IRIS
GRECO, GIOVANNI
 Distribuzione geografica
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Continente #
NA - Nord America 3.837
AS - Asia 3.557
EU - Europa 3.018
SA - Sud America 404
Continente sconosciuto - Info sul continente non disponibili 129
AF - Africa 74
OC - Oceania 5
Totale 11.024
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Nazione #
US - Stati Uniti d'America 3.678
SG - Singapore 1.695
RU - Federazione Russa 1.100
CN - Cina 586
IT - Italia 570
VN - Vietnam 541
BR - Brasile 335
HK - Hong Kong 275
UA - Ucraina 245
DE - Germania 227
NL - Olanda 227
FR - Francia 155
FI - Finlandia 123
IE - Irlanda 108
CA - Canada 99
IN - India 99
GB - Regno Unito 91
BD - Bangladesh 71
JP - Giappone 65
SE - Svezia 65
MX - Messico 36
AR - Argentina 29
IQ - Iraq 28
TR - Turchia 27
TH - Thailandia 26
PL - Polonia 24
ZA - Sudafrica 24
KR - Corea 21
PK - Pakistan 20
ES - Italia 19
EC - Ecuador 18
ID - Indonesia 16
PH - Filippine 16
BE - Belgio 10
CI - Costa d'Avorio 10
IR - Iran 9
LT - Lituania 9
AT - Austria 8
PT - Portogallo 8
IL - Israele 7
MA - Marocco 7
CO - Colombia 6
DZ - Algeria 6
JO - Giordania 6
KZ - Kazakistan 5
TT - Trinidad e Tobago 5
TW - Taiwan 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
JM - Giamaica 4
LB - Libano 4
PS - Palestinian Territory 4
PY - Paraguay 4
SA - Arabia Saudita 4
UZ - Uzbekistan 4
AU - Australia 3
CH - Svizzera 3
EG - Egitto 3
ET - Etiopia 3
KE - Kenya 3
NP - Nepal 3
PE - Perù 3
RO - Romania 3
RS - Serbia 3
SN - Senegal 3
VE - Venezuela 3
AL - Albania 2
AO - Angola 2
BA - Bosnia-Erzegovina 2
BB - Barbados 2
BW - Botswana 2
CL - Cile 2
CR - Costa Rica 2
CZ - Repubblica Ceca 2
EE - Estonia 2
KG - Kirghizistan 2
MY - Malesia 2
NI - Nicaragua 2
PA - Panama 2
SK - Slovacchia (Repubblica Slovacca) 2
SY - Repubblica araba siriana 2
TN - Tunisia 2
UY - Uruguay 2
AF - Afghanistan, Repubblica islamica di 1
AM - Armenia 1
BF - Burkina Faso 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BO - Bolivia 1
BY - Bielorussia 1
CD - Congo 1
CV - Capo Verde 1
DK - Danimarca 1
EU - Europa 1
GE - Georgia 1
GP - Guadalupe 1
GT - Guatemala 1
HN - Honduras 1
HR - Croazia 1
HT - Haiti 1
Totale 10.876
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Città #
Singapore 746
San Jose 469
Chandler 308
Hong Kong 269
Moscow 256
Jacksonville 246
Amsterdam 219
Ashburn 199
Beijing 186
Houston 170
Naples 164
Ho Chi Minh City 153
The Dalles 130
Hanoi 129
Santa Clara 121
Princeton 99
Lauterbourg 94
Woodbridge 87
Los Angeles 86
Millbury 82
Hefei 66
Dallas 63
Buffalo 62
Nanjing 54
Napoli 52
Ann Arbor 51
Boston 51
Wilmington 51
Tokyo 50
Ottawa 48
Council Bluffs 42
São Paulo 42
New York 41
Munich 35
Rome 33
Seattle 29
Frankfurt am Main 26
Redondo Beach 26
Mexico City 25
Brooklyn 24
Da Nang 23
Jiaxing 20
Warsaw 19
Denver 18
Kronberg 18
Milan 18
Nanchang 18
Orem 18
Chicago 17
Norwalk 17
Haiphong 16
Hebei 16
Montreal 16
Tianjin 16
Phoenix 15
Atlanta 14
Chennai 14
London 14
Toronto 14
Baghdad 13
Bangkok 13
Charlotte 12
Dearborn 12
Des Moines 12
Dong Ket 12
Johannesburg 12
Poplar 12
Seoul 12
Boardman 11
Delhi 11
Dublin 11
Helsinki 11
Redwood City 11
San Francisco 11
Shenyang 11
Orange 10
Biên Hòa 9
Turku 9
Casoria 8
Pune 8
Stockholm 8
Thái Nguyên 8
Ankara 7
Augusta 7
Bengaluru 7
Campinas 7
Changsha 7
Dhaka 7
Düsseldorf 7
Giugliano in Campania 7
Hải Dương 7
Rio de Janeiro 7
Brasília 6
Can Tho 6
Lahore 6
Manchester 6
Mumbai 6
New Delhi 6
Nuremberg 6
Pittsburgh 6
Totale 5.770
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Nome #
