UNICA IRIS Institutional Research Information System

MELEDDU, RITA
 Distribuzione geografica
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Continente #
EU - Europa 180.020
NA - Nord America 5.971
AS - Asia 2.578
SA - Sud America 361
AF - Africa 143
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 3
Totale 189.080
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Nazione #
IT - Italia 178.323
US - Stati Uniti d'America 5.874
SG - Singapore 985
CN - Cina 917
SE - Svezia 411
UA - Ucraina 380
BR - Brasile 277
DE - Germania 269
VN - Vietnam 220
FI - Finlandia 176
FR - Francia 129
GB - Regno Unito 126
HK - Hong Kong 111
IN - India 90
MA - Marocco 83
BD - Bangladesh 51
CA - Canada 48
KR - Corea 44
AT - Austria 34
NL - Olanda 34
MX - Messico 31
AR - Argentina 26
ZA - Sudafrica 25
PK - Pakistan 24
RU - Federazione Russa 24
PL - Polonia 21
IQ - Iraq 19
JP - Giappone 19
ID - Indonesia 16
TR - Turchia 15
VE - Venezuela 15
CO - Colombia 14
ES - Italia 14
IE - Irlanda 14
BE - Belgio 13
CZ - Repubblica Ceca 11
SA - Arabia Saudita 11
EC - Ecuador 9
PH - Filippine 9
EG - Egitto 8
UZ - Uzbekistan 8
KE - Kenya 7
PT - Portogallo 7
PY - Paraguay 7
LT - Lituania 6
TN - Tunisia 6
CL - Cile 5
ET - Etiopia 5
IR - Iran 5
JO - Giordania 5
RO - Romania 5
AL - Albania 4
MY - Malesia 4
NP - Nepal 4
PA - Panama 4
PE - Perù 4
BO - Bolivia 3
CR - Costa Rica 3
DZ - Algeria 3
EU - Europa 3
HU - Ungheria 3
JM - Giamaica 3
AE - Emirati Arabi Uniti 2
BA - Bosnia-Erzegovina 2
IL - Israele 2
IS - Islanda 2
KG - Kirghizistan 2
KH - Cambogia 2
KW - Kuwait 2
MD - Moldavia 2
NI - Nicaragua 2
NZ - Nuova Zelanda 2
SK - Slovacchia (Repubblica Slovacca) 2
TW - Taiwan 2
A1 - Anonimo 1
AU - Australia 1
AW - Aruba 1
AZ - Azerbaigian 1
BF - Burkina Faso 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BS - Bahamas 1
BY - Bielorussia 1
CM - Camerun 1
DJ - Gibuti 1
DO - Repubblica Dominicana 1
GE - Georgia 1
GR - Grecia 1
GT - Guatemala 1
HR - Croazia 1
IM - Isola di Man 1
LA - Repubblica Popolare Democratica del Laos 1
LB - Libano 1
LV - Lettonia 1
ME - Montenegro 1
MM - Myanmar 1
MN - Mongolia 1
NG - Nigeria 1
SC - Seychelles 1
Totale 189.074
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Città #
Cagliari 175.292
Uta 2.658
Ashburn 541
Singapore 515
Fairfield 463
Woodbridge 400
San Jose 364
Dallas 354
Chandler 348
Nyköping 261
Houston 251
Boardman 240
Ann Arbor 238
Wilmington 225
Seattle 207
Jacksonville 187
Beijing 184
Cambridge 149
Dearborn 136
New York 124
Los Angeles 122
Helsinki 108
Hong Kong 103
Shanghai 94
Santa Clara 90
Council Bluffs 86
Casablanca 78
Nanjing 75
Ho Chi Minh City 73
The Dalles 72
Lauterbourg 69
Boston 60
Hefei 50
Seoul 43
Hanoi 41
Munich 40
Redwood City 34
San Diego 32
Buffalo 31
Verona 30
Amsterdam 29
Vienna 28
Shenyang 27
São Paulo 27
Milan 25
Dong Ket 24
Frankfurt am Main 24
Orem 24
Chennai 23
Changsha 20
Nanchang 19
Warsaw 19
Guangzhou 18
Chicago 17
Jiaxing 17
London 17
Redondo Beach 17
Sassari 16
Toronto 16
Hebei 15
Herndon 14
Jinan 14
Nuremberg 14
Tokyo 14
Brooklyn 13
Dublin 13
Mountain View 13
Phoenix 13
Tianjin 13
Zhengzhou 13
Atlanta 12
Mexico City 12
Brussels 11
Gujranwala 11
Johannesburg 11
Kunming 11
Norwalk 11
Rome 11
Montreal 10
Rio de Janeiro 10
Washington 10
Haiphong 9
Mumbai 9
San Francisco 9
Auburn Hills 8
Da Nang 8
Denver 8
Tashkent 8
Turku 8
Wuhan 8
Bengaluru 7
Jakarta 7
Lappeenranta 7
Manchester 7
Ningbo 7
Baghdad 6
Brno 6
Caracas 6
Columbus 6
Durban 6
