KR101088848B1 - 피라졸로〔3,4―b〕피리딘 화합물, 및 이의포스포디에스테라제 억제제로서의 용도 - Google Patents
피라졸로〔3,4―b〕피리딘 화합물, 및 이의포스포디에스테라제 억제제로서의 용도 Download PDFInfo
- Publication number
- KR101088848B1 KR101088848B1 KR1020057011852A KR20057011852A KR101088848B1 KR 101088848 B1 KR101088848 B1 KR 101088848B1 KR 1020057011852 A KR1020057011852 A KR 1020057011852A KR 20057011852 A KR20057011852 A KR 20057011852A KR 101088848 B1 KR101088848 B1 KR 101088848B1
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- South Korea
- Prior art keywords
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- formula
- substituted
- unsubstituted
- ethyl
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- Expired - Fee Related
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- 0 CCCc(cc1)ccc1C(*=C)=O Chemical compound CCCc(cc1)ccc1C(*=C)=O 0.000 description 23
- PAFZNILMFXTMIY-UHFFFAOYSA-N NC1CCCCC1 Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- STHLKXRLHQOTOP-UHFFFAOYSA-N C=S(CC1)(CCC1=O)=C Chemical compound C=S(CC1)(CCC1=O)=C STHLKXRLHQOTOP-UHFFFAOYSA-N 0.000 description 1
- RJUSZBCFFPTAFP-UHFFFAOYSA-N CC(C)C1(CC1)S(c1ccccc1)(=O)=[ClH] Chemical compound CC(C)C1(CC1)S(c1ccccc1)(=O)=[ClH] RJUSZBCFFPTAFP-UHFFFAOYSA-N 0.000 description 1
- IKMHAKMFYVHZBP-UHFFFAOYSA-N CCC(C)c(cc1)ccc1OI Chemical compound CCC(C)c(cc1)ccc1OI IKMHAKMFYVHZBP-UHFFFAOYSA-N 0.000 description 1
- ZJMWRROPUADPEA-UHFFFAOYSA-N CCC(C)c1ccccc1 Chemical compound CCC(C)c1ccccc1 ZJMWRROPUADPEA-UHFFFAOYSA-N 0.000 description 1
- PBWHJRFXUPLZDS-UHFFFAOYSA-N CCC(CC)c1ccccc1 Chemical compound CCC(CC)c1ccccc1 PBWHJRFXUPLZDS-UHFFFAOYSA-N 0.000 description 1
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- QXQAPNSHUJORMC-UHFFFAOYSA-N CCCc(cc1)ccc1Cl Chemical compound CCCc(cc1)ccc1Cl QXQAPNSHUJORMC-UHFFFAOYSA-N 0.000 description 1
- WGBSGPXCMPGYBJ-UHFFFAOYSA-N CCCc(cc1)ccc1NS(C)(=O)=O Chemical compound CCCc(cc1)ccc1NS(C)(=O)=O WGBSGPXCMPGYBJ-UHFFFAOYSA-N 0.000 description 1
- IXSJJSCNLGAMQM-UHFFFAOYSA-N CCCc(cc1)ccc1S(C)(=C)=O Chemical compound CCCc(cc1)ccc1S(C)(=C)=O IXSJJSCNLGAMQM-UHFFFAOYSA-N 0.000 description 1
- ZSLXLRNHGFDCDH-UHFFFAOYSA-N CCCc1cc(C)cc(I)c1 Chemical compound CCCc1cc(C)cc(I)c1 ZSLXLRNHGFDCDH-UHFFFAOYSA-N 0.000 description 1
- FZJVYOOQGFZCSY-UHFFFAOYSA-N CCCc1ccc(C)c(C)c1 Chemical compound CCCc1ccc(C)c(C)c1 FZJVYOOQGFZCSY-UHFFFAOYSA-N 0.000 description 1
- IRUSTUOJENXLMN-UHFFFAOYSA-N CCCc1cccc(C)c1C Chemical compound CCCc1cccc(C)c1C IRUSTUOJENXLMN-UHFFFAOYSA-N 0.000 description 1
- AFYWHWCEKNKPAW-UHFFFAOYSA-N CCCc1cccc(I)c1 Chemical compound CCCc1cccc(I)c1 AFYWHWCEKNKPAW-UHFFFAOYSA-N 0.000 description 1
