IRIS
GRECO, GIOVANNI
 Distribuzione geografica
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Continente #
NA - Nord America 3.675
AS - Asia 3.517
EU - Europa 2.990
SA - Sud America 398
AF - Africa 73
OC - Oceania 5
Continente sconosciuto - Info sul continente non disponibili 2
Totale 10.660
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Nazione #
US - Stati Uniti d'America 3.526
SG - Singapore 1.693
RU - Federazione Russa 1.100
CN - Cina 585
IT - Italia 548
VN - Vietnam 540
BR - Brasile 330
HK - Hong Kong 275
UA - Ucraina 245
DE - Germania 227
NL - Olanda 227
FR - Francia 154
FI - Finlandia 123
IE - Irlanda 108
IN - India 99
CA - Canada 96
GB - Regno Unito 91
JP - Giappone 65
SE - Svezia 65
BD - Bangladesh 37
MX - Messico 35
AR - Argentina 29
IQ - Iraq 28
TR - Turchia 27
TH - Thailandia 26
PL - Polonia 24
ZA - Sudafrica 24
KR - Corea 21
PK - Pakistan 20
EC - Ecuador 17
ES - Italia 16
PH - Filippine 16
ID - Indonesia 14
CI - Costa d'Avorio 10
BE - Belgio 9
IR - Iran 9
LT - Lituania 9
AT - Austria 8
PT - Portogallo 8
IL - Israele 7
MA - Marocco 7
CO - Colombia 6
JO - Giordania 6
DZ - Algeria 5
KZ - Kazakistan 5
TW - Taiwan 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
LB - Libano 4
PS - Palestinian Territory 4
PY - Paraguay 4
SA - Arabia Saudita 4
TT - Trinidad e Tobago 4
UZ - Uzbekistan 4
AU - Australia 3
CH - Svizzera 3
EG - Egitto 3
ET - Etiopia 3
JM - Giamaica 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
BW - Botswana 2
CL - Cile 2
CZ - Repubblica Ceca 2
EE - Estonia 2
KG - Kirghizistan 2
MY - Malesia 2
NI - Nicaragua 2
PA - Panama 2
SY - Repubblica araba siriana 2
TN - Tunisia 2
UY - Uruguay 2
AF - Afghanistan, Repubblica islamica di 1
AM - Armenia 1
BB - Barbados 1
BF - Burkina Faso 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BO - Bolivia 1
BY - Bielorussia 1
CD - Congo 1
CR - Costa Rica 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
HU - Ungheria 1
Totale 10.641
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Città #
Singapore 744
San Jose 468
Chandler 308
Hong Kong 269
Moscow 256
Jacksonville 246
Amsterdam 219
Ashburn 186
Beijing 186
Houston 168
Naples 164
Ho Chi Minh City 153
The Dalles 130
Hanoi 128
Santa Clara 113
Princeton 99
Lauterbourg 94
Woodbridge 87
Los Angeles 83
Millbury 82
Hefei 66
Buffalo 62
Dallas 62
Nanjing 54
Napoli 52
Ann Arbor 51
Boston 51
Wilmington 51
Tokyo 50
Ottawa 48
São Paulo 41
Munich 35
New York 35
Rome 33
Seattle 29
Frankfurt am Main 26
Redondo Beach 26
Mexico City 24
Brooklyn 23
Da Nang 23
Jiaxing 20
Warsaw 19
Council Bluffs 18
Denver 18
Kronberg 18
Nanchang 18
Orem 18
Norwalk 17
Chicago 16
Haiphong 16
Hebei 16
Montreal 16
Tianjin 16
Milan 15
Phoenix 15
Chennai 14
London 14
Atlanta 13
Baghdad 13
Bangkok 13
Dearborn 12
Des Moines 12
Dong Ket 12
Johannesburg 12
Poplar 12
Seoul 12
Toronto 12
Boardman 11
Charlotte 11
Delhi 11
Dublin 11
Helsinki 11
Redwood City 11
Shenyang 11
Orange 10
Biên Hòa 9
San Francisco 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 5.696
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Nome #
4-amino-6-alkyloxy-2-alkylthiopyrimidine derivatives as novel non-nucleoside agonists for the adenosine A1 receptor 213
Clinical studies on topical Curcumin 207
Farmacocinetica e Farmacodinamica su Basi Chimico-Fisiche 155
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 151
Annurca Apple oleolite as functional ingredient for the formulation of cosmetics with skin-antiageing activity 148
NAD-Driven Sirtuin Activation by Cordiceps sinensis extract: exploring the adaptogenic potential to promote skin longeviti 145
[1,2,4]Triazino[4,3-a]benzimidazole Acetic Acid Derivatives: a New Series of Selective Aldose Reductase Inhibitors 145
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 145
Studies on enantioselectivity of chiral 4-acetylamino-6-alkyloxy-2-alkylthiopyrimidines acting as antagonists of the human A3 adenosine receptor 140
Study of Benzodiazepines Receptor Sites Using a Combined QSAR-CoMFA Approach. 137
Synthesis and antinociceptive Activity of Peptides Related to Interleukin-1b193-195 Lys-Pro-Thr. 136
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 133
New Fluorescent 2-Phenylindolglyoxylamide Derivatives as Probes Targeting the Peripheral-Type Benzodiazepine Receptor: Design, Synthesis and Biological Evaluation. 129
