NO20074853L - Smamolekylinhibitorer av MDM2 og anvendelser derav - Google Patents
Smamolekylinhibitorer av MDM2 og anvendelser deravInfo
- Publication number
- NO20074853L NO20074853L NO20074853A NO20074853A NO20074853L NO 20074853 L NO20074853 L NO 20074853L NO 20074853 A NO20074853 A NO 20074853A NO 20074853 A NO20074853 A NO 20074853A NO 20074853 L NO20074853 L NO 20074853L
- Authority
- NO
- Norway
- Prior art keywords
- mdm2
- inhibitors
- smamolecule
- applications
- relates
- Prior art date
Links
- 102000012199 E3 ubiquitin-protein ligase Mdm2 Human genes 0.000 title abstract 2
- 108050002772 E3 ubiquitin-protein ligase Mdm2 Proteins 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 230000025084 cell cycle arrest Effects 0.000 abstract 1
- 230000030833 cell death Effects 0.000 abstract 1
- 230000010261 cell growth Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000003993 interaction Effects 0.000 abstract 1
- 150000003384 small molecules Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/54—Spiro-condensed
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- C07D487/10—Spiro-condensed systems
-
- 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
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Indole Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65513505P | 2005-02-22 | 2005-02-22 | |
| PCT/US2006/006221 WO2006091646A2 (en) | 2005-02-22 | 2006-02-22 | Small molecule inhibitors of mdm2 and uses thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO20074853L true NO20074853L (no) | 2007-11-21 |
Family
ID=36927977
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20074853A NO20074853L (no) | 2005-02-22 | 2007-09-24 | Smamolekylinhibitorer av MDM2 og anvendelser derav |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP1856123B1 (pt) |
| JP (2) | JP5248866B2 (pt) |
| KR (1) | KR100944301B1 (pt) |
| CN (2) | CN102627649B (pt) |
| AU (2) | AU2006216780B8 (pt) |
| BR (1) | BRPI0609172A2 (pt) |
| CA (2) | CA2752738C (pt) |
| EA (2) | EA014445B1 (pt) |
| MX (1) | MX2007010272A (pt) |
| NO (1) | NO20074853L (pt) |
| WO (1) | WO2006091646A2 (pt) |
Families Citing this family (67)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SG176463A1 (en) | 2005-02-22 | 2011-12-29 | Univ Michigan | Small molecule inhibitors of mdm2 and uses thereof |
| MY158766A (en) | 2005-04-11 | 2016-11-15 | Xenon Pharmaceuticals Inc | Spiro-oxindole compounds and their uses as therapeutic agents |
| AR053710A1 (es) | 2005-04-11 | 2007-05-16 | Xenon Pharmaceuticals Inc | Compuestos espiroheterociclicos y sus usos como agentes terapeuticos |
| BRPI0715506A2 (pt) * | 2006-08-30 | 2014-07-08 | Univ Michigan | Novas moléculas pequenas inibidoras de mdm2 e usos das mesmas |
| US8222288B2 (en) | 2006-08-30 | 2012-07-17 | The Regents Of The University Of Michigan | Small molecule inhibitors of MDM2 and the uses thereof |
| WO2008034736A2 (en) * | 2006-09-21 | 2008-03-27 | F. Hoffmann-La Roche Ag | Oxindole derivatives as anticancer agents |
| CN103271906A (zh) | 2006-10-12 | 2013-09-04 | 泽农医药公司 | 螺-吲哚酮化合物作为治疗剂的用途 |
| US7638548B2 (en) * | 2006-11-09 | 2009-12-29 | Hoffmann-La Roche Inc. | Spiroindolinone derivatives |
| EP2103619A4 (en) | 2006-12-14 | 2011-11-23 | Daiichi Sankyo Co Ltd | IMIDAZOTHIAZOLDERIVATE |
