De Amici_2000_Farmaco_55_535

Reference

Title : Synthesis and pharmacological characterization of new chiral derivatives of muscarine and allo-muscarine - De Amici_2000_Farmaco_55_535
Author(s) : De Amici M , Dallanoce C , Angeli P , Marucci G , Cantalamessa F , De Micheli C
Ref : Farmaco , 55 :535 , 2000
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.

PubMedSearch : De Amici_2000_Farmaco_55_535
PubMedID: 11132731

Related information

Citations formats

De Amici M, Dallanoce C, Angeli P, Marucci G, Cantalamessa F, De Micheli C (2000)
Synthesis and pharmacological characterization of new chiral derivatives of muscarine and allo-muscarine
Farmaco 55 :535

De Amici M, Dallanoce C, Angeli P, Marucci G, Cantalamessa F, De Micheli C (2000)
Farmaco 55 :535