UniSa - IRIS Institutional Research Information System

BRUNO, Ines
 Distribuzione geografica
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Continente #
NA - Nord America 4.358
EU - Europa 1.521
AS - Asia 975
SA - Sud America 177
AF - Africa 11
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 3
Totale 7.051
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Nazione #
US - Stati Uniti d'America 4.329
IT - Italia 413
CN - Cina 349
SG - Singapore 319
UA - Ucraina 306
RU - Federazione Russa 223
DE - Germania 208
BR - Brasile 161
IE - Irlanda 109
SE - Svezia 86
TR - Turchia 83
FI - Finlandia 78
VN - Vietnam 68
HK - Hong Kong 63
KR - Corea 49
GB - Regno Unito 28
CA - Canada 21
IN - India 17
CZ - Repubblica Ceca 16
NL - Olanda 14
AT - Austria 11
UZ - Uzbekistan 7
ES - Italia 6
PL - Polonia 6
AR - Argentina 5
EU - Europa 5
MX - Messico 5
AZ - Azerbaigian 4
FR - Francia 4
JP - Giappone 4
ZA - Sudafrica 4
BG - Bulgaria 3
IQ - Iraq 3
PE - Perù 3
AE - Emirati Arabi Uniti 2
AU - Australia 2
CH - Svizzera 2
CO - Colombia 2
DZ - Algeria 2
EC - Ecuador 2
GT - Guatemala 2
IL - Israele 2
MA - Marocco 2
PK - Pakistan 2
RS - Serbia 2
TH - Thailandia 2
UY - Uruguay 2
VE - Venezuela 2
A2 - ???statistics.table.value.countryCode.A2??? 1
EG - Egitto 1
HU - Ungheria 1
LU - Lussemburgo 1
MK - Macedonia 1
NG - Nigeria 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PR - Porto Rico 1
PT - Portogallo 1
RO - Romania 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 7.051
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Città #
Ann Arbor 1.074
Woodbridge 439
Chandler 429
Houston 386
Jacksonville 372
Wilmington 324
Princeton 289
Ashburn 130
Singapore 118
Dublin 101
Salerno 101
Izmir 81
Nanjing 78
Beijing 68
Andover 67
Dearborn 67
Dong Ket 66
Boardman 64
Hong Kong 59
Munich 56
Pellezzano 54
Moscow 35
Fairfield 30
Mestre 27
Düsseldorf 25
Redwood City 25
Shenyang 25
Guangzhou 23
Jiaxing 21
Fisciano 20
Hebei 20
Changsha 17
Nanchang 15
Naples 15
Turku 15
Brno 14
Norwalk 14
The Dalles 14
Acerra 13
Nuremberg 13
Spinea 13
Washington 13
Columbus 12
New York 12
Seattle 12
Los Angeles 11
Pune 10
Tianjin 10
Dallas 9
Jinan 9
Montreal 9
São Paulo 9
San Francisco 8
Galway 7
Chicago 6
London 6
Tashkent 6
Warsaw 6
Amsterdam 5
Belo Horizonte 5
Boston 5
Brooklyn 5
Curitiba 5
Indiana 5
Nürnberg 5
Ottawa 5
Arzano 4
Caianello 4
Council Bluffs 4
Edinburgh 4
Johannesburg 4
Nocera Superiore 4
Pignola 4
Porto Alegre 4
Pozzuoli 4
Rome 4
Tappahannock 4
Tokyo 4
Vienna 4
Wuhan 4
Yubileyny 4
Baghdad 3
Baku 3
Cambridge 3
Campinas 3
Charlotte 3
Chennai 3
Cormano 3
Granada 3
Guarulhos 3
Haikou 3
Jundiaí 3
Manaus 3
Messina 3
Mexico City 3
Napoli 3
Palermo 3
Phoenix 3
San Diego 3
Santa Clara 3
Totale 5.129
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Nome #
9H-purine scaffold reveals induced-fit pocket plasticity of the BRD9 bromodomain 169
Bioactive Prenylhydroquinone Sulfates and a Novel C31 Furanoterpene Alcohol Sulfate from the Marine Sponge, Ircinia Sp. 139
40 th "A. Corbella" International Summer School on Organic Synthesis - ISOS 2015 137
Starfish Saponins, Part 50. Steroidal Glycosides from the Okinawan Starfish Nardoa tuberculata 136
(±)-Gelliusines A and B, Two Diastereomeric Brominated Tris-indole Alkaloids from a Deep Water New Caledonian Marine Sponge (Gellius or Orina sp.) 129
Biologically active guanidine alkaloids from the Mediterranean sponge Crambe crambe 126
