Showing papers on "Pharmacophore published in 1975"

A Theoretical and Experimental Study of the Semirigid Cholinergic Agonist 3-Acetoxyquinuclidine

Abstract: The interaction of the two enantiomens of 3-acetoxyquinuclidine (3-AcQ) and of its N-methyl derivative with the cholinergic receptor and with cholinesterases was investigated experimentally in systems which respond to acetylcholine (ACh) Molecular structural factors which are conducive to the well-defined ACh-like activity were studied by quantum mechanical methods The flexible moiety in the semirigid structure of 3-AcQ was shown to permit molecular rearrangements, as required for receptor activation, and to adopt an ACh-like conformation in the energetically preferred geometry The interaction pharmacophore of the active species, defined by the electrostatic potential fields generated in their surroundings, revealed a reactivity pattern identical with that of ACh The interaction pharmacophore of the N-methyl derivative of 3-AcQ was shown to be much less compatible with the requirements for ACh-like activity The structural correlation between the ACh-like pattern of the drugs and the biological activity of related psychotropic-anticholinergic amino esters is discussed