PL2308877T3 - Pochodne imidazopirydyn-2-onu - Google Patents
Pochodne imidazopirydyn-2-onuInfo
- Publication number
- PL2308877T3 PL2308877T3 PL09804973T PL09804973T PL2308877T3 PL 2308877 T3 PL2308877 T3 PL 2308877T3 PL 09804973 T PL09804973 T PL 09804973T PL 09804973 T PL09804973 T PL 09804973T PL 2308877 T3 PL2308877 T3 PL 2308877T3
- Authority
- PL
- Poland
- Prior art keywords
- imidazopyridin
- derivatives
- Prior art date
Links
- JXXWJMUPNZDILL-UHFFFAOYSA-N imidazo[4,5-b]pyridin-2-one Chemical class C1=CC=NC2=NC(=O)N=C21 JXXWJMUPNZDILL-UHFFFAOYSA-N 0.000 title 1
Classifications
-
- 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
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
-
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (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 (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2008201670 | 2008-08-05 | ||
| JP2009078540 | 2009-03-27 | ||
| PCT/JP2009/063807 WO2010016490A1 (ja) | 2008-08-05 | 2009-08-04 | イミダゾピリジン-2-オン誘導体 |
| EP09804973.7A EP2308877B1 (en) | 2008-08-05 | 2009-08-04 | Imidazopyridin-2-one derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL2308877T3 true PL2308877T3 (pl) | 2014-07-31 |
Family
ID=41663708
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL09804973T PL2308877T3 (pl) | 2008-08-05 | 2009-08-04 | Pochodne imidazopirydyn-2-onu |
Country Status (21)
| Country | Link |
|---|---|
| US (2) | US8436012B2 (pl) |
| EP (1) | EP2308877B1 (pl) |
| JP (1) | JP5630867B2 (pl) |
| KR (1) | KR20110039307A (pl) |
| CN (1) | CN102171210B (pl) |
| AU (1) | AU2009278442B2 (pl) |
| BR (1) | BRPI0917540A2 (pl) |
| CA (1) | CA2732950C (pl) |
| CO (1) | CO6300866A2 (pl) |
| DK (1) | DK2308877T3 (pl) |
| ES (1) | ES2459047T3 (pl) |
| IL (1) | IL211042A (pl) |
| MX (1) | MX2011001019A (pl) |
| MY (1) | MY153606A (pl) |
| NZ (1) | NZ590688A (pl) |
| PL (1) | PL2308877T3 (pl) |
| PT (1) | PT2308877E (pl) |
| RU (1) | RU2478636C2 (pl) |
| TW (1) | TWI436998B (pl) |
| WO (1) | WO2010016490A1 (pl) |
| ZA (1) | ZA201100799B (pl) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2554375T3 (es) * | 2008-11-25 | 2015-12-18 | University Of Rochester | Inhibidores de las MLK y métodos de uso |
| WO2011021678A1 (ja) * | 2009-08-21 | 2011-02-24 | 武田薬品工業株式会社 | 縮合複素環化合物 |
| US8846909B2 (en) | 2010-05-24 | 2014-09-30 | University Of Rochester | Bicyclic heteroaryl kinase inhibitors and methods of use |
| WO2012003576A1 (en) * | 2010-07-06 | 2012-01-12 | Université de Montréal | Imidazopyridine, imidazopyrimidine and imidazopyrazine derivatives as melanocortin-4 receptor modulators |
| CA2825098C (en) | 2011-01-27 | 2020-03-10 | Universite De Montreal | Pyrazolopyridine and pyrazolopyrimidine derivatives as melanocortin-4 receptor modulators |
| KR101274986B1 (ko) * | 2011-07-27 | 2013-06-17 | 한국과학기술원 | 이미다조피리딘 유도체, 이를 포함하는 PI3K 및/또는 mTOR 저해제용 약학 조성물 및 PI3K 및/또는 mTOR과 연관된 질환 치료용 약학 조성물 |
| CN102702196B (zh) * | 2012-06-13 | 2015-01-14 | 南京药石药物研发有限公司 | 3-甲基-7-氮杂吲哚的合成方法 |
| KR20150068956A (ko) * | 2012-10-16 | 2015-06-22 | 에프. 호프만-라 로슈 아게 | 세린/트레오닌 키나아제 억제제 |
| EP2925319B1 (en) | 2012-11-30 | 2019-01-09 | University Of Rochester | Mixed lineage kinase inhibitors for hiv/aids therapies |
