WO1999007731A1 - INHIBITEURS SELECTIFS DU FACTEUR Xa - Google Patents
INHIBITEURS SELECTIFS DU FACTEUR Xa Download PDFInfo
- Publication number
- WO1999007731A1 WO1999007731A1 PCT/US1998/016705 US9816705W WO9907731A1 WO 1999007731 A1 WO1999007731 A1 WO 1999007731A1 US 9816705 W US9816705 W US 9816705W WO 9907731 A1 WO9907731 A1 WO 9907731A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- alkyl
- compound
- aryl
- alkylaryl
- Prior art date
Links
- 0 CC*1=*(CC)C(N(C(*)(*)C(NC(C)*)=O)C(C(C*)N(C)*)=O)=C(C)*I=*1 Chemical compound CC*1=*(CC)C(N(C(*)(*)C(NC(C)*)=O)C(C(C*)N(C)*)=O)=C(C)*I=*1 0.000 description 9
- AGEZXYOZHKGVCM-UHFFFAOYSA-N BrCc1ccccc1 Chemical compound BrCc1ccccc1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 1
- OGVNPMYUTVZKML-UHFFFAOYSA-N CC(C)(C)OC(N(Cc(cc1)ccc1C(N)=N)C(OC(C)(C)C)=O)=O Chemical compound CC(C)(C)OC(N(Cc(cc1)ccc1C(N)=N)C(OC(C)(C)C)=O)=O OGVNPMYUTVZKML-UHFFFAOYSA-N 0.000 description 1
- UBBCBDIQXSNCEQ-UHFFFAOYSA-N CC(C)(C)OC(N(Cc1ccccc1)C(OC(C)(C)C)=O)=O Chemical compound CC(C)(C)OC(N(Cc1ccccc1)C(OC(C)(C)C)=O)=O UBBCBDIQXSNCEQ-UHFFFAOYSA-N 0.000 description 1
- TUUPVPTYVPFAKG-UHFFFAOYSA-N CC1=C(C)C=CCC1 Chemical compound CC1=C(C)C=CCC1 TUUPVPTYVPFAKG-UHFFFAOYSA-N 0.000 description 1
- DZSBAEDCIJUGHO-UHFFFAOYSA-N OC(CN(C1=C(CCC2NC(Cc3ccccc3)=O)C=CCC1)C2=O)=O Chemical compound OC(CN(C1=C(CCC2NC(Cc3ccccc3)=O)C=CCC1)C2=O)=O DZSBAEDCIJUGHO-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Definitions
- G is selected from the group consisting of a direct link, C 3 _ 8 cycloalkyl, aryl, and a five to ten membered heterocyclic ring system containing 1 -4 heteroatoms selected from the group consisting of N, O and S;
- alkyl refers to saturated aliphatic groups including straight-chain, branched-chain, cyclic groups, and combinations thereof, having the number of carbon atoms specified, or if no number is specified, having up to 12 carbon atoms.
- alkylaryl and alkenylaryl refer to an alkyl group or alkenyl group, respectively, having the number of carbon atoms designated, appended to one, two, or three aryl groups.
- benzyl refers to -CH -C 6 H 5 .
- alkyloxy refers to an alkyl group linked to an oxygen atom, such as methoxy, ethoxy, and so forth.
- halogen refer to Cl, Br, F or I substituents.
- direct link as used herein refers to a bond directly linking the substituents on each side of the direct link.
- “Pharmaceutically acceptable acid addition salt” refers to those salts which retain the biological effectiveness and properties of the free bases and which are not biologically or otherwise undesirable, formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid and the like, and organic acids such as acetic acid, propionic acid, glycolic acid, pyruvic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid and the like.
- inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid and the like
- organic acids such as acetic acid, propionic acid, glycolic acid, pyruvic acid
- K', K", K'" and K"" are -CH-; more preferably K', K", K"' and K"" are all -CH-.
- R 4 or R 5 is preferably halogen.
- the invention encompasses compounds of general structural formula VIII, where R , R 2 and R 3 are H; r is 3; s is 0; t is 1 ; A is H; D is phenyl; E is -SO 2 -; G is a direct link; J is
- Therapeutically effective dosages may be determined by either in vitro or in vivo methods. For each particular compound of the present invention, individual determinations may be made to determine the optimal dosage required.
