AR064154A1 - Compuestos inhibidores de fodfoinostida 3- quinasas y composiciones farmaceuticas - Google Patents
Compuestos inhibidores de fodfoinostida 3- quinasas y composiciones farmaceuticasInfo
- Publication number
- AR064154A1 AR064154A1 ARP070105448A ARP070105448A AR064154A1 AR 064154 A1 AR064154 A1 AR 064154A1 AR P070105448 A ARP070105448 A AR P070105448A AR P070105448 A ARP070105448 A AR P070105448A AR 064154 A1 AR064154 A1 AR 064154A1
- Authority
- AR
- Argentina
- Prior art keywords
- cr14r15
- nr10r11
- alkyl
- nr12c
- optionally substituted
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 108091000080 Phosphotransferase Proteins 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 102000020233 phosphotransferase Human genes 0.000 title abstract 2
- 230000002401 inhibitory effect Effects 0.000 title 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 8
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 7
- 125000003118 aryl group Chemical group 0.000 abstract 7
- 125000006653 (C1-C20) heteroaryl group Chemical group 0.000 abstract 6
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 6
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 6
- 125000004452 carbocyclyl group Chemical group 0.000 abstract 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000002632 lipids Chemical class 0.000 abstract 2
- 125000002950 monocyclic group Chemical group 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 102000038030 PI3Ks Human genes 0.000 abstract 1
- 108091007960 PI3Ks Proteins 0.000 abstract 1
- 102000001253 Protein Kinase Human genes 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 125000002837 carbocyclic group Chemical group 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- 125000000842 isoxazolyl group Chemical group 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
- 239000002207 metabolite Substances 0.000 abstract 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 108060006633 protein kinase Proteins 0.000 abstract 1
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- 125000002098 pyridazinyl group Chemical group 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000003831 tetrazolyl group Chemical group 0.000 abstract 1
- 125000000335 thiazolyl group Chemical group 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 125000001425 triazolyl group Chemical group 0.000 abstract 1
Classifications
-
- 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
-
- 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
- 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
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
- 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)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Emergency Medicine (AREA)
- Obesity (AREA)
- Immunology (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87342206P | 2006-12-07 | 2006-12-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR064154A1 true AR064154A1 (es) | 2009-03-18 |
Family
ID=39403189
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP070105448A AR064154A1 (es) | 2006-12-07 | 2007-12-05 | Compuestos inhibidores de fodfoinostida 3- quinasas y composiciones farmaceuticas |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US9487533B2 (OSRAM) |
| EP (1) | EP2114950B1 (OSRAM) |
| JP (1) | JP5500990B2 (OSRAM) |
| KR (1) | KR101507182B1 (OSRAM) |
