UNICA IRIS Institutional Research Information System

MELEDDU, RITA
 Distribuzione geografica
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Continente #
EU - Europa 180.271
NA - Nord America 6.061
AS - Asia 2.601
SA - Sud America 363
Continente sconosciuto - Info sul continente non disponibili 272
AF - Africa 143
OC - Oceania 3
Totale 189.714
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Nazione #
IT - Italia 178.563
US - Stati Uniti d'America 5.957
SG - Singapore 992
CN - Cina 926
SE - Svezia 411
UA - Ucraina 380
BR - Brasile 277
DE - Germania 270
VN - Vietnam 220
FI - Finlandia 176
FR - Francia 131
GB - Regno Unito 126
HK - Hong Kong 114
IN - India 90
MA - Marocco 83
BD - Bangladesh 54
CA - Canada 51
KR - Corea 44
NL - Olanda 35
AT - Austria 34
MX - Messico 34
AR - Argentina 26
ZA - Sudafrica 25
PK - Pakistan 24
RU - Federazione Russa 24
PL - Polonia 21
IQ - Iraq 19
JP - Giappone 19
ES - Italia 18
ID - Indonesia 16
VE - Venezuela 16
TR - Turchia 15
BE - Belgio 14
CO - Colombia 14
IE - Irlanda 14
CZ - Repubblica Ceca 11
SA - Arabia Saudita 11
EC - Ecuador 9
PH - Filippine 9
EG - Egitto 8
UZ - Uzbekistan 8
KE - Kenya 7
LT - Lituania 7
PT - Portogallo 7
PY - Paraguay 7
CL - Cile 6
TN - Tunisia 6
ET - Etiopia 5
IR - Iran 5
JO - Giordania 5
NP - Nepal 5
RO - Romania 5
AL - Albania 4
MY - Malesia 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
GR - Grecia 2
GT - Guatemala 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
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 189.440
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Città #
Cagliari 175.523
Uta 2.658
Ashburn 547
Singapore 519
Fairfield 463
Woodbridge 400
San Jose 369
Dallas 356
Chandler 348
Nyköping 261
Houston 252
Boardman 240
Ann Arbor 238
Wilmington 225
Seattle 207
Beijing 190
Jacksonville 187
Cambridge 149
Dearborn 136
Los Angeles 124
New York 124
Council Bluffs 113
Helsinki 108
Hong Kong 106
Santa Clara 95
Shanghai 95
Casablanca 78
Nanjing 75
Ho Chi Minh City 73
The Dalles 72
Lauterbourg 69
Boston 61
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 26
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
Phoenix 16
Sassari 16
Toronto 16
Hebei 15
Mexico City 15
Herndon 14
Jinan 14
Nuremberg 14
Tokyo 14
Brooklyn 13
Dublin 13
Mountain View 13
Rome 13
Tianjin 13
Zhengzhou 13
Atlanta 12
Columbus 12
Brussels 11
Gujranwala 11
Johannesburg 11
Kunming 11
Norwalk 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
Durban 6
Totale 185.593
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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 14.733
Exploring the thiazole scaffold for the identification of new agents for the treatment of fluconazole resistant Candida 5.068
Phenylpropenoids from Bupleurum fruticosum as Anti-Human Rhinovirus Species A Selective Capsid Binders 4.708
Natural product-inspired esters and amides of ferulic and caffeic acid as dual inhibitors of HIV-1 reverse transcriptase 4.694
Design, synthesis, and biological evaluation of 1,3-diarylpropenones as dual inhibitors of HIV-1 reverse transcriptase 4.541
Isatin: a privileged scaffold for the design of carbonic anhydrase inhibitors 4.451
2-(2-cycloalkylidene hydrazin-1-yl)-4-aryl-1,3-thiazoles: a promising class of antifungal agents 4.420
Ribonuclease H/DNA polymerase HIV-1 reverse transcriptase dual inhibitor: mechanistic studies on the allosteric mode of action of isatin-based compound RMNC6 4.336
3-Acetyl-2,5-diaryl-2,3-dihydro-1,3,4-oxadiazoles: A new scaffold for the selective inhibition of monoamine oxidase B 4.330
Isatin thiazoline hybrids as dual inhibitors of HIV-1 reverse transcriptase 4.198
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 3.947
A novel series of 3,4-disubstituted dihydropyrazoles: Synthesis and evaluation for MAO enzyme inhibition 3.788
