NO20084533L - Pyrimidin-derivat som PI3K-inhibitor og bruk av dette - Google Patents
Pyrimidin-derivat som PI3K-inhibitor og bruk av detteInfo
- Publication number
- NO20084533L NO20084533L NO20084533A NO20084533A NO20084533L NO 20084533 L NO20084533 L NO 20084533L NO 20084533 A NO20084533 A NO 20084533A NO 20084533 A NO20084533 A NO 20084533A NO 20084533 L NO20084533 L NO 20084533L
- Authority
- NO
- Norway
- Prior art keywords
- pi3k inhibitor
- pyrimidine derivative
- pyrimidine
- derivative
- pi3k
- Prior art date
Links
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)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (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)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006216108 | 2006-08-08 | ||
JP2007118631 | 2007-04-27 | ||
PCT/JP2007/065396 WO2008018426A1 (fr) | 2006-08-08 | 2007-08-07 | Dérivé de pyrimidine comme inhibiteur de la PI3K et son utilisation |
Publications (2)
Publication Number | Publication Date |
---|---|
NO20084533L true NO20084533L (no) | 2009-01-09 |
NO342978B1 NO342978B1 (no) | 2018-09-17 |
Family
ID=39032956
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO20084533A NO342978B1 (no) | 2006-08-08 | 2008-10-28 | Pyrimidin-derivat som PI3K-inhibitor og bruk av dette |
Country Status (26)
Country | Link |
---|---|
US (1) | US8022205B2 (no) |
EP (1) | EP2050749B1 (no) |
JP (1) | JP4450857B2 (no) |
KR (1) | KR101435692B1 (no) |
AR (1) | AR062292A1 (no) |
AU (1) | AU2007282535B9 (no) |
BR (1) | BRPI0714908B8 (no) |
CA (1) | CA2659604C (no) |
CL (1) | CL2007002316A1 (no) |
CY (1) | CY1119882T1 (no) |
DK (1) | DK2050749T3 (no) |
ES (1) | ES2657635T3 (no) |
HU (1) | HUE035116T2 (no) |
IL (1) | IL196601A (no) |
LT (1) | LT2050749T (no) |
MX (1) | MX2009001451A (no) |
MY (1) | MY145385A (no) |
NO (1) | NO342978B1 (no) |
NZ (1) | NZ575274A (no) |
PE (1) | PE20080527A1 (no) |
PL (1) | PL2050749T3 (no) |
PT (1) | PT2050749T (no) |
RU (1) | RU2448109C2 (no) |
SI (1) | SI2050749T1 (no) |
TW (1) | TWI394758B (no) |
WO (1) | WO2008018426A1 (no) |
Families Citing this family (67)
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DK2125822T3 (en) * | 2006-12-21 | 2015-01-12 | Nerviano Medical Sciences Srl | SUBSTITUTED PYRAZOLOQUINAZOLINDERIVATER, process for their preparation and their use as kinase inhibitors |
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. |
US9029408B2 (en) | 2008-06-16 | 2015-05-12 | Gtx, Inc. | Compounds for treatment of cancer |
DK3289876T3 (da) * | 2008-06-16 | 2022-10-10 | Univ Tennessee Res Found | Forbindelser til behandling af cancer |
US9447049B2 (en) | 2010-03-01 | 2016-09-20 | University Of Tennessee Research Foundation | Compounds for treatment of cancer |
US8822513B2 (en) | 2010-03-01 | 2014-09-02 | Gtx, Inc. | Compounds for treatment of cancer |
US8513221B2 (en) * | 2008-07-07 | 2013-08-20 | Xcovery Holding, LLC | PI3K isoform selective inhibitors |
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 |
ES2539478T3 (es) * | 2008-11-11 | 2015-07-01 | Xcovery Holding Company Llc | Inhibidores de PI3K/mTOR cinasa |
BRPI0918337A2 (pt) * | 2008-12-19 | 2017-05-30 | Abbott Lab | composto, composição farmacêutica, método de tratamento, método para tratar uma doença ou condição causada, exacerbada ou resultante de um excesso de plaquetas ou ativação indesejada de plaquetas em um paciente, método para reduzir a contagem de plaquetas circulantes em um paciente e uso |
NZ595372A (en) | 2009-03-27 | 2013-11-29 | 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 |
GEP20207129B (en) | 2009-06-17 | 2020-07-10 | Vertex Pharma | Inhibitors of influenza viruses replication |
MX2011013816A (es) | 2009-06-29 | 2012-04-11 | Incyte Corp | Pirimidinonas como inhibidores de pi3k. |
