JP2006507299A - Akt活性の阻害薬 - Google Patents
Akt活性の阻害薬 Download PDFInfo
- Publication number
- JP2006507299A JP2006507299A JP2004550130A JP2004550130A JP2006507299A JP 2006507299 A JP2006507299 A JP 2006507299A JP 2004550130 A JP2004550130 A JP 2004550130A JP 2004550130 A JP2004550130 A JP 2004550130A JP 2006507299 A JP2006507299 A JP 2006507299A
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- compound
- benzyl
- aryl
- inhibitor
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 0 C*C(*1)=C(C)*C2=C1[N+]CC(C)*2 Chemical compound C*C(*1)=C(C)*C2=C1[N+]CC(C)*2 0.000 description 8
- GTDRXSGQFSLDHR-UHFFFAOYSA-N CC(C)N1c(cccc2)c2NC1 Chemical compound CC(C)N1c(cccc2)c2NC1 GTDRXSGQFSLDHR-UHFFFAOYSA-N 0.000 description 1
- LKXLOGZBEFPAIJ-UHFFFAOYSA-N CC(C)[n]1c(C=CCC2)c2nc1 Chemical compound CC(C)[n]1c(C=CCC2)c2nc1 LKXLOGZBEFPAIJ-UHFFFAOYSA-N 0.000 description 1
- UMJVKPYTXOUBSB-UHFFFAOYSA-N CC(C)[n]1c2ccccc2nc1 Chemical compound CC(C)[n]1c2ccccc2nc1 UMJVKPYTXOUBSB-UHFFFAOYSA-N 0.000 description 1
- VATSEXCEOAFVSO-UHFFFAOYSA-N CNC(c1cnc[s]1)=O Chemical compound CNC(c1cnc[s]1)=O VATSEXCEOAFVSO-UHFFFAOYSA-N 0.000 description 1
- LNPDTQAFDNKSHK-UHFFFAOYSA-N Cc([o]nc1-c2ccccc2)c1-c(cc1)ccc1S(N)(=O)=O Chemical compound Cc([o]nc1-c2ccccc2)c1-c(cc1)ccc1S(N)(=O)=O LNPDTQAFDNKSHK-UHFFFAOYSA-N 0.000 description 1
- RZEKVGVHFLEQIL-UHFFFAOYSA-N Cc(cc1)ccc1-c1cc(C(F)(F)F)n[n]1-c(cc1)ccc1S(N)(=O)=O Chemical compound Cc(cc1)ccc1-c1cc(C(F)(F)F)n[n]1-c(cc1)ccc1S(N)(=O)=O RZEKVGVHFLEQIL-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- 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
-
- 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
-
- 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)
- 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)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US42230702P | 2002-10-30 | 2002-10-30 | |
| PCT/US2003/034007 WO2004041162A2 (en) | 2002-10-30 | 2003-10-24 | Inhibitors of akt activity |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006507299A true JP2006507299A (ja) | 2006-03-02 |
| JP2006507299A5 JP2006507299A5 (enExample) | 2006-09-14 |
Family
ID=32312489
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004550130A Pending JP2006507299A (ja) | 2002-10-30 | 2003-10-24 | Akt活性の阻害薬 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7399764B2 (enExample) |
| EP (1) | EP1558586B1 (enExample) |
| JP (1) | JP2006507299A (enExample) |
| AT (1) | ATE503483T1 (enExample) |
| AU (1) | AU2003284981B2 (enExample) |
| CA (1) | CA2501365C (enExample) |
| DE (1) | DE60336576D1 (enExample) |
| WO (1) | WO2004041162A2 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012517963A (ja) * | 2009-02-13 | 2012-08-09 | バイエル ファーマ アクチエンゲゼルシャフト | 縮合ピリミジン類 |
Families Citing this family (65)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2522435C (en) * | 2003-04-24 | 2011-04-12 | Merck & Co., Inc. | Inhibitors of akt activity |
| CA2522262A1 (en) * | 2003-04-24 | 2004-11-11 | Merck & Co., Inc. | Inhibitors of akt activity |
| EP1622616B1 (en) | 2003-04-24 | 2011-06-15 | Merck Sharp & Dohme Corp. | Inhibitors of akt activity |
| EP1620095A4 (en) * | 2003-04-24 | 2009-04-01 | Merck & Co Inc | HEMMER OF ACT ACTIVITY |
