SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

CACCIARI, Barbara
 Distribuzione geografica
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Continente #
NA - Nord America 10.289
AS - Asia 4.725
EU - Europa 2.546
SA - Sud America 859
AF - Africa 53
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 2
Totale 18.478
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Nazione #
US - Stati Uniti d'America 10.109
SG - Singapore 1.737
CN - Cina 1.520
BR - Brasile 716
UA - Ucraina 688
DE - Germania 501
TR - Turchia 469
HK - Hong Kong 450
GB - Regno Unito 342
VN - Vietnam 304
SE - Svezia 233
IT - Italia 186
FI - Finlandia 178
RU - Federazione Russa 148
MX - Messico 92
FR - Francia 79
CA - Canada 75
PL - Polonia 64
AR - Argentina 54
IN - India 54
ID - Indonesia 34
EC - Ecuador 32
BD - Bangladesh 29
ZA - Sudafrica 28
JP - Giappone 23
NL - Olanda 22
BE - Belgio 21
ES - Italia 17
PY - Paraguay 17
IQ - Iraq 15
LT - Lituania 13
PK - Pakistan 12
AT - Austria 10
CO - Colombia 9
VE - Venezuela 9
MA - Marocco 8
SA - Arabia Saudita 8
AE - Emirati Arabi Uniti 7
CL - Cile 7
IE - Irlanda 7
PE - Perù 7
UZ - Uzbekistan 7
JO - Giordania 6
TW - Taiwan 6
CZ - Repubblica Ceca 5
IR - Iran 5
KZ - Kazakistan 5
NP - Nepal 5
AL - Albania 4
AZ - Azerbaigian 4
BG - Bulgaria 4
KR - Corea 4
PA - Panama 4
TN - Tunisia 4
TT - Trinidad e Tobago 4
UY - Uruguay 4
BO - Bolivia 3
CH - Svizzera 3
EG - Egitto 3
KE - Kenya 3
KG - Kirghizistan 3
PS - Palestinian Territory 3
PT - Portogallo 3
SY - Repubblica araba siriana 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AU - Australia 2
BY - Bielorussia 2
CI - Costa d'Avorio 2
DK - Danimarca 2
LB - Libano 2
LV - Lettonia 2
MD - Moldavia 2
ME - Montenegro 2
MY - Malesia 2
NZ - Nuova Zelanda 2
PH - Filippine 2
RO - Romania 2
RS - Serbia 2
AF - Afghanistan, Repubblica islamica di 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
CR - Costa Rica 1
DZ - Algeria 1
GA - Gabon 1
GE - Georgia 1
GI - Gibilterra 1
GP - Guadalupe 1
GY - Guiana 1
HN - Honduras 1
KH - Cambogia 1
KW - Kuwait 1
MG - Madagascar 1
MK - Macedonia 1
NI - Nicaragua 1
NO - Norvegia 1
PR - Porto Rico 1
QA - Qatar 1
SD - Sudan 1
TH - Thailandia 1
Totale 18.478
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Città #
Singapore 1.012
Woodbridge 977
Ashburn 964
Fairfield 914
Dallas 849
Houston 777
Jacksonville 712
Chandler 593
Ann Arbor 488
Hong Kong 445
Santa Clara 420
Beijing 379
Seattle 364
Wilmington 358
Cambridge 264
Nanjing 243
Izmir 220
Princeton 158
Los Angeles 117
Boardman 112
Ho Chi Minh City 94
San Diego 89
Shenyang 77
São Paulo 69
Nanchang 67
Munich 62
Dong Ket 61
Hefei 60
Mexico City 60
Hanoi 55
New York 55
Warsaw 55
Shanghai 45
Ferrara 44
Milan 43
Jiaxing 41
Tianjin 41
San Mateo 37
Brooklyn 35
Falkenstein 34
Hebei 34
Kunming 32
Changsha 31
Chicago 31
Jinan 31
Zhengzhou 31
Dearborn 30
Helsinki 29
London 28
Falls Church 26
San Francisco 24
Orem 23
Philadelphia 23
Norwalk 22
Rio de Janeiro 22
Tokyo 22
Brussels 21
Chennai 21
Moscow 21
Montreal 20
Frankfurt am Main 19
Ningbo 19
Stockholm 19
Turku 19
Phoenix 18
San Jose 18
Toronto 18
Addison 17
Buffalo 17
Guangzhou 17
Jakarta 17
Denver 15
Manchester 15
The Dalles 15
Bremen 14
Istanbul 14
Johannesburg 14
Mountain View 14
Taizhou 14
Amsterdam 13
Atlanta 13
Da Nang 13
Verona 13
Boston 12
Curitiba 12
Montréal 12
Redwood City 12
Indiana 11
Poplar 11
Porto Alegre 11
Salvador 11
Washington 11
Augusta 10
Haiphong 10
Ankara 9
Brasília 9
Charlotte 9
Guayaquil 9
Mcallen 9
Orange 9
Totale 12.554
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Nome #
1,2,3-triazolo[5,4-e]1,2,4-triazolo[1,5-c]pyrimidine derivatives: A new class of A(2A) adenosine receptor antagonists 1.129
[2,1-c][1,4]benzodiazepine (PBD)-distamycin hybrid inhibits DNA binding to transcription factor Sp1 488
1-methyl-3-nitro-5-methoxycarbonyl pyrazole 262
5,7-Disubstituted-[1,2,4]triazolo[1,5-a][1,3,5]triazines as pharmacological tools to explore the antagonist selectivity profiles toward adenosine receptors 228
6-Amino-2-mercapto-3H-pyrimidin-4-one derivatives as new candidates for the antagonism at the P2Y12 receptors 214
