PE20010546A1 - USE OF A COMPOSITION OF BENZOHETERO CYCLES AS MEK INHIBITORS TO TREAT CHRONIC PAIN - Google Patents
USE OF A COMPOSITION OF BENZOHETERO CYCLES AS MEK INHIBITORS TO TREAT CHRONIC PAINInfo
- Publication number
- PE20010546A1 PE20010546A1 PE2000000704A PE0007042000A PE20010546A1 PE 20010546 A1 PE20010546 A1 PE 20010546A1 PE 2000000704 A PE2000000704 A PE 2000000704A PE 0007042000 A PE0007042000 A PE 0007042000A PE 20010546 A1 PE20010546 A1 PE 20010546A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- cycloalkyl
- phenyl
- composition
- methyl
- Prior art date
Links
- 208000000094 Chronic Pain Diseases 0.000 title 1
- 208000002193 Pain Diseases 0.000 title 1
- 239000002829 mitogen activated protein kinase inhibitor Substances 0.000 title 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 6
- BGKLFAQCHHCZRZ-UHFFFAOYSA-N 4-iodo-2-methylaniline Chemical compound CC1=CC(I)=CC=C1N BGKLFAQCHHCZRZ-UHFFFAOYSA-N 0.000 abstract 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 1
- 230000001684 chronic effect Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229940043355 kinase inhibitor Drugs 0.000 abstract 1
- 208000004296 neuralgia Diseases 0.000 abstract 1
- 208000021722 neuropathic pain Diseases 0.000 abstract 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 abstract 1
Classifications
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- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
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- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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- 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
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- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4192—1,2,3-Triazoles
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- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/423—Oxazoles condensed with carbocyclic rings
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- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4245—Oxadiazoles
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- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/428—Thiazoles condensed with carbocyclic rings
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- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/433—Thidiazoles
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- 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
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
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- 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
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- 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
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- 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
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- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
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- 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
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- 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
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- 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]
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- 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
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- 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
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- 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
