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OPTIMIZATION OF SCALE-UP SYNTHESIS OF ANTI-CANCER CERAMIDE ANALOG 315.
Foroozesh, Maryam; Goyal, Navneet; Jackson, Taylor; Do, Camilla; Booker, Sydney; Hill, Tarius; Liu, Jiawang.
Afiliación
  • Foroozesh M; Department of Chemistry, Xavier University of Louisiana, 1 Drexel Dr., New Orleans, LA, 70125.
  • Goyal N; Department of Chemistry, Xavier University of Louisiana, 1 Drexel Dr., New Orleans, LA, 70125.
  • Jackson T; Department of Chemistry, Xavier University of Louisiana, 1 Drexel Dr., New Orleans, LA, 70125.
  • Do C; Department of Chemistry, Xavier University of Louisiana, 1 Drexel Dr., New Orleans, LA, 70125.
  • Booker S; Department of Chemistry, Xavier University of Louisiana, 1 Drexel Dr., New Orleans, LA, 70125.
  • Hill T; Department of Chemistry, Xavier University of Louisiana, 1 Drexel Dr., New Orleans, LA, 70125.
  • Liu J; Department of Chemistry, Xavier University of Louisiana, 1 Drexel Dr., New Orleans, LA, 70125.
J Undergrad Chem Res ; 16(3): 89-90, 2017.
Article en En | MEDLINE | ID: mdl-30220887
ABSTRACT
Ceramides, serve as central mediators in sphingolipid metabolism and signaling pathways. They function in signaling events which induce apoptosis, cell cycle arrest, and autophagic responses. In cancer cells, ceramide levels are often suppressed by the up-regulation of ceramide-metabolizing enzymes or the down-regulation of ceramide-generating enzymes, resulting in increased cancer cell survival. Chemotherapeutic drugs and radiation therapy have been shown to increase intracellular ceramide levels leading to anti-cancer effects. Anti-cancer effects have also been seen in cancer cells with the use of exogenous short-chain ceramides. Our laboratory has synthesized a library of ceramide analogs and tested their effects on breast cancer cell lines. Analog 315 has been shown to be the most effective ceramide analog in our library. Here, we are reporting a large-scale synthesis of that analog is reported.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Undergrad Chem Res Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Undergrad Chem Res Año: 2017 Tipo del documento: Article