MANCUSO, Francesca
 Distribuzione geografica
Continente #
EU - Europa 110
NA - Nord America 29
AS - Asia 26
AF - Africa 3
Totale 168
Nazione #
IT - Italia 58
US - Stati Uniti d'America 29
IE - Irlanda 25
FR - Francia 13
PK - Pakistan 8
GB - Regno Unito 5
IN - India 5
PL - Polonia 4
VN - Vietnam 4
CN - Cina 3
IR - Iran 3
DE - Germania 2
DZ - Algeria 2
FI - Finlandia 2
EG - Egitto 1
JP - Giappone 1
MN - Mongolia 1
NL - Olanda 1
SG - Singapore 1
Totale 168
Città #
Messina 26
Dublin 25
Ashburn 9
Francofonte 7
Riesi 5
Council Bluffs 4
Dong Ket 4
Lahore 4
Reggio Calabria 4
Warsaw 4
London 3
New York 3
Paris 3
Delhi 2
Florence 2
Gwalior 2
Milan 2
Oran 2
Tampere 2
Amsterdam 1
Blackheath 1
Boardman 1
Chions 1
Columbus 1
Ferrara 1
Heliopolis 1
Los Angeles 1
Mountain View 1
Olbia 1
Otemae 1
Pacifica 1
Paderno Dugnano 1
Peshawar 1
Philadelphia 1
Scordia 1
Settingiano 1
Sikar 1
Southwark 1
Sunnyvale 1
Tehran 1
Ulan Bator 1
Washington 1
Totale 136
Nome #
Synthesis and biological evaluation of sulfonamide-based compounds as inhibitors of carbonic anhydrase from Vibrio cholerae, file a073709c-1d2b-43da-a48a-8957f90d8e18 40
Targeting Carbonic Anhydrases (CAs): Rational Design, Synthesis, Structural Studies and Biochemical Evaluation, file de3e52b3-a4b5-762d-e053-3705fe0a30e0 27
Seeking new approach for therapeutic treatment of cholera disease via inhibition of bacterial carbonic anhydrases: experimental and theoretical studies for sixteen benzenesulfonamide derivatives, file de3e52b2-1d3c-762d-e053-3705fe0a30e0 20
In Silico-Guided Identification of New Potent Inhibitors of Carbonic Anhydrases Expressed in Vibrio cholerae, file 48c1a758-16a7-41a3-aa91-c44b499a2dc7 19
Synthesis, computational studies and assessment of in vitro inhibitory activity of umbelliferon-based compounds against tumour-associated carbonic anhydrase isoforms IX and XII, file de3e52b3-50c0-762d-e053-3705fe0a30e0 19
Looking toward the Rim of the Active Site Cavity of Druggable Human Carbonic Anhydrase Isoforms, file bb71dea4-5919-4977-95c5-c66fbd10e415 16
Effetto in vitro di derivati di 1-(1H-indol-3-il) etanone e propan-1-one su Candida spp. and Aspergillus niger, file de3e52b4-bf2d-762d-e053-3705fe0a30e0 7
The in vitro potential of novel carbonic anhydrase Inhibitors against candida spp, file 0d9115ab-e71d-42ca-8664-8faaec89a331 6
Proton transfer mediated recognition of amines by ionizable macrocyclic receptors, file af59a3e9-9def-44d9-82c8-f46e3851eef6 3
Evaluation of the In Vitro Antifungal Activity of Novel Arylsulfonamides against Candida spp, file bf0695b8-4862-4531-8b1d-73eae380ef16 3
The In Vitro Potential of 1-(1H-indol-3-yl) Derivatives against Candida spp. and Aspergillus niger as Tyrosinase Inhibitors, file de3e52b4-fc75-762d-e053-3705fe0a30e0 3
Tetracationic-to-dianionic tetraamino-dihydroxy-tetraoxacalix[4]arene: A paraquat receptor for all seasons, file 707b3fa8-658b-4a61-b557-fc9de1027271 1
Simulated human digestion of N1-aryl-2-arylthioacetamidobenzimidazoles and their activity against Herpes-simplex virus 1 in vitro, file de3e52b2-63b5-762d-e053-3705fe0a30e0 1
Inhibitory effects and structural insights for a novel series of coumarin-based compounds that selectively target human CA IX and CA XII carbonic anhydrases, file de3e52b2-e8eb-762d-e053-3705fe0a30e0 1
null, file de3e52b3-cb22-762d-e053-3705fe0a30e0 1
Exploring structural properties of potent human carbonic anhydrase inhibitors bearing a 4-(cycloalkylamino-1-carbonyl)benzenesulfonamide moiety, file de3e52b4-3bfb-762d-e053-3705fe0a30e0 1
Totale 168
Categoria #
all - tutte 541
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 541


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201 0 0 0 0 0 0 0 0 0 1 0 0
2020/202120 1 0 0 0 0 0 2 1 7 4 0 5
2021/202212 0 1 3 0 1 1 6 0 0 0 0 0
2022/202362 1 0 1 2 7 2 1 2 33 2 11 0
2023/202473 2 2 4 15 3 4 23 8 6 5 1 0
Totale 168