| CN (1) | CN101675053B (OSRAM) |
| AR (1) | AR064154A1 (OSRAM) |
| AU (1) | AU2007333243B2 (OSRAM) |
| BR (1) | BRPI0717907A2 (OSRAM) |
| CA (1) | CA2671845C (OSRAM) |
| CL (1) | CL2007003523A1 (OSRAM) |
| ES (1) | ES2571028T3 (OSRAM) |
| IL (1) | IL199151A (OSRAM) |
| MX (1) | MX2009005925A (OSRAM) |
| NO (1) | NO342697B1 (OSRAM) |
| PE (1) | PE20081353A1 (OSRAM) |
| RU (1) | RU2470936C2 (OSRAM) |
| TW (1) | TW200829594A (OSRAM) |
| WO (1) | WO2008073785A2 (OSRAM) |
| ZA (1) | ZA200904531B (OSRAM) |
Families Citing this family (84)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69638122D1 (de) * | 1996-09-04 | 2010-03-18 | Intertrust Tech Corp | Zuverlässige Infrastrukturhilfssysteme, Verfahren und Techniken für sicheren elektronischen Handel, elektronische Transaktionen, Handelsablaufsteuerung und Automatisierung, verteilte Verarbeitung und Rechteverwaltung |
| AU2007329352B2 (en) | 2006-12-07 | 2013-01-17 | F. Hoffmann-La Roche Ag | Phosphoinositide 3-kinase inhibitor compounds and methods of use |
| EP2158207B1 (en) * | 2007-06-12 | 2011-05-25 | F. Hoffmann-La Roche AG | Thiazoliopyrimidines and their use as inhibitors of phosphatidylinositol-3 kinase |
| PE20090678A1 (es) * | 2007-09-12 | 2009-06-27 | Genentech Inc | Combinaciones de compuestos inhibidores de fosfoinositida 3-quinasa y agentes quimioterapeuticos y los metodos de uso |
| WO2009042607A1 (en) * | 2007-09-24 | 2009-04-02 | Genentech, Inc. | Thiazolopyrimidine p13k inhibitor compounds and methods of use |
| JP5348725B2 (ja) * | 2007-10-25 | 2013-11-20 | ジェネンテック, インコーポレイテッド | チエノピリミジン化合物の製造方法 |
| GB0721095D0 (en) * | 2007-10-26 | 2007-12-05 | Piramed Ltd | Pharmaceutical compounds |
| CA2710194C (en) | 2007-12-19 | 2014-04-22 | Amgen Inc. | Inhibitors of p13 kinase |
| JP2011529920A (ja) * | 2008-07-31 | 2011-12-15 | ジェネンテック, インコーポレイテッド | ピリミジン化合物、組成物及び使用方法 |
| WO2010027002A1 (ja) * | 2008-09-05 | 2010-03-11 | 塩野義製薬株式会社 | Pi3k阻害活性を有する縮環モルホリン誘導体 |
| TWI378933B (en) | 2008-10-14 | 2012-12-11 | Daiichi Sankyo Co Ltd | Morpholinopurine derivatives |
| CA2740484C (en) * | 2008-10-17 | 2021-09-21 | Akaal Pharma Pty Ltd | S1p receptors modulators and their use thereof |
| US9181182B2 (en) | 2008-10-17 | 2015-11-10 | Akaal Pharma Pty Ltd | S1P receptors modulators |
| WO2010080996A1 (en) | 2009-01-08 | 2010-07-15 | Curis, Inc. | Phosphoinositide 3-kinase inhibitors with a zinc binding moiety |
| US9090601B2 (en) | 2009-01-30 | 2015-07-28 | Millennium Pharmaceuticals, Inc. | Thiazole derivatives |
| EP2405916B1 (en) | 2009-03-12 | 2018-02-07 | Genentech, Inc. | Combinations of phosphoinositide 3-kinase inhibitor compounds and chemotherapeutic agents for the treatment of hematopoietic malignancies |
| EP2405973B1 (en) * | 2009-03-13 | 2015-04-22 | Katholieke Universiteit Leuven, K.U. Leuven R&D | Thiazolopyrimidine modulators as immunosuppressive agents |
| SG172951A1 (en) | 2009-03-24 | 2011-08-29 | Sumitomo Chemical Co | Method for manufacturing a boronic acid ester compound |
| CN102459272B (zh) | 2009-05-27 | 2014-08-06 | 健泰科生物技术公司 | 对P110δ具有选择性的为PI3K抑制剂的二环嘧啶化合物和使用方法 |
| EP2451811A1 (en) * | 2009-05-27 | 2012-05-16 | F. Hoffmann-La Roche AG | Bicyclic indole-pyrimidine pi3k inhibitor compounds selective for p110 delta, and methods of use |
| JP2012531422A (ja) * | 2009-06-24 | 2012-12-10 | ジェネンテック, インコーポレイテッド | オキソ−複素環縮合ピリミジン化合物、組成物及び使用方法 |