| AU2005233584B2 (en) * | 2004-04-09 | 2010-12-09 | Merck Sharp & Dohme Corp. | Inhibitors of Akt activity |
| AU2005233569B2 (en) * | 2004-04-09 | 2010-08-19 | Merck Sharp & Dohme Corp. | Inhibitors of Akt activity |
| JP2008510823A (ja) * | 2004-08-23 | 2008-04-10 | メルク エンド カムパニー インコーポレーテッド | Akt活性阻害剤 |
| CN101098872B (zh) * | 2004-11-22 | 2012-09-05 | 沃泰克斯药物股份有限公司 | 可用作蛋白激酶抑制剂的吡咯并吡嗪和吡唑并吡嗪 |
| ES2382814T3 (es) | 2005-05-17 | 2012-06-13 | Merck Sharp & Dohme Ltd. | Ácido cis-4-[(4-clorofenil)sulfonil]-4-(2,5-difluorofenil)ciclohexanopropanoico para el tratamiento del cáncer |
| DK1898903T3 (da) | 2005-06-10 | 2013-07-01 | Merck Sharp & Dohme | Inhibitorer af Akt-aktivitet |
| EP1978964A4 (en) | 2006-01-24 | 2009-12-09 | Merck & Co Inc | JAK2 tyrosine kinase Inhibition |
| CA2656618C (en) | 2006-07-06 | 2014-08-26 | Array Biopharma Inc. | Cyclopenta [d] pyrimidines as akt protein kinase inhibitors |
| CN101511842B (zh) * | 2006-07-06 | 2012-10-31 | 阵列生物制药公司 | 作为akt蛋白激酶抑制剂的二氢呋喃并嘧啶 |
| ATE532789T1 (de) | 2006-07-06 | 2011-11-15 | Array Biopharma Inc | Dihydrothienopyrimidine als akt-proteinkinase- inhibitoren |
| US8063050B2 (en) | 2006-07-06 | 2011-11-22 | Array Biopharma Inc. | Hydroxylated and methoxylated pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
| WO2008070134A1 (en) * | 2006-12-06 | 2008-06-12 | Merck & Co., Inc. | Inhibitors of akt activity |
| AR064010A1 (es) * | 2006-12-06 | 2009-03-04 | Merck & Co Inc | Inhibidores de la actividad de la akt |
| WO2008070823A2 (en) * | 2006-12-07 | 2008-06-12 | University Of South Florida | Substrate-mimetic akt inhibitor |
| WO2009006567A2 (en) | 2007-07-05 | 2009-01-08 | Array Biopharma Inc. | Pyrimidyl cyclopentanes as akt protein kinase inhibitors |
| SI2173723T1 (sl) | 2007-07-05 | 2011-12-30 | Array Biopharma Inc | Pirimidil ciklopentani kot inhibitorji AKT-protein-kinaze |
| US9409886B2 (en) | 2007-07-05 | 2016-08-09 | Array Biopharma Inc. | Pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
| US8846683B2 (en) | 2007-07-05 | 2014-09-30 | Array Biopharma, Inc. | Pyrimidyl cyclopentanes as Akt protein kinase inhibitors |
| NZ586346A (en) | 2008-01-09 | 2012-02-24 | Array Biopharma Inc | Hydroxylated pyrimidyl cyclopentanes as akt protein kinase inhibitors |
| WO2009089453A1 (en) | 2008-01-09 | 2009-07-16 | Array Biopharma Inc. | Hydroxylated pyrimidyl cyclopentane as akt protein kinase inhibitor |
| US20100048913A1 (en) | 2008-03-14 | 2010-02-25 | Angela Brodie | Novel C-17-Heteroaryl Steroidal CYP17 Inhibitors/Antiandrogens;Synthesis In Vitro Biological Activities, Pharmacokinetics and Antitumor Activity |
| EP2303269B1 (en) * | 2008-06-03 | 2014-07-30 | Merck Sharp & Dohme Corp. | Inhibitors of akt activity |
| EP2299825B1 (en) * | 2008-06-03 | 2013-07-31 | Merck Sharp & Dohme Corp. | Inhibitors of akt activity |
| EP2393827B1 (en) | 2009-02-05 | 2015-10-07 | Tokai Pharmaceuticals, Inc. | Novel prodrugs of steroidal cyp17 inhibitors/antiandrogens |
| US8168652B2 (en) | 2009-03-12 | 2012-05-01 | Merck Sharp & Dohme Corp. | Inhibitors of AKT activity |
| WO2010114780A1 (en) | 2009-04-01 | 2010-10-07 | Merck Sharp & Dohme Corp. | Inhibitors of akt activity |
