IRIS - Res&Arch Institutional Research Information System - Research & Archive

CAMAIONI, Emidio
 Distribuzione geografica
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Continente #
NA - Nord America 6.181
EU - Europa 3.937
AS - Asia 3.623
SA - Sud America 623
Continente sconosciuto - Info sul continente non disponibili 424
AF - Africa 97
OC - Oceania 2
Totale 14.887
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Nazione #
US - Stati Uniti d'America 5.971
SG - Singapore 1.699
IT - Italia 789
UA - Ucraina 675
IE - Irlanda 615
CN - Cina 505
RU - Federazione Russa 502
BR - Brasile 473
HK - Hong Kong 458
VN - Vietnam 299
DE - Germania 282
SE - Svezia 267
FR - Francia 202
FI - Finlandia 201
GB - Regno Unito 146
TR - Turchia 108
KR - Corea 97
BD - Bangladesh 91
IN - India 89
CA - Canada 87
PL - Polonia 58
AR - Argentina 49
MX - Messico 44
NL - Olanda 34
IQ - Iraq 33
JP - Giappone 33
CO - Colombia 31
CH - Svizzera 27
ID - Indonesia 27
UZ - Uzbekistan 26
BE - Belgio 23
PK - Pakistan 22
AT - Austria 21
CZ - Repubblica Ceca 20
ES - Italia 19
VE - Venezuela 19
EC - Ecuador 17
PH - Filippine 17
ZA - Sudafrica 17
CR - Costa Rica 14
JM - Giamaica 14
EG - Egitto 13
TN - Tunisia 13
CL - Cile 12
GR - Grecia 12
IL - Israele 12
MA - Marocco 12
RO - Romania 12
AZ - Azerbaigian 11
JO - Giordania 11
LB - Libano 11
SA - Arabia Saudita 11
MY - Malesia 10
PY - Paraguay 10
SV - El Salvador 10
LT - Lituania 9
NP - Nepal 8
TT - Trinidad e Tobago 8
HN - Honduras 7
SC - Seychelles 7
EU - Europa 6
OM - Oman 6
TH - Thailandia 6
CW - ???statistics.table.value.countryCode.CW??? 5
DZ - Algeria 5
GT - Guatemala 5
KZ - Kazakistan 5
LY - Libia 5
PA - Panama 5
PE - Perù 5
AE - Emirati Arabi Uniti 4
AM - Armenia 4
BG - Bulgaria 4
BO - Bolivia 4
ET - Etiopia 4
KE - Kenya 4
NI - Nicaragua 4
GP - Guadalupe 3
PR - Porto Rico 3
PT - Portogallo 3
RS - Serbia 3
SN - Senegal 3
AW - Aruba 2
BH - Bahrain 2
CI - Costa d'Avorio 2
DK - Danimarca 2
IR - Iran 2
KG - Kirghizistan 2
KW - Kuwait 2
LA - Repubblica Popolare Democratica del Laos 2
NE - Niger 2
NG - Nigeria 2
NO - Norvegia 2
PS - Palestinian Territory 2
TM - Turkmenistan 2
AF - Afghanistan, Repubblica islamica di 1
AL - Albania 1
AU - Australia 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
Totale 14.447
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Città #
Singapore 1.130
San Jose 621
Dublin 610
Chandler 556
Ashburn 505
Hong Kong 453
Jacksonville 410
San Mateo 336
Santa Clara 242
Boardman 214
Perugia 197
Council Bluffs 194
Moscow 173
Altamura 166
Princeton 160
Medford 156
Lauterbourg 140
Beijing 125
Dong Ket 119
Lawrence 105
Wilmington 104
Ann Arbor 97
Seoul 97
Los Angeles 96
Munich 87
Andover 86
New York 81
Izmir 77
The Dalles 62
Redmond 58
Des Moines 56
Ho Chi Minh City 51
São Paulo 50
Saint Petersburg 49
Dallas 45
Hanoi 42
Rome 42
Piscataway 39
Helsinki 35
Chicago 31
Milan 30
Washington 30
Tokyo 28
Montreal 27
Orem 27
Turku 27
Phoenix 26
Brooklyn 24
Norwalk 24
London 23
Brussels 21
Denver 21
San Paolo di Civitate 21
San Francisco 19
Woodbridge 19
Chennai 18
Mexico City 18
Nuremberg 18
Shanghai 17
Tashkent 17
Boston 16
Houston 16
Warsaw 16
Atlanta 15
Baghdad 15
Stockholm 15
Toronto 15
Bologna 14
Charlotte 14
Naples 14
Poplar 14
Rio de Janeiro 14
Johannesburg 13
Ankara 12
Buffalo 12
Belo Horizonte 11
Bucharest 11
Den Haag 11
Haiphong 11
Manchester 11
Redwood City 11
Seattle 11
Turin 11
Auburn Hills 10
North Bergen 10
Amsterdam 9
Baku 9
Bogotá 9
Florence 9
Medellín 9
San Diego 9
San José 9
Zhengzhou 9
Amman 8
Annapolis 8
Brasília 8
Falls Church 8
New Delhi 8
Olomouc 8
Quito 8
Totale 8.803
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Nome #
Advances in indoleamine 2,3-dioxygenase 1 medicinal chemistry 188
Computational studies in enantioselective liquid chromatography: Forty years of evolution in docking- and molecular dynamics-based simulations 175
Integrated Fragment-Based Approaches on the Route to Novel IDO1 Modulators 153
