CINECA IRIS Institutional Research Information System

MARINI, ANNA MARIA
 Distribuzione geografica
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Continente #
NA - Nord America 10.335
AS - Asia 4.935
EU - Europa 4.357
SA - Sud America 585
AF - Africa 181
OC - Oceania 24
Totale 20.417
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Nazione #
US - Stati Uniti d'America 10.036
IT - Italia 1.545
SG - Singapore 1.442
CN - Cina 1.399
SE - Svezia 805
HK - Hong Kong 718
BR - Brasile 475
DE - Germania 465
VN - Vietnam 395
TR - Turchia 351
BG - Bulgaria 329
GB - Regno Unito 256
CA - Canada 244
FI - Finlandia 189
UA - Ucraina 165
RU - Federazione Russa 162
FR - Francia 158
IN - India 148
KR - Corea 115
AT - Austria 108
JP - Giappone 96
CH - Svizzera 59
CI - Costa d'Avorio 51
BD - Bangladesh 39
AR - Argentina 35
IQ - Iraq 33
NG - Nigeria 33
ID - Indonesia 32
PK - Pakistan 29
BE - Belgio 27
MX - Messico 27
AU - Australia 20
ZA - Sudafrica 20
NL - Olanda 18
SA - Arabia Saudita 18
VE - Venezuela 18
ES - Italia 16
EG - Egitto 15
JO - Giordania 15
MY - Malesia 15
SN - Senegal 13
UZ - Uzbekistan 13
CO - Colombia 12
KE - Kenya 12
IE - Irlanda 11
CL - Cile 10
EC - Ecuador 10
PE - Perù 10
AZ - Azerbaigian 9
CZ - Repubblica Ceca 9
KZ - Kazakistan 8
MA - Marocco 8
OM - Oman 8
PL - Polonia 8
BJ - Benin 6
DZ - Algeria 6
IR - Iran 6
PA - Panama 6
PY - Paraguay 6
TW - Taiwan 6
LB - Libano 5
PH - Filippine 5
AL - Albania 4
CR - Costa Rica 4
NZ - Nuova Zelanda 4
PS - Palestinian Territory 4
QA - Qatar 4
TT - Trinidad e Tobago 4
UY - Uruguay 4
AE - Emirati Arabi Uniti 3
BO - Bolivia 3
ET - Etiopia 3
IL - Israele 3
JM - Giamaica 3
KH - Cambogia 3
LT - Lituania 3
MK - Macedonia 3
MN - Mongolia 3
PT - Portogallo 3
BN - Brunei Darussalam 2
DO - Repubblica Dominicana 2
GE - Georgia 2
GR - Grecia 2
HN - Honduras 2
NP - Nepal 2
RO - Romania 2
SO - Somalia 2
TN - Tunisia 2
AO - Angola 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BH - Bahrain 1
CG - Congo 1
CY - Cipro 1
DK - Danimarca 1
GA - Gabon 1
GD - Grenada 1
GT - Guatemala 1
GY - Guiana 1
HR - Croazia 1
Totale 20.396
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Città #
Woodbridge 1.262
Ann Arbor 992
Ashburn 947
Singapore 869
Houston 861
Hong Kong 705
Serra 612
Chandler 602
Fairfield 560
Santa Clara 530
San Jose 506
Milan 409
Sofia 327
Beijing 298
Izmir 273
Shanghai 257
Dallas 256
Seattle 238
Jacksonville 228
Wilmington 224
New York 207
Ottawa 199
Cambridge 167
Hefei 151
Boardman 145
Princeton 143
Los Angeles 135
Nanjing 132
Lawrence 130
Lauterbourg 116
Seoul 113
London 107
Medford 106
Ho Chi Minh City 95
Council Bluffs 90
Vienna 87
Dearborn 84
Des Moines 80
Tokyo 77
Hanoi 72
Dong Ket 68
Istanbul 63
Frankfurt am Main 57
Buffalo 53
Abidjan 51
Bern 51
Rome 47
Düsseldorf 46
Helsinki 46
Nanchang 42
Redondo Beach 41
Jüchen 39
Rho 38
São Paulo 38
San Diego 33
Kunming 30
Lagos 30
Shenyang 30
Boulder 29
Bremen 29
Columbus 29
Redwood City 29
The Dalles 29
Chicago 28
Pune 28
Brussels 27
Munich 24
Fuzhou 23
San Francisco 23
Hebei 21
Washington 20
Nürnberg 18
Ogden 18
Changsha 17
Da Nang 17
Auburn Hills 16
Norwalk 15
Orem 15
Pisa 15
Rio de Janeiro 15
Turku 15
Florence 14
Jakarta 14
Secaucus 14
Tianjin 14
Amman 13
Belo Horizonte 13
Dakar 13
Johannesburg 13
Lancaster 13
Toronto 13
Hangzhou 12
Jiaxing 12
Jinan 12
Manchester 12
Tashkent 12
Guangzhou 11
Mumbai 11
Porto Alegre 11
Curitiba 10
Totale 14.932
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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 416
Benzofuroxane Derivatives as Multi Effective Agents for the Treatment of Cardiovascular Diabetic Complications. Synthesis, Functional Evaluation, and Molecular Modeling Studies 279
Exploiting the Pyrazolo[3,4-d]pyrimidin-4-one ring system as a useful template to obtain potent adenosine deaminase inhibitors, 272