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- 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
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- 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
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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Endocrinology (AREA)
- Physical Education & Sports Medicine (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Addiction (AREA)
- Psychiatry (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Virology (AREA)
- Dermatology (AREA)
- Immunology (AREA)
- Oncology (AREA)
- Emergency Medicine (AREA)
- Communicable Diseases (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Abstract
SE REFIERE AL USO DE UNA COMPOSICION QUE COMPRENDE UN INHIBIDOR DE CINASA MEK DE FORMULA I, DONDE: W ES OR1, NR2OR1, NRARB, NR2NRARB, O(CH2)2-4NRARB, NR2(CH2)2-4, R1 ES H, ALQUILO C1-C8, ALQUENILO C3-C8, ALQUINILO C3-C8, CICLOALQUILO C3-C8, FENILO, FENIL(ALQUILO)C1-C4. FENILALQUENILO C3-C4, ENTRE OTROS; R2 ES H, ALQUILO C1-C4, FENILO, CICLOALQUILO C3-C6, HETEROCICLO C3-C6; RA ES H, ALQUILO C1-C6, ALQUENILO C3-C8, ALQUINILO C3-C8, CICLOALQUILO C3-C8, FENILO, (CICLOALQUILO C3-C8)ALQUILO C1-C4, ENTRE OTROS; RB ES H, ALQUILO C1-C8, CICLOALQUILO C3-C8, FENILO; Q ES EL GRUPO a, ENTRE OTROS; R3 ES H, F; R4 ES HALO, NO2, SO2NRo(CH2)2-4NREFE, ENTRE OTROS; T ES ALQUILO C1-C8, CICLOALQUILO C3-C8, ENTRE OTROS; Z ES EL GRUPO iv, ENTRE OTROS; UNO DE R5 Y R6 ES H, METILO Y EL OTRO ES H, ALQUILO C1-C6, ALQUENILO C2-C6, FENILO, ENTRE OTROS; R10 Y R11 SON H, METILO, HALO, NO2. SON COMPUESTOS PREFERIDOS ACIDO 7-FLUORO-6-(4-YODO-2-METIL-FENILAMINO)-1H-BENZOIMIDAZOL-5-CARBOXILICO, ACIDO 7-FLUORO-6-(4-YODO-2-METIL-FENILAMINO)-1H-BENZOIMIDAZOL-5-CARBOXILICO, ENTRE OTROS. LA COMPOSICION PUEDE SER UTIL PARA EL TRATAMIENTO DEL DOLOR CRONICO, NEUROPATICOIT REFERS TO THE USE OF A COMPOSITION INCLUDING A MEK KINASE INHIBITOR OF FORMULA I, WHERE: W IS OR1, NR2OR1, NRARB, NR2NRARB, O (CH2) 2-4NRARB, NR2 (CH2) 2-4, R1 IS H, C1-C8 ALKYL, C3-C8 ALKENYL, C3-C8 ALKYL, C3-C8 CYCLOALKYL, PHENYL, C1-C4 PHENYL (ALKYL). PHENYLALKENYL C3-C4, AMONG OTHERS; R2 IS H, C1-C4 ALKYL, PHENYL, C3-C6 CYCLOALKYL, C3-C6 HETEROCYCLE; RA IS H, C1-C6 ALKYL, C3-C8 ALKENYL, C3-C8 ALKYNYL, C3-C8 CYCLOALKYL, PHENYL, (C3-C8 CYCLOALKYL) C1-C4 ALKYL, AMONG OTHERS; RB IS H, C1-C8 ALKYL, C3-C8 CYCLOALKYL, PHENYL; Q IS THE GROUP a, AMONG OTHERS; R3 IS H, F; R4 IS HALO, NO2, SO2NRo (CH2) 2-4NREFE, AMONG OTHERS; T IS C1-C8 ALKYL, C3-C8 CYCLOALKYL, AMONG OTHERS; Z IS GROUP iv, AMONG OTHERS; ONE OF R5 AND R6 IS H, METHYL AND THE OTHER IS H, C1-C6 ALKYL, C2-C6 ALKENYL, PHENYL, AMONG OTHERS; R10 AND R11 ARE H, METHYL, HALO, NO2. PREFERRED COMPOUNDS ARE 7-FLUORO-6- (4-IODO-2-METHYL-PHENYLAMINE) -1H-BENZOIMIDAZOL-5-CARBOXYL ACID, 7-FLUORO-6- (4-IODO-2-METHYL-PHENYLAMINE) -1H -BENZOIMIDAZOLE-5-CARBOXYLICO, AMONG OTHERS. THE COMPOSITION MAY BE USEFUL FOR THE TREATMENT OF CHRONIC, NEUROPATHIC PAIN
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14441899P | 1999-07-16 | 1999-07-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20010546A1 true PE20010546A1 (en) | 2001-06-04 |
Family
ID=22508500
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2000000704A PE20010546A1 (en) | 1999-07-16 | 2000-07-14 | USE OF A COMPOSITION OF BENZOHETERO CYCLES AS MEK INHIBITORS TO TREAT CHRONIC PAIN |
Country Status (13)
| Country | Link |
|---|---|
| EP (1) | EP1202731A2 (en) |
| JP (1) | JP2003504398A (en) |
| KR (1) | KR20020015376A (en) |
| CN (1) | CN1358094A (en) |
