JP2006056881A5 - - Google Patents

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Publication number
JP2006056881A5
JP2006056881A5 JP2005210382A JP2005210382A JP2006056881A5 JP 2006056881 A5 JP2006056881 A5 JP 2006056881A5 JP 2005210382 A JP2005210382 A JP 2005210382A JP 2005210382 A JP2005210382 A JP 2005210382A JP 2006056881 A5 JP2006056881 A5 JP 2006056881A5
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JP
Japan
Prior art keywords
ring
optionally substituted
compound according
methylene group
agent
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Pending
Application number
JP2005210382A
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English (en)
Japanese (ja)
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JP2006056881A (ja
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Priority to JP2005210382A priority Critical patent/JP2006056881A/ja
Priority claimed from JP2005210382A external-priority patent/JP2006056881A/ja
Publication of JP2006056881A publication Critical patent/JP2006056881A/ja
Publication of JP2006056881A5 publication Critical patent/JP2006056881A5/ja
Pending legal-status Critical Current

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JP2005210382A 2004-07-21 2005-07-20 縮合環化合物 Pending JP2006056881A (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2005210382A JP2006056881A (ja) 2004-07-21 2005-07-20 縮合環化合物

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2004213523 2004-07-21
JP2005210382A JP2006056881A (ja) 2004-07-21 2005-07-20 縮合環化合物

Publications (2)

Publication Number Publication Date
JP2006056881A JP2006056881A (ja) 2006-03-02
JP2006056881A5 true JP2006056881A5 (https=) 2008-08-07

Family

ID=36104647

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2005210382A Pending JP2006056881A (ja) 2004-07-21 2005-07-20 縮合環化合物

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JP (1) JP2006056881A (https=)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9006288B2 (en) 2009-01-12 2015-04-14 Biokier, Inc. Composition and method for treatment of diabetes
US9314444B2 (en) 2009-01-12 2016-04-19 Biokier, Inc. Composition and method for treatment of NASH

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20080086917A (ko) * 2005-12-29 2008-09-26 노파르티스 아게 콜레스테릴 에스테르 전달 단백질 (cetp) 억제제로서의피리디닐 아민 유도체
EP2727585A1 (en) 2006-05-16 2014-05-07 Takeda Pharmaceutical Company Limited In-vivo screening method
AU2007276405A1 (en) * 2006-07-17 2008-01-24 Novartis Ag Sulphonylaminocarbonyl derivatives of bile acid amides for use as immunomodulators
AU2007325315A1 (en) * 2006-11-28 2008-06-05 Kalypsys Inc Heterocyclic modulators of TGR5
WO2008067219A2 (en) * 2006-11-29 2008-06-05 Kalypsys, Inc. Quinazolinone modulators of tgr5
US20080221161A1 (en) * 2007-02-09 2008-09-11 Kalypsys, Inc. Heterocyclic modulators of tgr5 for treatment of disease
US20090036425A1 (en) * 2007-08-02 2009-02-05 Pfizer Inc Substituted bicyclolactam compounds
WO2009063991A1 (ja) 2007-11-15 2009-05-22 Takeda Pharmaceutical Company Limited ピリドオキサゼピン誘導体およびその用途
EP2322222A4 (en) 2008-08-07 2011-12-21 Takeda Pharmaceutical THERAPEUTIC FOR IRRITATION SYNDROME
WO2010016846A1 (en) * 2008-08-08 2010-02-11 Kalypsys, Inc. Heterocyclic modulators of tgr5 for treatment of disease
KR20110120866A (ko) 2009-01-12 2011-11-04 바이오키어 인코포레이티드 당뇨병 치료 조성물 및 치료방법
WO2012151252A2 (en) 2011-05-02 2012-11-08 Biokier, Inc. Composition and method for treatment of diabetes
EA021079B1 (ru) 2009-06-15 2015-03-31 Такеда Фармасьютикал Компани Лимитед Производные пиразинооксазепина
EP2463290B1 (en) 2009-08-04 2014-03-05 Takeda Pharmaceutical Company Limited Thienooxazepine derivative
US9301938B2 (en) 2009-09-23 2016-04-05 Biokier, Inc. Composition and method for treatment of diabetes
EP2368886A1 (en) 2010-03-01 2011-09-28 Phenex Pharmaceuticals AG Novel compounds for modulation of orphan nuclear receptor RAR-related orphan receptor-gamma (ROR gamma, NR1F3) activity and for the treatment of chronic inflammatory and autoimmune desease
WO2013064231A1 (en) 2011-10-31 2013-05-10 Phenex Pharmaceuticals Ag SEVEN-MEMBERED SULFONAMIDES AS MODULATORS OF RAR-RELATED ORPHAN RECEPTOR-GAMMA (RORγ, NR1F3)
US20150073057A1 (en) 2013-09-06 2015-03-12 Biokier, Inc. Composition and method for treatment of diabetes
CN103739615B (zh) * 2013-12-20 2015-10-28 陕西理工学院 一种具有抗肿瘤活性的酮类化合物及其应用
JP6660668B2 (ja) * 2014-06-24 2020-03-11 花王株式会社 Ucp−1発現促進剤
WO2015199097A1 (ja) * 2014-06-24 2015-12-30 花王株式会社 Ucp-1発現促進剤
US10758519B2 (en) 2014-06-24 2020-09-01 Kao Corporation UCP-1 expression promoter
US12084472B2 (en) 2015-12-18 2024-09-10 Ardelyx, Inc. Substituted 4-phenyl pyridine compounds as non-systemic TGR5 agonists
TWI773657B (zh) * 2015-12-18 2022-08-11 美商亞德利克斯公司 作爲非全身tgr5促效劑之經取代之4-苯基吡啶化合物

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5137890A (en) * 1990-02-14 1992-08-11 Ortho Pharmaceutical Corporation 4-phenyl tetrahydropyrido(4,3-d)pyrimidines
JP2976097B2 (ja) * 1995-03-24 1999-11-10 武田薬品工業株式会社 環状化合物、その製造法および剤
JP2000038386A (ja) * 1997-06-30 2000-02-08 Nippon Kayaku Co Ltd 新規ナフチリジン誘導体またはその塩
JP2004521892A (ja) * 2000-12-20 2004-07-22 メルク エンド カムパニー インコーポレーテッド (ハロ−ベンゾカルボニル)複素環縮合フェニル系p38キナーゼ阻害剤
WO2002088079A2 (en) * 2001-05-01 2002-11-07 Bristol-Myers Squibb Company Dual inhibitors of pde 7 and pde 4
US7105667B2 (en) * 2001-05-01 2006-09-12 Bristol-Myers Squibb Co. Fused heterocyclic compounds and use thereof
SE0103644D0 (sv) * 2001-11-01 2001-11-01 Astrazeneca Ab Therapeutic isoquinoline compounds
JPWO2003104230A1 (ja) * 2002-06-07 2005-10-06 協和醗酵工業株式会社 二環性ピリミジン誘導体
JP2004346059A (ja) * 2003-01-28 2004-12-09 Takeda Chem Ind Ltd 受容体作動薬

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9006288B2 (en) 2009-01-12 2015-04-14 Biokier, Inc. Composition and method for treatment of diabetes
US9314444B2 (en) 2009-01-12 2016-04-19 Biokier, Inc. Composition and method for treatment of NASH

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