CINECA IRIS Institutional Research Information System

MARINI, ANNA MARIA
 Distribuzione geografica
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Continente #
NA - Nord America 7.408
EU - Europa 3.823
AS - Asia 1.189
AF - Africa 104
OC - Oceania 23
SA - Sud America 10
Totale 12.557
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Nazione #
US - Stati Uniti d'America 7.200
IT - Italia 1.520
SE - Svezia 809
CN - Cina 613
DE - Germania 408
BG - Bulgaria 329
TR - Turchia 274
CA - Canada 208
GB - Regno Unito 205
UA - Ucraina 155
FI - Finlandia 131
VN - Vietnam 124
AT - Austria 111
IN - India 67
CH - Svizzera 53
CI - Costa d'Avorio 52
HK - Hong Kong 45
RU - Federazione Russa 35
SG - Singapore 32
NG - Nigeria 30
BE - Belgio 24
AU - Australia 19
FR - Francia 19
SN - Senegal 12
EG - Egitto 10
JP - Giappone 10
NL - Olanda 9
IR - Iran 6
BR - Brasile 5
ID - Indonesia 5
EC - Ecuador 4
IE - Irlanda 4
NZ - Nuova Zelanda 4
KR - Corea 3
CZ - Repubblica Ceca 2
GR - Grecia 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
AZ - Azerbaigian 1
BD - Bangladesh 1
BN - Brunei Darussalam 1
CL - Cile 1
DK - Danimarca 1
ES - Italia 1
GE - Georgia 1
HR - Croazia 1
JO - Giordania 1
KZ - Kazakistan 1
MY - Malesia 1
PL - Polonia 1
RO - Romania 1
SA - Arabia Saudita 1
SI - Slovenia 1
TW - Taiwan 1
Totale 12.557
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Città #
Woodbridge 1.262
Ann Arbor 992
Houston 859
Serra 611
Chandler 606
Fairfield 563
Milan 404
Ashburn 372
Sofia 329
Izmir 270
Beijing 237
Seattle 237
Jacksonville 227
Wilmington 223
Ottawa 197
New York 192
Cambridge 167
Princeton 144
Nanjing 132
Lawrence 131
Medford 107
London 100
Vienna 92
Dearborn 84
Des Moines 80
Dong Ket 68
Abidjan 52
Bern 51
Hong Kong 45
Rome 45
Düsseldorf 43
Nanchang 42
Jüchen 39
Frankfurt am Main 38
Rho 38
San Diego 32
Bremen 30
Lagos 30
Boulder 29
Kunming 29
Redwood City 29
Los Angeles 28
Pune 28
Shenyang 25
Brussels 24
Hebei 21
Nürnberg 18
Washington 18
Ogden 17
Auburn Hills 16
Changsha 16
Hefei 16
Norwalk 15
Tianjin 14
Florence 13
Lancaster 13
Pisa 13
Dakar 12
Jiaxing 12
Boardman 11
Hangzhou 10
Jinan 10
Orange 10
Falls Church 9
San Francisco 9
Sydney 8
Tappahannock 8
Toronto 8
Guangzhou 7
Cascina 6
Indiana 6
Melbourne 6
Augusta 5
Citta 5
Dallas 5
Omaha 5
Vicopisano 5
Ardabil 4
Lucca 4
Marseille 4
Massa 4
Mumbai 4
Phoenix 4
San Mateo 4
Saronno 4
Singapore 4
Vercelli 4
Zhengzhou 4
Amsterdam 3
Auckland 3
Cecina 3
Chehalis 3
Chicago 3
Chiyoda-ku 3
Chongqing 3
Dublin 3
Helsinki 3
Kolkata 3
Lanzhou 3
Ningbo 3
Totale 9.790
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Nome #
1,2-Benzisothiazole Derivatives Bearing 4-, 5-, or 6-Alkyl/arylcarboxamide Moieties Inhibit Carbonic Anhydrase Isoform IX (CAIX) and Cell Proliferation under Hypoxic Conditions 313
Benzofuroxane Derivatives as Multi Effective Agents for the Treatment of Cardiovascular Diabetic Complications. Synthesis, Functional Evaluation, and Molecular Modeling Studies 197
Exploiting the Pyrazolo[3,4-d]pyrimidin-4-one ring system as a useful template to obtain potent adenosine deaminase inhibitors, 177
3-Aryl[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-ones: A New Class of Selective A1 Adenosine Receptor Antagonists 165
