PE20010545A1 - USE OF A COMPOSITION OF MEK INHIBITORS FOR THE TREATMENT OF CHRONIC PAIN - Google Patents
USE OF A COMPOSITION OF MEK INHIBITORS FOR THE TREATMENT OF CHRONIC PAINInfo
- Publication number
- PE20010545A1 PE20010545A1 PE2000000705A PE0007052000A PE20010545A1 PE 20010545 A1 PE20010545 A1 PE 20010545A1 PE 2000000705 A PE2000000705 A PE 2000000705A PE 0007052000 A PE0007052000 A PE 0007052000A PE 20010545 A1 PE20010545 A1 PE 20010545A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- composition
- treatment
- pain
- chronic pain
- Prior art date
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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
-
- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/196—Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
-
- 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
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/166—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
-
- 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
- A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/32—Alcohol-abuse
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/02—Nutrients, e.g. vitamins, minerals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/20—Antivirals for DNA viruses
- A61P31/22—Antivirals for DNA viruses for herpes viruses
-
- 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
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/14—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Virology (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Diabetes (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Addiction (AREA)
- Nutrition Science (AREA)
- AIDS & HIV (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Biotechnology (AREA)
- Dermatology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Urology & Nephrology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Psychiatry (AREA)
Abstract
SE REFIERE AL USO DE UNA COMPOSICION QUE COMPRENDE UN INHIBIDOR DE MEK TAL COMO DERIVADOS DEL ACIDO 4-BROMO Y 4-YODO FENILAMINOBENZHIDROXAMICO, DONDE R1 ES H, OH, ALQUILO C1-C8, ALCOXI C1-C8, HALO, TRIFLUOROMETILO, CN; R2 ES H; R3, R4, R5 SON H, OH, HALO, TRIFLUOROMETILO, ALQUILO C1-C8, ENTRE OTROS; n ES 0-4; m ES 0-1; R10 Y R11 SON H, ALQUILO C1-C8, JUNTO CON N FORMAN UN CICLO DE 3-10 MIEMBROS; R6 ES H, ALQUILO C1-C8, ENTRE OTROS; R7 ES H, ALQUILO C1-C8, ALQUENILO C2-C8, ENTRE OTROS; R6 Y R7 JUNTO CON N-O FORMAN UN CICLO DE 5-10 MIEMBROS. SON COMPUESTOS I PREFERIDOS 4-FLUORO-N-HIDROXI-2-(4-YODO-2-METIL-FENILAMINO)-BENZAMIDA, 3,4-DIFLUORO-2-(4-YODO-2-METIL-FENILAMINO)-N-(3-FURILMETOXI)BENZAMIDA, ENTRE OTROS. LA COMPOSICION PUEDE SER UTIL PARA EL TRATAMIENTO DE DOLOR CRONICO (DOLOR NEUROPATICO, DOLOR IDIOPATICO, DOLOR ASOCIADO AL ALCOHOLISMO CRONICO, DEFICIENCIA VITAMINICA, UREMIA, HIPOTIROIDISMOREFERS TO THE USE OF A COMPOSITION THAT INCLUDES A MEK INHIBITOR SUCH AS DERIVATIVES OF 4-BROMINE AND 4-IODINE PHENYLAMINOBENZHYDROXAMIC ACID, WHERE R1 IS H, OH, C1-C8 ALKYL, C1-C8 ALCOXY, HALOME, TRIFLUHYL, HALOMETHYL R2 IS H; R3, R4, R5 ARE H, OH, HALO, TRIFLUOROMETHYL, C1-C8 ALKYL, AMONG OTHERS; n IS 0-4; m IS 0-1; R10 AND R11 ARE H, C1-C8 ALKYL, TOGETHER WITH N, FORM A CYCLE OF 3-10 MEMBERS; R6 IS H, C1-C8 ALKYL, AMONG OTHERS; R7 IS H, C1-C8 ALKYL, C2-C8 ALKYL, AMONG OTHERS; R6 AND R7 TOGETHER WITH N-O FORM A CYCLE OF 5-10 MEMBERS. PREFERRED I COMPOUNDS ARE 4-FLUORO-N-HYDROXY-2- (4-IODO-2-METHYL-PHENYLAMINE) -BENZAMIDE, 3,4-DIFLUORO-2- (4-IODO-2-METHYL-PHENYLAMINE) -N- (3-FURILMETOXI) BENZAMIDE, AMONG OTHERS. THE COMPOSITION MAY BE USEFUL FOR THE TREATMENT OF CHRONIC PAIN (NEUROPATHIC PAIN, IDIOPATIC PAIN, PAIN ASSOCIATED WITH CHRONIC ALCOHOLISM, VITAMIN DEFICIENCY, UREMIA, HYPOTHYROIDISM
