| abstract |
The present invention is the use of a compound of formula (I) or a (pharmaceutically) acceptable salt thereof, wherein (a) X denotes CH=CH or CZ1=CZ2, wherein if Z1 is H then Z2 denotes a radical selected from the group consisting of OH, NH 2 , NHMe, NMe 2 , OMe and OEt and if Z2 is H then Z1 denotes a radical selected from the group consisting of OH, NH 2 , NHMe, NMe 2 , OMe and OEt, Y denotes a radical selected from the group consisting of NH 2 , NHMe, NMe 2 , NHEt, O-(CH 2 ) n -OH, wherein n is 2 to 5 and R denotes a radical selected from the group consisting of H, OH, Me, Et, OMe, OEt, NH 2 , NHMe, NMe 2 , NHEt and NEt 2 , or (b) X denotes O, Y denotes a radical selected from the group consisting of NH 2 , NHMe, NMe 2 , NHEt, O-(CH 2 ) n -OH and OMe, wherein n is 2 to 5 and R denotes H, OH, Me, Et, OMe, OEt, NH 2 , NHMe, NMe 2 , NHEt, NEt 2 as antimicrobial agent as well as to composition comprising said agent. |