JP2009510064A - 神経障害、精神障害または疼痛性障害の処置用の新規化合物 - Google Patents

神経障害、精神障害または疼痛性障害の処置用の新規化合物 Download PDF

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JP2009510064A
JP2009510064A JP2008533434A JP2008533434A JP2009510064A JP 2009510064 A JP2009510064 A JP 2009510064A JP 2008533434 A JP2008533434 A JP 2008533434A JP 2008533434 A JP2008533434 A JP 2008533434A JP 2009510064 A JP2009510064 A JP 2009510064A
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disease
pain
use according
disorder
compound
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JP2009510064A5 (enExample
Inventor
ミニディス，アレクサンダー
ウェンスボ，デイヴィッド
スラッシ，アブデルマリック
アイザック，メスヴィン
エリックソン，キャロライン
プロフィア，ベロニカ
バーグストロム，パー−オロブ
エドワーズ，ルイーズ
アロラ，ジャライ
ジン，タオ
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AstraZeneca AB
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AstraZeneca AB
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Diabetes (AREA)
  • Pain & Pain Management (AREA)
  • Pulmonology (AREA)
  • Psychiatry (AREA)
  • Obesity (AREA)
  • Endocrinology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Hematology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Cardiology (AREA)
  • Emergency Medicine (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Rheumatology (AREA)
  • Psychology (AREA)
  • Urology & Nephrology (AREA)
  • Virology (AREA)
  • Nutrition Science (AREA)
  • Child & Adolescent Psychology (AREA)
  • Oncology (AREA)
  • Vascular Medicine (AREA)
  • Tropical Medicine & Parasitology (AREA)
JP2008533434A 2005-09-29 2006-09-20 神経障害、精神障害または疼痛性障害の処置用の新規化合物 Pending JP2009510064A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US72152705P 2005-09-29 2005-09-29
PCT/US2006/036423 WO2007040982A1 (en) 2005-09-29 2006-09-20 5- (phenylisoxazolylethoxy) -triazol- 3 -yl substituted pyridine compounds for the treatment of neurological, psychiatric or pain disorders

Related Child Applications (1)

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JP2009211258A Division JP2010013476A (ja) 2005-09-29 2009-09-14 神経障害、精神障害または疼痛性障害の処置用の新規化合物

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JP2009510064A true JP2009510064A (ja) 2009-03-12
JP2009510064A5 JP2009510064A5 (enExample) 2009-11-05

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JP2008533434A Pending JP2009510064A (ja) 2005-09-29 2006-09-20 神経障害、精神障害または疼痛性障害の処置用の新規化合物
JP2009211258A Pending JP2010013476A (ja) 2005-09-29 2009-09-14 神経障害、精神障害または疼痛性障害の処置用の新規化合物

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JP2009211258A Pending JP2010013476A (ja) 2005-09-29 2009-09-14 神経障害、精神障害または疼痛性障害の処置用の新規化合物

Country Status (18)

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US (4) US20080227824A1 (enExample)
EP (1) EP1934209A1 (enExample)
JP (2) JP2009510064A (enExample)
KR (1) KR20080050421A (enExample)
CN (1) CN101273037A (enExample)
AR (1) AR058807A1 (enExample)
AU (1) AU2006297462A1 (enExample)
BR (1) BRPI0616228A2 (enExample)
CA (1) CA2623009A1 (enExample)
EC (1) ECSP088283A (enExample)
IL (1) IL189990A0 (enExample)
NO (1) NO20081434L (enExample)
RU (1) RU2008108219A (enExample)
TW (1) TW200800976A (enExample)
UA (1) UA92503C2 (enExample)
UY (1) UY29796A1 (enExample)
WO (1) WO2007040982A1 (enExample)
ZA (1) ZA200802163B (enExample)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2022532869A (ja) * 2019-05-15 2022-07-20 スーリン、クラース 動物の疼痛の予防及び／又は治療に使用するための４－［５－［（ｒａｃ）－１－［５－（３－クロロフェニル）－３－イソキサゾリル］エトキシ］－４－メチル－４ｈ－１，２，４－トリアゾール－３－イル］ピリジン
JP2023501114A (ja) * 2019-11-05 2023-01-18 スーリン、クラース 哺乳動物の過労の予防及び／又は治療に使用するための４－［５－［（ｒａｃ）－１－［５－（３－クロロフェニル）－３－イソキサゾリル］エトキシ］－４－メチル－４ｈ－１，２，４－トリアゾール－３－イル］ピリジン