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 3.787
Ferulic Acid Esters and Withanolides: in Search of Withania somnifera GABAA Receptor Modulators 3.622
Systemic lupus erythematosus occurring in a patient with Niemann-Pick type B disease. 3.550
Targeting tumor associated carbonic anhydrase IX and XII: Highly isozyme selective coumarin and psoralen inhibitors 3.546
Coumarins from Magydaris pastinacea as inhibitors of the tumour-associated carbonic anhydrases IX and XII: isolation, biological studies and in silico evaluation 3.434
Through scaffold modification to 3,5-diaryl-4,5-dihydroisoxazoles: new potent and selective inhibitors of monoamine oxidase B 3.384
Design and synthesis of new isatin derivatives as HIV-1 reverse transcriptase associated ribonuclease H inhibitors 3.363
Molecular Aspects of the RT/drug Interactions. Perspective of Dual Inhibitors 3.319
Synthesis and biological assessment of novel 2-thiazolylhydrazones and computational analysis of their recognition by monoamine oxidase B 3.299
Synthesis of new 3-aryl-4,5-dihydropyrazole-1-carbothioamide derivatives. An investigation on their ability to inhibit monoamine oxidase 3.231
N-Acylbenzenesulfonamide dihydro-1,3,4-oxadiazole hybrids: seeking selectivity toward carbonic anhydrase isoforms 3.217
Tuning the Dual Inhibition of Carbonic Anhydrase and Cyclooxygenase by Dihydrothiazole Benzensulfonamides 3.053
Design, Synthesis and Biological Evaluation of New 1,3-Diarylpropenones as Dual Inhibitors of HIV-1 RT. 3.048
Investigating the Anticancer Activity of Isatin/Dihydropyrazole Hybrids 3.044
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 2.987
Design, Synthesis and Biological Evaluation of New 1,3-Diarylpropenones as Single Site Dual Inhibitors of HIV-1 RT 2.939
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 2.931
Mutagenic study on HIV-1 reverse transcriptase to explore the mechanism of action of HIV-1 reverse transcriptase dual inhibitors 2.779
Synthesis and biological activity evaluation of new dual-inhibitors of both associated functions of HIV-1 RT 2.662
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 2.624
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 2.554
Chalcones as novel dual inhibitors of HIV-1 reverse transcriptase 2.469
New promising scaffolds for the inhibition of monoamine oxidase B 2.317
Exploring new scaffolds for the inibition of the Ribonuclease H function of RT HIV-1 2.280
Design and synthesis of new Isatin derivatives as HIV-1 Reverse Transcriptase associated Ribonuclease H inhibitors twenty-fourth 2.164
Isatin derivatives as new scaffolds for HIV-1 reverse transcriptase associated RNase H and RDDP dual inhibitors 2.155
Synthesis, biological evaluation and SAR study of novel pyrazole analogues as inhibitors of Mycobacterium tuberculosis 2.115
Design, synthesis and biolgical activity evaluation of new HIV-1 reverse transcriptase dual inhibitors 2.097
2-Acylhydrazino-5-arylpyrrole derivatives: Synthesis and antifungal activity evaluation 2.011
Design, synthesis and biological activity evaluation of new HIV-1 reverse transcriptase dual inhibitors 1.984
1,5-Diaryl-2-ethyl pyrrole derivatives as antimycobacterial agents: design, synthesis and microbiological evaluation 1.977
Synthesis, biological evaluation, and SAR study of novel pyrazole analogues as inhibitors of Mycobacterium tuberculosis: part 2. Synthesis of rigid pyrazolones 1.945
Design of new inhibitors of the HIV-1 Reverse Transcriptase associated Ribonuclease H function: a synthetic approach 1.893
1,5-Diphenylpyrrole derivatives as antimycobacterial agents. Probing the influence on antimycobacterial activity of lipophilic substituents at the phenyl rings 1.827
Identification of new scaffolds for the inhibition of HIV-1 Reverse Transcriptase associated Ribonuclease H function by means of shape based similarity screening 1.822
