NO20080150L - Inhibitorer av AKT-aktivitet - Google Patents
Inhibitorer av AKT-aktivitetInfo
- Publication number
- NO20080150L NO20080150L NO20080150A NO20080150A NO20080150L NO 20080150 L NO20080150 L NO 20080150L NO 20080150 A NO20080150 A NO 20080150A NO 20080150 A NO20080150 A NO 20080150A NO 20080150 L NO20080150 L NO 20080150L
- Authority
- NO
- Norway
- Prior art keywords
- akt activity
- inhibitors
- akt
- compounds
- inhibit
- Prior art date
Links
- 230000000694 effects Effects 0.000 title abstract 3
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 3
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 102000001708 Protein Isoforms Human genes 0.000 abstract 1
- 108010029485 Protein Isoforms Proteins 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 150000005054 naphthyridines Chemical class 0.000 abstract 1
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
-
- 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
- C07D471/12—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 three hetero rings
- C07D471/14—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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- 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
- C07D487/12—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 three hetero rings
- C07D487/14—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (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)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68972605P | 2005-06-10 | 2005-06-10 | |
| US73418805P | 2005-11-07 | 2005-11-07 | |
| PCT/US2006/022079 WO2006135627A2 (en) | 2005-06-10 | 2006-06-07 | Inhibitors of akt activity |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20080150L true NO20080150L (no) | 2008-03-10 |
Family
ID=37532789
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20080150A NO20080150L (no) | 2005-06-10 | 2008-01-09 | Inhibitorer av AKT-aktivitet |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US8008317B2 (pl) |
| EP (1) | EP1898903B8 (pl) |
| JP (1) | JP5055494B2 (pl) |
| KR (1) | KR100959771B1 (pl) |
| AU (1) | AU2006258124B8 (pl) |
| BR (1) | BRPI0611717A2 (pl) |
| CA (1) | CA2610888C (pl) |
| CR (1) | CR9580A (pl) |
| DK (1) | DK1898903T3 (pl) |
| EC (1) | ECSP077980A (pl) |
| ES (1) | ES2409168T3 (pl) |
| HR (1) | HRP20130429T1 (pl) |
| IL (1) | IL187690A (pl) |
| MX (1) | MX2007015578A (pl) |
| NI (1) | NI200700320A (pl) |
| NO (1) | NO20080150L (pl) |
| NZ (1) | NZ563423A (pl) |
| PL (1) | PL1898903T3 (pl) |
| PT (1) | PT1898903E (pl) |
| RU (1) | RU2421454C2 (pl) |
| TW (1) | TW200800166A (pl) |
| WO (1) | WO2006135627A2 (pl) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1784175A4 (en) | 2004-08-23 | 2009-07-22 | Merck & Co Inc | INHIBITORS OF ACT ACTIVITY |
| EP1898903B8 (en) | 2005-06-10 | 2013-05-15 | Merck Sharp & Dohme Corp. | Inhibitors of akt activity |
| TW200806670A (en) | 2006-04-25 | 2008-02-01 | Merck & Co Inc | Inhibitors of checkpoint kinases |
| AR064010A1 (es) | 2006-12-06 | 2009-03-04 | Merck & Co Inc | Inhibidores de la actividad de la akt |
