PE20080527A1 - Derivado de pirimidina como inhibidor de la fosfatidilinositol 3-quinasa (pi3k) - Google Patents
Derivado de pirimidina como inhibidor de la fosfatidilinositol 3-quinasa (pi3k)Info
- Publication number
- PE20080527A1 PE20080527A1 PE2007001059A PE2007001059A PE20080527A1 PE 20080527 A1 PE20080527 A1 PE 20080527A1 PE 2007001059 A PE2007001059 A PE 2007001059A PE 2007001059 A PE2007001059 A PE 2007001059A PE 20080527 A1 PE20080527 A1 PE 20080527A1
- Authority
- PE
- Peru
- Prior art keywords
- pi3k
- phosphatidylinositol
- kinase
- pyridin
- dihydro
- Prior art date
Links
- 108091007960 PI3Ks Proteins 0.000 title abstract 4
- 102000003993 Phosphatidylinositol 3-kinases Human genes 0.000 title abstract 4
- 108090000430 Phosphatidylinositol 3-kinases Proteins 0.000 title abstract 4
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical class C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical group 0.000 abstract 3
- JIQNWFBLYKVZFY-UHFFFAOYSA-N methoxycyclohexatriene Chemical class COC1=C[C]=CC=C1 JIQNWFBLYKVZFY-UHFFFAOYSA-N 0.000 abstract 3
- -1 PYRIMIDINE DERIVATIVE COMPOUNDS Chemical class 0.000 abstract 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000002062 proliferating effect Effects 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 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
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (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)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE PIRIMIDINA DE FORMULA (I) DONDE X ES UN ENLACE SIMPLE, -CO-, -SO2-, -CS- O -CH2-; Y ES UN ENLACE SIMPLE, BENCENO, PIRIDINA, PIRAZOL, TIAZOL, ENTRE OTROS; Z ES H, ALQUILO(C1-C6), ETINILO, HALOGENO, ENTRE OTROS; m ES 1 O 2; R1 ES UN COMPUESTO DE FORMULA (R1a), (R1b1), (R1c1), ENTRE OTROS, DONDE T ES ALQUILO(C1-C6), HALOGENO, O-HALOGENOALQUILO(C1-C6), CN, ENTRE OTROS; n ES DE 0 A 5. SON COMPUESTOS PREFERIDOS: 4-(3-METOXI-FENIL)-2-MORFOLIN-4-IL-7-PIRIDIN-4-IL-6,7-DIHIDRO-5H-PIRROLO[2,3-d]PIRIMIDINA, 4-(3-METOXI-FENIL)-2-MORFOLIN-4-IL-7-PIRIDIN-3-IL-6,7-DIHIDRO-5H-PIRROLO[2,3-d]PIRIMIDINA, 5-[4-(3-METOXI-FENIL)-2-MORFOLIN-4-IL-5,6-DIHIDRO-PIRROLO[2,3-d]PIRIMIDIN-7-IL]-PIRIDIN-2-OL, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA FOSFATIDILINOSITOL 3-QUINASA (PI3K) SIENDO UTILES EN EL TRATAMIENTO DE ENFERMEDADES PROLIFERATIVAS TALES COMO EL CANCER
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2006216108 | 2006-08-08 | ||
| JP2007118631 | 2007-04-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20080527A1 true PE20080527A1 (es) | 2008-07-09 |
Family
ID=39032956
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2007001059A PE20080527A1 (es) | 2006-08-08 | 2007-08-08 | Derivado de pirimidina como inhibidor de la fosfatidilinositol 3-quinasa (pi3k) |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US8022205B2 (es) |
| EP (1) | EP2050749B1 (es) |
| JP (1) | JP4450857B2 (es) |
| KR (1) | KR101435692B1 (es) |
| AR (1) | AR062292A1 (es) |
| AU (1) | AU2007282535B9 (es) |
