PE20020665A1 - ACIDO CICLOALQUIL FENIL ALCANOICO COMO ANTAGONISTA DE INTEGRINAS OVß3 - Google Patents
ACIDO CICLOALQUIL FENIL ALCANOICO COMO ANTAGONISTA DE INTEGRINAS OVß3Info
- Publication number
- PE20020665A1 PE20020665A1 PE2001000575A PE2001000575A PE20020665A1 PE 20020665 A1 PE20020665 A1 PE 20020665A1 PE 2001000575 A PE2001000575 A PE 2001000575A PE 2001000575 A PE2001000575 A PE 2001000575A PE 20020665 A1 PE20020665 A1 PE 20020665A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- ring
- cycloalkyl
- ovß3
- phenyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- 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
- A61P19/08—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
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
- A61P3/14—Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- A61P9/10—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
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/38—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/88—Nitrogen atoms, e.g. allantoin
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Hematology (AREA)
- Ophthalmology & Optometry (AREA)
- Urology & Nephrology (AREA)
- Oncology (AREA)
- Endocrinology (AREA)
- Diabetes (AREA)
- Neurology (AREA)
- Obesity (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
SE REFIERE A COMPUESTOS ACIDO CICLOALQUIL FENIL ALCANOICO DE FORMULA I DONDE EL ANILLO A ES UN ANILLO MONOCICLICO DE 4-8 MIEMBROS, ANILLO BICICLICO DE 7-12 MIEMBROS; A1 ES UN ANILLO MONOCICLICO DE 5-9 MIEMBROS, HETEROCICLO POLICICLICO DE 7-14 MIEMBROS, NR5-C(=Y1)-NR8R7, NR5C(Y2)(=NR7); CUANDO Z1 ES CO, SO2, EL ENLACE A1-Z2 INCLUYE PIRIDINA, IMIDAZOL, TIAZOL, OXAZOL, BENZIMIDAZOL, IMIDAZOPIRIDINA; Y1 ES NR2, O, S; R2 ES H, ALQUILO, ARILO, OH, ALCOXI; R7 Y R8 SON H, ALQUILO, ARALQUILO, AMINO, ALQUILAMINO; NR7 Y R8 FORMAN UN ANILLO MONOCICLICO, BICICLICO; R5, Rm, Rp, Rk, Rf SON H, ALQUILO; A ES NR5C(Y)=NR'; Y2 ES ALQUILO, CICLOALQUILO, BICICLOALQUILO, ENTRE OROS; Z1 ES CH2, O, NH, NRk, ENTRE OTROS; Z2 ES UN ENLAZANTE C2-C5; Z1-Z2 CONTIENE ADEMAS CARBOXAMIDA, SULFONA, ENLAZADO AL ANILLO A EN POSICION PARA O META EN RELACION A X1; n ES 0-1; Rc ES H, ALQUILO, HALOGENO, OH, ENTRE OTROS; X1 ES O, CO, SO2, NRm, (CHRp)q; Rp ES H, ALQUILO, ALCOXI, OH; q ES 0-1; X2 ES CHRe, CO, SO2, NRf, S. X o Y ES CRg, N; Rg ES H, ALQUILO, HALOALQUILO, FLUORO, ENTRE OTROS, X-X2-Y CONTIENE ACILO, ALQUILO, AMINO, ENTRE OTROS; Rb ES X3-Rh; X3 ES O, S, NRj; Rj Y Rh SON H, ALQUILO, ACILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS ACIDO 2-[4-[3-(2-PIRIDINILAMINO)PROPOXI]FENIL]CICLOPROPANO-ACETICO, ENTRE OTROS. LOS COMPUESTOS SON ANTAGONISTAS DE INTEGRINAS OVß3 Y PUEDEN SER UTILES PARA EL TRATAMIENTO DE METASTASIS TUMORAL, CRECIMIENTO TUMORAL, OSTEOPOROSIS, ENFERMEDAD DE PAGET, RETINOPATIA, DEGENERACION MACULAR
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21178100P | 2000-06-15 | 2000-06-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20020665A1 true PE20020665A1 (es) | 2002-08-14 |
Family
ID=22788343
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2001000575A PE20020665A1 (es) | 2000-06-15 | 2001-06-15 | ACIDO CICLOALQUIL FENIL ALCANOICO COMO ANTAGONISTA DE INTEGRINAS OVß3 |
Country Status (8)
Country | Link |
---|---|
US (2) | US6900232B2 (es) |
EP (1) | EP1289960A2 (es) |
JP (1) | JP2004525069A (es) |
AR (1) | AR030701A1 (es) |
