ZA200901477B - Pyrido (2,3-D) pyrimidinone compounds and their use as PI3 inhibitors - Google Patents
Pyrido (2,3-D) pyrimidinone compounds and their use as PI3 inhibitorsInfo
- Publication number
- ZA200901477B ZA200901477B ZA200901477A ZA200901477A ZA200901477B ZA 200901477 B ZA200901477 B ZA 200901477B ZA 200901477 A ZA200901477 A ZA 200901477A ZA 200901477 A ZA200901477 A ZA 200901477A ZA 200901477 B ZA200901477 B ZA 200901477B
- Authority
- ZA
- South Africa
- Prior art keywords
- pyrido
- inhibitors
- pyrimidinone compounds
- pyrimidinone
- compounds
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—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
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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)
- Health & Medical Sciences (AREA)
- Organic Chemistry (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)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US84506506P | 2006-09-15 | 2006-09-15 | |
US94785207P | 2007-07-03 | 2007-07-03 | |
US95262807P | 2007-07-30 | 2007-07-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200901477B true ZA200901477B (en) | 2010-07-28 |
Family
ID=38859750
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200901477A ZA200901477B (en) | 2006-09-15 | 2009-03-02 | Pyrido (2,3-D) pyrimidinone compounds and their use as PI3 inhibitors |
Country Status (42)
Families Citing this family (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4718637B2 (ja) | 2006-09-15 | 2011-07-06 | ファイザー・プロダクツ・インク | ピリド(2,3−d)ピリミジノン化合物およびpi3阻害剤としてのその使用 |
EA020022B1 (ru) * | 2007-04-10 | 2014-08-29 | Экселиксис, Инк. | Способы лечения с применением пиридопиримидиноновых ингибиторов pi3k-альфа |
JP2010523681A (ja) * | 2007-04-11 | 2010-07-15 | エクセリクシス, インク. | 癌の治療のためのPI3K−αの阻害剤としてのピリド[2,3−D]ピリミジン−7−オン化合物 |
MX336723B (es) * | 2008-07-11 | 2016-01-28 | Novartis Ag | Combinacion de (a) un inhibidor de fosfoinositido 3-cinasa y (b) un modulador de la ruta de ras/raf/mek. |
CA2734489C (fr) | 2008-08-20 | 2016-11-08 | Southern Research Institute | Derives de pyridine et de pyrimidine substitues par ethenyle et leur utilisation dans le traitement d'infections virales |
EP2326627A1 (fr) | 2008-08-20 | 2011-06-01 | Schering Corporation | Dérivés de pyridine et pyrimidine substituées et leur utilisation dans le traitement d'infections virales |
AR072940A1 (es) | 2008-08-20 | 2010-09-29 | Schering Corp | Derivados de piridina y pirimidina sustituidos con etinilo y su uso en el tratamiento de infecciones virales |
US8470834B2 (en) | 2008-08-20 | 2013-06-25 | Merck Sharp & Dohme Corp. | AZO-substituted pyridine and pyrimidine derivatives and their use in treating viral infections |
US8101622B2 (en) * | 2008-09-30 | 2012-01-24 | Exelixis, Inc. | Pyridopyrimidinone inhibitors of PI3Kα and mTOR |
US8628554B2 (en) | 2010-06-13 | 2014-01-14 | Virender K. Sharma | Intragastric device for treating obesity |
US10420665B2 (en) | 2010-06-13 | 2019-09-24 | W. L. Gore & Associates, Inc. | Intragastric device for treating obesity |