| BR (1) | BRPI0714908B8 (es) |
| CA (1) | CA2659604C (es) |
| CL (1) | CL2007002316A1 (es) |
| CY (1) | CY1119882T1 (es) |
| DK (1) | DK2050749T3 (es) |
| ES (1) | ES2657635T3 (es) |
| HU (1) | HUE035116T2 (es) |
| IL (1) | IL196601A (es) |
| LT (1) | LT2050749T (es) |
| MX (1) | MX2009001451A (es) |
| MY (1) | MY145385A (es) |
| NO (1) | NO342978B1 (es) |
| NZ (1) | NZ575274A (es) |
| PE (1) | PE20080527A1 (es) |
| PL (1) | PL2050749T3 (es) |
| PT (1) | PT2050749T (es) |
| RU (1) | RU2448109C2 (es) |
| SI (1) | SI2050749T1 (es) |
| TW (1) | TWI394758B (es) |
| WO (1) | WO2008018426A1 (es) |
Families Citing this family (69)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101512284B1 (ko) * | 2006-12-21 | 2015-04-15 | 네르비아노 메디칼 사이언시스 에스.알.엘. | 치환된 피라졸로-퀴나졸린 유도체, 이의 제조방법, 및 키나제 억제제로서의 이의 용도 |
| CL2009000241A1 (es) * | 2008-02-07 | 2010-09-03 | Chugai Pharmaceutical Co Ltd | Compuestos derivados de 5-(2-morfolin-4-il-7h-pirrolo[2,3-d]pirimidin-4-il)pirimidin-2-ilamina; proceso de preparacion; composicion farmaceutica; y uso de los compuestos para tratar o prevenir una enfermedad proliferativa tal como el cancer. |
| US8822513B2 (en) | 2010-03-01 | 2014-09-02 | Gtx, Inc. | Compounds for treatment of cancer |
| PL2303021T3 (pl) * | 2008-06-16 | 2019-10-31 | Univ Tennessee Res Found | Związki do leczenia nowotworu |
| US9029408B2 (en) | 2008-06-16 | 2015-05-12 | Gtx, Inc. | Compounds for treatment of cancer |
| US9447049B2 (en) | 2010-03-01 | 2016-09-20 | University Of Tennessee Research Foundation | Compounds for treatment of cancer |
| JP2011527342A (ja) * | 2008-07-07 | 2011-10-27 | エックスカバリー ホールディング カンパニー エルエルシー | Pi3kアイソフォーム選択的阻害剤 |
| TWI378933B (en) | 2008-10-14 | 2012-12-11 | Daiichi Sankyo Co Ltd | Morpholinopurine derivatives |
| GB2465405A (en) | 2008-11-10 | 2010-05-19 | Univ Basel | Triazine, pyrimidine and pyridine analogues and their use in therapy |
| KR20110098908A (ko) * | 2008-11-11 | 2011-09-02 | 엑스커버리 홀딩 컴퍼니 엘엘씨 | PI3K/mTOR 키나제 억제제 |
| ES2462715T3 (es) | 2008-12-19 | 2014-05-26 | Genentech, Inc. | Compuestos y métodos de uso |
| EP2411387B1 (en) | 2009-03-27 | 2015-08-19 | VetDC, Inc. | Pyrimidinyl and 1,3,5-triazinyl benzimidazole sulfonamides and their use in cancer therapy |
| WO2010114494A1 (en) * | 2009-04-03 | 2010-10-07 | S*Bio Pte Ltd | 8-substituted-2-morpholino purines for use as pi3k and/or mtor inhibitors in the treatment of proliferative disorders |
| NZ597059A (en) | 2009-06-17 | 2014-01-31 | Vertex Pharma | Inhibitors of influenza viruses replication |
| CN104945420A (zh) | 2009-06-29 | 2015-09-30 | 因塞特公司 | 作为pi3k抑制剂的嘧啶酮类 |
| EP2451802A1 (en) | 2009-07-07 | 2012-05-16 | Pathway Therapeutics, Inc. | Pyrimidinyl and 1,3,5-triazinyl benzimidazoles and their use in cancer therapy |
| TWI499592B (zh) * | 2009-09-09 | 2015-09-11 | Avila Therapeutics Inc | Pi3激酶抑制劑及其用途 |
| US8759359B2 (en) | 2009-12-18 | 2014-06-24 | Incyte Corporation | Substituted heteroaryl fused derivatives as PI3K inhibitors |