Clinical studies on topical Curcumin 219
4-amino-6-alkyloxy-2-alkylthiopyrimidine derivatives as novel non-nucleoside agonists for the adenosine A1 receptor 214
Annurca Apple oleolite as functional ingredient for the formulation of cosmetics with skin-antiageing activity 178
Clinical Studies Using Topical Melatonin 167
NAD-Driven Sirtuin Activation by Cordiceps sinensis extract: exploring the adaptogenic potential to promote skin longeviti 160
Farmacocinetica e Farmacodinamica su Basi Chimico-Fisiche 157
Design, synthesis and biological evaluation of novel N-alkyl- and N-acyl-(7-substituted-2-phenylimidazo[1,2-a][1,3,5]triazin-4-yl)amines (ITAs) as novel A1 adenosine receptor antagonists 154
Specific Targeting Highly Conserved Residues in the HIV-1 Reverse Transcriptase Primer Grip Region. Design, Synthesis, and Biological Evaluation of Novel, Potent, and Broad Spectrum NNRTIs with Antiviral Activity 149
[1,2,4]Triazino[4,3-a]benzimidazole Acetic Acid Derivatives: a New Series of Selective Aldose Reductase Inhibitors 147
Study of Benzodiazepines Receptor Sites Using a Combined QSAR-CoMFA Approach. 141
Studies on enantioselectivity of chiral 4-acetylamino-6-alkyloxy-2-alkylthiopyrimidines acting as antagonists of the human A3 adenosine receptor 140
Synthesis and antinociceptive Activity of Peptides Related to Interleukin-1b193-195 Lys-Pro-Thr. 137
3-Aryl-[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-one: a novel template for the design of highly selective A2B adenosine receptor antagonists 134
New Fluorescent 2-Phenylindolglyoxylamide Derivatives as Probes Targeting the Peripheral-Type Benzodiazepine Receptor: Design, Synthesis and Biological Evaluation. 132
Combined Use of Factorial Design and Comparative Molecular Field Analysis (CoMFA): a Case Study. 129
Synthesis and Biological Activity of Benzotriazole Derivatives Structurally Related to Trazodone. 127
Pyrrolobenzoxazepinone (PBO) Derivatives as Non-Nucleoside HIV-1 Reverse Transcriptase (RT) Inhibitors. Further Structure-Activity Relationship Studies and Identification of More Potent Broad Spectrum HIV-1 RT Inhibitors with Antiviral Activity. 125
Exploiting the indole scaffold to design compounds binding to different pharmacological targets 125
Synthesis and structure-activity relationships of 2-(substituted)-3-[3-(N,N-dimethylamino)propyl]-1,3-thiazolidin-4-ones and related analogues acting as H1-histamine antagonists 124
Quinoxalinylethylpyridylthioureas (QXPTs) as potent non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors. Further SAR studies and identification of a novel orally bioavailable hydrazine-based antiviral agent 122
Approaches to Three-Dimensional Structure-Activity Relationships, in "Reviews in Computational Chemistry", Lipkowitz, K.B. and Boyd, D.B. curatori 122
Identification of novel indole derivatives acting as inhibitors of the Keap1–Nrf2 interaction 121
Synthesis, Local Anesthetic Activity and QSAR Studies for a Set of N-[2-(alkylamino)-ethyl]benzotriazol-X-yl Acetamides. 120
Conformational studies on three Synthetic C-Terminal Fragments of the a-subunit of a Gs protein. 119
A Gα(s) carboxyl-terminal peptide prevents G(s) activation by the A(2A) adenosine receptor 116
3-Aryl-[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-one: a novel template for the design of highly selective A2B adenosine receptor antagonists 116
Novel N-(Arylalkyl)indol-3-ylglyoxylyamides Targeted as Ligands of the Benzodiazepine Receptor: Synthesis, Biological Evaluation, and Molecular Modeling Analysis of the Structure-Activity Relationships 114
