PE20040189A1 - Pirimidina y piridina biciclicos como inhibidores de p38 quinasa - Google Patents
Pirimidina y piridina biciclicos como inhibidores de p38 quinasaInfo
- Publication number
- PE20040189A1 PE20040189A1 PE2003000209A PE2003000209A PE20040189A1 PE 20040189 A1 PE20040189 A1 PE 20040189A1 PE 2003000209 A PE2003000209 A PE 2003000209A PE 2003000209 A PE2003000209 A PE 2003000209A PE 20040189 A1 PE20040189 A1 PE 20040189A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- pyrimidine
- ilamino
- tetrahydropyran
- aryl
- Prior art date
Links
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 title abstract 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 title abstract 3
- 229940043355 kinase inhibitor Drugs 0.000 title 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 title 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 title 1
- 208000011580 syndromic disease Diseases 0.000 abstract 3
- -1 2-CHLOROBENZOYL Chemical class 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 210000000936 intestine Anatomy 0.000 abstract 2
- 208000011231 Crohn disease Diseases 0.000 abstract 1
- 206010003246 arthritis Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000004064 dysfunction Effects 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 108010061159 protein kinase P Proteins 0.000 abstract 1
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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
-
- 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
-
- 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
- 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
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- 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
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Neurosurgery (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
SE REFIERE A DERIVADOS DE PIRIMIDINA Y PIRIDINA AMINO-BICICLICOS 2-SUSTITUIDOS DE FORMULA I DONDE A ES N O CH; R1 ES H, ALQUILO O ARILALQUILO; R2 ES ALQUILO, HIDROXIALQUILO, (R")2NCO-ALQUILENO, CICLOALQUILO, HETEROCICLILO, ARILO, HETEROARILO O HETEROALQUILO; R" ES H O ALQUILO; X ES O, NR3 O S, DONDE R3 ES H, ALQUILO O ARILO; Y ES ENLACE, O, NR', C(=O), CH(R'), CH(OR'), O S(O)n, DONDE n ES 0,1 O 2; R' ES H O ALQUILO; R ES ARILO O HETEROARILO. SON COMPUESTOS PREFERIDOS 2-(TETRAHIDROPIRAN-4-ILAMINO)-6-(2-CLOROBENZOIL)TIENO[2,3-d]PIRIMIDINA; 2-(TETRAHIDROPIRAN-4-ILAMINO)-6-(2-FLUOROBENZOIL)TIENO[2,3-d]PIRIMIDINA; 2-(TETRAHIDROPIRAN-4-ILAMINO)-6-(2-METOXIBENZOIL)-7-METIL-PIRROL[2,3-d]PIRIMIDINA; ENTRE OTROS.TAMBIEN SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION. LOS COMPUESTOS SON INHIBIDORES DE LA PROTEINQUINASA p 38 Y PUEDEN SER UTILES PARA EL TRATAMIENTO DE UN TRASTORNO MEDIADO POR PROTEINQUINASA p38 TAL COMO ARTRITIS, ENFERMEDAD DE CROHN, ALZHEIMER, SINDORME DE INTESTINO IRRITABLE, SINDROME DE DISTRESS RESPIRATORIO DEL ADULTO Y ENFERMEDAD OBSTRUCTIVA PULMONAR CRONICA
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US36237302P | 2002-03-07 | 2002-03-07 | |
| US43050802P | 2002-12-03 | 2002-12-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20040189A1 true PE20040189A1 (es) | 2004-05-01 |
Family
ID=27791709
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2003000209A PE20040189A1 (es) | 2002-03-07 | 2003-03-04 | Pirimidina y piridina biciclicos como inhibidores de p38 quinasa |