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- MMCPRBNOEBDGLZ-UHFFFAOYSA-N CC[n]1ncc2c1ncc(C(NC(C)(C)CO)=O)c2NC1CCOCC1 Chemical compound CC[n]1ncc2c1ncc(C(NC(C)(C)CO)=O)c2NC1CCOCC1 MMCPRBNOEBDGLZ-UHFFFAOYSA-N 0.000 description 1
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- JCXZKUZXVQKENT-UHFFFAOYSA-N CN1CCN(CC(O)=O)CC1 Chemical compound CN1CCN(CC(O)=O)CC1 JCXZKUZXVQKENT-UHFFFAOYSA-N 0.000 description 1
- RQEUFEKYXDPUSK-SSDOTTSWSA-N C[C@H](c1ccccc1)N Chemical compound C[C@H](c1ccccc1)N RQEUFEKYXDPUSK-SSDOTTSWSA-N 0.000 description 1
- KZKYCKOUODFYBV-UHFFFAOYSA-N NC(CC1)CCS1(=O)=O Chemical compound NC(CC1)CCS1(=O)=O KZKYCKOUODFYBV-UHFFFAOYSA-N 0.000 description 1
- IMLXLGZJLAOKJN-IZLXSQMJSA-N N[C@H](CC1)CC[C@@H]1O Chemical compound N[C@H](CC1)CC[C@@H]1O IMLXLGZJLAOKJN-IZLXSQMJSA-N 0.000 description 1
- MIPHRQMEIYLZFZ-SCSAIBSYSA-N N[C@H]1COCC1 Chemical compound N[C@H]1COCC1 MIPHRQMEIYLZFZ-SCSAIBSYSA-N 0.000 description 1
- OVRJVKCZJCNSOW-UHFFFAOYSA-N O=C1CCSCC1 Chemical compound O=C1CCSCC1 OVRJVKCZJCNSOW-UHFFFAOYSA-N 0.000 description 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
-
- 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/02—Nasal agents, e.g. decongestants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Rheumatology (AREA)
- Hospice & Palliative Care (AREA)
- Otolaryngology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Epidemiology (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 (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0230045.7A GB0230045D0 (en) | 2002-12-23 | 2002-12-23 | Compounds |
| GB0230045.7 | 2002-12-23 | ||
| GB0230165A GB0230165D0 (en) | 2002-12-24 | 2002-12-24 | Compounds |
| GB0230165.3 | 2002-12-24 | ||
| GB0307998A GB0307998D0 (en) | 2003-04-07 | 2003-04-07 | Compounds |
| GB0307998.5 | 2003-04-07 | ||
| PCT/EP2003/014867 WO2004056823A1 (en) | 2002-12-23 | 2003-12-19 | PYRAZOLO[3,4-b]PYRIDINE COMPOUNDS, AND THEIR USE AS PHOSPHODIESTERASE INHIBITORS |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20050088214A KR20050088214A (ko) | 2005-09-02 |
| KR101088848B1 true KR101088848B1 (ko) | 2011-12-06 |
Family
ID=32685762
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020057011852A Expired - Fee Related KR101088848B1 (ko) | 2002-12-23 | 2003-12-19 | 피라졸로〔3,4―b〕피리딘 화합물, 및 이의포스포디에스테라제 억제제로서의 용도 |
Country Status (28)
| Country | Link |
|---|---|
| US (1) | US7528148B2 (enExample) |
| EP (1) | EP1581532B1 (enExample) |
| JP (1) | JP4872068B2 (enExample) |
| KR (1) | KR101088848B1 (enExample) |
| CN (1) | CN1751042B (enExample) |
| AR (1) | AR043683A1 (enExample) |
| AT (1) | ATE466012T1 (enExample) |