| EP2142535A2 (en) | 2007-03-29 | 2010-01-13 | Novartis Ag | 3-imidazolyl-indoles for the treatment of proliferative diseases |
| WO2008144507A2 (en) * | 2007-05-16 | 2008-11-27 | President And Fellows Of Harvard College | Spirooxindole inhibitors of aurora kinase |
| US7834179B2 (en) * | 2007-05-23 | 2010-11-16 | Hoffmann-La Roche Inc. | Spiroindolinone derivatives |
| US7776875B2 (en) * | 2007-12-19 | 2010-08-17 | Hoffman-La Roche Inc. | Spiroindolinone derivatives |
| US7723372B2 (en) * | 2008-03-19 | 2010-05-25 | Hoffman-La Roche Inc. | Spiroindolinone derivatives |
| JPWO2009151069A1 (ja) | 2008-06-12 | 2011-11-17 | 第一三共株式会社 | 4,7−ジアザスピロ[2.5]オクタン環構造を有するイミダゾチアゾール誘導体 |
| KR101380013B1 (ko) * | 2008-09-18 | 2014-04-10 | 에프. 호프만-라 로슈 아게 | 치환 피롤리딘-2-카르복사미드 |
| US8354444B2 (en) * | 2008-09-18 | 2013-01-15 | Hoffmann-La Roche Inc. | Substituted pyrrolidine-2-carboxamides |
| WO2010045197A1 (en) | 2008-10-17 | 2010-04-22 | Xenon Pharmaceuticals, Inc. | Spiro-oxindole compounds and their use as therapeutic agents |
| JP5554337B2 (ja) | 2008-10-17 | 2014-07-23 | ゼノン・ファーマシューティカルズ・インコーポレイテッド | 治療剤としてのスピロオキシインドール化合物およびそれらの使用 |
| US7928233B2 (en) | 2009-02-10 | 2011-04-19 | Hoffmann-La Roche Inc. | Spiroindolinone pyridine derivatives |
| US8217051B2 (en) | 2009-02-17 | 2012-07-10 | Hoffmann-La Roche Inc. | Spiroindolinone derivatives |
| US8076482B2 (en) | 2009-04-23 | 2011-12-13 | Hoffmann-La Roche Inc. | 3,3′-spiroindolinone derivatives |
| AR077252A1 (es) | 2009-06-29 | 2011-08-10 | Xenon Pharmaceuticals Inc | Enantiomeros de compuestos de espirooxindol y sus usos como agentes terapeuticos |
| US8017607B2 (en) * | 2009-10-14 | 2011-09-13 | Hoffmann-La Roche Inc. | N-substituted-pyrrolidines as inhibitors of MDM2-P-53 interactions |
| RU2015103694A (ru) | 2009-10-14 | 2015-06-27 | Ксенон Фармасьютикалз Инк. | Способы синтеза спиро-оксиндольных соединений |
| KR20120099462A (ko) * | 2009-11-12 | 2012-09-10 | 더 리젠츠 오브 더 유니버시티 오브 미시건 | 스피로-옥신돌 mdm2 길항제 |
| US20110118283A1 (en) * | 2009-11-17 | 2011-05-19 | Qingjie Ding | Substituted Pyrrolidine-2-Carboxamides |
| US8088815B2 (en) | 2009-12-02 | 2012-01-03 | Hoffman-La Roche Inc. | Spiroindolinone pyrrolidines |
| US8288431B2 (en) | 2010-02-17 | 2012-10-16 | Hoffmann-La Roche Inc. | Substituted spiroindolinones |
| RU2016128400A (ru) | 2010-02-26 | 2018-12-06 | Ксенон Фармасьютикалз Инк. | Фармацевтические композиции спиро-оксиндольного соединения для местного введения и их применение в качестве терапевтических агентов |
| RU2012147597A (ru) * | 2010-04-09 | 2014-05-20 | Дзе Риджентс Оф Дзе Юниверсити Оф Мичиган | Биомаркеры для ингибиторов mdm2, использующиеся для лечения заболевания |
| US8217044B2 (en) | 2010-04-28 | 2012-07-10 | Hoffmann-La Roche Inc. | Spiroindolinone pyrrolidines |
| US20120046306A1 (en) * | 2010-08-18 | 2012-02-23 | David Joseph Bartkovitz | Substituted Heteroaryl Spiropyrrolidine MDM2 Antagonists |
| US20120065210A1 (en) * | 2010-09-15 | 2012-03-15 | Xin-Jie Chu | Substituted hexahydropyrrolo[1,2-c]imidazolones |
| US20120071499A1 (en) * | 2010-09-20 | 2012-03-22 | Xin-Jie Chu | Substituted Spiro[3H-Indole-3,6'(5'H)-[1H]Pyrrolo[1,2c]Imidazole-1',2(1H,2'H)-diones |
| FR2967072B1 (fr) | 2010-11-05 | 2013-03-29 | Univ Dundee | Procede pour ameliorer la production de virus et semences vaccinales influenza |
