IRIS
BUEMI, MARIAROSA
 Distribuzione geografica
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Continente #
EU - Europa 2.070
NA - Nord America 1.702
AS - Asia 1.055
SA - Sud America 304
AF - Africa 32
Totale 5.163
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Nazione #
US - Stati Uniti d'America 1.676
RU - Federazione Russa 1.133
SG - Singapore 412
CN - Cina 357
BR - Brasile 267
IE - Irlanda 256
SE - Svezia 233
IT - Italia 147
HK - Hong Kong 117
FR - Francia 66
DE - Germania 52
VN - Vietnam 48
GB - Regno Unito 46
FI - Finlandia 39
IN - India 39
UA - Ucraina 22
BE - Belgio 21
AR - Argentina 16
ZA - Sudafrica 13
IQ - Iraq 12
MX - Messico 12
MA - Marocco 11
BD - Bangladesh 10
CA - Canada 10
CZ - Repubblica Ceca 10
PL - Polonia 10
TR - Turchia 10
EC - Ecuador 8
JP - Giappone 7
SA - Arabia Saudita 6
AE - Emirati Arabi Uniti 5
ID - Indonesia 5
NL - Olanda 5
ES - Italia 4
MY - Malesia 4
AT - Austria 3
CH - Svizzera 3
CL - Cile 3
GR - Grecia 3
JO - Giordania 3
LK - Sri Lanka 3
LU - Lussemburgo 3
PK - Pakistan 3
PY - Paraguay 3
RO - Romania 3
UZ - Uzbekistan 3
AM - Armenia 2
AZ - Azerbaigian 2
BO - Bolivia 2
LV - Lettonia 2
NO - Norvegia 2
PE - Perù 2
TN - Tunisia 2
BG - Bulgaria 1
BH - Bahrain 1
CG - Congo 1
CO - Colombia 1
CR - Costa Rica 1
DZ - Algeria 1
EG - Egitto 1
GT - Guatemala 1
HU - Ungheria 1
JM - Giamaica 1
KE - Kenya 1
KR - Corea 1
LB - Libano 1
LT - Lituania 1
MK - Macedonia 1
ML - Mali 1
MN - Mongolia 1
NI - Nicaragua 1
NP - Nepal 1
PS - Palestinian Territory 1
PT - Portogallo 1
QA - Qatar 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
UY - Uruguay 1
VE - Venezuela 1
Totale 5.163
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Città #
Moscow 334
Ashburn 291
Dublin 256
Singapore 225
Dallas 196
Chandler 190
Nyköping 168
Beijing 131
Hong Kong 116
Ann Arbor 75
Jacksonville 70
Messina 70
The Dalles 56
Los Angeles 46
San Jose 41
Princeton 40
Lauterbourg 36
Medford 36
Cambridge 33
Des Moines 26
Dearborn 23
Jinan 23
New York 21
Boardman 20
Brussels 19
Hyderabad 16
São Paulo 16
Guangzhou 15
Munich 15
Orem 15
Tianjin 15
Redondo Beach 14
San Mateo 14
Shenyang 14
Wilmington 14
Buffalo 13
Denver 12
Catania 11
Ho Chi Minh City 11
Ningbo 11
Rio de Janeiro 11
Woodbridge 11
Francofonte 10
Johannesburg 10
Frankfurt am Main 9
Seattle 9
Taizhou 9
Belo Horizonte 8
Brasília 8
Brno 8
Brooklyn 8
Fuzhou 8
Haikou 8
Phoenix 8
Santa Clara 8
Hangzhou 7
Hanoi 7
Houston 7
London 7
Pune 7
Boston 6
Chicago 6
Düsseldorf 6
Hebei 6
Jiaxing 6
Montreal 6
Turku 6
Warsaw 6
Baghdad 5
Guayaquil 5
Helsinki 5
Lancaster 5
Nanjing 5
Porto Alegre 5
Shanghai 5
Tokyo 5
Zhengzhou 5
Agadir 4
Bexley 4
Biên Hòa 4
Helena 4
Manchester 4
Nanchang 4
Nova Iguaçu 4
Nuremberg 4
Riyadh 4
Rome 4
Salvador 4
Washington 4
Amman 3
Athens 3
Atlanta 3
Clearwater 3
Colombo 3
Dhaka 3
Guarulhos 3
Istanbul 3
Kuala Lumpur 3
Luxembourg 3
Mexico City 3
Totale 3.090
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Nome #
Chemical exploration of 4-(4-fluorobenzyl)piperidine fragment for the development of new tyrosinase inhibitors 254
Inhibitory effects and structural insights for a novel series of coumarin-based compounds that selectively target human CA IX and CA XII carbonic anhydrases 202
Targeting Tyrosinase: Development and Structural Insights of Novel Inhibitors Bearing Arylpiperidine and Arylpiperazine Fragments 194
Exploring structural properties of potent human carbonic anhydrase inhibitors bearing a 4-(cycloalkylamino-1-carbonyl)benzenesulfonamide moiety 185
InVivo Evaluation of Selective Carbonic Anhydrase Inhibitors as Potential Anticonvulsant Agents 181
Discovery of a new potent inhibitor of mushroom tyrosinase (Agaricus bisporus) containing 4-(4-hydroxyphenyl)piperazin-1-yl moiety 179
Discovery of benzimidazole-based Leishmania mexicana cysteine protease CPB2.8ΔCTE inhibitors as potential therapeutics for leishmaniasis 178
Design and optimization of isoquinoline-sulfonamides as potent and selective inhibitors of human carbonic anhydrase VII 177