Country Status (19)
| Country | Link |
|---|---|
| US (3) | US7091347B2 (es) |
| EP (1) | EP1485390B1 (es) |
| JP (1) | JP4187657B2 (es) |
| KR (1) | KR100714519B1 (es) |
| CN (1) | CN100386328C (es) |
| AR (1) | AR038864A1 (es) |
| AT (1) | ATE410429T1 (es) |
| AU (1) | AU2003210388B2 (es) |
| BR (1) | BR0308232A (es) |
| CA (1) | CA2477721A1 (es) |
| DE (1) | DE60323946D1 (es) |
| ES (1) | ES2314224T3 (es) |
| MX (1) | MXPA04008592A (es) |
| PA (1) | PA8568401A1 (es) |
| PE (1) | PE20040189A1 (es) |
| PL (1) | PL372886A1 (es) |
| RU (1) | RU2301233C2 (es) |
| TW (1) | TW200306194A (es) |
| WO (1) | WO2003074530A1 (es) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE60304718T2 (de) | 2002-08-06 | 2007-04-26 | Astrazeneca Ab | Kondensierte pyridine und pyrimidine mit tie2 (tek) aktivität |
| US7319102B1 (en) | 2003-12-09 | 2008-01-15 | The Procter & Gamble Company | Pyrrolo[2,3-d]pyrimidine cytokine inhibitors |
| AU2004309420B2 (en) * | 2003-12-23 | 2008-10-30 | Novartis Ag | Bicyclic heterocyclic p-38 kinase inhibitors |
| CN1918158B (zh) | 2004-02-14 | 2011-03-02 | Irm责任有限公司 | 作为蛋白激酶抑制剂的化合物和组合物 |
| RU2006134022A (ru) | 2004-02-27 | 2008-04-10 | Ф.Хоффманн-Ля Рош Аг (Ch) | Производные индазола и содержащие их фармацевтические композиции |
| WO2005085249A1 (en) * | 2004-02-27 | 2005-09-15 | F. Hoffmann-La Roche Ag | Fused derivatives of pyrazole |
| CN1934111A (zh) * | 2004-02-27 | 2007-03-21 | 霍夫曼-拉罗奇有限公司 | 杂芳基稠合的吡唑并衍生物 |
| WO2005107760A1 (en) * | 2004-04-30 | 2005-11-17 | Irm Llc | Compounds and compositions as inducers of keratinocyte differentiation |
| JP5118972B2 (ja) | 2004-10-29 | 2013-01-16 | テイボテク・フアーマシユーチカルズ | Hiv阻害性二環式ピリミジン誘導体 |
| GB0427604D0 (en) * | 2004-12-16 | 2005-01-19 | Novartis Ag | Organic compounds |
| KR101011956B1 (ko) * | 2005-08-25 | 2011-01-31 | 에프. 호프만-라 로슈 아게 | P38 mαp 키나아제 저해제 및 이의 사용 방법 |
| WO2007124181A2 (en) * | 2006-04-21 | 2007-11-01 | Amgen Inc. | Thieno-[2,3-d]pyrimidine and thieno-pyridazine compounds and methods of use |
| TWI398252B (zh) * | 2006-05-26 | 2013-06-11 | 諾華公司 | 吡咯并嘧啶化合物及其用途 |
| RU2540074C2 (ru) * | 2007-06-21 | 2015-01-27 | Кара Терапеутикс, Инк | Производные имидазопиразина или имидазодиазепина, активные в отношении рецептора св2 |
| RU2345996C1 (ru) * | 2007-07-17 | 2009-02-10 | Андрей Александрович Иващенко | Аннелированные азагетероциклические амиды, включающие пиримидиновый фрагмент, способ их получения и применения |
| RU2341527C1 (ru) * | 2007-07-17 | 2008-12-20 | Общество С Ограниченной Ответственностью "Исследовательский Институт Химического Разнообразия" | Аннелированные азагетероциклы, включающие пиримидиновый фрагмент, способ их получения и ингибиторы pi3k киназ |
| PE20091485A1 (es) | 2008-02-06 | 2009-10-26 | Novartis Ag | DERIVADOS DE PIRROLO-[2,3-d]-PIRIMIDINA COMO INHIBIDORES DE CINASAS |
| TW201002713A (en) | 2008-04-09 | 2010-01-16 | Organon Nv | Pyrrolo[2,3-d]pyrimidin-2-yl-amine derivatives as PKC-theta inhibitors |
| ES2522346T3 (es) | 2008-08-22 | 2014-11-14 | Novartis Ag | Compuestos de pirrolopirimidina como inhibidores de CDK |
| UY33227A (es) | 2010-02-19 | 2011-09-30 | Novartis Ag | Compuestos de pirrolopirimidina como inhibidores de la cdk4/6 |
| GB201104267D0 (en) | 2011-03-14 | 2011-04-27 | Cancer Rec Tech Ltd | Pyrrolopyridineamino derivatives |