US9526648B2 (en) | 2010-06-13 | 2016-12-27 | Synerz Medical, Inc. | Intragastric device for treating obesity |
US10010439B2 (en) | 2010-06-13 | 2018-07-03 | Synerz Medical, Inc. | Intragastric device for treating obesity |
SG190890A1 (en) | 2010-12-16 | 2013-07-31 | Hoffmann La Roche | Tricyclic pi3k inhibitor compounds and methods of use |
US8664230B2 (en) * | 2011-03-17 | 2014-03-04 | The Asan Foundation | Pyridopyrimidine derivatives and use thereof |
TW201306842A (zh) * | 2011-06-15 | 2013-02-16 | Exelixis Inc | 使用pi3k/mtor吡啶並嘧啶酮抑制劑及苯達莫司汀及/或利妥昔單抗治療惡性血液疾病之組合療法 |
WO2013066483A1 (fr) | 2011-08-31 | 2013-05-10 | Novartis Ag | Combinaisons synergiques d'inhibiteurs de pi3k et de mek |
CN104829609B (zh) * | 2014-02-11 | 2016-08-03 | 北大方正集团有限公司 | 取代的吡啶并嘧啶化合物及其制备方法和应用 |
JP6631616B2 (ja) | 2014-07-26 | 2020-01-15 | ノース・アンド・サウス・ブラザー・ファーマシー・インベストメント・カンパニー・リミテッド | CDK阻害剤としての2−アミノ−ピリド[2,3−d]ピリミジン−7(8H)−オン誘導体及びその使用 |
CN105330699B (zh) * | 2014-08-13 | 2018-12-04 | 山东汇睿迪生物技术有限公司 | 一种含磷吡啶并[2,3-d]嘧啶-7-酮类化合物或其药学上可接受的盐、药物组合物及其应用 |
KR20170058432A (ko) | 2014-10-10 | 2017-05-26 | 화이자 인코포레이티드 | 상승 효과적 아우리스타틴 조합 |
SI3302565T1 (sl) | 2015-06-04 | 2020-02-28 | Pfizer Inc. | Trdne farmacevtske oblike palbocikliba |
US10779980B2 (en) | 2016-04-27 | 2020-09-22 | Synerz Medical, Inc. | Intragastric device for treating obesity |
EP3481822B1 (fr) | 2016-07-06 | 2022-06-22 | The Regents of The University of Michigan | Inhibiteurs multifonctionnels des voies biologiques de mek/pi3k et mtor/mek/pi3k et procédés thérapeutiques les utilisant |
EP3497103B1 (fr) | 2016-08-15 | 2021-05-05 | Pfizer Inc. | Inhibiteurs de pyridopyrimidinone cdk2/4/6 |
AU2017376766A1 (en) * | 2016-12-14 | 2019-06-06 | Tva (Abc), Llc | HSP90-targeting conjugates and formulations thereof |
US10596165B2 (en) | 2018-02-12 | 2020-03-24 | resTORbio, Inc. | Combination therapies |
IL279329B1 (en) | 2018-06-15 | 2024-09-01 | Navitor Pharm Inc | Rapamycin analogs and their uses |
EP3902801A4 (fr) * | 2018-12-28 | 2022-12-14 | SPV Therapeutics Inc. | Inhibiteurs de kinases cycline-dépendantes |
US20220220103A1 (en) * | 2018-12-28 | 2022-07-14 | Spv Therapeutics Inc. | Cyclin-dependent kinase inhibitors |
US11583538B2 (en) | 2019-04-08 | 2023-02-21 | Venenum Biodesign, LLC | Substituted pyrrolo[1,2-a]pyrazines and pyrrolo[1,2-a][1,4]diazepines as TREX1 inhibitors |
US11819476B2 (en) | 2019-12-05 | 2023-11-21 | Janssen Pharmaceutica Nv | Rapamycin analogs and uses thereof |
WO2021139775A1 (fr) * | 2020-01-10 | 2021-07-15 | 江苏先声药业有限公司 | Composé de pyridone et son application |
WO2022075974A1 (fr) * | 2020-10-06 | 2022-04-14 | Venenum Biodesign, LLC | Inhibiteurs cycliques de trex1 |
KR20230121758A (ko) | 2020-11-18 | 2023-08-21 | 데시페라 파마슈티칼스, 엘엘씨. | Gcn2 및 perk 키나제 억제제 및 그의 사용 방법 |
CA3238551A1 (fr) * | 2021-11-18 | 2023-05-25 | Steven FRUCHTMAN | Methodes et compositions pour traitement du cancer |
Family Cites Families (45)
