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Farmaco (Societa Chimica Italiana : 1989)|June 26, 2001
Synthesis and antiplatelet activity of some 2,7-di(N-cycloamino)-3-phenyl-1,8-naphthyridine derivativesP L Ferrarini, M Badawneh, F Franconi, et al.Journal of the American Academy of Dermatology|June 1, 1994
Antinuclear antibodies are not induced by PUVA treatment in patients with uncomplicated psoriasisP Calzavara-Pinton, F Franceschini, M Rastrelli, et al.Journal of Medicinal Chemistry|March 26, 1998
Novel 3-aralkyl-7-(amino-substituted)-1,2,3-triazolo[4,5-d]pyrimidines with high affinity toward A1 adenosine receptorsL Betti, G Biagi, G Giannaccini, et al.European Journal of Medicinal Chemistry|January 5, 2002
Synthesis and evaluation of antihypertensive activity of 1,8-naphthyridine derivatives. Part XM Badawneh, P L Ferrarini, V Calderone, et al.Journal of the American Academy of Dermatology|June 12, 1999
Antiperinuclear factor in psoriatic arthropathyP G Calzavara-Pinton, F Franceschini, C Manera, et al.European Journal of Medicinal Chemistry|April 29, 2000
Substituted 1,2,3-triazolo[1,5-a]quinazolines: synthesis and binding to benzodiazepine and adenosine receptorsL Bertelli, G Biagi, I Giorgi, et al.European Journal of Medicinal Chemistry|September 28, 2000
Synthesis and beta-blocking activity of (R,S)-(E)-oximeethers of 2, 3-dihydro-1,8-naphthyridine and 2,3-dihydrothiopyrano[2, 3-b]pyridine:potential antihypertensive agents - part IXP L Ferrarini, C Mori, M Badawneh, et al.Journal of Medicinal Chemistry|October 15, 1993
Conformationally restrained analogs of sympathomimetic catecholamines. Synthesis, conformational analysis, and adrenergic activity of isochroman derivativesB Macchia, A Balsamo, M C Breschi, et al.Farmaco (Societa Chimica Italiana : 1989)|July 11, 1998
1,2,3-Triazolo[1,5-a][1,4]- and 1,2,3-triazolo[1,5-a]-[1,5]benzodiazepine derivatives: synthesis and benzodiazepine receptor bindingL Bertelli, G Biagi, I Giorgi, et al.Drug Design and Delivery|May 1, 1988
An anomalous effect of N-isopropyl substitution in determining beta-adrenergic activityB Macchia, A Balsamo, A Lapucci, et al.Pageof 3