE ON GASTRIC-SECRETION 69
Influence of urea-equivalent groups in position 5 of 2-amino, 2-(1-aminoethylidenamino) and 2-guanidino thiazole derivatives on H2-receptor antagonist activity in gastric fistula cat. 66
Pharmacological activities of two new histamine analogs 65
null 61
null 37
Totale 8.810
Categoria #
all - tutte 29.762
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 29.762


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212 0 0 0 0 0 0 0 0 0 0 0 2
2021/2022344 7 3 3 30 17 33 45 49 19 24 21 93
2022/20231.308 156 143 89 86 121 162 18 74 411 10 30 8
2023/2024410 22 45 3 10 31 137 39 17 14 19 27 46
2024/20251.468 51 78 89 93 105 183 42 60 197 144 132 294
2025/20263.055 276 300 287 291 433 208 304 120 473 227 82 54
Totale 8.810