| AU (1) | AU6068600A (en) |
| CA (1) | CA2377092A1 (en) |
| CO (1) | CO5190704A1 (en) |
| HU (1) | HUP0202319A3 (en) |
| IL (1) | IL147150A0 (en) |
| PE (1) | PE20010546A1 (en) |
| PL (1) | PL352835A1 (en) |
| WO (1) | WO2001005390A2 (en) |
| ZA (1) | ZA200109906B (en) |
Families Citing this family (69)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7018999B2 (en) | 2001-05-16 | 2006-03-28 | Cephalon, Inc. | Methods for the treatment and prevention of pain |
| AU2002310441A1 (en) * | 2001-06-14 | 2003-01-02 | The Regents Of The University Of California | A novel signaling pathway for the production of inflammatory pain and neuropathy |
| WO2003077914A1 (en) * | 2002-03-13 | 2003-09-25 | Array Biopharma, Inc | N3 alkylated benzimidazole derivatives as mek inhibitors |
| EP1482944A4 (en) * | 2002-03-13 | 2006-04-19 | 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 |
| GB0213383D0 (en) * | 2002-06-11 | 2002-07-24 | Cambridge Biotechnology Ltd | Therapeutic conditions |
| US20050004186A1 (en) * | 2002-12-20 | 2005-01-06 | Pfizer Inc | MEK inhibiting compounds |
| 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 |
| JP5042626B2 (en) | 2003-09-22 | 2012-10-03 | エス*バイオ プライベート リミティッド | Benzimidazole derivatives: production and pharmaceutical applications |
| AU2004293018B2 (en) | 2003-11-19 | 2010-02-18 | Array Biopharma Inc. | Heterocyclic 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 |
| US7732616B2 (en) | 2003-11-19 | 2010-06-08 | Array Biopharma Inc. | Dihydropyridine and dihydropyridazine derivatives as inhibitors of MEK and methods of use thereof |
| CA2546754A1 (en) | 2003-11-21 | 2005-06-09 | Array Biopharma Inc. | Akt protein kinase inhibitors |
| ES2378760T3 (en) | 2005-05-18 | 2012-04-17 | Array Biopharma, Inc. | MEK heterocyclic inhibitors and methods of use thereof |
| WO2007002157A2 (en) | 2005-06-23 | 2007-01-04 | Array Biopharma Inc. | Process for preparing benzimidazole compounds |
| NZ567140A (en) | 2005-10-07 | 2011-09-30 | Exelixis Inc | Azetidines as MEK inhibitors for the treatment of proliferative diseases |
| ATE532789T1 (en) | 2006-07-06 | 2011-11-15 | Array Biopharma Inc | DIHYDROTHIENOPYRIMIDINES AS ACT 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 |
| KR20150041164A (en) | 2006-07-06 | 2015-04-15 | 어레이 바이오파마 인크. | Cyclopenta〔d〕pyrimidines as akt protein kinase inhibitors |
| 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 |
| US8846683B2 (en) | 2007-07-05 | 2014-09-30 | Array Biopharma, Inc. | Pyrimidyl cyclopentanes as Akt protein kinase inhibitors |
| KR101624361B1 (en) | 2007-07-05 | 2016-05-25 | 어레이 바이오파마 인크. | 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 |
| AR067413A1 (en) | 2007-07-05 | 2009-10-07 | Genentech Inc | HETEROCICLICAL COMPOUNDS CONTAINING CYCLOPENTA [D] PYRIMIDINE INHIBITORS OF AKT PROTEINQUINASES, PHARMACEUTICAL COMPOSITIONS CONTAINING THEM, METHOD OF PREPARATION AND USE OF THE SAME FOR THE TREATMENT OF HYPER-TROLIFERATIVE TIPERIFERATIVE AS-ISSUES |
| JP5421925B2 (en) | 2007-12-19 | 2014-02-19 | ジェネンテック, インコーポレイテッド | 5-Anilinoimidazopyridine and method of use |
| US8293763B2 (en) | 2007-12-19 | 2012-10-23 | Genentech, Inc. | 8-anilinoimidazopyridines and their use as anti-cancer and/or anti-inflammatory agents |
| EP2220092B1 (en) | 2007-12-21 | 2012-06-06 | Genentech, Inc. | Azaindolizines and methods of use |
| US8853216B2 (en) | 2008-01-09 | 2014-10-07 | Array Biopharma, Inc. | Hydroxylated pyrimidyl cyclopentane as AKT protein kinase inhibitor |
| AU2009204025B2 (en) | 2008-01-09 | 2014-02-20 | Array Biopharma Inc. | Hydroxylated pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
