WO1993020099A3 - Cck and/or gastrin receptor ligands - Google Patents
Cck and/or gastrin receptor ligands Download PDFInfo
- Publication number
- WO1993020099A3 WO1993020099A3 PCT/GB1993/000614 GB9300614W WO9320099A3 WO 1993020099 A3 WO1993020099 A3 WO 1993020099A3 GB 9300614 W GB9300614 W GB 9300614W WO 9320099 A3 WO9320099 A3 WO 9320099A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- cck
- compounds
- treatment
- receptor ligands
- medicinal compositions
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/18—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/12—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
- C07D217/14—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
- C07K5/0202—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-X-X-C(=0)-, X being an optionally substituted carbon atom or a heteroatom, e.g. beta-amino acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
- C07K5/0205—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -NH-(X)3-C(=0)-, e.g. statine or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06078—Dipeptides with the first amino acid being neutral and aromatic or cycloaliphatic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06139—Dipeptides with the first amino acid being heterocyclic
- C07K5/06156—Dipeptides with the first amino acid being heterocyclic and Trp-amino acid; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0821—Tripeptides with the first amino acid being heterocyclic, e.g. His, Pro, Trp
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/10—Tetrapeptides
- C07K5/1024—Tetrapeptides with the first amino acid being heterocyclic
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Biophysics (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Crystallography & Structural Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9206757.8 | 1992-03-27 | ||
GB929206757A GB9206757D0 (en) | 1992-03-27 | 1992-03-27 | Novel peptide receptor ligands |
Publications (2)
Publication Number | Publication Date |
---|---|
WO1993020099A2 WO1993020099A2 (en) | 1993-10-14 |
WO1993020099A3 true WO1993020099A3 (en) | 1993-11-25 |
Family
ID=10712996
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB1993/000614 WO1993020099A2 (en) | 1992-03-27 | 1993-03-25 | Cck and/or gastrin receptor ligands |
Country Status (3)
Country | Link |
---|---|
AU (1) | AU3764593A (en) |
GB (1) | GB9206757D0 (en) |
WO (1) | WO1993020099A2 (en) |
Cited By (1)
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---|---|---|---|---|
CN107922428A (en) * | 2015-06-25 | 2018-04-17 | 普洛麦格公司 | Thienopyrroles compound and its purposes as the inhibitor for piercing shrimp source property luciferase |
Families Citing this family (79)
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EP0720601B1 (en) * | 1993-08-10 | 2000-10-25 | James Black Foundation Limited | Gastrin and cck receptor ligands |
US5795907A (en) * | 1994-05-27 | 1998-08-18 | James Black Foundation Limited | Gastin and CCK receptor ligands |
WO1996039385A1 (en) | 1995-06-06 | 1996-12-12 | Pfizer Inc. | Substituted n-(indole-2-carbonyl-) amides and derivatives as glycogen phosphorylase inhibitors |
KR100241643B1 (en) | 1995-06-06 | 2000-03-02 | 디. 제이. 우드 | Substituted N- (indole-2-carbonyl) -β-alanimamide and its derivatives for treating diabetes |
MX9709875A (en) * | 1995-06-06 | 1998-03-31 | Pfizer | Substituted n-(indole-2-carbonyl)-glycinamides and derivatives as glycogen phosphorylase inhibitors. |
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WO1999062514A1 (en) * | 1998-06-03 | 1999-12-09 | Cortech Inc. | INDOLE AND TETRAHYDROISOQUINOLINE CONTAINING α-KETO OXADIAZOLES AS SERINE PROTEASE INHIBITORS |
EP1114822A3 (en) * | 1998-06-03 | 2002-11-13 | Cortech Inc. | Indoles and tetrahydroisoquinolines containing alpha-keto oxadiazoles as serine protease inhibitors |
ID28385A (en) | 1998-10-08 | 2001-05-17 | Smithkline Beecham Plc | TETRAHIDROBENZAZEPINA DECREASED USING AS DOPAMINA D3 RECEPTOR MODULATOR (ANTIPSICOTIC MATERIAL) |