Combined Use of Factorial Design and Comparative Molecular Field Analysis (CoMFA): a Case Study. 128
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
Synthesis and Biological Activity of Benzotriazole Derivatives Structurally Related to Trazodone. 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
Exploiting the indole scaffold to design compounds binding to different pharmacological targets 123
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
Synthesis, Local Anesthetic Activity and QSAR Studies for a Set of N-[2-(alkylamino)-ethyl]benzotriazol-X-yl Acetamides. 119
Conformational studies on three Synthetic C-Terminal Fragments of the a-subunit of a Gs protein. 118
Identification of novel indole derivatives acting as inhibitors of the Keap1–Nrf2 interaction 117
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
A Gα(s) carboxyl-terminal peptide prevents G(s) activation by the A(2A) adenosine receptor 115
Synthesis and Structure-Activity Relationships of Antiinflammatory 1-Methyl-2-(4-X-benzoyl)imidazole-5-acetic Acids. 114
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 113
Anxiolytic-like Effects of N,N-Dialkyl-2-phenylindol-3-ylglyoxylamides by Modulation of Translocator Protein Promoting Neurosteroid Biosynthesis. 113
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
Lezioni di Chimica Farmaceutica e Tossicologica I 111
Synthesis and Antiinflammatory-Analgesic Profile of 1-Methyl-2-(4-X-benzoyl)imidazole-5-carboxylic Acids. 111
Novel, Highly Potent Aldose Reductase Inhibitors: Cyano-(2-oxo-2,3-dihydroindol-3-yl)-acetic Acid Derivatives 110
N,N-Dialkyl-2-phenylindol-3-ylglyoxylamides. A new class of Potent and Selective Ligands at the Peripheral Benzodiazepine Receptor. 110
A Comparative Molecular Field Analysis Model for 6-Arylpyrrolo[2,1-d][1,5]benzothiazepines Binding Selectively to the Mitochondrial Benzodiazepine Receptor. 109
3-Aryl[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-ones: A New Class of Selective A1 Adenosine Receptor Antagonists. 108
Comparative Molecular Field Analysis on a Set of Muscarinic Agonists. 108
Clinical Studies Using Topical Melatonin 107
5-Alkyl-2-alkylthio-6-(2,6-dihalophenylmethyl)-3,4-dihydropyrimidin-4(3H)-ones: Novel Potent and Selective Dihydro-alkoxy-benzyl-oxopyrimidine Derivatives. 107
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
Pyrroloquinoxaline Derivatives as a New Class of Potent and Selective 5-HT3 Receptor Agonists. Synthesis, Further Structure-Activity Relationhsips and Biological Studies. 106
Synthesis and biological evaluation of 4-phenylquinazoline-2-carboxamides designed as a novel class of potent ligands of the translocator protein 105
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. 105
Allosteric Modulators of Human A2B Adenosine Receptor 105
Conformational analysis of the Galpha(s) protein C-terminal region 104
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
Novel N2-substituted pyrazolo[3,4-d]pyrimidine adenosine A3 receptor antagonists: inhibition of A3-mediated human glioblastoma cell proliferation 102
Deepening the Topology of the Translocator Protein Binding Site by Novel N,N-Dialkyl-2-arylindol-3-ylglyoxylamides 101
Refinement of the Benzodiazepine Receptor Site Topology by Structure-Activity Relationships of New N-(Heteroarylmethyl)indol-3-ylglyoxylamides. 100
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
Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitors. Synthesis and Biological Evaluation of Novel Quinoxalinylethylpyridylthioureas (QXPTs) as Potent Antiviral Agents. 99
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
Farmaci Antibatterici 96
Structure-Affinity Relationship Studies on Benzotriazole Derivatives Binding to 5-HT Receptor Subtypes. 95
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. 95
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
Molecular Structure and Conformation of the (Z) and (E) Geometric Isomers of 2-(2-Phenylbenzylidene)-3-quinuclidinone. 93
New Pyrrolobenzothiazepine Derivatives as Molecular Probes of the "Peripheral-Type" Benzodiazepine Receptor (PBR) Binding Site. 92
Modeling of k-Opioid Receptor/Agonists Interactions Using Pharmacophore-Based and Docking Simulations 90
