Novel α,β-dicarboximide derivatives which selectively inhibit binding to the α-
,1A? adrenergic receptor, a receptor which has been shown to be important in the treatment of benign prostatic hyperplasia. The compounds of the present invention are potentially useful in the treatment of benign prostatic hyperplasia.
新型α,β-二甲
酰亚胺衍
生物可选择性地抑制与α-,1A?
1A?
肾上腺素能受体的结合,该受体已被证明在治疗良性前列腺增生症中具有重要作用。本发明的化合物可用于治疗良性前列腺增生症。