Journal of Combinatorial Chemistry · 2001 · 27 citations · 19 references
Combinatorial ChemistryMedicinal ChemistryBioorganic ChemistrySolid-phase SynthesisNovel Piperazine ScaffoldsNatural SciencesMedicineOrganic ChemistryCompound LibraryChemistry160-Member LibraryPharmacologyPharmaceutical ChemistrySynthetic ChemistryDrug DiscoveryNatural Product Synthesis
Strategies for finding novel structures of therapeutical interest are discussed. The rationale for the selection of the two scaffolds N4-(m-aminophenyl)-piperazine-2-carboxylic acid E and N4-(o-aminophenyl)-piperazine-2-carboxylic F is described. The synthesis of the appropriate precursors to scaffold E and F and their use in solid-phase chemistry are described. A 160-member library was produced combining these novel piperazine scaffolds with eight sulfonyl chlorides/acid chlorides and 10 amines. The compound library prepared was analyzed using LC-MS, showing the expected base peak in all wells at an average purity of 82%.
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Christopher A. Lipinski, Franco Lombardo, Beryl W. Dominy et al. · Advanced Drug Delivery Reviews · 1997 · 11K citations
Development Settings, Pharmaceutical Science, Drug Target +8
Benzodiazepine Peptidomimetics: Potent Inhibitors of Ras Farnesylation In Animal Cells
Guy L. James, Joseph L. Goldstein, Michael S. Brown et al. · Science · 1993 · 629 citations