Deepening the Topology of the Translocator Protein Binding Site by Novel N,N-Dialkyl-2-arylindol-3-ylglyoxylamides 164
3-aryl-[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-ones: Tricyclic heteroaromatic derivatives as a new class of benzodiazepine receptor ligands 162
Identification of Anxiolytic/Nonsedative Agents among Indol-3-ylglyoxylamides Acting as Functionally Selective Agonists at the γ-Aminobutyric Acid-A (GABAA) α2 Benzodiazepine Receptor 159
Synthesis of a Novel Purine-Containing Heterocyclic Ring System: 8,10-Dimethylindolo[2',3':5,6][1,2,4]triazino[4,3-f]purine-9,11(8H,10H,13H)dione 144
SPECIFIC-INHIBITION OF BENZODIAZEPINE RECEPTOR-BINDING BY SOME N-(INDOL-3-YLGLYOXYLYL)AMINO ACID-DERIVATIVES 143
Synthesis of some Substituted Pyrido[1,2-a]pyrimidin-4-ones and 1,8-Naphthyridines. 142
Refinement of Structure-activity Relationships of the Triazinobenzimidazole A1AR Antagonists 142
Geometrically Constrained Analogues N-Benzylindolylglyoxylylamides: [1,2,4]Triazino[4,3-a]benzimidazol-4(10H)-one Derivatives as Potential New Ligands at the Benzodiazepine Receptor. 141
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 138
FACILE SYNTHESIS OF 3-SUBSTITUTED[1,2,4]TRIAZINO[3,4-F]PURINE-4,6,8-TRIONE DERIVATIVES 137
N '-phenylindol-3-ylglyoxylohydrazide derivatives: Synthesis, structure-activity relationships, molecular modeling studies, and pharmacological action on brain benzodiazepine receptors 135
Recent Advances in the Development of Dual Topoisomerase I and II Inhibitors as Anticancer Drugs 135
Synthesis of Purinobenzodiazepine and Purinobenzotriazocine derivatives, two new heterocyclic ring systems. 133
“Synthesis and antiproliferative evaluation of new substituted Benzothiopyrano[4,3-c] condensed ring systems” 132
Benzothiopyranoindole-Based Antiproliferative Agents: Synthesis, Cytotoxicity, Nucleic Acids Interaction, and Topoisomerases Inhibition Properties. 132
N-(Indol-3-ylglyoxylyl)methionine derivatives: preparation and gastric anti-secretory activity. 131
Benzo[d]isothiazoles and Matrix Metalloproteinases. Searching for Novel and Selective Inhibitors of MMP9 131
Sulfonamides incorporating heteropolycyclic scaffolds show potent inhibitory action against carbonic anhydrase isoforms I, II, IX and XII 129
Medicinal chemistry of indolylglyoxylamide TSPO high affinity ligands with anxiolytic-like effects 128
An approach to novel fused triazole or tetrazole derivatives starting from Benzimidazo[1,2-a]quinazoline-5(7H)-one and 5,7-Dihydro-5-oxopyrido[3',2':5,6]pyrimido[1,2-a]benzimidazole 127
Novel N(2)-Substituted Pyrazolo[3,4-d]pyrimidine Adenosine A(3) Receptor Antagonists: Inhibition of A(3)-Mediated Human Glioblastoma Cell Proliferation (dagger) 125
SPECIFIC-INHIBITION OF BENZODIAZEPINE RECEPTOR-BINDING BY SOME N-(INDOL-3-YLGLYOXYLYL)AMINO ACID-DERIVATIVES - STEREOSELECTIVE INTERACTIONS 124
Synthesis of Pyrimido[1,2-a]benzimidazol-4(10H)-one Derivatives and Evaluation of their Interactions with DNA 123
Novel Potent and Selective Human Adenosine A3 Receptor Antagonists Containing the Pyrazolo[3,4-d]pyrimidine Ring System. Synthesis and Biological Evaluation 122
Phenylpyrazolo[1,5-a]quinazolin-5(4H)-one: a suitable scaffold for the development of non-camptothecin Topoisomerase I (Top1) inhibitors 122
