SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

PRETI, Delia
 Distribuzione geografica
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Continente #
NA - Nord America 7.536
EU - Europa 2.861
AS - Asia 1.221
SA - Sud America 12
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 3
AF - Africa 2
Totale 11.641
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Nazione #
US - Stati Uniti d'America 7.525
DE - Germania 1.073
CN - Cina 735
UA - Ucraina 473
IT - Italia 404
TR - Turchia 374
GB - Regno Unito 264
RU - Federazione Russa 218
SE - Svezia 183
FI - Finlandia 107
VN - Vietnam 66
PL - Polonia 58
BE - Belgio 35
FR - Francia 22
HK - Hong Kong 16
CA - Canada 10
IN - India 9
KR - Corea 9
EU - Europa 6
NL - Olanda 6
BR - Brasile 4
CL - Cile 4
AR - Argentina 3
AU - Australia 3
LT - Lituania 3
PK - Pakistan 3
IE - Irlanda 2
IL - Israele 2
IR - Iran 2
JP - Giappone 2
PT - Portogallo 2
AT - Austria 1
BG - Bulgaria 1
CH - Svizzera 1
DK - Danimarca 1
EG - Egitto 1
ES - Italia 1
GR - Grecia 1
HR - Croazia 1
ID - Indonesia 1
KH - Cambogia 1
MA - Marocco 1
MC - Monaco 1
MN - Mongolia 1
MX - Messico 1
PE - Perù 1
RO - Romania 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 11.641
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Città #
Fairfield 1.094
Woodbridge 1.028
Ann Arbor 603
Ashburn 560
Houston 530
Jacksonville 530
Chandler 496
Seattle 414
Wilmington 399
Cambridge 335
Ferrara 193
Izmir 181
Beijing 176
Nanjing 151
Princeton 130
San Diego 107
Boardman 85
Shanghai 83
Dong Ket 64
Warsaw 58
Milan 57
Bremen 56
Nanchang 49
Shenyang 49
New York 41
Brussels 35
Dearborn 35
Tianjin 34
San Mateo 32
Changsha 31
Hebei 30
Falls Church 27
Jiaxing 27
Mountain View 25
Redwood City 24
London 21
Addison 20
Philadelphia 18
Zhengzhou 18
Washington 17
Kunming 16
Jinan 15
Auburn Hills 14
Hong Kong 14
Munich 14
Duncan 13
Indiana 13
Norwalk 12
Orange 12
Des Moines 11
Ferrara di Monte Baldo 11
Tappahannock 10
Guangzhou 9
Bari 8
Helsinki 8
Kilburn 8
Mcallen 8
Montréal 8
Los Angeles 7
Ningbo 7
Verona 7
Chicago 6
Haikou 6
Lanzhou 6
Hangzhou 5
Padova 5
Prescot 5
Bologna 4
Düsseldorf 4
Grassano 4
Rome 4
West Jordan 4
Xian 4
Yellow Springs 4
Augusta 3
Bournemouth 3
Chongqing 3
Leawood 3
Mysore 3
Taizhou 3
Waban 3
Wandsworth 3
Aversa 2
Buenos Aires 2
Calvizzano 2
Dublin 2
Frankfurt am Main 2
Hanoi 2
Hefei 2
Hyderabad 2
Isola della Scala 2
Rimini 2
San Jose 2
Torino 2
Toronto 2
Triggiano 2
Walnut 2
Acton 1
Amsterdam 1
Andover 1
Totale 8.206
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Nome #
1,3-Dipropyl-8-(1-phenylacetamide-1H-pyrazol-3-yl)-xanthine derivatives as highly potent and selective human A2B adenosine receptor antagonists 283
History and perspectives of A2A adenosine receptor antagonists as potential therapeutic agents 140
Synthesis and biological evaluation of 2-and 3-aminobenzo[b]thiophene derivatives as antimitotic agents and inhibitors of tubulin polymerization 137
Synthesis and preliminary biological evaluation of new anti-tubulin agents containing different benzoheterocycles 135
Naphthoquinone amino acid derivatives, synthesis and biological activity as proteasome inhibitors 134
Design, synthesis and growth inhibition activity of bis-epoxyethyl derivatives of stallimycin modified on the amidino moiety 132
New heterocyclic ligands for the adenosine receptors P1 and for the ATP receptors P2. 131
Water-Soluble Pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidines as Human A3 Adenosine Receptor Antagonists 131
Design, synthesis, and biological evaluation of novel 2-((2-(4-(substituted)phenylpiperazin-1-yl)ethyl)amino)-5'-N-ethylcarboxamidoadenosines as potent and selective agonists of the A2A adenosine receptor 131
Discovery and Optimization of a Series of 2-Aryl-4-Amino-5-(3 ',4 ',5 '-trimethoxybenzoyl)Thiazoles as Novel Anticancer Agents 130
DNA minor groove binders as potential antitumor and antimicrobial agents 129
New 2-heterocyclyl-imidazo[2,1- i ]purin-5-one derivatives as potent and selective human A 3 adenosine receptor antagonists 129
The involvement of the TRPA1 receptor in a mouse model of sympathetically maintained neuropathic pain 128
From tyrosine to glycine: Synthesis and biological activity of potent antagonists of the purinergic P2X(7) receptor 127
Hybrid molecules based on distamycin A as potential antitumor agents 127
1,3,8-Triazaspiro compounds and their use as medicaments for the treatment of reperfusion injury. 127