| US20160008356A1 (en) * | 2013-02-28 | 2016-01-14 | Signal Pharmaceuticals, Llc | Treatment of cancer with tor kinase inhibitors |
| EP3024457A4 (en) | 2013-07-26 | 2017-06-28 | Update Pharma Inc. | Compositions to improve the therapeutic benefit of bisantrene |
| WO2015016195A1 (ja) | 2013-07-29 | 2015-02-05 | 協和発酵キリン株式会社 | Wntシグナル阻害剤 |
| DK3180315T3 (da) | 2014-08-15 | 2020-04-06 | Janssen Pharmaceuticals Inc | Pyrazoler |
| ES2791186T3 (es) | 2014-08-15 | 2020-11-03 | Janssen Pharmaceuticals Inc | Triazoles como inhibidores de receptores NR2B |
| JP6964576B2 (ja) | 2015-07-09 | 2021-11-10 | ヤンセン ファーマシューティカ エヌ.ベー. | 置換4−アザインドール及びglun2b受容体調節因子としてのそれらの使用 |
| KR20180108822A (ko) | 2016-02-10 | 2018-10-04 | 얀센 파마슈티카 엔.브이. | Nr2b-선택적 nmda 조절제로서 치환된 1,2,3-트라이아졸 |
| WO2017188374A1 (ja) * | 2016-04-28 | 2017-11-02 | 武田薬品工業株式会社 | 縮合複素環化合物 |
| CN106187899B (zh) * | 2016-06-28 | 2019-07-16 | 绍兴文理学院 | 一种氟代氮杂芳烃的合成方法 |
| TW201819376A (zh) * | 2016-10-06 | 2018-06-01 | 比利時商健生藥品公司 | 經取代之1H-咪唑並[4,5-b]吡啶-2(3H)-酮及其作為GLUN2B受體調節劑之用途 |
| CN107118084B (zh) * | 2017-06-27 | 2021-06-08 | 江苏合泰新材料科技有限公司 | 一种两步法合成1,3-双取代基-2-丙醇的方法 |
| CN107550905B (zh) * | 2017-09-11 | 2020-07-17 | 浙江永宁药业股份有限公司 | 多取代吡咯并吡啶类化合物的药物用途及其制备方法 |
| MA52244A (fr) | 2018-04-04 | 2021-02-17 | Janssen Pharmaceutica Nv | Pyridine et pyrimidines substituées et leur utilisation en tant que modulateurs du récepteur glun2b |
| EP3801499B1 (en) | 2018-06-07 | 2024-02-28 | Disarm Therapeutics, Inc. | Inhibitors of sarm1 |
| TWI837231B (zh) | 2018-11-29 | 2024-04-01 | 日商第一三共股份有限公司 | 含有ezh1/2雙重抑制劑之醫藥組合及其用途 |
| CN113164508B (zh) | 2018-12-19 | 2025-07-08 | 达萨玛治疗公司 | 与神经保护剂组合的sarm1抑制剂 |
| PH12021552839A1 (en) | 2019-06-14 | 2022-10-03 | Janssen Pharmaceutica Nv | Substituted pyrazolo-pyridine amides and their use as glun2b receptor modulators |
| AU2020291188A1 (en) | 2019-06-14 | 2022-01-20 | Janssen Pharmaceutica Nv | Substituted heteroaromatic Pyrazolo-pyridines and their use as GluN2B receptor modulators |
| MX2021015510A (es) | 2019-06-14 | 2022-04-11 | Janssen Pharmaceutica Nv | Pirazolo[4,3-b]piridinas sustituidas y su uso como moduladores del receptor glun2b. |
| CA3143105A1 (en) | 2019-06-14 | 2020-12-17 | Janssen Pharmaceutica Nv | Substituted pyrazolo-pyrazines and their use as glun2b receptor modulators |
| MA56196A (fr) | 2019-06-14 | 2022-04-20 | Janssen Pharmaceutica Nv | Pyrazolo-pyridine amides substitués et leur utilisation en tant que modulateurs du récepteur glun2b |
| CN113950357A (zh) | 2019-06-14 | 2022-01-18 | 詹森药业有限公司 | 吡嗪氨基甲酸酯及其作为GluN2B受体调节剂的用途 |
| CN114007691A (zh) | 2019-06-14 | 2022-02-01 | 詹森药业有限公司 | 吡啶氨基甲酸酯及其作为GluN2B受体调节剂的用途 |
| WO2022166920A1 (zh) * | 2021-02-08 | 2022-08-11 | 杭州中美华东制药有限公司 | 一种吡咯并哒嗪类化合物及其制备方法和用途 |
| EP4074712A1 (en) | 2021-04-13 | 2022-10-19 | Siegfried AG | Process for the synthesis of 1,3-dihydro-imidazo[4,5-b]pyridin-2-one and/or derivatives thereof |
| WO2024081889A1 (en) | 2022-10-14 | 2024-04-18 | Genesis Therapeutics, Inc. | 4h-pyrido[1,2-a]pyrimidin-4-one derivatives for treating cancer |
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|---|---|---|---|---|
| US4294837A (en) | 1980-03-28 | 1981-10-13 | Sterling Drug Inc. | 1,3-Dihydro-6-(pyridinyl)-2H-imidazo[4,5-b]pyridin-2-ones and -imidazo[4,5-b]pyridine-2-thiones and their cardiotonic use |
