CINECA IRIS Institutional Research Information System

MARINI, ANNA MARIA
 Distribuzione geografica
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Continente #
NA - Nord America 9.445
AS - Asia 4.321
EU - Europa 4.140
SA - Sud America 530
AF - Africa 167
OC - Oceania 24
Totale 18.627
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Nazione #
US - Stati Uniti d'America 9.175
IT - Italia 1.537
CN - Cina 1.336
SG - Singapore 1.281
SE - Svezia 804
HK - Hong Kong 697
DE - Germania 453
BR - Brasile 448
TR - Turchia 348
BG - Bulgaria 328
GB - Regno Unito 248
CA - Canada 229
VN - Vietnam 170
UA - Ucraina 164
RU - Federazione Russa 161
FI - Finlandia 149
IN - India 124
KR - Corea 115
AT - Austria 107
CH - Svizzera 53
CI - Costa d'Avorio 51
JP - Giappone 49
FR - Francia 33
NG - Nigeria 32
BD - Bangladesh 30
AR - Argentina 28
BE - Belgio 27
ID - Indonesia 24
MX - Messico 21
AU - Australia 20
IQ - Iraq 19
PK - Pakistan 17
SA - Arabia Saudita 17
NL - Olanda 16
EG - Egitto 14
ZA - Sudafrica 14
SN - Senegal 13
VE - Venezuela 13
KE - Kenya 12
MY - Malesia 12
ES - Italia 11
UZ - Uzbekistan 11
CO - Colombia 10
CZ - Repubblica Ceca 9
IE - Irlanda 9
AZ - Azerbaigian 8
EC - Ecuador 8
JO - Giordania 8
KZ - Kazakistan 8
PL - Polonia 8
CL - Cile 7
OM - Oman 7
BJ - Benin 6
IR - Iran 6
MA - Marocco 6
PE - Perù 6
TW - Taiwan 6
DZ - Algeria 5
AL - Albania 4
LB - Libano 4
NZ - Nuova Zelanda 4
PA - Panama 4
PY - Paraguay 4
QA - Qatar 4
AE - Emirati Arabi Uniti 3
ET - Etiopia 3
LT - Lituania 3
PH - Filippine 3
PS - Palestinian Territory 3
TT - Trinidad e Tobago 3
UY - Uruguay 3
BN - Brunei Darussalam 2
DO - Repubblica Dominicana 2
GR - Grecia 2
HN - Honduras 2
JM - Giamaica 2
KH - Cambogia 2
MK - Macedonia 2
MN - Mongolia 2
PT - Portogallo 2
RO - Romania 2
SO - Somalia 2
AO - Angola 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BH - Bahrain 1
BO - Bolivia 1
CR - Costa Rica 1
CY - Cipro 1
DK - Danimarca 1
GA - Gabon 1
GD - Grenada 1
GE - Georgia 1
GY - Guiana 1
HR - Croazia 1
IL - Israele 1
LC - Santa Lucia 1
LK - Sri Lanka 1
LR - Liberia 1
LU - Lussemburgo 1
Totale 18.613
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Città #
Woodbridge 1.262
Ann Arbor 992
Ashburn 874
Houston 861
Singapore 728
Hong Kong 692
Serra 612
Chandler 602
Fairfield 560
Santa Clara 523
Milan 409
Sofia 327
Beijing 289
Izmir 272
Shanghai 257
Dallas 247
Seattle 237
Jacksonville 228
Wilmington 224
New York 203
Ottawa 199
Cambridge 167
Hefei 151
Boardman 144
Princeton 143
Nanjing 132
Los Angeles 131
Lawrence 130
Seoul 113
London 107
Medford 106
Vienna 86
Dearborn 84
Des Moines 80
Dong Ket 68
Istanbul 63
Buffalo 52
Abidjan 51
Bern 51
Frankfurt am Main 48
Düsseldorf 46
Rome 45
Nanchang 42
Redondo Beach 41
Jüchen 39
Rho 38
São Paulo 37
Council Bluffs 35
San Diego 32
Kunming 30
Lagos 30
Shenyang 30
Tokyo 30
Boulder 29
Bremen 29
Columbus 29
Redwood City 29
The Dalles 29
Brussels 27
Pune 27
Chicago 24
Munich 24
Fuzhou 23
San Francisco 22
Hebei 21
Washington 19
Nürnberg 18
Ogden 18
San Jose 18
Changsha 17
Ho Chi Minh City 17
Auburn Hills 16
Norwalk 15
Turku 15
Florence 14
Jakarta 14
Pisa 14
Secaucus 14
Tianjin 14
Belo Horizonte 13
Dakar 13
Lancaster 13
Rio de Janeiro 13
Jiaxing 12
Jinan 12
Guangzhou 11
Hangzhou 11
Porto Alegre 11
Toronto 11
Curitiba 10
Hanoi 10
Manchester 10
Orange 10
Tashkent 10
Falls Church 9
Johannesburg 9
Nairobi 9
Osaka 9
Amman 8
Dhaka 8
Totale 13.738
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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 383
Benzofuroxane Derivatives as Multi Effective Agents for the Treatment of Cardiovascular Diabetic Complications. Synthesis, Functional Evaluation, and Molecular Modeling Studies 266
Exploiting the Pyrazolo[3,4-d]pyrimidin-4-one ring system as a useful template to obtain potent adenosine deaminase inhibitors, 257
N '-phenylindol-3-ylglyoxylohydrazide derivatives: Synthesis, structure-activity relationships, molecular modeling studies, and pharmacological action on brain benzodiazepine receptors 230
