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公开(公告)号:FI882456A
公开(公告)日:1988-11-29
申请号:FI882456
申请日:1988-05-25
Applicant: UCB SA
Inventor: BOLLEN ALEX , GOBERT JEAN , WUELFERT ERNST
IPC: C12N15/09 , A61K38/00 , C07K4/12 , C07K14/775 , C12N1/16 , C12N1/20 , C12N5/10 , C12N15/00 , C12N15/12 , C12P21/00 , C12P21/02 , C12R1/19 , C12R1/865 , C12N
Abstract: The present invention provides recombinant DNA sequences comprising a sequence which codes for human proapolipoprotein A-I wherein part of the natural coding sequence has been replaced by a DNA fragment coding for the same amino acids but consisting of a different nucleotide sequence such as to reduce or prevent formation of hairpins, cloning and expression vectors containing these DNA sequences, cell cultures or microorganisms transformed with these expression vectors and processes using the same for the production of proapolipoprotein A-I.
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公开(公告)号:DK289688A
公开(公告)日:1988-11-29
申请号:DK289688
申请日:1988-05-27
Applicant: UCB SA
Inventor: BOLLEN ALEX , GOBERT JEAN , WUELFERT ERNST
IPC: C12N15/09 , A61K38/00 , C07K4/12 , C07K14/775 , C12N1/16 , C12N1/20 , C12N5/10 , C12N15/00 , C12N15/12 , C12P21/00 , C12P21/02 , C12R1/19 , C12R1/865 , C07H21/04
Abstract: The present invention provides recombinant DNA sequences comprising a sequence which codes for human proapolipoprotein A-I wherein part of the natural coding sequence has been replaced by a DNA fragment coding for the same amino acids but consisting of a different nucleotide sequence such as to reduce or prevent formation of hairpins, cloning and expression vectors containing these DNA sequences, cell cultures or microorganisms transformed with these expression vectors and processes using the same for the production of proapolipoprotein A-I.
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公开(公告)号:NO874572L
公开(公告)日:1988-05-05
申请号:NO874572
申请日:1987-11-03
Applicant: UCB SA
Inventor: COSSEMENT ERIC , GEERTS JEAN-PIERRE , GOBERT JEAN , MICHEL PHILIPPE
IPC: A61K31/415 , A61K31/4164 , A61K31/495 , A61P9/08 , A61P9/10 , A61P9/12 , C07D233/54 , C07D233/58 , C07D233/64 , C07D405/06 , C07D413/06 , C07D233/00
Abstract: New substituted 1H-imidazoles and their salts, processes for the preparation thereof and pharmaceutical compositions. These compounds have the formula wherein R1, R2, R3 and R5=hydrogen or C1-C4-alkyl; R4=hydrogen, C1-C4-alkyl or C1-C4-alkoxy; Y1=hydrogen and Y2=OZ2 or the reverse; Z1=Z2=hydrogen or C1-C4-alkyl or Z1 and Z2=-CH2- or -C(CH3)2-. These compounds are prepared either by reducing a corresponding imidazole compound having a hydroxyl or alkoxy group on the methyl bridge between the imidazole and phenyl rings, or by hydrolyzing a 4-[[2,2-dimethyl-4H-1,3-benzodioxin-6(or 8)-yl]methyl]-1H-imidazole, or yet by reducing an alkyl 3-[(1H-imidazol-4-yl)methyl]-2-hydroxybenzoate. These compounds have cardiac, cerebral and tissular anti-ischemic activities.
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公开(公告)号:PT86040A
公开(公告)日:1987-11-01
申请号:PT8604087
申请日:1987-10-30
Applicant: UCB SA
Inventor: COSSEMENT ERIC , GEERTS JEAN-PIERRE , GOBERT JEAN , MICHEL PHILIPPE
IPC: A61K31/415 , A61K31/4164 , A61K31/495 , A61P9/08 , A61P9/10 , A61P9/12 , C07D233/54 , C07D233/58 , C07D233/64 , C07D405/06 , C07D413/06 , C07D233/00
Abstract: New substituted 1H-imidazoles and their salts, processes for the preparation thereof and pharmaceutical compositions. These compounds have the formula wherein R1, R2, R3 and R5=hydrogen or C1-C4-alkyl; R4=hydrogen, C1-C4-alkyl or C1-C4-alkoxy; Y1=hydrogen and Y2=OZ2 or the reverse; Z1=Z2=hydrogen or C1-C4-alkyl or Z1 and Z2=-CH2- or -C(CH3)2-. These compounds are prepared either by reducing a corresponding imidazole compound having a hydroxyl or alkoxy group on the methyl bridge between the imidazole and phenyl rings, or by hydrolyzing a 4-[[2,2-dimethyl-4H-1,3-benzodioxin-6(or 8)-yl]methyl]-1H-imidazole, or yet by reducing an alkyl 3-[(1H-imidazol-4-yl)methyl]-2-hydroxybenzoate. These compounds have cardiac, cerebral and tissular anti-ischemic activities.