Enantioselective HPLC analysis to assist the chemical exploration of chiral imidazolines 144
Biochemical Studies on Human Ornithine Aminotransferase Support a Cell-Based Enzyme Replacement Therapy in the Gyrate Atrophy of the Choroid and Retina 143
Dexpramipexole blocks Nav1.8 sodium channels and provides analgesia in multiple nociceptive and neuropathic pain models 143
3alpha-6alpha-Dihydroxy-7alpha-fluoro-5beta-cholanoate (UPF-680), physicochemical and physiological properties of a new fluorinated bile acid that prevents 17alpha-ethynyl-estradiol-induced cholestasis in rats.. 142
Critical Assessment of a Structure-Based Screening Campaign for IDO1 Inhibitors: Tips and Pitfalls 141
1μs Molecular Dynamics Simulations to study the poisoning effect of the PARP-1 full length enzyme 136
N-Decyl-S-trityl-(R)-cysteine, a new chiral selector for "green" ligand-exchange chromatography applications 136
Spiro[2.2]pentane as a dyssymetric scaffold for conformationally constrained analogues of glutamic acid: diastereodivergent synthesis of 1-aminospiro[2.2]pentyl-1,4-dicarboxylic acids 135
6a-Ethyl-chenodeoxycholic acid (6-ECDCA), a potent and selective FXR agonist endowed with anticholestatic activity. 135
Structure-activity relationships of bisphophonate nucleotide derivatives as P2Y1 receptor antagonists and partial agonists 134
Binding Mode of 6ECDCA, a Potent Bile Acid Agonist of the Farnesoid X Receptor (FXR) 134
New Insights from Crystallographic Data: Diversity of Structural Motifs and Molecular Recognition Properties between Groups of IDO1 Structures 132
2-Substituted N-ethylcarboxamidoadenosine derivatives as high-affinity agonists at human A3 adenosine receptors 127
Spiro[2.2]pentane as a Dissymmetric Scaffold for Conformationally Constrained Analogues of Glutamic Acid: Focus on Racemic 1-Aminospiro[2.2]pentyl-1,4-dicarboxylic Acids 127
Towards New Neuroprotective Agents: Design and Synthesis of Thieno[2,3-c]-isoquinolinon-5-one as a Potent PARP-1 Inhibitor. 125
Targeting the FXR nuclear receptor through a virtual screening approach 125
BF3·Et2O-Promoted Decomposition of Cyclic α-Diazo-β-Hydroxy Ketones: Novel Insights into Mechanistic Aspects 123
Circular Hazelnut Protection by Lignocellulosic Waste Valorization for Nanopesticides Development 123
Preparation and use of nucleotide bisphosphate as P2Y antagonists 122
On the way to selective PARP-2 inhibitors. Design, synthesis, and preliminary evaluation of a series of isoquinolinone derivatives. 120
Design and synthesis of 4H-thieno[2,3-c]isoquinolin-5-one derivatives as potent PARP-1 inhibitors, on route of new antiischemic agents 120
PARP inhibitors: polypharmacology versus selective inhibition 120
Adenosine receptor agonists: Synthesis and biological evaluation of the diastereoisomers of 2-(3-hydroxy-3-phenyl-1-propyn-1-yl)NECA 119
Chiral separation of helical chromenes with chloromethyl phenylcarbamate polysaccharide-based stationary phases 119
One Key and Multiple Locks: Substrate Binding in Structures of Tryptophan Dioxygenases and Hydroxylases 119
Estimating the hydrophobicity extent of molecular fragments using reversed‐phase liquid chromatography 117
Metabotropic glutamate receptors: structure and new subtype-selective ligands 116
2-Alkenyl and 2-alkyl derivatives of adenosine and adenosine-5'-N-ethyluronamide: different affinity and selectivity of E- and Z-diastereomers at A2A adenosine receptors. 116
Adenosine deaminase inhibitors: synthesis and structure-activity relationships of 2-hydroxy-3-nonyl derivatives of azoles. 114
Design, Molecular Modeling Studies, Synthesis and Preliminary Evaluation of Novel PARP-1 Inhibitors on the Road of Antiischemic Agents 113
Chromatographic hydrophobicity index: a high-throughput tool to estimate the critical micellar concentration of bile acids 113
Targeting Wnt-driven cancers: Discovery of novel tankyrase inhibitors 113
Fragment based drug design and diversity-oriented synthesis of carboxylic acid isosteres 113