| US4532337A (en) | 1984-02-28 | 1985-07-30 | Basf Aktiengesellschaft | Preparation of 3-formyl-5,6-dihydro-2H-pyran |
| JPH0678327B2 (ja) | 1989-07-20 | 1994-10-05 | ファイザー製薬株式会社 | 4,5,6,7,―四置換ベンゾオキサゾロン類 |
| IN188411B (pl) | 1997-03-27 | 2002-09-21 | Yuhan Corp | |
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| US7019026B1 (en) | 1999-09-10 | 2006-03-28 | Novo Nordisk A/S | Modulators of Protein Tyrosine Phosphatases (PTPases) |
| ES2319970T3 (es) | 2001-09-07 | 2009-05-18 | Kaken Pharmaceutical Co., Ltd. | Derivados de acido hidroxamico inverso. |
| WO2003028724A1 (en) | 2001-10-04 | 2003-04-10 | Smithkline Beecham Corporation | Chk1 kinase inhibitors |
| JP2003221386A (ja) | 2001-11-26 | 2003-08-05 | Takeda Chem Ind Ltd | 二環性誘導体、その製造法およびその用途 |
| DE10228103A1 (de) | 2002-06-24 | 2004-01-15 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
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| MXPA05005983A (es) * | 2002-12-04 | 2005-08-18 | Eisai Co Ltd | Compuestos de anillo fusionado 1,3-dihidroimidazol. |
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| BRPI0413740A (pt) * | 2003-08-21 | 2006-10-24 | Osi Pharm Inc | composto ou um seu n-óxido ou seu sal farmaceuticamente aceitável, composição, e, método de tratamento de distúrbio hiperproliferativo |
| ES2241496B1 (es) | 2004-04-15 | 2006-12-01 | Almirall Prodesfarma, S.A. | Nuevos derivados de piridina. |
| EP1769092A4 (en) | 2004-06-29 | 2008-08-06 | Europ Nickel Plc | IMPROVED LIXIVIATION OF BASE METALS |
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| BRPI0611707A2 (pt) | 2005-06-29 | 2012-04-24 | Compumedics Ltd | conjunto de sensor com ponte condutiva |
| GB0513840D0 (en) | 2005-07-07 | 2005-08-10 | Medivir Ab | Cysteine protease inhibitors |
| TWI411607B (zh) | 2005-11-14 | 2013-10-11 | Vitae Pharmaceuticals Inc | 天門冬胺酸蛋白酶抑制劑 |
| KR20080104351A (ko) | 2006-03-31 | 2008-12-02 | 노파르티스 아게 | 유기 화합물 |
| EP2029593A1 (en) | 2006-05-22 | 2009-03-04 | AstraZeneca AB | Indole derivatives |
| TW200801513A (en) | 2006-06-29 | 2008-01-01 | Fermiscan Australia Pty Ltd | Improved process |
| WO2008011557A2 (en) | 2006-07-20 | 2008-01-24 | Borchardt Allen J | Heteroaryl inhibitors of rho kinase |
| HRP20170627T1 (hr) | 2006-08-23 | 2017-06-30 | Kudos Pharmaceuticals Limited | Derivati 2-metilmorfolin pirido-, pirazo- i pirimido-pirimidina kao inhibitori mtor |
| WO2008029825A1 (en) | 2006-09-05 | 2008-03-13 | Kyowa Hakko Kirin Co., Ltd. | Imidazole derivative |
| WO2008051494A1 (en) * | 2006-10-19 | 2008-05-02 | Signal Pharmaceuticals, Llc | Heteroaryl compounds, compositions thereof, and use thereof as protein kinase inhibitors |
| CN101573360A (zh) * | 2006-10-19 | 2009-11-04 | 西格诺药品有限公司 | 杂芳基化合物、其组合物以及它们作为蛋白激酶抑制剂的用途 |
| TW200901998A (en) | 2007-03-06 | 2009-01-16 | Astrazeneca Ab | Novel 2-heteroaryl substituted benzothiophenes and benzofuranes |
| AP2010005167A0 (en) | 2007-08-01 | 2010-02-28 | Pfizer | Pyrazole compounds and their use as RAF inhibitors |
| EP2311842A3 (en) | 2008-06-24 | 2011-07-13 | Takeda Pharmaceutical Company Limited | PI3K/M TOR inhibitors |
| WO2010000020A1 (en) | 2008-06-30 | 2010-01-07 | Cathrx Ltd | A catheter |