| JP2010512312A (ja) * | 2006-12-06 | 2010-04-22 | メルク エンド カムパニー インコーポレーテッド | Ａｋｔ活性の阻害剤 |
| EP2139333A4 (en) * | 2007-03-28 | 2010-11-10 | Merck Sharp & Dohme | SUBSTITUTED PYRID- [3,2-E] - [1,2,4] -TRIAZOL- [4,3-C] -PYRIMIDINE DERIVATIVES AS CANNABINOID-1 RECEPTOR MODULATORS |
| WO2009006567A2 (en) | 2007-07-05 | 2009-01-08 | Array Biopharma Inc. | Pyrimidyl cyclopentanes as akt protein kinase inhibitors |
| US9409886B2 (en) | 2007-07-05 | 2016-08-09 | Array Biopharma Inc. | Pyrimidyl cyclopentanes as AKT protein kinase inhibitors |
| NZ583267A (en) | 2007-08-14 | 2012-03-30 | Bayer Schering Pharma Ag | Fused bicyclic pyrimidines |
| 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 |
| JP2011522048A (ja) * | 2008-06-03 | 2011-07-28 | メルク・シャープ・エンド・ドーム・コーポレイション | Ａｋｔ活性の阻害剤 |
| US8536193B2 (en) * | 2008-06-03 | 2013-09-17 | Merck Sharp & Dohme Corp. | Inhibitors of AKT activity |
| EP2583556B1 (de) | 2008-07-17 | 2016-01-20 | Bayer CropScience AG | Heterocyclische Verbindungen als Schädlingsbekämpfungsmittel |
| AU2010208480A1 (en) * | 2009-02-02 | 2011-07-28 | Msd K.K. | Inhibitors of Akt activity |
| CN102686600A (zh) | 2009-02-05 | 2012-09-19 | 托凯药业股份有限公司 | 甾体cyp17抑制剂/抗雄激素物质的新型药物前体 |
| CN102361872B (zh) | 2009-02-13 | 2014-12-03 | 拜耳知识产权有限责任公司 | 作为akt抑制剂的稠合嘧啶 |
| EA201101186A1 (ru) | 2009-02-13 | 2012-04-30 | Байер Фарма Акциенгезельшафт | Конденсированные пиримидины |
| WO2010101734A1 (en) * | 2009-03-06 | 2010-09-10 | Merck Sharp & Dohme Corp. | Combination cancer therapy with an akt inhibitor and other anticancer agents |
| US8614221B2 (en) * | 2009-03-11 | 2013-12-24 | Merck Sharp & Dohme Corp. | Inhibitors of Akt activity |
| 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 |
| EP2266985A1 (en) * | 2009-06-26 | 2010-12-29 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Tricyclic Pyrimidine Derivatives as Wnt antagonists |
| EP2473495A1 (en) | 2009-09-18 | 2012-07-11 | Almac Discovery Limited | Pharmaceutical compounds |
| EP2513059A4 (en) * | 2009-12-17 | 2013-06-05 | Merck Sharp & Dohme | HAMMER OF ACT ACTIVITY |
| GB0922589D0 (en) * | 2009-12-23 | 2010-02-10 | Almac Discovery Ltd | Pharmaceutical compounds |
| EP2593451B1 (en) * | 2010-07-12 | 2015-08-19 | Bayer Intellectual Property GmbH | Substituted imidazo[1,2-a]pyrimidines and -pyridines |
| JP5996532B2 (ja) * | 2010-07-15 | 2016-09-21 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ ＧｍｂＨ | 有害生物防除剤としての新規複素環式化合物 |
| HUE026323T2 (en) | 2011-04-07 | 2016-05-30 | Bayer Ip Gmbh | Imidazopyridazines as akt kinase inhibitors |
| US9408885B2 (en) | 2011-12-01 | 2016-08-09 | Vib Vzw | Combinations of therapeutic agents for treating melanoma |
| EP2850200A1 (en) * | 2012-05-17 | 2015-03-25 | Genentech, Inc. | Process of making hydroxylated cyclopentapyrimidine compounds and salts thereof |
| RS56680B1 (sr) | 2012-11-28 | 2018-03-30 | Merck Sharp & Dohme | Kompozicije i postupci za lečenje kancera |
| CA2897279C (en) | 2013-01-23 | 2020-12-29 | Astrazeneca Ab | Aminopyrazine derivatives and pharmaceutical compositions thereof for use in the treatment of cancer |
