Abstract:
:Tethered dimers incorporating natural alpha-amino acid end groups were synthesized, including examples in which the previously reported esterase-sensitive ester linker was replaced with more stable amide or ether linkers. These compounds remained effective both as inhibitors of NAD synthetase and as potent antibacterial agents for Gram-positive strains. Studies on nonspecific effects, including detergent properties and promiscuous inhibition, suggested little contribution to observed activities.
journal_name
J Med Chemjournal_title
Journal of medicinal chemistryauthors
Velu SE,Mou L,Luan CH,Yang ZW,DeLucas LJ,Brouillette CG,Brouillette WJdoi
10.1021/jm061349lsubject
Has Abstractpub_date
2007-05-31 00:00:00pages
2612-21issue
11eissn
0022-2623issn
1520-4804journal_volume
50pub_type
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