Some totally aliphatic 3-(acyloxy)propanolamines were synthesized with the aim of testing whether @blocking activity could be obtained from this class of drugs, even in the absence of an aromatic group. The significant and, in most cases, competitive P-blocking activity shown by the compounds under examination, together with the results of a theoretical study in which their reactivity was compared with that of other adrenergic 0-blocking drugs, seems to confirm a hypothesis previously advanced on the basis of knowledge about the action mechanism of adrenergic P-blocking drugs and of the results of structural studies. It was also possible to suggest some considerations about the role played by the (acy1oxy)methyl portion of 3-(acyloxy)propanolamines in eliciting their adrenergic P-blocking activity.

ROLE OF THE (ACYLOXY)METHYL MOIETY IN ELICITING THE ADRENERGIC BETA-BLOCKING ACTIVITY OF 3-(ACYLOXY)PROPANOLAMINES

LAPUCCI, ANNALINA;MARTINELLI, ADRIANO;BRESCHI, MARIA CRISTINA;DUCCI, MICHELE;
1987-01-01

Abstract

Some totally aliphatic 3-(acyloxy)propanolamines were synthesized with the aim of testing whether @blocking activity could be obtained from this class of drugs, even in the absence of an aromatic group. The significant and, in most cases, competitive P-blocking activity shown by the compounds under examination, together with the results of a theoretical study in which their reactivity was compared with that of other adrenergic 0-blocking drugs, seems to confirm a hypothesis previously advanced on the basis of knowledge about the action mechanism of adrenergic P-blocking drugs and of the results of structural studies. It was also possible to suggest some considerations about the role played by the (acy1oxy)methyl portion of 3-(acyloxy)propanolamines in eliciting their adrenergic P-blocking activity.
1987
Macchia, B; Balsamo, A; Lapucci, Annalina; Macchia, F; Martinelli, Adriano; Ammon, H. L.; Prasad, S. M.; Breschi, MARIA CRISTINA; Ducci, Michele; Martinotti, E.
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/172778
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? 18
social impact