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{{articleissues|deadend=January 2009|original research=January 2009|unreferenced=January 2009}}
{{articleissues|deadend=January 2009|original research=January 2009|unreferenced=January 2009}}
Chemical Postevolution is the structural optimization of (already evolutionary optimized) [[natural product]]s by synthetic chemical means. It is additional and often structurally orthogonal to natural [[evolution]].
Chemical Postevolution is the structural optimization of (already evolutionary optimized) [[natural product]]s by synthetic chemical means. It is additional and often structurally orthogonal to natural [[evolution]]. Whereas the term "[[Chemical Evolution]]" refers to an iterative optimization of chemical structures, Chemical Postevolution only refers to the biological improvement of antibiotic natural products.


== Application ==  
== Application ==  
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== Exploring Orthogonal Chemical Space Than Nature ==  
== Exploring Orthogonal Chemical Space Than Nature ==  
To create a drug, nature’s blueprints often have to be improved by [[semisynthesis]] or [[de novo synthesis]] to repair typical deficiencies such as limited stability, low solubility, narrow [[antibacterial spectrum]], poor in vivo efficacy, etc. Chemical structure defines biological activity. Complementary to nature, a chemist can explore white spots in structural space and biological activity that have never been explored by any organism over the entire period of evolution.
To create a drug, nature’s blueprints often have to be improved by [[semisynthesis]] or [[de novo synthesis]] to repair typical deficiencies such as limited stability, low solubility, narrow [[antibacterial spectrum]], poor in vivo efficacy, etc. Chemical structure defines biological activity. Complementary to nature, a chemist can explore white spots in structural space and biological activity that have never been explored by any organism over the entire period of evolution.
== Examples ==
Various natural antibiotics have already been optimized


== References ==  
== References ==  
<references/>
<references/>

Revision as of 22:28, 24 January 2009

Template:Articleissues Chemical Postevolution is the structural optimization of (already evolutionary optimized) natural products by synthetic chemical means. It is additional and often structurally orthogonal to natural evolution. Whereas the term "Chemical Evolution" refers to an iterative optimization of chemical structures, Chemical Postevolution only refers to the biological improvement of antibiotic natural products.

Application

Natural products have provided the majority of lead structures for marketed antibiotics. But, only a few “pure” natural products fulfill the complex profile required for a pharmaceutical drug. A drug has to match additional physicochemical, pharmacological, toxicological and technical requirements that have not been selectors in the evolution of antibacterial secondary metabolites. On the other hand, natural products offer excellent starting points for medicinal chemistry.[1]

Exploring Orthogonal Chemical Space Than Nature

To create a drug, nature’s blueprints often have to be improved by semisynthesis or de novo synthesis to repair typical deficiencies such as limited stability, low solubility, narrow antibacterial spectrum, poor in vivo efficacy, etc. Chemical structure defines biological activity. Complementary to nature, a chemist can explore white spots in structural space and biological activity that have never been explored by any organism over the entire period of evolution.

Examples

Various natural antibiotics have already been optimized

References

  1. ↑ F. von Nussbaum, M. Brands, B. Hinzen, S. Weigand, D. Häbich, Angew. Chem. 2006, 118, 5194–5254; Angew. Chem. Int. Ed. 2006, 45, 5072–5129. Antibacterial Natural Products in Medicinal Chemistry—Exodus or Revival? PMID 16881035