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PCT No. PCT/JP85/00445 Sec. 371 Date Apr. 10, 1986 Sec. 102(e) Date Apr. 10, 1986 PCT Filed Aug. 9, 1985 PCT Pub. No. WO86/01203 PCT Pub. Date Feb. 27, 1986.Compounds of the formula: wherein A means an alkylene; Y-Z means -CH=CH-, -CH2CH2-, or R1 and R2 are each a substituent; R3 is hydrogen atom, a...

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Bibliographic Details
Main Authors MIKIO KUROKAWA, FUMINORI SATO, NAONOBU HATANO, HITOSHI UNO
Format Patent
LanguageEnglish
Published 12.05.1988
Edition4
Subjects
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Summary:PCT No. PCT/JP85/00445 Sec. 371 Date Apr. 10, 1986 Sec. 102(e) Date Apr. 10, 1986 PCT Filed Aug. 9, 1985 PCT Pub. No. WO86/01203 PCT Pub. Date Feb. 27, 1986.Compounds of the formula: wherein A means an alkylene; Y-Z means -CH=CH-, -CH2CH2-, or R1 and R2 are each a substituent; R3 is hydrogen atom, alkyl, or alkoxy; R4 is phenyl, phenylalkyl, phenylalkenyl, diphenylmethyl, naphthyl, thiazolyl, optionally substituted pyridyl, optionally substituted pyrimidinyl, quinolyl, benzoylalkyl, benzoyl, furoyl, thenoyl, phenyloxycarbonyl, phenyloxysulfonyl, or phenylsulfonyl; a is 2 or 3, b and c are each 1 or 2, and d is an integer of 0 to 2, provided that the phenyl, phenyl moiety and naphthyl may optionally be substituted, and a pharmaceutically acceptable salt thereof, process for the preparation thereof, and pharmaceutical composition containing the same. The compounds and salt thereof show potent calcium antagonistic activity and are useful for prophylaxis and treatment of hypertension and/or ischemic heart disease.
Bibliography:Application Number: AU19850000472