Publication | Closed Access

Synthesis and in vitro profile of a novel series of catechol benzimidazoles. The discovery of potent, selective phosphodiesterase type IV inhibitors with greatly attenuated affinity for the [3H]rolipram binding site

Catechol BenzimidazolesMedicinal ChemistryNovel SeriesBiochemistryNatural SciencesVitro ProfileMedicineRational Drug DesignPharmacological AgentDrug DevelopmentChemical BiologyPharmacologyPharmaceutical ChemistryDrug Discovery