Synthesis of novel pyrido[3',2':5,6]thiopyrano[3,2-b]indol-5(6H)-ones and 6H-pyrido[3',2':5,6]thiopyrano[4,3-b]quinolines,two new heterocyclic systems. 121
Structure-Based Optimization of Tyrosine Kinase Inhibitor CLM3. Design, Synthesis, Functional Evaluation, and Molecular Modeling Studies. 120
"2-Phenyl[1,2,3]triazole[1,2-a][1,2,4]triazin-1,5(6H)-dione: a derivative of a new tricyclic heteroaromatic system with high affinity at the benzodiazepine receptor" 119
Studies in search for selective ligands for GABAA/BzR receptor subtypes: synthesis and biological evaluation of 4'-modified N-(benzyl)indol-3-ylglyoxylamides 119
Synthesis of novel 1,4-dihydropyrido[3’,2’:5,6]thiopyrano[4,3-c]-pyrazoles and 5H-pyrido[3’,2’:5,6]thiopyrano[4,3-d]pyrimidines as potential antiproliferative agents 117
Acetic acid aldose reductase inhibitors bearing a five-membered heterocyclic core with potent topical activity in a visual impairment rat model 117
Medicinal chemistry of indolylglyoxylamide GABAA/BzR high affinity ligands: identification of novel anxiolytic/non sedative agents 117
Synthesis of New Heterocyclic Ring Systems via [1,3,5]Triazino[1,2-a]benzimidazole Derivatives 116
Novel Pyrazolo[3,4-d]pyrimidine Derivatives as ATP-competitive Inhibitors of the Epidermal Growth Factor Receptor Protein Tyrosine Kinase 115
Synthesis and antiinflammatory Properties of 2-Methylaminobenzimidazole Derivatives 114
Synthesis, DNA binding and in vitro antiproliferative activity of purinoquinazoline, pyridopyrimidopurine and pyridopyrimidobenzimidazole derivatives as potential antitumor agents 114
Pyrido[1,2-a]pyrimidin-4-one derivatives as a novel class of selective aldose reductase inhibitors exhibiting antioxidant activity 114
Synthesis and biological activity of 1,4-dihydrobenzothiopyrano[4,3-c]pyrazole derivatives, novel pro-apoptotic mitochondrial targeted agents 112
Investigation of new 2-aryl substituted Benzothiopyrano[4,3-d]pyrimidines as kinase inhibitors targeting vascular endothelial growth factor receptor 2 112
Naphtho[1,2-d]isothiazole Acetic Acid Derivatives as a Novel Class of Selective Aldose Reductase Inhibitors 111
Pyrazolo[3,4,-d]pyrimidine-4-one Derivatives as Novel and Potent Inhibitors of Adenosine Deaminase 110
Synthesis of purinobenzothiazine and pyridothiazinopurine derivatives. Two new heterocyclic ring systems 110
Mitochondrial permeability transition induced by novel pyridothiopyranopyrimidine derivatives: Potential new antimitochondrial antitumour agents. 110
Small Molecules Containing the Benzo[d]isotiazole Ring System as Novel ATP-Competitive Inhibitors of Epidermal Growth Factor Receptor protein Tyrosine Kinase 107
Arylsulfonamide inhibitors of aggrecanases as potential therapeutic agents for osteoarthritis: Synthesis and biological evaluation. 107
Microwave-assisted Suzuki Coupling in Aqueous Media: a Useful Tool for the Synthesis of 3-Arylindazole Derivatives 106
Novel N-substituted indol-3-ylglyoxylamides probing the LDi and L1L2 lipophilic regions of the benzodiazepine receptor site in search for subtype-selective ligands 106
Novel Irreversible Fluorescent Probes Targeting the 18 kDa Translocator Protein: Synthesis and Biological Characterization 104
3-Aryl-[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-one: a novel template for the design of highly selective A(2B) adenosine receptor antagonists 104
