SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

SPALLUTO, Giampiero
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 1.995
AS - Asia 534
EU - Europa 502
AF - Africa 1
Totale 3.032
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 1.994
CN - Cina 315
UA - Ucraina 163
TR - Turchia 133
DE - Germania 88
GB - Regno Unito 74
SE - Svezia 72
SG - Singapore 50
FI - Finlandia 42
IT - Italia 29
HK - Hong Kong 16
AT - Austria 13
FR - Francia 7
JP - Giappone 7
IN - India 6
CZ - Repubblica Ceca 4
PL - Polonia 4
RU - Federazione Russa 4
IR - Iran 3
TW - Taiwan 3
NL - Olanda 2
BD - Bangladesh 1
CA - Canada 1
MA - Marocco 1
Totale 3.032
Salva come PNG Salva come JPEG
Città #
Chandler 241
Woodbridge 239
Houston 219
Fairfield 193
Jacksonville 187
Ann Arbor 150
Ashburn 93
Nanjing 84
Wilmington 77
Izmir 72
Beijing 66
Seattle 51
Cambridge 47
Princeton 44
Dearborn 35
Boardman 34
Singapore 30
Shanghai 22
Shenyang 21
Nanchang 18
San Diego 17
Hong Kong 16
Addison 14
Milan 14
New York 13
San Mateo 13
Vienna 13
Changsha 12
Tianjin 11
Jiaxing 10
Hebei 9
Jinan 9
Los Angeles 9
Falls Church 8
Kunming 8
Norwalk 8
Bremen 7
Taizhou 7
Helsinki 6
Zhengzhou 6
Ningbo 5
Philadelphia 5
Olomouc 4
Verona 4
Des Moines 3
Düsseldorf 3
Lanzhou 3
London 3
Orange 3
Redwood City 3
Taipei 3
Urbana 3
Auburn Hills 2
Bielefeld 2
Cosenza 2
Ferrara 2
Haikou 2
Hiroshima 2
Kilburn 2
Kraskovo 2
Mountain View 2
Munich 2
Queens 2
Redmond 2
Taiyuan 2
Amsterdam 1
Ardabil 1
Augusta 1
Bangalore 1
Berlin 1
Casablanca 1
Chengdu 1
Clifton 1
Delhi 1
Durham 1
Edinburgh 1
Flensburg 1
Guangzhou 1
Hefei 1
Irvine 1
Leawood 1
Moscow 1
Mumbai 1
New Bedfont 1
New Delhi 1
Nottingham 1
Parma 1
Pasadena 1
Pune 1
San Francisco 1
Summerside 1
Tallahassee 1
Tappahannock 1
Tower Hamlets 1
Wandsworth 1
Weihai 1
Wenzhou 1
Totale 2.233
Salva come PNG Salva come JPEG
Nome #
4-Isopropyl-2-oxazolin-5-one anion as a new convenient formyl anion equivalent for conjugate addition and aldol reactions 194
Enantioselective synthesis of (-)-meroquinene through tandem Michael reaction methodology 139
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 136
A formal total synthesis (±)-forskolin through [3+2] nitrile oxide cycloaddition chemistry 135
MASTERING BETA-KETO-ESTERS 122
4-Isopropyl-2-oxazolin-5-one anion as masked umpoled synthon for both formyl and hydroxycarbonyl anions: generation, reactivity and synthetic applications 119
5-Hydroxytryptamine-mediated effects of nicotine on endogenous GABA efflux from guinea-pig cortical slices. 117
Changes in cortical ACh and GABA outflow during morphine withdrawal involve alpha-1 and alpha-2 receptors 112
Effect of acute and subchronic nicotine treatment on cortical efflux of [3H]-D-aspartate and endogenous GABA in freely moving guinea-pigs. 110
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 104
Pharmacological and biochemical characterization of A3 adenosine receptors in Jurkat T cells. 102
New potent and selective human adenosine A3 receptor antagonists 93
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. 86
Alpha-2 adrenoreceptor-mediated decrease in gamma-aminobutyric acid outflow in cortical slices and synaptosomes during morphine tolerance. 79
[3H]-MRE 3008-F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A3 adenosine receptors. 77
Generation and cycloaddition reactions of 3-substituted-2-nitro-1,3- dienes 76
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. 76
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. 73
[H-3]MRE 3008F20: A novel antagonist radioligand for the pharmacological and biochemical characterization of human A(3) adenosine receptors 73
Alpha-1 adrenoreceptor-mediated increase in ACh release in brain slices during morphine tolerance 73
Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]-pyrimidine derivatives as highly potent and selective human A(3) adenosine receptor antagonists 70
[3H]MRE3008-F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A3 adenosine receptors. 70
Synthesis, binding and thermodynamic studies of new highly selective A2A adenosine receptor antagonists 68
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. 67
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. 65
Pharmacological and biochemical characterization of A3 adenosine receptor in Jurkat T cells. 63
Synthesis and preliminary biological evaluation of [3H]-MRE 3008F20: the first high affinity radioligand antagonist for the human A3 adenosine receptors 59
Synthesis, biological properties and molecular modelling investigation of the first potent, selective and water soluble human A3 adenosine receptor antagonist. 58
Second generation of A2A adenosine receptor antagonist: synthesis and biological evaluation 58
Synthesis and pharmacological characterization of [3H]-MRE3008F20: the first radioligand antagonist for the human A3 adenosine receptors. 57
Pyrazolo-triazolo-pyrimidine derivates as adenosine receptor ligands: a search for A2B adenosine receptor antagonists. 55
Pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine derivatives: A new pharmacological tool for the characterization of the human A(3) adenosine receptor 54
Pyrazolo [4,3-E]1,2,4-trazolo[1,5-c]pyrimidine derivatives a new class of potent and selective human A3 adenosine receptor antagonists 53
Pyrazolo[4,3-e]1,2,4-triazolo[1,5]pyrimidine derivates as irreversible antagonists at the human A3 adenosine receptor 50
Pyrazolo-triazolo-pyrimidine as human A3 adenosine receptor antagonists: influence of the substitutent at N8 pyrazole nucleus. 50
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 45
An efficient synthesis of 4-oxo-2,5-hexadienoates via Δ2-isoxazoline intermediates 10
Totale 3.048
Salva come PNG Salva come JPEG
Categoria #
all - tutte 12.846
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 12.846
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020491 0 0 23 79 47 64 66 53 38 90 22 9
2020/2021333 37 26 5 39 5 35 10 38 13 38 66 21
2021/2022375 9 40 18 26 19 10 11 21 15 30 44 132
2022/2023465 39 42 6 76 76 73 15 48 57 2 17 14
2023/2024193 21 24 10 5 27 26 8 11 5 3 1 52
2024/202534 13 20 1 0 0 0 0 0 0 0 0 0
Totale 3.048