IRIS
MANCUSO, Francesca
 Distribuzione geografica
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Continente #
NA - Nord America 403
EU - Europa 321
AS - Asia 77
SA - Sud America 3
AF - Africa 1
OC - Oceania 1
Totale 806
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Nazione #
US - Stati Uniti d'America 403
IE - Irlanda 130
SE - Svezia 86
IT - Italia 71
CN - Cina 44
IN - India 23
PL - Polonia 8
CZ - Repubblica Ceca 4
SG - Singapore 4
VN - Vietnam 4
AT - Austria 3
DE - Germania 3
GB - Regno Unito 3
NL - Olanda 3
BE - Belgio 2
FI - Finlandia 2
FR - Francia 2
GR - Grecia 2
AU - Australia 1
BO - Bolivia 1
BR - Brasile 1
CL - Cile 1
DZ - Algeria 1
EE - Estonia 1
NO - Norvegia 1
PH - Filippine 1
PK - Pakistan 1
Totale 806
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Città #
Chandler 192
Dublin 130
Nyköping 49
Messina 42
Ashburn 34
Hyderabad 20
Princeton 13
Beijing 11
Medford 11
Ann Arbor 10
Des Moines 10
Francofonte 8
Warsaw 8
Falls Church 7
Catania 5
Haikou 5
Jacksonville 5
Shenyang 5
Wilmington 5
Brno 4
Cagliari 4
Dearborn 4
Dong Ket 4
Seattle 4
Taizhou 4
Tianjin 4
Hangzhou 3
Jinan 3
Milan 3
Vienna 3
Woodbridge 3
Brussels 2
Larne 2
Munich 2
Nanchang 2
Paris 2
Pune 2
San Francisco 2
Singapore 2
Amsterdam 1
Boardman 1
Caltanissetta 1
Cambridge 1
Cedar Knolls 1
Chicago 1
Den Haag 1
Frigento 1
Fuzhou 1
Guangzhou 1
Hebei 1
Helsinki 1
Islamabad 1
Jiaxing 1
Los Angeles 1
Manila 1
Modica 1
Nanjing 1
Norfolk 1
Norwalk 1
Oran 1
Phoenix 1
Rome 1
Sortino 1
Southend 1
Stockholm 1
Sucre 1
São Paulo 1
Tallinn 1
Zhengzhou 1
Totale 659
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Nome #
Inhibitory effects and structural insights for a novel series of coumarin-based compounds that selectively target human CA IX and CA XII carbonic anhydrases 91
Targeting Carbonic Anhydrases (CAs): Rational Design, Synthesis, Structural Studies and Biochemical Evaluation 89
Seeking new approach for therapeutic treatment of cholera disease via inhibition of bacterial carbonic anhydrases: experimental and theoretical studies for sixteen benzenesulfonamide derivatives 88
Looking toward the Rim of the Active Site Cavity of Druggable Human Carbonic Anhydrase Isoforms 70
In Silico-Guided Identification of New Potent Inhibitors of Carbonic Anhydrases Expressed in Vibrio cholerae 66
Exploring structural properties of potent human carbonic anhydrase inhibitors bearing a 4-(cycloalkylamino-1-carbonyl)benzenesulfonamide moiety 59
Simulated human digestion of N1-aryl-2-arylthioacetamidobenzimidazoles and their activity against Herpes-simplex virus 1 in vitro 58
Synthesis, computational studies and assessment of in vitro inhibitory activity of umbelliferon-based compounds against tumour-associated carbonic anhydrase isoforms IX and XII 54
P158-DEVELOPMENT OF FLEXIBLE ARYLSULFONAMIDES AS POTENTIAL MULTITARGET ANTICANCER AGENTS 45
Effetto in vitro di derivati di 1-(1H-indol-3-il) etanone e propan-1-one su Candida spp. and Aspergillus niger 44
4-Sulfamoylphenylalkylamides as Inhibitors of Carbonic Anhydrases Expressed in Vibrio cholerae 40
null 29
The In Vitro Potential of 1-(1H-indol-3-yl) Derivatives against Candida spp. and Aspergillus niger as Tyrosinase Inhibitors 28
Synthesis and biological evaluation of sulfonamide-based compounds as inhibitors of carbonic anhydrase from Vibrio cholerae 23
The in vitro potential of novel carbonic anhydrase Inhibitors against candida spp 20
Tetracationic-to-dianionic tetraamino-dihydroxy-tetraoxacalix[4]arene: A paraquat receptor for all seasons 18
Proton transfer mediated recognition of amines by ionizable macrocyclic receptors 16
Evaluation of the In Vitro Antifungal Activity of Novel Arylsulfonamides against Candida spp 9
Decamethyl-pillar[5]arene: Synthesis and Recognition Properties 4
Screening Campaign and Docking Investigations in Identifying New Hit Compounds as Inhibitors of Human Carbonic Anhydrases Expressed In Tumour Cells 4
One oxacalix[4]arene, seven protonated species: a macrocyclic receptor for paraquat 4
Protonation equilibria of the tryptophan metabolite 8-hydroxyquinoline-2-carboxylic acid (8-HQA) and its precursors: A potentiometric and calorimetric comparative study 2
The In Vitro Potential of 1-(1H-indol-3-yl) Derivatives against Candida spp. and Aspergillus niger as Tyrosinase Inhibitors 2
Tetraamino-dihydroxy-tetraoxacalix[4]arene as a versatile paraquat receptor 2
KCNT1 Channel Blockers: A Medicinal Chemistry Perspective 1
Transition‐Metal‐Mediated versus Tetrazine‐Triggered Bioorthogonal Release Reactions: Direct Comparison and Combinations Thereof 1
Totale 867
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Categoria #
all - tutte 3.531
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 3.531
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202032 3 1 1 2 0 3 6 0 0 10 5 1
2020/2021109 2 0 21 2 7 4 19 11 21 4 12 6
2021/2022138 0 18 4 1 6 5 22 5 0 27 16 34
2022/2023440 19 35 11 139 13 27 1 15 160 3 7 10
2023/2024122 5 16 7 28 6 18 2 8 3 21 2 6
2024/202511 11 0 0 0 0 0 0 0 0 0 0 0
Totale 867