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14429299P | 1999-07-16 | 1999-07-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20010545A1 true PE20010545A1 (en) | 2001-06-04 |
Family
ID=22507940
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2000000705A PE20010545A1 (en) | 1999-07-16 | 2000-07-14 | USE OF A COMPOSITION OF MEK INHIBITORS FOR THE TREATMENT OF CHRONIC PAIN |
Country Status (16)
| Country | Link |
|---|---|
| EP (1) | EP1202726A2 (en) |
| JP (1) | JP2003504400A (en) |
| KR (1) | KR20020012315A (en) |
| CN (1) | CN1373660A (en) |
| AR (1) | AR024732A1 (en) |
| AU (1) | AU5786000A (en) |
| CA (1) | CA2374052A1 (en) |
| CO (1) | CO5300398A1 (en) |
| HU (1) | HUP0202623A3 (en) |
| IL (1) | IL147619A0 (en) |
| NZ (1) | NZ515567A (en) |
| PE (1) | PE20010545A1 (en) |
| PL (1) | PL352684A1 (en) |
| TR (1) | TR200200082T2 (en) |
| WO (1) | WO2001005392A2 (en) |
| ZA (1) | ZA200109907B (en) |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1219753C (en) | 2000-07-19 | 2005-09-21 | 沃尼尔·朗伯公司 | Oxygenated esters of 4-iodoanilinophenylhydroxamic acid |
| IL149462A0 (en) | 2001-05-09 | 2002-11-10 | Warner Lambert Co | Method of treating or inhibiting neutrophil chemotaxis by administering a mek inhibitor |
| IL163995A0 (en) | 2002-03-13 | 2005-12-18 | Array Biopharma Inc | N3 alkylated benzimidazole derivatives as mek inhibitors |
| US7235537B2 (en) | 2002-03-13 | 2007-06-26 | Array Biopharma, Inc. | N3 alkylated benzimidazole derivatives as MEK inhibitors |
| US7632866B2 (en) | 2002-10-21 | 2009-12-15 | Ramot At Tel Aviv University | Derivatives of N-phenylanthranilic acid and 2-benzimidazolone as potassium channel and/or neuron activity modulators |
| WO2005009975A2 (en) | 2003-07-24 | 2005-02-03 | Warner-Lambert Company Llc | Benzimidazole derivatives as mek inhibitors |
| US7144907B2 (en) | 2003-09-03 | 2006-12-05 | Array Biopharma Inc. | Heterocyclic inhibitors of MEK and methods of use thereof |
| US7538120B2 (en) | 2003-09-03 | 2009-05-26 | Array Biopharma Inc. | Method of treating inflammatory diseases |
| JPWO2005035493A1 (en) * | 2003-10-08 | 2006-12-21 | 帝人ファーマ株式会社 | Process for producing aminopyrrolidine derivative and intermediate compound |
| RU2352558C2 (en) | 2003-10-21 | 2009-04-20 | Уорнер-Ламберт Компани Ллс | Polymorphic form of n-[(r)-2,3-dihydroxypropoxy]-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)benzamide |
| WO2005051300A2 (en) | 2003-11-19 | 2005-06-09 | Array Biopharma Inc. | Bicyclic inhibitors of mek and methods of use thereof |
| US7732616B2 (en) | 2003-11-19 | 2010-06-08 | Array Biopharma Inc. | Dihydropyridine and dihydropyridazine derivatives as inhibitors of MEK and methods of use thereof |
| US7517994B2 (en) | 2003-11-19 | 2009-04-14 | Array Biopharma Inc. | Heterocyclic inhibitors of MEK and methods of use thereof |
| PH12012501891A1 (en) | 2003-11-21 | 2013-09-02 | Array Biopharma Inc | Akt protein kinase inhibitors |
| MY144232A (en) * | 2004-07-26 | 2011-08-15 | Chugai Pharmaceutical Co Ltd | 5-substituted-2-phenylamino benzamides as mek inhibitors |
