Analysis of highly potent amidine containing inhibitors of serine proteases and their N-hydroxylated prodrugs (amidoximes)
| Autor: | Joscha Kotthaus, Bernd Clement, Andreas van de Locht, Torsten Steinmetzer |
|---|---|
| Rok vydání: | 2010 |
| Předmět: |
Proteases
Serine Proteinase Inhibitors Amidines Administration Oral Biological Availability Hydroxylation High-performance liquid chromatography Sensitivity and Specificity Mass Spectrometry Amidine Serine chemistry.chemical_compound Structure-Activity Relationship Drug Discovery Organic chemistry Structure–activity relationship Humans Prodrugs Chromatography High Pressure Liquid Pharmacology General Medicine Prodrug Bioavailability chemistry Intestinal Absorption Serine Proteases |
| Zdroj: | Journal of enzyme inhibition and medicinal chemistry. 26(1) |
| ISSN: | 1475-6374 |
| Popis: | The development of serine protease inhibitors often results in the discovery of new lead compounds containing strong basic amidine functions that usually suffer from poor absorption from the intestine. In order to improve oral bioavailability of these drugs, prodrug principles such as the conversion of amidines into amidoximes may be applied. In this work, two HPLC-based separation methods of serine protease inhibitors (amidines) and their N-hydroxylated prodrugs have been developed and characterised. This was performed by evaluating 11 distinct amidine-amidoxime pairs with different physicochemical parameters (clogP: -3 to 5.1). The HPLC methods developed allowed excellent separation of the compound pairs examined. Also, the possible selection of different separation techniques (i.e. adsorption- and ion-pair-chromatography) permits universal application. Moreover, both techniques are compatible with mass spectrometry and are superior to the previously described methods. In summary, both HPLC methods are suitable for the separation of most amidoxime-prodrugs currently in clinical or preclinical development. |
| Databáze: | OpenAIRE |
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