CA2243507A1 - Inhibiteurs de la farnesyl-proteine transferase - Google Patents
Inhibiteurs de la farnesyl-proteine transferase Download PDFInfo
- Publication number
- CA2243507A1 CA2243507A1 CA 2243507 CA2243507A CA2243507A1 CA 2243507 A1 CA2243507 A1 CA 2243507A1 CA 2243507 CA2243507 CA 2243507 CA 2243507 A CA2243507 A CA 2243507A CA 2243507 A1 CA2243507 A1 CA 2243507A1
- Authority
- CA
- Canada
- Prior art keywords
- hydrogen
- alkyl
- substituted
- aryl
- unsubstituted
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
Abstract
Composés inhibants la farnésyl-protéine transférase (FTase) et la farnésylation du Ras protéique oncogène. L'invention porte en outre sur des compositions chimiothérapeutiques renfermant les composés de cette invention et sur des méthodes d'inhibitions de la farnésyl-protéine transférase et de la farnésylation du Ras protéique oncogène.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US1086096P | 1996-01-30 | 1996-01-30 | |
US60/010,860 | 1996-01-30 | ||
GB9605699.9 | 1996-03-19 | ||
GBGB9605699.9A GB9605699D0 (en) | 1996-03-19 | 1996-03-19 | Inhibitors of farnesyl-protein transferase |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2243507A1 true CA2243507A1 (fr) | 1997-08-07 |
Family
ID=26308951
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA 2243507 Abandoned CA2243507A1 (fr) | 1996-01-30 | 1997-01-27 | Inhibiteurs de la farnesyl-proteine transferase |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0880320A4 (fr) |
AU (1) | AU712504B2 (fr) |
CA (1) | CA2243507A1 (fr) |
WO (1) | WO1997027752A1 (fr) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5929250A (en) * | 1997-01-23 | 1999-07-27 | Smithkline Beecham Corporation | IL-8 receptor antagonists |
WO2000001382A1 (fr) | 1998-07-02 | 2000-01-13 | Merck & Co., Inc. | Inhibiteurs de prenyl-proteine transferase |
JP2002519427A (ja) | 1998-07-02 | 2002-07-02 | メルク エンド カムパニー インコーポレーテッド | プレニル蛋白トランスフェラーゼ阻害薬 |
FR2780892B1 (fr) * | 1998-07-08 | 2001-08-17 | Sod Conseils Rech Applic | Utilisation d'inhibiteurs de prenyltransferases pour preparer un medicament destine a traiter les pathologies qui resultent de la fixation membranaire de la proteine g heterotrimerique |
US6525069B1 (en) | 1998-12-18 | 2003-02-25 | Bristol-Myers Squibb Pharma Co. | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
AU3126700A (en) | 1998-12-18 | 2000-07-03 | Du Pont Pharmaceuticals Company | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
AU2056700A (en) | 1998-12-18 | 2000-07-03 | Du Pont Pharmaceuticals Company | 2-substituted-4-nitrogen heterocycles as modulators of chemokine receptor activity |
EP1158980B1 (fr) | 1998-12-18 | 2005-08-24 | Bristol-Myers Squibb Pharma Company | N-ureidoalkyl-piperidines utilisees en tant que modulateurs de l'activite des recepteurs des chimiokines |
US6331541B1 (en) | 1998-12-18 | 2001-12-18 | Soo S. Ko | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
TR200101859T2 (tr) | 1998-12-18 | 2001-12-21 | Dupont Pharmaceuticals Company | Kemokin alıcı aktivitesinin modülatörleri olarak N-üreidoalkil-piperidinler |
US6897234B2 (en) | 1999-12-17 | 2005-05-24 | Bristol-Myers Squibb Pharma Company | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
AU2001251444A1 (en) | 2000-04-10 | 2001-10-23 | Merck And Co., Inc. | Inhibitors of prenyl-protein transferase |
DE10025782A1 (de) | 2000-05-26 | 2001-12-06 | Basf Ag | Flüssigkristalline Stoffgemenge |
