UA92169C2 - Fused heterocyclic compounds, process for the preparation thereof, pharmaceutical composition, crf receptor antagonist, tretment method and use of crf receptor antagonist - Google Patents

Fused heterocyclic compounds, process for the preparation thereof, pharmaceutical composition, crf receptor antagonist, tretment method and use of crf receptor antagonist

Info

Publication number
UA92169C2
UA92169C2 UAA200711851A UAA200711851A UA92169C2 UA 92169 C2 UA92169 C2 UA 92169C2 UA A200711851 A UAA200711851 A UA A200711851A UA A200711851 A UAA200711851 A UA A200711851A UA 92169 C2 UA92169 C2 UA 92169C2
Authority
UA
Ukraine
Prior art keywords
optionally substituted
receptor antagonist
crf receptor
preparation
pharmaceutical composition
Prior art date
Application number
UAA200711851A
Other languages
Russian (ru)
Ukrainian (uk)
Inventor
Казуйоши Асо
Мичийо Мочизуки
Альберт Чарльз Гиоркос
Кристофер Питер Корритт
Сук Янг Чо
Скотт Алан Пратт
Кристофер Стивен Сидем
Original Assignee
Такеда Фармасьютикал Компани Лимитед
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Такеда Фармасьютикал Компани Лимитед filed Critical Такеда Фармасьютикал Компани Лимитед
Publication of UA92169C2 publication Critical patent/UA92169C2/en

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

There is provided a CRF receptor antagonist comprising a compound of the formula (I): wherein R1 is an optionally substituted hydrocarbyl, an optionally substituted C-linked heterocyclic group, an optionally substituted N-linked heteroaryl group, a cyano or an acyl; R2 is an optionally substituted cyclic hydrocarbyl or an optionally substituted heterocyclic group; X is oxygen, sulfur or -NR3-(wherein R3 is a hydrogen, an optionally substituted hydrocarbyl or an acyl); Y1, Y2 and Y3 are each an optionally substituted carbon or a nitrogen, provided that one or less of Y1, Y2 and Y3 is nitrogen; and Z is a bond, -CO-, oxygen, sulfur, -SO-, -SO-, -NR4-, -NR4-alk-, -CONR4- or -NR4CO- (wherein alk is an optionally substituted C3-4 alkylene and R4 is a hydrogen, an optionally substituted hydrocarbyl or an acyl); or a salt thereof or a prodrug thereof.(I)
UAA200711851A 2005-04-27 2006-04-26 Fused heterocyclic compounds, process for the preparation thereof, pharmaceutical composition, crf receptor antagonist, tretment method and use of crf receptor antagonist UA92169C2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US67511305P 2005-04-27 2005-04-27

Publications (1)

Publication Number Publication Date
UA92169C2 true UA92169C2 (en) 2010-10-11

Family

ID=39334842

Family Applications (1)

Application Number Title Priority Date Filing Date
UAA200711851A UA92169C2 (en) 2005-04-27 2006-04-26 Fused heterocyclic compounds, process for the preparation thereof, pharmaceutical composition, crf receptor antagonist, tretment method and use of crf receptor antagonist

Country Status (3)

Country Link
CN (1) CN101166729B (en)
UA (1) UA92169C2 (en)
ZA (1) ZA200708844B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102153538B (en) * 2010-02-11 2013-12-11 山东轩竹医药科技有限公司 Benzocyclodirivative

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6124463A (en) * 1998-07-02 2000-09-26 Dupont Pharmaceuticals Benzimidazoles as corticotropin release factor antagonists
US6365589B1 (en) * 1998-07-02 2002-04-02 Bristol-Myers Squibb Pharma Company Imidazo-pyridines, -pyridazines, and -triazines as corticotropin releasing factor antagonists

Also Published As

Publication number Publication date
ZA200708844B (en) 2009-08-26
CN101166729B (en) 2011-08-31
CN101166729A (en) 2008-04-23

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