UniSa - IRIS Institutional Research Information System

RAMUNNO, Anna
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
AS - Asia 4.687
NA - Nord America 2.707
EU - Europa 1.137
SA - Sud America 203
AF - Africa 44
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 2
Totale 8.788
Salva come PNG Salva come JPEG
Nazione #
HK - Hong Kong 3.377
US - Stati Uniti d'America 2.657
SG - Singapore 626
IT - Italia 490
CN - Cina 294
VN - Vietnam 189
UA - Ucraina 162
BR - Brasile 145
RU - Federazione Russa 144
DE - Germania 74
IE - Irlanda 60
FR - Francia 56
KR - Corea 39
FI - Finlandia 38
IN - India 38
TR - Turchia 35
GB - Regno Unito 32
AR - Argentina 22
SE - Svezia 22
CA - Canada 21
MX - Messico 19
NL - Olanda 17
ZA - Sudafrica 17
BD - Bangladesh 14
JP - Giappone 14
CO - Colombia 10
ES - Italia 10
ID - Indonesia 10
MA - Marocco 10
EC - Ecuador 9
IQ - Iraq 9
PL - Polonia 8
UZ - Uzbekistan 7
AT - Austria 6
AU - Australia 5
CL - Cile 5
PK - Pakistan 5
PY - Paraguay 5
SA - Arabia Saudita 5
CZ - Repubblica Ceca 4
DZ - Algeria 4
TN - Tunisia 4
VE - Venezuela 4
IL - Israele 3
LB - Libano 3
NZ - Nuova Zelanda 3
OM - Oman 3
PH - Filippine 3
SK - Slovacchia (Repubblica Slovacca) 3
BY - Bielorussia 2
EU - Europa 2
GR - Grecia 2
JM - Giamaica 2
JO - Giordania 2
KE - Kenya 2
KW - Kuwait 2
MY - Malesia 2
PE - Perù 2
SN - Senegal 2
AE - Emirati Arabi Uniti 1
AL - Albania 1
AZ - Azerbaigian 1
BO - Bolivia 1
BZ - Belize 1
CH - Svizzera 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
EG - Egitto 1
ET - Etiopia 1
GH - Ghana 1
GT - Guatemala 1
HN - Honduras 1
HR - Croazia 1
HU - Ungheria 1
IR - Iran 1
LT - Lituania 1
LU - Lussemburgo 1
MN - Mongolia 1
MQ - Martinica 1
NG - Nigeria 1
NI - Nicaragua 1
PA - Panama 1
PT - Portogallo 1
SY - Repubblica araba siriana 1
TH - Thailandia 1
TW - Taiwan 1
ZM - Zambia 1
Totale 8.788
Salva come PNG Salva come JPEG
Città #
Hong Kong 3.375
Ann Arbor 450
Singapore 340
San Jose 234
Milan 213
Chandler 197
Jacksonville 183
Woodbridge 178
Ashburn 174
Princeton 145
Dallas 121
Wilmington 106
Houston 79
Dong Ket 77
Beijing 64
The Dalles 64
Council Bluffs 58
Dublin 58
Ho Chi Minh City 54
Salerno 51
Lauterbourg 49
Los Angeles 41
Nanjing 39
Rome 39
Boardman 36
Moscow 36
Andover 34
New York 31
Pellezzano 26
Hanoi 19
Izmir 18
Fairfield 16
Figino 15
Orem 15
Santa Clara 14
São Paulo 14
Tokyo 14
Amsterdam 13
Chennai 13
Chicago 12
Dearborn 12
Hebei 12
Munich 12
Seoul 12
Shenyang 12
Frankfurt am Main 11
Johannesburg 11
Atlanta 10
Brooklyn 10
Changsha 10
Nanchang 10
Jiaxing 9
Mexico City 9
Naples 8
Phoenix 8
Redwood City 8
Rio de Janeiro 8
Tianjin 8
Turin 8
Washington 8
London 7
Nuremberg 7
Tashkent 7
Warsaw 7
Boston 6
Brasília 6
City of London 6
Da Nang 6
Düsseldorf 6
Fisciano 6
Florence 6
Montreal 6
San Francisco 6
Sarno 6
Seattle 6
Stockholm 6
Denver 5
Irpin 5
Manchester 5
Menlo Park 5
New Delhi 5
Norwalk 5
Poplar 5
Pune 5
Quito 5
Toronto 5
Ankara 4
Asunción 4
Bari 4
Brisbane 4
Brno 4
Jakarta 4
Querétaro 4
Turku 4
Vienna 4
Agadir 3
Bogotá 3
Bologna 3
Bratislava 3
Campina Grande 3
Totale 7.112
Salva come PNG Salva come JPEG
Nome #
Non-nucleoside HIV-1 reverse transcriptase (RT) inhibitors: Past, present, and future perspectives. 796
Antioxidant activity of diphenylpropionamide derivatives: synthesis, biologicalevaluation and computational analysis. 619
First dual AK​/GSK-​3β inhibitors endowed with antioxidant properties as multifunctional, potential neuroprotective agents 587
Inhibition of human topoisomerase I and anti-proliferative effects on MCF-7 cells by new titanocene complexes 548
