BARRESI, ELISABETTA
 Distribuzione geografica
Continente #
NA - Nord America 869
EU - Europa 660
AS - Asia 244
OC - Oceania 23
SA - Sud America 17
AF - Africa 14
Totale 1.827
Nazione #
US - Stati Uniti d'America 857
IT - Italia 292
CN - Cina 118
FR - Francia 95
DE - Germania 59
ES - Italia 51
IN - India 29
AT - Austria 23
GB - Regno Unito 23
AU - Australia 22
NL - Olanda 22
VN - Vietnam 21
UA - Ucraina 18
JP - Giappone 17
RU - Federazione Russa 17
HK - Hong Kong 16
CZ - Repubblica Ceca 15
EC - Ecuador 13
CA - Canada 11
FI - Finlandia 9
SG - Singapore 9
CH - Svizzera 8
KR - Corea 7
EG - Egitto 6
PT - Portogallo 6
ZA - Sudafrica 6
IE - Irlanda 5
IR - Iran 5
LB - Libano 4
AE - Emirati Arabi Uniti 3
GR - Grecia 3
HU - Ungheria 3
ID - Indonesia 3
PL - Polonia 3
SE - Svezia 3
TH - Thailandia 3
TW - Taiwan 3
BR - Brasile 2
CL - Cile 2
TR - Turchia 2
BE - Belgio 1
DZ - Algeria 1
IL - Israele 1
IQ - Iraq 1
JO - Giordania 1
LT - Lituania 1
MY - Malesia 1
NZ - Nuova Zelanda 1
PA - Panama 1
RO - Romania 1
SI - Slovenia 1
SK - Slovacchia (Repubblica Slovacca) 1
TN - Tunisia 1
Totale 1.827
Città #
Serra 109
Ashburn 81
Ann Arbor 67
Fairfield 65
Houston 65
Madrid 49
Buffalo 48
Seattle 46
Santa Cruz 42
Woodbridge 30
Beijing 24
Boardman 22
Vienna 22
Columbus 20
Chicago 17
Pisa 17
Sydney 15
Wilmington 15
Cambridge 13
Dong Ket 13
Milan 13
Quito 13
Shanghai 13
Cedar Knolls 12
Dallas 12
Fuzhou 12
Mountain View 12
Hangzhou 11
Vicopisano 11
Wuhan 11
Council Bluffs 10
Des Moines 10
Pistoia 10
Bremen 9
Paris 9
Colle di Val d'Elsa 8
Hong Kong 8
University Park 8
Bengaluru 7
Florence 7
Grenoble 7
Las Vegas 7
Naples 7
Rome 7
Amsterdam 6
Aversa 6
Helsinki 6
Los Angeles 6
Cerro Maggiore 5
Clearwater 5
Frankfurt am Main 5
Guangzhou 5
Muizenberg 5
Salerno 5
San Diego 5
Beirut 4
Casarza Ligure 4
Central 4
Centre Hall 4
Chengdu 4
Chongqing 4
Dublin 4
Kolkata 4
Livorno 4
London 4
Madison 4
Ottawa 4
Phoenix 4
Provo 4
Quarrata 4
Singapore 4
Toronto 4
Viterbo 4
Geneva 3
Henderson 3
Miami 3
Modena 3
Palo Alto 3
Parsippany 3
Pignone 3
San Francisco 3
Tokyo 3
Turin 3
Zurich 3
Annandale 2
Atlanta 2
Bangkok 2
Calci 2
Cascina 2
Crugers 2
East Ham 2
Esslingen am Neckar 2
Fisciano 2
Geumjeong-gu 2
Glasgow 2
Lappeenranta 2
Leeds 2
Messina 2
Milpitas 2
Mohali 2
Totale 1.210
Nome #
TSPO PIGA ligands promote neurosteroidogenesis and human astrocyte well-being, file e0d6c927-910c-fcf8-e053-d805fe0aa794 226
TSPO ligand residence time influences human glioblastoma multiforme cell death/life balance, file e0d6c926-900d-fcf8-e053-d805fe0aa794 219
TSPO ligand residence time: a new parameter to predict compound neurosteroidogenic efficacy, file e0d6c926-d013-fcf8-e053-d805fe0aa794 218
Novel fluorescent triazinobenzimidazole derivatives as probes for labelling human A1 and A2B adenosine receptor subtypes, file e0d6c92b-c55e-fcf8-e053-d805fe0aa794 183
Long lasting MDM2/Translocator protein modulator: a new strategy for irreversible apoptosis of human glioblastoma cells, file e0d6c927-c866-fcf8-e053-d805fe0aa794 165
Long lasting inhibition of Mdm2-p53 interaction potentiates mesenchymal stem cell differentiation into osteoblasts, file e0d6c92c-354e-fcf8-e053-d805fe0aa794 100
Iminothioethers as Hydrogen Sulfide Donors: From the Gasotransmitter Release to the Vascular Effects, file e0d6c92b-82e4-fcf8-e053-d805fe0aa794 99