Design, Synthesis and Biological Evaluation of Heteroaryl Diketohexenoic and Diketobutanoic Acids as HIV-1 Integrase Inhibitors Endowed with Antiretroviral Activity. 90
Design of novel nicotinic ligands through 3D database searching. 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
Allosteric modulation of A2B adenosine receptors potentiate the effects of orthosteric receptor agonists to promote mesenchymal stem cell differentiation to osteoblasts 88
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 88
Synthesis and Pharmacological Evaluation of a Set of N-[2-(Alkylamino)ethyl]benzotriazol-X-yl Isobutyramides Acting as Local Anesthetics. 88
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
Derivatives of 4-Amino-6-hydroxy-2-mercaptopyrimidine as Novel, Potent, and Selective A3 Adenosine Receptor Antagonists 85
Synthesis and neurokinin antagonist activity of 2-benzylidene- and 2- benzyl-3-benzylamino quinuclidines 85
Synthesis and muscarinic receptor binding profiles of antagonist benzotriazole derivatives 85
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
Conformational studies on a synthetic C-terminal fragment of the alpha subunit of G(S) proteins. 81
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. 80
Novel Ligands Specific for Mitochondrial Benzodiazepine Receptor: 6-Arylpyrrolo[2,1-d][1,5]benzothiazepine Derivatives. Synthesis, Structure-Activity Relationships and Molecular Modeling Studies. 80
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
Synthesis, Structure-Activity Relationships and Molecular Modeling Studies of N-(Indol-3-ylglyoxylyl)benzylamine Derivatives Acting at the Benzodiazepine Receptor. 79
Novel Irreversible Fluorescent Probes Targeting the 18kDa Translocator Protein: Synthesis and Biological Characterization. 79
High Affinity Central Benzodiazepine Receptor Ligands: Synthesis and Biological Evaluation of a Series of Phenyltriazolobenzotriazindione Derivatives (PTBTs) 78
Use of the Hydrogen Bond Potential Function in a Comparative Molecular Field Analysis (CoMFA) on a Set of Benzodiazepines. 77
Spirohydantoin Derivatives of Thiopyrano[2,3-b]pyridin-4(4H)-one as Potent In Vitro and In Vivo Aldose Reductase Inhibitors 76
Linking CoMFA and Protein Homology Models of Enzyme-Inhibitor Interactions: an Application to Non-Steroidal Aromatase Inhibitors. 76
Synthesis and in Vitro Activities of Highly Potent Selective Tripeptide Antagonists of the Neurokinin NK-1 Receptor. 76
Modulation of A2B adenosine receptor by 1-Benzyl-3-ketoindole derivatives 76
Structure-Based Design, Synthesis and Biological Evaluation of Novel Pyrrolyl Aryl Sulfones: HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitors Active at Nanomolar Concentrations. 74
Use of comparative molecular field analysis and cluster analysis in series design. 73
N’-Phenylindol-3-ylglyoxylohydrazide Derivatives: Synthesis, Structure-Activity Relationships, Molecular Modeling Studies and Pharmacological Action on Brain Benzodiazepine Receptors. 73
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. 73
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
Biomimetic Peptides in Dermatology Interfering with Neurotransmission 69
Synthesis and biological evaluation on human glioblastoma cells of novel pyrazolo[3,4-d]pyrimidine adenosine A(3) receptor antagonists 69
Synthesis of 3-(2'-Furoyl)indole Derivatives as Potential New Ligands at the Benzodiazepine Receptor, Structurally More Restrained Analogues of Indoleglyoxylylamides. 68
Novel positive allosteric modulators of A2B adenosine receptor acting as bone mineralisation promoters 67
Allosterism vs. Orthosterism: Recent Findings and Future Perspectives on A2B AR Physio-Pathological Implications 67
Osteoblast differentiation and survival: A role for A2B adenosine receptor allosteric modulators 67
Totale 10.225
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Categoria #
all - tutte 36.190
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 36.190
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202113 0 0 0 0 0 0 0 0 0 0 0 13
2021/2022514 11 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
2025/20264.554 564 309 486 442 852 203 491 251 526 280 134 16
Totale 10.787