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公开(公告)号:ES2149159T3
公开(公告)日:2000-11-01
申请号:ES92102197
申请日:1992-02-10
Applicant: HOECHST AG
Inventor: SEEMANN GERHARD , BOSSLET KLAUS , CZECH JORG , KOLAR CENEK , HOFFMANN DIETER , SEDLACEK HANS-HARALD
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公开(公告)号:DK0501215T3
公开(公告)日:2000-09-18
申请号:DK92102197
申请日:1992-02-10
Applicant: HOECHST AG
Inventor: SEEMANN GERHARD , BOSSLET KLAUS , CZECH JOERG , KOLAR CENEK , HOFFMANN DIETER , SEDLACEK HANS-HARALD
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公开(公告)号:IE62873B1
公开(公告)日:1995-03-08
申请号:IE399089
申请日:1989-12-13
Applicant: HOECHST AG
Inventor: KOLAR CENEK , KOENIG WOLFGANG , SANDOW JUERGEN KURT
Abstract: Peptides of the formula Ac-D-Nal(2)-D-Phe-D-Phe-Ser-X-D-Ser(Rha)-Leu-Arg-Pro-Y in which X represents Tyr or His and Y represents Gly-NH2, D-Ala-NH2, Azgly-NH2 or NH-C2H5 are competitive antagonists of Gn-RH. They are used for the treatment of gonadotropin- and steroid-dependent diseases and are prepared by known methods of peptide chemistry.
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公开(公告)号:FI86863B
公开(公告)日:1992-07-15
申请号:FI874401
申请日:1987-10-07
Applicant: HOECHST AG
Inventor: KOENIG WOLFGNG , SANDOW JUERGEN KURT , KOLAR CENEK
Abstract: The invention relates to peptides of the formula in which X is absent or is hydrogen or acyl; A is Pgl, de-hydro-Pro, Pro, D-Thi or D-Pgl or represents optionally substituted D-Nal(2), D-Phe or D-Trp; B is His or optionally substituted D-Phe; C is Trp, D-Thi, D-Pal(3) or optionally substituted D-Trp; D is Tyr, Arg of His; E is D-Ser(R1), beta -Asn, beta -Asp-OMe, D-Thi or -NH-CH(CH2R2)-CO-; F is Ser(R1), Leu, Trp or Phe; G is Gly-NH2, Aza-Gly-NH2, D-Ala-NH2 or NH-alkyl; R1 is glycosyl and R2 is hydrogen, acyl, aryl or heteroaryl. The invention also relates to methods for the preparation of these peptides, agents containing them and their use.
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公开(公告)号:PT85881B
公开(公告)日:1990-07-31
申请号:PT8588187
申请日:1987-10-08
Applicant: HOECHST AG
Inventor: KOLAR CENEK , KONIG WOLFGANG , SANDOW JURGEN KURT
IPC: A61K38/00 , A61K38/04 , A61P5/00 , A61P9/12 , C07K7/06 , C07K7/23 , C07K9/00 , C07K14/575 , A61K37/02
Abstract: The invention relates to peptides of the formula in which X is absent or is hydrogen or acyl; A is Pgl, de-hydro-Pro, Pro, D-Thi or D-Pgl or represents optionally substituted D-Nal(2), D-Phe or D-Trp; B is His or optionally substituted D-Phe; C is Trp, D-Thi, D-Pal(3) or optionally substituted D-Trp; D is Tyr, Arg of His; E is D-Ser(R1), beta -Asn, beta -Asp-OMe, D-Thi or -NH-CH(CH2R2)-CO-; F is Ser(R1), Leu, Trp or Phe; G is Gly-NH2, Aza-Gly-NH2, D-Ala-NH2 or NH-alkyl; R1 is glycosyl and R2 is hydrogen, acyl, aryl or heteroaryl. The invention also relates to methods for the preparation of these peptides, agents containing them and their use.
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公开(公告)号:ZA877561B
公开(公告)日:1988-05-25
申请号:ZA877561
申请日:1987-10-08
Applicant: HOECHST AG
Inventor: KOENIG WOLFGANG , WOLFGANG KOENIG , SANDOW JUERGEN KURT , JUERGEN KURT SANDOW , KOLAR CENEK , CENEK KOLAR
IPC: A61K38/00 , A61K38/04 , A61P5/00 , A61P9/12 , C07K7/06 , C07K7/23 , C07K9/00 , C07K14/575 , C07K , A61K
Abstract: The invention relates to peptides of the formula in which X is absent or is hydrogen or acyl; A is Pgl, de-hydro-Pro, Pro, D-Thi or D-Pgl or represents optionally substituted D-Nal(2), D-Phe or D-Trp; B is His or optionally substituted D-Phe; C is Trp, D-Thi, D-Pal(3) or optionally substituted D-Trp; D is Tyr, Arg of His; E is D-Ser(R1), beta -Asn, beta -Asp-OMe, D-Thi or -NH-CH(CH2R2)-CO-; F is Ser(R1), Leu, Trp or Phe; G is Gly-NH2, Aza-Gly-NH2, D-Ala-NH2 or NH-alkyl; R1 is glycosyl and R2 is hydrogen, acyl, aryl or heteroaryl. The invention also relates to methods for the preparation of these peptides, agents containing them and their use.
