SURNAME
|
Name
|
Title
|
ALTERIO
|
Vincenzo
|
X-ray crystal structure of carbonic anhydrase XII complexed with a theranostic monoclonal antibody fragment
|
AMBROSIO
|
Francesca Alessandra
|
Compounds Targeting the RNA-Binding Protein HuR. Structure-Based Design, Synthesis and Interaction Studies.
|
BARBAROSSA
|
Alexia
|
Benzothienoquinazolinones as new inhibitor of Topoisomerases and Tubulin
|
BARONISSI
|
Giuliana
|
Design, synthesis and pharmacological characterization of novel potent non-steroidal agonists of the farnesoid X receptor
|
BARROS SILVA
|
Tiago
|
Hydroxypyridin-4-ones are a versatile scaffold to develop copper(II)-chelating COMT inhibitors with neuroprotective properties
|
BOU PETIT
|
Elisabeth
|
Study of pyrazolo[3,4-b]pyridin-6-one and pyrazolo[3,4-b]-pyridine scaffolds as MNK inhibitors
|
BOUTON
|
Jakob
|
3’-Deoxy-3’-fluoro-7-deazapurine nucleosides: synthesis and evaluation against kinetoplastid parasites
|
CAGIDE
|
Fernando
|
Development of new antibiotics based on natural scaffolds
|
CATALANO
|
Raffaella
|
Metabolites prediction at the Mu.Ta.Lig. Chemotheca
|
CERAMELLA
|
Jessica
|
Interesting biological properties of Anchusa azurea Mill. (Boraginaceae) methanol extract
|
CORICELLO
|
Adriana
|
Upcoming targets in neurodegenerative diseases: a molecular recognition study.
|
COSTANZO
|
Paola
|
New donepezil-like multi-target directed ligands for Alzheimer’s Disease based on hydroxytyrosol
|
DI FIORE
|
Anna
|
Exploring conformational variability of benzoxaborole derivatives for the development of selective carbonic anhydrase inhibitors
|
ELEK
|
Milica
|
The SF5 moiety as promising substituent for the design of novel D2 and D3 receptors ligands
|
FILIPOVIC
|
Nenad
|
A novel binuclear hydrazone-based Cd(II) complex is a strong pro-apoptotic inducer with significant activity against 2D and 3D pancreatic cancer stem cells
|
FOIS
|
Benedetta
|
Heterocyclic amides as selective inhibitors of HRV-B replication
|
HYERACI
|
Mariafrancesca
|
New complexes of platinum(II): effects on sensitive and resistant cells New complexes of platinum(II): effects on sensitive and resistant cells
|
JUHAS
|
Martin
|
Design, synthesis and biological evaluation of pyrazine derivatives
|
KRATKY
|
Martin
|
Conjugates of tuftsin-based peptide carriers and phenolic antitubercular molecules
|
LANZILLOTTA
|
Daria
|
The CD98hc oncoprotein as a target of novel anticancer therapeutic approachesagents
|
LIN
|
Cai
|
Discovery of pyrrolo[2,3-b]pyridine nucleoside analogues as anti-Trypanosomacruzi agents
|
MANCUSO
|
Francesca
|
Design and synthesis of new potential theranostic agents targeting tumor-expressed carbonic anhydrase IX and XII
|
MANCUSO
|
Stefano
|
New strategies for the multistep synthesis of oleocanthal
|
MARTINS
|
Daniel
|
Toxicological profile of phenethylamine-based psychoactive drugs
|
MARUCA
|
Annalisa
|
Computational methods to identify bioactive food constituents with potential Multi-Targeting profile
|
MELEDDU
|
Rita
|
Identification of potent and selective MAO-B inhibitors
|
MORACA
|
Federica
|
Design, synthesis and biological evaluation of Exemestane derivatives as potent inhibitors of Aromatase
|
NOVELLI
|
Paolo
|
Synthesis of a new cross-bridged cyclam radiotracer for PET detection of PD-L1 cancer expression.
|
OBLAK
|
Domen
|
3D pharmacophore modeling of DHODH as an antimalarial target using LigandScout
|
OCCHIUZZI
|
Maria Antonietta
|
Lipid lowering and antiglycaemic properties of Tacle®
by in vitro and in vivo investigation
|
OLIVEIRA
|
Catarina
|
Benzoic acid-derived nitrones: a new class of acetylcholinesterase inhibitors and potential neuroprotective agents
|
PARISE
|
Angela
|
Arsenous acid-platinum(II) a new dual pharmacophore anti-cancer agent: computational insights
|
PETROU
|
Anthi
|
Molecular docking and design of novel 2, 3-aryl-thiazolidin-4-ones as potent NNRTIs inhibitors
|
PFLEGR
|
Vaclav
|
Synthesis and evaluation of novel antimycobacterial isoniazid analogues
|
PINTO
|
Miguel
|
De-risking tolcapone hepatotoxicity for repurposing therapy using a nanotechnological approach
|
PROCOPIO
|
Anna Caterina
|
In silico
identification of new aromatase inhibitors
|
PUIG DE LA BELLACASA
|
Raimon
|
An in vivo biologically active pyrido[2,3-d]pyrimidine as a KRAS and tyrosine kinase inhibitor for the potential treatment of lung cancer
|
RITACCA
|
Alessandra
|
Can boron-containing compounds be considered new structural scaffolds for the treatment of Alzheimer’s disease?
|
ROCCA
|
Roberta
|
Identification of small molecules with specific interference to lncRNA activity through different computational approaches
|
ROMEO
|
Isabella
|
Mechanistic insights of hydrolytic activity into a de novo functional protein framework.
|
SEQUEIRA
|
Lisa
|
Synthesis of furochromone derivatives with potential anticancer activity
|
SESTITO
|
Simona
|
Computational conception and chemical synthesis of dual BTK-TCL1 inhibitors
|
STRASZAK
|
Dominik
|
New route for the synthesis of 1-(arylimidazolin-2-yl)-3-arylureas
|
TALLARICO
|
Sofia
|
Combined ultrasound/microwave chemocatalytic method for selective conversion of cellulose into lactic acid
|
TORRES VARGAS
|
Jose Antonio
|
Biological activity of toluquinol derivatives
|
VITTORIO
|
Serena
|
In silico
studies for the discovery of MUC1/CIN85 protein-protein interaction inhibitors as anti-metastatic agents
|
YETIK ANACAK
|
Gunay
|
A new synthesized AChE inhibitor induces H2S formation in the brain
|