Makaluvamine P: a New Cytotoxic Pyrroloiminoquinone from Zyzzya cf. fuliginosa 125
Dimeric and trimeric triazole based molecules as a new class of Hsp90 molecular chaperone inhibitors 121
Targeting the Hsp90 C-terminal domain by the chemically accessible dihydropyrimidinone scaffold 121
Anti-inflammatory and analgesic activity of a novel inhibitor of microsomal prostaglandin E synthase-1 expression 119
Design and Synthesis of cyclopeptide analogues of the potent Histone deacetylase inhibitor FR235222 117
Design, Synthesis, and Biological Activity of Hydroxamic Tertiary Amines as Histone Deacetylase Inhibitors 115
Synthesis, Conformational Analysis, and Cytotoxicity of New Analogues of the Natural Cyclodepsipeptide Jaspamide 114
Design and synthesis of a second series of triazole-based compounds as potent dual mPGES-1 and 5-lipoxygenase inhibitors 113
Crambines C1 and C2: two further ichthyotoxic guanidine alkaloids from the sponge Crambe crambe 112
Correction: Identification of the key structural elements of a dihydropyrimidinone core driving toward more potent Hsp90 C-terminal inhibitors 109
New dihydropyrimidin-2(1H)-one based Hsp90 C-terminal inhibitors 108
STARFISH SAPONINS .38. STEROIDAL GLYCOSIDES FROM THE STARFISH PYCNOPODIA-HELIANTHOIDES 107
Isolation and structure of new polyhydroxylated sterols from a deep-water starfish of the genus Rosaster 106
Bioactive Macrolides and Cylopeptides from South Pacific Sponges 105
Design,virtual Screening and Synthesis of Potential Microsomal Prostaglandine E2 Synthase-1 (mPGES-1)Inhibitors 103
Exploration of the dihydropyrimidine scaffold for the development of new potential anti-inflammatory agents blocking prostaglandin E2 synthase-1 enzyme (mPGES-1) 102
Elucidating new structural features of the triazole scaffold for the development of mPGES-1 inhibitors 102
Molecular modeling studies toward the structural optimization of new cyclopeptide-based HDAC inhibitors modeled on the natural product FR235222 101
Total Synthesis, NMR Solution Structure, and Binding Model of the Potent Histone Deacetylase Inhibitor FR235222 100
Edwardsolides A, B and C. New Sesquiterpenoid Lactones from the Mediterranean OctocoralMaasella edwardsi 99
Novel HIV-Inhibitory Halistanol Sulfates F-H from a Marine Sponge, Pseudoaxinissa digitata 99
Structural Insights for the Optimization of Dihydropyrimidin-2(1H)-one Based mPGES-1 Inhibitors 98
Targeting Microsomal Prostaglanding E2 Synthase 1 for the Development of new potential Anti-Inflammatory Drugs 98
New Bisindole Alkaloids of the Topsentin and Hamacanthin classes from the Mediterranean marine sponge Rhaphisia lacazei. 95
Synthesis of new mono and bis amides projected as potential histone deacetylase (HDAC) inhibitors 94
Further brominated bis- and tris-indole alkaloids from the deep water New Caledonian marine sponge Orina sp. 94
Polycyclic guanidine alkaloids from the marine sponge Crambe crambe and calcium channel blocker activity of crambescidin 816 92
Dactylolide, a New Cytotoxic Macrolide from the Vanuatu Sponge Dactylospongia sp. 91
Toward the Discovery of New Agents Able to Inhibit the Expression of Microsomal Prostaglandin E Synthase-1 Enzyme as Promising Tools in Drug Development 91
Structure-Based Discovery of Inhibitors of Microsomal Prostaglandin E2 Synthase-1, 5-Lipoxygenase and 5-Lipoxygenase-Activating Protein: Promising Hits for the Development of New Anti-inflammatory Agents 91