Deepening the Topology of the Translocator Protein Binding Site by Novel N,N-Dialkyl-2-arylindol-3-ylglyoxylamides, file e0d6c92b-cb7f-fcf8-e053-d805fe0aa794 75
Lead Optimization of 2-Phenylindolylglyoxylyldipeptide Murine Double Minute (MDM)2/Translocator Protein (TSPO) Dual Inhibitors for the Treatment of Gliomas, file e0d6c930-9943-fcf8-e053-d805fe0aa794 64
Apoptosis Therapy in Cancer: The First Single-molecule Co-activating p53 and the Translocator Protein in Glioblastoma, file e0d6c929-3740-fcf8-e053-d805fe0aa794 55
Exploiting the 4-Phenylquinazoline Scaffold for the Development of High Affinity Fluorescent Probes for the Translocator Protein (TSPO), file e0d6c930-7bf9-fcf8-e053-d805fe0aa794 55
Sulfonamides incorporating heteropolycyclic scaffolds show potent inhibitory action against carbonic anhydrase isoforms I, II, IX and XII, file e0d6c92b-b770-fcf8-e053-d805fe0aa794 53
4-Substituted Benzenesulfonamides Incorporating Bi/Tricyclic Moieties Act as Potent and Isoform-Selective Carbonic Anhydrase II/IX Inhibitors, file e0d6c92b-b587-fcf8-e053-d805fe0aa794 50
New insights in the structure-activity relationships of 2-phenylamino-substituted benzothiopyrano[4,3-d]pyrimidines as kinase inhibitors, file e0d6c92b-9166-fcf8-e053-d805fe0aa794 47
A mixed-valence diruthenium(ii,iii) complex endowed with high stability: from experimental evidence to theoretical interpretation, file e0d6c92f-13e4-fcf8-e053-d805fe0aa794 29
Phenylpyrazolo[1,5-a]quinazolin-5(4H)-one: a suitable scaffold for the development of non-camptothecin Topoisomerase I (Top1) inhibitors, file e0d6c92c-5c4f-fcf8-e053-d805fe0aa794 26
Multiple Topoisomerase I (TopoI), Topoisomerase II (TopoII) and Tyrosyl-DNA Phosphodiesterase (TDP) inhibitors in the development of anticancer drugs, file e0d6c92f-81fc-fcf8-e053-d805fe0aa794 26
Residence Time (RT), a new parameter to predict neurosteroidogenic efficacy of Translocator Protein (TSPO) ligands: N,N-dialkyl-2-arylindol-3-ylglyoxylamides, a case study, file e0d6c92b-a2b1-fcf8-e053-d805fe0aa794 20
The Alpha Keto Amide Moiety as a Privileged Motif in Medicinal Chemistry: Current Insights and Emerging Opportunities, file e0d6c931-a390-fcf8-e053-d805fe0aa794 13
Allosterism vs. Orthosterism: Recent Findings and Future Perspectives on A2B AR Physio-Pathological Implications, file e0d6c931-8347-fcf8-e053-d805fe0aa794 11
Diruthenium(ii,iii) paddlewheel complexes: effects of bridging and axial ligands on anticancer properties, file 1d659f7e-9987-44cd-a572-ec80b421a21c 9
A complex bearing TSPO PIGA ligand coordinated to the [Au(PEt3)]+ pharmacophore is highly cytotoxic against ovarian cancer cells, file e4741689-3cec-44c5-b0ae-3aa643dd4dca 9
Benzothiopyranoindole- and pyridothiopyranoindole-based antiproliferative agents targeting topoisomerases, file e0d6c92e-466c-fcf8-e053-d805fe0aa794 8
Exploiting the 4-Phenylquinazoline Scaffold for the Development of High Affinity Fluorescent Probes for the Translocator Protein (TSPO), file e0d6c92a-0b3b-fcf8-e053-d805fe0aa794 7
Novel 2-substituted-benzimidazole-6-sulfonamides as carbonic anhydrase inhibitors: synthesis, biological evaluation against isoforms I, II, IX and XII and molecular docking studies, file e0d6c92e-8301-fcf8-e053-d805fe0aa794 6