| AU (2) | AU2003293999B2 (enExample) |
| BR (1) | BR0317645A (enExample) |
| CA (1) | CA2511340C (enExample) |
| CO (1) | CO5690642A2 (enExample) |
| CY (1) | CY1110676T1 (enExample) |
| DE (1) | DE60332396D1 (enExample) |
| DK (1) | DK1581532T3 (enExample) |
| ES (1) | ES2345385T3 (enExample) |
| GB (1) | GB0230045D0 (enExample) |
| IL (1) | IL169335A0 (enExample) |
| IS (1) | IS2795B (enExample) |
| MA (1) | MA27615A1 (enExample) |
| MX (1) | MXPA05006923A (enExample) |
| NO (1) | NO332354B1 (enExample) |
| NZ (2) | NZ570085A (enExample) |
| PL (2) | PL377880A1 (enExample) |
| PT (1) | PT1581532E (enExample) |
| SI (1) | SI1581532T1 (enExample) |
| TW (2) | TWI354671B (enExample) |
| WO (1) | WO2004056823A1 (enExample) |
| ZA (1) | ZA200605901B (enExample) |
Families Citing this family (126)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2165768B1 (es) | 1999-07-14 | 2003-04-01 | Almirall Prodesfarma Sa | Nuevos derivados de quinuclidina y composiciones farmaceuticas que los contienen. |
| GB0230045D0 (en) | 2002-12-23 | 2003-01-29 | Glaxo Group Ltd | Compounds |
| EP1539753B1 (en) * | 2002-09-16 | 2009-09-09 | Glaxo Group Limited | Pyrazolo(3,4-b)pyridine compounds, and their use as phosphodiesterase inhibitors |
| GB0316290D0 (en) | 2003-07-11 | 2003-08-13 | Glaxo Group Ltd | Novel compounds |
| WO2005058892A1 (en) * | 2003-12-19 | 2005-06-30 | Glaxo Group Limited | Pyrazolo [3,4-b] pyridine compounds, and their use as phosphodiesterase inhibitors |
| GB0405933D0 (en) * | 2004-03-16 | 2004-04-21 | Glaxo Group Ltd | Compounds |
| CA2559629A1 (en) * | 2004-03-16 | 2005-09-29 | Glaxo Group Limited | Pyrazolo[3,4-b]pyridine compound, and its use as a pde4 inhibitor |
| WO2005118543A1 (ja) * | 2004-06-03 | 2005-12-15 | Ono Pharmaceutical Co., Ltd. | キナーゼ阻害薬およびその用途 |
| WO2006072599A2 (en) | 2005-01-10 | 2006-07-13 | Glaxo Group Limited | Androstane 17-alpha carbonate derivatives for use in the treatment of allergic and inflammatory conditions |
| CN103467471A (zh) | 2005-06-06 | 2013-12-25 | 武田药品工业株式会社 | 有机化合物 |
| EP1906958A4 (en) * | 2005-06-27 | 2010-12-22 | Ambrilia Biopharma Inc | PYRAZOLO [3,4-B] PYRIDIN-2-YL] -BENZOIC DERIVATIVES AS HIV INTEGRASE INHIBITORS |
| EP1907383A1 (en) * | 2005-06-30 | 2008-04-09 | Prosidion Limited | Gpcr agonists |
| WO2007003961A2 (en) * | 2005-06-30 | 2007-01-11 | Prosidion Limited | Gpcr agonists |
| EP1931668A2 (en) | 2005-09-16 | 2008-06-18 | Ranbaxy Laboratories Limited | Substituted pyrazolo [3,4-b]pyridines as phosphodiesterase inhibitors |
| US7915286B2 (en) | 2005-09-16 | 2011-03-29 | Ranbaxy Laboratories Limited | Substituted pyrazolo [3,4-b] pyridines as phosphodiesterase inhibitors |
