Journal
REVISTA VIRTUAL DE QUIMICA
Volume 8, Issue 3, Pages 1020-1031Publisher
BRAZILIAN CHEMICAL SOC
DOI: 10.5935/1984-6835.20160073
Keywords
Borneol ester; antiproliferative activity; antioedematogenic activity
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Funding
- Conselho Nacional de Desenvolvimento Cientifico e Tecnologico
- Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior
- Fundacao de Amparo a Pesquisa do Estado de Minas Gerais
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Borneol derivatives have been regarded as promising anti-inflammatory and antimicrobial agents. In this work, eight borneol esters (1-8) were synthesized using DIC/DMAP or SOCl2 method and the products characterized by means of spectroscopic techniques. Six of them are new compounds and the DIC/DMAP method was faster and resulted in high reaction yields. Compounds 1-8 were subjected to in vitro antiproliferative assay using normal and tumor human cell lines and to antioedematogenic activity evaluation. Compound 6 [(1S, 2R, 4S)-1,7,7trimethylbicyclo[2.2.1] heptan-2-yl 3,4,5-trimethoxybenzoate] presented a promisor cytotoxic activity against various tumor cell lines and 7 [(1S, 2R, 4S)-1,7,7-trimethylbicyclo[2.2.1] heptan2-yl benzoate] was effective in the reduction of oedematogenic response in all period of time evaluated.
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