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US5264437A (en) * | 1992-03-20 | 1993-11-23 | Syntex (U.S.A.) Inc. | Optionally substituted pyrido[2,3-d]pyridine-2,4(1H,3H)-diones and pyrido[2,]pyrimidine-2(1H,3H)-ones |
MD1861G2 (ro) | 1994-11-14 | 2002-09-30 | Уорнер-Ламберт Кампэни | Derivaţi ai 6-arilpirido[2,3-d]pirimidinelor şi naftiridinelor, compoziţie farmaceutică pe baza lor, metode de tratament şi de inhibare a proliferării şi migraţiei celulei receptorului tirozinkinazei |
CN1177960A (zh) * | 1995-03-10 | 1998-04-01 | 圣诺菲药品有限公司 | 6-取代的吡唑并[3,4-d]嘧啶-4-酮及其组合物和使用方法 |
IL117923A (en) | 1995-05-03 | 2000-06-01 | Warner Lambert Co | Anti-cancer pharmaceutical compositions containing polysubstituted pyrido¬2,3-d¾pyrimidine derivatives and certain such novel compounds |
US5925761A (en) | 1997-02-04 | 1999-07-20 | Sepracor Inc. | Synthesis of terfenadine and derivatives |
WO1998033798A2 (fr) | 1997-02-05 | 1998-08-06 | Warner Lambert Company | Pyrido[2,3d]pyrimidines et 4-aminopyrimidines en tant qu'inhibiteurs de la proliferation cellulaire |
US6498163B1 (en) | 1997-02-05 | 2002-12-24 | Warner-Lambert Company | Pyrido[2,3-D]pyrimidines and 4-aminopyrimidines as inhibitors of cellular proliferation |
GB9904932D0 (en) | 1999-03-04 | 1999-04-28 | Glaxo Group Ltd | Composition and method for preventing/reducing the severity of side effects of chemotherapy and/or radiation therapy |
SK10772002A3 (sk) | 2000-01-27 | 2004-01-08 | Warner-Lambert Company | Pyridopyrimidinónové deriváty na liečbu neurodegeneratívnych ochorení |
AP2002002643A0 (en) | 2000-03-06 | 2002-12-31 | Warner Lambert Co | 5-alkylpyrido[2,3-d]pyrimidines tyrosine kinase inhibitors |
ES2360933T3 (es) | 2000-04-27 | 2011-06-10 | Astellas Pharma Inc. | Derivados de heteroarilo condensados. |
EP1364950A4 (fr) | 2001-02-26 | 2005-03-09 | Tanabe Seiyaku Co | Derive de pyridopyrimidine ou naphthyridine |
US7019002B2 (en) * | 2001-12-11 | 2006-03-28 | Pharmacia & Upjohn, S.P.A. | Pyridopyrimidinones derivatives as telomerase inhibitors |
GEP20063909B (en) | 2002-01-22 | 2006-08-25 | Warner Lambert Co | 2-(PYRIDIN-2-YLAMINO)-PYRIDO[2,3d] PYRIMIDIN-7-ONES |
JP2003321472A (ja) | 2002-02-26 | 2003-11-11 | Takeda Chem Ind Ltd | Grk阻害剤 |
BR0309053A (pt) | 2002-04-19 | 2005-02-22 | Smithkline Beecham Corp | Compostos |
KR20050006221A (ko) | 2002-05-06 | 2005-01-15 | 제네랩스 테크놀로지스, 인코포레이티드 | C형 간염 바이러스 감염 치료용의 뉴클레오시드 유도체 |
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JP2004203751A (ja) | 2002-12-24 | 2004-07-22 | Pfizer Inc | 置換6,6−ヘテロ二環式誘導体 |
US20050009849A1 (en) | 2003-01-03 | 2005-01-13 | Veach Darren R. | Pyridopyrimidine kinase inhibitors |
WO2004089930A1 (fr) | 2003-04-02 | 2004-10-21 | Imclone Systems Incorporated | Derives de 4- fluoroquinolone et leur utilisation comme inhibiteurs de kinase |
WO2005040337A2 (fr) | 2003-05-20 | 2005-05-06 | The Regents Of The University Of California | Procedes permettant de lier des agents a des plaques $g(b)-amyloides |