| AU2011326395B2 (en) * | 2010-11-12 | 2016-01-07 | Ascenta Licensing Corporation | Spiro-oxindole MDM2 antagonists |
| TR201807311T4 (tr) | 2011-03-10 | 2018-06-21 | Daiichi Sankyo Co Ltd | Dispiropirolidin derivesi. |
| ES2624808T3 (es) | 2011-05-11 | 2017-07-17 | The Regents Of The University Of Michigan | Antagonistas de MDM2 espirooxindólicos |
| CN102627650B (zh) * | 2012-03-08 | 2015-07-08 | 徐州师范大学 | 手性四氢吡咯-3,2′-氧化吲哚螺环化合物及其合成方法 |
| TWI586668B (zh) * | 2012-09-06 | 2017-06-11 | 第一三共股份有限公司 | 二螺吡咯啶衍生物之結晶 |
| ES2707305T3 (es) | 2012-12-20 | 2019-04-03 | Merck Sharp & Dohme | Imidazopiridinas sustituidas como inhibidores de HDM2 |
| CN103435622B (zh) * | 2013-07-31 | 2015-11-18 | 陕西科技大学 | 一种螺环吲哚二酮哌嗪类生物碱及其合成方法和应用 |
| WO2015033974A1 (ja) | 2013-09-04 | 2015-03-12 | 第一三共株式会社 | スピロオキシインドール誘導体の製造方法 |
| TW201613576A (en) | 2014-06-26 | 2016-04-16 | Novartis Ag | Intermittent dosing of MDM2 inhibitor |
| JP6503386B2 (ja) | 2014-07-03 | 2019-04-17 | 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 | MDM2−p53阻害剤としての新しいスピロ[3H−インドール−3,2’−ピロリジン]−2(1H)−オン化合物および誘導体 |
| CA2956129C (en) | 2014-08-21 | 2022-10-25 | Boehringer Ingelheim International Gmbh | New spiro[3h-indole-3,2'-pyrrolidin]-2(1h)-one compounds and derivatives as mdm2-p53 inhibitors |
| TW201636017A (zh) | 2015-02-05 | 2016-10-16 | 梯瓦製藥國際有限責任公司 | 以螺吲哚酮化合物之局部調配物治療帶狀疱疹後遺神經痛之方法 |
| CN107427501B (zh) * | 2015-02-20 | 2023-12-01 | 第一三共株式会社 | 通过联合使用治疗癌症的方法 |
| EP3277677B9 (en) * | 2015-03-30 | 2021-07-14 | Mission Therapeutics Limited | 1-cyano-pyrrolidine compounds as usp30 inhibitors |
| KR20170134462A (ko) | 2015-04-13 | 2017-12-06 | 다이이찌 산쿄 가부시키가이샤 | Mdm2 저해제와 btk 저해제의 병용 치료법 |
| GB201517216D0 (en) | 2015-09-29 | 2015-11-11 | Cancer Res Technology Ltd And Astex Therapeutics Ltd | Pharmaceutical compounds |
| GB201517217D0 (en) | 2015-09-29 | 2015-11-11 | Astex Therapeutics Ltd And Cancer Res Technology Ltd | Pharmaceutical compounds |
| PL3359542T3 (pl) | 2015-10-09 | 2021-09-20 | Boehringer Ingelheim International Gmbh | Związki i pochodne spiro[3h-indolo-3,2’-pirolidyno]-2(1h)-onowe jako inhibitory mdm2-p53 |
| CN105585570B (zh) * | 2015-12-15 | 2019-10-15 | 贵州大学 | 异恶唑拼接吡咯螺环氧化吲哚化合物及其制备方法及应用 |
| AU2017246452C1 (en) | 2016-04-06 | 2021-06-03 | The Regents Of The University Of Michigan | MDM2 protein degraders |
| EP3458101B1 (en) | 2016-05-20 | 2020-12-30 | H. Hoffnabb-La Roche Ag | Protac antibody conjugates and methods of use |
| WO2018074387A1 (ja) | 2016-10-17 | 2018-04-26 | 第一三共株式会社 | Mdm2阻害剤とdnaメチルトランスフェラーゼ阻害剤との併用治療法 |
| GB201704965D0 (en) | 2017-03-28 | 2017-05-10 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| GB201704966D0 (en) | 2017-03-28 | 2017-05-10 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| CN107353292B (zh) * | 2017-08-23 | 2018-07-10 | 山东博苑医药化学有限公司 | 螺环氧化吲哚乙内酰(硫)脲衍生物及其制备方法和在防治植物病毒、杀菌、杀虫方面的应用 |
| CN108486041A (zh) * | 2018-03-28 | 2018-09-04 | 华南农业大学 | PI3K/Akt信号通路在鸡胚成纤维细胞内对马立克氏病毒增殖的应用及其检测方法 |
| CN110680838B (zh) * | 2019-11-21 | 2021-10-01 | 海门茂发美术图案设计有限公司 | 一种素心腊梅碱的抗前列腺癌用途 |
| CN112876488B (zh) * | 2021-02-18 | 2021-12-21 | 苏州大学 | 螺环吲哚啉衍生物及其制备方法和应用 |
| WO2023056069A1 (en) | 2021-09-30 | 2023-04-06 | Angiex, Inc. | Degrader-antibody conjugates and methods of using same |
