| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5229506 | Tetrahedron | 2006 | 10 Pages |
Abstract
Four dendrimeric fragments (FPs) were designed to encapsulate, mainly by H-bonding, a family of drugs known as salicylanilides (acaricides). All geometries were optimized at DFT/LAV3Pâ level of theory. Amide and alcohol groups were the most efficient to interact with salicylanilides (e.g., FP2-chlosantel complex).
Related Topics
Physical Sciences and Engineering
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Authors
Delia Soto-Castro, Aurelio Evangelista-Lara, Patricia Guadarrama,