Rr. Wilkening et al., Synthesis and activity of 2-(sulfonamido)methylcarbapenems: Discovery of anovel, anti-MRSA 1,8-naphthosultam pharmacophore, BIOORG MED, 9(5), 1999, pp. 673-678
A series of 1 beta-methyl carbapenems substituted at the IL-position with l
ipophilic, acyclic and cyclic (sulfonamido)methyl groups was prepared and e
valuated for activity against resistant gram-positive bacteria. From these
studies, the 1,8-naphthosultamyl group emerged as a novel, PBP2a-binding, a
nti-MRSA pharmacophore worthy of further exploration. (C) 1999 Elsevier Sci
ence Ltd. All rights reserved.