CO5300398A1 - METHOD FOR THE TREATMENT OF CHRONIC PAIN THROUGH THE USE OF MEK INHIBITORS - Google Patents
METHOD FOR THE TREATMENT OF CHRONIC PAIN THROUGH THE USE OF MEK INHIBITORSInfo
- Publication number
- CO5300398A1 CO5300398A1 CO00053304A CO00053304A CO5300398A1 CO 5300398 A1 CO5300398 A1 CO 5300398A1 CO 00053304 A CO00053304 A CO 00053304A CO 00053304 A CO00053304 A CO 00053304A CO 5300398 A1 CO5300398 A1 CO 5300398A1
- Authority
- CO
- Colombia
- Prior art keywords
- alkyl
- cycloalkyl
- hydrogen
- optionally contains
- hydroxy
- 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
-
- 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
Abstract
Un método para tratar el dolor crónico, dicho método comprende administrar a un individuo que necesita dicho tratamiento una composición que comprende un inhibidor MEK seleccionado de un compuesto que se define en la Fórmula I<EMI FILE="00053304_1" ID="1" IMF=JPEG >donde:R1 es hidrógeno, hidroxi, alquilo de C1-C8, alcoxi de C1-C8, halo, trifluorometilo, o CN;R2 es hidrógeno;R3, R4, y R5 son independientemente hidrógeno, hidroxi, halo, trifluorometilo, alquilo de C1-C8, alcoxi de C1-C8, nitro, CN, o (O o NH)m -(CH2)n-R9, donde R9 es hidrógeno, hidroxi, CO2H, o NR10R11;n es 0-4;m es 0 ó 1;R10 y R11 son independientemente hidrógeno o alquilo de C1-C8, o tomados juntos con el nitrógeno al que están unidos pueden completar un anillo cíclico de 3-10 miembros que opcionalmente contienen 1, 2, o 3 heteroátomos adicionales seleccionados de O, S, NH, o alquilo de N-C1-C8; O ||R6 es hidrógeno, alquilo de C1-C8, alquilo de C -C1-C8 arilo, aralquilo o cicloalquilo de C3-C10;R7 es hidrógeno, alquilo de C1-C8, alquenilo de C2-C8, alquinilo de C2-C8, cicloalquilo de C3-C10, (cicloalquilo o cicloalquilo que opcionalmente contiene un heteroátomo seleccionado de O, S, o NR9);y donde cualquiera de los grupos alquilo, alquenilo, y alquinilo que anteceden pueden ser no sustituidos o sustituidos por cicloalquilo (o cicloalquilo que opcionalmente contiene un heteroátomo seleccionado de O, S, o NR9), arilo, ariloxi, heteroarilo, o heteroariloxi; o R6 y R7 tomados juntos con el N-O al que están unidos pueden completar un anillo cíclico de 5 a 10 miembros, que opcionalmente contiene uno, dos o tres heteroátomos adicionales seleccionados de O, S, o NR10R11.A method for treating chronic pain, said method comprises administering to an individual in need of said treatment a composition comprising a MEK inhibitor selected from a compound defined in Formula I <EMI FILE = "00053304_1" ID = "1" IMF = JPEG> where: R1 is hydrogen, hydroxy, C1-C8 alkyl, C1-C8 alkoxy, halo, trifluoromethyl, or CN; R2 is hydrogen; R3, R4, and R5 are independently hydrogen, hydroxy, halo, trifluoromethyl, C1-C8 alkyl, C1-C8 alkoxy, nitro, CN, or (O or NH) m - (CH2) n-R9, where R9 is hydrogen, hydroxy, CO2H, or NR10R11; n is 0-4; m is 0 or 1; R10 and R11 are independently hydrogen or C1-C8 alkyl, or taken together with the nitrogen to which they are attached can complete a 3-10 membered cyclic ring that optionally contains 1, 2, or 3 additional heteroatoms selected of O, S, NH, or N-C1-C8 alkyl; O || R6 is hydrogen, C1-C8 alkyl, C-C1-C8 aryl alkyl, aralkyl or C3-C10 cycloalkyl; R7 is hydrogen, C1-C8 alkyl, C2-C8 alkenyl, C2- alkynyl C8, C3-C10 cycloalkyl, (cycloalkyl or cycloalkyl which optionally contains a heteroatom selected from O, S, or NR9); and where any of the above alkyl, alkenyl, and alkynyl groups may be unsubstituted or substituted by cycloalkyl ( or cycloalkyl which optionally contains a heteroatom selected from O, S, or NR9), aryl, aryloxy, heteroaryl, or heteroaryloxy; or R6 and R7 taken together with the N-O to which they are attached can complete a 5 to 10 membered cyclic ring, which optionally contains one, two or three additional heteroatoms selected from O, S, or NR10R11.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14429299P | 1999-07-16 | 1999-07-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CO5300398A1 true CO5300398A1 (en) | 2003-07-31 |
