Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Vincenzo Olgiati"'
Autor:
Paride Grisenti, Vincenzo Villani, Vincenzo Olgiati, Patrizia Ferraboschi, Rachele Pucciariello, Ada Manzocchi, Ambrogio Magni, Fabio Celotti
A series of steroidal compounds were synthesized in order to evaluate the possible influence of the configuration of a stereocenter in the 17β-side chain on the inhibitory activity on the enzyme 5α-reductase (5AR). For this purpose diastereomerical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63d1190559cf2431d710b333779b768c
http://hdl.handle.net/2434/5341
http://hdl.handle.net/2434/5341
Autor:
Vincenzo Olgiati, Germano Coppi, Maurizio Sabbatini, I. Panocka, Anselmo Maggioni, Francesco Amenta
Publikováno v:
Mechanisms of ageing and development. 104(2)
The effect of 4 and 8 weeks of treatment with the thyrotropin releasing hormone (TRH), analogue posatirelin ( l -6-ketopiperidine-2-carbonyl- l -leucyl-proline amide), on the changes of cholinergic neurotransmission enzymes, choline acetyltransferase
Autor:
Vincenzo Tortorella, Stefano Govoni, Nicola Antonio Colabufo, Marcello Leopoldo, Alberto Ghiglieri, Francesco Fiorentini, Roberto Perrone, Francesco Berardi, Vincenzo Olgiati
Publikováno v:
Journal of medicinal chemistry. 38(6)
Several 4-alkyl-1-arylpiperazines that present a tetralin moiety on the terminal part of the side chain were synthesized in order to increase the selectivity on the 5-HT1A versus D-2, alpha 1, sigma, and other 5-HT receptors. Many changes have been e
Autor:
Vincenzo Tortorella, Roberto Perrone, Francesco Fiorentini, Nicola Antonio Colabufo, Ermes Vanotti, Vincenzo Olgiati, Stefano Govoni, Francesco Berardi
Publikováno v:
Scopus-Elsevier
A new model of 4-alkyl-1-arylpiperazines containing a terminal dihydronaphthalene fragment on the alkyl chain was synthesized in order to have mixed serotonergic and dopaminergic activity and to pursue the recent alternative approaches to the discove
Publikováno v:
Scopus-Elsevier
[ 3 ]Haloperidol and [ 3 H]spiroperidol binding studies after kainate injection into the striatum indicate the presence of dopamine receptive sites not located on post-synaptic membranes. However, the physiological meaning of these “presynaptic”