US6331541B1 (en) | 1998-12-18 | 2001-12-18 | Soo S. Ko | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
US6525069B1 (en) | 1998-12-18 | 2003-02-25 | Bristol-Myers Squibb Pharma Co. | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
US6444686B1 (en) | 1998-12-18 | 2002-09-03 | Brsitol-Myers Squibb Pharma Company | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
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US6331545B1 (en) | 1998-12-18 | 2001-12-18 | Soo S. Ko | Heterocycyclic piperidines as modulators of chemokine receptor activity |
US6897234B2 (en) | 1999-12-17 | 2005-05-24 | Bristol-Myers Squibb Pharma Company | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
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US6277877B1 (en) | 2000-08-15 | 2001-08-21 | Pfizer, Inc. | Substituted n-(indole-2-carbonyl)glycinamides and derivates as glycogen phosphorylase inhibitors |
AU2002357692A1 (en) | 2001-11-09 | 2003-05-26 | Bristol-Myers Squibb Company | Tetrahydroisoquinoline analogs as modulators of chemokine receptor activity |
AU2003245453B2 (en) | 2002-06-14 | 2008-08-14 | Merck Sharp & Dohme Corp. | Mitotic kinesin inhibitors |
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DE602004019229D1 (en) | 2003-08-15 | 2009-03-12 | Merck & Co Inc | INHIBITORS OF MITOTIC KINESINE |
WO2005018547A2 (en) | 2003-08-15 | 2005-03-03 | Merck & Co., Inc. | Mitotic kinesin inhibitors |
US7638549B2 (en) | 2003-08-15 | 2009-12-29 | Merck & Co. Inc. | Mitotic kinesin inhibitors |
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0215297A2 (en) * | 1985-08-14 | 1987-03-25 | G.D. Searle & Co. | Substituted dipeptide amides |
EP0288965A2 (en) * | 1987-04-29 | 1988-11-02 | Hoechst Aktiengesellschaft | Peptides with a phospholipase A2 inhibiting activity |
EP0337774A2 (en) * | 1988-04-12 | 1989-10-18 | Biomeasure, Inc. | CCK antagonists |
EP0405506A1 (en) * | 1989-06-30 | 1991-01-02 | Abbott Laboratories | Tetrapeptide type-B CCK receptor ligands |
US4997950A (en) * | 1989-04-20 | 1991-03-05 | Richard Finbar Murphy | Novel C-terminal gastrin antagonists |
WO1991012264A1 (en) * | 1990-02-09 | 1991-08-22 | Rhone-Poulenc Rorer S.A. | N-phenyl n-acetamido glycinamides, preparation method and drugs containing them |
-
1992
- 1992-03-27 GB GB929206757A patent/GB9206757D0/en active Pending
-
1993
- 1993-03-25 WO PCT/GB1993/000614 patent/WO1993020099A2/en active Application Filing
- 1993-03-25 AU AU37645/93A patent/AU3764593A/en not_active Abandoned
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0215297A2 (en) * | 1985-08-14 | 1987-03-25 | G.D. Searle & Co. | Substituted dipeptide amides |
EP0288965A2 (en) * | 1987-04-29 | 1988-11-02 | Hoechst Aktiengesellschaft | Peptides with a phospholipase A2 inhibiting activity |
EP0337774A2 (en) * | 1988-04-12 | 1989-10-18 | Biomeasure, Inc. | CCK antagonists |
US4997950A (en) * | 1989-04-20 | 1991-03-05 | Richard Finbar Murphy | Novel C-terminal gastrin antagonists |
EP0405506A1 (en) * | 1989-06-30 | 1991-01-02 | Abbott Laboratories | Tetrapeptide type-B CCK receptor ligands |
WO1991012264A1 (en) * | 1990-02-09 | 1991-08-22 | Rhone-Poulenc Rorer S.A. | N-phenyl n-acetamido glycinamides, preparation method and drugs containing them |
Non-Patent Citations (1)
Title |
---|
J.A.SMITH ET AL 'PEPTIDES,CHEMISTRY AND BIOLOGY; Proceedings 12th American Peptide Symposium, June 16-21, 1991,Cambridge,U.S.A.' 1992 , ESCOM , LEIDEN A.M.NADZAN; "Design of cholecystokinin analogs with high affinity and selectivity for brain CCK receptors" * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107922428A (en) * | 2015-06-25 | 2018-04-17 | 普洛麦格公司 | Thienopyrroles compound and its purposes as the inhibitor for piercing shrimp source property luciferase |
CN107922428B (en) * | 2015-06-25 | 2021-02-05 | 普洛麦格公司 | Thienopyrrole compounds and their use as inhibitors of oplophorus-derived luciferase |
Also Published As
Publication number | Publication date |
---|---|
AU3764593A (en) | 1993-11-08 |
GB9206757D0 (en) | 1992-05-13 |
WO1993020099A2 (en) | 1993-10-14 |
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