Deepening the Topology of the Translocator Protein Binding Site by Novel N,N-Dialkyl-2-arylindol-3-ylglyoxylamides 219
3-aryl-[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-ones: Tricyclic heteroaromatic derivatives as a new class of benzodiazepine receptor ligands 205
3-Aryl[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-ones: A New Class of Selective A1 Adenosine Receptor Antagonists 200
Sulfonamides incorporating heteropolycyclic scaffolds show potent inhibitory action against carbonic anhydrase isoforms I, II, IX and XII 199
Identification of Anxiolytic/Nonsedative Agents among Indol-3-ylglyoxylamides Acting as Functionally Selective Agonists at the γ-Aminobutyric Acid-A (GABAA) α2 Benzodiazepine Receptor 196
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. 193
Synthesis of some Substituted Pyrido[1,2-a]pyrimidin-4-ones and 1,8-Naphthyridines. 192
Medicinal chemistry of indolylglyoxylamide TSPO high affinity ligands with anxiolytic-like effects 189
Structure-Based Optimization of Tyrosine Kinase Inhibitor CLM3. Design, Synthesis, Functional Evaluation, and Molecular Modeling Studies. 189
N-(Indol-3-ylglyoxylyl)methionine derivatives: preparation and gastric anti-secretory activity. 187
SPECIFIC-INHIBITION OF BENZODIAZEPINE RECEPTOR-BINDING BY SOME N-(INDOL-3-YLGLYOXYLYL)AMINO ACID-DERIVATIVES 187
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 186
Pyrido[1,2-a]pyrimidin-4-one derivatives as a novel class of selective aldose reductase inhibitors exhibiting antioxidant activity 183
Benzothiopyranoindole-Based Antiproliferative Agents: Synthesis, Cytotoxicity, Nucleic Acids Interaction, and Topoisomerases Inhibition Properties. 183
Investigation of new 2-aryl substituted Benzothiopyrano[4,3-d]pyrimidines as kinase inhibitors targeting vascular endothelial growth factor receptor 2 183
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 182
Phenylpyrazolo[1,5-a]quinazolin-5(4H)-one: a suitable scaffold for the development of non-camptothecin Topoisomerase I (Top1) inhibitors 182
Refinement of Structure-activity Relationships of the Triazinobenzimidazole A1AR Antagonists 181
Benzo[d]isothiazoles and Matrix Metalloproteinases. Searching for Novel and Selective Inhibitors of MMP9 181
Synthesis, DNA binding and in vitro antiproliferative activity of purinoquinazoline, pyridopyrimidopurine and pyridopyrimidobenzimidazole derivatives as potential antitumor agents 179
"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" 178
Studies in search for selective ligands for GABAA/BzR receptor subtypes: synthesis and biological evaluation of 4'-modified N-(benzyl)indol-3-ylglyoxylamides 177
N-(indole-3-ylglyoxyl) aminoacid derivatives. preparation and pharmacological properties. 175
Medicinal chemistry of indolylglyoxylamide GABAA/BzR high affinity ligands: identification of novel anxiolytic/non sedative agents 175
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 174
“Synthesis and antiproliferative evaluation of new substituted Benzothiopyrano[4,3-c] condensed ring systems” 173
Synthesis of Purinobenzodiazepine and Purinobenzotriazocine derivatives, two new heterocyclic ring systems. 173
Novel Pyrazolo[3,4-d]pyrimidine Derivatives as ATP-competitive Inhibitors of the Epidermal Growth Factor Receptor Protein Tyrosine Kinase 172
Novel N(2)-Substituted Pyrazolo[3,4-d]pyrimidine Adenosine A(3) Receptor Antagonists: Inhibition of A(3)-Mediated Human Glioblastoma Cell Proliferation (dagger) 172
SPECIFIC-INHIBITION OF BENZODIAZEPINE RECEPTOR-BINDING BY SOME N-(INDOL-3-YLGLYOXYLYL)AMINO ACID-DERIVATIVES - STEREOSELECTIVE INTERACTIONS 172
Recent Advances in the Development of Dual Topoisomerase I and II Inhibitors as Anticancer Drugs 172
Synthesis and antiinflammatory Properties of 2-Methylaminobenzimidazole Derivatives 171
Novel Potent and Selective Human Adenosine A3 Receptor Antagonists Containing the Pyrazolo[3,4-d]pyrimidine Ring System. Synthesis and Biological Evaluation 170
