首页> 外国专利> PIPERAZINE DERIVATIVES AS ALPHA 1A-ADRENERGIC RECEPTOR ANTAGONISTS

PIPERAZINE DERIVATIVES AS ALPHA 1A-ADRENERGIC RECEPTOR ANTAGONISTS

机译:哌嗪衍生物作为α1A-肾上腺素受体拮抗剂

摘要

There are disclosed compounds of general formula (I). Y is a linking group, chosen from a wide range, but including -COO-, -CH2COO-, -CONH-, -CON(CH3)-, -CH2CONH-, -SO2NH-, -SO2N(CH3)- and -PO(OC2H5)NH-. W is an alkylene chain. A is a substituted phenyl group or a benzofuran or benzodioxan group. R and R1 may have many values, but R is preferably a bulky group. These compounds and their prodrugs, enantiomers, diastereoisomers, N-oxides and pharmaceutically acceptable salts block alpha 1A-adrenergic receptors and are thus useful for the prevention of contractions of the prostate, urethra and lower urinary tract, without affecting blood pressure.
机译:公开了通式(I)的化合物。 Y是连接基团,其选自广泛的范围,但包括-COO-,-CH 2 COO-,-CONH-,-CON(CH 3)-,-CH 2 CONH-,-SO 2 NH-,-SO 2 N(CH 3)-和-PO (OC2H5)NH-。 W是亚烷基链。 A是取代的苯基或苯并呋喃或苯并二恶烷基。 R和R1可以具有许多值,但是R优选为大基团。这些化合物及其前药,对映异构体,非对映异构体,N-氧化物和药学上可接受的盐可阻断α1A-肾上腺素能受体,因此可用于预防前列腺,尿道和下尿路的收缩,而不影响血压。

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