ES2706185T3 (es) | 2009-07-07 | 2019-03-27 | Mei Pharma Inc | Pirimidinil y 1,3,5-triazinil bencimidazoles y sus usos en la terapia contra el cáncer |
EP2475375A4 (en) * | 2009-09-09 | 2013-02-20 | Avila Therapeutics Inc | PI3 KINASE INHIBITORS AND USES THEREOF |
WO2011075643A1 (en) | 2009-12-18 | 2011-06-23 | Incyte Corporation | Substituted heteroaryl fused derivatives as pi3k inhibitors |
CN104592205A (zh) | 2010-03-01 | 2015-05-06 | Gtx公司 | 用于治疗癌的化合物 |
JP2013529212A (ja) * | 2010-05-19 | 2013-07-18 | エクスカバリー ホールディング カンパニー,エルエルシー | mTOR選択的キナーゼ阻害剤 |
CA2822070C (en) | 2010-12-20 | 2019-09-17 | Incyte Corporation | N-(1-(substituted-phenyl)ethyl)-9h-purin-6-amines as pi3k inhibitors |
RU2013138835A (ru) * | 2011-02-09 | 2015-03-20 | Ф. Хоффманн-Ля Рош Аг | Гетероциклические соединения в качестве ингибиторов pi3 киназы |
TWI572599B (zh) | 2011-03-28 | 2017-03-01 | Mei製藥公司 | (α-經取代之芳烷胺基及雜芳烷胺基)嘧啶基及1,3,5-三基苯并咪唑,其醫藥組合物及其在治療增生性疾病之用途 |
MX2013015147A (es) * | 2011-07-05 | 2014-03-27 | Vertex Pharma | Procesos y compuestos intermediarios para producir azaindoles. |
UA118010C2 (uk) | 2011-08-01 | 2018-11-12 | Вертекс Фармасьютікалз Інкорпорейтед | Інгібітори реплікації вірусів грипу |
DK2751109T3 (en) | 2011-09-02 | 2017-01-23 | Incyte Holdings Corp | HETEROCYCLYLAMINES AS PI3K INHIBITORS |
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 |
KR20150009540A (ko) | 2012-05-16 | 2015-01-26 | 노파르티스 아게 | Pi-3 키나제 억제제에 대한 투여 요법 |
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 |
PL2868660T3 (pl) * | 2012-07-02 | 2018-05-30 | Taiho Pharmaceutical Co., Ltd. | Środek wzmacniający działanie przeciwnowotworowe zawierający związek imidazooksazynowy |
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 |
EP2914260A1 (en) | 2012-10-31 | 2015-09-09 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for preventing antiphospholipid syndrome (aps) |
BR112015010035A2 (pt) * | 2012-11-01 | 2017-07-11 | Infinity Pharmaceuticals Inc | tratamento de câncer usando moduladores de isoformas quinase pi3 |
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 |
LT3421468T (lt) | 2013-11-13 | 2021-01-11 | Vertex Pharmaceuticals Incorporated | Gripo virusų replikacijos inhibitorių paruošimo būdai |
US10683550B2 (en) | 2014-04-04 | 2020-06-16 | Crown Bioscience, Inc. (Taicang) | HNF4G-RSPO2 fusion gene and use thereof in treatment of cancer |
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 |
RS63963B1 (sr) | 2015-02-27 | 2023-03-31 | Incyte Holdings Corp | Postupak pripreme pi3k inhibitora |
JPWO2016136928A1 (ja) | 2015-02-27 | 2017-08-31 | 大鵬薬品工業株式会社 | イミダゾオキサジンの結晶、当該結晶を含む医薬組成物、及び当該結晶の製造方法 |
US9988401B2 (en) | 2015-05-11 | 2018-06-05 | Incyte Corporation | Crystalline forms of a PI3K inhibitor |
WO2016183060A1 (en) | 2015-05-11 | 2016-11-17 | Incyte Corporation | Process for the synthesis of a phosphoinositide 3-kinase inhibitor |
WO2016183116A1 (en) | 2015-05-13 | 2016-11-17 | Vertex Pharmaceuticals Incorporated | Methods of preparing inhibitors of influenza viruses replication |
EP3294735B8 (en) | 2015-05-13 | 2022-01-05 | Vertex Pharmaceuticals Incorporated | 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 |
EP3484884B1 (en) | 2016-07-14 | 2021-01-27 | 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 |
WO2018051306A1 (en) | 2016-09-19 | 2018-03-22 | 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 |
PL3618875T3 (pl) | 2017-05-02 | 2023-10-23 | Novartis Ag | Terapia skojarzona obejmująca inhibitor raf i trametynib |
CN110996959A (zh) | 2017-05-23 | 2020-04-10 | 梅制药公司 | 联合疗法 |
MA49921A (fr) | 2017-08-14 | 2021-05-12 | Mei Pharma Inc | Polythérapie |
US11414420B2 (en) | 2017-11-27 | 2022-08-16 | Hoffmann-La Roche Inc. | Pyrimidine derivatives |