Synthesis and Structure-Activity Relationships of Antiinflammatory 1-Methyl-2-(4-X-benzoyl)imidazole-5-acetic Acids. 114
Anxiolytic-like Effects of N,N-Dialkyl-2-phenylindol-3-ylglyoxylamides by Modulation of Translocator Protein Promoting Neurosteroid Biosynthesis. 113
Lezioni di Chimica Farmaceutica e Tossicologica I 112
Structure-Activity Relationships of 2-(Substituted)-3-[3-(N,N-Dimethylamino)Propyl]-1,3-Thiazolidin-4-ones and Related Analogues Acting as H1-Histamine Antagonists. 112
Comparative Molecular Field Analysis on a Set of Muscarinic Agonists. 112
A Comparative Molecular Field Analysis Model for 6-Arylpyrrolo[2,1-d][1,5]benzothiazepines Binding Selectively to the Mitochondrial Benzodiazepine Receptor. 111
Conformational analysis of the Galpha(s) protein C-terminal region 111
Novel, Highly Potent Aldose Reductase Inhibitors: Cyano-(2-oxo-2,3-dihydroindol-3-yl)-acetic Acid Derivatives 111
N,N-Dialkyl-2-phenylindol-3-ylglyoxylamides. A new class of Potent and Selective Ligands at the Peripheral Benzodiazepine Receptor. 111
Synthesis and Antiinflammatory-Analgesic Profile of 1-Methyl-2-(4-X-benzoyl)imidazole-5-carboxylic Acids. 111
3-Aryl[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-ones: A New Class of Selective A1 Adenosine Receptor Antagonists. 110
5-Alkyl-2-alkylthio-6-(2,6-dihalophenylmethyl)-3,4-dihydropyrimidin-4(3H)-ones: Novel Potent and Selective Dihydro-alkoxy-benzyl-oxopyrimidine Derivatives. 108
2-Phenyl[1,2,3]triazolo[1,2-a][1,2,4]benzotriazin-1-one derivatives as a new class of adenosine receptor antagonists 107
Synthesis and biological evaluation of 4-phenylquinazoline-2-carboxamides designed as a novel class of potent ligands of the translocator protein 106
2-(Benzimidazol-2-yl)quinoxalines: a Movel Class of Selective Antagonists at Human A(1) and A(3) Adenosine Receptors Designed by 3D Database Searching. 106
Pyrroloquinoxaline Derivatives as a New Class of Potent and Selective 5-HT3 Receptor Agonists. Synthesis, Further Structure-Activity Relationhsips and Biological Studies. 106
Novel N2-substituted pyrazolo[3,4-d]pyrimidine adenosine A3 receptor antagonists: inhibition of A3-mediated human glioblastoma cell proliferation 105
Allosteric Modulators of Human A2B Adenosine Receptor 105
5-Amino-2-phenyl[1,2,3]triazolo[1,2-a][1,2,4]benzotriazin-1-one: A Versatile Scaffold to Obtain Potent and Selective A3 Adenosine Receptor Antagonists. 103
Refinement of the Benzodiazepine Receptor Site Topology by Structure-Activity Relationships of New N-(Heteroarylmethyl)indol-3-ylglyoxylamides. 101
Deepening the Topology of the Translocator Protein Binding Site by Novel N,N-Dialkyl-2-arylindol-3-ylglyoxylamides 101
Identification of anxiolytic/non sedative agents among indol-3-ylglyoxylamides acting as functionally selective agonists at the GABAA alfa2 benzodiazepine receptor 100
Novel N-Substituted Indol-3-ylglyoxylamides Probing the LDi and L1/L2 Lipophilic Regions of the Benzodiazepine Receptor Site in Search for Subtype-Selective Ligands. 99
Structure-Affinity Relationship Studies on Benzotriazole Derivatives Binding to 5-HT Receptor Subtypes. 99
Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors. Synthesis and Biological Evaluation of Novel Quinoxalinylethylpyridylthioureas (QXPTs) as Potent Antiviral Agents. 99
Farmaci Antibatterici 98
