The stereoselectivity of the interaction with muscarinic receptors of enantiomers of a series of chiral antagonists is receptor subtype dependent. There is no overall relationship between stereoselectivity and receptor affinity. Depending on the antagonist studied, receptor stereoselectivity may indeed reflect: (1) the weakening or loss of a single interaction involving one of the four groups bound to the asymmetric carbon; (2) steric hindrance preventing optimum interaction of the low affinity steroisomer with the receptor; and/or (3) the inversion of the relative positions of two moieties of the ligand with similar structural and electronic properties i.e. comparable affinities for the two corresponding subsites in the receptor.SCOPUS: cp...
The enantiomers desoxymuscarine 6 were tested in vitro on guinea pig tissues, and their muscarinic p...
Allosteric modulators of ligand-receptor interactions are found for a variety of receptors (Christop...
The preparation and the biological activities of the four stereoisomers of 3-[5-(3-amino-1,2,5-oxadi...
The chemical structure corresponding to 1-hydroxy[1,1'-bicyclohexyl]-2-carboxylic acid 2-(diethylami...
This review continues a general presentation of the principles of stereochemistry with special refer...
1 Tbc affinities of the (R)- and (S)-enantiomers of hexahydro-difenidol (1) and its acetylenie analo...
The goals of the present study were: (1) to investigate thc binding properlies oi (R)- and (S)-procy...
<p>(A) Traditional three-point concept of chiral ligand recognition with non-equivalent interacting ...
The results of a study concerning the enantioselectivity of chiral colinergic agonists and antagonis...
. Cis-2-phenyl-2-cyclohexyl-r-5 [(dimethylamino)-methyl]-1,3-oxathiolane cis [(±)1] and trans [(±)2]...
We investigated the binding and pharmacological properties of the esters of 3,3-dimethylbutan-1-ol (...
By further steric complication of previously studied highly chiral muscarinic agonists, we have obta...
The synthesis of the eight stereoisomers of muscarine has been efficiently accomplished by utiliz...
(R)-Hexahydro-difenidol has a higher affinity for M1 receptors in NB-OK 1 cells, pancreas M3 and str...
Division of Medicinal Chemistry, Central Drug Research Institute, Lucknow-226 001, Uttar Pradesh Ind...
The enantiomers desoxymuscarine 6 were tested in vitro on guinea pig tissues, and their muscarinic p...
Allosteric modulators of ligand-receptor interactions are found for a variety of receptors (Christop...
The preparation and the biological activities of the four stereoisomers of 3-[5-(3-amino-1,2,5-oxadi...
The chemical structure corresponding to 1-hydroxy[1,1'-bicyclohexyl]-2-carboxylic acid 2-(diethylami...
This review continues a general presentation of the principles of stereochemistry with special refer...
1 Tbc affinities of the (R)- and (S)-enantiomers of hexahydro-difenidol (1) and its acetylenie analo...
The goals of the present study were: (1) to investigate thc binding properlies oi (R)- and (S)-procy...
<p>(A) Traditional three-point concept of chiral ligand recognition with non-equivalent interacting ...
The results of a study concerning the enantioselectivity of chiral colinergic agonists and antagonis...
. Cis-2-phenyl-2-cyclohexyl-r-5 [(dimethylamino)-methyl]-1,3-oxathiolane cis [(±)1] and trans [(±)2]...
We investigated the binding and pharmacological properties of the esters of 3,3-dimethylbutan-1-ol (...
By further steric complication of previously studied highly chiral muscarinic agonists, we have obta...
The synthesis of the eight stereoisomers of muscarine has been efficiently accomplished by utiliz...
(R)-Hexahydro-difenidol has a higher affinity for M1 receptors in NB-OK 1 cells, pancreas M3 and str...
Division of Medicinal Chemistry, Central Drug Research Institute, Lucknow-226 001, Uttar Pradesh Ind...
The enantiomers desoxymuscarine 6 were tested in vitro on guinea pig tissues, and their muscarinic p...
Allosteric modulators of ligand-receptor interactions are found for a variety of receptors (Christop...
The preparation and the biological activities of the four stereoisomers of 3-[5-(3-amino-1,2,5-oxadi...