WO2008133192A1 - Fused imidazole compound and use thereof - Google Patents
Fused imidazole compound and use thereof Download PDFInfo
- Publication number
- WO2008133192A1 WO2008133192A1 PCT/JP2008/057566 JP2008057566W WO2008133192A1 WO 2008133192 A1 WO2008133192 A1 WO 2008133192A1 JP 2008057566 W JP2008057566 W JP 2008057566W WO 2008133192 A1 WO2008133192 A1 WO 2008133192A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- optionally substituted
- nitrogen
- oxide
- containing heterocyclic
- imidazole compound
- Prior art date
Links
- -1 imidazole compound Chemical class 0.000 title abstract 2
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 title 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 229940126560 MAPK inhibitor Drugs 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 102000002574 p38 Mitogen-Activated Protein Kinases Human genes 0.000 abstract 1
- 108010068338 p38 Mitogen-Activated Protein Kinases Proteins 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 230000006433 tumor necrosis factor production Effects 0.000 abstract 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
-
- 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
-
- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- 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
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Immunology (AREA)
- Physical Education & Sports Medicine (AREA)
- Neurosurgery (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Hospice & Palliative Care (AREA)
- Cardiology (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Heart & Thoracic Surgery (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Disclosed is a compound represented by the formula (I) below or a salt thereof. The compound is useful as a p38 MAPK inhibitor and/or a TNF-α production inhibitor. (In the formula, Xa, Xb and Xc may be the same or different and each represents an optionally substituted CH or a nitrogen atom, and either one of them represents a nitrogen atom; Xd represents an optionally substituted CH; Ra represents an optionally substituted phenyl or an optionally substituted heterocyclic group; Rb represents a hydrogen atom; Rc represents an optionally substituted nitrogen-containing heterocyclic N-oxide, an N-(optionally substituted nitrogen-containing heterocyclic N-oxide-C1-6-alkyl)amino or an optionally substituted nitrogen-containing heterocyclic N-oxide-carbonylamino-C1-6- alkyl.)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007-111032 | 2007-04-19 | ||
JP2007111032 | 2007-04-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2008133192A1 true WO2008133192A1 (en) | 2008-11-06 |
Family
ID=39925646
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2008/057566 WO2008133192A1 (en) | 2007-04-19 | 2008-04-18 | Fused imidazole compound and use thereof |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2008133192A1 (en) |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7820665B2 (en) | 2007-12-19 | 2010-10-26 | Amgen Inc. | Imidazopyridazine inhibitors of PI3 kinase for cancer treatment |
US7928140B2 (en) | 2007-08-02 | 2011-04-19 | Amgen Inc. | Benzothiazole PI3 kinase modulators for cancer treatment |
JP2013521320A (en) * | 2010-03-09 | 2013-06-10 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Imidazo [1,2-a] pyrazine derivatives and their use for the prevention or treatment of neurological, mental and metabolic disorders and diseases |