FACILE SYNTHESIS OF 3-SUBSTITUTED[1,2,4]TRIAZINO[3,4-F]PURINE-4,6,8-TRIONE DERIVATIVES 170
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. 169
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 168
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. 168
Arylsulfonamide inhibitors of aggrecanases as potential therapeutic agents for osteoarthritis: Synthesis and biological evaluation. 166
Synthesis of Pyrimido[1,2-a]benzimidazol-4(10H)-one Derivatives and Evaluation of their Interactions with DNA 164
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 163
4-Substituted Benzenesulfonamides Incorporating Bi/Tricyclic Moieties Act as Potent and Isoform-Selective Carbonic Anhydrase II/IX Inhibitors 160
Synthesis and biological activity of 1,4-dihydrobenzothiopyrano[4,3-c]pyrazole derivatives, novel pro-apoptotic mitochondrial targeted agents 158
Novel N-substituted indol-3-ylglyoxylamides probing the LDi and L1L2 lipophilic regions of the benzodiazepine receptor site in search for subtype-selective ligands 158
Synthesis and antiproliferative evaluation of new aryl substituted Pyrido[3’,2’:5,6]thiopyrano[4,3-c]pyrazoles 157
Synthesis and antiinflammatory activity of some N-(5-substituted indole-3-ylglyoxylyl)amine derivatives. 156
Mitochondrial permeability transition induced by novel pyridothiopyranopyrimidine derivatives: Potential new antimitochondrial antitumour agents. 155
Acetic acid aldose reductase inhibitors bearing a five-membered heterocyclic core with potent topical activity in a visual impairment rat model 154
Synthesis of New Heterocyclic Ring Systems via [1,3,5]Triazino[1,2-a]benzimidazole Derivatives 152
Synthesis and Biological Evaluation of Pyrido[1,2-d]pyrimidin-4-one Derivatives as Novel Aldose Reductase Inhibitors Exhibiting Antioxidant Activity 151
Pyrazolo[3,4,-d]pyrimidine-4-one Derivatives as Novel and Potent Inhibitors of Adenosine Deaminase 151
Small Molecules Containing the Benzo[d]isotiazole Ring System as Novel ATP-Competitive Inhibitors of Epidermal Growth Factor Receptor protein Tyrosine Kinase 150
Naphtho[1,2-d]isothiazole Acetic Acid Derivatives as a Novel Class of Selective Aldose Reductase Inhibitors 150
Microwave-assisted Suzuki Coupling in Aqueous Media: a Useful Tool for the Synthesis of 3-Arylindazole Derivatives 148
Geometrically Constrained Derivatives of Indolylglyoxylamides as Ligands Binding the GABAA/BzR Complex. 148
Novel Aldose Reductase Acetic acid Inhibitors Bearing a Five Membered heterocyclic core 147
Synthesis and Antihypertensive activity of some 2-aminobenzimidazole and indole derivatives. 144
Novel Antitumoral Pyrazolopyrimidines Based on Inhibition of Protein Tyrosine Kinase 143
Inhibition studies on carbonic anhydrase isoforms I, II, IV and IX with N-arylsubstituted secondary sulfonamides featuring a bicyclic tetrahydroindazole scaffold 143
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 142
Synthesis of purinobenzothiazine and pyridothiazinopurine derivatives. Two new heterocyclic ring systems 138
Refinement of the Benzodiazepine Receptor Site Topology by Structure-Activity Relationships of New N-(Heteroarylmethyl)indol-3-ylglyoxylamides 138
N-(Indol-3-ylglyoxylyl)dopamine derivatives: preparation and antidepressant activity 138
1-(PHENYLSULPHONAMIDO)-PYRAZOLE DERIVATIVES AS CARBONIC ANHYDRASE INHIBITORS. 137
"Synthesis of purinobenzodiazepine and purinobenzotriazocine derivatives, two new heterocyclic ring system" 136
2-(phenylsulphonamido)-pyrazole derivatives as carbonic anhydrase inhibitors 136
INDOLE AMIDE DERIVATIVES: SYNTHESIS, STUCTURE-ACTIVITY RELATIONSHIPS AND MOLECULAR MODELLING STUDIES OF A NEW SERIES OF HISTAMINE H1-RECEPTOR ANTAGONISTS. 135
New insights in the structure-activity relationships of 2-phenylamino-substituted benzothiopyrano[4,3-d]pyrimidines as kinase inhibitors 135
Novel Irreversible Fluorescent Probes Targeting the 18 kDa Translocator Protein: Synthesis and Biological Characterization 134