- the range of therapeutically effective dosages will be influenced by the route of administration, the therapeutic objectives and the condition of the patient. For injection by hypodermic needle, it may be assumed the dosage is delivered into the body's fluids. For other routes of administration, the absorption efficiency must be individually determined for each compound by methods well known in pharmacology. Accordingly, it may be necessary for the therapist to titer the dosage and modify the route of administration as required to obtain the optimal therapeutic effect.
- the determination of effective dosage levels that is, the dosage levels necessary to achieve the desired result, will be readily determined by one skilled in the art.
- the compounds of the invention can be administered orally or parenterally in an effective amount within the dosage range of about 0.1 to 100 mg/kg, preferably about 0.5 to 50 mg/kg and more preferably about 1 to 20 mg/kg on a regimen in a single or 2 to 4 divided daily doses and/or continuous infusion.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Hematology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Diabetes (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Abstract
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002299610A CA2299610A1 (fr) | 1997-08-11 | 1998-08-11 | Inhibiteurs selectifs du facteur xa |
JP2000506233A JP2001515842A (ja) | 1997-08-11 | 1998-08-11 | 選択的Xa因子阻害剤 |
AU88270/98A AU744626B2 (en) | 1997-08-11 | 1998-08-11 | Selective factor Xa inhibitors |
NZ502876A NZ502876A (en) | 1997-08-11 | 1998-08-11 | Fused bicyclic lactam selective factor Xa inhibitors for treating thrombosis related diseases |
EP98939912A EP0994894A1 (fr) | 1997-08-11 | 1998-08-11 | INHIBITEURS SELECTIFS DU FACTEUR Xa |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US8418497P | 1997-08-11 | 1997-08-11 | |
US90803197A | 1997-08-11 | 1997-08-11 | |
US60/084,184 | 1997-08-11 | ||
US08/908,031 | 1997-08-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1999007731A1 true WO1999007731A1 (fr) | 1999-02-18 |
Family
ID=26770690
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1998/016705 WO1999007731A1 (fr) | 1997-08-11 | 1998-08-11 | INHIBITEURS SELECTIFS DU FACTEUR Xa |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0994894A1 (fr) |
JP (1) | JP2001515842A (fr) |
CA (1) | CA2299610A1 (fr) |
NZ (1) | NZ502876A (fr) |
WO (1) | WO1999007731A1 (fr) |
Cited By (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6133256A (en) * | 1997-04-14 | 2000-10-17 | Cor Therapeutics Inc | Selective factor Xa inhibitors |
US6194435B1 (en) | 1996-10-11 | 2001-02-27 | Cor Therapeutics, Inc. | Lactams as selective factor Xa inhibitors |
US6204268B1 (en) | 1997-04-14 | 2001-03-20 | Cor Therapeutics, Inc | Selective factor Xa inhibitors |
US6211183B1 (en) | 1997-04-14 | 2001-04-03 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6218382B1 (en) | 1997-08-11 | 2001-04-17 | Cor Therapeutics, Inc | Selective factor Xa inhibitors |
US6228854B1 (en) | 1997-08-11 | 2001-05-08 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6262047B1 (en) | 1996-10-11 | 2001-07-17 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6297233B1 (en) | 1999-02-09 | 2001-10-02 | Bristol-Myers Squibb Company | Lactam inhibitors of FXa and method |
WO2001079261A1 (fr) * | 2000-04-14 | 2001-10-25 | Corvas International, Inc. | Derives de tetrahydro-azepinone servant d'inhibiteurs de la thrombine |