Totale 185.284
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Nome #
(3Z)-3-(2-[4-(aryl)-1,3-thiazol-2-yl]hydrazin-1-ylidene)-2,3-dihydro- 1H -indol-2-one derivatives as dual inhibitors of HIV-1 reverse transcriptase 14.730
Exploring the thiazole scaffold for the identification of new agents for the treatment of fluconazole resistant Candida 5.066
Phenylpropenoids from Bupleurum fruticosum as Anti-Human Rhinovirus Species A Selective Capsid Binders 4.704
Natural product-inspired esters and amides of ferulic and caffeic acid as dual inhibitors of HIV-1 reverse transcriptase 4.691
Design, synthesis, and biological evaluation of 1,3-diarylpropenones as dual inhibitors of HIV-1 reverse transcriptase 4.533
Isatin: a privileged scaffold for the design of carbonic anhydrase inhibitors 4.447
2-(2-cycloalkylidene hydrazin-1-yl)-4-aryl-1,3-thiazoles: a promising class of antifungal agents 4.418
Ribonuclease H/DNA polymerase HIV-1 reverse transcriptase dual inhibitor: mechanistic studies on the allosteric mode of action of isatin-based compound RMNC6 4.332
3-Acetyl-2,5-diaryl-2,3-dihydro-1,3,4-oxadiazoles: A new scaffold for the selective inhibition of monoamine oxidase B 4.325
Isatin thiazoline hybrids as dual inhibitors of HIV-1 reverse transcriptase 4.192
New 4-[(3-cyclohexyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzene-1-sulfonamides, synthesis and inhibitory activity toward carbonic anhydrase I, II, IX, XII 3.946
Drug design, synthesis, in vitro and in silico evaluation of selective monoaminoxidase B inhibitors based on 3-acetyl-2-dichlorophenyl-5-aryl-2,3-dihydro-1,3,4-oxadiazole chemical scaffold 3.786
A novel series of 3,4-disubstituted dihydropyrazoles: Synthesis and evaluation for MAO enzyme inhibition 3.782
Ferulic Acid Esters and Withanolides: in Search of Withania somnifera GABAA Receptor Modulators 3.615
Systemic lupus erythematosus occurring in a patient with Niemann-Pick type B disease. 3.544
Targeting tumor associated carbonic anhydrase IX and XII: Highly isozyme selective coumarin and psoralen inhibitors 3.544
Coumarins from Magydaris pastinacea as inhibitors of the tumour-associated carbonic anhydrases IX and XII: isolation, biological studies and in silico evaluation 3.430
Through scaffold modification to 3,5-diaryl-4,5-dihydroisoxazoles: new potent and selective inhibitors of monoamine oxidase B 3.380
Design and synthesis of new isatin derivatives as HIV-1 reverse transcriptase associated ribonuclease H inhibitors 3.354
Molecular Aspects of the RT/drug Interactions. Perspective of Dual Inhibitors 3.316
Synthesis and biological assessment of novel 2-thiazolylhydrazones and computational analysis of their recognition by monoamine oxidase B 3.293
Synthesis of new 3-aryl-4,5-dihydropyrazole-1-carbothioamide derivatives. An investigation on their ability to inhibit monoamine oxidase 3.226
N-Acylbenzenesulfonamide dihydro-1,3,4-oxadiazole hybrids: seeking selectivity toward carbonic anhydrase isoforms 3.211
Tuning the Dual Inhibition of Carbonic Anhydrase and Cyclooxygenase by Dihydrothiazole Benzensulfonamides 3.049
Design, Synthesis and Biological Evaluation of New 1,3-Diarylpropenones as Dual Inhibitors of HIV-1 RT. 3.043
Investigating the Anticancer Activity of Isatin/Dihydropyrazole Hybrids 3.041
Site directed mutagenesis studies on HIV-1 reverse transcriptase (RT) enlighten the mechanism of action of a new Ribonuclease H/DNA polymerase RT dual inhibitor 2.981