Two new guanidine alkaloids from the Mediterranean sponge Crambe crambe 91
Starfish saponins, part 43. Structures of two new sulfated steroidal fucofuranosides (imbricatosides A and B) and six new polyhydroxysteroids from the starfish Dermasterias imbricata 91
Development of a second generation of inhibitors of microsomal prostaglandin E synthase 1 expression bearing the gamma-hydroxybutenolide scaffold 88
Discovery of new potent molecular entities able to inhibit mPGES-1 88
A Combinatorial Virtual Screening Approach Driving the Synthesis of 2,4-Thiazolidinedione-Based Molecules as New Dual mPGES-1/5-LO Inhibitors 87
Synthesis of 2-Amino-8-oxodecanoic Acids (Aodas) Present in Natural Histone Deacetylase Inhibitors. 86
Synthesis and Pharmacological Evaluation of a Selected Library of New Potential Anti-Inflammatory Agents Bearing the gamma-hydroxybutenolide Scaffold: a New Class of Inhibitors of Prostanoid Production Through the Selective Modulation of Microsomal prostaglandin E Synthase-1 Expression (mPGES-1). 86
Structure-Based Design of Microsomal Prostaglandin E2 Synthase-1 (mPGES-1) Inhibitors using a Virtual Fragment Growing Optimization Scheme 86
Marine eicosanoids: occurrence of 8,11,12-trihydroxylated eicosanoic acids in starfishes 83
Synthesis, structural aspects and cytotoxicity of the natural cyclopeptides yunnanins A, C and phakellistatins 1, 10 82
Synthesis and biological activity of cyclotetrapeptide analogues of the natural HDAC inhibitor FR235222 81
Identification of the key structural elements of a dihydropyrimidinone core driving toward more potent Hsp90 C-terminal inhibitors 81
Cyclic Peptoids as Mycotoxin Mimics: An Exploration of Their Structural and Biological Properties 80
Discovery and synthesis of the first selective BAG domain modulator of BAG3 as an attractive candidate for the development of a new class of chemotherapeutics 79
Discovery of new molecular entities able to strongly interfere with Hsp90 C-terminal domain 78
Structural basis for the design and synthesis of selective HDAC inhibitors 77
Synthetic approach to bioactive marine Cyclopeptide Halipeptin A 77
Critical Surveys Covering the Year 2004:Total Synthesis of Natural Products 76
Synthetic and pharmacological studies on new simplified analogues of the potent actin-targeting Jaspamide 74
Chemistry and Biology of Chromatin Remodeling Agents: State of Art and Future Perspectives of HDAC Inhibitors 74
Dragmacidin F: a New Antiviral Bromo-indole Alkaloid from the Mediterranean Sponge Halicortex sp. 73
Synthesis, structure, and biological aspects of cyclopeptides related to marine phakellistatins 7-9 72
Inhibition of Microsomal Prostaglandin E2 Synthase 1: focused design of new anti-inflammatory and anti-cancer drugs 72
Isolation and NMR characterization of rosacelose, a novel sulfated polysaccharide from the sponge Mixylla rosacea. 70
Effects of FR235222, a novel HDAC inhibitor, in proliferation and apoptosis of human leukaemia cell lines: role of annexin A1 70
Starfish saponins. Part 14. Structures of the steroidal glycoside sufates from the starfish Marthasterias glacialis 69
Identification of 2,4,5-trisubstituted-2,4-dihydro-3H-1,2,4-triazol-3-one-based small molecules as selective BRD9 binders 68
Tossine marine: nuove affascinanti molecole bioattive da invertebrati e microrganismi marini. Recenti acquisizioni e prospettive 68
Identification of new γ-hydroxybutenolides that preferentially inhibit the activity of mPGES-1 67