An update into the medicinal chemistry of translocator protein (TSPO) ligands, file e0d6c92f-2892-fcf8-e053-d805fe0aa794 6
Novel positive allosteric modulators of A2B adenosine receptor acting as bone mineralisation promoters, file e0d6c930-154d-fcf8-e053-d805fe0aa794 6
Strategies for the improvement of metal-based chemotherapeutic treatments, file e0d6c931-2203-fcf8-e053-d805fe0aa794 6
Carbonic Anhydrase Activators for Neurodegeneration: An Overview, file e0d6c932-4879-fcf8-e053-d805fe0aa794 6
null, file 318ef464-8aa7-4b1d-be28-6012267ab7c9 4
Unbinding of Translocator Protein 18 kDa (TSPO) Ligands: From in Vitro Residence Time to in Vivo Efficacy via in Silico Simulations, file e0d6c92e-1981-fcf8-e053-d805fe0aa794 4
Multiple Topoisomerase I (TopoI), Topoisomerase II (TopoII) and Tyrosyl-DNA Phosphodiesterase (TDP) inhibitors in the development of anticancer drugs, file e0d6c92f-81fb-fcf8-e053-d805fe0aa794 4
Carbonic anhydrase activation profile of indole-based derivatives, file e0d6c931-882d-fcf8-e053-d805fe0aa794 4
De novo neurosteroidogenesis in human microglia: Involvement of the 18 kda translocator protein, file e0d6c931-a2a0-fcf8-e053-d805fe0aa794 4
New antiproliferative agents derived from tricyclic 3,4-dihydrobenzo[4,5]imidazo[1,2-a][1,3,5]triazine scaffold: synthesis and pharmacological effects, file 05bf5b55-6e3d-4623-9d95-6ae5ff165e7e 3
Phenylpyrazolo[1,5-a]quinazolin-5(4H)-one: a suitable scaffold for the development of non-camptothecin Topoisomerase I (Top1) inhibitors, file e0d6c926-3fe9-fcf8-e053-d805fe0aa794 3
Deepening the Topology of the Translocator Protein Binding Site by Novel N,N-Dialkyl-2-arylindol-3-ylglyoxylamides, file e0d6c927-1b29-fcf8-e053-d805fe0aa794 3
Iminothioethers as Hydrogen Sulfide Donors: From the Gasotransmitter Release to the Vascular Effects, file e0d6c929-afb4-fcf8-e053-d805fe0aa794 3
Residence Time (RT), a new parameter to predict neurosteroidogenic efficacy of Translocator Protein (TSPO) ligands: N,N-dialkyl-2-arylindol-3-ylglyoxylamides, a case study, file e0d6c92b-a2ae-fcf8-e053-d805fe0aa794 3
Sulfonamides incorporating heteropolycyclic scaffolds show potent inhibitory action against carbonic anhydrase isoforms I, II, IX and XII, file e0d6c92b-b585-fcf8-e053-d805fe0aa794 3
Discovery of Pyrido[3′,2′:5,6]thiopyrano[4,3- d]pyrimidine-Based Antiproliferative Multikinase Inhibitors, file e0d6c92d-026d-fcf8-e053-d805fe0aa794 3
Discovery of Pyrido[3′,2′:5,6]thiopyrano[4,3- d]pyrimidine-Based Antiproliferative Multikinase Inhibitors, file e0d6c92e-4a2e-fcf8-e053-d805fe0aa794 3
Tetrahydroquinazole-based secondary sulphonamides as carbonic anhydrase inhibitors: synthesis, biological evaluation against isoforms I, II, IV, and IX, and computational studies, file e0d6c931-7dee-fcf8-e053-d805fe0aa794 3
Two mixed valence diruthenium(ii,iii) isomeric complexes show different anticancer properties, file e0d6c931-a464-fcf8-e053-d805fe0aa794 3
Target-Based Anticancer Indole Derivatives for the Development of Anti-Glioblastoma Agents, file 837fe3a1-a2c5-4f2c-9446-9b13643af92a 2
A cyanine-based NIR fluorescent Vemurafenib analog to probe BRAFV600E in cancer cells, file 8f951b78-6e7e-49d1-aaba-0cff216cb1f3 2