Design, Synthesis and Biological Evaluation of New 1,3-Diarylpropenones as Single Site Dual Inhibitors of HIV-1 RT 2.933
Site directed mutagenesis studies on HIV-1 reverse transcriptase (RT) shed light on the mechanism of action of a new Ribonuclease H/ DNA polymerase RT dual inhibitor 2.923
Mutagenic study on HIV-1 reverse transcriptase to explore the mechanism of action of HIV-1 reverse transcriptase dual inhibitors 2.776
Synthesis and biological activity evaluation of new dual-inhibitors of both associated functions of HIV-1 RT 2.659
3-[2-(4-aryl-1,3-thiazol-2-yl)hydrazin-1-ylidene]-1H-indol-2-ones as new potential dual inhibitors of polimerase and ribonuclease HIV-1 RT associated function 2.621
Exploring new structural features of the 4-[(3-methyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzenesulphonamide scaffold for the inhibition of human carbonic anhydrases 2.552
Chalcones as novel dual inhibitors of HIV-1 reverse transcriptase 2.466
New promising scaffolds for the inhibition of monoamine oxidase B 2.311
Exploring new scaffolds for the inibition of the Ribonuclease H function of RT HIV-1 2.273
Design and synthesis of new Isatin derivatives as HIV-1 Reverse Transcriptase associated Ribonuclease H inhibitors twenty-fourth 2.157
Isatin derivatives as new scaffolds for HIV-1 reverse transcriptase associated RNase H and RDDP dual inhibitors 2.151
Synthesis, biological evaluation and SAR study of novel pyrazole analogues as inhibitors of Mycobacterium tuberculosis 2.114
Design, synthesis and biolgical activity evaluation of new HIV-1 reverse transcriptase dual inhibitors 2.091
2-Acylhydrazino-5-arylpyrrole derivatives: Synthesis and antifungal activity evaluation 2.008
Design, synthesis and biological activity evaluation of new HIV-1 reverse transcriptase dual inhibitors 1.979
1,5-Diaryl-2-ethyl pyrrole derivatives as antimycobacterial agents: design, synthesis and microbiological evaluation 1.973
Synthesis, biological evaluation, and SAR study of novel pyrazole analogues as inhibitors of Mycobacterium tuberculosis: part 2. Synthesis of rigid pyrazolones 1.940
Design of new inhibitors of the HIV-1 Reverse Transcriptase associated Ribonuclease H function: a synthetic approach 1.889
1,5-Diphenylpyrrole derivatives as antimycobacterial agents. Probing the influence on antimycobacterial activity of lipophilic substituents at the phenyl rings 1.824
Identification of new scaffolds for the inhibition of HIV-1 Reverse Transcriptase associated Ribonuclease H function by means of shape based similarity screening 1.817
SITE DIRECT MUTAGENESIS AND KINETIC STUDIES TO EXPLORE THE MECHANISM OF ACTION OF ISATIN DERIVATIVES AS HIV-1 REVERSE TRANSCRIPTASE DUAL INHIBITORS 1.803
New Dihydrothiazole Benzensulfonamides: Looking for Selectivity toward Carbonic Anhydrase Isoforms I, II, IX, and XII 1.741
Exploring new scaffolds for the inhibition of the Ribonuclease H function of RT HIV-1 1.711
SYNTHESIS, MOLECULAR MODELLING, INHIBITORY ACTIVITY, AND SELECTIVITY TOWARDS MONOAMINE OXIDASE OF NEW HETEROCYCLIC SCAFFOLDS 1.690
Semicarbazide-sensitive amine oxidase/vascular adhesion protein-1: a patent survey 1.644
Flavonoids and Acid-Hydrolysis derivatives of Neo-Clerodane diterpenes from Teucrium flavum subsp. glaucum as inhibitors of the HIV-1 reverse transcriptase–associated RNase H function 1.638
Synthesis and biological evaluation of new enantiomerically pure azole derivatives as inhibitors of Mycobacterium tuberculosis 1.626
