Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.15/443
Título: Synthesis of sugars embodying conjugated carbonyl systems and related triazole derivatives from carboxymethyl glycoside lactones: evaluation of their antimicrobial activity and toxicity
Autor: Xavier, N. M.
Goulart, Margarida
Neves, Ana
Justino, Jorge
Chambert, S.
Rauter, A. P.
Queneau, Y.
Palavras-chave: Bicyclic sugar lactones
Sugar enones
Diene pyranosides
Antimicrobial activity
Data: 15-Jan-2011
Editora: Elsevier
Citação: XAVIER; N.M.;GOULART, M. ; NEVES, A.; JUSTINO, J. CHAMBERT, S. RAUTER, A.P. ; Queneau, Y. (2011) - Synthesis of sugars embodying conjugated carbonyl systems and related triazole derivatives from carboxymethyl glycoside lactones. Evaluation of their antimicrobial activity and toxicity. Bioorganic & medicinal chemistry 19 (2): 926-938
Resumo: The synthesis of a series of pyranoid derivatives comprising a conjugated carbonyl function and related triazole derivatives, structurally suitable for bioactivity evaluation, was achieved in few steps starting from readily available carboxymethyl glycoside lactones (CMGL). 3-Enopyranosid-2-uloses were generated by oxidation/elimination of tri-O-acylated 2-hydroxy pyranosides. Subsequent Wittig olefination provided stereoselectively 2-C-branched-chain conjugated dienepyranosides with (E)-configuration around the exocyclic double bond. A heterogeneous CuI/Amberlyst-catalyzed 'click' chemistry protocol was used to convert glycosides bearing a propargyl moiety into the corresponding 1,2,3-triazoles. These new molecules were screened for their in vitro antibacterial and antifungal activities and those containing conjugated carbonyl systems demonstrated the best efficacy. (N-Dodecylcarbamoyl)methyl enone glycerosides were the most active ones among the enones tested. The alpha-anomer displayed very strong activities against Bacillus cereus and Bacillus subtilis and strong activity toward Enterococcus faecalis and the fungal pathogen Penicillium aurantiogriseum. The corresponding beta-anomer presented a very strong inhibitory effect against two fungal species (Aspergillus niger and P. aurantiogriseum). (N-Dodecyl-/N-propargyl/or N-benzylcarbamoyl) methyl dienepyranosides exhibited selectively a strong activity toward E. faecalis. Further acute toxicity evaluation indicated low toxic effect of the (N-dodecylcarbamoyl)methyl enone glyceroside alpha-anomer and of the carbamoylmethyl dienepyranosides N-protected with propargyl or benzyl groups
Peer review: yes
URI: http://hdl.handle.net/10400.15/443
ISSN: 0968-0896
Versão do Editor: http://www.elsevier.com/locate/bmc
Aparece nas colecções:Artigos em revistas internacionais_ESAS

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