EP1162194A1 (fr) * | 2000-06-06 | 2001-12-12 | Aventis Pharma Deutschland GmbH | Dérivés de (thio)-urée inhibiteurs du facteur VIIa, procédé de leur préparation et leur utilisation |
EP1296978A2 (fr) | 2000-06-30 | 2003-04-02 | Bristol-Myers Squibb Company | N-ureidoheterocycloaklyl-piperidines utilises comme modulateurs de l'activite du recepteur de la chimiokine |
AU2002326948A1 (en) | 2001-09-18 | 2003-04-01 | Bristol-Myers Squibb Company | Piperizinones as modulators of chemokine receptor activity |
TW200409630A (en) | 2002-09-12 | 2004-06-16 | Bristol Myers Squibb Co | N-ureidoalkyl-piperidines as modulators of chemokine receptor activity |
US6919356B2 (en) | 2002-09-26 | 2005-07-19 | Bristol Myers Squibb Company | N-substituted heterocyclic amines as modulators of chemokine receptor activity |
AU2003259007A1 (en) | 2002-10-31 | 2004-05-25 | Amersham Biosciences Ab | Use of urea variants as affinity ligands |
EP2095819A1 (fr) | 2008-02-28 | 2009-09-02 | Maastricht University | Dérivés de N-benzyle imidazole et leur utilisation comme inhibiteurs de l'aldosterone synthase |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4576957A (en) * | 1984-07-05 | 1986-03-18 | American Cyanamid Company | N-(Substituted phenyl)-N'-[(1H-imidazol-1-yl) and (1H-1,2,4-triazol-1-yl)alkyl]ureas |
WO1995009001A1 (fr) * | 1993-09-30 | 1995-04-06 | Merck & Co., Inc. | Inhibiteurs de farnesyl-proteine transferase |
IL111235A (en) * | 1993-10-15 | 2001-03-19 | Schering Plough Corp | Medicinal preparations for inhibiting protein G activity and for the treatment of malignant diseases, containing tricyclic compounds, some such new compounds and a process for the preparation of some of them |
AU1615895A (en) * | 1994-03-31 | 1995-10-12 | Bristol-Myers Squibb Company | Imidazole-containing inhibitors of farnesyl protein transferase |
EP0783517A2 (fr) * | 1994-09-29 | 1997-07-16 | Merck & Co. Inc. | Inhibiteurs de la transferase de proteines farnesylees exempts de thiol |
US5756528A (en) * | 1995-06-06 | 1998-05-26 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
CA2238081A1 (fr) * | 1995-11-22 | 1997-05-29 | S. Jane Desolms | Inhibiteurs de la farnesyl-proteine transferase |
US6066738A (en) * | 1996-01-30 | 2000-05-23 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
EP0877610A4 (fr) * | 1996-01-30 | 1999-09-15 | Merck & Co Inc | Inhibiteurs de farnesyl-proteine transferase |
AU704087B2 (en) * | 1996-01-30 | 1999-04-15 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
AU716153B2 (en) * | 1996-04-03 | 2000-02-17 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
EP0891334A1 (fr) * | 1996-04-03 | 1999-01-20 | Merck & Co., Inc. | Inhibiteurs de la farnesyl-proteine transferase |
AU715604B2 (en) * | 1996-04-03 | 2000-02-03 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
EP0935464A1 (fr) * | 1996-04-03 | 1999-08-18 | Merck & Co., Inc. | Inhibiteurs de transferase de farnesyl-proteine |
-
1997
- 1997-01-27 CA CA 2243507 patent/CA2243507A1/fr not_active Abandoned
- 1997-01-27 EP EP97904147A patent/EP0880320A4/fr not_active Withdrawn
- 1997-01-27 WO PCT/US1997/001599 patent/WO1997027752A1/fr not_active Application Discontinuation
- 1997-01-27 AU AU18516/97A patent/AU712504B2/en not_active Ceased
Also Published As
Publication number | Publication date |
---|---|
EP0880320A4 (fr) | 1999-06-16 |
AU712504B2 (en) | 1999-11-11 |
EP0880320A1 (fr) | 1998-12-02 |
AU1851697A (en) | 1997-08-22 |
WO1997027752A1 (fr) | 1997-08-07 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FZDE | Dead |