| RU2557658C2 (ru) | 2009-09-28 | 2015-07-27 | Ф.Хоффманн-Ля Рош Аг | Бензоксепиновые ингибиторы pi3 и способы применения |
| WO2011049625A1 (en) | 2009-10-20 | 2011-04-28 | Mansour Samadpour | Method for aflatoxin screening of products |
| HUE035059T2 (hu) | 2009-11-05 | 2018-05-02 | Rhizen Pharmaceuticals S A | Új benzopirán-kinát modulátorok |
| WO2011058025A1 (en) * | 2009-11-12 | 2011-05-19 | F. Hoffmann-La Roche Ag | N-7 substituted purine and pyrazolopyrimidine compounds, compositions and methods of use |
| CA2778686C (en) * | 2009-11-12 | 2015-07-21 | F. Hoffmann-La Roche Ag | N-9-substituted purine compounds, compositions and methods of use |
| CN102762565A (zh) | 2010-02-22 | 2012-10-31 | 弗·哈夫曼-拉罗切有限公司 | 吡啶并[3,2-d]嘧啶PI3δ抑制剂化合物及使用方法 |
| JP2013525308A (ja) * | 2010-04-16 | 2013-06-20 | キュリス,インコーポレイテッド | K−ras変異を有する癌の治療 |
| BR122014012788B1 (pt) | 2010-06-23 | 2022-04-19 | Hanmi Science Co., Ltd | Derivados de pirimidina fundidos, seus usos, e composição farmacêutica para inibição da atividade de tirosina quinase |
| WO2012007493A1 (en) | 2010-07-14 | 2012-01-19 | F. Hoffmann-La Roche Ag | Purine compounds selective for ρi3κ p110 delta, and methods of use |
| DE102010049595A1 (de) * | 2010-10-26 | 2012-04-26 | Merck Patent Gmbh | Chinazolinderivate |
| KR20140099556A (ko) | 2010-12-16 | 2014-08-12 | 에프. 호프만-라 로슈 아게 | 트라이사이클릭 pi3k 억제제 화합물 및 이의 사용 방법 |
| EA201300867A1 (ru) * | 2011-01-27 | 2014-03-31 | Дзе Трастиз Оф Принстон Юнивесити | ИНГИБИТОРЫ КИНАЗЫ mTOR В КАЧЕСТВЕ АНТИВИРУСНЫХ АГЕНТОВ |
| CA2825028A1 (en) | 2011-02-09 | 2012-08-16 | F. Hoffman-La Roche Ag | Heterocyclic compounds as pi3 kinase inhibitors |
| US20120258967A1 (en) * | 2011-03-09 | 2012-10-11 | Avila Therapeutics, Inc. | Pi3 kinase inhibitors and uses thereof |
| WO2012126901A1 (en) | 2011-03-21 | 2012-09-27 | F. Hoffmann-La Roche Ag | Benzoxazepin compounds selective for pi3k p110 delta and methods of use |
| KR20180108848A (ko) * | 2011-04-01 | 2018-10-04 | 쿠리스 인코퍼레이션 | 아연 결합 모이어티를 갖는 포스포이노시티드 3-키나아제 억제제 |
| CN103608335B (zh) | 2011-04-08 | 2018-02-23 | 爱尔兰詹森科学公司 | 用于治疗病毒感染的嘧啶衍生物 |
| ES2710874T3 (es) | 2011-05-04 | 2019-04-29 | Rhizen Pharmaceuticals S A | Compuestos novedosos como moduladores de proteína cinasas |
| EP2524918A1 (en) | 2011-05-19 | 2012-11-21 | Centro Nacional de Investigaciones Oncológicas (CNIO) | Imidazopyrazines derivates as kinase inhibitors |
| BR122019020718B1 (pt) | 2011-11-09 | 2021-07-06 | Janssen Sciences Ireland Uc | Derivados purínicos para o tratamento de infecções virais e composição farmacêutica que os compreende |
| JP6206926B2 (ja) * | 2011-11-23 | 2017-10-04 | キャンサー・リサーチ・テクノロジー・リミテッド | 異常なプロテインキナーゼcのチエノピリミジン阻害剤 |
| JP6077642B2 (ja) | 2012-04-10 | 2017-02-08 | シャンハイ インリ ファーマシューティカル カンパニー リミティド | 縮合ピリミジン化合物、その調製法、中間体、組成物、及び使用 |
| KR20160027217A (ko) | 2012-05-23 | 2016-03-09 | 에프. 호프만-라 로슈 아게 | 내배엽 및 간세포를 수득하고 사용하는 조성물 및 방법 |
| KR101915942B1 (ko) | 2012-06-08 | 2018-11-06 | 에프. 호프만-라 로슈 아게 | 암의 치료를 위한 포스포이노시타이드 3 키나제 억제제 화합물 및 화학치료제의 돌연변이체 선택성 및 조합물 |
| SMT201900334T1 (it) * | 2012-07-04 | 2019-07-11 | Rhizen Pharmaceuticals S A | Inibitori selettivi di pi3k delta |
| MX360718B (es) | 2012-07-13 | 2018-11-13 | Janssen Sciences Ireland Uc | Purinas macrocíclicas para el tratamiento de infecciones víricas. |
