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2000
Volume 3, Issue 1
  • ISSN: 1570-1808
  • E-ISSN: 1875-628X

Abstract

Enantiomerically pure (2R,3S)-disubstituted tetrahydropyrans with diverse functional groups were synthesized. These derivatives were used as a model to study the influence of the tert-butyl dimethyl silyl group in the anticancer activity. The in vitro cytotoxicity was evaluated against a panel of six human cancer cells from diverse origin (MCF7, T-47D, HeLa, SW1573, WiDr and A2780). The structure-activity relationship study shows the relevant role of the silyl protecting group in the enhancement of the observed cytotoxic activity.

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/content/journals/lddd/10.2174/157018006775240944
2006-02-01
2025-09-22
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