发明名称 |
Interfuranylene prostacyclins |
摘要 |
The invention relates to novel interfuranylene-prostacyclin derivatives of the general formula (I) <IMAGE> (I) wherein R1 stands for hydrogen or a straight or branched chain C1-6 alkyl group, an inorganic cation or for the protonated form of a base containing an amino group; R2 stands for hydrogen, a C1-4 alkanoyl or benzoyl group, a monosubstituted benzoyl, trialkylsilyl or an alkoxyalkyl group; R3 stands for a straight or branched chain C1-6 alkyl group, a phenyl group optionally substituted by halogen or by a C1-4 alkyl group, a heteroaryl group optionally substituted by halogen or by a C1-4 alkyl group or a cycloalkyl group; A stands for an ethylene or for a cis- or trans-vinylene or -C 3BOND C- group; B means a chemical bond, a -CHR5-, -CHR5-CH2- or a -CH2-O- group: and R5 means hydrogen or a C1-4 alkyl group. The compounds of the formula (I) can be used therapeutically as platelet aggregation inhibiting, anti-thrombotic, hypotensive and anti-antherosclerotic agents; they are much more stable than the natural prostacyclin derivatives.
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申请公布号 |
US4740523(A) |
申请公布日期 |
1988.04.26 |
申请号 |
US19860820434 |
申请日期 |
1986.01.17 |
申请人 |
CHINOIN GYOGYSZER ES VEGYESZETI TERMEKEK GYAR RT |
发明人 |
GALAMBOS, GEZA;IVANICS, JOZSEF;DORMAN, GYOERGY;KANAY, KAROLY;TOEMOESKOEZY, ISTVAN;KOVACS, GABOR;STADLER, ISTVAN;KOERMOECZI, PETER;HADHAZY, PAL;VIRAG, SANDOR;KISS, MIKLOS |
分类号 |
C07C405/00;A61K31/35;A61K31/557;A61K31/5585;A61P7/02;A61P9/12;A61P9/14;A61P11/08;A61P35/00;C07D307/935;C07D311/02;C07D407/04;C07D407/14;(IPC1-7):A61K31/35;C07D311/00 |
主分类号 |
C07C405/00 |
代理机构 |
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代理人 |
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主权项 |
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地址 |
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