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Chiral Cognisance: A Road to Safer and More Effective Medicinal Products
A quarter of all synthetic medicinal drugs contain a mixture of equal proportions of two molecules that have the same chemical constitution but differ in the spatial arrangement of their constituent atoms such that each is a mirror-image of the other, like the right and left hand. Biologically, rece...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal College of Physicians of London
1994
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5401007/ https://www.ncbi.nlm.nih.gov/pubmed/7807424 |
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author | Ariëns, E J Wuis, E W |
author_facet | Ariëns, E J Wuis, E W |
author_sort | Ariëns, E J |
collection | PubMed |
description | A quarter of all synthetic medicinal drugs contain a mixture of equal proportions of two molecules that have the same chemical constitution but differ in the spatial arrangement of their constituent atoms such that each is a mirror-image of the other, like the right and left hand. Biologically, receptors which are stereospecific react with only one of the two components of the mixture to produce the desired therapeutic effect, while the other is inactive or may interact with different receptors to cause undesirable, even toxic, effects. Development of syntheses that produce a preponderance of the required form, and efficient separation of mixtures, will result in safer and more effective medicinal products. |
format | Online Article Text |
id | pubmed-5401007 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1994 |
publisher | Royal College of Physicians of London |
record_format | MEDLINE/PubMed |
spelling | pubmed-54010072019-01-22 Chiral Cognisance: A Road to Safer and More Effective Medicinal Products Ariëns, E J Wuis, E W J R Coll Physicians Lond Overviews A quarter of all synthetic medicinal drugs contain a mixture of equal proportions of two molecules that have the same chemical constitution but differ in the spatial arrangement of their constituent atoms such that each is a mirror-image of the other, like the right and left hand. Biologically, receptors which are stereospecific react with only one of the two components of the mixture to produce the desired therapeutic effect, while the other is inactive or may interact with different receptors to cause undesirable, even toxic, effects. Development of syntheses that produce a preponderance of the required form, and efficient separation of mixtures, will result in safer and more effective medicinal products. Royal College of Physicians of London 1994 /pmc/articles/PMC5401007/ /pubmed/7807424 Text en © Journal of the Royal College of Physicians of London 1994 http://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) , which permits non-commercial use and redistribution provided that the original author and source are credited. |
spellingShingle | Overviews Ariëns, E J Wuis, E W Chiral Cognisance: A Road to Safer and More Effective Medicinal Products |
title | Chiral Cognisance: A Road to Safer and More Effective Medicinal Products |
title_full | Chiral Cognisance: A Road to Safer and More Effective Medicinal Products |
title_fullStr | Chiral Cognisance: A Road to Safer and More Effective Medicinal Products |
title_full_unstemmed | Chiral Cognisance: A Road to Safer and More Effective Medicinal Products |
title_short | Chiral Cognisance: A Road to Safer and More Effective Medicinal Products |
title_sort | chiral cognisance: a road to safer and more effective medicinal products |
topic | Overviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5401007/ https://www.ncbi.nlm.nih.gov/pubmed/7807424 |
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