Novel 8-heterocyclyl xanthine derivatives in drug development - An update 126
The TRPA1 channel mediates the analgesic action of dipyrone and pyrazolone derivatives 126
Synthesis of a new series of pyrazolo[1,5-a]pyrimidines structurally related to zaleplon 125
null 124
Discovery of Novel 1,3,8-Triazaspiro[4.5]decane Derivatives That Target the c Subunit of F1/FO-Adenosine Triphosphate (ATP) Synthase for the Treatment of Reperfusion Damage in Myocardial Infarction 123
Synthesis and biological evaluation of 2-amino-3-(4-chlorobenzoyl)-4-[(4- arylpiperazin-1-yl)methyl]-5-substituted-thiophenes. Effect of the 5-modification on allosteric enhancer activity at the A1 adenosine receptor 123
New heterocyclic ligands for the adenosine receptors P1 and for the ATP receptors P2. 122
Synthesis and biological evaluation of 2-(3 ',4 ',5 '-trimethoxybenzoyl)-3-amino 5-aryl thiophenes as a new class of tubulin inhibitors 121
Synthesis and biological evaluation of 2-amino-3-(3',4',5'-trimethoxyphenylsulfonyl)-5-aryl thiophenes as a new class of antitubulin agents 121
null 121
Pyrazolo [4,3-e][1,2,4]triazolo[1,5-c]pyrimidine template: Organic and medicinal chemistry approach 120
Recent improvements in the development of A2B adenosine receptor agonists. 120
7-Substituted-pyrrolo[3,2-d]pyrimidine-2,4-dione derivatives as antagonists of the transient receptor potential ankyrin 1 (TRPA1) channel: A promising approach for treating pain and inflammation 120
null 120
null 118
A3 adenosine receptor antagonists: History and future perspectives 117
Structure-and conformation-Activity studies of nociceptin/orphanin FQ receptor dimeric ligands 117
N-6-[(Hetero)aryl/(cyclo)alkyl-carbamoyi-methoxy-phenyl]-(2chloro)-5 '-N-ethylearboxamido-adenosines: The first example of adenosine-related structures with potent agonist activity at the human A(2B) adenosine receptor 116
Synthesis and Biological Evaluation of 1-Methyl-2-(3’,4’,5’-Trimethoxybenzoyl)-3-Amino Indoles as a New Class of Antimitotic Agents and Tubulin Inhibitors 114
Transient receptor potential ankyrin receptor 1 is a novel target for pro-tussive agents 113
Microwave-assisted synthesis of substituted 2,4-diarylthiazoles and their evaluation as anticancer agents 112
null 112
Medicinal Chemistry of A3 Adenosine Receptor Modulators: Pharmacological Activities and Therapeutic Implications 111
Synthesis and biological evaluation of 2-amino-3-(4-chlorobenzoyl)-4-[N- (substituted) piperazin-1-yl]thiophenes as potent allosteric enhancers of the A1 adenosine receptor 111
Allosteric enhancers for A(1) adenosine receptor 110
null 110
Recent improvements in the development of A2B adenosine receptor agonists 110
Transient Receptor Potential Ankyrin 1 (TRPA1) Channel as Emerging Target for Novel Analgesics and Anti-Inflammatory Agents 110
7-Oxo-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxamides as Selective CB2 Cannabinoid Receptor Ligands: Structural Investigations around a Novel Class of Full Agonists 110
Oxaliplatin elicits mechanical and cold allodynia in rodents via TRPA1 receptor stimulation 109
null 109
Structure-activity relationship studies of a new series of imidazo[2,1-f]purinones as potent and selective A(3) adenosine receptor antagonists. 108
Concise Synthesis and Biological Evaluation of 2-Aroyl-5-Amino Benzo[b]thiophene Derivatives As a Novel Class of Potent Antimitotic Agents 108
Synthesis and Biological Evaluation of Novel Allosteric Enhancers of the A1 Adenosine Receptor Based on 2-Amino-3-(4’-Chlorobenzoyl)-4-Substituted-5-Arylethynyl Thiophene 108
Hybrid molecules between distamycin A and active moieties of antitumor agents 108
The blockade of transient receptor potential ankirin 1 (TRPA1) signalling mediates antidepressant- and anxiolytic-like actions in mice 108
Ozone-induced hypertussive responses in rabbits and guinea pigs 105
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 103
null 103
Activation of TRPA1 on dural afferents: a potential mechanism of headache pain 102
Neuropeptide S receptor ligands: a patent review (2005-2016) 102
The P2X7 receptor as a therapeutic target. 101
Structure-activity relationships of 2-amino-3-aroyl-4-[(4-arylpiperazin-1- yl)methyl]thiophenes. Part 2: Probing the influence of diverse substituents at the phenyl of the arylpiperazine moiety on allosteric enhancer activity at the A 1 adenosine receptor 101