| RU2015137617A (ru) | 2013-03-14 | 2017-04-18 | Юниверсити Оф Мэриленд, Балтимор Офис Оф Текнолоджи Трансфер | Агенты, подавляющие андрогенные рецепторы, и их применение |
| CN105636594A (zh) | 2013-08-12 | 2016-06-01 | 托凯药业股份有限公司 | 使用雄激素靶向疗法用于治疗肿瘤性疾病的生物标记物 |
| EP3091016A1 (en) | 2015-05-05 | 2016-11-09 | Technische Universität Dortmund | Kinase inhibitors and their use in cancer therapy |
| EP3388428B1 (en) * | 2015-12-07 | 2021-08-04 | Suzhou Sinovent Pharmaceuticals Company | Five-membered heterocyclic amides wnt pathway inhibitor |
| TW201822637A (zh) | 2016-11-07 | 2018-07-01 | 德商拜耳廠股份有限公司 | 用於控制動物害蟲的經取代磺醯胺類 |
| MX2020002611A (es) | 2017-09-07 | 2020-07-13 | Univ Res Inst Inc Augusta | Activador especifico de akt3 y usos del mismo. |
| CN118767143A (zh) | 2019-12-12 | 2024-10-15 | 听治疗有限责任公司 | 用于预防和治疗听力损失的组合物和方法 |
| GB2600384A (en) | 2020-09-30 | 2022-05-04 | Vaderis Therapeutics Ag | Allosteric AKT inhibitors for use in the treatment of hereditary hemorrhagic telangiectasia |
| MX2024005207A (es) * | 2021-11-05 | 2024-07-24 | Georgiamune Inc | Moduladores de akt3. |
| WO2025196161A2 (en) | 2024-03-20 | 2025-09-25 | Specialty Operations France | Cosmetic compositions, use thereof, and methods for using such compositions |
| WO2025196160A1 (en) | 2024-03-20 | 2025-09-25 | Specialty Operations France | Cosmetic compositions, use thereof, and methods for using such compositions |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4831013A (en) * | 1986-03-20 | 1989-05-16 | Ciba-Geigy Corporation | 2-substituted-e-fused-[1,2,4]triazolo[1,5-c]pyrimidines, pharmaceutical compositions, and uses thereof |
| ES2172583T3 (es) * | 1995-06-06 | 2002-10-01 | Pfizer | 5,6-dihidro-9h-pirazol(3,4-c)-1,2,4-triazol(4,3-alfa)piridinas triciclicas. |
| ES2137113B1 (es) * | 1997-07-29 | 2000-09-16 | Almirall Prodesfarma Sa | Nuevos derivados de triazolo-piridazinas heterociclicos. |
| UA67760C2 (uk) * | 1997-12-11 | 2004-07-15 | Міннесота Майнінг Енд Мануфакчурінг Компані | Імідазонафтиридин та тетрагідроімідазонафтиридин, фармацевтична композиція, спосіб індукування біосинтезу цитокінів та спосіб лікування вірусної інфекції, проміжні сполуки |
| GB9824897D0 (en) * | 1998-11-12 | 1999-01-06 | Merck Sharp & Dohme | Therapeutic compounds |
| GB9904933D0 (en) * | 1999-03-04 | 1999-04-28 | Glaxo Group Ltd | Compounds |
| US7034026B2 (en) | 2001-04-10 | 2006-04-25 | Merck & Co., Inc. | Inhibitors of Akt activity |
| US20030187026A1 (en) | 2001-12-13 | 2003-10-02 | Qun Li | Kinase inhibitors |
| US7223738B2 (en) | 2002-04-08 | 2007-05-29 | Merck & Co., Inc. | Inhibitors of Akt activity |
| JP4394959B2 (ja) | 2002-04-08 | 2010-01-06 | メルク エンド カムパニー インコーポレーテッド | Ａｋｔ活性の阻害剤 |
| US7273869B2 (en) | 2002-04-08 | 2007-09-25 | Merck & Co., Inc. | Inhibitors of Akt activity |
| EP1496906A4 (en) | 2002-04-08 | 2006-05-03 | Merck & Co Inc | HEMMER OF ACT ACTIVITY |
| EP1539754A4 (en) * | 2002-08-23 | 2009-02-25 | Novartis Vaccines & Diagnostic | BENZIMIDAZOCHINOLINONE AND ITS USE |
| JP2006507299A (ja) | 2002-10-30 | 2006-03-02 | メルク エンド カムパニー インコーポレーテッド | Ａｋｔ活性の阻害薬 |