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公开(公告)号:AU7945987A
公开(公告)日:1988-04-14
申请号:AU7945987
申请日:1987-10-08
Applicant: HOECHST AG
Inventor: KONIG WOLFGANG , SANDOW JURGEN KURT , KOLAR CENEK
IPC: A61K38/00 , A61K38/04 , A61P5/00 , A61P9/12 , C07K7/06 , C07K7/23 , C07K9/00 , C07K14/575 , C07K7/20 , A61K37/43
Abstract: The invention relates to peptides of the formula in which X is absent or is hydrogen or acyl; A is Pgl, de-hydro-Pro, Pro, D-Thi or D-Pgl or represents optionally substituted D-Nal(2), D-Phe or D-Trp; B is His or optionally substituted D-Phe; C is Trp, D-Thi, D-Pal(3) or optionally substituted D-Trp; D is Tyr, Arg of His; E is D-Ser(R1), beta -Asn, beta -Asp-OMe, D-Thi or -NH-CH(CH2R2)-CO-; F is Ser(R1), Leu, Trp or Phe; G is Gly-NH2, Aza-Gly-NH2, D-Ala-NH2 or NH-alkyl; R1 is glycosyl and R2 is hydrogen, acyl, aryl or heteroaryl. The invention also relates to methods for the preparation of these peptides, agents containing them and their use.
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公开(公告)号:AT193326T
公开(公告)日:2000-06-15
申请号:AT92102197
申请日:1992-02-10
Applicant: HOECHST AG
Inventor: SEEMANN GERHARD , BOSSLET KLAUS , CZECH JOERG , KOLAR CENEK , HOFFMANN DIETER , SEDLACEK HANS-HARALD
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公开(公告)号:PT98533B
公开(公告)日:1999-01-29
申请号:PT9853391
申请日:1991-08-01
Applicant: HOECHST AG
Inventor: KOLAR CENEK , KONIG WOLFGANG , SANDOW JURGEN
IPC: A61K38/00 , A61P5/00 , A61P5/24 , C07K7/06 , C07K7/23 , C07K9/00 , C07K14/575 , C07K14/00 , A61K38/04
Abstract: Peptides of the formula in which X is alkanoyl, A is optionally substituted D-Na(2), D-Phe or D-Trp, B is optionally substituted D-Phe, C is D-Pal(3) or optionally substituted D-Phe or D-Trp, and D is Tyr or His, E is D-Ser(R ), F is Leu, Trp or Phe, G is L-Ser(R ), H is Gly-NH2, D-Ala-NH2 or azagly-NH2 and R is a glycosyl radical, have inhibitory effects on the formation of the gonadotropins lutropin and follitropin and thus also on the synthesis of testosterone and oestrogen. A process for the preparation of these peptides is described.
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公开(公告)号:CA1314656C
公开(公告)日:1993-03-16
申请号:CA548918
申请日:1987-10-08
Applicant: HOECHST AG
Inventor: KOENIG WOLFGANG , SANDOW JUERGEN K , KOLAR CENEK
IPC: A61K38/00 , A61K38/04 , A61P5/00 , A61P9/12 , C07K7/06 , C07K7/23 , C07K9/00 , C07K14/575 , C07K7/20 , A61K37/43
Abstract: HOE 86/F 253 of the disclosure: Analogs of gonadoliberin with improved solubility, methods for their preparation, agents containing them and their use The invention relates to peptides of the formula in which X is absent or is hydrogen or acyl; A is Pgl, dehydro-Pro, Pro, D-Thi or D-Pgl or represents optionally substituted D-Nal(2), D-Phe or D-Trp; .beta. is His or optionally substituted D-Phe; C is Trp, D-Thi, D-Pal(3) or optionally substituted D-Trp; D is Tyr, Arg or His; E is D-Ser(R1), .beta.Asn, .beta.-Asp-OMe, D-Thi or -NH-CH(CH2R2)-CO-; F is Ser(R1), Leu, Trp or Phe; G is Gly-NH2, Aza-Gly-NH2, D-Ala-NH2 or NHalkyl; R1 is glycosyl and R2 is hydrogen, acyl, aryl or heteroaryl. The invention also relates to methods for the preparation of these peptides, agents containing them and their use.
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