Recent developments in the field of adenosine receptor ligands. 99
The 'headache tree' via umbellulone and TRPA1 activates the trigeminovascular system. 99
Design, synthesis, and biological evaluation of new 8-heterocyclic xanthine derivatives as highly potent and selective human A(2B) adenosine receptor antagonists 98
New 2-arylpyrazolo[4,3-c]quinoline derivates as potent and selective human A3 adenosine receptor antagonists 97
Structure-activity relationships around the KN-62, a potent antagonist of the P2X(7)receptor 96
null 96
Pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidines and linked heterocycles as template for the adenosine receptor antagonism: medicinal chemistry approach and SAR considerations. 95
Synthesis and biological evaluation of 2-substituted-4-(3 ',4 ',5 '-trimethoxyphenyl)-5-aryl thiazoles as anticancer agents 94
Acetaminophen, via its reactive metabolite N-acetyl-p-benzo-quinoneimine and transient receptor potential ankyrin-1 stimulation, causes neurogenic inflammation in the airways and other tissues in rodents 94
Biased Agonism at Nociceptin/Orphanin FQ Receptors: A Structure Activity Study on N/OFQ(1-13)-NH2 94
[H-3]-MRE 2029-F20, a selective antagonist radioligand for the human A(2B) adenosine receptors 92
null 92
Synthesis and biological evaluation of novel N-6-[4-(substituted) sulfonamidophenylcarbamoyl]adenosine-5 '-uronamides as A(3) adenosine receptor agonists 91
Synthesis and biological evaluation of 2-aroyl-4-phenyl-5-hydroxybenzofurans as a new class of antitubulin agents 91
Tetrabranched Hetero-Conjugated Peptides as Bifunctional Agonists of the NOP and Mu Opioid Receptors 90
Microwave-assisted synthesis of thieno[2,3-c]pyridine derivatives as a new series of allosteric enhancers at the adenosine A(1) receptor 89
Recent developments in the field of A(2A) and A(3) adenosine receptor antagonists 87
null 87
New strategies for the synthesis of A(3) adenosine receptor antagonists 87
null 87
Hybrid molecules containing benzo[4,5]imidazo[1,2-d][1,2,4]thiadiazole and alpha-bromoacryloyl moieties as potent apoptosis inducers on human myeloid leukaemia cells 86
Synthesis and Biological Activity of Peptide α-Ketoamide Derivatives as Proteasome Inhibitors 86
TRP channels as therapeutic targets in airway disorders: a patent review 85
Design, synthesis, and biological evaluation of C-9- and C-2-substituted pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c] pyrimidines as new A(2A) and A(3) adenosine receptors antagonists 84
null 84
New pyrrolo[2,1-f]purine-2,4-dione and imidazo[2,1-f]purine-2,4-dione derivatives as potent and selective human A(3) adenosine receptor antagonists 83
Preparation of fused purine derivatives as adenosine A3 receptor modulators. 83
null 83
null 82
Preparation of fused purine derivatives as adenosine A3 receptor modulators. 81
Design, synthesis and biological evaluation of hybrid molecules containing conjugated styryl ketone and α-bromoacryloyl moieties 80
Discovery of novel fetal hemoglobin inducers for β-thalassemia by small chemical library screening 80
Recent developments in the field of A2B and A3 adenosine receptors antagonists 79
Pharmacological profile of the neuropeptide S receptor: Dynamic mass redistribution studies 77
Adenosine Modulates HIF-1 alpha, VEGF, IL-8, and Foam Cell Formation in a Human Model of Hypoxic Foam Cells 75
New 2-arylpyrazolo[4,3-c]quinoline derivatives as potent and selective human A(3) adenosine receptor antagonists 75
The acyl-glucuronide metabolite of ibuprofen has analgesic and anti-inflammatory effects via the TRPA1 channel 75
Recent improvements in the field of A(3) adenosine receptor ligands 74
Role of TRPA1 receptors in skin inflammation induced by volatile chemical irritants in mice 74
null 73
Ligands for A(2B) adenosine receptor subtype 72
Totale 10.655
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Categoria #
all - tutte 39.431
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.019
Totale 40.450
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20191.145 0 0 0 0 0 0 0 0 0 255 355 535
2019/20202.441 374 93 79 352 178 284 223 237 206 228 141 46
2020/20211.838 181 130 90 183 85 179 83 215 59 280 185 168
2021/20221.345 60 127 137 54 80 61 84 57 46 104 139 396
2022/20231.259 130 84 23 180 238 169 52 92 169 9 63 50
2023/2024584 58 96 49 25 60 131 40 88 25 12 0 0
Totale 11.814