| EP1620095A4 (en) * | 2003-04-24 | 2009-04-01 | Merck & Co Inc | HEMMER OF ACT ACTIVITY |
| CN1809354A (zh) | 2003-04-24 | 2006-07-26 | 麦克公司 | Akt活性抑制剂 |
| ATE461179T1 (de) | 2003-04-24 | 2010-04-15 | Merck Sharp & Dohme | Hemmer der akt aktivität |
| US7414055B2 (en) | 2003-04-24 | 2008-08-19 | Merck & Co., Inc. | Inhibitors of Akt activity |
| WO2005007099A2 (en) | 2003-07-10 | 2005-01-27 | Imclone Systems Incorporated | Pkb inhibitors as anti-tumor agents |
| EP1679308B1 (en) | 2003-10-15 | 2013-07-24 | Ube Industries, Ltd. | Novel indazole derivative |
| EP1737861A4 (en) | 2004-04-09 | 2010-04-28 | Merck Sharp & Dohme | HEMMER OF ACT ACTIVITY |
| EP1784175A4 (en) | 2004-08-23 | 2009-07-22 | Merck & Co Inc | INHIBITORS OF ACT ACTIVITY |
| US20080015212A1 (en) | 2004-12-02 | 2008-01-17 | Barnett Stanley F | Inhibitors Of Akt Activity |
| US7910561B2 (en) | 2004-12-15 | 2011-03-22 | Merck Sharp & Dohme Corp. | Inhibitors of Akt activity |
| AU2006216998B2 (en) | 2005-02-14 | 2010-12-23 | Merck Sharp & Dohme Corp. | Inhibitors of Akt activity |
| AU2006235314B2 (en) | 2005-04-12 | 2011-01-20 | Merck Sharp & Dohme Corp. | Inhibitors of Akt activity |
| EP1898903B8 (en) | 2005-06-10 | 2013-05-15 | Merck Sharp & Dohme Corp. | Inhibitors of akt activity |
| AR064010A1 (es) | 2006-12-06 | 2009-03-04 | Merck & Co Inc | Inhibidores de la actividad de la akt |
-
2006
- 2006-06-07 EP EP06772406.2A patent/EP1898903B8/en active Active
- 2006-06-07 RU RU2008100045/04A patent/RU2421454C2/ru not_active IP Right Cessation
- 2006-06-07 JP JP2008515861A patent/JP5055494B2/ja not_active Expired - Fee Related
- 2006-06-07 HR HRP20130429TT patent/HRP20130429T1/hr unknown
- 2006-06-07 PL PL06772406T patent/PL1898903T3/pl unknown
- 2006-06-07 BR BRPI0611717-1A patent/BRPI0611717A2/pt active Search and Examination
- 2006-06-07 ES ES06772406T patent/ES2409168T3/es active Active
- 2006-06-07 US US11/921,352 patent/US8008317B2/en active Active
- 2006-06-07 PT PT67724062T patent/PT1898903E/pt unknown
- 2006-06-07 DK DK06772406.2T patent/DK1898903T3/da active
- 2006-06-07 CA CA2610888A patent/CA2610888C/en not_active Expired - Fee Related
- 2006-06-07 MX MX2007015578A patent/MX2007015578A/es active IP Right Grant
- 2006-06-07 WO PCT/US2006/022079 patent/WO2006135627A2/en not_active Ceased
- 2006-06-07 KR KR1020077028878A patent/KR100959771B1/ko not_active Expired - Fee Related
- 2006-06-07 AU AU2006258124A patent/AU2006258124B8/en not_active Ceased
- 2006-06-07 NZ NZ563423A patent/NZ563423A/en not_active IP Right Cessation
- 2006-10-30 TW TW095140060A patent/TW200800166A/zh unknown
-
2007
- 2007-11-27 IL IL187690A patent/IL187690A/en not_active IP Right Cessation
- 2007-12-03 EC EC2007007980A patent/ECSP077980A/es unknown
- 2007-12-06 NI NI200700320A patent/NI200700320A/es unknown
- 2007-12-07 CR CR9580A patent/CR9580A/es unknown
-
2008
- 2008-01-09 NO NO20080150A patent/NO20080150L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| RU2421454C2 (ru) | 2011-06-20 |
| MX2007015578A (es) | 2008-03-06 |
| EP1898903A4 (en) | 2010-07-21 |
| AU2006258124B2 (en) | 2009-09-03 |
| CA2610888C (en) | 2011-02-08 |
