FERRO, Stefania
 Distribuzione geografica
Continente #
EU - Europa 44
AS - Asia 4
Totale 48
Nazione #
IT - Italia 40
GB - Regno Unito 4
PK - Pakistan 2
VN - Vietnam 2
Totale 48
Città #
Messina 13
Francofonte 9
Catania 3
Borghetto Santo Spirito 2
Carini 2
Dong Ket 2
Islamabad 2
Woking 2
Fiorenzuola D'arda 1
London 1
Villamagna 1
Totale 38
Nome #
Searching for indole derivatives as potential mushroom tyrosinase inhibitors, file de3e52b4-9788-762d-e053-3705fe0a30e0 12
Graphene Quantum Dots Based Systems As HIV Inhibitors, file de3e52b1-9612-762d-e053-3705fe0a30e0 6
NOVEL N1-ARYL-2- ARYLTHIOACETAMIDOBENZIMIDAZOLES WERE EFFECTIVE AGAINST HERPES SIMPLEX VIRUS 1 (HSV-1) REPLICATION IN VITRO, file de3e52b1-3470-762d-e053-3705fe0a30e0 5
Novel 3-(4-benzylpiperidin-1-yl)-1-(1H-indol-3-yl)propan-1-one derivates were effective in vitro against clinical isolates of Candida spp. and Aspergillus niger, file de3e52b1-a688-762d-e053-3705fe0a30e0 5
Targeting Tyrosinase: Development and Structural Insights of Novel Inhibitors Bearing Arylpiperidine and Arylpiperazine Fragments, file de3e52b4-1ede-762d-e053-3705fe0a30e0 3
AMPA receptor antagonists: Synthesis and pharmacological evaluation, file de3e52b4-e060-762d-e053-3705fe0a30e0 3
Computational Studies to Discover a New NR2B/NMDA Receptor Antagonist and Evaluation of Pharmacological Profile, file de3e52ae-b83d-762d-e053-3705fe0a30e0 2
Discovery of benzimidazole-based Leishmania mexicana cysteine protease CPB2.8ΔCTE inhibitors as potential therapeutics for leishmaniasis, file de3e52b3-33b1-762d-e053-3705fe0a30e0 2
Design and synthesis of N1-aryl-benzimidazoles 2-substituted as novel HIV-1 non-nucleoside reverse transcriptase inhibitors, file de3e52ae-ef4f-762d-e053-3705fe0a30e0 1
null, file de3e52b1-9366-762d-e053-3705fe0a30e0 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
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, file de3e52b3-0102-762d-e053-3705fe0a30e0 1
Structure-guided design of new indoles as negative allosteric modulators (NAMs) of N-methyl-d-aspartate receptor (NMDAR) containing GluN2B subunit, file de3e52b3-36be-762d-e053-3705fe0a30e0 1
Probing Molecular Interactions between Human Carbonic Anhydrases (hCAs) and a Novel Class of Benzenesulfonamides, file de3e52b3-5adf-762d-e053-3705fe0a30e0 1
Chemical exploration of 4-(4-fluorobenzyl)piperidine fragment for the development of new tyrosinase inhibitors, file de3e52b4-1070-762d-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
Carbonic anhydrase inhibitors: Design, synthesis and structural characterization of new heteroaryl-N-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms, file de3e52b4-b101-762d-e053-3705fe0a30e0 1
Totale 48
Categoria #
all - tutte 79
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 79


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20192 0 0 0 0 0 0 0 0 0 0 2 0
2019/20203 0 0 0 0 0 0 0 0 0 1 1 1
2020/202130 0 0 0 0 2 0 1 4 10 7 2 4
2021/20226 0 0 0 0 0 0 6 0 0 0 0 0
2022/20234 0 2 0 0 0 0 0 2 0 0 0 0
Totale 48