| US20130102601A1 (en) * | 2011-10-21 | 2013-04-25 | F. Hoffmann-La Roche Ltd | Pyrimidin-4-one derivatives and their use in the treatment, amelioration or prevention of a viral disease |
| GB201216017D0 (en) | 2012-09-07 | 2012-10-24 | Cancer Rec Tech Ltd | Inhibitor compounds |
| GB201216018D0 (en) | 2012-09-07 | 2012-10-24 | Cancer Rec Tech Ltd | Pharmacologically active compounds |
| CN103254194B (zh) * | 2013-05-17 | 2015-07-08 | 浙江师范大学 | 一种8-硫杂黄嘌呤化合物的制备方法 |
| CN105828822B (zh) | 2013-08-14 | 2019-10-18 | 诺华股份有限公司 | 用于治疗癌症的组合疗法 |
| GB201403536D0 (en) | 2014-02-28 | 2014-04-16 | Cancer Rec Tech Ltd | Inhibitor compounds |
| US10259816B2 (en) * | 2015-04-24 | 2019-04-16 | Guangzhou Maxinovel Pharmaceuticals Co., Ltd. | Condensed-ring pyrimidylamino derivative, preparation method therefor, and intermediate, pharmaceutical composition and applications thereof |
| US20190060286A1 (en) | 2016-02-29 | 2019-02-28 | University Of Florida Research Foundation, Incorpo | Chemotherapeutic Methods |
| GB201709840D0 (en) | 2017-06-20 | 2017-08-02 | Inst Of Cancer Research: Royal Cancer Hospital | Methods and medical uses |
| BR112020006677A2 (pt) | 2017-10-05 | 2020-10-06 | Fulcrum Therapeutics, Inc. | uso de inibidores p38 para reduzir a expressão de dux4 |
| US10342786B2 (en) | 2017-10-05 | 2019-07-09 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
| SG11202004971YA (en) * | 2017-12-21 | 2020-06-29 | Gliapharm Sa | Compositions and methods of treatment for neurological disorders comprising motor neuron diseases |
| US20200339591A1 (en) * | 2017-12-21 | 2020-10-29 | Gliapharm Sa | Compositions and methods of treatment for neurological disorders comprising a dementia |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4835157A (en) * | 1988-03-15 | 1989-05-30 | Ortho Pharmaceutical Corporation | Thieno- and furopyrimidine-2,4-dione piperidine derivatives as serotonin antagonists and alpha adrenergic blocking agents |
| WO1995029897A1 (en) | 1994-04-29 | 1995-11-09 | G.D. Searle & Co. | METHOD OF USING (H+/K+) ATPase INHIBITORS AS ANTIVIRAL AGENTS |
| US5834469A (en) | 1994-06-09 | 1998-11-10 | Smithkline Beecham Corporation | Endothelin receptor antagonists |
| JPH10510510A (ja) | 1994-06-09 | 1998-10-13 | スミスクライン・ビーチャム・コーポレイション | エンドセリン受容体拮抗物質 |
| JP3290666B2 (ja) * | 1995-06-07 | 2002-06-10 | ファイザー・インコーポレーテッド | 複素環式の縮合環ピリミジン誘導体 |
| JP2002514162A (ja) | 1996-07-08 | 2002-05-14 | デュポン ファーマシューティカルズ カンパニー | Xa因子阻害薬およびトロンビン阻害薬としてのアミジノインドール類、アミジノアゾール類、およびそれらの類似体 |
| JP2001506230A (ja) * | 1996-08-09 | 2001-05-15 | スミスクライン・ビーチャム・コーポレイション | 新規ピペラジン含有化合物 |
| WO1998008382A1 (en) | 1996-08-30 | 1998-03-05 | Eli Lilly And Company | Nonclassical pyrrolo[2,3-d]pyrimidine antifolates |
| BR9812944A (pt) * | 1997-10-20 | 2000-08-08 | Hoffmann La Roche | Inibidores bicìclicos da cinase |
| US6232320B1 (en) * | 1998-06-04 | 2001-05-15 | Abbott Laboratories | Cell adhesion-inhibiting antiinflammatory compounds |
| CA2348740A1 (en) | 1998-12-23 | 2000-07-06 | Ruth R. Wexler | Thrombin or factor xa inhibitors |
| CZ27399A3 (cs) | 1999-01-26 | 2000-08-16 | Ústav Experimentální Botaniky Av Čr | Substituované dusíkaté heterocyklické deriváty, způsob jejich přípravy, tyto deriváty pro použití jako léčiva, farmaceutická kompozice a kombinovaný farmaceutický přípravek tyto deriváty obsahující a použití těchto derivátů pro výrobu léčiv |
