JP2006519258A - ピリジン、ピリミジン、キノリン、キナゾリンおよびナフタレン系のウロテンシン−ii受容体拮抗薬 - Google Patents
ピリジン、ピリミジン、キノリン、キナゾリンおよびナフタレン系のウロテンシン−ii受容体拮抗薬 Download PDFInfo
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- JP2006519258A JP2006519258A JP2006508787A JP2006508787A JP2006519258A JP 2006519258 A JP2006519258 A JP 2006519258A JP 2006508787 A JP2006508787 A JP 2006508787A JP 2006508787 A JP2006508787 A JP 2006508787A JP 2006519258 A JP2006519258 A JP 2006519258A
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- Prior art keywords
- methylquinolin
- compound
- ethyl
- ylamino
- amine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 108050002984 Urotensin II receptors Proteins 0.000 title claims description 11
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- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 title description 5
- 239000002464 receptor antagonist Substances 0.000 title description 3
- 229940044551 receptor antagonist Drugs 0.000 title description 3
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- RJUCSJZWSQCMNR-UHFFFAOYSA-N 1-[1-[2-[3-[(2-methylquinolin-4-yl)amino]phenoxy]ethyl]-4-phenylpiperidin-4-yl]ethanone Chemical compound C1CN(CCOC=2C=C(NC=3C4=CC=CC=C4N=C(C)C=3)C=CC=2)CCC1(C(=O)C)C1=CC=CC=C1 RJUCSJZWSQCMNR-UHFFFAOYSA-N 0.000 claims description 2
- 125000004898 2,2-dimethylpropylamino group Chemical group CC(CN*)(C)C 0.000 claims description 2
- MUEUNYKUKXVLEE-UHFFFAOYSA-N 4-[[2-[[3-[(2-methylquinolin-4-yl)amino]benzoyl]amino]ethylamino]methyl]benzoic acid Chemical compound C=12C=CC=CC2=NC(C)=CC=1NC(C=1)=CC=CC=1C(=O)NCCNCC1=CC=C(C(O)=O)C=C1 MUEUNYKUKXVLEE-UHFFFAOYSA-N 0.000 claims description 2
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- CEWQKUDAXBICPI-UHFFFAOYSA-N [1-[2-[3-[(2-methylquinolin-4-yl)amino]phenoxy]ethyl]piperidin-4-yl]-diphenylmethanol Chemical compound C=12C=CC=CC2=NC(C)=CC=1NC(C=1)=CC=CC=1OCCN(CC1)CCC1C(O)(C=1C=CC=CC=1)C1=CC=CC=C1 CEWQKUDAXBICPI-UHFFFAOYSA-N 0.000 claims description 2
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Classifications
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
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- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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Applications Claiming Priority (2)
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| US45108903P | 2003-02-28 | 2003-02-28 | |
| PCT/US2004/005150 WO2004078114A2 (en) | 2003-02-28 | 2004-02-20 | Pyridine, pyrimidine, quinoline, quinazoline, and naphthalene urotensin-ii receptor antagonists. |
Publications (2)
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| JP2006519258A true JP2006519258A (ja) | 2006-08-24 |
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| EP (1) | EP1603884A4 (enExample) |
| JP (1) | JP2006519258A (enExample) |
| AU (1) | AU2004218456A1 (enExample) |
| CA (1) | CA2517166A1 (enExample) |
| WO (1) | WO2004078114A2 (enExample) |
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| CN111170897A (zh) * | 2019-12-18 | 2020-05-19 | 荆门市丽康源纺织科技有限公司 | 一种间位酯的制备方法及间位酯 |
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| JP2005508852A (ja) | 2001-05-07 | 2005-04-07 | スミスクライン・ビーチャム・コーポレイション | スルホンアミド |
| JP2004535390A (ja) | 2001-05-07 | 2004-11-25 | スミスクライン・ビーチャム・コーポレイション | スルホンアミド |
| JP2004529170A (ja) | 2001-05-07 | 2004-09-24 | スミスクライン・ビーチャム・コーポレイション | スルホンアミド |
| AR033879A1 (es) | 2001-05-07 | 2004-01-07 | Smithkline Beecham Corp | Compuesto sulfonamida, composicion farmaceutica que lo comprende, su uso para preparar dicha composicion y procedimiento para la obtencion de dicho compuesto |
| PL371587A1 (en) * | 2002-01-17 | 2005-06-27 | Neurogen Corporation | Substituted quinazolin-4-ylamine analogues as modulators of capsaicin receptors |
| NZ566263A (en) | 2002-05-24 | 2009-09-25 | Millennium Pharm Inc | CCR9 inhibitors and methods of use thereof |
| KR20050043967A (ko) | 2002-09-17 | 2005-05-11 | 액테리온 파마슈티칼 리미티드 | 1-피리딘-4-일-요소 유도체 |
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- 2004-02-20 CA CA002517166A patent/CA2517166A1/en not_active Abandoned
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2007
- 2007-05-25 US US11/807,047 patent/US20080004312A1/en not_active Abandoned
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2013060473A (ja) * | 2006-01-10 | 2013-04-04 | Janssen Pharmaceutica Nv | ウロテンシンii受容体拮抗薬 |
| JP2009544623A (ja) * | 2006-07-20 | 2009-12-17 | スミスクライン・ビーチャム・コーポレイション | モルホリニルおよびピロリジニル類似体 |
| JP2010529126A (ja) * | 2007-06-07 | 2010-08-26 | 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 | ウロテンシンii受容体拮抗薬 |
| JP2011511046A (ja) * | 2008-02-07 | 2011-04-07 | サノフイ−アベンテイス | 5,6−ビスアリール−2−ピリジン−カルボキシアミド誘導体、この調製、およびウロテンシンii受容体の拮抗剤としてのこの治療的用途 |
| JP2015127304A (ja) * | 2013-12-27 | 2015-07-09 | 日本サプリメント株式会社 | 糖取り込み促進剤 |
| JP2017501205A (ja) * | 2013-12-30 | 2017-01-12 | ライフサイ ファーマシューティカルズ,インク. | 治療用阻害化合物 |
| JP2020509088A (ja) * | 2017-02-24 | 2020-03-26 | 深▲チェン▼市霊蘭生物医薬科技有限公司Shenzhen Linglan Bio−Pharmaceutical Technology Co., Ltd | 新規なドーパミンd3受容体選択的リガンド及びびその調製方法並びに医薬使用 |
| JP7017797B2 (ja) | 2017-02-24 | 2022-02-09 | 深▲チェン▼市霊蘭生物医薬科技有限公司 | 新規なドーパミンd3受容体選択的リガンド及びびその調製方法並びに医薬使用 |
| JP2023542541A (ja) * | 2020-09-25 | 2023-10-10 | エサイエント ファーマシューティカルズ,インコーポレイティド | Mas関連gタンパク質受容体x2のモジュレーター、並びに関連製品及び方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| US20080004312A1 (en) | 2008-01-03 |
| US20040186102A1 (en) | 2004-09-23 |
| WO2004078114A3 (en) | 2005-02-17 |
| AU2004218456A1 (en) | 2004-09-16 |
| CA2517166A1 (en) | 2004-09-16 |
| US7265122B2 (en) | 2007-09-04 |
| WO2004078114A2 (en) | 2004-09-16 |
| EP1603884A4 (en) | 2008-05-28 |
| EP1603884A2 (en) | 2005-12-14 |
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