Synthesis, structural aspects and bioactivity of the marine cyclopeptide hymenamide C. 64
Synthesis, structural aspects and bioactivity of the marine cyclopeptide hymenamide C. 61
Identification of the 2-Benzoxazol-2-yl-phenol Scaffold as New Hit for JMJD3 Inhibition 61
Discovery of noscapine derivatives as potential β-tubulin inhibitors 61
Synthesis And Biological Properties Of The Seven Alanine-Modified Analogues Of The Marine Cyclopeptide Hymenamide C 57
Synthesis, solution structure, and bioactivity of six new simplified analogues of the natural cyclodepsipeptide jaspamide 56
Identification by Inverse Virtual Screening of magnolol-based scaffold as new tankyrase-2 inhibitors 56
Spongidepsin, a new cytotoxic macrolide from Spongia sp. 55
Tuning the biomimetic performances of 4-hydroxyproline-containing cyclic peptoids 55
Regioselective Entry to Bromo-γ -hydroxybutenolides: Useful Building Blocks for Assemblying Natural Product-Like Libraries. 54
Structural Refinement of 2,4-Thiazolidinedione Derivatives as New Anticancer Agents Able to Modulate the BAG3 Protein 51
Glucopyranosylbianthrones from the Algerian Asphodelus tenuifolius: Structural Insights and Biological Evaluation on Melanoma Cancer Cells 45
Repositioning of Quinazolinedione-Based Compounds on Soluble Epoxide Hydrolase (sEH) through 3D Structure-Based Pharmacophore Model-Driven Investigation 42
Introducing structure-based three-dimensional pharmacophore models for accelerating the discovery of selective BRD9 binders 41
Targeting mPGES-1 by a Combinatorial Approach: Identification of the Aminobenzothiazole Scaffold to Suppress PGE2Levels 29
A multidisciplinary functional proteomics-aided strategy as a tool for the profiling of a novel cytotoxic thiadiazolopyrimidone 29
From Natural Compounds to Bioactive Molecules through NMR and In Silico Methodologies 26
Identification of 2,4-Dinitro-Biphenyl-Based Compounds as MAPEG Inhibitors 26
Identification of 2-(thiophen-2-yl)acetic Acid-Based Lead Compound for mPGES-1 Inhibition 25
Identification of a New Promising BAG3 Modulator Featuring the Imidazopyridine Scaffold 19
Exploring the chemical space of functionalized [1,2,4]triazolo[4,3-a]quinoxaline-based compounds targeting the bromodomain of BRD9 16
Identification of the first-in-class dual inhibitor targeting BAG3 and HSP70 proteins to disrupt multiple chaperone pathways 12
In Silico Design, Chemical Synthesis, Biophysical and in Vitro Evaluation for the Identification of 1-Ethyl-1H-Pyrazolo[3,4-b]Pyridine-Based BRD9 Binders 11
Identification of 2-Aminoacyl-1,3,4-thiadiazoles as Prostaglandin E2 and Leukotriene Biosynthesis Inhibitors 11
Identification of Novel Bromodomain-Containing Protein 4 (BRD4) Binders through 3D Pharmacophore-Based Repositioning Screening Campaign 11
Identification of Honokiol-Based Scaffold to Design Tankyrase 1/2 Inhibitors by In Silico and In Vitro Studies 8
Totale 7.234
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Categoria #
all - tutte 26.506
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 26.506
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021610 4 61 65 5 73 36 74 6 111 7 78 90
2021/2022528 4 0 0 14 13 14 12 14 81 68 68 240
2022/20231.000 90 92 22 143 121 192 6 105 131 0 64 34
2023/2024392 37 59 26 16 48 75 19 19 6 15 12 60
2024/20251.172 47 9 7 59 29 112 239 98 184 52 146 190
2025/202632 32 0 0 0 0 0 0 0 0 0 0 0
Totale 7.234