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公开(公告)号:PT80460B
公开(公告)日:1987-08-19
申请号:PT8046085
申请日:1985-05-14
Applicant: UCB SA
Inventor: GEERTS JEAN-PIERRE , GOBERT JEAN , BODSON GUY
IPC: A61K31/40 , A61K31/4015 , C07D207/26 , A61P7/06 , A61P9/00 , A61P9/10 , C07D207/12 , C07D207/27 , C07D207/277 , C07D295/185
Abstract: (S)-alpha-ethyl-2-oxo-1-pyrrolidineacetamide, its preparation and pharmaceutical compositions containing the same. It can be prepared either by reacting (S)-alpha-ethyl-2-oxo-1-pyrrolidineacetic acid successively with an alkyl haloformate and with ammonia, or, by cyclizing an (S)-2-amino-butanamide of the formula X-CH2CH2-NHCH (C2H5)CONH2 wherein Y is a -CH2-radical when X represents a ZOOC-radical and Y is a -CO- radical when X represents a HalCH2-radical, Z being a C1-C4 alkyl radical and Hal a halogen atom. This laevorotatory enantiomer has been found to have significantly higher protective activity against hypoxia and ischemia than the corresponding racemate.
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公开(公告)号:NO851934L
公开(公告)日:1985-11-18
申请号:NO851934
申请日:1985-05-14
Applicant: UCB SA
Inventor: GOBERT JEAN , GIURGEA CORNELIU , GEERTS JEAN-PIERRE , BODSON GUY
IPC: C07D207/26 , A61K31/40 , A61K31/4015 , A61P25/28 , C07D207/27 , C07D295/185 , C07D
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公开(公告)号:DK212985D0
公开(公告)日:1985-05-14
申请号:DK212985
申请日:1985-05-14
Applicant: UCB SA
Inventor: GOBERT JEAN , GEERTS JEAN-PIERRE , BODSON GUY
IPC: C07D207/26 , A61K31/40 , A61K31/4015 , A61P7/06 , A61P9/00 , A61P9/10 , C07D207/12 , C07D207/27 , C07D207/277 , C07D295/185 , C07D
Abstract: (S)-alpha-ethyl-2-oxo-1-pyrrolidineacetamide, its preparation and pharmaceutical compositions containing the same. It can be prepared either by reacting (S)-alpha-ethyl-2-oxo-1-pyrrolidineacetic acid successively with an alkyl haloformate and with ammonia, or, by cyclizing an (S)-2-amino-butanamide of the formula X-CH2CH2-NHCH (C2H5)CONH2 wherein Y is a -CH2-radical when X represents a ZOOC-radical and Y is a -CO- radical when X represents a HalCH2-radical, Z being a C1-C4 alkyl radical and Hal a halogen atom. This laevorotatory enantiomer has been found to have significantly higher protective activity against hypoxia and ischemia than the corresponding racemate.
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公开(公告)号:DK212885D0
公开(公告)日:1985-05-14
申请号:DK212885
申请日:1985-05-14
Applicant: UCB SA
Inventor: GOBERT JEAN , GIURGEA CORNELIU , GEERTS JEAN-PIERRE , BODSON GUY
IPC: C07D207/26 , A61K31/40 , A61K31/4015 , A61P25/28 , C07D207/27 , C07D295/185 , C07D
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公开(公告)号:HU224070B1
公开(公告)日:2005-05-30
申请号:HU9901848
申请日:1994-03-11
Applicant: UCB SA
Inventor: BODSON GUY , COSSEMENT ERIC , GOBERT JEAN
IPC: C07D295/06 , C07D295/073
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公开(公告)号:DK174289B1
公开(公告)日:2002-11-18
申请号:DK586589
申请日:1989-11-22
Applicant: UCB SA
Inventor: BODSON GUY , COSSEMENT ERIC , GOBERT JEAN
IPC: C07D295/08 , C07D295/088
Abstract: A process for the preparation of 2-[2-[4-[(4-chlorophenyl) phenylmethyl]-1-piperazinyl]ethoxy]-acetic acid and its dihydrochloride, wherein 2-[4-[(4-chlorophenyl-phenylmethyl]-1-piperazinyl]1-1ethanol is reacted with an alkali metal halogenoacetate in the presence of an alkali metal alcoholate, the alkali metal salt thus obtained is converted into the corresponding acid and, if appropriate, into its dihydrochloride.
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