TNSN02009A1 - Pyrimidinones bicycliques condensees nouvelles, inhibitrices de mmp, et compositions les contenant. - Google Patents
Pyrimidinones bicycliques condensees nouvelles, inhibitrices de mmp, et compositions les contenant.Info
- Publication number
- TNSN02009A1 TNSN02009A1 TNTNSN02009A TNSN02009A TNSN02009A1 TN SN02009 A1 TNSN02009 A1 TN SN02009A1 TN TNSN02009 A TNTNSN02009 A TN TNSN02009A TN SN02009 A TNSN02009 A TN SN02009A TN SN02009 A1 TNSN02009 A1 TN SN02009A1
- Authority
- TN
- Tunisia
- Prior art keywords
- mmp
- inhibitors
- compositions containing
- condensed bicyclic
- new condensed
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/04—Drugs for skeletal disorders for non-specific disorders of the connective tissue
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Biomedical Technology (AREA)
- Epidemiology (AREA)
- Vascular Medicine (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Immunology (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Enzymes And Modification Thereof (AREA)
Abstract
L’INVENTION A POUR OBJET DES COMPOSES DE FORMULE : DANS LAQUELLE R1, R4,ET Y REPRESENTENT DIVERS RADICAUX, ET W, CONJOINTEMENT AVEC LES ATOMES DE CARBONE AUQUEL IL EST FIXE, FORME UN DIRADICAL A NOYAU PENTAGONAL. ELLE CONCERNE EGALEMENT DES COMPOSITIONS PHARMACEUTIQUES LES CONTENANT. APPLICATION : UTILISATION DE CES COMPOSES ET COMPOSITIONS, COMME INHIBITEURS DE MMP-13, POUR LE TRAITEMENT DE DIVERSES MALADIES.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US26875601P | 2001-02-14 | 2001-02-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
TNSN02009A1 true TNSN02009A1 (fr) | 2005-12-23 |
Family
ID=23024328
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TNTNSN02009A TNSN02009A1 (fr) | 2001-02-14 | 2002-02-13 | Pyrimidinones bicycliques condensees nouvelles, inhibitrices de mmp, et compositions les contenant. |
Country Status (15)
Country | Link |
---|---|
US (1) | US20030004172A1 (fr) |
EP (1) | EP1370562A1 (fr) |
JP (1) | JP2004518732A (fr) |
BR (1) | BR0207216A (fr) |
CA (1) | CA2433778A1 (fr) |
DO (1) | DOP2002000337A (fr) |
GT (1) | GT200200017A (fr) |
HN (1) | HN2002000029A (fr) |
MX (1) | MXPA03004926A (fr) |
PA (1) | PA8538301A1 (fr) |
PE (1) | PE20020957A1 (fr) |
SV (1) | SV2003000882A (fr) |
TN (1) | TNSN02009A1 (fr) |
UY (1) | UY27159A1 (fr) |
WO (1) | WO2002064598A1 (fr) |
Families Citing this family (60)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DOP2002000334A (es) * | 2001-02-14 | 2002-08-30 | Warner Lambert Co | Pirimidinas biciclicas como inhibidores de metaloproteinasas de matriz |
US8329924B2 (en) * | 2001-06-11 | 2012-12-11 | Vertex Pharmaceuticals (Canada) Incorporated | Compounds and methods for the treatment or prevention of Flavivirus infections |
OA12622A (en) * | 2001-06-11 | 2006-06-12 | Shire Biochem Inc | Thiophene derivatives as antiviral agents for flavivirus infection. |
US6924276B2 (en) | 2001-09-10 | 2005-08-02 | Warner-Lambert Company | Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors |
EP1434585A1 (fr) | 2001-10-12 | 2004-07-07 | Warner-Lambert Company LLC | Inhibiteurs de metalloproteinase matricielle (mmp) a base d'alkyne |
US6962922B2 (en) | 2001-10-12 | 2005-11-08 | Warner-Lambert Company Llc | Alkynylated quinazoline compounds |
US6894057B2 (en) | 2002-03-08 | 2005-05-17 | Warner-Lambert Company | Oxo-azabicyclic compounds |
US6747147B2 (en) | 2002-03-08 | 2004-06-08 | Warner-Lambert Company | Oxo-azabicyclic compounds |
US20040006077A1 (en) * | 2002-06-25 | 2004-01-08 | Bernard Gaudilliere | Thiazine and oxazine derivatives as MMP-13 inhibitors |
