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Synthesis and antiproliferative activity of flavonoid triazolyl glycosides.
- Source :
-
Heterocyclic Communications . 2018, Vol. 24 Issue 2, p119-124. 6p. - Publication Year :
- 2018
-
Abstract
- Sixteen flavonoid triazolyl glycosides <bold>4–19</bold> were synthesized in good yields <italic>via</italic> Cu(I)-catalyzed azide-alkyne cycloadditions of terminal alkynes of flavonoids <bold>1–3</bold> with acetylated sugar azides followed by deacetylation with sodium methoxide in anhydrous methanol. The antiproliferative activity of the synthesized compounds against three human cancer cell lines (Hela, HCC1954 and SK-OV-3) <italic>in vitro</italic> was evaluated. Flavonoids <bold>1</bold>, <bold>2</bold> and flavonoid triazolyl glycosides <bold>7</bold>, <bold>12</bold>, <bold>17</bold> exhibit potent antiproliferative activity against these cancer cell lines. [ABSTRACT FROM AUTHOR]
- Subjects :
- *FLAVONOIDS
*GLYCOSIDES
*RING formation (Chemistry)
*DEACETYLATION
*CANCER cells
Subjects
Details
- Language :
- English
- ISSN :
- 07930283
- Volume :
- 24
- Issue :
- 2
- Database :
- Academic Search Index
- Journal :
- Heterocyclic Communications
- Publication Type :
- Academic Journal
- Accession number :
- 129097766
- Full Text :
- https://doi.org/10.1515/hc-2017-0241