AU (1) | AU2001269821A1 (es) |
PE (1) | PE20020665A1 (es) |
UY (1) | UY26780A1 (es) |
WO (1) | WO2001096307A2 (es) |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7176322B2 (en) | 2002-05-23 | 2007-02-13 | Amgen Inc. | Calcium receptor modulating agents |
US6908935B2 (en) | 2002-05-23 | 2005-06-21 | Amgen Inc. | Calcium receptor modulating agents |
US7589199B2 (en) | 2002-06-12 | 2009-09-15 | Chemocentryx, Inc. | Substituted piperazines |
US7842693B2 (en) * | 2002-06-12 | 2010-11-30 | Chemocentryx, Inc. | Substituted piperazines |
CA2488202C (en) | 2002-06-12 | 2011-03-08 | Chemocentryx, Inc. | 1-aryl-4-substituted piperazine derivatives for use as ccr1 antagonists for the treatment of inflammation and immune disorders |
US20050256130A1 (en) * | 2002-06-12 | 2005-11-17 | Chemocentryx, Inc. | Substituted piperazines |
US20040259669A1 (en) * | 2003-06-20 | 2004-12-23 | Seaway Plastics Ltd. | Volleyball net pretensioned with rigid side strips |
TW200526626A (en) | 2003-09-13 | 2005-08-16 | Astrazeneca Ab | Chemical compounds |
US7435831B2 (en) * | 2004-03-03 | 2008-10-14 | Chemocentryx, Inc. | Bicyclic and bridged nitrogen heterocycles |
CA2558211C (en) * | 2004-03-03 | 2013-09-03 | Chemocentryx, Inc. | Bicyclic and bridged nitrogen heterocycles |
EP2394662B1 (en) * | 2004-04-02 | 2018-03-21 | The Regents of The University of California | Methods and compositions for treating and preventing disease associated with alpha v beta 5 integrin |
KR101478933B1 (ko) | 2004-12-28 | 2015-01-02 | 키넥스 파마슈티컬즈, 엘엘씨 | 세포 증식 질환의 치료를 위한 조성물 및 방법 |
US7968574B2 (en) | 2004-12-28 | 2011-06-28 | Kinex Pharmaceuticals, Llc | Biaryl compositions and methods for modulating a kinase cascade |
KR20070113233A (ko) | 2005-02-18 | 2007-11-28 | 아스트라제네카 아베 | 항균성 피페리딘 유도체 |
EP2041071B1 (en) | 2006-06-29 | 2014-06-18 | Kinex Pharmaceuticals, LLC | Biaryl compositions and methods for modulating a kinase cascade |
US7935697B2 (en) | 2006-12-28 | 2011-05-03 | Kinex Pharmaceuticals, Llc | Compositions for modulating a kinase cascade and methods of use thereof |
US7939529B2 (en) | 2007-05-17 | 2011-05-10 | Kinex Pharmaceuticals, Llc | Process for the preparation of compositions for modulating a kinase cascade and methods of use thereof |
PL2195312T3 (pl) | 2007-10-09 | 2013-04-30 | Merck Patent Gmbh | Pochodne pirydynowe użyteczne jako aktywatory glukokinazowe |
EP2217238B1 (en) * | 2007-11-08 | 2014-03-12 | The General Hospital Corporation | Methods and compositions for the treatment of proteinuric diseases |
US10087252B2 (en) | 2009-07-24 | 2018-10-02 | The Regents Of The University Of California | Methods and compositions for treating and preventing disease associated with αvβ5 integrin |
CN102905700A (zh) | 2010-04-16 | 2013-01-30 | 金克斯医药品有限公司 | 用于预防和治疗癌症的组合物以及方法 |
JP6499076B2 (ja) | 2012-08-30 | 2019-04-10 | アセネックス インコーポレイテッド | タンパク質チロシンキナーゼ調節因子としてのn−(3−フルオロベンジル)−2−(5−(4−モルホリノフェニル)ピリジン−2−イル)アセトアミド |
JP6215335B2 (ja) | 2013-09-24 | 2017-10-18 | 富士フイルム株式会社 | 新規な含窒素化合物もしくはその塩またはそれらと金属との錯体 |
BR112017003745A2 (pt) | 2014-08-29 | 2017-12-05 | Tes Pharma S R L | inibidores de semialdeído descarboxilase de ácido alfa-amino-beta-carboximucônico |
CN116041169A (zh) * | 2022-07-29 | 2023-05-02 | 北京先通国际医药科技股份有限公司 | 一种合成修饰脂肪酸型pet试剂前体关键中间体的工艺路线及其用途 |
Family Cites Families (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3654306A (en) | 1970-01-26 | 1972-04-04 | Robins Co Inc A H | 5-azaspiro(2.4)heptane-4 6-diones |
