Author(s): Manda, Bhaskar R. ; Prasad, Avvari N. ; Thatikonda, Narendar R. ; Lacerda, Valdemar ; Barbosa, Layla R. ; Santos, Heloa ; Romao, Wanderson ; Pavan, Fernando R. [UNESP] ; Ribeiro, Camila M. [UNESP] ; Santos, Edson A. dos ; Marques, Maria R. ; Lima, Denis P. de ; Micheletti, Ana C. ; Beatriz, Adilson
Date: 2018
Persistent ID: http://hdl.handle.net/11449/165973
Origin: Oasisbr
Subject(s): CNSL; cardanol; amino alcohols; epoxide ring opening; antimicrobial activity
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FUNDECT (PRONEM)
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
Kardol Ind. Quimica Ltda.
The synthesis of novel amino alcohol derivatives based on cardanol and glycerol were achieved in good yields and characterized by H-1 and C-13 NMR (nuclear magnetic resonance) and MS (mass spectrometry). In addition, we evaluated the in vitro antimicrobial activity against Gram-positive (Staphylococcus aureus, standard and clinical strains), Gram-negative (Escherichia coli) and M. tuberculosis bacterial strains. The bioassay results indicated that four compounds showed activity against S. aureus, including the clinical resistant strain, with MIC (minimum inhibitory concentration) ranging from 3.90 to 15.60 mu g mL(-1) and M. tuberculosis, with MIC90 (minimum inhibitory concentration required to inhibit the growth of 90% of organisms) ranging from 3.18 to 7.36 mu g mL(-1).
Univ Fed Mato Grosso Do Sul, Inst Quim INQUI, Av Senador Felinto Muller 1555, BR-79074460 Campo Grande, MS, Brazil
Univ Fed Espirito Santo, Dept Quim, BR-29075910 Vitoria, ES, Brazil
Univ Estadual Paulista, Fac Ciencias Farmaceut, BR-14801902 Araraquara, SP, Brazil
Univ Fed Mato Grosso Do Sul, Inst Biociencias INBIO, Cidade Univ S-N,CP 549, BR-79070900 Campo Grande, MS, Brazil
Univ Estadual Paulista, Fac Ciencias Farmaceut, BR-14801902 Araraquara, SP, Brazil
FUNDECT (PRONEM): 054/12