| EP1967516B1 (en) | 2005-05-18 | 2009-11-04 | Array Biopharma, Inc. | 4-(phenylamino)-6-oxo-1,6-dihydropyridazine-3-carboxamide derivatives as MEK inhibitors for the treatment of hyperproliferative diseases |
| CA2622755C (en) | 2005-10-07 | 2017-01-31 | Exelixis, Inc. | Azetidines as mek inhibitors |
| DK2054418T3 (en) | 2006-07-06 | 2012-02-27 | Array Biopharma Inc | Dihydrothienopyrimidines as AKT protein kinase inhibitors |
| US8329701B2 (en) | 2006-07-06 | 2012-12-11 | Array Biopharma Inc. | Dihydrofuro pyrimidines as AKT protein kinase inhibitors |
| US8063050B2 (en) | 2006-07-06 | 2011-11-22 | Array Biopharma Inc. | Hydroxylated and methoxylated pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
| SI2049500T1 (en) | 2006-07-06 | 2012-01-31 | Array Biopharma Inc | CYCLOPENTA ?áD?å PYRIMIDINES AS AKT PROTEIN KINASE INHIBITORS |
| EP2101759B1 (en) | 2006-12-14 | 2018-10-10 | Exelixis, Inc. | Methods of using mek inhibitors |
| MX2009014013A (en) | 2007-07-05 | 2010-01-28 | Array Biopharma Inc | Pyrimidyl cyclopentanes as akt protein kinase inhibitors. |
| US9409886B2 (en) | 2007-07-05 | 2016-08-09 | Array Biopharma Inc. | Pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
| NZ582692A (en) | 2007-07-05 | 2012-05-25 | Array Biopharma Inc | Pyrimidyl cyclopentanes as akt protein kinase inhibitors |
| US8846683B2 (en) | 2007-07-05 | 2014-09-30 | Array Biopharma, Inc. | Pyrimidyl cyclopentanes as Akt protein kinase inhibitors |
| CN101868443A (en) * | 2007-09-20 | 2010-10-20 | 特拉维夫大学拉莫特有限公司 | N-phenyl anthranilic acid derivatives and uses thereof |
| NZ586418A (en) | 2007-12-19 | 2012-09-28 | Cancer Rec Tech Ltd | Pyrido[2,3-b]pyrazine-8-substituted compounds and their use |
| ES2422733T3 (en) | 2008-01-09 | 2013-09-13 | Array Biopharma Inc | Hydroxylated pyrimidylcyclopentanes as AKT protein kinase inhibitors |
| AU2009204019B2 (en) | 2008-01-09 | 2014-02-20 | Array Biopharma Inc. | Hydroxylated pyrimidyl cyclopentane as AKT protein kinase inhibitor |
| EP2346818B1 (en) | 2008-11-10 | 2012-12-05 | Bayer Intellectual Property GmbH | Substituted sulphonamido phenoxybenzamides |
| CA2777430A1 (en) | 2009-10-21 | 2011-04-28 | Bayer Pharma Aktiengesellschaft | Substituted benzosulphonamides |
| EP2491015A1 (en) | 2009-10-21 | 2012-08-29 | Bayer Pharma Aktiengesellschaft | Substituted benzosulphonamides |
| WO2011047796A1 (en) | 2009-10-21 | 2011-04-28 | Bayer Schering Pharma Aktiengesellschaft | Substituted halophenoxybenzamide derivatives |
| PL2531502T3 (en) | 2010-02-01 | 2014-08-29 | Cancer Research Tech Ltd | 1-(5-tert-butyl-2-phenyl-2h-pyrazol-3-yl)-3-[2-fluoro-4-(1-methyl-2-oxo-2,3-dihydro-1h-imidazo[4,5-b]pyridin-7-yloxy)-phenyl]-urea and related compounds and their use in therapy |
| EP2632899A1 (en) | 2010-10-29 | 2013-09-04 | Bayer Intellectual Property GmbH | Substituted phenoxypyridines |
| WO2012135779A1 (en) | 2011-04-01 | 2012-10-04 | Genentech, Inc. | Combinations of akt and mek inhibitor compounds, and methods of use |
| BR112013025353A8 (en) | 2011-04-01 | 2018-01-02 | Genentech Inc | combination of a) a compound of formula ia, compound of formula ia or a pharmaceutically acceptable salt thereof, method for treating a hyperproliferative disorder in a mammal, use of a compound of formula ia or a pharmaceutically acceptable salt thereof, kit and product |
| GEP201706690B (en) | 2012-10-12 | 2017-06-26 | Exelixis Inc | Novel process for making compounds for use in treatment of cancer |