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US7160888B2 (en) | 2003-08-22 | 2007-01-09 | Warner Lambert Company Llc | [1,8]naphthyridin-2-ones and related compounds for the treatment of schizophrenia |
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 |
WO2005082903A1 (fr) | 2004-02-18 | 2005-09-09 | Warner-Lambert Company Llc | 2-(pyridin-3-ylamino)-pyrido[2,3-d]pyrimidin-7-ones |
WO2005094830A1 (fr) | 2004-03-30 | 2005-10-13 | Pfizer Products Inc. | Combinaisons d'inhibiteurs de transduction de signaux |
WO2005105097A2 (fr) | 2004-04-28 | 2005-11-10 | Gpc Biotech Ag | Derives de pyridopyrimidine |
EP1749004B1 (fr) * | 2004-05-04 | 2007-09-19 | Warner-Lambert Company LLC | Pyrid[2,3-d]pyrimidin-7-ones pyrrolyl-substituees et derives de ces dernieres utilises comme agents therapeutiques |
EP1761281A1 (fr) | 2004-06-04 | 2007-03-14 | Pfizer Products Incorporated | Methode de traitement de croissances cellulaires anormales |
JP2008510770A (ja) | 2004-08-26 | 2008-04-10 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Plk阻害剤としての新規プテリジノン |
WO2006050501A2 (fr) | 2004-11-03 | 2006-05-11 | University Of Kansas | Analogues de novobiocine en tant qu'agents anticancereux |
CA2590294A1 (fr) | 2004-12-13 | 2006-06-22 | Sunesis Pharmaceuticals, Inc. | Pyridopyrimidinones, dihydropyrimidopyrimidinones et pteridinones utiles en tant qu'inhibiteurs des kinases raf |
US20060142312A1 (en) | 2004-12-23 | 2006-06-29 | Pfizer Inc | C6-aryl and heteroaryl substituted pyrido[2,3-D] pyrimidin-7-ones |
EP1940839B1 (fr) * | 2005-10-07 | 2013-07-31 | Exelixis, Inc. | INHIBITEURS DE PI3Kalpha DE TYPE PYRIDOPYRIMIDINONE |
AU2006302148B2 (en) * | 2005-10-07 | 2012-12-06 | Exelixis, Inc. | Pyridopyrimidinone inhibitors of PI3Kalpha |
EP1872922A1 (fr) * | 2006-06-27 | 2008-01-02 | Nederlandse Organisatie voor Toegepast-Natuuurwetenschappelijk Onderzoek TNO | Procédé et dispositif de fabrication d'un article en matière plastique |
AU2007284562B2 (en) | 2006-08-16 | 2013-05-02 | Exelixis, Inc. | Using PI3K and MEK modulators in treatments of cancer |
JP4718637B2 (ja) | 2006-09-15 | 2011-07-06 | ファイザー・プロダクツ・インク | ピリド(2,3−d)ピリミジノン化合物およびpi3阻害剤としてのその使用 |
BRPI0808772A2 (pt) * | 2007-03-14 | 2014-08-12 | Exelixis Inc | Inibidores da via de hedgehog |
JP2010523681A (ja) | 2007-04-11 | 2010-07-15 | エクセリクシス, インク. | 癌の治療のためのPI3K−αの阻害剤としてのピリド[2,3−D]ピリミジン−7−オン化合物 |
US8101622B2 (en) | 2008-09-30 | 2012-01-24 | Exelixis, Inc. | Pyridopyrimidinone inhibitors of PI3Kα and mTOR |
CN102970868A (zh) * | 2010-04-16 | 2013-03-13 | 柯瑞斯公司 | 具有k-ras突变的癌症的治疗 |
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2007
- 2007-09-03 JP JP2009527908A patent/JP4718637B2/ja active Active
- 2007-09-03 MX MX2009002927A patent/MX2009002927A/es active IP Right Grant
- 2007-09-03 ES ES07804890T patent/ES2366489T3/es active Active
- 2007-09-03 EP EP07804890.7A patent/EP2074122B9/fr active Active
- 2007-09-03 SI SI200730715T patent/SI2074122T1/sl unknown
- 2007-09-03 KR KR1020097005342A patent/KR101099926B1/ko active IP Right Grant