Carbonic anhydrase inhibitors: Design, synthesis and structural characterization of new heteroaryl-N-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms 177
DISCOVERY OF NEW INDOLE DERIVATES AS NEUROPROTECTIVE AGENTS 161
Graphene Quantum Dots Based Systems As HIV Inhibitors 159
Nuovi ligandi del recettore NR2B/NMDA a struttura indolica 152
From NMDA receptor antagonists to discovery of selective σ2 receptor ligands 149
Probing the molecular interactions between the human Carbonic Anhydrases (hCAs) and a novel class of benzenesulfonamides 143
Serendipitous discovery of indole derivatives as potent tyrosinase inhibitors 142
Discovery and optimization of isoquinoline-derived inhibitors of human Carbonic Anhydrases (hCAs) 138
Computational and synthetic approaches for developing Lavendustin B derivatives as allosteric inhibitors of HIV-1 integrase 134
Structural optimization of N1-aryl-benzimidazoles for the discovery of new non-nucleoside reverse transcriptase inhibitors active against wild-type and mutant HIV-1 strains 133
New indole derivatives as promising ligands for ifenprodil site of NR2B/NMDA receptors 132
Probing Molecular Interactions between Human Carbonic Anhydrases (hCAs) and a Novel Class of Benzenesulfonamides 131
Searching for novel N1-substituted benzimidazol-2-ones as non-nucleoside HIV-1 RT inhibitors 130
Design, Synthesis and Biostructural Characterization of Carbonic Anhydrase Inhibitors 125
Indole derivatives as dual-effective agents for the treatment of neurodegenerative diseases: Synthesis, biological evaluation, and molecular modeling studies 123
Synthesis and biological characterization of novel potent arylsulfonamides as human carbonic anhydrase inhibitors (hCAIs) targeting central nervous system 123
Rational design, synthesis and evaluation of coumarin derivatives as protein-protein interaction inhibitors 122
Identification of 3-substituted-1H-indoles as ligands of GluN2B containing N-methyl-D-aspartate receptors 121
Searching for NR2B/NMDA Receptor Antagonists As Neuroprotective Agents 120
Inhibition of HIV-1 RT activity by a new series of 3-(1,3,4-thiadiazol-2-yl)thiazolidin-4-one derivatives 118
Synthesis, biological evaluation and docking studies of NR2B/NMDA receptor antagonists 114
Identification of influenza PA-Nter endonuclease inhibitors using pharmacophore- and docking-based virtual screening 110
Synthesis and Biological Characterization of 3-Substituted-1H-indoles as Ligands of GluN2B-Containing N-Methyl-d-aspartate Receptors 101
Progettazione e sintesi di antagonisti non competitivi del recettore NR2B/NMDA 99
Structure-guided design of new indoles as negative allosteric modulators (NAMs) of N-methyl-d-aspartate receptor (NMDAR) containing GluN2B subunit 89
Synthesis, Modelling and Biological Characterization of 3-Substituted-1H-indoles as Ligands of GluN2B-containing N-Methyl-d-Aspartate Receptors 87
SYNTHESIS AND BIOLOGICAL CHARACTERIZATION OF NEW NR2B/NMDA RECEPTOR LIGANDS 86
SYNTHESIS AND BIOLOGICAL CHARACTERIZATION OF 3-SUBSTITUTED-1H-INDOLES AS LIGANDS OF GLUN2B-CONTAINING N-METHYL-D-ASPARTATE RECEPTORS 78
Synthesis and Biological Characterization of 3-Substituted-1H-indoles as Ligands of GluN2B-containing N-Methyl-D-Aspartate Receptors. Part. 2. 76
Rational Design and synthesis of new GluN2B/NMDA receptor ligands as neuroprotective agents. 75
Targeting GluN2B-containing N-Methyl-D-aspartate receptors: design, synthesis, and binding affinity evaluation of novel 3-substituted indoles. 73
Totale 5.271
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Categoria #
all - tutte 15.834
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 15.834
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202160 0 0 0 0 0 0 0 0 0 40 10 10
2021/2022341 4 54 2 19 1 1 46 16 5 8 106 79
2022/2023730 46 65 33 75 57 61 14 30 328 2 16 3
2023/2024188 11 25 9 48 11 44 0 8 0 17 0 15
2024/2025752 15 8 15 45 42 14 12 164 182 52 81 122
2025/20262.526 109 207 156 214 237 585 283 319 306 110 0 0
Totale 5.271