| RU2581367C2 (ru) | 2010-03-01 | 2016-04-20 | Джи Ти Икс, ИНК. | Соединения для лечения рака |
| EP2571884A4 (en) | 2010-05-19 | 2014-03-19 | Xcovery Holding Co Llc | SELECTIVE MTOR KINASE HEMMER |
| CA2822070C (en) | 2010-12-20 | 2019-09-17 | Incyte Corporation | N-(1-(substituted-phenyl)ethyl)-9h-purin-6-amines as pi3k inhibitors |
| CA2825028A1 (en) * | 2011-02-09 | 2012-08-16 | F. Hoffman-La Roche Ag | Heterocyclic compounds as pi3 kinase inhibitors |
| ES2608967T3 (es) | 2011-03-28 | 2017-04-17 | Mei Pharma, Inc. | (Aralquilamino sustituido en alfa y heteroarilalquilamino)pirimidinil y 1,3,5-triazinil benzimidazoles, composiciones farmacéuticas que los contienen, y estos compuestos para usar en el tratamiento de enfermedades proliferativas |
| PL3141548T3 (pl) * | 2011-07-05 | 2020-09-07 | Vertex Pharmaceuticals Incorporated | Sposoby i związki pośrednie do wytwarzania azaindoli |
| UA118010C2 (uk) | 2011-08-01 | 2018-11-12 | Вертекс Фармасьютікалз Інкорпорейтед | Інгібітори реплікації вірусів грипу |
| ES2873001T3 (es) | 2011-09-02 | 2021-11-03 | Incyte Holdings Corp | Heterociclaminas como inhibidores de PI3K |
| US20130123255A1 (en) * | 2011-11-10 | 2013-05-16 | Chugai Seiyaku Kabushiki Kaisha | Combination of a pi3k inhibitor and a mek inhibitor |
| EP2788500A1 (en) | 2011-12-09 | 2014-10-15 | F.Hoffmann-La Roche Ag | Identification of non-responders to her2 inhibitors |
| AR090548A1 (es) | 2012-04-02 | 2014-11-19 | Incyte Corp | Azaheterociclobencilaminas biciclicas como inhibidores de pi3k |
| MX360892B (es) | 2012-05-16 | 2018-11-20 | Novartis Ag | Régimen de dosificación para un inhibidor de cinasa pi-3. |
| CN103450204B (zh) * | 2012-05-31 | 2016-08-17 | 中国科学院上海药物研究所 | 吡咯[2,1-f][1,2,4]并三嗪类化合物,其制备方法及用途 |
| NO2868660T3 (es) * | 2012-07-02 | 2018-05-26 | ||
| WO2014022728A1 (en) | 2012-08-02 | 2014-02-06 | Endo Pharmaceuticals, Inc | Substituted 5 - (quinazolin - 2 - yl) pyrimidin- 2 -amine derivatives useful as pi3k/mtor inhibitors for the treatment of cancer |
| US20150258127A1 (en) | 2012-10-31 | 2015-09-17 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for preventing antiphospholipid syndrome (aps) |
| HUE040126T2 (hu) * | 2012-11-01 | 2019-02-28 | Infinity Pharmaceuticals Inc | Rákok kezelése PI3 kináz izoform modulátorok alkalmazásával |
| CN103588792B (zh) | 2013-03-04 | 2016-03-23 | 中国科学院上海药物研究所 | 吡啶并嘧啶或嘧啶并嘧啶类化合物、其制备方法、药物组合物及其用途 |
| US9242969B2 (en) * | 2013-03-14 | 2016-01-26 | Novartis Ag | Biaryl amide compounds as kinase inhibitors |
| US9296727B2 (en) | 2013-10-07 | 2016-03-29 | Vertex Pharmaceuticals Incorporated | Methods of regioselective synthesis of 2,4-disubstituted pyrimidines |
| CN104557872B (zh) * | 2013-10-16 | 2017-05-24 | 上海璎黎药业有限公司 | 稠合杂环化合物、其制备方法、药物组合物和用途 |
| WO2015073481A1 (en) | 2013-11-13 | 2015-05-21 | Vertex Pharmaceuticals Incorporated | Methods of preparing inhibitors of influenza viruses replication |
| CN111808957A (zh) | 2014-04-04 | 2020-10-23 | 中美冠科生物技术(太仓)有限公司 | 用于确定对mek/erk抑制剂的应答性的方法 |