| PH12012500713A1 (en) | 2009-10-14 | 2012-11-26 | Merck Sharp & Dohme | Substituted piperidines that increase p53 activity and the uses thereof |
| MX2012008641A (es) * | 2010-01-27 | 2012-11-23 | Vertex Pharma | Inhibidores de cinasas de pirazolopirazinas. |
| EP2584903B1 (en) | 2010-06-24 | 2018-10-24 | Merck Sharp & Dohme Corp. | Novel heterocyclic compounds as erk inhibitors |
| CA2806655A1 (en) * | 2010-07-28 | 2012-02-02 | Bayer Intellectual Property Gmbh | Substituted imidazo[1,2-b]pyridazines |
| US8518907B2 (en) | 2010-08-02 | 2013-08-27 | Merck Sharp & Dohme Corp. | RNA interference mediated inhibition of catenin (cadherin-associated protein), beta 1 (CTNNB1) gene expression using short interfering nucleic acid (siNA) |
| RU2624045C2 (ru) | 2010-08-17 | 2017-06-30 | Сирна Терапьютикс,Инк | ОПОСРЕДУЕМОЕ РНК-ИНТЕРФЕРЕНЦИЕЙ ИНГИБИРОВАНИЕ ЭКСПРЕССИИ ГЕНОВ ВИРУСА ГЕПАТИТА B (HBV) С ПРИМЕНЕНИЕМ МАЛОЙ ИНТЕРФЕРИРУЮЩЕЙ НУКЛЕИНОВОЙ КИСЛОТЫ (миНК) |
| WO2012030685A2 (en) | 2010-09-01 | 2012-03-08 | Schering Corporation | Indazole derivatives useful as erk inhibitors |
| EP3327125B1 (en) | 2010-10-29 | 2020-08-05 | Sirna Therapeutics, Inc. | Rna interference mediated inhibition of gene expression using short interfering nucleic acids (sina) |
| EP2654748B1 (en) | 2010-12-21 | 2016-07-27 | Merck Sharp & Dohme Corp. | Indazole derivatives useful as erk inhibitors |
| RU2013148817A (ru) | 2011-04-01 | 2015-05-10 | Дженентек, Инк. | Комбинации соединений-ингибиторов акт и мек и способы их применения |
| ES2620644T3 (es) | 2011-04-01 | 2017-06-29 | Genentech, Inc. | Combinaciones de compuestos inhibidores de AKT y agentes quimioterapéuticos, y métodos de uso |
| WO2013063214A1 (en) | 2011-10-27 | 2013-05-02 | Merck Sharp & Dohme Corp. | Novel compounds that are erk inhibitors |
| US9408885B2 (en) | 2011-12-01 | 2016-08-09 | Vib Vzw | Combinations of therapeutic agents for treating melanoma |
| EP3358013B1 (en) | 2012-05-02 | 2020-06-24 | Sirna Therapeutics, Inc. | Short interfering nucleic acid (sina) compositions |
| US9233979B2 (en) | 2012-09-28 | 2016-01-12 | Merck Sharp & Dohme Corp. | Compounds that are ERK inhibitors |
| ME02925B (me) | 2012-11-28 | 2018-04-20 | Merck Sharp & Dohme | Kompozicije i postupci za liječenje kancera |
| CA2895504A1 (en) | 2012-12-20 | 2014-06-26 | Merck Sharp & Dohme Corp. | Substituted imidazopyridines as hdm2 inhibitors |
| KR101470115B1 (ko) * | 2013-01-09 | 2014-12-05 | 동국대학교 산학협력단 | 2-(페닐에티닐)티에노[3,4-b]피라진 유도체 및 이를 포함하는 암의 예방 또는 치료용 약학적 조성물 |
| WO2014120748A1 (en) | 2013-01-30 | 2014-08-07 | Merck Sharp & Dohme Corp. | 2,6,7,8 substituted purines as hdm2 inhibitors |
| SG11201507093WA (en) | 2013-03-14 | 2015-10-29 | Univ Maryland Baltimore Office Of Technology Transfer | Androgen receptor down-regulating agents and uses thereof |
| SG11201600525XA (en) | 2013-08-12 | 2016-02-26 | Tokai Pharmaceuticals Inc | Biomarkers for treatment of neoplastic disorders using androgen-targeted therapies |
| US20160194368A1 (en) | 2013-09-03 | 2016-07-07 | Moderna Therapeutics, Inc. | Circular polynucleotides |
| JOP20190055A1 (ar) | 2016-09-26 | 2019-03-24 | Merck Sharp & Dohme | أجسام مضادة ضد cd27 |
| WO2018071283A1 (en) | 2016-10-12 | 2018-04-19 | Merck Sharp & Dohme Corp. | Kdm5 inhibitors |