| MX349551B (es) | 2012-10-10 | 2017-08-02 | Hoffmann La Roche | Proceso para preparar compuestos tienopirimidinas. |
| TR201807076T4 (tr) | 2012-10-10 | 2018-06-21 | Janssen Sciences Ireland Uc | Viral enfeksiyonların ve diğer hastalıkların tedavisine yönelik pirolo[3,2-d]pirimidin derivatları. |
| 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) |
| SG11201503042QA (en) | 2012-11-16 | 2015-06-29 | Janssen Sciences Ireland Uc | Heterocyclic substituted 2-amino-quinazoline derivatives for the treatment of viral infections |
| EA035174B1 (ru) | 2013-02-21 | 2020-05-12 | Янссен Сайенсиз Айрлэнд Юси | Производные 2-аминопиримидина в качестве модуляторов толл-подобных рецепторов tlr7 и/или tlr8 |
| HRP20170654T1 (hr) | 2013-03-29 | 2017-06-30 | Janssen Sciences Ireland Uc | Makrociklički deaza-purinoni za liječenje virusnih infekcija |
| DE102013008118A1 (de) * | 2013-05-11 | 2014-11-13 | Merck Patent Gmbh | Arylchinazoline |
| DK3004074T3 (da) | 2013-05-24 | 2018-01-29 | Janssen Sciences Ireland Uc | Pyridonderivater til behandling af virusinfektioner og yderligere sygdomme |
| WO2014203129A1 (en) | 2013-06-19 | 2014-12-24 | Olema Pharmaceuticals, Inc. | Combinations of benzopyran compounds, compositions and uses thereof |
| HRP20171720T1 (hr) | 2013-06-27 | 2017-12-29 | Janssen Sciences Ireland Uc | Derivati pirolo [3,2-d] pirimidina za liječenje virusnih infekcija i drugih bolesti |
| EP3027624B1 (en) | 2013-07-30 | 2018-09-12 | Janssen Sciences Ireland UC | Thieno[3,2-d]pyrimidines derivatives for the treatment of viral infections |
| US9745321B2 (en) | 2013-09-30 | 2017-08-29 | Shanghai Yingli Pharmaceutical Co., Ltd | Fused pyrimidine compound, intermediate, preparation method therefor, and composition and application thereof |
| FR3015483B1 (fr) * | 2013-12-23 | 2016-01-01 | Servier Lab | Nouveaux derives de thienopyrimidine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| US9708341B2 (en) | 2014-06-09 | 2017-07-18 | Sumitomo Chemical Company, Limited | Method for producing pyridine compound |
| TWI678369B (zh) | 2014-07-28 | 2019-12-01 | 美商基利科學股份有限公司 | 用於治療呼吸道合胞病毒感染之噻吩並[3,2-d]嘧啶、呋喃並[3,2-d]嘧啶及吡咯並[3,2-d]嘧啶化合物類 |
| KR20160082062A (ko) | 2014-12-30 | 2016-07-08 | 한미약품 주식회사 | 싸이옥소 퓨로피리미디논 유도체의 제조방법 및 이에 사용되는 중간체 |
| AR104068A1 (es) | 2015-03-26 | 2017-06-21 | Hoffmann La Roche | Combinaciones de un compuesto inhibidor de fosfoinosítido 3-cinasa y un compuesto inhibidor de cdk4/6 para el tratamiento del cáncer |
| KR20180012324A (ko) | 2015-06-29 | 2018-02-05 | 에프. 호프만-라 로슈 아게 | 타셀리십을 사용하는 치료 방법 |
| CN106467545B (zh) * | 2015-08-20 | 2018-10-16 | 北大方正集团有限公司 | 一种噻吩并嘧啶化合物 |
| AU2016378723B2 (en) | 2015-12-22 | 2021-09-30 | SHY Therapeutics LLC | Compounds for the treatment of cancer and inflammatory disease |
| EP3478680B1 (en) | 2016-06-29 | 2020-04-22 | H. Hoffnabb-La Roche Ag | Novel tetrahydropyridopyrimidines for the treatment and prophylaxis of hbv infection |
| US11053256B2 (en) | 2016-07-01 | 2021-07-06 | Janssen Sciences Ireland Unlimited Company | Dihydropyranopyrimidines for the treatment of viral infections |
| MA46340A (fr) | 2016-09-29 | 2019-08-07 | Janssen Sciences Ireland Unlimited Co | Promédicaments de pyrimidine pour le traitement d'infections virales et d'autres maladies |
| CN110573518A (zh) | 2017-01-26 | 2019-12-13 | 尤拉·S·赞特里佐斯 | 被取代的双环嘧啶基化合物及其组合物和用途 |
