Gian Filippo Ruda
Postdoctoral Research Assistant
Gian Filippo Ruda graduated in Organic Chemistry at the University of Sassari in 2002. During his thesis project he worked on the synthesis of peptides supported on polyethylene glycol under the supervision of Prof. Maurizio Taddei (University of Siena).
In February 2002 he joined the group of Prof. Ian Gilbert at the Welsh School of Pharmacy in Cardiff (UK) where he worked on the synthesis of inhibitors of the enzyme dUTPase for the treatment of infectious diseases. During his PhD study he spent few months at the Pharmacy Department of the Brighton University under the supervision of Prof. Jean-Yves Maillard. In July 2005 he received his PhD in Medicinal Chemistry.
In August 2005 Dr. Ruda moved with Prof. Gilbert to the Division of Chemical Biology and Drug Discovery of the University of Dundee (UK) where he worked as postdoctoral medicinal chemist collaborating to several projects on the field of neglected diseases in particular Human African Trypanosomiasis, Malaria and Aspergillosis. He also collaborated with Prof. Andrew Hopkins (University of Dundee) to test the proof-of -concept of new computational methods for rationally design of multi-target drugs with polypharmacology.
Gian Filippo Ruda joined the Department of Drug Discovery and Development D3 at the IIT in June 2010 as Senior Postdoc, until June 2013.
Then, he joined Prof. Paul Brennan Group at the Target Discovery Institute, focussing his research interests in lysine demethylase (KDM) inhibitors as novel epigenetic chemical probes.
C8-substituted pyrido[3,4-d]pyrimidin-4(3H)-ones: Studies towards the identification of potent, cell penetrant Jumonji C domain containing histone lysine demethylase 4 subfamily (KDM4) inhibitors, compound profiling in cell-based target engagement assays.
Le Bihan Y-V. et al, (2019), Eur J Med Chem, 177, 316 - 337
Assessing histone demethylase inhibitors in cells: lessons learned
Hatch SB. et al, (2017), Epigenetics & Chromatin, 10
Design, Synthesis, Structure–Activity Relationship Studies, and Three-Dimensional Quantitative Structure–Activity Relationship (3D-QSAR) Modeling of a Series of O-Biphenyl Carbamates as Dual Modulators of Dopamine D3 Receptor and Fatty Acid Amide Hydrolase
De Simone A. et al, (2017), Journal of Medicinal Chemistry, 60, 2287 - 2304
Potent and Selective KDM5 Inhibitor Stops Cellular Demethylation of H3K4me3 at Transcription Start Sites and Proliferation of MM1S Myeloma Cells
Tumber A. et al, (2017), Cell Chemical Biology, 24, 371 - 380
Kernel-Based, Partial Least Squares Quantitative Structure-Retention Relationship Model for UPLC Retention Time Prediction: A Useful Tool for Metabolite Identification
Falchi F. et al, (2016), Analytical Chemistry, 88, 9510 - 9517