SITE DIRECT MUTAGENESIS AND KINETIC STUDIES TO EXPLORE THE MECHANISM OF ACTION OF ISATIN DERIVATIVES AS HIV-1 REVERSE TRANSCRIPTASE DUAL INHIBITORS 1.810
New Dihydrothiazole Benzensulfonamides: Looking for Selectivity toward Carbonic Anhydrase Isoforms I, II, IX, and XII 1.745
Exploring new scaffolds for the inhibition of the Ribonuclease H function of RT HIV-1 1.715
SYNTHESIS, MOLECULAR MODELLING, INHIBITORY ACTIVITY, AND SELECTIVITY TOWARDS MONOAMINE OXIDASE OF NEW HETEROCYCLIC SCAFFOLDS 1.693
Semicarbazide-sensitive amine oxidase/vascular adhesion protein-1: a patent survey 1.648
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 1.642
Synthesis and biological evaluation of new enantiomerically pure azole derivatives as inhibitors of Mycobacterium tuberculosis 1.628
Synthesis and biological evaluation of new dual inhibitors of HIV-1 associated functions 1.618
From classic to innovative approaches in HIV-1 infection treatment 1.571
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 1.570
2-methoxynaphthalen thiazole derivate : a new HIV-1 RT Ribonuclease H/DNA polymerase dual inhibitor active on viral replication 1.538
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 1.536
Exploring new scaffolds for the dual inhibition of HIV-1 RT polymerase and ribonuclease associated functions 1.212
Synthesis, molecular modelling, inhibitory acivity, and selectivity towards monoamine oxidase of new heterocyclic scaffold 1.122
Design and synthesis of 1,5-diaryl-2-ethyl pyrrole derivatives and their evaluation as antimycobacterial agents 1.100
L’OLIO ESSENZIALE DI ARTEMISIA ARBORESCENS INATTIVA HSV1 E HSV2 E INIBISCE LA DIFFUSIONE LATERALE DI CELLULE VERO 1.017
Synthesis of different series of small molecules targeting HIV-1 RT, Candida albicans, MAO and G-Quadruplex 1.011
Tri-substituted thiazolines as promising scaffolds for the design of efficient COX inhibitors 949
5-Nitro-3-(2-(4-phenylthiazol-2-yl)hydrazineylidene)indolin-2-one derivatives inhibit HIV-1 replication by a multitarget mechanism of action 877
L’olio essenziale di Artemisia arborescens inattiva HSV-1 e HSV-2 e inibisce la diffusione laterale in cellule Vero 808
Selective inhibition of carbonic anhydrase IX and XII by coumarin and psoralen derivatives 769
Suppression of lipopolysaccharide-induced COX-2 expression via p38MAPK, JNK, and C/EBPβ phosphorylation inhibition by furomagydarin A, a benzofuran glycoside from Magydaris pastinacea 656
2H-chromene and 7H-furo-chromene derivatives selectively inhibit tumour associated human carbonic anhydrase IX and XII isoforms 442
New Structural Features of Isatin Dihydrothiazole Hybrids for Selective Carbonic Anhydrase Inhibitors 307
Privileged Scaffold Hybridization in the Design of Carbonic Anhydrase Inhibitors 302
Exploring the 1-(4-Nitrophenyl)-3-arylprop-2-en-1-one Scaffold for the Selective Inhibition of Monoamine Oxidase B 297
Tiazolidinoni come agenti antivirali 187
Synthesis and Evaluation of Thiazolidinone-Isatin Hybrids for Selective Inhibition of Cancer-Related Carbonic Anhydrases 175
Identifying potential allosteric inhibitors of ZIKV NS3pro through a combined computational and biochemical approach 81
Chromones as Nonclassical Inhibitors of Carbonic Anhydrase IX and XII Isoforms: Probing Chromone-Based Derivatives 45
Totale 189.714
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Categoria #
all - tutte 220.079
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 220.079
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20227.060 0 734 401 542 710 557 445 382 689 764 894 942
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
2025/20266.523 471 253 755 549 535 362 800 586 456 937 505 314
2026/2027349 121 228 0 0 0 0 0 0 0 0 0 0
Totale 189.714