JP2006503811A (ja) * | 2002-07-17 | 2006-02-02 | ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー | アロステリックカルボキシルマトリックスメタロプロテイナーゼ−13阻害薬とセレコキシブまたはバルデコキシブとの組み合わせ |
BR0312727A (pt) * | 2002-07-17 | 2005-04-19 | Warner Lambert Co | Combinação de um inibidor alostérico da metaloproteinase-13 de matriz com celecoxib ou valdecoxib |
CA2492391A1 (fr) * | 2002-07-17 | 2004-01-22 | Warner-Lambert Company Llc | Combinaison d'un inhibiteur allosterique de metalloproteinase matricielle 13 avec un inhibiteur selectif de cyclooxygenase-2, a l'exception du celecoxib ou du valdecoxib |
MXPA05001783A (es) | 2002-08-13 | 2005-04-25 | Warner Lambert Co | Derivados de pirimidina-2,4-diona como inhibidores de las metaloproteinasas de matriz. |
WO2004014923A1 (fr) | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | Inhibiteurs de metalloprotease bicycliques condenses avec la pyrimidinone |
WO2004014378A1 (fr) | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | Derives de 3-isoquinolinone utilises comme inhibiteurs de metalloprotease de matrice |
AU2003250465A1 (en) * | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | 5,6-fused uracil derivatives as matrix metalloproteinase inhibitors |
AU2003253165A1 (en) * | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | Pyrimidine fused bicyclic metalloproteinase inhibitors |
AU2003249535A1 (en) * | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | 1,6-fused uracil derivatives as matrix metalloproteinase inhibitors |
AU2003253176A1 (en) | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | Monocyclic derivatives as matrix metalloproteinase inhibitors |
CA2492019A1 (fr) * | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | Derives d'isoquinoleine utilises comme inhibiteurs de metalloprotease de matrice |
WO2004014375A2 (fr) | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | Inhibiteurs de metalloprotease bicycliques condenses |
AU2003249539A1 (en) * | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | Cyclic compounds containing zinc binding groups as matrix metalloproteinase inhibitors |
EP1539709A1 (fr) | 2002-08-13 | 2005-06-15 | Warner-Lambert Company LLC | Derives d'azaisoquinoline utilises comme inhibiteurs de metalloproteases matricielles |
AU2003253186A1 (en) | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | Fused tetrahydropyridine derivatives as matrix metalloproteinase inhibitors |
WO2004014869A2 (fr) * | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | Derives de 3,4-dihydropyrimidine-2-one 5,6-fondue, utilise comme inhibiteurs de metalloproteinase matricielle |
EP1394159A1 (fr) * | 2002-08-13 | 2004-03-03 | Warner-Lambert Company LLC | Nouveaux dérivés de thiophène, leur procédé de préparation et les compositions pharmaceutiques qui les contiennent |
AU2003250482A1 (en) * | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | Phthalimide derivatives as matrix metalloproteinase inhibitors |
WO2004014908A1 (fr) * | 2002-08-13 | 2004-02-19 | Warner-Lambert Company Llc | Inhibiteurs de metalloproteinases heterobicycliques |
JP2005539020A (ja) | 2002-08-13 | 2005-12-22 | ワーナー−ランバート カンパニー リミティド ライアビリティー カンパニー | マトリクスメタロプロテイナーゼ阻害物質としてのクロモン誘導体 |
PA8578101A1 (es) | 2002-08-13 | 2004-05-07 | Warner Lambert Co | Derivados de heterobiarilo como inhibidores de metaloproteinasa de la matriz |
US20040142950A1 (en) * | 2003-01-17 | 2004-07-22 | Bunker Amy Mae | Amide and ester matrix metalloproteinase inhibitors |
DK1591446T3 (da) * | 2003-01-29 | 2013-06-10 | Takeda Pharmaceutical | Thienopyrimidinforbindelser og anvendelse deraf. |