US6333321B1 (en) | 1997-08-11 | 2001-12-25 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6369063B1 (en) | 1997-04-14 | 2002-04-09 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6369080B2 (en) | 1996-10-11 | 2002-04-09 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6469029B1 (en) | 1999-09-13 | 2002-10-22 | 3-Dimensional Pharmaceuticals, Inc. | Azacycloalkanone serine protease inhibitors |
US6495540B2 (en) | 2000-03-28 | 2002-12-17 | Bristol - Myers Squibb Pharma Company | Lactams as inhibitors of A-β protein production |
US6503902B2 (en) | 1999-09-13 | 2003-01-07 | Bristol-Myers Squibb Pharma Company | Hydroxyalkanoylaminolactams and related structures as inhibitors of a β protein production |
US6503901B1 (en) | 1999-10-08 | 2003-01-07 | Bristol Myers Squibb Pharma Company | Amino lactam sulfonamides as inhibitors of Aβ protein production |
US6509333B2 (en) | 2000-06-01 | 2003-01-21 | Bristol-Myers Squibb Pharma Company | Lactams substituted by cyclic succinates as inhibitors of Aβ protein production |
US6511973B2 (en) | 2000-08-02 | 2003-01-28 | Bristol-Myers Squibb Co. | Lactam inhibitors of FXa and method |
US6525044B2 (en) | 2000-02-17 | 2003-02-25 | Bristol-Myers Squibb Company | Succinoylamino carbocycles and heterocycles as inhibitors of a-β protein production |
US6525076B1 (en) | 1996-10-11 | 2003-02-25 | Millennium Pharmaceuticals, Inc. | Selective factor Xa inhibitors |
US6713476B2 (en) | 2000-04-03 | 2004-03-30 | Dupont Pharmaceuticals Company | Substituted cycloalkyls as inhibitors of a beta protein production |
US6759404B2 (en) | 2000-04-03 | 2004-07-06 | Richard E. Olson | Cyclic malonamides as inhibitors of aβ protein production |
US6900199B2 (en) | 2000-04-11 | 2005-05-31 | Bristol-Myers Squibb Pharma Company | Substituted lactams as inhibitors of Aβ protein production |
US6960576B2 (en) | 1999-09-13 | 2005-11-01 | Bristol-Myers Squibb Pharma Company | Hydroxyalkanoylaminolactams and related structures as inhibitors of Aβ protein production |
US7053084B1 (en) | 1998-12-24 | 2006-05-30 | Bristol-Myers Squibb Company | Succinoylamino benzodiazepines as inhibitors of Aβ protein production |
EP2982668A2 (fr) | 2002-12-03 | 2016-02-10 | Pharmacyclics LLC | Dérivés de 2-(2-hydroxybiphényl-3-yl)-1h-benzoimidazole-5-carboxamidine en tant qu'inhibiteurs du facteur viia inhibitors pour le traitement de maladies thromboemboliques |
US9815850B2 (en) | 2016-02-05 | 2017-11-14 | Denali Therapeutics Inc. | Compounds, compositions and methods |
US11072618B2 (en) | 2016-12-09 | 2021-07-27 | Denali Therapeutics Inc. | Compounds, compositions and methods |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005011611A2 (fr) * | 2003-07-31 | 2005-02-10 | Irm, Llc | Composes bicycliques et compositions utilisees comme inhibiteurs pdf |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995035311A1 (fr) * | 1994-06-17 | 1995-12-28 | Corvas International, Inc. | Derives de l'acide 3-amino-2-oxo-1-piperidineacetique |
WO1996019491A1 (fr) * | 1994-12-22 | 1996-06-27 | Biochem Pharma Inc. | Peptides de cetoarginine heterocycliques utilises comme inhibiteurs de thrombine |
WO1998016523A2 (fr) * | 1996-10-11 | 1998-04-23 | Cor Therapeutics, Inc. | Inhibiteurs competitifs du facteur xa |
-
1998
- 1998-08-11 EP EP98939912A patent/EP0994894A1/fr not_active Withdrawn
- 1998-08-11 JP JP2000506233A patent/JP2001515842A/ja active Pending
- 1998-08-11 WO PCT/US1998/016705 patent/WO1999007731A1/fr not_active Application Discontinuation
- 1998-08-11 NZ NZ502876A patent/NZ502876A/en unknown
- 1998-08-11 CA CA002299610A patent/CA2299610A1/fr not_active Abandoned