| DE602006021044D1 (de) * | 2005-09-29 | 2011-05-12 | Glaxo Group Ltd | Pyrazoloä3,4-büpyridinverbindungen und ihre verwendung als pde4-inhibitoren |
| PE20071068A1 (es) | 2005-12-20 | 2007-12-13 | Glaxo Group Ltd | Acido 3-(4-{[4-(4-{[3-(3,3-dimetil-1-piperidinil)propil]oxi}fenil)-1-piperidinil]carbonil}-1-naftalenil)propanoico o propenoico, sales de los mismos, como antagonistas de los receptores h1 y h3 |
| WO2007103308A2 (en) * | 2006-03-07 | 2007-09-13 | Array Biopharma Inc. | Heterobicyclic pyrazole compounds and methods of use |
| EA200801997A1 (ru) | 2006-04-20 | 2009-04-28 | Глаксо Груп Лимитед | Новые соединения |
| WO2007135026A2 (de) * | 2006-05-24 | 2007-11-29 | Boehringer Ingelheim International Gmbh | Substituierte pteridine als therapeutika |
| US9255099B2 (en) | 2006-06-06 | 2016-02-09 | Intra-Cellular Therapies, Inc. | Pyrazolo[3,4-D]pyrimidine-4,6(5H,7H)-diones as phosphodiesterase 1 inhibitors |
| GB0611587D0 (en) | 2006-06-12 | 2006-07-19 | Glaxo Group Ltd | Novel compounds |
| TW200817006A (en) | 2006-06-23 | 2008-04-16 | Smithkline Beecham Corp | IL-8 receptor antagonist |
| GB0614570D0 (en) * | 2006-07-21 | 2006-08-30 | Glaxo Group Ltd | Compounds |
| JP2009545579A (ja) | 2006-08-01 | 2009-12-24 | グラクソ グループ リミテッド | ピラゾロ[3,4−b]ピリジン化合物、及びpde4阻害薬としてのその使用 |
| US8492378B2 (en) * | 2006-08-03 | 2013-07-23 | Takeda Pharmaceutical Company Limited | GSK-3β inhibitor |
| WO2008070095A1 (en) | 2006-12-05 | 2008-06-12 | Intra-Cellular Therapies, Inc. | Novel uses |
| JP5671236B2 (ja) * | 2007-03-14 | 2015-02-18 | ランバクシー ラボラトリーズ リミテッド | ホスホジエステラーゼ阻害剤としてのピラゾロ(3,4−b)ピリジン誘導体 |
| EP2124943A1 (en) * | 2007-03-14 | 2009-12-02 | Ranbaxy Laboratories Limited | Pyrazolo [3, 4-b]pyridine derivatives as phosphodiesterase inhibitors |
| PE20081889A1 (es) | 2007-03-23 | 2009-03-05 | Smithkline Beecham Corp | Indol carboxamidas como inhibidores de ikk2 |
| CN101801954B (zh) | 2007-09-20 | 2013-10-09 | Irm责任有限公司 | 作为gpr119活性调节剂的化合物和组合物 |
| WO2009055033A1 (en) * | 2007-10-26 | 2009-04-30 | Amgen Inc. | Pyrazolo-pyridinone derivatives and methods of use |
| ES2588238T3 (es) * | 2007-12-06 | 2016-10-31 | Intra-Cellular Therapies, Inc. | Derivados de pirazolopirimidin-4,6-diona y su uso como producto farmacéutico |
| AR070563A1 (es) | 2008-02-06 | 2010-04-21 | Glaxo Group Ltd | Compuesto de un biciclo condensado pirazol-piridin-amina, composicion farmaceutica que lo comprende y su uso para preparar un medicamento util para el tratamiento de enfermedades respiratorias. |
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