TY - JOUR
T1 - Design and synthesis of two brucine derivatives and evaluation of its antibacterial activity against Escherichia coli and Salmonella typhi
AU - Figueroa-Valverde, Lauro
AU - Díaz-Cedillo, Francisco
AU - López-Ramos, María
AU - García-Cervera, Elodia
AU - Pool-Gómez, Eduardo
PY - 2012
Y1 - 2012
N2 - In this study two brucine derivatives were synthesized. The first step was achieved by the reaction of brucine with ethylenediamine using boric acid as catalyst to form an imine group (Schiff base) involved in the compound 3. The second step involves the coupling of ethylenediamine to brucine by the method reported by Mannich, using formaldehyde to form the compound 4. The antibacterial activity of both brucine derivatives was evaluated in vitro on Escherichia coli and Salmonella typhi using the dilution method and the minimum inhibitory concentration. The results showed that bacterial growth of Escherichia coli was inhibited by the compounds 3 and 4 in a dosedependent manner. Nevertheless, the bacterial growth of Salmonella typhi only was blocked by the compound 3. These data suggest that functional groups involved in the structure of 3 are specific for its antibacterial activity.
AB - In this study two brucine derivatives were synthesized. The first step was achieved by the reaction of brucine with ethylenediamine using boric acid as catalyst to form an imine group (Schiff base) involved in the compound 3. The second step involves the coupling of ethylenediamine to brucine by the method reported by Mannich, using formaldehyde to form the compound 4. The antibacterial activity of both brucine derivatives was evaluated in vitro on Escherichia coli and Salmonella typhi using the dilution method and the minimum inhibitory concentration. The results showed that bacterial growth of Escherichia coli was inhibited by the compounds 3 and 4 in a dosedependent manner. Nevertheless, the bacterial growth of Salmonella typhi only was blocked by the compound 3. These data suggest that functional groups involved in the structure of 3 are specific for its antibacterial activity.
KW - Brucine derivatives
KW - Escherichia coli
KW - Salmonella typhi
UR - http://www.scopus.com/inward/record.url?scp=84861642858&partnerID=8YFLogxK
M3 - Artículo
SN - 0970-7077
VL - 24
SP - 2173
EP - 2176
JO - Asian Journal of Chemistry
JF - Asian Journal of Chemistry
IS - 5
ER -