| CN107163061A (zh) * | 2017-04-14 | 2017-09-15 | 江西科技师范大学 | 含吡唑啉结构的噻吩并嘧啶类化合物的制备及应用 |
| MX2019014875A (es) | 2017-06-21 | 2021-01-29 | SHY Therapeutics LLC | Compuestos que interaccionan con la superfamilia ras para el tratamiento de cancer, enfermedades inflamatorias, rasopatias y enfermedad fibrotica. |
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| CN113087718B (zh) * | 2020-01-09 | 2024-02-09 | 四川科伦博泰生物医药股份有限公司 | 噻吩并嘧啶酮类化合物及其医药应用 |
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| DE2050814A1 (de) * | 1970-10-16 | 1972-04-20 | Dr. Karl Thomae Gmbh, 7950 Biberach | Neue Verfahren zur Herstellung von 2-(5-Nitro-2-furyl)-thieno eckige Klammer auf 3,2-d eckige Klammer zu pyrimidinen |
| DE1959403A1 (de) * | 1969-11-26 | 1971-06-03 | Thomae Gmbh Dr K | Neue 2-(5-Nitro-2-furyl)-thieno[3,2-d]pyrimidine und Verfahren zu ihrer Herstellung |
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| EP2041139B1 (en) * | 2006-04-26 | 2011-11-09 | F. Hoffmann-La Roche AG | Pharmaceutical compounds |
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| AU2007246793B2 (en) | 2006-04-26 | 2013-02-07 | F. Hoffmann-La Roche Ag | Thieno [3, 2-D] pyrimidine derivative useful as PI3K inhibitor |
| GB0608820D0 (en) | 2006-05-04 | 2006-06-14 | Piramed Ltd | Pharmaceutical compounds |
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- 2007-12-05 KR KR1020097014132A patent/KR101507182B1/ko not_active Expired - Fee Related
- 2007-12-05 ZA ZA200904531A patent/ZA200904531B/xx unknown
- 2007-12-05 AR ARP070105448A patent/AR064154A1/es unknown
- 2007-12-05 RU RU2009125916/04A patent/RU2470936C2/ru not_active IP Right Cessation
- 2007-12-05 CA CA2671845A patent/CA2671845C/en not_active Expired - Fee Related
- 2007-12-05 TW TW096146408A patent/TW200829594A/zh unknown
- 2007-12-05 ES ES07865255T patent/ES2571028T3/es active Active
- 2007-12-05 AU AU2007333243A patent/AU2007333243B2/en not_active Ceased
- 2007-12-05 JP JP2009540457A patent/JP5500990B2/ja active Active
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- 2007-12-05 MX MX2009005925A patent/MX2009005925A/es active IP Right Grant
- 2007-12-05 PE PE2007001727A patent/PE20081353A1/es not_active Application Discontinuation
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|---|---|
| RU2009125916A (ru) | 2011-01-20 |
| JP5500990B2 (ja) | 2014-05-21 |
| MX2009005925A (es) | 2009-08-12 |
| EP2114950B1 (en) | 2016-03-09 |
| CL2007003523A1 (es) | 2008-08-22 |
| US20080269210A1 (en) | 2008-10-30 |
| CN101675053B (zh) | 2014-03-12 |
| TW200829594A (en) | 2008-07-16 |
| ES2571028T3 (es) | 2016-05-23 |
| IL199151A (en) | 2017-01-31 |
| KR20090106508A (ko) | 2009-10-09 |
| CN101675053A (zh) | 2010-03-17 |
| NO342697B1 (no) | 2018-07-09 |
| BRPI0717907A2 (pt) | 2013-11-05 |
| EP2114950A2 (en) | 2009-11-11 |
| KR101507182B1 (ko) | 2015-03-30 |
| RU2470936C2 (ru) | 2012-12-27 |
| AU2007333243A1 (en) | 2008-06-19 |
| IL199151A0 (en) | 2010-03-28 |
| JP2010512337A (ja) | 2010-04-22 |
| CA2671845C (en) | 2015-03-24 |
| ZA200904531B (en) | 2010-09-29 |
| US9487533B2 (en) | 2016-11-08 |
| CA2671845A1 (en) | 2008-06-19 |
| NO20092565L (no) | 2009-09-07 |
| PE20081353A1 (es) | 2008-11-12 |
| WO2008073785A3 (en) | 2008-08-28 |
| WO2008073785A2 (en) | 2008-06-19 |
| AU2007333243B2 (en) | 2013-03-14 |
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