Publication | Open Access
Discovery of an Orally-Active Nonsteroidal Androgen Receptor Pure Antagonist and the Structure-Activity Relationships of Its Derivatives
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Citations
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References
2008
Year
Androgen Receptor-5,5-Dimethylthiohydantoin DerivativesOrganic ChemistryPharmacotherapyHeterocycle ChemistryPharmaceutical ChemistryChemical DerivativeMedicinal ChemistrySteroid MetabolismCompound 13BBiochemistryHormonal ReceptorReceptor (Biochemistry)Structure-activity RelationshipsMechanism Of ActionNon-peptide LigandEndocrinologyPharmacologyNatural SciencesAnabolic SteroidsMedicineDerivative (Chemistry)Drug Discovery
The 3-(4-cyano-3-trifluoromethylphenyl)-5,5-dimethylthiohydantoin derivatives which have carboxy-terminal side chains were synthesized and their agonistic/antagonistic activities against androgen receptor (AR) measured. Among them, compound 13b showed antagonistic activity (IC50=130 nM) with no agonistic activity even at 10000 nM. This compound exhibited significant metabolic stability and oral antiandrogenic activity (ED50=7 mg/kg).
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