1H-pyrazolo[2,3-d][1,2,4]triazine-3,7-diones as a new class of human leukocyte elastase inhibitors 204
Synthesis, in vitro antiproliferative activity, and DNA-binding properties of hybrid molecules containing pyrrolo[2,1-c][1,4] benzodiazepine and minor-groove-binding oligopyrrole carriers 191
8-(2-Furyl)adenine derivatives as A₂A adenosine receptor ligands 184
Design, synthesis, in vitro antiproliferative activity and apoptosis-inducing studies of 1-(3',4',5'-trimethoxyphenyl)-3-(2'-alkoxycarbonylindolyl)-2-propen-1-one derivatives obtained by a molecular hybridisation approach 184
A new synthetic approach to indazole synthesis 183
[H-3]MRE 3008F20: A novel antagonist radioligand for the pharmacological and biochemical characterization of human A(3) adenosine receptors 182
5-heteroarylcarbamoylamino-pyrazolo-triazolo pyrimidines as hA3 adenosine receptor antagonists. 178
7-substituted-5-amino-2-(furyl)-pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidines as A2A adenosine receptor antagonists: importance of modifications at the side chain on the activity and solubility. 178
7-substituted 5-amino-2-(2-furyl)pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as A(2A) adenosine receptor antagonists: A study on the importance of modifications at the side chain on the activity and solubility 176
1H-pyrazolo[4,3-d]pyrimidine-7(6H)-one and 5H-pyrazolo[4,3-d] 1,2,3-triazin-4(3H)-one derivatives. Synthesis and in vitro biological activity at adenosine A1 and A2a receptors 166
Pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidines and Structurally Simplified Analogs. Chemistry and SAR Profile as Adenosine Receptor Antagonists 166
Schematic overview of oligosaccharides, with survey on their major physiological effects and a focus on milk ones 165
New potent and selective human adenosine A3 receptor antagonists. 165
Antiproliferative effects of novel synthetic nucleobase analogues on U937 Histiocytic lymphoma cell line 163
Resolution of a CPzI precursor, synthesis and biological evaluation of (+) and (-)-N-Boc-CPzI: A further validation of the relationship between chemical solvolytic stability and cytotoxicity 162
Solid lipid microparticles for the stability enhancement of a dopamine prodrug 160
Synthesis and antitumor activity of novel distamycin derivatives 159
[3H]-MRE 3008-F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A3 adenosine receptors. 157
The influence of the 1-(3-Trifluoromethyl-Benzyl)-1H-Pyrazole-4-yl moiety on the adenosine receptors affinity profile of pyrazolo[4,3-e][1,2,4]Triazolo[1,5-c] pyrimidine derivatives 156
[3H]MRE3008-F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A3 adenosine receptors. 155
7-sobstituted-5-amino-2-(furyl)-pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidines as A2A adenosine receptor antagonist: importance of modifications at the side chain on the activity and solubility. 154
DNA minor groove alkylating agents structurally related to distamycin A 152
New potent and selective human adenosine A3 receptor antagonists 151
Synthesis and calcium antagonist activity of dialkyl 1,4-dihydro-2,6-dimethyl-4-(nitrogenous heteroaryl)-3,5-pyridine dicarboxylates. 151
Synthesis and antitumor activity of a new class of pyrazolo[4,3-e]pyrrolo[1,2-a][1,4]diazepinone analogs of pyrrolo[1,4]benzodiazepines (PBDs) 149
Oligonucleotides and oligonucleotide conjugates: A new approach for cancer treatment 147
A(1) and A(3) adenosine receptor agonists: an overview 146
Carbon nanotube substrates boost neuronal electrical signaling 145
A2A-adenosine receptor reserve for coronary vasodilation 145
Binding affinity of adenosine receptor agonists and antagonists at human cloned A3 adenosine receptors 143
Synthesis and properties of substituted CBI analogs of CC-1065 and the duocarmycins incorporating the 7-methoxy-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (MCBI) alkylation subunit: Magnitude of electronic effects on the functional reactivity 143
Synthesis and Biological Evaluation of a New Series of 1,2,4-Triazolo[1,5-a]-1,3,5-triazines as Human A(2A) Adenosine Receptor Antagonists with Improved Water Solubility 142