Modulation of A2B Adenosine Receptor by 1-Benzyl-3-ketoindole Derivatives, file e0d6c926-3fe8-fcf8-e053-d805fe0aa794 2
4-Substituted Benzenesulfonamides Incorporating Bi/Tricyclic Moieties Act as Potent and Isoform-Selective Carbonic Anhydrase II/IX Inhibitors, file e0d6c92a-e588-fcf8-e053-d805fe0aa794 2
Lead Optimization of 2-Phenylindolylglyoxylyldipeptide Murine Double Minute (MDM)2/Translocator Protein (TSPO) Dual Inhibitors for the Treatment of Gliomas, file e0d6c930-69b9-fcf8-e053-d805fe0aa794 2
Targeting the 18-kDa translocator protein: Recent perspectives for neuroprotection, file e0d6c930-eab8-fcf8-e053-d805fe0aa794 2
Inhibition studies on carbonic anhydrase isoforms I, II, IV and IX with N-arylsubstituted secondary sulfonamides featuring a bicyclic tetrahydroindazole scaffold, file e0d6c931-21c9-fcf8-e053-d805fe0aa794 2
New antiproliferative agents derived from tricyclic 3,4-dihydrobenzo[4,5]imidazo[1,2-a][1,3,5]triazine scaffold: synthesis and pharmacological effects, file 8e91915f-52da-40bb-baa1-f895bec21f13 1
Indol-3-ylglyoxylamide as Privileged Scaffold in Medicinal Chemistry, file ae326778-5fa6-4d4f-8327-9a65144e090d 1
Structure-Activity Relationship Refinement and Further Assessment of 4-Phenylquinazoline-2-carboxamide Translocator Protein Ligands as Antiproliferative Agents in Human Glioblastoma Tumors., file e0d6c929-31e8-fcf8-e053-d805fe0aa794 1
Benzothiopyranoindole- and pyridothiopyranoindole-based antiproliferative agents targeting topoisomerases, file e0d6c92b-8836-fcf8-e053-d805fe0aa794 1
New insights in the structure-activity relationships of 2-phenylamino-substituted benzothiopyrano[4,3-d]pyrimidines as kinase inhibitors, file e0d6c92b-e71c-fcf8-e053-d805fe0aa794 1
Unbinding of Translocator Protein 18 kDa (TSPO) Ligands: From in Vitro Residence Time to in Vivo Efficacy via in Silico Simulations, file e0d6c92d-ecd7-fcf8-e053-d805fe0aa794 1
A mixed-valence diruthenium(ii,iii) complex endowed with high stability: from experimental evidence to theoretical interpretation, file e0d6c92f-2b3e-fcf8-e053-d805fe0aa794 1
Enriching the arsenal of pharmacological tools against mical2, file e0d6c931-722b-fcf8-e053-d805fe0aa794 1
Two mixed valence diruthenium(ii,iii) isomeric complexes show different anticancer properties, file e0d6c931-76d6-fcf8-e053-d805fe0aa794 1
Drug repurposing meets DNA independent pathways: targeting alternative substrates for anticancer therapy, file e0d6c931-9cca-fcf8-e053-d805fe0aa794 1
Tetrahydroquinazole-based secondary sulphonamides as carbonic anhydrase inhibitors: synthesis, biological evaluation against isoforms I, II, IV, and IX, and computational studies, file e0d6c931-a0eb-fcf8-e053-d805fe0aa794 1
Cancer Immunotherapy: An Overview on Small Molecules as Inhibitors of the Immune Checkpoint PD-1/PD-L1 (2015-2021), file e0d6c932-3d0e-fcf8-e053-d805fe0aa794 1
Totale 1.873
Categoria #
all - tutte 5.330
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 5.330


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201975 0 0 0 0 0 0 0 0 0 0 29 46
2019/2020164 23 19 4 10 16 12 14 11 20 11 9 15
2020/2021257 8 20 2 14 18 12 23 7 62 30 34 27
2021/2022390 40 21 23 59 46 20 12 18 16 5 107 23
2022/2023423 28 30 58 59 39 28 18 27 40 38 35 23
2023/2024439 15 22 43 30 51 39 58 47 17 48 69 0
Totale 1.873