JP2008094846A (ja) * | 2003-01-29 | 2008-04-24 | Takeda Chem Ind Ltd | チエノピリミジン化合物およびその用途 |
US7247654B2 (en) | 2003-06-04 | 2007-07-24 | Bristol-Myers Squibb Company | 3,4-disubstituted benzamidines and benzylamines, and analogues thereof, useful as serine protease inhibitors |
WO2005002585A1 (fr) * | 2003-07-02 | 2005-01-13 | Warner-Lambert Company Llc | Combinaison d'un inhibiteur allosterique de la metalloproteinase-13 matricielle et d'un ligand au recepteur alpha-2-delta |
WO2005016926A1 (fr) * | 2003-08-19 | 2005-02-24 | Warner-Lambert Company Llc | Derives de pyrido[3,4-d]pyrimidine utiles comme inhibiteurs de la metalloproteinase-13 de matrice |
US20060247231A1 (en) * | 2003-12-18 | 2006-11-02 | Warner-Lambert Company Llc | Amide and ester matrix metalloproteinase inhibitors |
US7570259B2 (en) | 2004-06-01 | 2009-08-04 | Intel Corporation | System to manage display power consumption |
ATE405553T1 (de) | 2004-12-08 | 2008-09-15 | Bristol Myers Squibb Co | Heterocyclische verbindungen als inhibitoren von faktor viia |
CA2644996A1 (fr) * | 2006-03-02 | 2007-09-13 | Cv Therapeutics, Inc. | Antagonistes du recepteur a2a de l'adenosine |
ZA200901163B (en) * | 2006-08-23 | 2010-08-25 | Neurogen Corp | 2-Phenoxy pyrimidinone analogues |
CA2670788A1 (fr) * | 2006-12-01 | 2008-06-12 | Cv Therapeutics, Inc. | Antagonistes du recepteur d'adenosine a2a |
EP1939197A1 (fr) | 2006-12-22 | 2008-07-02 | Schwarz Pharma Ag | Derivés de 8-éthinylxanthine comme antagonistes selectives du recepteur A2A |
CA2685753A1 (fr) * | 2007-05-09 | 2008-11-20 | Neuromed Pharmaceuticals Ltd. | Derives bicycliques de pyrimidine en tant que bloqueurs des canaux calciques |
AR077898A1 (es) | 2009-08-26 | 2011-09-28 | Nycomed Gmbh | Metilpirrolopirimidincarboxamidas |
CA2855372C (fr) | 2011-11-11 | 2022-03-22 | Nimbus Apollo, Inc. | Derives de 2,4-dioxo-thieno-[2,3-d]pyrimidinyle et compositions pharmaceutiques connexes utilisees comme inhibiteurs d'acc |
SG11201602397XA (en) | 2013-10-07 | 2016-05-30 | Bayer Pharma AG | Cyclic thienouracil-carboxamides and use thereof |
UY36586A (es) | 2015-03-26 | 2016-10-31 | Bayer Pharma AG | Heterociclilmetiltienouracilos y uso de los mismos |
AR106472A1 (es) * | 2015-10-26 | 2018-01-17 | Gilead Apollo Llc | Inhibidores de acc y usos de los mismos |
JP2019503338A (ja) | 2015-11-25 | 2019-02-07 | ギリアド アポロ, エルエルシー | 2,4−ジオキソ−1,4−ジヒドロチエノ[2,3−d]ピリミジンの誘導体を含む殺真菌組成物 |
US20170166583A1 (en) | 2015-11-25 | 2017-06-15 | Gilead Apollo, Llc | Ester acc inhibitors and uses thereof |
WO2017091600A1 (fr) | 2015-11-25 | 2017-06-01 | Gilead Apollo, Llc | Inhibiteurs de l'acc à base de pyrazole et utilisations associées |
EP3380479B1 (fr) | 2015-11-25 | 2022-12-07 | Gilead Apollo, LLC | Inhibiteurs d'acc à base de triazole et utilisations associées |
KR102700008B1 (ko) | 2016-03-02 | 2024-08-29 | 길리어드 아폴로, 엘엘씨 | 티에노피리미딘디온 acc 억제제의 고체 형태 및 그의 제조 방법 |
WO2018041771A1 (fr) | 2016-09-02 | 2018-03-08 | Bayer Pharma Aktiengesellschaft | Thiéno-uraciles substitués par un groupe (1-méthylcyclopropyl)méthyle et leur utilisation |
RU2019111357A (ru) | 2016-09-23 | 2020-10-23 | Байер Акциенгезельшафт | N3-циклически замещенные тиеноурацилы и их применение |
EP3600309B1 (fr) | 2017-03-28 | 2022-06-22 | Gilead Sciences, Inc. | Combinaisons thérapeutiques pour le traitement de maladies du foie |
CN110183464B (zh) * | 2019-05-31 | 2021-08-31 | 淮阴工学院 | 一种抗癌化合物艾斯替尼及其合成方法和应用 |
KR102649886B1 (ko) * | 2021-07-21 | 2024-03-22 | 충남대학교산학협력단 | 신규한 피리미딘-4-온 화합물 및 이를 포함하는 항암제 조성물 |
WO2024036183A1 (fr) * | 2022-08-09 | 2024-02-15 | Vanderbilt University | Antagonistes de récepteurs 5-hydroxytryptamine de sous-type 2b |