Adenosine Deaminase: Functional Implications and Different Classes of Inhibitors 111
The relationship between s. Aureus and branched-chain amino acids content in composite cow milk 111
Dexpramipexole improves bioenergetics and outcome in experimental stroke 111
2-Aralkynyl and 2-heteroalkynyl derivatives of adenosine-5'-N-ethyluronamide as selective A2a adenosine receptor agonists. 110
Chiral ligand-exchange separation and resolution ofextremely rigid glutamate analogs: 1-aminospiro[2.2]pentyl-1,4-dicarboxylicacids. 109
Investigating the allosteric reverse signalling of PARP inhibitors with microsecond molecular dynamic simulations and fluorescence anisotropy. 109
Selective PARP-2 inhibitors increase apoptosis in hippocampal slices but protect cortical cells in models of post-ischaemic brain damage 107
The Janus-faced nature of IDO1 in infectious diseases: Challenges and therapeutic opportunities 107
Effects of Molecular Dynamics and Replica Exchange Molecular Dynamics in Sampling the Conformational Space of PARP-1 107
2-Alkynyl derivatives of adenosine-5'-N-ethyluronamide: selective A2 adenosine receptor agonists with potent inhibitory activity on platelet aggregation. 107
Rat Brain Guanosine Binding Site:Biological Studies and Pseudo Receptor Construction 106
Modeling of Poly(ADP-ribose)polymerase (PARP) Inhibitors. Docking of Ligands and QSAR 106
Molecular recognition in P2 receptors: Ligand development aided by molecular modeling and mutagenesis 106
Novel PARP Inhibitors: Synthesis and Molecular Modeling Studies 105
6α-Ethyl-Chenodeoxycholic Acid (6-ECDCA), a Potent and Selective FXR Agonist Endowed with Anticholestatic Activity 105
Recent advances in urea- and thiourea-containing compounds: focus on innovative approaches in medicinal chemistry and organic synthesis 105
Rat brain guanosine binding site. Biological studies and pseudo-Receptor construction 104
Pharmacology of the highly selective A1 adenosine receptor agonist2-chloro-N6-cyclopentyladenosine. 103
Molecular determinats for metabotropic glutamate receptor activation and blockade. Molecular dynamics and electrostatic potential analysis studies 103
Investigating the allosteric reverse signalling of PARP inhibitors with microsecond molecular dynamic simulations and fluorescence anisotropy 103
Insights in the PARP1 poisoning effect 103
A Green Nanostructured Pesticide to Control Tomato Bacterial Speck Disease 103
Boosting Immunity and Management against Wheat Fusarium Diseases by a Sustainable, Circular Nanostructured Delivery Platform 102
Molecular docking and spatial coarse graining simulations as tools to investigate substrate recognition, enhancer binding and conformational transitions in indoleamine-2,3-dioxygenase (IDO). 102
Bile acids: property-activity relationship and molecular modelling studies 102
Chiral ligand-exchange separation and resolution of extremely rigid glutamate analogues: 1-aminospiro[2.2]pentyl-1,4-dicarboxylic acids 102
Dual species sphingosine-1-phosphate lyase inhibitors to combine antifungal and anti-inflammatory activities in cystic fibrosis: a feasibility study 101
Adenosine deaminase inhibitors: Structure-activity relationships in 1-deazaadenosine and erythro-9-(2-hydroxy-3-nonyl)adenine analogues 101
Discovery and characterization of novel potent PARP-1 inhibitors endowed with neuroprotective properties: From TIQ-A to HYDAMTIQ 100
Derived chromatographic indices as effective tools to study the self-aggregation process of bile acids 99
Adenosine deaminase inhibitors: synthesis, diastereoisomeric resolution and biological activity of 1-(2-hydroxy-3-nonyl)-1,2,4-triazole-3-carboxamide. 99
8-Bromo-9-etiladenine come tools per l’ottenimento di antagonisti selettivi per il recettore adenosinico A2B 99
Synthesis of New Nucleosides by coupling of chloropurines with 2- and 3-deoxy derivatives of N-methyl-D-ribofuranuronamide 98
Highlights at the gate of tryptophan catabolism: a review on the mechanism of activation and regulation of indoleamine 2,3-dioxigenase (IDO), a novel target in cancer disease 95