| KR100959771B1 (ko) | 2010-05-28 |
| EP1898903B8 (en) | 2013-05-15 |
| EP1898903B1 (en) | 2013-03-27 |
| ES2409168T3 (es) | 2013-06-25 |
| BRPI0611717A2 (pt) | 2009-01-13 |
| US8008317B2 (en) | 2011-08-30 |
| AU2006258124B8 (en) | 2010-01-07 |
| ECSP077980A (es) | 2008-01-23 |
| WO2006135627A3 (en) | 2008-07-31 |
| PT1898903E (pt) | 2013-06-28 |
| JP2009501698A (ja) | 2009-01-22 |
| IL187690A0 (en) | 2008-11-03 |
| CA2610888A1 (en) | 2006-12-21 |
| JP5055494B2 (ja) | 2012-10-24 |
| PL1898903T3 (pl) | 2013-08-30 |
| HRP20130429T1 (en) | 2013-06-30 |
| IL187690A (en) | 2012-06-28 |
| KR20080016627A (ko) | 2008-02-21 |
| DK1898903T3 (da) | 2013-07-01 |
| RU2008100045A (ru) | 2009-07-20 |
| WO2006135627A2 (en) | 2006-12-21 |
| AU2006258124A1 (en) | 2006-12-21 |
| EP1898903A2 (en) | 2008-03-19 |
| TW200800166A (en) | 2008-01-01 |
| NZ563423A (en) | 2010-05-28 |
| CR9580A (es) | 2008-09-23 |
| NI200700320A (es) | 2008-06-17 |
| US20100222321A1 (en) | 2010-09-02 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO20080150L (no) | Inhibitorer av AKT-aktivitet | |
| NO20092569L (no) | Inhibitorer av Akt-aktivitet | |
| WO2006091395A3 (en) | Inhibitors of akt activity | |
| NO20063449L (no) | Substituerte heterocykler og deres anvendelse | |
| NO20061194L (no) | Mitotiske kinesininbibitorer | |
| NO20081454L (no) | Met-kinaseinhibitorer | |
| NO20065847L (no) | Difenylimidazopyrimidiner og -imidazolaminer som inhibitorer av B-sekretase | |
| EA200970486A1 (ru) | Соединения для ингибирования митоза | |
| WO2006106326A8 (en) | Substituted heterocycles and their use as chk1, pdk1 and pak inhibitors | |
| EA200870380A1 (ru) | Аминотетрагидропираны в качестве ингибиторов дипептидилпептидазы-vi для лечения или предупреждения диабета | |
| EA201170670A1 (ru) | Аминотетрагидропираны в качестве ингибиторов дипептидилпептидазы-iv для лечения или предупреждения диабета | |
| NO20084652L (no) | Deazapuriner anvendelige som inhibitorer av januskinaser | |
| NO20091605L (no) | Pyridinonforbindelser | |
| NO20080785L (no) | Behandling av kreft | |
| NO20073791L (no) | Pyrazolylaminopyridinderivater anvendbare som kinaseinhibitorer | |
| NO20073170L (no) | Kaspaseinhibitorer og anvendelse derav | |
| NO20056192L (no) | Kapaseinhibitorer og anvendelse derav | |
| NO20092691L (no) | 4-hydroksy-2-okso-2,3-dihydro-1,3-benzotiazol-7yl-forbindelser for modulering av B2-adrenoreseptoraktivitet | |
| BRPI0806789B8 (pt) | composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, e, uso de um composto ou de um sal farmaceuticamente aceitável do mesmo | |
| TW200736229A (en) | Substituted 1H-benzimidazole-4-carboxamides are potent PARP inhibitors | |
| WO2006110638A3 (en) | Inhibitors of akt activity | |
| ATE443044T1 (de) | Tace inhibitoren | |
| NO20064351L (no) | Caspaseinhibitorer og anvendelser derav | |
| WO2006068796A3 (en) | Inhibitors of akt activity | |
| NO20080839L (no) | Isotopsubstituerte protonpumpeinhibitorer |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC2A | Withdrawal, rejection or dismissal of laid open patent application |