Family
ID=22507940
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CO00053304A CO5300398A1 (en) | 1999-07-16 | 2000-07-14 | METHOD FOR THE TREATMENT OF CHRONIC PAIN THROUGH THE USE OF MEK INHIBITORS |
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 (45)
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DZ3401A1 (en) | 2000-07-19 | 2002-01-24 | Warner Lambert Co | OXYGEN ESTERS OF 4-IODOPHENYLAMINO BENZHYDROXAMIC ACIDS |
IL149462A0 (en) | 2001-05-09 | 2002-11-10 | Warner Lambert Co | Method of treating or inhibiting neutrophil chemotaxis by administering a mek inhibitor |
US7235537B2 (en) | 2002-03-13 | 2007-06-26 | Array Biopharma, Inc. | N3 alkylated benzimidazole derivatives as MEK inhibitors |
SI1482932T1 (en) | 2002-03-13 | 2010-02-26 | 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 |
ES2331246T3 (en) | 2003-07-24 | 2009-12-28 | Warner-Lambert Company Llc | DERIVATIVES OF BENZAMIDAZOL AS INHIBITORS OF THE MEK. |
US7538120B2 (en) | 2003-09-03 | 2009-05-26 | Array Biopharma Inc. | Method of treating inflammatory diseases |
US7144907B2 (en) | 2003-09-03 | 2006-12-05 | Array Biopharma Inc. | Heterocyclic inhibitors of MEK and methods of use thereof |
EP1676837A4 (en) * | 2003-10-08 | 2008-09-10 | Teijin Pharma Ltd | 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 |
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 |
AU2004293436B2 (en) | 2003-11-19 | 2010-12-09 | Array Biopharma Inc. | Heterocyclic inhibitors of MEK and methods of use thereof |
CN1882347A (en) | 2003-11-21 | 2006-12-20 | 阿雷生物药品公司 | AKT protein kinase inhibitors |
TWI361066B (en) * | 2004-07-26 | 2012-04-01 | Chugai Pharmaceutical Co Ltd | 5-substituted-2-phenylamino benzamides as mek inhibitors |
DK1922307T3 (en) | 2005-05-18 | 2012-04-02 | Array Biopharma Inc | Heterocyclic Inhibitors of MEK and Methods for Using Them |
CA3052368A1 (en) | 2005-10-07 | 2007-04-19 | Exelixis, Inc. | Azetidines as mek inhibitors |
US8063050B2 (en) | 2006-07-06 | 2011-11-22 | Array Biopharma Inc. | Hydroxylated and methoxylated pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
US9303040B2 (en) | 2006-07-06 | 2016-04-05 | Array Biopharma Inc. | Substituted piperazines as AKT inhibitors |
CA2656618C (en) | 2006-07-06 | 2014-08-26 | Array Biopharma Inc. | Cyclopenta [d] pyrimidines as akt protein kinase inhibitors |
JP5231410B2 (en) | 2006-07-06 | 2013-07-10 | アレイ バイオファーマ、インコーポレイテッド | Dihydrofuropyrimidine as an AKT protein kinase inhibitor |
CN105106199A (en) | 2006-12-14 | 2015-12-02 | 埃克塞利希斯股份有限公司 | Methods of using MEK inhibitors |
US9409886B2 (en) | 2007-07-05 | 2016-08-09 | Array Biopharma Inc. | Pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
EP2173723B3 (en) | 2007-07-05 | 2014-11-19 | Array Biopharma Inc. | Pyrimidyl cyclopentanes as akt protein kinase inhibitors |
TWI450720B (en) | 2007-07-05 | 2014-09-01 | 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 |
US8198279B2 (en) | 2007-12-19 | 2012-06-12 | Institute Of Cancer Research: Royal Cancer Hospital (The) | Pyrido[2,3-b]pyrazin-8-substituted compounds and their use |
EP2247578B1 (en) | 2008-01-09 | 2013-05-22 | Array Biopharma, Inc. | Hydroxylated pyrimidyl cyclopentanes as akt protein kinase inhibitors |
JP5539225B2 (en) | 2008-01-09 | 2014-07-02 | アレイ バイオファーマ、インコーポレイテッド | Hydroxylated pyrimidylcyclopentane as an AKT protein kinase inhibitor |