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WO2004014881A2 (en) * 2002-08-09 2004-02-19 Astra Zeneca Ab '1,2,4'oxadiazoles as modulators of metabotropic glutamate receptor-5
US7585881B2 (en) * 2004-02-18 2009-09-08 Astrazeneca Ab Additional heteropolycyclic compounds and their use as metabotropic glutamate receptor antagonists
UY29796A1 (es) * 2005-09-29 2007-04-30 Astrazeneca Ab Nuevos compuestos para el tratamiento de trastornos neurológicos, psiquiátricos o del dolor
TW200821305A (en) * 2006-10-05 2008-05-16 Astrazeneca Ab MGluR5 modulators
BRPI0818448A2 (pt) * 2007-10-19 2015-05-12 Astrazeneca Ab Composto, composição farmacêutica, uso de um composto, e, métodos para o tratamento ou prevenção de um distúrbio madiano pelo receptor mglur5.
CA2702974A1 (en) * 2007-10-26 2009-04-30 Astrazeneca Ab Amino 1,2,4-triazole derivatives as modulators of mglur5
MX2011001549A (es) * 2008-08-12 2011-03-15 Astrazeneca Ab Forma cristalina de 4-(5-{(1r)-1-[5-(3-clorofenil)isoxazol-3-il]et oxi}-4-metil-4h-1,2,4-triazol-3-il)piridina.
TW201011015A (en) * 2008-08-12 2010-03-16 Astrazeneca Ab New compounds 500
CA2751761A1 (en) 2008-10-22 2010-04-29 House Ear Institute Treatment and/or prevention of inner ear conditions by modulation of a metabotropic glutamate receptor
CN102245592A (zh) * 2008-12-12 2011-11-16 阿斯利康(瑞典)有限公司 制备4-[4-甲基-5-(c1-10 烷基硫基/c5-10芳基-c1-6 烷基硫基)-4h-1,2,4-三唑-3-基]吡啶的新方法
EP2379531A1 (en) * 2008-12-18 2011-10-26 AstraZeneca AB Processes for the manufacture of 3-{4-methyl-5- [ (ir) -1- (2- (3-methylphenyl) -2h-tetrazol-5-yl) -ethoxy]-4h- [1,2, 4]triazol-3-yl} -pyridine, 4-methyl-3-methylthio-5- (3- pyridyl)-l,2,4-triazole, and (ir) -1- [2- (3-methylphenyl) -2h- tetrazol-5-yl]ethanol
US20110313172A1 (en) * 2008-12-18 2011-12-22 Astrazeneca Ab Process for the preparation of 1-[5-(3-chloro-phenyl)-isooxazol-3-yl]-ethanone and (r)-1-[5-(3-chloro-phenyl)-isooxazol-3-yl]-ethanol
US8349852B2 (en) 2009-01-13 2013-01-08 Novartis Ag Quinazolinone derivatives useful as vanilloid antagonists
EP2438052A1 (en) * 2009-06-05 2012-04-11 Oslo University Hospital HF Azole derivatives as wtn pathway inhibitors
JP5775094B2 (ja) 2009-12-29 2015-09-09 イーライ リリー アンド カンパニー 統合失調症の処置に有用な選択的ｍＧｌｕ５受容体増強因子としてのテトラヒドロトリアゾロピリジン化合物
CN102762572A (zh) 2010-02-01 2012-10-31 诺瓦提斯公司 作为CRF-1受体拮抗剂的吡唑并[5,1b]*唑衍生物
AR080056A1 (es) 2010-02-01 2012-03-07 Novartis Ag Derivados de ciclohexil-amida como antagonistas de los receptores de crf
EP2531490B1 (en) 2010-02-02 2014-10-15 Novartis AG Cyclohexyl amide derivatives as crf receptor antagonists
US8080568B1 (en) * 2010-06-29 2011-12-20 Ewha University - Industry Collaboration Foundation 2-pyridyl substituted imidazoles as therapeutic ALK5 and/or ALK4 inhibitors
UA112418C2 (uk) * 2010-09-07 2016-09-12 Астеллас Фарма Інк. Терапевтичний болезаспокійливий засіб
CN103429583A (zh) 2010-12-08 2013-12-04 奥斯陆大学医院公司 作为wnt信号通路抑制剂的三唑衍生物
EA201391348A8 (ru) 2011-03-18 2014-11-28 Новартис Аг КОМБИНАЦИИ АКТИВАТОРОВ АЛЬФА-7 НИКОТИНОВОГО АЦЕТИЛХОЛИНОВОГО РЕЦЕПТОРА И АНТАГОНИСТОВ mGluR5, ПРЕДНАЗНАЧЕННЫЕ ДЛЯ ПРИМЕНЕНИЯ ПРИ ВЫЗВАННОЙ ДОПАМИНОМ ДИСКИНЕЗИИ, СВЯЗАННОЙ С БОЛЕЗНЬЮ ПАРКИНСОНА
WO2016163754A1 (en) * 2015-04-07 2016-10-13 Medpacto Inc. Pharmaceutical composition for preventing or treating cancer and method using thereof
KR20160120157A (ko) 2015-04-07 2016-10-17 주식회사 메드팩토 암 예방 또는 치료용 약학적 조성물 및 이를 이용한 방법
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US20070129408A1 (en) 2007-06-07
TW200800976A (en) 2008-01-01
IL189990A0 (en) 2008-08-07
ECSP088283A (es) 2008-04-28
WO2007040982A1 (en) 2007-04-12
US20070270468A1 (en) 2007-11-22
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RU2008108219A (ru) 2009-11-10
AU2006297462A1 (en) 2007-04-12
JP2010013476A (ja) 2010-01-21
US20080227824A1 (en) 2008-09-18
EP1934209A1 (en) 2008-06-25
AR058807A1 (es) 2008-02-27
US20070270469A1 (en) 2007-11-22
CA2623009A1 (en) 2007-04-12
CN101273037A (zh) 2008-09-24
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US7476684B2 (en) 2009-01-13
UY29796A1 (es) 2007-04-30

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