N-(indole-3-ylglyoxyl) aminoacid derivatives. preparation and pharmacological properties. 103
Novel Aldose Reductase Acetic acid Inhibitors Bearing a Five Membered heterocyclic core 102
Refinement of the Benzodiazepine Receptor Site Topology by Structure-Activity Relationships of New N-(Heteroarylmethyl)indol-3-ylglyoxylamides 101
N-(Indol-3-ylglyoxylyl)dopamine derivatives: preparation and antidepressant activity 101
Synthesis and Biological Evaluation of Pyrido[1,2-d]pyrimidin-4-one Derivatives as Novel Aldose Reductase Inhibitors Exhibiting Antioxidant Activity 100
INDOLE AMIDE DERIVATIVES: SYNTHESIS, STUCTURE-ACTIVITY RELATIONSHIPS AND MOLECULAR MODELLING STUDIES OF A NEW SERIES OF HISTAMINE H1-RECEPTOR ANTAGONISTS. 100
1-(PHENYLSULPHONAMIDO)-PYRAZOLE DERIVATIVES AS CARBONIC ANHYDRASE INHIBITORS. 99
Geometrically Constrained Derivatives of Indolylglyoxylamides as Ligands Binding the GABAA/BzR Complex. 99
3-Aryl-[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-one: A Novel Template for the Design of Highly Selective A(2B) Adenosine Receptor Antagonists. 98
Synthesis and antiinflammatory activity of some N-(5-substituted indole-3-ylglyoxylyl)amine derivatives. 97
Synthesis and Benzodiazepine Receptor Affinity of Derivatives of the New Tricyclic Heteroaromatic System Pyrido[3’,2’:5,6]thiopyrano[4,3-c]pyridazin-3(2H,5H)-one 97
Novel Antitumoral Pyrazolopyrimidines Based on Inhibition of Protein Tyrosine Kinase 95
4-Substituted Benzenesulfonamides Incorporating Bi/Tricyclic Moieties Act as Potent and Isoform-Selective Carbonic Anhydrase II/IX Inhibitors 95
Synthesis of some 5H,12H-[1]benzoxepino[4,3-b]indol-6-ones. A new heterocyclic ring system 93
Synthesis and biological evaluation of Modified 2-Phenylindol-3-ylglyoxylamides as good candidates for the development of radioligands for the visualization of peripheral benzodiazepine receptor 92
2-Phenyl[1,2,3]triazolo[1,2-a][1,2,4]benzotriazin-1-one derivatives as a new class of adenosine receptor antagonists 90
New oxazole and 1,2,4-oxadiazole derivatives as selective ligands at the Translocator Protein (TSPO) 90
Design, Synthesis, and Biological Evaluation of 3-Arylindazole Acetic Acid Derivatives as Aldose Reductase Inhibitors 89
"Synthesis of pyridothiopyranoindole and of pyridothiopyranoquinoline derivatives as novel tetracyclic ring system" 89
Synthesis and local anaesthetic activity of some 7-amino-2-dialkylaminoalkylpyrrolo[3,4-c]pyridine derivatives 88
Exploiting the pyrazolo[3,4-d]pyrimidinone ring system as a useful template for the obtainment of potent adenosine deaminase inhibitors 87
"Synthesis, DNA binding and in vitro antiproliferative activity of quinazobenzimidazole derivatives as potential antitumor agents". 86
Novel N-(Arylalkyl)indol-3-ylglyoxylamides targeted as ligands of the benzodiazepine receptor : synthesis, biological evaluation, and molecular modeling analysis of the Structure-Activity Relationships. 86
Synthesis and Antihypertensive activity of some 2-aminobenzimidazole and indole derivatives. 85
Synthesis of some 3,7-DisubstitutedQuino[3,2-c][1,8]naphthyridines. 85
Anxiolytic-like Effects of N,N-Dialkyl-2-phenylindol-3-ylglyoxylamides by Modulation of Translocator Protein Promoting Neurosteroid Biosynthesis 85
