-
公开(公告)号:CZ90999A3
公开(公告)日:1999-06-16
申请号:CZ90999
申请日:1997-09-15
Applicant: HOECHST AG
Inventor: ERTL JOHANN , PREIBISCH GERALD , MULLER GUNTER
IPC: C12N15/09 , A61K38/00 , A61K38/17 , A61K38/22 , A61K45/00 , A61P3/10 , A61P5/50 , C07K14/575 , C07K16/26 , C07K19/00 , C12P21/02
Abstract: The invention relates to pharmaceutical agents containing leptin antagonists for treating Type II diabetes. One leptin antagonist is based on a murine leptin fragment and comprises amino acids 116 to 167 or 116 to 166. Methods of treating Type II diabetes are also disclosed.
-
公开(公告)号:AU4458697A
公开(公告)日:1998-04-14
申请号:AU4458697
申请日:1997-09-15
Applicant: HOECHST AG
Inventor: MUELLER GUENTER , PREIBISCH GERALD , ERTL JOHANN
IPC: C12N15/09 , A61K38/00 , A61K38/17 , A61K38/22 , A61K45/00 , A61P3/10 , A61P5/50 , C07K14/575 , C07K16/26 , C07K19/00 , C12P21/02
Abstract: The invention relates to pharmaceutical agents containing leptin antagonists for treating Type II diabetes. One leptin antagonist is based on a murine leptin fragment and comprises amino acids 116 to 167 or 116 to 166. Methods of treating Type II diabetes are also disclosed.
-
公开(公告)号:FI881268A
公开(公告)日:1988-09-21
申请号:FI881268
申请日:1988-03-17
Applicant: HOECHST AG
Inventor: RAGG HERMANN , PREIBISCH GERALD , HEIN FRIEDRICH , UHLMANN EUGEN , LINDENMAIER WERNER
IPC: G01N33/50 , A61K38/00 , A61K38/55 , C07K14/00 , C07K14/435 , C07K14/575 , C07K14/81 , C07K19/00 , C12N5/10 , C12N15/09 , C12P21/02 , C12Q1/68 , C12Q1/6876 , C12R1/91 , C12N
Abstract: Human leuserpine-2 (hLS2) has the same gene structure as alpha -antitrypsin or angiotensinogen. By combination of exons from serpine genes which have this gene structure, recombinant genes can be produced which code for hybrid serpines. By expression of the recombinant genes in eukaryotic cells, the corresponding hybrid serpines can be obtained.
-
公开(公告)号:ZA9708455B
公开(公告)日:1998-03-20
申请号:ZA9708455
申请日:1997-09-19
Applicant: HOECHST AG
Inventor: MUELLER GUENTER , PREIBISCH GERALD , ERTL JOHANN
IPC: C12N15/09 , A61K38/00 , A61K38/17 , A61K38/22 , A61K45/00 , A61P3/10 , A61P5/50 , C07K14/575 , C07K16/26 , C07K19/00 , C12P21/02 , A61K
CPC classification number: C07K14/5759 , A61K38/00
-
公开(公告)号:AU1328888A
公开(公告)日:1988-09-22
申请号:AU1328888
申请日:1988-03-18
Applicant: HOECHST AG
Inventor: RAGG HERMANN , PREIBISCH GERALD , HEIN FRIEDRICH , UHLMANN EUGEN , LINDENMAIER WERNER
IPC: G01N33/50 , A61K38/00 , A61K38/55 , C07K14/00 , C07K14/435 , C07K14/575 , C07K14/81 , C07K19/00 , C12N5/10 , C12N15/09 , C12P21/02 , C12Q1/68 , C12Q1/6876 , C12R1/91 , C07G17/00 , C07H21/04 , C07K3/28 , C07K13/00 , C12N5/00 , C12N9/64 , C12N15/00 , G01N33/53
Abstract: Human leuserpine-2 (hLS2) has the same gene structure as alpha -antitrypsin or angiotensinogen. By combination of exons from serpine genes which have this gene structure, recombinant genes can be produced which code for hybrid serpines. By expression of the recombinant genes in eukaryotic cells, the corresponding hybrid serpines can be obtained.