- 2007-09-03 EA EA200970207A patent/EA016388B1/ru not_active IP Right Cessation
- 2007-09-03 ME MEP-80/09A patent/MEP8009A/xx unknown
- 2007-09-03 WO PCT/IB2007/002578 patent/WO2008032162A1/fr active Application Filing
- 2007-09-03 RS RSP-2009/0104A patent/RS20090104A/sr unknown
- 2007-09-03 MY MYPI20091013A patent/MY146420A/en unknown
- 2007-09-03 GE GEAP200711157A patent/GEP20115306B/en unknown
- 2007-09-03 AT AT07804890T patent/ATE514695T1/de active
- 2007-09-03 CN CN2007800342100A patent/CN101573358B/zh not_active Expired - Fee Related
- 2007-09-03 DK DK07804890.7T patent/DK2074122T5/da active
- 2007-09-03 BR BRPI0716749A patent/BRPI0716749B8/pt not_active IP Right Cessation
- 2007-09-03 NZ NZ575167A patent/NZ575167A/en not_active IP Right Cessation
- 2007-09-03 RS RS20110379A patent/RS51927B/en unknown
- 2007-09-03 CA CA2663401A patent/CA2663401C/fr not_active Expired - Fee Related
- 2007-09-03 PT PT07804890T patent/PT2074122E/pt unknown
- 2007-09-03 AU AU2007297212A patent/AU2007297212B8/en not_active Ceased
- 2007-09-03 PL PL07804890T patent/PL2074122T3/pl unknown
- 2007-09-03 AP AP2009004790A patent/AP2710A/xx active
- 2007-09-12 UY UY30588A patent/UY30588A1/es not_active Application Discontinuation
- 2007-09-13 AR ARP070104059A patent/AR062785A1/es not_active Application Discontinuation
- 2007-09-13 PE PE2007001238A patent/PE20080670A1/es not_active Application Discontinuation
- 2007-09-13 GT GT200700077A patent/GT200700077A/es unknown
- 2007-09-13 US US11/854,999 patent/US7696213B2/en not_active Expired - Fee Related
- 2007-09-14 TW TW096134605A patent/TWI334353B/zh not_active IP Right Cessation
- 2007-09-14 CL CL200702682A patent/CL2007002682A1/es unknown
- 2007-09-17 HN HN2007000267A patent/HN2007000267A/es unknown
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2009
- 2009-02-25 IL IL197243A patent/IL197243A/en active IP Right Grant
- 2009-03-02 ZA ZA200901477A patent/ZA200901477B/xx unknown
- 2009-03-11 DO DO2009000039A patent/DOP2009000039A/es unknown
- 2009-03-13 CU CU20090040A patent/CU23783B7/es not_active IP Right Cessation
- 2009-03-13 TN TN2009000085A patent/TN2009000085A1/fr unknown
- 2009-03-13 MA MA31707A patent/MA30709B1/fr unknown
- 2009-03-13 CR CR10662A patent/CR10662A/es unknown
- 2009-03-13 NI NI200900032A patent/NI200900032A/es unknown
- 2009-03-18 NO NO20091141A patent/NO342357B1/no not_active IP Right Cessation
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2010
- 2010-02-09 US US12/702,937 patent/US8273755B2/en active Active
- 2010-05-03 HK HK10104328.3A patent/HK1138589A1/xx not_active IP Right Cessation
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2011
- 2011-07-20 CY CY20111100714T patent/CY1111911T1/el unknown
- 2011-08-24 HR HRP20110621TT patent/HRP20110621T2/hr unknown
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2012
- 2012-08-16 US US13/587,825 patent/US8633204B2/en not_active Expired - Fee Related
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