Journal of Medicinal Chemistry · 2002 · 23 citations · 15 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryNeuropharmacologyDrug-receptor InteractionsLead Compound DesignLigand BindingPotency OptimizationReceptor PharmacologyStructure-activity Relationship AnalysisChemical SubstituentsLead Chemistry
The arylamidrazones have been found to be potent corticotropin releasing factor (CRF) receptor antagonists structurally distinct from previously reported CRF1 antagonists. Attempts to modify the arylamidrazone core suggested an important role for the anilino NH moiety. The right-hand-side 2-nitro feature in lead 1 could be replaced with substituents methyl, chloro, cyano, or trifluoromethyl with a 4- to 10-fold reduction in receptor binding. With appropriate left-hand-side modifications, this potency loss could be recovered.
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Teresa M. Reyes, Kathleen Lewis, Marilyn H. Perrin et al. · Proceedings of the National Academy of Sciences · 2001 · 892 citations · Full text
Kamal E. Habib, Katherine P Weld, Kenner C. Rice et al. · Proceedings of the National Academy of Sciences · 2000 · 402 citations