| CN115417871B (zh) * | 2022-09-21 | 2023-06-02 | 成都理工大学 | 双螺环吡咯螺氧化吲哚化合物及其合成方法和抗真菌活性 |
| WO2024240858A1 (en) | 2023-05-23 | 2024-11-28 | Valerio Therapeutics | Protac molecules directed against dna damage repair system and uses thereof |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3219661A (en) * | 1962-12-14 | 1965-11-23 | Warner Lambert Pharmaceutical | Spirooxindole and spirodehydroindole alkaloids and process therefor |
| GB1056537A (en) * | 1963-07-16 | 1967-01-25 | Smith Kline French Lab | Improvements in or relating to crystalline alkaloids of mitragyna citiata and compositions thereof |
| JPH0423184A (ja) * | 1990-05-18 | 1992-01-27 | Toshiba Corp | 光学的文字読取装置 |
| JP3074281B2 (ja) * | 1990-05-30 | 2000-08-07 | 住友大阪セメント株式会社 | フレキシブルコンテナ |
| JPH07238069A (ja) * | 1994-02-28 | 1995-09-12 | Daicel Chem Ind Ltd | 環状アミド化合物の製造方法 |
| RU2084449C1 (ru) * | 1994-03-02 | 1997-07-20 | Всероссийский научный центр по безопасности биологически активных веществ | 1-бензил-2-оксотриптамин гидрохлорид и его производные, обладающие гепатозащитной активностью |
| US5773455A (en) * | 1996-06-28 | 1998-06-30 | Biomeasure, Incorporated | Inhibitors of prenyl transferases |
| ATE467418T1 (de) * | 1997-01-20 | 2010-05-15 | Immodal Pharmaka Gmbh | Verfahren und stoffe zur freisetzung eines wachstumsfaktors aus endothelzellen, und nach dem verfahren freigesetzter wachstumsfaktor sowie seine verwendung |
| EA002305B1 (ru) * | 1997-06-10 | 2002-02-28 | Глэксо Гроуп Лимитед | Производные бензимидазола |
| WO1999012904A1 (en) * | 1997-09-08 | 1999-03-18 | Arqule, Inc. | Spiro[pyrrolidine-2,3'-oxindole] compounds and methods of use |
| CN1182083C (zh) * | 2001-10-08 | 2004-12-29 | 廖宜芳 | 一种杀虫灭菌的配位肥及其制造方法 |
| JP4361798B2 (ja) * | 2001-12-18 | 2009-11-11 | エフ.ホフマン−ラ ロシュ アーゲー | Mdm2インヒビターとしてのシス−イミダゾリン |
-
2006
- 2006-02-22 AU AU2006216780A patent/AU2006216780B8/en not_active Ceased
- 2006-02-22 EP EP06735754.1A patent/EP1856123B1/en not_active Expired - Lifetime
- 2006-02-22 CN CN201210066457.3A patent/CN102627649B/zh not_active Expired - Fee Related
- 2006-02-22 KR KR1020077021939A patent/KR100944301B1/ko not_active Expired - Fee Related
- 2006-02-22 CN CN2006800129073A patent/CN101160314B/zh not_active Expired - Fee Related
- 2006-02-22 JP JP2007556414A patent/JP5248866B2/ja not_active Expired - Fee Related
- 2006-02-22 BR BRPI0609172-5A patent/BRPI0609172A2/pt not_active IP Right Cessation
- 2006-02-22 WO PCT/US2006/006221 patent/WO2006091646A2/en not_active Ceased
- 2006-02-22 CA CA2752738A patent/CA2752738C/en not_active Expired - Fee Related
- 2006-02-22 EA EA200701771A patent/EA014445B1/ru not_active IP Right Cessation
- 2006-02-22 EA EA201001255A patent/EA019566B1/ru not_active IP Right Cessation
- 2006-02-22 MX MX2007010272A patent/MX2007010272A/es active IP Right Grant
- 2006-02-22 CA CA2598690A patent/CA2598690C/en not_active Expired - Fee Related
-
2007
- 2007-09-24 NO NO20074853A patent/NO20074853L/no not_active Application Discontinuation
-
2010
- 2010-06-30 AU AU2010202759A patent/AU2010202759B2/en not_active Ceased
-
2012
- 2012-04-06 JP JP2012086927A patent/JP5638023B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EA014445B1 (ru) | 2010-12-30 |
| AU2006216780B8 (en) | 2010-04-22 |