Family Cites Families (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3155665A (en) | 1961-04-26 | 1964-11-03 | Searle & Co | 4, 6-dialkyl-5, 7-diketothiazolo [4, 5-d] pyrimidine-2-carboxylic acid and derivatives thereof |
US3277093A (en) | 1965-08-02 | 1966-10-04 | Searle & Co | (optionally-2-substituted) 4-halophenyl-5, 7-diketo-6-alkylthiazolo[4, 5-d]pyrimidines |
GB8601371D0 (en) | 1986-01-21 | 1986-02-26 | Beecham Group Plc | Compounds |
US6140325A (en) * | 1993-08-19 | 2000-10-31 | Takeda Chemical Industries, Ltd. | Thienopyrimidine derivatives, their production and use |
US6048863A (en) * | 1994-04-19 | 2000-04-11 | Takeda Chemical Industries, Ltd. | Condensed-ring thiophene derivatives and thienopyrimidine derivatives, their production and use |
WO1996014319A1 (fr) * | 1994-11-08 | 1996-05-17 | Takeda Chemical Industries, Ltd. | Derives de thienopyridine ou de thienopyrimidine et leur utilisation |
US5792767A (en) | 1995-01-27 | 1998-08-11 | Abbott Laboratories | Bicyclic substituted hexahydrobenz e! isoindole alpha-1 adrenergic antagonists |
CN1066448C (zh) * | 1996-06-06 | 2001-05-30 | 株式会社大塚制药工场 | 酰胺衍生物 |
US6469014B1 (en) * | 1997-05-28 | 2002-10-22 | Astrazeneca Ab | Thieno[2,3-d] pyrimidinediones, their preparation and use in therapy |
SE9702001D0 (sv) * | 1997-05-28 | 1997-05-28 | Astra Pharma Prod | Novel compounds |
US6166019A (en) * | 1998-07-16 | 2000-12-26 | Abbott Laboratories | Piperazinyl pyrimidine dione compounds selective for adrenoceptors |
NZ509809A (en) * | 1998-08-28 | 2002-11-26 | Astrazeneca Ab | Thienol[2,3-d]pyrimidinediones which exhibit immunosuppressive activity |
DE19940494C1 (de) * | 1999-08-26 | 2001-02-15 | Ibfb Gmbh Privates Inst Fuer B | Mehrcyclische Pyrimidin-2,4(1H,3H)-dione mit funktionalisierten Alkylresten in 1- und/oder 3-Position, Verfahren zu ihrer Herstellung und pharmazeutische Zubereitungen |
PA8539501A1 (es) * | 2001-02-14 | 2002-09-30 | Warner Lambert Co | Compuestos triazolo como inhibidores de mmp |
US6924276B2 (en) * | 2001-09-10 | 2005-08-02 | Warner-Lambert Company | Diacid-substituted heteroaryl derivatives as matrix metalloproteinase inhibitors |
AU2003253165A1 (en) * | 2002-08-13 | 2004-02-25 | Warner-Lambert Company Llc | Pyrimidine fused bicyclic metalloproteinase inhibitors |
US20050004111A1 (en) * | 2003-01-03 | 2005-01-06 | Aventis Pharma Deutschland Gmbh | Selective MMP-13 inhibitors |
-
2002
- 2002-01-18 EP EP02711123A patent/EP1370562A1/fr not_active Withdrawn
- 2002-01-18 BR BR0207216-5A patent/BR0207216A/pt not_active IP Right Cessation
- 2002-01-18 WO PCT/IB2002/000204 patent/WO2002064598A1/fr not_active Application Discontinuation
- 2002-01-18 CA CA002433778A patent/CA2433778A1/fr not_active Abandoned
- 2002-01-18 JP JP2002564529A patent/JP2004518732A/ja not_active Abandoned
- 2002-01-18 MX MXPA03004926A patent/MXPA03004926A/es unknown
- 2002-02-01 DO DO2002000337A patent/DOP2002000337A/es unknown
- 2002-02-05 PA PA20028538301A patent/PA8538301A1/es unknown
- 2002-02-07 GT GT200200017A patent/GT200200017A/es unknown
- 2002-02-08 UY UY27159A patent/UY27159A1/es not_active Application Discontinuation
- 2002-02-11 HN HN2002000029A patent/HN2002000029A/es unknown
- 2002-02-12 PE PE2002000110A patent/PE20020957A1/es not_active Application Discontinuation
- 2002-02-13 SV SV2002000882A patent/SV2003000882A/es unknown
- 2002-02-13 US US10/075,073 patent/US20030004172A1/en not_active Abandoned
- 2002-02-13 TN TNTNSN02009A patent/TNSN02009A1/fr unknown
Also Published As
Publication number | Publication date |
---|---|