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CN102574782B (en) | 2009-10-21 | 2014-10-08 | 拜耳知识产权有限责任公司 | Substituted halophenoxybenzamide derivatives |
WO2011047795A1 (en) | 2009-10-21 | 2011-04-28 | Bayer Schering Pharma Aktiengesellschaft | Substituted benzosulphonamides |
US8962606B2 (en) | 2009-10-21 | 2015-02-24 | Bayer Intellectual Property Gmbh | Substituted benzosulphonamides |
AU2011209586B2 (en) | 2010-02-01 | 2016-01-21 | Cancer Research Technology Limited | 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 |
WO2012055953A1 (en) | 2010-10-29 | 2012-05-03 | Bayer Pharma Aktiengesellschaft | Substituted phenoxypyridines |
RS56759B1 (en) | 2011-04-01 | 2018-04-30 | Genentech Inc | Combination of akt inhibitor compound and abiraterone for use in therapeutic treatments |
EP2694073B1 (en) | 2011-04-01 | 2018-08-08 | Genentech, Inc. | Combinations of akt and mek inhibitors for treating cancer |
MY186549A (en) | 2012-10-12 | 2021-07-26 | Exelixis Inc | Novel process for making compounds for use in the treatment of cancer |
AU2014318748B2 (en) | 2013-09-11 | 2019-02-28 | Duquesne University Of The Holy Ghost | Novel anthranilic amides and the use thereof |
GB201320732D0 (en) | 2013-11-25 | 2014-01-08 | Cancer Rec Tech Ltd | Methods of chemical synthesis |
GB201320729D0 (en) | 2013-11-25 | 2014-01-08 | Cancer Rec Tech Ltd | Therapeutic compounds and their use |
EP3368026A1 (en) * | 2015-10-27 | 2018-09-05 | Acetylon Pharmaceuticals, Inc. | Hdac inhibitors for the treatment of diabetic peripheral neuropathy |
AU2018351475A1 (en) | 2017-10-17 | 2020-04-30 | Atriva Therapeutics Gmbh | Novel mek-inhibitor for the treatment of viral and bacterial infections |
WO2020259787A1 (en) * | 2019-06-28 | 2020-12-30 | University Of Copenhagen | Treatment of cns disorders with sleep disturbances |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
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WO1998037881A1 (en) * | 1997-02-28 | 1998-09-03 | Warner Lambert Company | Method of treating or preventing septic shock by administering a mek inhibitor |
EP0993439B1 (en) * | 1997-07-01 | 2004-09-29 | Warner-Lambert Company LLC | 4-bromo or 4-iodo phenylamino benzhydroxamic acid derivatives and their use as mek inhibitors |
WO1999001421A1 (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 JP JP2001510449A patent/JP2003504400A/en active Pending
- 2000-07-05 CA CA002374052A patent/CA2374052A1/en not_active Abandoned
- 2000-07-05 HU HU0202623A patent/HUP0202623A3/en unknown
- 2000-07-05 KR KR1020027000609A patent/KR20020012315A/en not_active Application Discontinuation
- 2000-07-05 EP EP00943383A patent/EP1202726A2/en not_active Withdrawn
- 2000-07-05 PL PL00352684A patent/PL352684A1/en not_active Application Discontinuation
- 2000-07-05 NZ NZ515567A patent/NZ515567A/en unknown
- 2000-07-05 CN CN00809801A patent/CN1373660A/en active Pending
- 2000-07-05 TR TR2002/00082T patent/TR200200082T2/en unknown
- 2000-07-05 IL IL14761900A patent/IL147619A0/en unknown
- 2000-07-05 WO PCT/US2000/018347 patent/WO2001005392A2/en not_active Application Discontinuation
- 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 |
---|---|
NZ515567A (en) | 2004-03-26 |
TR200200082T2 (en) | 2002-04-22 |
ZA200109907B (en) | 2003-02-28 |
AU5786000A (en) | 2001-02-05 |
WO2001005392A3 (en) | 2001-07-19 |
JP2003504400A (en) | 2003-02-04 |
KR20020012315A (en) | 2002-02-15 |
PL352684A1 (en) | 2003-09-08 |
EP1202726A2 (en) | 2002-05-08 |
CN1373660A (en) | 2002-10-09 |
PE20010545A1 (en) | 2001-06-04 |
WO2001005392A2 (en) | 2001-01-25 |
IL147619A0 (en) | 2002-08-14 |
CA2374052A1 (en) | 2001-01-25 |
HUP0202623A3 (en) | 2003-03-28 |
HUP0202623A2 (en) | 2002-11-28 |
AR024732A1 (en) | 2002-10-23 |
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