Concepts and Molecular Aspects in the Polypharmacology of PARP-1 Inhibitors 95
Branched-chain amino acids as potential diagnostic and prognostic disease biomarkers 95
Multi-Gram Scale Synthesis and Characterization of Mometasone Furoate EP Impurity C 95
Pharmacological inhibition of poly(ADP-ribose) polymerase (PARP) activity in PARP-1 silenced tumour cells increases chemosensitivity to temozolomide and to a N3-adenine selective methylating agent 93
Bile Acid Derivatives as Ligands of the Farnesoid X Receptor. Synthesis, Evaluation, and Structure Activity Relationship of a Series of Body and Side Chain Modified Analogs of Chenodeoxycholic Acid 93
Hydrophobic Amino Acid Content in Onions as Potential Fingerprints of Geographical Origin: The Case of Rossa da Inverno sel. Rojo Duro 93
Effects of new arylazido compounds of pyridoxal phosphate on ecto-ATPase activity of guinea pig tissues 92
Thymoquinone, a potential therapeutic agent of Nigella sativa, binds to site I of human serum albumin 92
Inhibitory Effects of 1-Deazaadenosine Analogues on HIV Replication and Adenosine Deaminase 92
On the Way to Selective PARP-2 Inhibitors: Design, Synthesis and Preliminary Evaluation of a Series of Isoquinolinone Derivatives 92
Quantitative analysis of cucurbitane-type triterpenes in Ibervillea sonorae extracts: Relationship study with their antiproliferative activity 90
Synthesis and biological activity of 3'-deoxy derivative of adenosine (5'-N-methylcarboxamide) (MECA) 89
Poly(ADP-ribose) catabolism triggers AMP-dependent mitochondrial energy failure 86
Synthesis, molecular modelling and preliminary evaluation of a series of new thioidantoine derivatives as inhibitors of indoleamine-2,3-dioxygenase (IDO) 86
Design, Synthesis, Crystallographic Studies and Preliminary Biological Appraisal of New Substituted Triazolo[4,3-b]pyridazin-8-amine Derivatives as Tankyrase Inhibitors. 86
The relationships between somatic cells and isoleucine, leucine and tyrosine content in cow milk 86
Synthesis and Biological Evaluation of 2-(3’-(1H-tetrazol-5-yl)bicyclo[1.1.1]pent-1-yl)glycine (S-TBPG), a novel mGlu1 Receptor 85
Synthesis and Receptor Affinity of Polysubstituted Adenosines 85
New insights into the evaluation of the bile salt critical micellar concentration 85
Identification of the Nicotinamide Salvage Pathway as a New Toxification Route for Antimetabolites 85
HYDAMTIQ: A New, Potent PARP-1 Inhibitor with Neuroprotective Properties 84
Combined strategies toward the design and synthesis, of novel inhibitors of indoleamine-2,3-dioxygenase (IDO) 84
Continuous Flow Synthesis of the PARP-1/2 Inhibitor HYDAMTIQ: Synthetic Strategy, Optimization, and Green Metrics Evaluation 82
Dominant Factors Affecting the Chromatographic Behaviour of Bile Acids 82
Heterocycles as Companions on Route to Drug Discovery 81
Use of RP-HPLC on a Dynamically Coated Artificial Membrane to Predict Intestinal Absorption of Bile Acids 80
Fast chromatographic determination of the bile salt critical micellar concentration 80
Sustainable Protocols for Cellulose Nanocrystals Synthesis from Tomato Waste and Their Antimicrobial Properties against Pseudomonas syringae pv. tomato 79
Exploring the effect of PARP-1 flexibility in docking studies 79
Therapeutic Potential of a Novel Poly(ADP-ribose) Polymerase Inhibitor, Hydamtiq, in Human Pancreatic and Colon Cancers 79
Totale 10.821
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Categoria #
all - tutte 68.141
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 68.141
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022958 0 0 0 54 37 11 13 405 43 51 138 206
2022/20232.058 165 391 30 121 178 215 3 83 760 7 76 29
2023/2024851 47 104 44 12 7 15 182 29 88 28 132 163
2024/20252.064 22 202 73 62 252 105 122 93 442 154 319 218
2025/20264.558 339 357 251 529 591 360 829 175 527 389 133 78
2026/20271.499 102 127 307 963 0 0 0 0 0 0 0 0
Totale 14.887