C. Cusan

发表

Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: Effect of the N-5 bond type on the affinity and selectivity at the four adenosine receptor subtypes

S. Moro, K. Klotz, G. Spalluto, 2007, Purinergic Signalling.

Arachidonic Acid Released by Phospholipase A2 Activation Triggers Ca2+-dependent Apoptosis through the Mitochondrial Pathway*

M. Prato, L. Scorrano, C. Cusan, 2004, Journal of Biological Chemistry.

Versatile Selective α‐Carboxylic Acid Esterification of N‐Protected Amino Acids and Peptides by Alcalase.

C. Cusan, R. Liskamp, D. Rijkers, 2009 .

Fully Enzymatic Peptide Synthesis using C‐Terminal tert‐Butyl Ester Interconversion

C. Cusan, R. Liskamp, D. Rijkers, 2010 .

Enzymatic synthesis of activated esters and their subsequent use in enzyme-based peptide synthesis

C. Cusan, R. Liskamp, D. Rijkers, 2011 .

A New Multi‐Charged C60 Derivative: Synthesis and Biological Properties

M. Prato, L. Ferraro, G. Spalluto, 2002 .

Stereoselective and efficient synthesis of (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-ol.

C. Cusan, P. Quaedflieg, P. Wigerinck, 2005, Organic letters.

Enzymatic synthesis of C-terminal arylamides of amino acids and peptides.

C. Cusan, R. Liskamp, D. Rijkers, 2009, The Journal of organic chemistry.

Lysosomally cleavable peptide-containing polymersomes modified with anti-EGFR antibody for systemic cancer chemotherapy.

J. Feijen, D. Mink, C. Cusan, 2011, Biomaterials.

Novel versatile fullerene synthons.

M. Prato, G. Spalluto, C. Cusan, 2001, The Journal of organic chemistry.

Synthesis and biological evaluation of new phenidone analogues as potential dual cyclooxygenase (COX-1 and COX-2) and human lipoxygenase (5-LOX) inhibitors.

M. Prato, R. Bauer, G. Spalluto, 2005, Il Farmaco.

A versatile and selective chemo-enzymatic synthesis of β-protected aspartic and γ-protected glutamic acid derivatives

C. Cusan, R. Liskamp, D. Rijkers, 2009 .

Synthesis and Biological Evaluation of New Phenidone Analogues as Potential Dual Cyclooxygenase (COX‐1 and COX‐2) and Human Lipoxygenase (5‐LOX) Inhibitors.

M. Prato, R. Bauer, G. Spalluto, 2005 .

Anti-inflammatory and anti-oxidant activity of a new class of phenyl-pyrazolone derivatives.

G. Spalluto, C. Cusan, M. Prato, 2006, Current drug discovery technologies.

Synthesis and biological evaluation of a new class of acyl derivatives of 3-amino-1-phenyl-4,5-dihydro-1H-pyrazol-5-one as potential dual cyclooxygenase (COX-1 and COX-2) and human lipoxygenase (5-LOX) inhibitors.

M. Prato, R. Bauer, G. Spalluto, 2005, Farmaco.

Mitochondria Are Direct Targets of the Lipoxygenase Inhibitor MK886

M. Prato, L. Scorrano, C. Cusan, 2002, The Journal of Biological Chemistry.

The Associative Properties of Some Amphiphilic Fullerene Derivatives

M. Prato, M. Maggini, C. Cusan, 2005 .

The application of a 3D-QSAR (autoMEP/PLS) approach as an efficient pharmacodynamic-driven filtering method for small-sized virtual library: application to a lead optimization of a human A3 adenosine receptor antagonist.

Magdalena Bacilieri, Barbara Cacciari, Giampiero Spalluto, 2006, Bioorganic & medicinal chemistry.

Fullerene non-linear excited state absorption induced by gold nanoparticles light harvesting

M. Prato, C. Cusan, G. Mattei, 2005 .

Enzymatic Fragment Condensation of Side Chain‐Protected Peptides using Subtilisin A in Anhydrous Organic Solvents: A General Strategy for Industrial Peptide Synthesis

C. Cusan, R. Liskamp, D. Rijkers, 2013 .