A Concerted Study Using Binding Measurements, X-ray Structural Data and Molecular Modeling on the Stereochemical Features Responsible for the Affinity of 6-Arylpyrrolo[2,1-d][1,5]benzothiazepines toward Mitochondrial Benzodiazepine Receptors. 98
Solid-State Structure and Conformation of (Z)-2-(Phenylbenzylidene)-3-quinuclidinone, an Intermediate in the Synthesis of Quinuclidine Derivatives 97
3D-QSAR Methods in "Design of Bioactive Molecules. Three-Dimensional Techniques and Applications", Martin, Y.C. e Willet, P. curatori. 96
Molecular Structure and Conformation of the (Z) and (E) Geometric Isomers of 2-(2-Phenylbenzylidene)-3-quinuclidinone. 94
Use of Hydrophobic Substituent Constant in a Comparative Molecular Field Analysis (CoMFA) on a Set of Anilides Inhibiting the Hill Reaction. 94
3-Aryl-[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-ones: Tricyclic Heteroaromatic Derivatives as a New Class of Benzodiazepine Receptor Ligands. 93
Design, Synthesis and Biological Evaluation of Heteroaryl Diketohexenoic and Diketobutanoic Acids as HIV-1 Integrase Inhibitors Endowed with Antiretroviral Activity. 93
New Pyrrolobenzothiazepine Derivatives as Molecular Probes of the "Peripheral-Type" Benzodiazepine Receptor (PBR) Binding Site. 92
Design of novel nicotinic ligands through 3D database searching. 91
Modeling of k-Opioid Receptor/Agonists Interactions Using Pharmacophore-Based and Docking Simulations 90
A1 adenosine receptor antagonists, 3-aryl[1,2,4]triazino[4,3-a]benzimidazol-4-(10H)-ones (ATBIs) and N-alkyl and N-acyl-(7-substituted-2-phenylimidazo[1,2-a][1,3,5]triazin-4-yl)amines (ITAs): Different recognition of bovine and human binding sites 90
Computer-Assisted Design, Synthesis and Biological Evaluation of Novel Pyrrolyl Heteroaryl Sulfones Targeted at HIV-1 Reverse Transcriptase as Non-Nucleoside Inhibitors. 89
Novel ligands specific mitochondrial benzodiazepines receptors 89
Synthesis and Pharmacological Evaluation of a Set of N-[2-(Alkylamino)ethyl]benzotriazol-X-yl Isobutyramides Acting as Local Anesthetics. 89
Allosteric modulation of A2B adenosine receptors potentiate the effects of orthosteric receptor agonists to promote mesenchymal stem cell differentiation to osteoblasts 88
Derivatives of 4-Amino-6-hydroxy-2-mercaptopyrimidine as Novel, Potent, and Selective A3 Adenosine Receptor Antagonists 87
Modification of the Potent Peptide FK888 with Unusual Aminoacids: Effects on Activity on Neurokinin Receptors. 87
Shape-dependent effects in a series of aromatic nitro compounds acting as mutagenic agents on S.typhimurium TA98. 86
Synthesis and neurokinin antagonist activity of 2-benzylidene- and 2- benzyl-3-benzylamino quinuclidines 86
Synthesis and muscarinic receptor binding profiles of antagonist benzotriazole derivatives 86
Enantiomeric 4-Acylamino-6-alkyloxy-2 Alkylthiopyrimidines As Potential A3 Adenosine Receptor Antagonists: HPLC Chiral Resolution and Absolute Configuration Assignment by a Full Set of Chiroptical Spectroscopy 85
Synthesis, Structure-Activity Relationships and Molecular Modeling Studies of N-(Indol-3-ylglyoxylyl)benzylamine Derivatives Acting at the Benzodiazepine Receptor. 84
Novel Ligands Specific for Mitochondrial Benzodiazepine Receptor: 6-Arylpyrrolo[2,1-d][1,5]benzothiazepine Derivatives. Synthesis, Structure-Activity Relationships and Molecular Modeling Studies. 83
Geometrically Constrained Analogues of N-Benzylindolylglyoxylyl amides: [1,2,4]Triazino[4,3-a]benzimidazol-4(10H)-one Derivatives as Potential New Ligands at the Benzodiazepine Receptor. 81
