Review of chirality and its importance in pharmacology
- 1 January 1991
- journal article
- review article
- Published by Wiley in Drug Development Research
- Vol. 24 (2) , 149-156
- https://doi.org/10.1002/ddr.430240202
Abstract
While many pharmacologists have become increasingly aware of the importance of chirality and the role it plays in accounting for the oftentimes dramatic differences in the pharmacodynamics and pharmacokinetics of pure enantiomeric forms of therapeutic agents, there continues to be a significant lack of diligence regarding the need for properly identified stereochemicals in the scientific literature. All too frequently published reports and textbooks fail to adequately identify the stereochemical nature of the drugs utilized in a study Since the individual components of an enantiomeric pair typically have significant differences in their pharmacologic activities, the need for unambiguous descriptive nomenclature is evident. This review presents a summary of the various types of nomenclature utilized in the pharmacologic literature and their chemical bases. Several examples are described which illustrate the significant differences between enantiomeric forms of drugs and suggest possible theoretical bases for such differences. The need for continued awareness on the part of pharmacologists and the proper, unambiguous identification of stereolsomers in the scientific literature and labeling is stressed.Keywords
This publication has 15 references indexed in Scilit:
- Racemic mixtures and single stereoisomers: Industrial concerns and issues in drug developmentChirality, 1991
- Enantiomer specific pharmacokineticsPharmacology & Therapeutics, 1990
- RACEMATES OR ENANTIOMERS: REGULATORY APPROACHESClinical and Experimental Pharmacology and Physiology, 1989
- Chirality in bioactive agents and its pitfallsTrends in Pharmacological Sciences, 1986
- Stereoisomerism and drug actionTrends in Pharmacological Sciences, 1986
- Importance of Drug Enantiomers in Clinical PharmacologyDrugs, 1985
- The optical isomers of the 1,4-dihydropyridine BAY K 8644 show opposite effects on Ca channelsEuropean Journal of Pharmacology, 1985
- Separate site(s) of action of optical isomers of 1-methyl-5-phenyl-5-propylbarbituric acid with opposite pharmacological activities at the GABA receptor complexEuropean Journal of Pharmacology, 1985
- Remarkable substrate-inhibitor properties of nicotine enantiomers towards a guinea pig lung aromatic azaheterocycle N-methyltransferaseBiochemical and Biophysical Research Communications, 1985
- THE α‐ AND β‐ADRENOCEPTOR BLOCKING POTENCIES OF LABETALOL AND ITS INDIVIDUAL STEREOISOMERS IN ANAESTHETIZED DOGS AND IN ISOLATED TISSUESBritish Journal of Pharmacology, 1982