DNA minor-groove binders: results and design of new antitumor agents 141
Nitrile oxide [3 + 2] cycloaddition: application to the synthesis of 6-substituted 3(2H)-pyridazinones and 6-substituted 4,5-dihydro-4-hydroxy-3(2H)-pyridazinones 140
Ethyl (R,S)-5-acetyl-4,5-dihydro-3-isoxazoleacetate 139
An efficient procedure for the synthesis of 5H-6-substituted-pyrazolo[1,5-d]-1,2,4-triazine-4,7-diones 138
Recent developments in the field of adenosine receptor ligands 138
New 9-methyl-8-(4-hydroxyphenyl)adenine derivatives as A1 adenosine receptor antagonists 138
Structure Activity Relationship of 4-Amino-2-thiopyrimidine Derivatives as Platelet Aggregation Inhibitors 138
Structure-activity relationship of novel tallimustine derivatives: Synthesis and antitumor activity 137
Ethyl-(R,S)-5-acetyl-4,5-dihydro-3-isoxazole acetate 137
Design, synthesis and biological activity of a pyrrolo[2,1-c][1,4]benzodiazepine (PBD)-distamycin hybrid 137
Selective binding to human genomic sequences of two synthetic analogues structurally related to U-71184 and adozelesin 135
Synthesis and Antitumor Activity of a New Class of Pyrazolo[4,3-e]pyrrolo[1,2-a][1,4]diazepinone Analogs of Pyrrolo[1,4][2,1-c]benzodiazepines 135
A novel class of pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidines as A3 adenosine receptor antagonists 133
Effect of A-ring modifications on the DNA-binding behavior and cytotoxicity of pyrrolo[2,1-c] [1,4]benzodiazepines 133
Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: A complete structure-activity profile 131
Linear and nonlinear 3D-QSAR approaches in tandem with ligand-based homology modeling as a computational strategy to depict the pyrazolo-triazolo- pyrimidine antagonists binding site of the human adenosine A2A receptor 131
Facile and versatile route to the synthesis of fused 2-pyridones: Useful intermediates for polycyclic sytems 131
Chemical Synthesis of [13C]Daidzein 131
Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: Effect of the N-5 bond type on the affinity and selectivity at the four adenosine receptor subtypes 130
A(3) adenosine receptor ligands: History and perspectives 129
The Significance of 2-Furyl Ring Substitution with a 2-(para-substituted) Aryl Group in a New Series of Pyrazolo-triazolo-pyrimidines as Potent and Highly Selective hA3 Adenosine Receptors Antagonists: New Insights into Structure-Affinity Relationship and Receptor-Antagonist Recognition 129
Cosmetic preservation and structure-activity relationships of 4-diazo-pyrazole-5-carboxamides 128
Synthesis and biological evaluation of new antitubulin agents containing 2-(30,40,50-trimethoxyanilino)-3,6-disubstituted-4,5,6,7-tetrahydrothieno[2,3-c]pyridine Scaffold 128
Synthesis and preliminary biological evaluation of [H-3]-MRE 3008-F20: the first high affinity radioligand antagonist for the human A(3) adenosine receptors 127
Synthesis, biological studies and molecular modeling investigation of 1,3-dimethyl-2,4-dioxo-6-methyl-8-(substituted) 1,2,3,4-tetrahydro [1,2,4]-triazolo [3,4-f]-purines as potential adenosine receptor antagonists 126
Synthesis, biological activity, and molecular modeling investigation of new pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives as human A(3) adenosine receptor antagonists 124
Carbon Nanotubes Carrying Cell-Adhesion Peptides do not Interfere with Neuronal Functionality 123
Synthesis of pyridazine derivatives through the unexpected intermediate 5-amino-4-cyano-2,3-dihydro-furan-2,3-disulfonic acid disodium salt 123
Unusual Ring-Opening Reaction of 6,7-Dihydrothieno[3,2-d]pyrimidine- 2,4-dione Derivatives Leading to 5-(Alkylthio)-6-vinyluracils 123
CC-1065 and the duocarmycins: recent developments 121
Exploring Potency and Selectivity Receptor Antagonist Profiles Using a Multilabel Classification Approach: The Human Adenosine Receptors as a Key Study 121
Binding affinity of adenosine receptor agonists and antagonists at human cloned A3 adenosine receptors 120
Pyridazine nucleus: a pharmacophoric moiety for bio-active compounds 119
A Novel Conjugated Agent between Dopamine and an A(2A) Adenosine Receptor Antagonist as a Potential Anti-Parkinson Multitarget Approach. 119