US8716282B2 (en) | 2009-10-30 | 2014-05-06 | Janssen Pharmaceutica Nv | Imidazo[1,2-b]pyridazine derivatives and their use as PDE10 inhibitors |
US8729074B2 (en) | 2009-03-20 | 2014-05-20 | Amgen Inc. | Inhibitors of PI3 kinase |
JP2014518223A (en) * | 2011-06-20 | 2014-07-28 | アルツハイマーズ・インスティテュート・オブ・アメリカ・インコーポレイテッド | Compounds and their therapeutic uses |
JP2015513559A (en) * | 2012-03-14 | 2015-05-14 | 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 | Substituted imidazopyridazine |
WO2015086501A1 (en) * | 2013-12-09 | 2015-06-18 | Ucb Biopharma Sprl | Imidazopyridazine derivatives as modulators of tnf activity |
US9145419B2 (en) | 2010-04-28 | 2015-09-29 | Bristol-Myers Squibb Company | Imidazopyridazinyl compounds |
JP2016531126A (en) * | 2013-08-23 | 2016-10-06 | 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 | New bisamide pyridine |
US9550784B2 (en) | 2012-07-09 | 2017-01-24 | Beerse Pharmaceutica NV | Inhibitors of phosphodiesterase 10 enzyme |
US9669035B2 (en) | 2012-06-26 | 2017-06-06 | Janssen Pharmaceutica Nv | Combinations comprising PDE 2 inhibitors such as 1-aryl-4-methyl-[1,2,4]triazolo-[4,3-A]]quinoxaline compounds and PDE 10 inhibitors for use in the treatment of neurological of metabolic disorders |
JP2018522869A (en) * | 2015-06-29 | 2018-08-16 | アストラゼネカ・アクチエボラーグAstrazeneca Aktiebolag | Polycyclic amide derivatives as CDK9 inhibitors |
US10604523B2 (en) | 2011-06-27 | 2020-03-31 | Janssen Pharmaceutica Nv | 1-aryl-4-methyl-[1,2,4]triazolo[4,3-a]quinoxaline derivatives |
WO2023247552A1 (en) | 2022-06-21 | 2023-12-28 | Syngenta Crop Protection Ag | Microbiocidal bicyclic heterocyclic carboxamide derivatives |
EP4096657A4 (en) * | 2020-01-29 | 2024-07-10 | Foghorn Therapeutics Inc. | COMPOUNDS AND THEIR USES |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07503017A (en) * | 1992-01-13 | 1995-03-30 | スミスクライン・ビーチャム・コーポレイション | Imidazole derivatives and their use as cytokine inhibitors |
JP2003513977A (en) * | 1999-11-10 | 2003-04-15 | オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド | Substituted 2-aryl-3- (heteroaryl) -imidazo [1,2-α] pyrimidines and related pharmaceutical compositions and methods |
WO2005066177A1 (en) * | 2003-12-31 | 2005-07-21 | Schering-Plough Ltd. | Control of parasites in animals by the use of imidazo[1,2-b]pyridazine derivatives |
JP2006502164A (en) * | 2002-09-06 | 2006-01-19 | バイオジェン・アイデック・エムエイ・インコーポレイテッド | Imidazopyridine and its production and use |
WO2006070943A1 (en) * | 2004-12-28 | 2006-07-06 | Takeda Pharmaceutical Company Limited | Condensed imidazole compound and use thereof |
JP2006519249A (en) * | 2003-03-04 | 2006-08-24 | ファイザー・プロダクツ・インク | Novel condensed heteroaromatic compounds as transforming growth factor (TGF) inhibitors |
-
2008
- 2008-04-18 WO PCT/JP2008/057566 patent/WO2008133192A1/en active Application Filing
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07503017A (en) * | 1992-01-13 | 1995-03-30 | スミスクライン・ビーチャム・コーポレイション | Imidazole derivatives and their use as cytokine inhibitors |
JP2003513977A (en) * | 1999-11-10 | 2003-04-15 | オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド | Substituted 2-aryl-3- (heteroaryl) -imidazo [1,2-α] pyrimidines and related pharmaceutical compositions and methods |
JP2006502164A (en) * | 2002-09-06 | 2006-01-19 | バイオジェン・アイデック・エムエイ・インコーポレイテッド | Imidazopyridine and its production and use |
JP2006519249A (en) * | 2003-03-04 | 2006-08-24 | ファイザー・プロダクツ・インク | Novel condensed heteroaromatic compounds as transforming growth factor (TGF) inhibitors |