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1995035311A1 (fr) * | 1994-06-17 | 1995-12-28 | Corvas International, Inc. | Derives de l'acide 3-amino-2-oxo-1-piperidineacetique |
WO1996019491A1 (fr) * | 1994-12-22 | 1996-06-27 | Biochem Pharma Inc. | Peptides de cetoarginine heterocycliques utilises comme inhibiteurs de thrombine |
WO1998016523A2 (fr) * | 1996-10-11 | 1998-04-23 | Cor Therapeutics, Inc. | Inhibiteurs competitifs du facteur xa |
Non-Patent Citations (2)
Title |
---|
J. E. SEMPLE: "Design, synthesis, and evolution of a novel, selective, and orally bioavailable class of thrombin inhibitors: P1-argininal derivatives incorporating P3-4 lactam sulfonamide moieties", JOURNAL OF MEDICINAL CHEMISTRY, vol. 39, no. 23, 1996, pages 4531 - 36, XP002081550 * |
KUNITADA S ET AL: "FACTOR XA INHIBITORS", CURRENT PHARMACEUTICAL DESIGN, vol. 2, no. 5, October 1996 (1996-10-01), pages 531 - 542, XP002057653 * |
Cited By (43)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6369080B2 (en) | 1996-10-11 | 2002-04-09 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6194435B1 (en) | 1996-10-11 | 2001-02-27 | Cor Therapeutics, Inc. | Lactams as selective factor Xa inhibitors |
US6262047B1 (en) | 1996-10-11 | 2001-07-17 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6525076B1 (en) | 1996-10-11 | 2003-02-25 | Millennium Pharmaceuticals, Inc. | Selective factor Xa inhibitors |
US6204268B1 (en) | 1997-04-14 | 2001-03-20 | Cor Therapeutics, Inc | Selective factor Xa inhibitors |
US6211183B1 (en) | 1997-04-14 | 2001-04-03 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6133256A (en) * | 1997-04-14 | 2000-10-17 | Cor Therapeutics Inc | Selective factor Xa inhibitors |
US6369063B1 (en) | 1997-04-14 | 2002-04-09 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6218382B1 (en) | 1997-08-11 | 2001-04-17 | Cor Therapeutics, Inc | Selective factor Xa inhibitors |
US6228854B1 (en) | 1997-08-11 | 2001-05-08 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US6333321B1 (en) | 1997-08-11 | 2001-12-25 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US7718795B2 (en) | 1998-12-24 | 2010-05-18 | Bristol-Myers Squibb Pharma Company | Succinoylamino benzodiazepines as inhibitors of aβ protein production |
US7456172B2 (en) | 1998-12-24 | 2008-11-25 | Bristol-Myers Squibb Pharma Company | Succinoylamino benzodiazepines as inhibitors of Aβ protein production |
US7304049B2 (en) | 1998-12-24 | 2007-12-04 | Bristol-Myers Squibb Pharma Company | Succinoylaminobenzodiazepines as inhibitors of Aβ protein production |
US7053084B1 (en) | 1998-12-24 | 2006-05-30 | Bristol-Myers Squibb Company | Succinoylamino benzodiazepines as inhibitors of Aβ protein production |
US6297233B1 (en) | 1999-02-09 | 2001-10-02 | Bristol-Myers Squibb Company | Lactam inhibitors of FXa and method |
US7342008B2 (en) | 1999-09-13 | 2008-03-11 | Bristol-Myers Squibb Pharma Company | Hydroxyalkanoylaminolactams and related structures as inhibitors of Aβ protein production |
US6503902B2 (en) | 1999-09-13 | 2003-01-07 | Bristol-Myers Squibb Pharma Company | Hydroxyalkanoylaminolactams and related structures as inhibitors of a β protein production |
US6469029B1 (en) | 1999-09-13 | 2002-10-22 | 3-Dimensional Pharmaceuticals, Inc. | Azacycloalkanone serine protease inhibitors |
US7423033B2 (en) | 1999-09-13 | 2008-09-09 | Bristol-Myers Squibb Pharma Company | Hydroxyalkanoylaminolactams and related structures as inhibitors of aβ protein production |