IL99537A (en) | 1990-09-27 | 1995-11-27 | Merck & Co Inc | Fibrinogen receptor antagonists and pharmaceutical compositions containing them |
GB9202792D0 (en) | 1992-02-11 | 1992-03-25 | British Bio Technology | Compounds |
WO1993021166A1 (en) | 1992-04-10 | 1993-10-28 | Smithkline Beecham Plc | Heterocyclic compounds and their use in the treatment of type ii-diabetes |
GB9311282D0 (en) | 1993-06-01 | 1993-07-21 | Rhone Poulenc Rorer Ltd | New compositions of matter |
GB9315148D0 (en) | 1993-07-22 | 1993-09-08 | Smithkline Beecham Plc | Novel compounds |
US5665754A (en) | 1993-09-20 | 1997-09-09 | Glaxo Wellcome Inc. | Substituted pyrrolidines |
US5849736A (en) * | 1993-11-24 | 1998-12-15 | The Dupont Merck Pharmaceutical Company | Isoxazoline and isoxazole fibrinogen receptor antagonists |
DE4408082A1 (de) | 1994-03-10 | 1995-09-14 | Hoechst Ag | Substituierte Propan-Derivate, Verfahren zu ihrer Herstellung und die Anwendung der Verbindungen zur Behandlung von Krankheiten |
US5741796A (en) | 1994-05-27 | 1998-04-21 | Merck & Co., Inc. | Pyridyl and naphthyridyl compounds for inhibiting osteoclast-mediated bone resorption |
US5710171A (en) * | 1995-05-24 | 1998-01-20 | Merck & Co., Inc. | Bisphenyl inhibitors of farnesyl-protein transferase |
CA2176854A1 (en) * | 1995-06-07 | 1996-12-08 | Daniel J. Keavy | N-acyl-2 aryl cyclopropylmethylamine derivatives as melatonergics |
GB9511694D0 (en) | 1995-06-09 | 1995-08-02 | Fujisawa Pharmaceutical Co | Benzamide derivatives |
DE19536891A1 (de) | 1995-10-04 | 1997-04-10 | Basf Ag | Neue Aminosäurederivate, ihre Herstellung und Verwendung |
IT1276153B1 (it) | 1995-11-17 | 1997-10-27 | Roberto Pellicciari | Derivati di glicina ad attivita' antagonista dei recettori metabotropi del glutammato |
DE69713582T2 (de) * | 1996-03-29 | 2003-01-09 | G.D. Searle & Co., Chicago | Zimtsäurederivate und deren verwendung als integrin-antagonisten |
CA2250695A1 (en) * | 1996-03-29 | 1997-10-09 | G.D. Searle & Co. | Cyclopropyl alkanoic acid derivatives |
DK0889877T3 (da) | 1996-03-29 | 2001-10-01 | Searle & Co | Meta-substituerede phenylenderivater og deres anvendelse som alfav-beta3-integrin-antagonister eller -inhibitorer |
EP0974348B1 (en) | 1996-11-08 | 2008-07-02 | Nippon Chemiphar Co., Ltd. | Visceral fat lowering agent |
EP1007026A4 (en) | 1997-01-17 | 2002-08-07 | Merck & Co Inc | INTEGRIN ANTAGONISTS |
JPH10287634A (ja) | 1997-04-11 | 1998-10-27 | Otsuka Pharmaceut Co Ltd | ベンゼン誘導体 |
WO1999045927A1 (en) | 1998-03-10 | 1999-09-16 | Smithkline Beecham Corporation | Vitronectin receptor antagonists |
UA71586C2 (en) * | 1998-12-04 | 2004-12-15 | Smithkline Beecham Corp | A vitronectin receptor antagonist |
BR9916518A (pt) | 1998-12-23 | 2002-01-29 | Searle & Co | Método para tratar ou prevenir um distúrbio de neoplasia em um mamìfero em necessidade de tal tratamento ou prevenção, e, combinação compreendendo um inibidor de ciclooxigenase-2 e um ou mais agentes anti-neoplásticos |
CN1331862C (zh) | 1999-04-28 | 2007-08-15 | 萨诺费-阿文蒂斯德国有限公司 | 作为ppar受体配体的二芳基酸衍生物 |
ES2226832T3 (es) | 1999-05-05 | 2005-04-01 | Aventis Pharma Limited | Pirrolidinas sustituidas como inhibidores de la adhesion celular. |
DE19939981A1 (de) | 1999-08-24 | 2001-03-01 | Merck Patent Gmbh | Neue Inhibitoren des Integrins alphavß3 |