null 118
Pyrazolo [4,3-E]1,2,4-triazolo[1,5-c]pyrimidine derivates a new class of potent and selective human A3 adenosine receptor antagonists. 117
Demystifying the three dimensional structure of G protein-coupled receptors (GPCRs) with the aid of molecular modeling 117
Substituted 6-amino-thiouracils as new P2Y(12) receptor antagonists 115
Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives: Potent and selective A2A adenosine antagonists 115
Novel N-6-(substituted-phenylcarbamoyl)adenosine-5'-uronamides as potent agonists for A(3) adenosine receptors 113
Synthesis and cardiodepressant activity of dialkyl 1,4-dihydro-2,6-dimethyl-4-(pentatomic-heteroaryl)-3,5-pyridinedicarboxylates. 2 110
Synthesis and Biological Evaluation of Highly Active 7-Anilino Triazolopyrimidines as Potent Antimicrotubule Agents 110
Comparative molecular field analysis (CoMFA) of a series of selective adenosine receptor A(2A) antagonists 109
Synthesis and pharmacological characterization of a new series of 5,7-disubstituted-[1,2,4]triazolo[1,5-a][1,3,5]triazine derivatives as adenosine receptor antagonists: A preliminary inspection of ligand-receptor recognition process 109
Synthesis and Biological Activity of a New Series of N6-Arylcarbamoyl, 2-(Ar)alkynyl-N6-arylcarbamoyl, and N6-Carboxamido Derivatives of Adenosine-5'-N-ethyluronamide as A1 and A3 Adenosine Receptor Agonists 109
Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]-pyrimidine derivatives as highly potent and selective human A(3) adenosine receptor antagonists 108
Synthesis and molecular investigation of new pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine derivates as human A3 adenosine receptor antagonists. 108
Fluorosulfonyl- and bis-(beta-chloroethyl)amino-phenylamino functionalized pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine derivatives: Irreversible antagonists at the human A(3) adenosine receptor and molecular modeling studies 108
Synthesis, biological and modeling studies of new water soluble hA3 adenosine receptor antagonists. 105
Conjugation of Dopamine and an A2A Adenosine Receptor Antagonist: a possible approach for the treatment of Parkinson’s Disease. 105
null 104
Synthesis and molecular investigation of new pyrazolo[4,3-e]1,2,4,-triazolo[1,5-c]pyrimidine derivates as human A3 adenosine receptor antagonists. 104
Synthesis, antibacterial activity and structure-activity relationships of N-substituted 4-diazopyrazole-5-carboxamides. 2 103
Current developments of A(2a) adenosine receptor antagonists 103
Synthesis, binding and thermodynamic studies of new highly selective A2A adenosine receptor antagonists 103
Heterocyclic analogs of DNA minor groove alkylating agents 102
Synthesis of the tritium labeled SCH 58261, a new non-xanthine A(2A) adenosine receptor antagonist 101
A2Aadenosine receptor antagonists as therapeutic candidates: Are they still an interesting challenge? 100
Synthesis, biological properties, and molecular modeling investigation of the first potent, selective, and water-soluble human A(3) adenosine receptor antagonist 99
Rationale design of new human adenosione A3 receptor antagonists through a CoMFA model. 98
Binding affinity of adenosine receptor agonists and antagonists at human A3 adenosine receptors 98
Synthesis, antiviral and antiproliferative activity of a new class of 5-(alkyl or arylthio)-6-vinyl uracils 98
Synthesis, cytotoxicity and antitumor activity of some new simplified pyrazole analogs of the antitumor agent CC-1065. Effect of an hydrophobic group on antitumor activity 97
Totale 15.042
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Categoria #
all - tutte 84.919
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 477
Totale 85.396
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.007 0 0 0 0 0 167 32 199 36 188 232 153
2021/20221.361 39 138 78 135 85 51 42 83 38 98 153 421
2022/20231.317 158 63 26 171 220 223 31 118 173 8 73 53
2023/2024810 70 92 34 21 71 60 20 260 12 12 10 148
2024/20252.595 75 134 196 79 329 171 55 201 395 316 379 265
2025/20264.798 660 559 1.299 1.011 901 368 0 0 0 0 0 0
Totale 18.599