| MX2011001872A (es) | 2008-08-18 | 2011-05-23 | Univ Yale | Moduladores de mif. |
| ES2554375T3 (es) | 2008-11-25 | 2015-12-18 | University Of Rochester | Inhibidores de las MLK y métodos de uso |
| WO2011000020A1 (en) | 2009-06-12 | 2011-01-06 | Sbc Research Pty Ltd | Enhanced method of detection |
| WO2011096490A1 (ja) * | 2010-02-04 | 2011-08-11 | 第一三共株式会社 | イミダゾピリジン-2-オン誘導体 |
-
2009
- 2009-08-04 BR BRPI0917540A patent/BRPI0917540A2/pt not_active IP Right Cessation
- 2009-08-04 JP JP2010523864A patent/JP5630867B2/ja not_active Expired - Fee Related
- 2009-08-04 PL PL09804973T patent/PL2308877T3/pl unknown
- 2009-08-04 CN CN200980139552.8A patent/CN102171210B/zh not_active Expired - Fee Related
- 2009-08-04 KR KR1020117002441A patent/KR20110039307A/ko not_active Ceased
- 2009-08-04 DK DK09804973.7T patent/DK2308877T3/da active
- 2009-08-04 EP EP09804973.7A patent/EP2308877B1/en not_active Not-in-force
- 2009-08-04 AU AU2009278442A patent/AU2009278442B2/en not_active Ceased
- 2009-08-04 PT PT98049737T patent/PT2308877E/pt unknown
- 2009-08-04 WO PCT/JP2009/063807 patent/WO2010016490A1/ja not_active Ceased
- 2009-08-04 RU RU2011108453/04A patent/RU2478636C2/ru not_active IP Right Cessation
- 2009-08-04 MX MX2011001019A patent/MX2011001019A/es active IP Right Grant
- 2009-08-04 MY MYPI2011000134A patent/MY153606A/en unknown
- 2009-08-04 CA CA2732950A patent/CA2732950C/en not_active Expired - Fee Related
- 2009-08-04 NZ NZ590688A patent/NZ590688A/xx not_active IP Right Cessation
- 2009-08-04 ES ES09804973.7T patent/ES2459047T3/es active Active
- 2009-08-05 TW TW098126301A patent/TWI436998B/zh not_active IP Right Cessation
-
2010
- 2010-11-24 US US12/954,408 patent/US8436012B2/en not_active Expired - Fee Related
-
2011
- 2011-01-31 ZA ZA2011/00799A patent/ZA201100799B/en unknown
- 2011-02-03 IL IL211042A patent/IL211042A/en not_active IP Right Cessation
- 2011-02-15 CO CO11017787A patent/CO6300866A2/es active IP Right Grant
-
2013
- 2013-03-13 US US13/800,907 patent/US8785438B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CO6300866A2 (es) | 2011-07-21 |
| JP5630867B2 (ja) | 2014-11-26 |
| RU2011108453A (ru) | 2012-09-10 |
| BRPI0917540A2 (pt) | 2015-11-17 |
| MY153606A (en) | 2015-02-27 |
| EP2308877A4 (en) | 2012-03-14 |
| ZA201100799B (en) | 2011-10-26 |
| AU2009278442A1 (en) | 2010-02-11 |
| IL211042A (en) | 2014-12-31 |
| WO2010016490A1 (ja) | 2010-02-11 |
| TWI436998B (zh) | 2014-05-11 |
| US20130338156A1 (en) | 2013-12-19 |
| PT2308877E (pt) | 2014-05-02 |
| CA2732950C (en) | 2013-10-01 |
| CN102171210A (zh) | 2011-08-31 |
| AU2009278442B2 (en) | 2013-09-26 |
| RU2478636C2 (ru) | 2013-04-10 |
| US20110082138A1 (en) | 2011-04-07 |
| IL211042A0 (en) | 2011-04-28 |
| EP2308877B1 (en) | 2014-01-22 |
| KR20110039307A (ko) | 2011-04-15 |
| ES2459047T3 (es) | 2014-05-07 |
| EP2308877A1 (en) | 2011-04-13 |
| NZ590688A (en) | 2012-09-28 |
| CA2732950A1 (en) | 2010-02-11 |
| US8436012B2 (en) | 2013-05-07 |
| MX2011001019A (es) | 2011-03-25 |
| CN102171210B (zh) | 2014-04-23 |
| JPWO2010016490A1 (ja) | 2012-01-26 |
| US8785438B2 (en) | 2014-07-22 |
| TW201011021A (en) | 2010-03-16 |
| HK1155444A1 (en) | 2012-05-18 |
| DK2308877T3 (da) | 2014-04-22 |
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