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Eur J Med Chem. 2012 Sep;55:455-61. doi: 10.1016/j.ejmech.2012.06.057. Epub 2012 Jul 7.

Azide-alkyne cycloaddition en route to novel 1H-1,2,3-triazole tethered isatin conjugates with in vitro cytotoxic evaluation.

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1
Department of Chemistry, Guru Nanak Dev University, Amritsar 143005, India.

Abstract

1H-1,2,3-triazole tethered isatin conjugates have been synthesized and evaluated for cytotoxicity on four human cancer cell lines. The results revealed 5a, 5c, 5e and 5n proved to be twice as potent as 5-fluorouracil on THP-1 cell line with 5a and 5c being most active exhibiting IC(50) values of <1 against all cell lines except Caco-2. Activity profiles showed dependence on the substituents on isatin rings with a preference for hydrogen while a strong electron withdrawing fluoro as well as nitro substituents on either ring decreased the anticancer activity.

PMID:
22818042
DOI:
10.1016/j.ejmech.2012.06.057
[Indexed for MEDLINE]

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