Synthesis and antiproliferative evaluation of new aryl substituted Pyrido[3’,2’:5,6]thiopyrano[4,3-c]pyrazoles 84
SYNTHESIS OF NOVEL 5H,11H-PYRIDO[2',3':2,3]THIOPIRANO[4,3-B]-INDOLES BY FISCHER-INDOLE CYCLIZATION. 83
Synthesis, in vitro antiproliferative activity and DNA-interaction of benzimidazoquinazoline derivatives as potential anti-tumor agents 82
Design, synthesis, and biological evaluation of novel fluorescent probes targeting the Translocator Protein (18 kDa) (TSPO) 82
N-(Indol-3-ylglyoxylyl)amino acid ester derivatives. Synthesis and interaction properties at the benzodiazepine receptor 80
Tricyclic Sulfonamides Incorporating Benzothiopyrano[4,3-c]pyrazole and Pyridothiopyrano[4,3-c]pyrazole Effectively Inhibit a- and ß-Carbonic Anhydrase: X-ray Crystallography and Solution Investigations on 15 Isoforms 78
Isosteric replacement of amide by ester function. Synthesis and benzodiazepine receptor affinity of indol-3-ylglyoxylyl ester derivatives 76
NOVEL KINASE INHIBITORS IN THYROID CANCER TREATMENT: SYNTHESIS AND BIOLOGICAL EVALUATION 75
Isosteric replacement of the indole nucleus by benzothiophene and benzofuran in a series of indolylglyoxylylamine derivatives with partial agonist activity at the benzodiazepine receptor. 74
Synthesis and Antiproliferative Activity of New Aminoalkyl Substituted Benzothiopyranoindoles 74
Synthesis of 3-(2'-furoyl)indole derivatives as potential new ligands at the benzodiazepine receptor, structurally more restrained analogues of indoleglyoxylylamides. 74
Novel Pyrazolopyrimidine Derivatives as Therapeutic Agents for the Treatment of Medullary Thyroid Carcinoma 73
New insights in the structure-activity relationships of 2-phenylamino-substituted benzothiopyrano[4,3-d]pyrimidines as kinase inhibitors 73
SPECIFIC INHIBITION OF 3H FLUNITRAZEPAM BINDING BY SOME N-(INDOL-3-YLGLYOXYLYL)AMINO ACID DERIVATIVES AND SOME N-(2-METHYL OR 1,2-DIMETHYLINDOL-3-YLGLYOXYLYL)AMINO ACID DERIVATIVES. 72
Carbonic anhydrase activation profile of indole-based derivatives 72
Benzoxadiazole Derivatives: Atypical Inhibitors of Aldose Reductase 71
Targeting the Translocator protein (TSPO) with 2-phenylindol-3-ylglyoxylamide derivatives 71
2-(phenylsulphonamido)-pyrazole derivatives as carbonic anhydrase inhibitors 71
Phenylpyrazolo[1,5-a]quinazolin-5(4H)-one: a suitable scaffold for the development of noncamptothecin Topoisomerase I (top1) inhibitors 71
"Sintesi e attività antiproliferativa di sistemi Pirido[3’,2’:5,6]tiopirano[4,3-c]pirazolici 2-aril sostituiti" 70
Novel Highly Potent Adenosine Deaminase Inhibitors Containing the Pyrazolo[3,4-d]pyrimidine Ring System. Synthesis, Structure-Activity Relationships and Molecular Modeling Studies 70
Totale 10.963
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Categoria #
all - tutte 28.751
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 28.751
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019377 0 0 0 0 0 0 0 0 0 0 219 158
2019/20202.207 258 183 518 107 171 197 207 117 156 109 166 18
2020/2021944 173 32 65 42 113 32 45 94 67 59 69 153
2021/20221.512 35 115 57 106 262 191 24 70 58 54 86 454
2022/20232.003 262 362 138 192 240 263 21 143 273 7 81 21
2023/20241.310 218 180 170 110 226 293 34 30 22 27 0 0
Totale 12.755