| CA2752738A1 (en) | 2006-08-31 |
| WO2006091646A2 (en) | 2006-08-31 |
| KR20070108917A (ko) | 2007-11-13 |
| AU2010202759A1 (en) | 2010-07-22 |
| CN101160314B (zh) | 2012-05-23 |
| BRPI0609172A2 (pt) | 2010-02-23 |
| JP2008531504A (ja) | 2008-08-14 |
| CA2752738C (en) | 2014-05-27 |
| AU2010202759B2 (en) | 2012-07-19 |
| EA201001255A1 (ru) | 2011-02-28 |
| CN102627649A (zh) | 2012-08-08 |
| KR100944301B1 (ko) | 2010-02-24 |
| EP1856123A4 (en) | 2010-12-29 |
| CN101160314A (zh) | 2008-04-09 |
| JP2012162550A (ja) | 2012-08-30 |
| CA2598690C (en) | 2011-11-15 |
| EA200701771A1 (ru) | 2008-06-30 |
| JP5638023B2 (ja) | 2014-12-10 |
| EA019566B1 (ru) | 2014-04-30 |
| WO2006091646A3 (en) | 2006-11-30 |
| JP5248866B2 (ja) | 2013-07-31 |
| CA2598690A1 (en) | 2006-08-31 |
| MX2007010272A (es) | 2008-03-12 |
| CN102627649B (zh) | 2015-03-25 |
| AU2006216780B2 (en) | 2010-04-01 |
| EP1856123B1 (en) | 2016-02-17 |
| EP1856123A2 (en) | 2007-11-21 |
| AU2006216780A1 (en) | 2006-08-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO20074853L (no) | Smamolekylinhibitorer av MDM2 og anvendelser derav | |
| MX2009002306A (es) | Nuevos inhibidores de mdm2 de molecula pequeña y sus usos. | |
| NO20065502L (no) | Farmasoytiske sammensetninger. | |
| NO20062649L (no) | Biarylsulfonamider og metoder for anvendelse av disse | |
| CL2008002478A1 (es) | Compuestos derivados de n-fenil-5-(4 haloalcoxi)fenil) pirimidin-2-amino, inhibidores de c-kit y pdgfr; composicion farmaceutica; y su uso en el tratmiento de asma, dermatitis atopica, hipertension pulmonar o arterial, fibrosis renal, pulmonar o cardiaca, entre otras. | |
| GT200600407A (es) | Compuestos ppar activos | |
| NO20076001L (no) | Tigecyklin og metoder for deres fremstilling | |
| NO20082298L (no) | Kaliumkanalinhibitorer | |
| CY1109916T1 (el) | Βενζιμιδαζολο-θειοφαινικες ενωσεις ως plk αναστολεις | |
| NO20075693L (no) | Modulerende forbindelser av indolamin-2,3-dioksygenase og fremgangsmater for anvendelse av samme | |
| NO20075200L (no) | Fremstilling av karotenoider i oljeaktige gjaer og fungi | |
| EA200701396A1 (ru) | Триазолофталазины в качестве ингибиторов pde-2 | |
| NO20082482L (no) | Karbonylamino pyrrolpyrazoler, samt anvendelse som kinase inhibitorer | |
| CY1111151T1 (el) | Αναστολεις φωσφολιπασης α2 του κυτταροδιαλυματος | |
| NO20075998L (no) | Tigecyklin og metoder til fremstilling av 9-aminominocyklin | |
| NO20075997L (no) | Methoder til furifysering av tigecyklin | |
| NO20083153L (no) | Kjemiske forbindelser | |
| DE602004006433D1 (de) | Pyrrol-substituierte indole als inhibitoren von pai-1 | |
| NO20076391L (no) | Sammensetninger og metoder for behandling av tilstander relatert til efrinsignaler med cupredoxin | |
| NO20091990L (no) | Substituerte pyrazoler, sammensetninger inneholdende disse, fremgangsmate for fremstilling og anvendelse | |
| ATE524482T1 (de) | Ionische flüssigkeiten mit niedriger viskosität | |
| AR061542A1 (es) | Masa de absorcion y procedimiento para eliminar mercurio | |
| SE0400208D0 (sv) | Chemical compounds | |
| DE602006009789D1 (de) | Acetylenderivate | |
| EA200801413A1 (ru) | Гетероциклические сетр ингибиторы |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC2A | Withdrawal, rejection or dismissal of laid open patent application |