Selective cytotoxicity of Pancratistatin-related natural <it>Amaryllidaceae </it>alkaloids: evaluation of the activity of two new compounds

• Main Authors: McNulty James, Nair Jerald, Sood Divya, Sharda Natasha, Griffin Carly, Pandey Siyaram
• Format: Article
• Language: English
• Published: BMC 2007-06-01
• Series: Cancer Cell International
• Online Access: http://www.cancerci.com/content/7/1/10

<p>Abstract</p> <p>Background</p> <p>Pancratistatin (PST), a compound extracted from an <it>Amaryllidaceae </it>(AMD) family plant, has been shown to specifically induce apoptosis in cancer cells with no/minimal toxic effect on normal cells. A systematic synthetic approach has indicated that the minimum cytotoxic pharmacophore comprises the <it>trans</it>-fused b/c-ring system containing the 2, 3, 4-triol unit in the C-ring. To further explore the structure-activity relationship of this group of compounds we have investigated the anti-cancer efficacy and specificity of two PST-related natural compounds, AMD4 and AMD5. Both of these compounds lack the polyhydroxylated lycorane element of PST instead having a methoxy-substuituted crinane skeleton.</p> <p>Results</p> <p>Our results indicate that AMD5 has efficacy and selectivity similar to PST, albeit at a 10-fold increased concentration. Interestingly AMD4 lacks apoptotic activity.</p> <p>Conclusion</p> <p>Our results indicate that the phenanthridone skeleton in natural <it>Amaryllidaceae </it>alkaloids may be a significant common element for selectivity against cancer cells; furthermore, the configuration of the methoxy-side groups is responsible for higher binding affinity to the target protein/s thus making for a more efficient anti-cancer agent.</p>