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公开(公告)号:EP1093460A1
公开(公告)日:2001-04-25
申请号:EP99930569.1
申请日:1999-06-23
发明人: RITTER, Kurt , JANSSEN, Bernd , HAUPT, Andreas , KLING, Andreas , BARLOZZARI, Teresa , AMBERG, Wilhelm
CPC分类号: C07K7/02 , A61K38/00 , C07K5/101 , C07K5/1024
摘要: Compounds of the present invention include cell growth inhibitors which are peptides of Formula (I): A - B - D - E - F - G and acid salts thereof, wherein A, D and E are α-amino acid residues, B is an α-amino acid residue or an α-hydroxy acid residue, F is an aminobenzoic acid residue or an aminocycloalkanecarboxylic acid residue, and G is a monovalent radical, such as, for example, a hydrogen atom, an amino group, an alkyl group, an alkylene alkyl ether, an alkylene alkyl thioether, an alkylene aldehyde, an alkylene amide, a β-hydroxylamino group, a hydrazido group, an alkoxy group, a thioalkoxy group, an aminoxy group, an oximato group, an alkylene aryl group, an alkylene ester, an alkylene sulfoxide or an alkylene sulfone. Another aspect of the present invention includes pharmaceutical compositions comprising a compound of Formula (I) and a pharmaceutically acceptable carrier. An additional embodiment of the present invention is a method for treating cancer in a mammal, such as a human, comprising administering to the mammal an effective amount of a compound of Formula (I) in a pharmaceutically acceptable composition.
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公开(公告)号:EP0674652B1
公开(公告)日:2000-09-13
申请号:EP94902676.9
申请日:1993-12-04
发明人: HAUPT, Andreas , JANSSEN, Bernd , RITTER, Kurt , KLINGE, Dagmar , KEILHAUER, Gerhard , ROMERDAHL, Cynthia , BARLOZZARI, Teresa , QIAN, Xiao-Dong
CPC分类号: C07K7/02 , A61K38/00 , C07K5/0205
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公开(公告)号:EP0991658A1
公开(公告)日:2000-04-12
申请号:EP98935531.8
申请日:1998-07-07
摘要: Compounds of the present invention include cell growth inhibitors which are peptides of Formula (I):, A - B - D - E - F - (G)r - (K)s - L and acid salts thereof, wherein A, B, D, E, F, G and K are α-amino acid residues, and s and r are each, independently, 0 or 1. L is a monovalent radical, such as, for example, an amino group, an N-substituted amino group, a β-hydroxylamino group, a hydrazido group, an alkoxy group, a thioalkoxy group, an aminoxy group, or an oximato group. The present invention also includes a method for treating cancer in a mammal, such as a human, comprising administering to the mammal an effective amount of a compound of Formula (I) in a pharmaceutically acceptable composition.
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公开(公告)号:EP0871656A1
公开(公告)日:1998-10-21
申请号:EP96918661.0
申请日:1996-06-03
摘要: Novel dolasstatin derivatives of the formula (I): R1R2N-CHX-CO-A-B-D-E-(F)¿t?K, in which R?1, R2¿, A, B, D, E, F, K, X and t have the meanings stated in the description, and the preparation thereof are described. The novel substances have an antineoplastic effect.
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公开(公告)号:EP0859786A1
公开(公告)日:1998-08-26
申请号:EP96937291.0
申请日:1996-10-30
发明人: KLING, Andreas , JANSSEN, Bernd , AMBERG, Wilhelm , HAUPT, Andreas , RITTER, Kurt , BUSCHMANN, Ernst , BERNARD, Harald , MÜLLER, Stefan , ZIERKE, Thomas , BARLOZZARI, Teresa , DE ARRUDA, Monika , ROBINSON, Simon
摘要: Novel peptides of the formula A-B-D-E-F-L, wherein A, B, D, E, F, and L have the meanings stated in the specification, and their preparation are disclosed. The novel compounds are suitable for controlling diseases.
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公开(公告)号:EP1021200B1
公开(公告)日:2002-02-06
申请号:EP98948455.5
申请日:1998-09-24
IPC分类号: A61K38/08 , A61K39/395
CPC分类号: A61K38/08 , A61K39/395 , A61K2300/00
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7.
公开(公告)号:EP0915908A1
公开(公告)日:1999-05-19
申请号:EP97934502.0
申请日:1997-07-21
发明人: BARLOZZARI, Teresa , HAUPT, Andreas , JANSSEN, Bernd , GRIESINGER, Christian , BELIK, Daniel , BORETZKY, Michael , PETTIT, George, Robert
摘要: The present invention provides anti-tumor peptides of the Formula (I), A-B-N(CH3)-CHD-CH(OCH3)-CH2CO-Pro-Pro-K, and the acid salts thereof. A is an amino acid residue of the formula (CH3)2N-CHX-CO, wherein X is a normal or branched alkyl group. B is an amino acid residue selected from the group consisting of valyl, isoleucyl, leucyl, and 2-t-butylglycyl. D is a normal or branched C3-C4-alkyl group. K is a t-butoxy group or a substituted amino group. An additional embodiment of the present invention is a method for treating a malignancy in a mammal, such as a human, comprising administering to the mammal an effective amount of a compound or compounds of Formula (I) in a pharmaceutically acceptable composition.
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公开(公告)号:EP0866800A2
公开(公告)日:1998-09-30
申请号:EP96943076.0
申请日:1996-12-11
发明人: AMBERG, Wilhelm , BARLOZZARI, Teresa , BERNARD, Harald , BUSCHMANN, Ernst , HAUPT, Andreas , HEGE, Hans-Guenther , JANSSEN, Bernd , KLING, Andreas , LIETZ, Helmut , RITTER, Kurt , ULLRICH, Martina , WEYMANN, Jürgen , ZIERKE, Thomas
CPC分类号: A61K38/08
摘要: Novel peptides of the following formula (I): R1R2N-CHX-CO-A-B-D-E-(G)¿s?-K in which R?1, R2¿, A, B, D, E, G, K, X, and s have the meanings stated in the description, and the preparation thereof are described. The novel peptides have an antineoplastic effect.
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公开(公告)号:EP0832104A1
公开(公告)日:1998-04-01
申请号:EP96918660.0
申请日:1996-06-03
摘要: Novel dolastatin derivatives of the formula (I): R1R2N-CHX-CO-A-B-D-E-(F)¿t?-K in which R?1, R2¿, A, B, D, E, F, K, X and t have the meanings stated in the description, and the preparation thereof are described. The novel substances have an antineoplastic effect.
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公开(公告)号:EP0642530A1
公开(公告)日:1995-03-15
申请号:EP93909931.0
申请日:1993-05-10
摘要: Novel derivates of dolastatin of formula (I) in which R1, R2, A, B, D, E, F, G, K, X, t, u, v, and w have the meanings stated in the description, and the preparation thereof are described. The novel substances have an antineoplastic effect.
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