Abstract
A series of substituted pyrazolines were synthesized and evaluated for their anticancer activity and for their ability to inhibit P-glycoprotein-mediated multidrug resistance by direct binding to a purified protein domain containing an ATP-binding site and a modulator interacting region. Compounds 2a and e have been found to bind to P-glycoprotein with greater affinity
| Lingua originale | Inglese |
|---|---|
| pagine (da-a) | 4632-4635 |
| Numero di pagine | 4 |
| Rivista | BIOORGANIC & MEDICINAL CHEMISTRY LETTERS |
| Stato di pubblicazione | Pubblicato - 2005 |
Keywords
- P-GLYCOPROTEIN
- PYRAZOLE DERIVATES
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