MXPA03004926A (es) | 2005-02-14 |
HN2002000029A (es) | 2003-02-14 |
US20030004172A1 (en) | 2003-01-02 |
SV2003000882A (es) | 2003-01-13 |
WO2002064598A1 (fr) | 2002-08-22 |
GT200200017A (es) | 2002-11-15 |
DOP2002000337A (es) | 2002-08-15 |
UY27159A1 (es) | 2002-09-30 |
CA2433778A1 (fr) | 2002-08-22 |
PA8538301A1 (es) | 2002-09-17 |
JP2004518732A (ja) | 2004-06-24 |
PE20020957A1 (es) | 2002-11-08 |
EP1370562A1 (fr) | 2003-12-17 |
BR0207216A (pt) | 2004-03-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
TNSN02009A1 (fr) | Pyrimidinones bicycliques condensees nouvelles, inhibitrices de mmp, et compositions les contenant. | |
TNSN99006A1 (fr) | 4-(2-ceto-1-benzimidazolinyl) piperidines nouvelles, procede pour leur preparation et compositions pharmaceutiques les contenant | |
TNSN02010A1 (fr) | Derives de pyrimidine nouveaux inhibiteurs de mmp, et compositions les contenant | |
TNSN02011A1 (fr) | Derives de pyrimidine bicycliques nouveaux, inhibiteurs de mmp, et compositions les contenant | |
TNSN02022A1 (fr) | Triazolopyridines anti-inflammatoires nouvelles, et compositions les contenant | |
TNSN01149A1 (fr) | Spiro-pyrimidine-2,4,6-triones inhibitrices de metalloproteinases, et compositions les contenant. | |
TNSN01150A1 (fr) | Pyrimidine-2,4,6- triones inhibitrices de metalloproteinases, et compositions les contenant. | |
TNSN99125A1 (fr) | Pyrrolo(2,3-d) pyrimidines nouvelles, procede pour leur preparation et compositions pharmaceutiques les contenant | |
TNSN01145A1 (fr) | Derives d'imidazole a noyau aryle ou heteroaryle condense, et compositions les contenant. | |
TNSN01048A1 (fr) | Acides malonamiques et leurs derives, et compositions les contenant | |
TNSN98216A1 (fr) | Derives d'acide hydrauxamique, compositions pharmaceutiques les contenant et procede pour leur preparation | |
TNSN98017A1 (fr) | Derives de sulfonyluree, procede pour leur preparation et compositions pharmaceutiques les contenant. | |
TNSN00169A1 (fr) | Pyrimidine-2,4,6-triones inhibitrices de metalloproteinases, et compositions pharmaceutiques les contenant | |
TNSN99172A1 (fr) | 4-carboxyamino-2-methyl-1,2,3,4-tetrahydroquinoleines, procede pour leur preparation et compositions pharmaceutiques les contenant | |
TR200001973T2 (tr) | 11 ß-halojen-7alfa-ile ikame edilmiş-estratrienler, bu 11ß-halojen-7alfa-ile ikame edilmiş-estratrienleri içeren farmasötik terkiplerin üretimi için yöntem ve ilaç üretiminde kullanımları. | |
TNSN01019A1 (fr) | Pyrimidinecarboxamides utiles comme inhibiteurs d'iso-ezymes pde4, et compositions les contenant | |
TNSN99171A1 (fr) | 4-carboxyamino-2-substitue-1,2,3,4-tetrahydroquinoleines, procede pour leur preparation et compositions pharmaceutiques les contenant | |
TNSN99106A1 (fr) | Derives d'isothiazole nouveaux, procede pour leur preparation et compositions pharmaceutiques les contenant. | |
TNSN99073A1 (fr) | Pyrazolopyrimidinones nouvelles, procede pour leur preparation et compositions pharmaceutiques les contenant | |
TNSN02015A1 (fr) | Composes nouveaux antagonistes de ppar, et compositions les contenant | |
TNSN00121A1 (fr) | Composes nouveaux inhibiteurs de metalloproteases, procede pour leur preparation et compositions pharmaceutiques les contenant | |
BR9806296A (pt) | Derivados de ácido sulfìnico e sua preparação e uso | |
TNSN99170A1 (fr) | Derives de tetrahydroquinoleine substitues nouveaux, procede pour leur preparation et compositions pharmaceutiques les contenant | |
MA27774A1 (fr) | Inhibiteurs de phosphatidylinositol 3-kinase | |
TNSN98084A1 (fr) | Derives de macrolides substitues en position c-4 |