Tetrasubstituted Pyrrole Derivative Mimetics of Protein–Protein Interaction Hot-Spot Residues: A Promising Class of Anticancer Agents Targeting Melanoma Cells 537
Anti-Inflammatory, Antioxidant and Crystallographic Studies of N-Palmitoyl-ethanol Amine (PEA) Derivatives 455
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. 299
Interaction between Alzheimer's Abeta(25-35) peptide and phospholipid bilayers: The role of cholesterol. 216
Tuning the folding states of beta-amyloid fragment A beta(16-35) with different charge of micelle aggregates 186
Effect of flavonoids on A beta(25-35)/DLPC vesicle interaction. 167
Synthesis and biological investigation of peptidomimetic SARS-CoV-2 main protease inhibitors bearing quinoline-based heterocycles at P3 164
Interaction of a beta-sheet breaker peptide with lipid membranes. 159
Characterization of the 1H-cyclopentapyrimidine-2,4(1H,3H)-dione derivative (S)-CPW399 as a novel, potent, and subtype-selective AMPA receptor full agonist with partial desensitization properties. 151
Exploring the Photodynamic Properties of Two Antiproliferative Benzodiazopyrrole Derivatives 148
New anticancer agents mimicking protein recognition motifs 144
A rational approach to the design of selective substrates and potent nontransportable inhibitors of the excitatory amino acid transporter EAAC1 (EAAT3). new glutamate and aspartate analogues as potential neuroprotective agents. 143
Membrane charge dependent states of the beta-amyloid fragment Abeta (16-35) with differently charged micelle aggregates. 143
Tetra-substituted pyrrole derivatives act as potent activators of p53 in melanoma cells 143
Progresses in the pursuit of aldose reductase inhibitors: The structure-based lead optimization step 138
Specific Targeting of Highly Conserved Residues in the HIV-1 Reverse Transcriptase Primer Grip Region. 2. Stereoselective Interaction to Overcome the Effects of Drug Resistant Mutations 135
Targeting Relevant HDACs to Support the Survival of Cone Photoreceptors in Inherited Retinal Diseases: Identification of a Potent Pharmacological Tool with In Vitro and In Vivo Efficacy 125
Activation of the c-Jun N-terminal kinase (JNK) signaling pathway is essential during PBOX-6-induced apoptosis in chronic myelogenous leukemia (CML) cells. 124
Pyrrolo[1,5]benzoxa(thia)zepines as a New Class of Potent Apoptotic Agents. Biological Studies and Identification of an Intracellular Location of Their Drug Target. 120
6-(2-Phenylethyl)nicotine: A novel nicotinic cholinergic receptor ligand. 113
Effects of drug resistance mutations L100I and V106A on the binding of pyrrolobenzoxazepinone nonnucleoside inhibitors to the human immunodeficiency virus type 1 reverse transcriptase catalytic complex. 110
5-methyl-2-carboxamidepyrrole-based novel dual mPGES-1/sEH inhibitors as promising anticancer candidates 107
3-(2-Aminoethyl)pyridine analogs as a4b2 nicotinic cholinergic receptor ligands. 107
Activation of the Wnt Pathway by Small Peptides: Rational Design, Synthesis and Biological Evaluation. 106
Caspase-3 is not essential for DNA fragmentation in MCF-7 cells during apoptosis induced by the pyrrolo-1,5-benzoxazepine, PBOX-6. 103
Novel sterically hindered cannabinoid CB1 receptor ligands 102
Exploring the chemical space around chrysin to develop novel vascular CaV1.2 channel blockers, promising vasorelaxant agents 99
Design, Synthesis and Biological Evaluation of Novel 2-(N-Aryl or Heteroarylphenylsulfonamido)acetic Acids as Aldose Reductase Inhibitors 96
Pyrrolo-1,5-benzoxazepines: a new class of apoptotic agents. 91
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 90
Design and synthesis of multifunctional microtubule targeting agents endowed with dual pro-apoptotic and anti-autophagic efficacy 90