| CA3058134A1 (en) | 2017-04-13 | 2018-10-18 | Aduro Biotech Holdings, Europe B.V. | Anti-sirp alpha antibodies |
| WO2019094311A1 (en) | 2017-11-08 | 2019-05-16 | Merck Sharp & Dohme Corp. | Prmt5 inhibitors |
| US11098059B2 (en) | 2017-11-08 | 2021-08-24 | Merck Sharp & Dohme Corp. | PRMT5 inhibitors |
| WO2019148412A1 (en) | 2018-02-01 | 2019-08-08 | Merck Sharp & Dohme Corp. | Anti-pd-1/lag3 bispecific antibodies |
| AU2019317549A1 (en) | 2018-08-07 | 2021-02-25 | Msd International Gmbh | PRMT5 inhibitors |
| EP3833668B1 (en) | 2018-08-07 | 2025-03-19 | Merck Sharp & Dohme LLC | Prmt5 inhibitors |
| EP3833667B1 (en) | 2018-08-07 | 2024-03-13 | Merck Sharp & Dohme LLC | Prmt5 inhibitors |
| WO2021118924A2 (en) | 2019-12-12 | 2021-06-17 | Ting Therapeutics Llc | Compositions and methods for the prevention and treatment of hearing loss |
| WO2021126729A1 (en) | 2019-12-17 | 2021-06-24 | Merck Sharp & Dohme Corp. | Prmt5 inhibitors |
| WO2021126728A1 (en) | 2019-12-17 | 2021-06-24 | Merck Sharp & Dohme Corp. | Prmt5 inhibitors |
| EP4077282A4 (en) | 2019-12-17 | 2023-11-08 | Merck Sharp & Dohme LLC | Prmt5 inhibitors |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999007701A1 (en) * | 1997-08-05 | 1999-02-18 | Sugen, Inc. | Tricyclic quinoxaline derivatives as protein tyrosine kinase inhibitors |
| WO2002041896A2 (de) * | 2000-11-25 | 2002-05-30 | Merck Patent Gmbh | Verwendung von thienopyrimidinen |
| JP2002220338A (ja) * | 2001-01-26 | 2002-08-09 | Banyu Pharmaceut Co Ltd | ビアリールウレア化合物又はその塩を有効成分として含有するCdk4及び/又はCdk6阻害剤 |
| JP2002284684A (ja) * | 2001-01-16 | 2002-10-03 | Japan Science & Technology Corp | チエノイソキノロン含有抗菌抗ウィルス剤および抗腫瘍剤 |
| WO2002083138A1 (en) * | 2001-04-10 | 2002-10-24 | Merck & Co., Inc. | Inhibitors of akt activity |
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| US3431262A (en) * | 1968-03-26 | 1969-03-04 | American Home Prod | Pyrazolo quinoxalines |
| JPS5416497A (en) * | 1977-07-08 | 1979-02-07 | Nippon Soda Co Ltd | Aminooxopyrrolopyrazine compounds and their preparation |
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| US5474995A (en) | 1993-06-24 | 1995-12-12 | Merck Frosst Canada, Inc. | Phenyl heterocycles as cox-2 inhibitors |
| CN1151147C (zh) | 1995-02-02 | 2004-05-26 | 史密丝克莱恩比彻姆有限公司 | 作为5-ht受体拮抗剂的吲哚衍生物 |
| WO1996023769A2 (en) | 1995-02-02 | 1996-08-08 | Smithkline Beecham Plc | Heterocyclic compounds possessing 5ht2c receptor antagonist activity |
| US20020132326A1 (en) | 1995-12-15 | 2002-09-19 | Hemmings Brian A. | Process for activating a kinase |
| US20020127214A1 (en) | 1995-11-16 | 2002-09-12 | Hemmings Brian Arthur | RAC-protein kinase as therapeutic agent or in diagnostics |
| DE69633186T2 (de) | 1995-11-16 | 2005-08-18 | Novartis Ag | Methode zur Identifizierung von Verbindungen die mit RAC Proteine Kinase interagieren |
| GB9525702D0 (en) | 1995-12-15 | 1996-02-14 | Ciba Geigy Ag | Process for activating a kinase |
| AU1200497A (en) | 1995-12-20 | 1997-07-14 | Medical Research Council | Control of protein synthesis, and screening method for agents |
| CZ297769B6 (cs) | 1996-06-27 | 2007-03-28 | Janssen Pharmaceutica N. V. | N-[4-(heteroarylmetyl)fenyl]-heteroarylaminy, zpusob jejich prípravy a jejich pouzití jako léciva |
