Synthesis and properties of novel lipopeptides and lipid mimetics
β Scribed by Anna Nicolaou; George Kokotos; Violetta Constantinou-Kokotou; Christos Charitos; Caterina Noula; Robert Verger; William A. Gibbons
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 113 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1075-2617
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β¦ Synopsis
Lipid mimetics, synthetic molecules that resemble natural lipids either structurally or functionally, have been developed as potential medicinal substances. They have been successfully applied in the development of drug and peptide delivery systems and for the development of inhibitors or lipid metabolizing enzymes. Phospholipase A2 is considered to be involved as the rate-limiting step in the production of lipid mediators of inflammatory responses and, as such, it has been a target for drug design. A series of lipid mimetics including lipopeptides, amides and alcohols of lipidic alpha-amino acids, have been tested by bulk and monolayer assay techniques. The findings suggested the direct interaction of the tested compounds with porcine pancreatic phospholipase A2. The inactivation of the enzyme occurred in a competitive manner. The most active compound I (2-amino-N-hexadecyl-L-hexanamide) showed an apparent IC50 of 12 microM and inhibitory power Z = 13 in the monolayer assay.
π SIMILAR VOLUMES
## Abstract Dendrimer chemistry is an attractive concept for mimicry of the highly branched character of the bioactive carbohydrates found as part of a cell's sugar coat, called the glycocalyx. Glycodendrimers have thus been used to study biological processes occurring on cell surfaces, such as bac