| US11465978B2 (en) | 2013-09-11 | 2022-10-11 | The Administrators Of The Tulane Educational Fund | Anthranilic amides and the use thereof |
| GB201320729D0 (en) | 2013-11-25 | 2014-01-08 | Cancer Rec Tech Ltd | Therapeutic compounds and their use |
| GB201320732D0 (en) | 2013-11-25 | 2014-01-08 | Cancer Rec Tech Ltd | Methods of chemical synthesis |
| JP7080812B2 (en) | 2015-10-27 | 2022-06-06 | アセチロン ファーマシューティカルズ インコーポレイテッド | HDAC inhibitors for the treatment of diabetic peripheral neuropathy |
| EP3973960B1 (en) | 2017-10-17 | 2025-09-03 | Atriva Therapeutics GmbH | Novel mek-inhibitor for the treatment of viral and bacterial infections |
| LU101183B1 (en) * | 2019-04-16 | 2020-10-16 | Atriva Therapeutics Gmbh | Novel mek-inhibitor for the treatment of viral and bacterial infections |
| AU2020306249B2 (en) * | 2019-06-28 | 2025-06-26 | University Of Copenhagen | Treatment of CNS disorders with sleep disturbances |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU5610398A (en) * | 1997-02-28 | 1998-09-18 | Warner-Lambert Company | Method of treating or preventing septic shock by administering a mek inhibitor |
| ES2229515T3 (en) * | 1997-07-01 | 2005-04-16 | Warner-Lambert Company Llc | 4-BROMO OR 4-IODINE DERIVATIVES OF BENZHYDROXAMIC PHENYLAMINE ACID AND ITS USE AS INHIBITORS OF THE MEK. |
| CA2290509A1 (en) * | 1997-07-01 | 1999-01-14 | Warner-Lambert Company | 2-(4-bromo or 4-iodo phenylamino) benzoic acid derivatives and their use as mek inhibitors |
| CA2346448A1 (en) * | 1998-12-16 | 2000-06-22 | Warner-Lambert Company | Treatment of arthritis with mek inhibitors |
-
2000
- 2000-07-05 TR TR2002/00082T patent/TR200200082T2/en unknown
- 2000-07-05 CN CN00809801A patent/CN1373660A/en active Pending
- 2000-07-05 EP EP00943383A patent/EP1202726A2/en not_active Withdrawn
- 2000-07-05 IL IL14761900A patent/IL147619A0/en unknown
- 2000-07-05 NZ NZ515567A patent/NZ515567A/en unknown
- 2000-07-05 WO PCT/US2000/018347 patent/WO2001005392A2/en not_active Ceased
- 2000-07-05 JP JP2001510449A patent/JP2003504400A/en active Pending
- 2000-07-05 CA CA002374052A patent/CA2374052A1/en not_active Abandoned
- 2000-07-05 KR KR1020027000609A patent/KR20020012315A/en not_active Withdrawn
- 2000-07-05 PL PL00352684A patent/PL352684A1/en not_active Application Discontinuation
- 2000-07-05 HU HU0202623A patent/HUP0202623A3/en unknown
- 2000-07-05 AU AU57860/00A patent/AU5786000A/en not_active Abandoned
- 2000-07-13 AR ARP000103604A patent/AR024732A1/en unknown
- 2000-07-14 PE PE2000000705A patent/PE20010545A1/en not_active Application Discontinuation
- 2000-07-14 CO CO00053304A patent/CO5300398A1/en not_active Application Discontinuation
-
2001
- 2001-11-30 ZA ZA200109907A patent/ZA200109907B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| HUP0202623A3 (en) | 2003-03-28 |
| HUP0202623A2 (en) | 2002-11-28 |
| AU5786000A (en) | 2001-02-05 |
| WO2001005392A2 (en) | 2001-01-25 |
| PL352684A1 (en) | 2003-09-08 |
| ZA200109907B (en) | 2003-02-28 |
| IL147619A0 (en) | 2002-08-14 |
| WO2001005392A3 (en) | 2001-07-19 |
| KR20020012315A (en) | 2002-02-15 |
| EP1202726A2 (en) | 2002-05-08 |
| CN1373660A (en) | 2002-10-09 |
| NZ515567A (en) | 2004-03-26 |
| TR200200082T2 (en) | 2002-04-22 |
| CA2374052A1 (en) | 2001-01-25 |
| CO5300398A1 (en) | 2003-07-31 |
| AR024732A1 (en) | 2002-10-23 |
| JP2003504400A (en) | 2003-02-04 |
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