N '-phenylindol-3-ylglyoxylohydrazide derivatives: Synthesis, structure-activity relationships, molecular modeling studies, and pharmacological action on brain benzodiazepine receptors 249
Deepening the Topology of the Translocator Protein Binding Site by Novel N,N-Dialkyl-2-arylindol-3-ylglyoxylamides 244
Sulfonamides incorporating heteropolycyclic scaffolds show potent inhibitory action against carbonic anhydrase isoforms I, II, IX and XII 233
Investigation of new 2-aryl substituted Benzothiopyrano[4,3-d]pyrimidines as kinase inhibitors targeting vascular endothelial growth factor receptor 2 214
3-aryl-[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-ones: Tricyclic heteroaromatic derivatives as a new class of benzodiazepine receptor ligands 213
Identification of Anxiolytic/Nonsedative Agents among Indol-3-ylglyoxylamides Acting as Functionally Selective Agonists at the γ-Aminobutyric Acid-A (GABAA) α2 Benzodiazepine Receptor 210
3-Aryl[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-ones: A New Class of Selective A1 Adenosine Receptor Antagonists 209
Phenylpyrazolo[1,5-a]quinazolin-5(4H)-one: a suitable scaffold for the development of non-camptothecin Topoisomerase I (Top1) inhibitors 209
Synthesis of some Substituted Pyrido[1,2-a]pyrimidin-4-ones and 1,8-Naphthyridines. 208
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. 207
Structure-Based Optimization of Tyrosine Kinase Inhibitor CLM3. Design, Synthesis, Functional Evaluation, and Molecular Modeling Studies. 205
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. 202
Medicinal chemistry of indolylglyoxylamide TSPO high affinity ligands with anxiolytic-like effects 201
New insights in the structure-activity relationships of 2-phenylamino-substituted benzothiopyrano[4,3-d]pyrimidines as kinase inhibitors 201
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 199
Studies in search for selective ligands for GABAA/BzR receptor subtypes: synthesis and biological evaluation of 4'-modified N-(benzyl)indol-3-ylglyoxylamides 198
Pyrido[1,2-a]pyrimidin-4-one derivatives as a novel class of selective aldose reductase inhibitors exhibiting antioxidant activity 198
SPECIFIC-INHIBITION OF BENZODIAZEPINE RECEPTOR-BINDING BY SOME N-(INDOL-3-YLGLYOXYLYL)AMINO ACID-DERIVATIVES 196
Synthesis, DNA binding and in vitro antiproliferative activity of purinoquinazoline, pyridopyrimidopurine and pyridopyrimidobenzimidazole derivatives as potential antitumor agents 194
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 194
Benzothiopyranoindole-Based Antiproliferative Agents: Synthesis, Cytotoxicity, Nucleic Acids Interaction, and Topoisomerases Inhibition Properties. 194
Medicinal chemistry of indolylglyoxylamide GABAA/BzR high affinity ligands: identification of novel anxiolytic/non sedative agents 194
N-(Indol-3-ylglyoxylyl)methionine derivatives: preparation and gastric anti-secretory activity. 193
Refinement of Structure-activity Relationships of the Triazinobenzimidazole A1AR Antagonists 193
"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" 192
N-(indole-3-ylglyoxyl) aminoacid derivatives. preparation and pharmacological properties. 191
Benzo[d]isothiazoles and Matrix Metalloproteinases. Searching for Novel and Selective Inhibitors of MMP9 191
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 191
Inhibition studies on carbonic anhydrase isoforms I, II, IV and IX with N-arylsubstituted secondary sulfonamides featuring a bicyclic tetrahydroindazole scaffold 189
“Synthesis and antiproliferative evaluation of new substituted Benzothiopyrano[4,3-c] condensed ring systems” 188
Recent Advances in the Development of Dual Topoisomerase I and II Inhibitors as Anticancer Drugs 186
Novel N(2)-Substituted Pyrazolo[3,4-d]pyrimidine Adenosine A(3) Receptor Antagonists: Inhibition of A(3)-Mediated Human Glioblastoma Cell Proliferation (dagger) 184