DE19939980A1 (de) | 1999-08-24 | 2001-03-01 | Merck Patent Gmbh | Inhibitoren des Integrins alphavbeta¶3¶ |
-
2001
- 2001-06-15 JP JP2002510450A patent/JP2004525069A/ja not_active Withdrawn
- 2001-06-15 PE PE2001000575A patent/PE20020665A1/es not_active Application Discontinuation
- 2001-06-15 US US09/882,186 patent/US6900232B2/en not_active Expired - Fee Related
- 2001-06-15 UY UY26780A patent/UY26780A1/es not_active Application Discontinuation
- 2001-06-15 WO PCT/US2001/019104 patent/WO2001096307A2/en active Application Filing
- 2001-06-15 AU AU2001269821A patent/AU2001269821A1/en not_active Abandoned
- 2001-06-15 EP EP01948363A patent/EP1289960A2/en not_active Withdrawn
- 2001-06-19 AR ARP010102897A patent/AR030701A1/es unknown
-
2004
- 2004-07-14 US US10/891,361 patent/US6949578B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
WO2001096307A2 (en) | 2001-12-20 |
US6949578B2 (en) | 2005-09-27 |
US20040259869A1 (en) | 2004-12-23 |
AU2001269821A1 (en) | 2001-12-24 |
WO2001096307A3 (en) | 2002-08-15 |
EP1289960A2 (en) | 2003-03-12 |
US20020077321A1 (en) | 2002-06-20 |
AR030701A1 (es) | 2003-09-03 |
UY26780A1 (es) | 2002-01-31 |
US6900232B2 (en) | 2005-05-31 |
JP2004525069A (ja) | 2004-08-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20020665A1 (es) | ACIDO CICLOALQUIL FENIL ALCANOICO COMO ANTAGONISTA DE INTEGRINAS OVß3 | |
PE20060374A1 (es) | Inhibidores de cinasa heterociclicos fusionados | |
EA200400830A1 (ru) | ПИРИМИДИНОВЫЕ СОЕДИНЕНИЯ, ОТНОСЯЩИЕСЯ К A2b-СЕЛЕКТИВНЫМ АНТАГОНИСТАМ, ИХ СИНТЕЗ И ПРИМЕНЕНИЕ | |
PE20050132A1 (es) | Piperazinas heterociclicas sustituidas | |
PE20020917A1 (es) | Derivados de imidazol como bloqueadores del receptor n-metil-d-aspartato | |
RU2010131833A (ru) | Способы получения производных хиназолинона | |
PE20050765A1 (es) | DERIVADOS DE SULFONAMIDA COMO AGONISTAS DE LOS RECEPTORES ß2 ADRENERGICOS | |
PE58399A1 (es) | Atropisomeros de 3-aril-4(3h)-quinazolinonas | |
DE60228406D1 (de) | PYRAZOLOÄ3,4-dÜPYRIMIDINDERIVATE UND IHRE VERWENDUNG ALS ANTAGONISTEN DES PURINERGEN REZEPTORS | |
PE20051046A1 (es) | Derivados de diaril-urea en el tratamiento de enfermedades dependientes de la quinasa de proteina | |
PE20120814A1 (es) | Compuestos y composiciones como inhibidores de la proteina cinasa | |
PE20010219A1 (es) | AGONISTAS ß-ADRENORRECEPTORES | |
JP2005508966A5 (es) | ||
EP0242709A3 (en) | Antagonists of specific excitatory amino acid neurotransmitter receptors | |
PE20020298A1 (es) | Derivados de 1,3,8-triaza-espiro[4,5]decan-4-ona como antagonistas de receptores de neuroquinina nk-1 | |
CA2624602A1 (en) | Process for preparing 6-substituted-7-azaindoles | |
CA2078810A1 (en) | Leukotriene biosynthesis inhibitors | |
PE20060693A1 (es) | Nuevos derivados de trifluorometansulfonanilida oxamida eter | |
RU2008110917A (ru) | ПРОИЗВОДНЫЕ 7-(2-АМИНО-1-ГИДРОКСИ-ЭТИЛ)-4-ГИДРОКСИБЕНЗОТИАЗОЛ-2(3Н)-ОНА В КАЧЕСТВЕ АГОНИСТОВ β2-АДРЕНЕРГИЧЕСКИХ РЕЦЕПТОРОВ | |
JP2005509622A5 (es) | ||
PE20020483A1 (es) | Peptidos ciclicos selectivos como agonistas de los receptores de melanocortina 4 | |
PE20010753A1 (es) | DERIVADOS DE PURINA COMO AGONISTAS DEL RECEPTOR DE ADENOSINA A2a | |
JPH04330073A (ja) | アンギオテンシンii拮抗薬としての置換ピリドピリミジノン類及び関連複素環類 | |
PE20021158A1 (es) | Derivados de sulfonamida como antagonistas del receptor de bradiquinina | |
PE20100093A1 (es) | Derivados de acetileno |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC | Refusal |