Synthesis of some 5H,12H-[1]benzoxepino[4,3-b]indol-6-ones. A new heterocyclic ring system 132
N-(Indol-3-ylglyoxylyl)amino acid ester derivatives. Synthesis and interaction properties at the benzodiazepine receptor 131
Phenylpyrazolo[1,5-a]quinazolin-5(4H)-one: a suitable scaffold for the development of noncamptothecin Topoisomerase I (top1) inhibitors 131
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 129
Anxiolytic-like Effects of N,N-Dialkyl-2-phenylindol-3-ylglyoxylamides by Modulation of Translocator Protein Promoting Neurosteroid Biosynthesis 129
Tetrahydroquinazole-based secondary sulphonamides as carbonic anhydrase inhibitors: synthesis, biological evaluation against isoforms I, II, IV, and IX, and computational studies 128
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. 127
Design, Synthesis, and Biological Evaluation of 3-Arylindazole Acetic Acid Derivatives as Aldose Reductase Inhibitors 127
Exploiting the pyrazolo[3,4-d]pyrimidinone ring system as a useful template for the obtainment of potent adenosine deaminase inhibitors 127
Synthesis and local anaesthetic activity of some 7-amino-2-dialkylaminoalkylpyrrolo[3,4-c]pyridine derivatives 126
New oxazole and 1,2,4-oxadiazole derivatives as selective ligands at the Translocator Protein (TSPO) 126
Refinement of the translocator protein pharmacophore/receptor model via structure-activity relationships of novel N,N-dialkylindolylglyoxylamides 125
Benzoxadiazole Derivatives: Atypical Inhibitors of Aldose Reductase 124
"Synthesis of pyridothiopyranoindole and of pyridothiopyranoquinoline derivatives as novel tetracyclic ring system" 124
Novel Highly Potent Adenosine Deaminase Inhibitors Containing the Pyrazolo[3,4-d]pyrimidine Ring System. Synthesis, Structure-Activity Relationships and Molecular Modeling Studies 123
2-Phenyl[1,2,3]triazolo[1,2-a][1,2,4]benzotriazin-1-one derivatives as a new class of adenosine receptor antagonists 122
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. 121
SYNTHESIS OF NOVEL 5H,11H-PYRIDO[2',3':2,3]THIOPIRANO[4,3-B]-INDOLES BY FISCHER-INDOLE CYCLIZATION. 120
Isosteric replacement of amide by ester function. Synthesis and benzodiazepine receptor affinity of indol-3-ylglyoxylyl ester derivatives 120
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 119
Synthesis of some 3,7-DisubstitutedQuino[3,2-c][1,8]naphthyridines. 119
Design, synthesis, and biological evaluation of novel fluorescent probes targeting the Translocator Protein (18 kDa) (TSPO) 119
Novel Pyrazolopyrimidine Derivatives as Therapeutic Agents for the Treatment of Medullary Thyroid Carcinoma 118
"Synthesis, DNA binding and in vitro antiproliferative activity of quinazobenzimidazole derivatives as potential antitumor agents". 116
Novel, Highly Potent Adenosine Deaminase Inhibitors Containing the Pyrazolo[3,4-d]pyrimidine Ring System. Synhesis, Structure-Activity Relationships, and Molecular Modeling Studies 116
NOVEL KINASE INHIBITORS IN THYROID CANCER TREATMENT: SYNTHESIS AND BIOLOGICAL EVALUATION 113
Synthesis, in vitro antiproliferative activity and DNA-interaction of benzimidazoquinazoline derivatives as potential anti-tumor agents 113
Isosteric replacement of the indole nucleus by benzothiophene and benzofuran in a series of indolylglyoxylylamine derivatives with partial agonist activity at the benzodiazepine receptor. 112
Totale 15.885
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Categoria #
all - tutte 49.702
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 49.702
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021519 0 0 0 0 0 32 45 94 67 59 69 153
2021/20221.488 35 109 55 102 260 188 23 70 58 54 84 450
2022/20231.964 258 354 134 190 236 260 21 142 264 7 78 20
2023/20241.459 217 178 168 110 225 290 34 30 22 27 21 137
2024/20253.904 31 150 41 245 472 374 264 204 327 495 411 890
2025/20262.090 218 461 411 261 365 374 0 0 0 0 0 0
Totale 18.835