Synthesis of Purinobenzodiazepine and Purinobenzotriazocine derivatives, two new heterocyclic ring systems. 184
Novel Pyrazolo[3,4-d]pyrimidine Derivatives as ATP-competitive Inhibitors of the Epidermal Growth Factor Receptor Protein Tyrosine Kinase 183
Synthesis and antiinflammatory Properties of 2-Methylaminobenzimidazole Derivatives 180
SPECIFIC-INHIBITION OF BENZODIAZEPINE RECEPTOR-BINDING BY SOME N-(INDOL-3-YLGLYOXYLYL)AMINO ACID-DERIVATIVES - STEREOSELECTIVE INTERACTIONS 180
Novel Potent and Selective Human Adenosine A3 Receptor Antagonists Containing the Pyrazolo[3,4-d]pyrimidine Ring System. Synthesis and Biological Evaluation 179
FACILE SYNTHESIS OF 3-SUBSTITUTED[1,2,4]TRIAZINO[3,4-F]PURINE-4,6,8-TRIONE DERIVATIVES 179
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. 178
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 177
Arylsulfonamide inhibitors of aggrecanases as potential therapeutic agents for osteoarthritis: Synthesis and biological evaluation. 177
4-Substituted Benzenesulfonamides Incorporating Bi/Tricyclic Moieties Act as Potent and Isoform-Selective Carbonic Anhydrase II/IX Inhibitors 177
Mitochondrial permeability transition induced by novel pyridothiopyranopyrimidine derivatives: Potential new antimitochondrial antitumour agents. 172
Synthesis and antiinflammatory activity of some N-(5-substituted indole-3-ylglyoxylyl)amine derivatives. 171
Synthesis of Pyrimido[1,2-a]benzimidazol-4(10H)-one Derivatives and Evaluation of their Interactions with DNA 171
Synthesis and antiproliferative evaluation of new aryl substituted Pyrido[3’,2’:5,6]thiopyrano[4,3-c]pyrazoles 171
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 170
Pyrazolo[3,4,-d]pyrimidine-4-one Derivatives as Novel and Potent Inhibitors of Adenosine Deaminase 170
Geometrically Constrained Derivatives of Indolylglyoxylamides as Ligands Binding the GABAA/BzR Complex. 170
Acetic acid aldose reductase inhibitors bearing a five-membered heterocyclic core with potent topical activity in a visual impairment rat model 169
Synthesis and Biological Evaluation of Pyrido[1,2-d]pyrimidin-4-one Derivatives as Novel Aldose Reductase Inhibitors Exhibiting Antioxidant Activity 167
Synthesis and biological activity of 1,4-dihydrobenzothiopyrano[4,3-c]pyrazole derivatives, novel pro-apoptotic mitochondrial targeted agents 167
Small Molecules Containing the Benzo[d]isotiazole Ring System as Novel ATP-Competitive Inhibitors of Epidermal Growth Factor Receptor protein Tyrosine Kinase 165
Novel N-substituted indol-3-ylglyoxylamides probing the LDi and L1L2 lipophilic regions of the benzodiazepine receptor site in search for subtype-selective ligands 165
Naphtho[1,2-d]isothiazole Acetic Acid Derivatives as a Novel Class of Selective Aldose Reductase Inhibitors 161
Refinement of the translocator protein pharmacophore/receptor model via structure-activity relationships of novel N,N-dialkylindolylglyoxylamides 159
Synthesis of New Heterocyclic Ring Systems via [1,3,5]Triazino[1,2-a]benzimidazole Derivatives 159
2-(phenylsulphonamido)-pyrazole derivatives as carbonic anhydrase inhibitors 158
Synthesis and Antihypertensive activity of some 2-aminobenzimidazole and indole derivatives. 156
Microwave-assisted Suzuki Coupling in Aqueous Media: a Useful Tool for the Synthesis of 3-Arylindazole Derivatives 156
Novel Aldose Reductase Acetic acid Inhibitors Bearing a Five Membered heterocyclic core 156
Novel Antitumoral Pyrazolopyrimidines Based on Inhibition of Protein Tyrosine Kinase 154
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 154
Tetrahydroquinazole-based secondary sulphonamides as carbonic anhydrase inhibitors: synthesis, biological evaluation against isoforms I, II, IV, and IX, and computational studies 154
Refinement of the Benzodiazepine Receptor Site Topology by Structure-Activity Relationships of New N-(Heteroarylmethyl)indol-3-ylglyoxylamides 150
