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Results: 1-8 |
Results: 8
A new class of nonsteroidal aromatase inhibitors: Design and synthesis of chromone and xanthone derivatives and inhibition of the P450 enzymes aromatase and 17 alpha-hydroxylase/C17,20-lyase
Authors: Recanatini, M Bisi, A Cavalli, A Belluti, F Gobbi, S Rampa, A Valenti, P Palzer, M Palusczak, A Hartmann, RW
Citation: M. Recanatini et al., A new class of nonsteroidal aromatase inhibitors: Design and synthesis of chromone and xanthone derivatives and inhibition of the P450 enzymes aromatase and 17 alpha-hydroxylase/C17,20-lyase, J MED CHEM, 44(5), 2001, pp. 672-680
Acetylcholinesterase inhibitors: SAR and kinetic studies on omega-[N-methyl-N-(3-alkylcarbamoyloxyphenyl)methyl]aminoalkoxyaryl derivatives
Authors: Rampa, A Piazzi, L Belluti, F Gobbi, S Bisi, A Bartolini, M Andrisano, V Cavrini, V Cavalli, A Recanatini, M Valenti, P
Citation: A. Rampa et al., Acetylcholinesterase inhibitors: SAR and kinetic studies on omega-[N-methyl-N-(3-alkylcarbamoyloxyphenyl)methyl]aminoalkoxyaryl derivatives, J MED CHEM, 44(23), 2001, pp. 3810-3820
Acetylcholinesterase inhibitors for potential use in Alzheimer's disease: Molecular modeling, synthesis and kinetic evaluation of 11H-indeno-[1,2-b]-quinolin-10-ylamine derivatives
Authors: Rampa, A Bisi, A Belluti, F Gobbi, S Valenti, P Andrisano, V Cavrini, V Cavalli, A Recanatini, M
Citation: A. Rampa et al., Acetylcholinesterase inhibitors for potential use in Alzheimer's disease: Molecular modeling, synthesis and kinetic evaluation of 11H-indeno-[1,2-b]-quinolin-10-ylamine derivatives, BIO MED CH, 8(3), 2000, pp. 497-506
Synthesis and biological activity of some rigid analogues of flavone-8-acetic acid
Authors: Valenti, P Bisi, A Rampa, A Belluti, F Gobbi, S Zampiron, A Carrara, M
Citation: P. Valenti et al., Synthesis and biological activity of some rigid analogues of flavone-8-acetic acid, BIO MED CH, 8(1), 2000, pp. 239-246
In vitro evaluation of newly developed chalcone analogues in human cancer cells
Authors: De Vincenzo, R Ferlini, C Distefano, M Gaggini, C Riva, A Bombardelli, E Morazzoni, P Valenti, P Belluti, F Ranelletti, FO Mancuso, S Scambia, G
Citation: R. De Vincenzo et al., In vitro evaluation of newly developed chalcone analogues in human cancer cells, CANC CHEMOT, 46(4), 2000, pp. 305-312
SAR of 9-amino-1,2,3,4-tetrahydroacridine-based acetylcholinesterase inhibitors: Synthesis, enzyme inhibitory activity, QSAR, and structure-based CoMFA of tacrine analogues
Authors: Recanatini, M Cavalli, A Belluti, F Piazzi, L Rampa, A Bisi, A Gobbi, S Valenti, P Andrisano, V Bartolini, M Cavrini, V
Citation: M. Recanatini et al., SAR of 9-amino-1,2,3,4-tetrahydroacridine-based acetylcholinesterase inhibitors: Synthesis, enzyme inhibitory activity, QSAR, and structure-based CoMFA of tacrine analogues, J MED CHEM, 43(10), 2000, pp. 2007-2018
A simple one-pot synthesis of isoflavanones
Authors: Valenti, P Belluti, F Rampa, A Bisi, A
Citation: P. Valenti et al., A simple one-pot synthesis of isoflavanones, SYN COMMUN, 29(22), 1999, pp. 3895-3899
Synthesis of flavone-2 '-carboxylic acid analogues as potential antitumor agents
Authors: Valenti, P Bisi, A Rampa, A Gobbi, S Belluti, F Da Re, P Cima, L Carrara, M
Citation: P. Valenti et al., Synthesis of flavone-2 '-carboxylic acid analogues as potential antitumor agents, ANTI-CAN DR, 13(8), 1998, pp. 881-892
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