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Chemistry & Biodiversity|April 19, 2008
Synthesis of novel pyrrolo[3,4-d]pyrazole-dicarboxylic acids and evaluation of their interaction with glutamate receptorsPaola Conti, Samuele Joppolo di Ventimiglia, Andrea Pinto, et al.
Molecular Cancer Therapeutics|March 24, 2012
Evading Pgp activity in drug-resistant cancer cells: a structural and functional study of antitubulin furan metotica compoundsTam Luong Nguyen, Maria Rosaria Cera, Andrea Pinto, et al.
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|April 14, 2023
Discovery of a spirocyclic 3-bromo-4,5-dihydroisoxazole covalent inhibitor of hGAPDH with antiproliferative activity against pancreatic cancer cellsAndrea Galbiati, Stefania Bova, Raffaella Pacchiana, 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.
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.
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