WO2005066177A1 (en) * | 2003-12-31 | 2005-07-21 | Schering-Plough Ltd. | Control of parasites in animals by the use of imidazo[1,2-b]pyridazine derivatives |
WO2006070943A1 (en) * | 2004-12-28 | 2006-07-06 | Takeda Pharmaceutical Company Limited | Condensed imidazole compound and use thereof |
Cited By (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7928140B2 (en) | 2007-08-02 | 2011-04-19 | Amgen Inc. | Benzothiazole PI3 kinase modulators for cancer treatment |
US7820665B2 (en) | 2007-12-19 | 2010-10-26 | Amgen Inc. | Imidazopyridazine inhibitors of PI3 kinase for cancer treatment |
US8729074B2 (en) | 2009-03-20 | 2014-05-20 | Amgen Inc. | Inhibitors of PI3 kinase |
US8716282B2 (en) | 2009-10-30 | 2014-05-06 | Janssen Pharmaceutica Nv | Imidazo[1,2-b]pyridazine derivatives and their use as PDE10 inhibitors |
US8859543B2 (en) | 2010-03-09 | 2014-10-14 | Janssen Pharmaceutica Nv | Imidazo[1,2-a]pyrazine derivatives and their use for the prevention or treatment of neurological, psychiatric and metabolic disorders and diseases |
JP2013521320A (en) * | 2010-03-09 | 2013-06-10 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Imidazo [1,2-a] pyrazine derivatives and their use for the prevention or treatment of neurological, mental and metabolic disorders and diseases |
US9145419B2 (en) | 2010-04-28 | 2015-09-29 | Bristol-Myers Squibb Company | Imidazopyridazinyl compounds |
JP2014518223A (en) * | 2011-06-20 | 2014-07-28 | アルツハイマーズ・インスティテュート・オブ・アメリカ・インコーポレイテッド | Compounds and their therapeutic uses |
US10604523B2 (en) | 2011-06-27 | 2020-03-31 | Janssen Pharmaceutica Nv | 1-aryl-4-methyl-[1,2,4]triazolo[4,3-a]quinoxaline derivatives |
JP2015513559A (en) * | 2012-03-14 | 2015-05-14 | 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 | Substituted imidazopyridazine |
US9669035B2 (en) | 2012-06-26 | 2017-06-06 | Janssen Pharmaceutica Nv | Combinations comprising PDE 2 inhibitors such as 1-aryl-4-methyl-[1,2,4]triazolo-[4,3-A]]quinoxaline compounds and PDE 10 inhibitors for use in the treatment of neurological of metabolic disorders |
US9550784B2 (en) | 2012-07-09 | 2017-01-24 | Beerse Pharmaceutica NV | Inhibitors of phosphodiesterase 10 enzyme |
JP2016531126A (en) * | 2013-08-23 | 2016-10-06 | 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 | New bisamide pyridine |
CN105814061A (en) * | 2013-12-09 | 2016-07-27 | Ucb生物制药私人有限公司 | Imidazopyridazine derivatives as modulators of TNF activity |
JP2016539975A (en) * | 2013-12-09 | 2016-12-22 | ユーシービー バイオファルマ エスピーアールエル | Imidazopyridazine derivatives as modulators of TNF activity |
US9873703B2 (en) | 2013-12-09 | 2018-01-23 | Ucb Biopharma Sprl | Imidazopyridazine derivatives as modulators of TNF activity |
RU2679609C1 (en) * | 2013-12-09 | 2019-02-12 | Юсб Байофарма Спрл | Imidazopyridazine derivatives as modulators of tnf activity |
WO2015086501A1 (en) * | 2013-12-09 | 2015-06-18 | Ucb Biopharma Sprl | Imidazopyridazine derivatives as modulators of tnf activity |
JP2018522869A (en) * | 2015-06-29 | 2018-08-16 | アストラゼネカ・アクチエボラーグAstrazeneca Aktiebolag | Polycyclic amide derivatives as CDK9 inhibitors |
JP6997627B2 (en) | 2015-06-29 | 2022-01-17 | アストラゼネカ・アクチエボラーグ | Polycyclic amide derivative as a CDK9 inhibitor |
EP4096657A4 (en) * | 2020-01-29 | 2024-07-10 | Foghorn Therapeutics Inc. | COMPOUNDS AND THEIR USES |
WO2023247552A1 (en) | 2022-06-21 | 2023-12-28 | Syngenta Crop Protection Ag | Microbiocidal bicyclic heterocyclic carboxamide derivatives |
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