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pierfausto seneci
pierfausto seneci
Professor of Chemistry, University of Milan
Verified email at unimi.it
Title
Cited by
Cited by
Year
An inhibitor of tau hyperphosphorylation prevents severe motor impairments in tau transgenic mice
S Le Corre, HW Klafki, N Plesnila, G Hübinger, A Obermeier, H Sahagún, ...
Proceedings of the National Academy of Sciences 103 (25), 9673-9678, 2006
2902006
Solid-phase synthesis and combinatorial technologies
P Seneci
John Wiley & Sons, 2003
2812003
Novel SMAC-mimetics synergistically stimulate melanoma cell death in combination with TRAIL and Bortezomib
D Lecis, C Drago, L Manzoni, P Seneci, C Scolastico, E Mastrangelo, ...
British journal of cancer 102 (12), 1707-1716, 2010
1032010
A combinatorial approach to [1, 5] benzothiazepine derivatives as potential antibacterial agents
F Micheli, F Degiorgis, A Feriani, A Paio, A Pozzan, P Zarantonello, ...
Journal of Combinatorial Chemistry 3 (2), 224-228, 2001
992001
Solid supported chiral auxiliaries in asymmetric synthesis. Part 2: Catalysis of 1, 3-dipolar cycloadditions by Mg (II) cation
G Faita, A Paio, P Quadrelli, F Rancati, P Seneci
Tetrahedron 57 (39), 8313-8322, 2001
912001
Dihydrotanshinone-I interferes with the RNA-binding activity of HuR affecting its post-transcriptional function
VG D’Agostino, P Lal, B Mantelli, C Tiedje, C Zucal, N Thongon, ...
Scientific reports 5 (1), 16478, 2015
832015
Regulation of HuR structure and function by dihydrotanshinone-I
P Lal, L Cerofolini, VG D’Agostino, C Zucal, C Fuccio, I Bonomo, E Dassi, ...
Nucleic acids research 45 (16), 9514-9527, 2017
752017
Peptide aldehydes as inhibitors of HIV protease
E Sarubbi, PF Seneci, MR Angelastro, NP Peet, M Denaro, K Islam
FEBS letters 319 (3), 253-256, 1993
751993
Designing Smac-mimetics as antagonists of XIAP, cIAP1, and cIAP2
F Cossu, E Mastrangelo, M Milani, G Sorrentino, D Lecis, D Delia, ...
Biochemical and biophysical research communications 378 (2), 162-167, 2009
722009
(4S)-p-Hydroxybenzyl-1, 3-oxazolidin-2-one as a solid-supported chiral auxiliary in asymmetric 1, 3-dipolar cycloadditions
G Faita, A Paio, P Quadrelli, F Rancati, P Seneci
Tetrahedron Letters 41 (8), 1265-1269, 2000
712000
Stimulus-responsive liposomes for biomedical applications
AI Antoniou, S Giofrè, P Seneci, D Passarella, S Pellegrino
Drug discovery today 26 (8), 1794-1824, 2021
682021
Synthesis and antimicrobial activity of oxazolidin-2-ones and related heterocycles
P Seneci, M Caspani, F Ripamonti, R Ciabatti
Journal of the Chemical Society, Perkin Transactions 1, 2345-2351, 1994
591994
Immobilized benzylpenicillin acylase: application to the synthesis of optically active forms of carnitin and propranalol
C Fuganti, P Grasselli, PF Seneci, S Servi, P Casati
Tetrahedron letters 27 (18), 2061-2062, 1986
581986
Smac mimetics induce inflammation and necrotic tumour cell death by modulating macrophage activity
D Lecis, M De Cesare, P Perego, A Conti, E Corna, C Drago, P Seneci, ...
Cell death & disease 4 (11), e920-e920, 2013
542013
Stereoselective synthesis of conformationally constrained cyclohexanediols: a set of molecular scaffolds for the synthesis of glycomimetics
A Bernardi, D Arosio, L Manzoni, F Micheli, A Pasquarello, P Seneci
The Journal of Organic Chemistry 66 (19), 6209-6216, 2001
542001
Structural basis for bivalent Smac-mimetics recognition in the IAP protein family
F Cossu, M Milani, E Mastrangelo, P Vachette, F Servida, D Lecis, ...
Journal of molecular biology 392 (3), 630-644, 2009
522009
Rational design, synthesis and characterization of potent, non-peptidic Smac mimics/XIAP inhibitors as proapoptotic agents for cancer therapy
P Seneci, A Bianchi, C Battaglia, L Belvisi, M Bolognesi, A Caprini, ...
Bioorganic & medicinal chemistry 17 (16), 5834-5856, 2009
502009
Targeting the X-linked inhibitor of apoptosis protein through 4-substituted azabicyclo [5.3. 0] alkane smac mimetics. Structure, activity, and recognition principles
E Mastrangelo, F Cossu, M Milani, G Sorrentino, D Lecis, D Delia, ...
Journal of molecular biology 384 (3), 673-689, 2008
492008
Interfering with HuR–RNA interaction: design, synthesis and biological characterization of tanshinone mimics as novel, effective HuR inhibitors
L Manzoni, C Zucal, DD Maio, VG D’Agostino, N Thongon, I Bonomo, ...
Journal of Medicinal Chemistry 61 (4), 1483-1498, 2018
472018
Application of combinatorial technologies for catalyst design and development
F Gennari, P Seneci, S Miertus
Catalysis Reviews 42 (3), 385-402, 2000
462000
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