Page 43 - AR2012-13.pdf
P. 43
!!
!
$
%
%&%&
$!&& % &
' ( !
$!&& %
"
"#
"
"
"
"
" $!%#
)##
#
Fig. 32 Chemical structures of phenylpropenes and cinnamyl derivatives
Table 8. Screening of methoxylated phenylpropenes (1-4) and their benzaldehyde derivatives
(5-7) for antimicrobial activity
1.-# #&&'$(&)* )'#&+&#% ),)&-# -#) )$ &'$(&)* '*#$.- /
0
!
"#$% )'#.$&) ,&
"
CSIR-IHBT Annual Report 2012-13
A= E. coli; B= E. cloacae; C= B. subtilis; D= B. cepacea; E= M. luteus; F= S. aureus; G= P. aeruginosa; H= K. pneumoniae; I= A. niger;
J= A. sydowii; K= A. parasiticus; L= T. rubrum; M= C. albicans and N= I. orientalis; R= resistant; Ampicillin and nystatin were
standard controls for anti-bacterial and anti-fungal, respectively.
33