-
公开(公告)号:FI881268A0
公开(公告)日:1988-03-17
申请号:FI881268
申请日:1988-03-17
Applicant: HOECHST AG
Inventor: RAGG HERMANN , PREIBISCH GERALD , HEIN FRIEDRICH , UHLMANN EUGEN , LINDENMAIER WERNER
IPC: G01N33/50 , A61K38/00 , A61K38/55 , C07K14/00 , C07K14/435 , C07K14/575 , C07K14/81 , C07K19/00 , C12N5/10 , C12N15/09 , C12P21/02 , C12Q1/68 , C12Q1/6876 , C12R1/91 , C12N
Abstract: Human leuserpine-2 (hLS2) has the same gene structure as alpha -antitrypsin or angiotensinogen. By combination of exons from serpine genes which have this gene structure, recombinant genes can be produced which code for hybrid serpines. By expression of the recombinant genes in eukaryotic cells, the corresponding hybrid serpines can be obtained.
-
公开(公告)号:ZA978455B
公开(公告)日:1998-03-20
申请号:ZA978455
申请日:1997-09-19
Applicant: HOECHST AG
Inventor: MUELLER GUENTER , PREIBISCH GERALD , ERTL JOHANN
IPC: C12N15/09 , A61K38/00 , A61K38/17 , A61K38/22 , A61K45/00 , A61P3/10 , A61P5/50 , C07K14/575 , C07K16/26 , C07K19/00 , C12P21/02 , A61K
Abstract: The invention relates to pharmaceutical agents containing leptin antagonists for treating Type II diabetes. One leptin antagonist is based on a murine leptin fragment and comprises amino acids 116 to 167 or 116 to 166. Methods of treating Type II diabetes are also disclosed.
-
公开(公告)号:DK151788D0
公开(公告)日:1988-03-18
申请号:DK151788
申请日:1988-03-18
Applicant: HOECHST AG
Inventor: RAGG HERMANN , PREIBISCH GERALD , HEIN FRIEDRICH , UHLMANN EUGEN , LINDENMAIER WERNER
IPC: G01N33/50 , A61K38/00 , A61K38/55 , C07K14/00 , C07K14/435 , C07K14/575 , C07K14/81 , C07K19/00 , C12N5/10 , C12N15/09 , C12P21/02 , C12Q1/68 , C12Q1/6876 , C12R1/91 , C07K15/04 , C07H21/04 , C12N5/00 , C12N15/00 , C12P19/34
Abstract: Human leuserpine-2 (hLS2) has the same gene structure as alpha -antitrypsin or angiotensinogen. By combination of exons from serpine genes which have this gene structure, recombinant genes can be produced which code for hybrid serpines. By expression of the recombinant genes in eukaryotic cells, the corresponding hybrid serpines can be obtained.
-
公开(公告)号:AU735178B2
公开(公告)日:2001-07-05
申请号:AU4458697
申请日:1997-09-15
Applicant: HOECHST AG
Inventor: MUELLER GUENTER , PREIBISCH GERALD , ERTL JOHANN
IPC: C12N15/09 , A61K38/00 , A61K38/17 , A61K38/22 , A61K45/00 , A61P3/10 , A61P5/50 , C07K14/575 , C07K16/26 , C07K19/00 , C12P21/02
Abstract: The invention relates to pharmaceutical agents containing leptin antagonists for treating Type II diabetes. One leptin antagonist is based on a murine leptin fragment and comprises amino acids 116 to 167 or 116 to 166. Methods of treating Type II diabetes are also disclosed.
-
10.
公开(公告)号:PL332458A1
公开(公告)日:1999-09-13
申请号:PL33245897
申请日:1997-09-15
Applicant: HOECHST AG
Inventor: ERTL JOHANN , PREIBISCH GERALD , MUELLER GUENTER
IPC: C12N15/09 , A61K38/00 , A61K38/17 , A61K38/22 , A61K45/00 , A61P3/10 , A61P5/50 , C07K14/575 , C07K16/26 , C07K19/00 , C12P21/02
Abstract: The invention relates to pharmaceutical agents containing leptin antagonists for treating Type II diabetes. One leptin antagonist is based on a murine leptin fragment and comprises amino acids 116 to 167 or 116 to 166. Methods of treating Type II diabetes are also disclosed.
-
-
-
-
-
-
-
-
-