N-(Indol-3-ylglyoxylyl)dopamine derivatives: preparation and antidepressant activity 150
Phenylpyrazolo[1,5-a]quinazolin-5(4H)-one: a suitable scaffold for the development of noncamptothecin Topoisomerase I (top1) inhibitors 149
"Synthesis of purinobenzodiazepine and purinobenzotriazocine derivatives, two new heterocyclic ring system" 148
1-(PHENYLSULPHONAMIDO)-PYRAZOLE DERIVATIVES AS CARBONIC ANHYDRASE INHIBITORS. 146
N-(Indol-3-ylglyoxylyl)amino acid ester derivatives. Synthesis and interaction properties at the benzodiazepine receptor 145
3-Aryl-1,2,4-triazino-4,3-abenzimidazol-4(10H)-one: a novel template for the design of highly selective A2B adenosine receptor antagonists 145
Synthesis of some 5H,12H-[1]benzoxepino[4,3-b]indol-6-ones. A new heterocyclic ring system 144
Synthesis of purinobenzothiazine and pyridothiazinopurine derivatives. Two new heterocyclic ring systems 143
INDOLE AMIDE DERIVATIVES: SYNTHESIS, STUCTURE-ACTIVITY RELATIONSHIPS AND MOLECULAR MODELLING STUDIES OF A NEW SERIES OF HISTAMINE H1-RECEPTOR ANTAGONISTS. 143
New oxazole and 1,2,4-oxadiazole derivatives as selective ligands at the Translocator Protein (TSPO) 142
Anxiolytic-like Effects of N,N-Dialkyl-2-phenylindol-3-ylglyoxylamides by Modulation of Translocator Protein Promoting Neurosteroid Biosynthesis 142
Novel Irreversible Fluorescent Probes Targeting the 18 kDa Translocator Protein: Synthesis and Biological Characterization 141
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. 140
Design, Synthesis, and Biological Evaluation of 3-Arylindazole Acetic Acid Derivatives as Aldose Reductase Inhibitors 140
"Synthesis of pyridothiopyranoindole and of pyridothiopyranoquinoline derivatives as novel tetracyclic ring system" 140
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 139
Exploiting the pyrazolo[3,4-d]pyrimidinone ring system as a useful template for the obtainment of potent adenosine deaminase inhibitors 138
Benzoxadiazole Derivatives: Atypical Inhibitors of Aldose Reductase 135
Design, synthesis, and biological evaluation of novel fluorescent probes targeting the Translocator Protein (18 kDa) (TSPO) 135
2-Phenyl[1,2,3]triazolo[1,2-a][1,2,4]benzotriazin-1-one derivatives as a new class of adenosine receptor antagonists 133
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. 132
Novel Highly Potent Adenosine Deaminase Inhibitors Containing the Pyrazolo[3,4-d]pyrimidine Ring System. Synthesis, Structure-Activity Relationships and Molecular Modeling Studies 131
Novel Pyrazolopyrimidine Derivatives as Therapeutic Agents for the Treatment of Medullary Thyroid Carcinoma 130
Synthesis and local anaesthetic activity of some 7-amino-2-dialkylaminoalkylpyrrolo[3,4-c]pyridine derivatives 130
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 130
Synthesis of some 3,7-DisubstitutedQuino[3,2-c][1,8]naphthyridines. 130
SYNTHESIS OF NOVEL 5H,11H-PYRIDO[2',3':2,3]THIOPIRANO[4,3-B]-INDOLES BY FISCHER-INDOLE CYCLIZATION. 129
Targeting the Translocator protein (TSPO) with 2-phenylindol-3-ylglyoxylamide derivatives 128
"Synthesis, DNA binding and in vitro antiproliferative activity of quinazobenzimidazole derivatives as potential antitumor agents". 127
NOVEL KINASE INHIBITORS IN THYROID CANCER TREATMENT: SYNTHESIS AND BIOLOGICAL EVALUATION 126
Isosteric replacement of amide by ester function. Synthesis and benzodiazepine receptor affinity of indol-3-ylglyoxylyl ester derivatives 125
Synthesis, in vitro antiproliferative activity and DNA-interaction of benzimidazoquinazoline derivatives as potential anti-tumor agents 124
Totale 17.356
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Categoria #
all - tutte 55.389
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 55.389
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20263.859 218 461 411 261 365 380 751 212 261 340 131 68
2026/202724 24 0 0 0 0 0 0 0 0 0 0 0
Totale 20.628