Conformational studies on a synthetic C-terminal fragment of the alpha subunit of G(S) proteins. 81
Synthesis, Biological Activity, and SARs of Pyrrolobenzoxazine Derivatives, a New Class of Specific "Peripheral-Type" Benzodiazepine Receptor Ligands. 80
From the Pharmacophore to the Homology Model of the Benzodiazepine Receptor: The Indolyglyoxylamides Affair. 80
Computer-Aided Structure-Affinity Relationships in a Set of Piperazine and 3,8-Diazabicyclo[3.2.1]octane Derivatives Binding to the mu Opioid Receptor. 80
High Affinity Central Benzodiazepine Receptor Ligands: Synthesis and Biological Evaluation of a Series of Phenyltriazolobenzotriazindione Derivatives (PTBTs) 79
Novel Irreversible Fluorescent Probes Targeting the 18kDa Translocator Protein: Synthesis and Biological Characterization. 79
Use of the Hydrogen Bond Potential Function in a Comparative Molecular Field Analysis (CoMFA) on a Set of Benzodiazepines. 78
Synthesis and in Vitro Activities of Highly Potent Selective Tripeptide Antagonists of the Neurokinin NK-1 Receptor. 78
Spirohydantoin Derivatives of Thiopyrano[2,3-b]pyridin-4(4H)-one as Potent In Vitro and In Vivo Aldose Reductase Inhibitors 77
Linking CoMFA and Protein Homology Models of Enzyme-Inhibitor Interactions: an Application to Non-Steroidal Aromatase Inhibitors. 77
Structure-Based Design, Synthesis and Biological Evaluation of Novel Pyrrolyl Aryl Sulfones: HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitors Active at Nanomolar Concentrations. 77
Modulation of A2B adenosine receptor by 1-Benzyl-3-ketoindole derivatives 77
Structure-Based Design, Synthesis and Biological Evaluation of Conformationally Restricted Novel 2-Alkylthio-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones (S-DABOs) as Non-Nucleoside Inhibitors of HIV-1 Reverse Transcriptase. 76
Use of comparative molecular field analysis and cluster analysis in series design. 75
N’-Phenylindol-3-ylglyoxylohydrazide Derivatives: Synthesis, Structure-Activity Relationships, Molecular Modeling Studies and Pharmacological Action on Brain Benzodiazepine Receptors. 74
Synthesis of 3-(2'-Furoyl)indole Derivatives as Potential New Ligands at the Benzodiazepine Receptor, Structurally More Restrained Analogues of Indoleglyoxylylamides. 73
Biomimetic Peptides in Dermatology Interfering with Neurotransmission 72
A Critical Review of Recent CoMFA Applications. 72
Derivatives of benzimidazol-2-ylquinoline and benzimidazol-2-ylisoquinoline as selective A1 adenosine receptor antagonists with stimulant activity on human colon motility 72
Allosterism vs. Orthosterism: Recent Findings and Future Perspectives on A2B AR Physio-Pathological Implications 69
Synthesis and biological evaluation on human glioblastoma cells of novel pyrazolo[3,4-d]pyrimidine adenosine A(3) receptor antagonists 69
Novel positive allosteric modulators of A2B adenosine receptor acting as bone mineralisation promoters 68
Indole Derivatives as Probes to Study Benzodiazepine Binding Site in GABA Receptor Complex. 67
Totale 10.458
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Categoria #
all - tutte 38.675
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 38.675
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022503 0 2 5 7 4 17 1 28 106 41 117 175
2022/2023848 112 65 15 83 70 69 5 69 110 206 29 15
2023/2024499 25 67 106 17 12 21 3 61 13 15 96 63
2024/20252.584 183 170 27 31 67 96 298 150 192 261 879 230
2025/20264.622 564 309 486 442 852 203 491 251 526 280 134 84
2026/2027169 144 25 0 0 0 0 0 0 0 0 0 0
Totale 11.024