US6960576B2 (en) | 1999-09-13 | 2005-11-01 | Bristol-Myers Squibb Pharma Company | Hydroxyalkanoylaminolactams and related structures as inhibitors of Aβ protein production |
US6962942B2 (en) | 1999-09-13 | 2005-11-08 | 3-Dimensional Pharmaceuticals, Inc. | Azacycloalkanone serine protease inhibitors |
US7112583B2 (en) | 1999-09-13 | 2006-09-26 | Bristol-Myers Squibb Pharma Company | Hydroxyalkanoylaminolactams and related structures as inhibitors of Aβ protein production |
US6503901B1 (en) | 1999-10-08 | 2003-01-07 | Bristol Myers Squibb Pharma Company | Amino lactam sulfonamides as inhibitors of Aβ protein production |
US6525044B2 (en) | 2000-02-17 | 2003-02-25 | Bristol-Myers Squibb Company | Succinoylamino carbocycles and heterocycles as inhibitors of a-β protein production |
US6495540B2 (en) | 2000-03-28 | 2002-12-17 | Bristol - Myers Squibb Pharma Company | Lactams as inhibitors of A-β protein production |
US6713476B2 (en) | 2000-04-03 | 2004-03-30 | Dupont Pharmaceuticals Company | Substituted cycloalkyls as inhibitors of a beta protein production |
US6759404B2 (en) | 2000-04-03 | 2004-07-06 | Richard E. Olson | Cyclic malonamides as inhibitors of aβ protein production |
US7655647B2 (en) | 2000-04-11 | 2010-02-02 | Bristol-Myers Squibb Pharma Company | Substituted lactams as inhibitors of Aβ protein production |
US7390802B2 (en) | 2000-04-11 | 2008-06-24 | Bristol-Myers Squibb Pharma Corporation | Substituted lactams as inhibitors of Aβ protein production |
US6900199B2 (en) | 2000-04-11 | 2005-05-31 | Bristol-Myers Squibb Pharma Company | Substituted lactams as inhibitors of Aβ protein production |
US7498324B2 (en) | 2000-04-11 | 2009-03-03 | Bristol-Myers Squibb Pharma Company | Substituted lactams as inhibitors of Aβ protein production |
US7276495B2 (en) | 2000-04-11 | 2007-10-02 | Bristol-Myers Squibb Pharma Company | Substituted lactams as inhibitors of Aβ protein production |
WO2001079261A1 (fr) * | 2000-04-14 | 2001-10-25 | Corvas International, Inc. | Derives de tetrahydro-azepinone servant d'inhibiteurs de la thrombine |
US6958329B2 (en) | 2000-06-01 | 2005-10-25 | Bristol-Myers Squibb Pharma Company | Lactams substituted by cyclic succinates as inhibitors of A-β protein production |
US6509333B2 (en) | 2000-06-01 | 2003-01-21 | Bristol-Myers Squibb Pharma Company | Lactams substituted by cyclic succinates as inhibitors of Aβ protein production |
US6511973B2 (en) | 2000-08-02 | 2003-01-28 | Bristol-Myers Squibb Co. | Lactam inhibitors of FXa and method |
EP2982668A2 (fr) | 2002-12-03 | 2016-02-10 | Pharmacyclics LLC | Dérivés de 2-(2-hydroxybiphényl-3-yl)-1h-benzoimidazole-5-carboxamidine en tant qu'inhibiteurs du facteur viia inhibitors pour le traitement de maladies thromboemboliques |
US9815850B2 (en) | 2016-02-05 | 2017-11-14 | Denali Therapeutics Inc. | Compounds, compositions and methods |
US9896458B2 (en) | 2016-02-05 | 2018-02-20 | Denali Therapeutics Inc. | Compounds, compositions and methods |
US10131676B2 (en) | 2016-02-05 | 2018-11-20 | Denali Therapeutics Inc. | Compounds, compositions and methods |
US10604535B2 (en) | 2016-02-05 | 2020-03-31 | Denali Therapeutics Inc. | Compounds, compositions and methods |
US11072618B2 (en) | 2016-12-09 | 2021-07-27 | Denali Therapeutics Inc. | Compounds, compositions and methods |
Also Published As
Publication number | Publication date |
---|---|
NZ502876A (en) | 2001-11-30 |
CA2299610A1 (fr) | 1999-02-18 |
EP0994894A1 (fr) | 2000-04-26 |
JP2001515842A (ja) | 2001-09-25 |
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