| IL150594A0 (en) | 2000-01-07 | 2003-02-12 | Ustav Ex Botan Adademie Ved Ce | Purine derivatives, process for their preparation and use |
| HK1052705B (en) * | 2000-08-14 | 2006-09-29 | Ortho-Mcneil Pharmaceutical, Inc. | Substituted pyrazole |
| AU2002333524A1 (en) * | 2001-09-11 | 2003-03-24 | Glaxosmithkline K.K. | Furo-and thienopyrimidine derivatives as angiogenesis inhibitors |
-
2003
- 2003-02-28 ES ES03743361T patent/ES2314224T3/es not_active Expired - Lifetime
- 2003-02-28 RU RU2004129768/04A patent/RU2301233C2/ru active
- 2003-02-28 AT AT03743361T patent/ATE410429T1/de not_active IP Right Cessation
- 2003-02-28 CN CNB038054191A patent/CN100386328C/zh not_active Expired - Fee Related
- 2003-02-28 BR BR0308232-6A patent/BR0308232A/pt not_active IP Right Cessation
- 2003-02-28 PL PL03372886A patent/PL372886A1/xx not_active Application Discontinuation
- 2003-02-28 KR KR1020047013677A patent/KR100714519B1/ko not_active Expired - Fee Related
- 2003-02-28 JP JP2003572998A patent/JP4187657B2/ja not_active Expired - Fee Related
- 2003-02-28 AU AU2003210388A patent/AU2003210388B2/en not_active Ceased
- 2003-02-28 EP EP03743361A patent/EP1485390B1/en not_active Expired - Lifetime
- 2003-02-28 WO PCT/EP2003/002090 patent/WO2003074530A1/en not_active Ceased
- 2003-02-28 CA CA002477721A patent/CA2477721A1/en not_active Abandoned
- 2003-02-28 MX MXPA04008592A patent/MXPA04008592A/es active IP Right Grant
- 2003-02-28 DE DE60323946T patent/DE60323946D1/de not_active Expired - Fee Related
- 2003-03-04 TW TW092104537A patent/TW200306194A/zh unknown
- 2003-03-04 AR ARP030100718A patent/AR038864A1/es not_active Application Discontinuation
- 2003-03-04 PE PE2003000209A patent/PE20040189A1/es not_active Application Discontinuation
- 2003-03-06 US US10/383,392 patent/US7091347B2/en not_active Expired - Fee Related
- 2003-03-06 PA PA20038568401A patent/PA8568401A1/es unknown
-
2005
- 2005-08-12 US US11/202,611 patent/US7449472B2/en not_active Expired - Fee Related
- 2005-11-30 US US11/292,217 patent/US7439247B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20050288312A1 (en) | 2005-12-29 |
| TW200306194A (en) | 2003-11-16 |
| KR20040091084A (ko) | 2004-10-27 |
| US7439247B2 (en) | 2008-10-21 |
| WO2003074530A1 (en) | 2003-09-12 |
| US7449472B2 (en) | 2008-11-11 |
| AR038864A1 (es) | 2005-02-02 |
| JP2005526057A (ja) | 2005-09-02 |
| US7091347B2 (en) | 2006-08-15 |
| US20030207900A1 (en) | 2003-11-06 |
| ES2314224T3 (es) | 2009-03-16 |
| CN1639168A (zh) | 2005-07-13 |
| KR100714519B1 (ko) | 2007-05-07 |
| PL372886A1 (en) | 2005-08-08 |
| RU2004129768A (ru) | 2005-08-27 |
| RU2301233C2 (ru) | 2007-06-20 |
| DE60323946D1 (de) | 2008-11-20 |
| CN100386328C (zh) | 2008-05-07 |
| EP1485390B1 (en) | 2008-10-08 |
| ATE410429T1 (de) | 2008-10-15 |
| MXPA04008592A (es) | 2004-12-06 |
| PA8568401A1 (es) | 2003-12-10 |
| AU2003210388B2 (en) | 2007-05-17 |
| US20060084803A1 (en) | 2006-04-20 |
| CA2477721A1 (en) | 2003-09-12 |
| AU2003210388A1 (en) | 2003-09-16 |
| EP1485390A1 (en) | 2004-12-15 |
| JP4187657B2 (ja) | 2008-11-26 |
| BR0308232A (pt) | 2004-12-28 |
Similar Documents
| Publication | Publication Date | Title |
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