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New piperazinyl polyazacyclophane scaffolds, libraries and biological activities
Bioorganic & Medicinal Chemistry Letters
|January 5, 1999
Abstract:
Four novel unsymmetric piperazinyl polyazacyclophane scaffolds 1-4 were synthesized in high yields by an efficient cyclization strategy. Twenty-six libraries 12-37 (total 16,000 compounds) were generated by a solution-phase combinatorial approach from 1-4 and thirty-eight functional groups. Potent antibacterial and HIV-1 tat/TAR protein-RNA disrupting activities were discovered.