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Journal of Enzyme Inhibition and Medicinal Chemistry|March 26, 2015
Bicyclic γ-amino acids as inhibitors of γ-aminobutyrate aminotransferaseAndrea Pinto, Lucia Tamborini, Eugenia Pennacchietti, et al.
European Journal of Medicinal Chemistry|March 10, 2007
Synthesis and pharmacological evaluation of novel conformationally constrained homologues of glutamic acidPaola Conti, Antonio Caligiuri, Andrea Pinto, et al.
Chemmedchem|November 19, 2013
Development of rhodesain inhibitors with a 3-bromoisoxazoline warheadRoberta Ettari, Lucia Tamborini, Ilenia C Angelo, et al.
European Journal of Medicinal Chemistry|October 12, 2010
Synthesis of novel chiral Δ2-isoxazoline derivatives related to ABT-418 and estimation of their affinity at neuronal nicotinic acetylcholine receptor subtypesClelia Dallanoce, Pietro Magrone, Carlo Matera, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 2, 2017
Structural basis of subunit selectivity for competitive NMDA receptor antagonists with preference for GluN2A over GluN2B subunitsGenevieve E Lind, Tung-Chung Mou, Lucia Tamborini, et al.
Journal of Medicinal Chemistry|March 15, 2008
Synthesis and pharmacological characterization at glutamate receptors of the four enantiopure isomers of tricholomic acidAndrea Pinto, Paola Conti, Marco De Amici, et al.
Chemmedchem|September 13, 2007
Synthesis of conformationally constrained glutamic acid homologues and investigation of their pharmacological profilesPaola Conti, Andrea Pinto, Lucia Tamborini, et al.
Journal of Medicinal Chemistry|August 20, 2014
Discovery of covalent inhibitors of glyceraldehyde-3-phosphate dehydrogenase, a target for the treatment of malariaStefano Bruno, Andrea Pinto, Gianluca Paredi, et al.
European Journal of Medicinal Chemistry|February 18, 2014
Synthesis of (3-hydroxy-pyrazolin-5-yl)glycine based ligands interacting with ionotropic glutamate receptorsAndrea Pinto, Lucia Tamborini, Federica Mastronardi, et al.
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