US20230271965A1 (en) * | 2020-06-03 | 2023-08-31 | Kineta, 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 |
CA3215002A1 (en) | 2021-04-09 | 2022-10-13 | Christian Gege | Deuterated dhodh inhibitors |
MX2024007009A (es) * | 2021-12-08 | 2024-08-22 | Kineta Inc | Heteroarenos bicíclicos y métodos para su uso. |
MX2024007010A (es) * | 2021-12-08 | 2024-08-26 | Kineta Inc | Pirimidinas y metodos para su uso. |
WO2024023766A1 (en) | 2022-07-28 | 2024-02-01 | Berlin-Chemie Ag | P13k inhibitor combination therapy |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002059083A2 (en) * | 2000-10-23 | 2002-08-01 | Smithkline Beecham Corporation | Novel compounds |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
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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 |
EP0257102B1 (en) | 1986-02-24 | 1997-11-19 | Mitsui Petrochemical Industries, Ltd. | Agents for treating neurophathy |
CA2067221C (en) * | 1989-10-11 | 1997-04-15 | Yasuji Sakuma | Fused pyrimidine derivative, process for preparation of same and pharmaceutical preparation comprising same as active ingredient |
TW574214B (en) * | 1994-06-08 | 2004-02-01 | Pfizer | Corticotropin releasing factor antagonists |
US7384937B2 (en) * | 2002-11-06 | 2008-06-10 | Bristol-Myers Squibb Co. | Fused heterocyclic compounds and use thereof |
EA013811B1 (ru) | 2002-11-21 | 2010-08-30 | Новартис Вэксинес Энд Дайэгностикс, Инк. | 2,4,6-тризамещённые пиримидины, являющиеся ингибиторами фосфотидилинозитол(pi)-3-киназы, и их применение при лечении рака |
RU2328497C2 (ru) | 2003-05-05 | 2008-07-10 | Ф.Хоффманн-Ля Рош Аг | Конденсированные производные пиримидина и лекарственное средство, обладающее активностью в отношении crf |
-
2007
- 2007-08-07 HU HUE07792065A patent/HUE035116T2/hu unknown
- 2007-08-07 KR KR1020097002650A patent/KR101435692B1/ko active IP Right Grant
- 2007-08-07 MY MYPI20090459A patent/MY145385A/en unknown
- 2007-08-07 RU RU2009108328/04A patent/RU2448109C2/ru active
- 2007-08-07 PT PT77920650T patent/PT2050749T/pt unknown
- 2007-08-07 LT LTEP07792065.0T patent/LT2050749T/lt unknown
- 2007-08-07 WO PCT/JP2007/065396 patent/WO2008018426A1/ja active Search and Examination
- 2007-08-07 AU AU2007282535A patent/AU2007282535B9/en active Active
- 2007-08-07 JP JP2008528817A patent/JP4450857B2/ja active Active
- 2007-08-07 US US12/376,039 patent/US8022205B2/en active Active
- 2007-08-07 ES ES07792065T patent/ES2657635T3/es active Active
- 2007-08-07 PL PL07792065T patent/PL2050749T3/pl unknown
- 2007-08-07 MX MX2009001451A patent/MX2009001451A/es active IP Right Grant
- 2007-08-07 CA CA2659604A patent/CA2659604C/en active Active
- 2007-08-07 DK DK07792065.0T patent/DK2050749T3/en active
- 2007-08-07 BR BRPI0714908A patent/BRPI0714908B8/pt active IP Right Grant
- 2007-08-07 EP EP07792065.0A patent/EP2050749B1/en active Active
- 2007-08-07 NZ NZ575274A patent/NZ575274A/en unknown
- 2007-08-07 SI SI200731994T patent/SI2050749T1/en unknown
- 2007-08-08 CL CL200702316A patent/CL2007002316A1/es unknown
- 2007-08-08 AR ARP070103510A patent/AR062292A1/es active IP Right Grant
- 2007-08-08 PE PE2007001059A patent/PE20080527A1/es active IP Right Grant
- 2007-08-08 TW TW096129165A patent/TWI394758B/zh active
-
2008
- 2008-10-28 NO NO20084533A patent/NO342978B1/no unknown
-
2009
- 2009-01-20 IL IL196601A patent/IL196601A/en active IP Right Grant
-
2017
- 2017-12-28 CY CY20171101353T patent/CY1119882T1/el unknown
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002059083A2 (en) * | 2000-10-23 | 2002-08-01 | Smithkline Beecham Corporation | Novel compounds |
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