| BRPI0910200A2 (en) | 2008-07-01 | 2015-09-29 | Genentech Inc | compound, pharmaceutical composition, method of inhibiting abnormal cell growth or treating a hyperproliferative disorder in a mammal and method of treating an inflammatory disease in a mammal |
| CA2742945A1 (en) | 2008-11-10 | 2010-05-14 | Bayer Schering Pharma Aktiengesellschaft | Substituted sulphonamido phenoxybenzamides |
| 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 |
| WO2011047788A1 (en) | 2009-10-21 | 2011-04-28 | Bayer Schering Pharma Aktiengesellschaft | Substituted benzosulphonamides |
| CN103282351A (en) | 2010-10-29 | 2013-09-04 | 拜耳知识产权有限责任公司 | Substituted phenoxypyridines |
| EP2694072B2 (en) | 2011-04-01 | 2024-08-07 | Genentech, Inc. | Combination of akt inhibitor compound and abiraterone for use in therapeutic treatments |
| CN103841976A (en) | 2011-04-01 | 2014-06-04 | 基因泰克公司 | Combinations of AKT and MEK inhibitor compounds and methods of use thereof |
| ES2396764B1 (en) | 2011-11-02 | 2013-12-19 | Universidad Autónoma de Madrid | P38 INHIBITING DRUGS AND APPLICATIONS. |
| JP5977837B2 (en) | 2011-12-21 | 2016-08-24 | ノヴィラ・セラピューティクス・インコーポレイテッド | Hepatitis B antiviral agent |
| CN103204822B (en) | 2012-01-17 | 2014-12-03 | 上海科州药物研发有限公司 | Benzoxazole compounds as protein kinase inhibitors, and preparation method and application thereof |
| NZ743463A (en) | 2012-08-28 | 2019-09-27 | Janssen Sciences Ireland Uc | Sulfamoyl-arylamides and the use thereof as medicaments for the treatment of hepatitis b |
| NZ706723A (en) | 2012-10-12 | 2018-07-27 | Exelixis Inc | Novel process for making compounds for use in the treatment of cancer |
| FI3702351T3 (en) * | 2012-10-19 | 2024-01-24 | Array Biopharma Inc | Formulation comprising a mek inhibitor |
| MX366123B (en) | 2013-02-28 | 2019-06-27 | Janssen Sciences Ireland Uc | Sulfamoyl-arylamides and the use thereof as medicaments for the treatment of hepatitis b. |
| US8993771B2 (en) | 2013-03-12 | 2015-03-31 | Novira Therapeutics, Inc. | Hepatitis B antiviral agents |
| EA027068B1 (en) | 2013-04-03 | 2017-06-30 | Янссен Сайенсиз Айрлэнд Юси | N-phenyl-carboxamide derivatives and the use thereof as medicaments for the treatment of hepatitis b |
| JO3603B1 (en) | 2013-05-17 | 2020-07-05 | Janssen Sciences Ireland Uc | Sulfamoyl pyrolamide derivatives and their use as medicines to treat hepatitis B |
| PL3024819T3 (en) | 2013-07-25 | 2018-08-31 | Janssen Sciences Ireland Uc | Glyoxamide substituted pyrrolamide derivatives and the use thereof as medicaments for the treatment of hepatitis b |
| EP3060547B1 (en) | 2013-10-23 | 2017-10-11 | Janssen Sciences Ireland UC | Carboxamide derivatives and the use thereof as medicaments for the treatment of hepatitis b |
| CN104774188B (en) * | 2014-01-15 | 2019-10-11 | 江苏恒瑞医药股份有限公司 | Benzoheterocycles or benzoheteroaromatic derivatives, their preparation method and their application in medicine |
| US9169212B2 (en) | 2014-01-16 | 2015-10-27 | Novira Therapeutics, Inc. | Azepane derivatives and methods of treating hepatitis B infections |
| US10392349B2 (en) | 2014-01-16 | 2019-08-27 | Novira Therapeutics, Inc. | Azepane derivatives and methods of treating hepatitis B infections |
| US9181288B2 (en) | 2014-01-16 | 2015-11-10 | Novira Therapeutics, Inc. | Azepane derivatives and methods of treating hepatitis B infections |
| US20150216938A1 (en) | 2014-02-05 | 2015-08-06 | Novira Therapeutics Inc. | Combination therapy for treatment of hbv infections |
