发明名称 CONDENSED PYRIDAZINE-BASED COMPOUND
摘要 <p>PURPOSE: To obtain a new condensed pyridazine compound useful for preventing and treating cardio-vascular insufficiency, having excellent inhibitory action on CGMP-PDE(cyclic GMP phosphodiesterase), high watersolubility, excellent absorption in body and low toxicity. CONSTITUTION: This condensed pyridazine-based compound is shown by formula I (ring C is a 5- to 6-membered ring which may contain a hetero atom; (n) is an integer of 0 or 1-4; R<1> is a halogen, nitro, cyano, etc.,; A is H, a halogen, an aryl, etc.; X is a group of the formula N, etc.; Y is group of the formula CO, etc.; an alternate long and short dash line is a double bond or a single bond with the proviso that a case where (n) is 0 is omitted when the ring C is a benzene ring) or its pharmacologically permissible salt. The most preferable example is a compound of formula II. The compound of formula I, for example, is obtained by halogenating a 1,4-phthalazinedione derivative.</p>
申请公布号 JPH08225541(A) 申请公布日期 1996.09.03
申请号 JP19950203102 申请日期 1995.08.09
申请人 EISAI CO LTD 发明人 WATANABE NOBUHISA;KABASAWA YASUHIRO;TAKASE YASUTAKA;OZAKI FUMIHIRO;ISHIBASHI KEIJI;MIYAZAKI KAZUSHIRO;MATSUKURA MASAYUKI;SODA SHIGERU;MIYAKE KAZUTOSHI;ISHIHARA HIROKI;KODAMA KOTARO;ADACHI HIDEYUKI
分类号 C07D237/30;A61K31/50;A61K31/502;A61P7/02;A61P9/00;A61P9/12;A61P11/00;A61P43/00;C07D209/48;C07D237/32;C07D237/34;C07D401/04;C07D401/12;C07D403/04;C07D403/12;C07D405/12;C07D405/14;(IPC1-7):C07D237/30 主分类号 C07D237/30
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