Photo-​control of cancer cell growth by benzodiazo N-​substituted pyrrole derivatives 87
Phosphonium Salt Displays Cytotoxic Effects Against Human Cancer Cell Lines 86
Development of 1-(2-aminophenyl)pyrrole-based amides acting as human topoisomerase I inhibitors 85
Pyrrolo-1,5-benzoxazepines induce apoptosis in chronic myelogenous leukemia (CML) cells by bypassing the apoptotic suppressor Bcr-Abl. 85
Development of potent and selective FAAH inhibitors with improved drug-like properties as potential tools to treat neuroinflammatory conditions 84
The stereoselective targeting of a specific enzyme-substrate complex is the molecular mechanism for the synergic inhibition of HIV-1 reverse transcriptase by (R)-(-)-PPO464. A novel generation of nonnucleoside inhibitors. 83
Pyrrolobenzoxazepinone derivatives as non-nucleoside HIV-1 RT inhibitors: Further structure-activity relationship studies and identification of more potent broad-spectrum HIV-1 RT inhibitors with antiviral activity. 83
Development of Epigenetic Modifiers with Therapeutic Potential in FMS-Related Tyrosine Kinase 3/Internal Tandem Duplication (FLT3/ITD) Acute Myeloid Leukemia and Other Blood Malignancies 80
Azetidin-2-one-based small molecules as dual hHDAC6/HDAC8 inhibitors: Investigation of their mechanism of action and impact of dual inhibition profile on cell viability 80
Inhibition of G1 cyclin-dependent kinase activity during growth arrest of human astrocytoma cells by the pyrrolo-1,5-benzoxazepine, PBOX-21. 79
Phenol-derived CVFM analog inhibitors of ras farnesyltransferase possessing cellular in vitro activity. 75
Synthesis of New Molecular Probes for Investigation of Steroid Biosynthesis Induced by Selective Interaction with Peripheral Type Benzodiazepine Receptors (PBR). 69
Discovery of p-Trifluoromethylbenzohydrazide Derivatives as Potent Antiviral Agents against Monkeypox Virus 68
Ultrasound-Assisted Extraction, Chemical Characterization, and Impact on Cell Viability of Food Wastes Derived from Southern Italy Autochthonous Citrus Fruits 65
Development of Potent and Selective Monoacylglycerol Lipase Inhibitors. SARs, Structural Analysis, and Biological Characterization 63
Bioguided Identification of Polymethoxyflavones as Novel Vascular CaV1.2 Channel Blockers from Citrus Peel 60
Optimization of Potent and Specific Trypanothione Reductase Inhibitors: A Structure-Based Drug Discovery Approach 52
Extra Virgin Olive Oil Extracts of Indigenous Southern Tuscany Cultivar Act as Anti-Inflammatory and Vasorelaxant Nutraceuticals 49
Pioneering first‐in‐class FAAH‐HDAC inhibitors as potentialmultitarget neuroprotective agents 47
Synthetic derivatives of natural cinnamic acids as potential anti-colorectal cancer agents 46
Synthesis, bioactivity and docking studies of chrysin derivatives as iNOS inhibitors 37
Targeting Class I Histone Deacetylases Triggers Antitumor Responses in Colorectal Cancer In Vitro and In Vivo 15
Extra Virgin Olive Oils from Minuta cv. Display a Characteristic Volatilomic Profile and Their Phytocomplexes Exert Antioxidant Activity in CaCo-2 Cells 3
Totale 8.942
Salva come PNG Salva come JPEG
Categoria #
all - tutte 23.268
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 23.268
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022248 0 0 0 0 9 2 3 9 36 38 29 122
2022/2023456 43 45 10 60 72 88 1 30 73 1 22 11
2023/2024305 20 24 15 20 21 39 19 28 46 19 11 43
2024/2025613 23 6 13 23 30 58 131 44 120 30 63 72
2025/20265.640 308 1.820 1.580 178 326 159 405 102 131 240 76 315
2026/20271 1 0 0 0 0 0 0 0 0 0 0 0
Totale 8.942