Synthesis and biological evaluation of new dual inhibitors of HIV-1 associated functions 1.614
From classic to innovative approaches in HIV-1 infection treatment 1.566
Novel N-aryl- and N-heteryl-phenazine-1-carboxamides as potential agents for the treatment of infections sustained by drug-resistant and MDR Mycobacterium tuberculosis 1.564
2-methoxynaphthalen thiazole derivate : a new HIV-1 RT Ribonuclease H/DNA polymerase dual inhibitor active on viral replication 1.535
Novel N-aryl- and N-heteryl phenazine-1-carboxamides as potential agents for the treatment of infections sustained by drug-resistant and multidrug-resistant Mycobacterium tuberculosis 1.528
Exploring new scaffolds for the dual inhibition of HIV-1 RT polymerase and ribonuclease associated functions 1.208
Synthesis, molecular modelling, inhibitory acivity, and selectivity towards monoamine oxidase of new heterocyclic scaffold 1.117
Design and synthesis of 1,5-diaryl-2-ethyl pyrrole derivatives and their evaluation as antimycobacterial agents 1.096
L’OLIO ESSENZIALE DI ARTEMISIA ARBORESCENS INATTIVA HSV1 E HSV2 E INIBISCE LA DIFFUSIONE LATERALE DI CELLULE VERO 1.014
Synthesis of different series of small molecules targeting HIV-1 RT, Candida albicans, MAO and G-Quadruplex 1.005
Tri-substituted thiazolines as promising scaffolds for the design of efficient COX inhibitors 944
5-Nitro-3-(2-(4-phenylthiazol-2-yl)hydrazineylidene)indolin-2-one derivatives inhibit HIV-1 replication by a multitarget mechanism of action 875
L’olio essenziale di Artemisia arborescens inattiva HSV-1 e HSV-2 e inibisce la diffusione laterale in cellule Vero 806
Selective inhibition of carbonic anhydrase IX and XII by coumarin and psoralen derivatives 767
Suppression of lipopolysaccharide-induced COX-2 expression via p38MAPK, JNK, and C/EBPβ phosphorylation inhibition by furomagydarin A, a benzofuran glycoside from Magydaris pastinacea 651
2H-chromene and 7H-furo-chromene derivatives selectively inhibit tumour associated human carbonic anhydrase IX and XII isoforms 435
New Structural Features of Isatin Dihydrothiazole Hybrids for Selective Carbonic Anhydrase Inhibitors 302
Privileged Scaffold Hybridization in the Design of Carbonic Anhydrase Inhibitors 297
Exploring the 1-(4-Nitrophenyl)-3-arylprop-2-en-1-one Scaffold for the Selective Inhibition of Monoamine Oxidase B 293
Tiazolidinoni come agenti antivirali 174
Synthesis and Evaluation of Thiazolidinone-Isatin Hybrids for Selective Inhibition of Cancer-Related Carbonic Anhydrases 160
Identifying potential allosteric inhibitors of ZIKV NS3pro through a combined computational and biochemical approach 73
Chromones as Nonclassical Inhibitors of Carbonic Anhydrase IX and XII Isoforms: Probing Chromone-Based Derivatives 35
Totale 189.348
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Categoria #
all - tutte 218.007
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 218.007
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.333 0 0 0 0 0 0 0 0 0 0 0 1.333
2021/20228.064 1.004 734 401 542 710 557 445 382 689 764 894 942
2022/202312.945 1.117 1.853 1.685 1.379 868 1.346 675 1.036 762 691 1.076 457
2023/202411.424 523 367 816 816 1.081 2.108 1.464 934 723 706 858 1.028
2024/202536.787 13.803 11.583 4.410 2.369 1.081 1.764 831 114 261 184 147 240
2025/20266.506 471 253 755 549 535 362 800 586 456 937 505 297
Totale 189.348