Synthesis and pharmacological characterization of new chiral derivatives of muscarine and allo-muscarine
Articolo
Data di Pubblicazione:
2000
Citazione:
Synthesis and pharmacological characterization of new chiral derivatives
of muscarine and allo-muscarine / M. De Amici, C. Dallanoce, C. De Micheli, P. Angeli, G. Marucci, F. Cantalamessa, L. Sparapassi. - In: IL FARMACO. - ISSN 0014-827X. - 55:8(2000), pp. 535-543.
Abstract:
Novel derivatives of natural muscarine and allo-muscarine, i.e. the benzyl ethers (-)-10 and (-)-12 and the benzoate (-)-13, were synthesized in very high enantiomeric excess. Target compounds were tested in vitro on guinea pig tissues, and their muscarinic potency was evaluated at M2 (heart force and rate) and M3 (ileum and bladder) receptor subtypes. The derivatives under study were also assayed in vivo on pithed rat. In addition, muscarinic receptor heterogeneity was investigated by determining the affinity and the relative efficacy of compounds (-)-10, (-)-12 and (-)-13 at M2 (heart force and rate) and M3 (ileum and bladder) receptor subtypes.
Tipologia IRIS:
01 - Articolo su periodico
Elenco autori:
M. De Amici, C. Dallanoce, C. De Micheli, P. Angeli, G. Marucci, F. Cantalamessa, L. Sparapassi
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