| WO2015155624A1 (en) | 2014-04-10 | 2015-10-15 | Pfizer Inc. | Dihydropyrrolopyrimidine derivatives |
| WO2015191677A1 (en) | 2014-06-11 | 2015-12-17 | Incyte Corporation | Bicyclic heteroarylaminoalkyl phenyl derivatives as pi3k inhibitors |
| HK1245794A1 (zh) | 2015-02-27 | 2018-08-31 | 大鹏药品工业株式会社 | 咪唑并恶嗪晶体、含有所述晶体的药物组合物和制备所述晶体的方法 |
| JP6816005B2 (ja) | 2015-02-27 | 2021-01-20 | インサイト・コーポレイションIncyte Corporation | Pi3k阻害剤の塩及びその調製のためのプロセス |
| WO2016183060A1 (en) | 2015-05-11 | 2016-11-17 | Incyte Corporation | Process for the synthesis of a phosphoinositide 3-kinase inhibitor |
| US9988401B2 (en) | 2015-05-11 | 2018-06-05 | Incyte Corporation | Crystalline forms of a PI3K inhibitor |
| WO2016183120A1 (en) | 2015-05-13 | 2016-11-17 | Vertex Pharmaceuticals Incorporated | Inhibitors of influenza viruses replication |
| EP3294717B1 (en) | 2015-05-13 | 2020-07-29 | Vertex Pharmaceuticals Inc. | Methods of preparing inhibitors of influenza viruses replication |
| JP6616244B2 (ja) * | 2015-05-29 | 2019-12-04 | 北興化学工業株式会社 | 新規なヒドロキシフェニルボロン酸エステルとその製造方法、およびヒドロキシビフェニル化合物の製造法 |
| US11883404B2 (en) | 2016-03-04 | 2024-01-30 | Taiho Pharmaceuticals Co., Ltd. | Preparation and composition for treatment of malignant tumors |
| SI3458067T1 (sl) * | 2016-05-18 | 2021-07-30 | Torqur Ag | Zdravljenje nevroloških obolenj |
| WO2018007331A1 (en) | 2016-07-08 | 2018-01-11 | F. Hoffmann-La Roche Ag | Fused pyrimidine derivatives |
| WO2018011164A1 (en) | 2016-07-14 | 2018-01-18 | F. Hoffmann-La Roche Ag | Fused pyrimidine derivatives |
| IT201600092469A1 (it) * | 2016-09-14 | 2018-03-14 | Lundbeck Pharmaceuticals Italy S P A | Processo per la produzione di Blonanserina |
| AU2017329090B9 (en) | 2016-09-19 | 2019-09-05 | Novartis Ag | Therapeutic combinations comprising a RAF inhibitor and a ERK inhibitor |
| EP3523304B1 (en) | 2016-10-04 | 2021-01-27 | H. Hoffnabb-La Roche Ag | Bicyclic heteroaryl derivatives |
| KR20240032157A (ko) | 2017-05-02 | 2024-03-08 | 노파르티스 아게 | 병용 요법 |
| CN117860758A (zh) | 2017-05-23 | 2024-04-12 | 梅制药公司 | 联合疗法 |
| US11351176B2 (en) | 2017-08-14 | 2022-06-07 | Mei Pharma, Inc. | Combination therapy |
| JP7335242B2 (ja) | 2017-11-27 | 2023-08-29 | エフ. ホフマン-ラ ロシュ アーゲー | ピリミジン誘導体 |
| MA52761A (fr) | 2018-06-01 | 2021-04-14 | Incyte Corp | Schéma posologique destiné au traitement de troubles liés à la pi3k |
| CN113795490A (zh) | 2019-05-13 | 2021-12-14 | 诺华股份有限公司 | N-(3-(2-(2-羟基乙氧基)-6-吗啉代吡啶-4-基)-4-甲基苯基)-2(三氟甲基)异烟酰胺的新结晶形式作为Raf抑制剂治疗癌症 |
| WO2021247862A1 (en) * | 2020-06-03 | 2021-12-09 | Yumanity Therapeutics, Inc. | Bicyclic heteroarenes and methods of their use |
| TW202220661A (zh) | 2020-08-07 | 2022-06-01 | 德商柏林化學股份公司 | 包含pi3k抑制劑之經改良醫藥調配物 |
| BR112023020806A2 (pt) | 2021-04-09 | 2023-12-12 | Immunic Ag | Inibidores de dhodh deuterados |
| EP4444309A1 (en) * | 2021-12-08 | 2024-10-16 | Kineta, Inc. | Pyrimidines and methods of their use |
| US20250145642A1 (en) * | 2021-12-08 | 2025-05-08 | Kineta, Inc. | Bicyclic heteroarenes and methods of their use |