| CN110483484A (en) | 2014-02-06 | 2019-11-22 | 爱尔兰詹森科学公司 | Sulfamoyl pyrrole amides derivative and its purposes for being used to treat hepatitis B as drug |
| US9400280B2 (en) | 2014-03-27 | 2016-07-26 | Novira Therapeutics, Inc. | Piperidine derivatives and methods of treating hepatitis B infections |
| CN107847762A (en) | 2015-03-19 | 2018-03-27 | 诺维拉治疗公司 | Azacyclooctane and azacyclononane derivatives and methods of treating hepatitis B infection |
| US10875876B2 (en) | 2015-07-02 | 2020-12-29 | Janssen Sciences Ireland Uc | Cyclized sulfamoylarylamide derivatives and the use thereof as medicaments for the treatment of hepatitis B |
| HK1259410A1 (en) | 2015-09-29 | 2019-11-29 | 诺维拉治疗公司 | Crystalline forms of a hepatitis b antiviral agent |
| CN109640980A (en) | 2016-04-15 | 2019-04-16 | 诺维拉治疗公司 | Combination and method comprising shell assembly inhibitor |
| AR108257A1 (en) | 2016-05-02 | 2018-08-01 | Mei Pharma Inc | POLYMORPHIC FORMS OF 3- [2-BUTIL-1- (2-DIETILAMINO-ETIL) -1H-BENCIMIDAZOL-5-IL] -N-HYDROXY-ACRYLAMIDE AND USES OF THE SAME |
| CA3090125A1 (en) | 2018-03-14 | 2019-09-19 | Janssen Sciences Ireland Unlimited Company | Capsid assembly modulator dosing regimen |
| JP2022521081A (en) | 2019-02-22 | 2022-04-05 | ヤンセン・サイエンシズ・アイルランド・アンリミテッド・カンパニー | Amide derivatives useful in the treatment of HBV infections or HBV-induced diseases |
| MA55879A (en) | 2019-05-06 | 2022-03-16 | Janssen Sciences Ireland Unlimited Co | AMIDE DERIVATIVES USEFUL IN THE TREATMENT OF HEPATITIS B VIRUS INFECTION OR DISEASES INDUCED BY HEPATITIS B VIRUS |
| CN110981819B (en) * | 2019-12-24 | 2022-07-01 | 广西师范大学 | Quinoxaline signal channel inhibitor and preparation method and application thereof |
| CN114788867A (en) * | 2022-04-24 | 2022-07-26 | 天津医科大学总医院 | Application of Map2k1 as a therapeutic target for post-chemotherapy neuralgia |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6251943B1 (en) * | 1997-02-28 | 2001-06-26 | Warner-Lambert Company | Method of treating or preventing septic shock by administering a MEK inhibitor |
| HK1041697A1 (en) * | 1999-01-13 | 2002-07-19 | 沃尼尔‧朗伯公司 | Benzoheterocycles and their use as mek inhibitors |
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2000
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- 2000-07-05 IL IL14715000A patent/IL147150A0/en unknown
- 2000-07-05 CN CN00809478A patent/CN1358094A/en active Pending
- 2000-07-05 EP EP00947013A patent/EP1202731A2/en not_active Withdrawn
- 2000-07-05 HU HU0202319A patent/HUP0202319A3/en unknown
- 2000-07-05 JP JP2001510447A patent/JP2003504398A/en active Pending
- 2000-07-05 WO PCT/US2000/018345 patent/WO2001005390A2/en not_active Ceased
- 2000-07-05 AU AU60686/00A patent/AU6068600A/en not_active Abandoned
- 2000-07-05 PL PL00352835A patent/PL352835A1/en unknown
- 2000-07-05 KR KR1020027000589A patent/KR20020015376A/en not_active Withdrawn
- 2000-07-14 PE PE2000000704A patent/PE20010546A1/en not_active Application Discontinuation
- 2000-07-14 CO CO00053306A patent/CO5190704A1/en not_active Application Discontinuation
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| CA2377092A1 (en) | 2001-01-25 |
| EP1202731A2 (en) | 2002-05-08 |
| HUP0202319A2 (en) | 2002-10-28 |
| PL352835A1 (en) | 2003-09-08 |
| HUP0202319A3 (en) | 2004-12-28 |
| IL147150A0 (en) | 2002-08-14 |
| CN1358094A (en) | 2002-07-10 |
| AU6068600A (en) | 2001-02-05 |
| JP2003504398A (en) | 2003-02-04 |
| WO2001005390A2 (en) | 2001-01-25 |
| WO2001005390A3 (en) | 2001-05-17 |
| CO5190704A1 (en) | 2002-08-29 |
| ZA200109906B (en) | 2003-05-28 |
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