Abstract |
Novel bicyclo[3.3.1]nonane derivatives were synthesized by an efficient methodology from acetoacetanilide, 2-methoxy and 4-methoxyacetoacetanilides, 1,3,5-trinitrobenzene and triethylamine. The structures of the compounds were characterized by UV/Visible, FTIR, (1)H NMR and 2D-correlation spectroscopy analysis. The in vitro cytotoxic studies were performed using Ehrlich Ascites Carcinoma cell line by Trypan blue dye exclusion assay and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide cell proliferation assay. The IC50 values of the 8-(4'-/2'-methoxy/unsubstituted phenylcarbamoyl)bicyclo[3.3.1]nonanes were found to be 110.65 μg/ml, 148.23 μg/ml and 151.71 μg/ml, respectively. Thus (4-methoxyphenylcarbomyl) bicyclo[3.3.1]nonane was more potent compared to other two bicyclic adducts.
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Authors | Dhivya Chandrasekaran, S A A Vandarkuzhali, G Sridharan, Radha Natarajan, P Brindha |
Journal | Indian journal of pharmaceutical sciences
(Indian J Pharm Sci)
Vol. 76
Issue 4
Pg. 370-4
(Jul 2014)
ISSN: 0250-474X [Print] India |
PMID | 25284936
(Publication Type: Journal Article)
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