| US6060491A (en) | 1997-06-19 | 2000-05-09 | Dupont Pharmaceuticals | 6-membered aromatics as factor Xa inhibitors |
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| IL136458A0 (en) | 2000-05-30 | 2001-06-14 | Peptor Ltd | Protein kinase inhibitors |
| US6958334B2 (en) | 2001-04-10 | 2005-10-25 | Merck & Co., Inc. | Inhibitors of Akt activity |
| WO2002083064A2 (en) | 2001-04-10 | 2002-10-24 | Merck & Co., Inc. | A method of treating cancer |
| AU2002251266A1 (en) | 2001-04-10 | 2002-10-28 | Merck Sharp And Dohme Limited | Inhibitors of akt activity |
| US20040116433A1 (en) | 2002-04-08 | 2004-06-17 | Owens Andrew Pate | Inhibitors of akt activity |
| US20060142178A1 (en) | 2002-04-08 | 2006-06-29 | Barnett Stanley F | Method of treating cancer |
| WO2003086403A1 (en) | 2002-04-08 | 2003-10-23 | Merck & Co., Inc. | Inhibitors of akt activity |
| US7273869B2 (en) | 2002-04-08 | 2007-09-25 | Merck & Co., Inc. | Inhibitors of Akt activity |
| CA2481229C (en) | 2002-04-08 | 2010-09-21 | Merck & Co., Inc. | Substituted pyrazine inhibitors of akt |
| AU2003223467B2 (en) | 2002-04-08 | 2007-10-04 | Merck Sharp & Dohme Corp. | Inhibitors of Akt activity |
| US20040102360A1 (en) | 2002-10-30 | 2004-05-27 | Barnett Stanley F. | Combination therapy |
-
2003
- 2003-10-24 CA CA2501365A patent/CA2501365C/en not_active Expired - Fee Related
- 2003-10-24 AT AT03779301T patent/ATE503483T1/de not_active IP Right Cessation
- 2003-10-24 JP JP2004550130A patent/JP2006507299A/ja active Pending
- 2003-10-24 EP EP03779301A patent/EP1558586B1/en not_active Expired - Lifetime
- 2003-10-24 WO PCT/US2003/034007 patent/WO2004041162A2/en not_active Ceased
- 2003-10-24 DE DE60336576T patent/DE60336576D1/de not_active Expired - Lifetime
- 2003-10-24 AU AU2003284981A patent/AU2003284981B2/en not_active Ceased
- 2003-10-24 US US10/530,252 patent/US7399764B2/en not_active Expired - Fee Related
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999007701A1 (en) * | 1997-08-05 | 1999-02-18 | Sugen, Inc. | Tricyclic quinoxaline derivatives as protein tyrosine kinase inhibitors |
| WO2002041896A2 (de) * | 2000-11-25 | 2002-05-30 | Merck Patent Gmbh | Verwendung von thienopyrimidinen |
| JP2002284684A (ja) * | 2001-01-16 | 2002-10-03 | Japan Science & Technology Corp | チエノイソキノロン含有抗菌抗ウィルス剤および抗腫瘍剤 |
| JP2002220338A (ja) * | 2001-01-26 | 2002-08-09 | Banyu Pharmaceut Co Ltd | ビアリールウレア化合物又はその塩を有効成分として含有するCdk4及び/又はCdk6阻害剤 |
| WO2002083138A1 (en) * | 2001-04-10 | 2002-10-24 | Merck & Co., Inc. | Inhibitors of akt activity |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012517963A (ja) * | 2009-02-13 | 2012-08-09 | バイエル ファーマ アクチエンゲゼルシャフト | 縮合ピリミジン類 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2004041162A2 (en) | 2004-05-21 |
| EP1558586A4 (en) | 2007-06-27 |
| EP1558586A2 (en) | 2005-08-03 |
| EP1558586B1 (en) | 2011-03-30 |
| DE60336576D1 (de) | 2011-05-12 |
| WO2004041162A3 (en) | 2004-07-29 |
| ATE503483T1 (de) | 2011-04-15 |
| AU2003284981B2 (en) | 2009-05-28 |
| US20050288294A1 (en) | 2005-12-29 |
| CA2501365C (en) | 2011-05-31 |
| US7399764B2 (en) | 2008-07-15 |
| AU2003284981A1 (en) | 2004-06-07 |
| CA2501365A1 (en) | 2004-05-21 |
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