| WO2024023766A1 (en) | 2022-07-28 | 2024-02-01 | Berlin-Chemie Ag | P13k inhibitor combination therapy |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH08325268A (ja) | 1986-02-24 | 1996-12-10 | Mitsui Petrochem Ind Ltd | ピロロ〔3,4−d〕ピリミジン誘導体 |
| EP0799617A3 (en) * | 1986-02-24 | 1997-11-12 | Mitsui Petrochemical Industries, Ltd. | Therapeutic agent for neurological diseases |
| AU645504B2 (en) * | 1989-10-11 | 1994-01-20 | Teijin Limited | Bicyclic pyrimidine derivative, method of producing the same, and pharmaceutical preparation containing the same as active ingredient |
| TW530047B (en) * | 1994-06-08 | 2003-05-01 | Pfizer | Corticotropin releasing factor antagonists |
| ATE521353T1 (de) | 2000-10-23 | 2011-09-15 | Glaxosmithkline Llc | Neues trisubstitutiertes 8h-pyridoä2,3- düpyrimidin-7-onderivat zur behandlung von durch csbp/p38kinase vermittelten krankheiten |
| AU2003291310A1 (en) * | 2002-11-06 | 2004-06-03 | Bristol-Myers Squibb Company | Fused heterocyclic compounds and use thereof |
| MXPA05005477A (es) * | 2002-11-21 | 2005-07-25 | Chiron Corp | Pirimidinas 2,4,6-trisustituidas como inhibidores de fosfotidilinositol (pi) 3-cinasa y su uso en el tratamiento del cancer. |
| BRPI0409986A (pt) | 2003-05-05 | 2006-05-09 | Hoffmann La Roche | derivados de pirimidina fundida com atividade de crf |
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2007
- 2007-08-07 ES ES07792065T patent/ES2657635T3/es active Active
- 2007-08-07 NZ NZ575274A patent/NZ575274A/en unknown
- 2007-08-07 HU HUE07792065A patent/HUE035116T2/hu unknown
- 2007-08-07 PT PT77920650T patent/PT2050749T/pt unknown
- 2007-08-07 US US12/376,039 patent/US8022205B2/en active Active
- 2007-08-07 DK DK07792065.0T patent/DK2050749T3/en active
- 2007-08-07 PL PL07792065T patent/PL2050749T3/pl unknown
- 2007-08-07 LT LTEP07792065.0T patent/LT2050749T/lt unknown
- 2007-08-07 CA CA2659604A patent/CA2659604C/en active Active
- 2007-08-07 MY MYPI20090459A patent/MY145385A/en unknown
- 2007-08-07 AU AU2007282535A patent/AU2007282535B9/en active Active
- 2007-08-07 JP JP2008528817A patent/JP4450857B2/ja active Active
- 2007-08-07 EP EP07792065.0A patent/EP2050749B1/en active Active
- 2007-08-07 BR BRPI0714908A patent/BRPI0714908B8/pt active IP Right Grant
- 2007-08-07 MX MX2009001451A patent/MX2009001451A/es active IP Right Grant
- 2007-08-07 SI SI200731994T patent/SI2050749T1/en unknown
- 2007-08-07 WO PCT/JP2007/065396 patent/WO2008018426A1/ja not_active Ceased
- 2007-08-07 RU RU2009108328/04A patent/RU2448109C2/ru active
- 2007-08-07 KR KR1020097002650A patent/KR101435692B1/ko active Active
- 2007-08-08 CL CL200702316A patent/CL2007002316A1/es unknown
- 2007-08-08 PE PE2007001059A patent/PE20080527A1/es active IP Right Grant
- 2007-08-08 AR ARP070103510A patent/AR062292A1/es active IP Right Grant
- 2007-08-08 TW TW096129165A patent/TWI394758B/zh active
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2008
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