JP2008516004A5 - - Google Patents

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Publication number
JP2008516004A5
JP2008516004A5 JP2007543041A JP2007543041A JP2008516004A5 JP 2008516004 A5 JP2008516004 A5 JP 2008516004A5 JP 2007543041 A JP2007543041 A JP 2007543041A JP 2007543041 A JP2007543041 A JP 2007543041A JP 2008516004 A5 JP2008516004 A5 JP 2008516004A5
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JP
Japan
Prior art keywords
pharmaceutical composition
salt
radioisotope
granule
capsule
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.)
Granted
Application number
JP2007543041A
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English (en)
Japanese (ja)
Other versions
JP2008516004A (ja
JP5635727B2 (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/US2005/035921 external-priority patent/WO2007050050A2/en
Publication of JP2008516004A publication Critical patent/JP2008516004A/ja
Publication of JP2008516004A5 publication Critical patent/JP2008516004A5/ja
Application granted granted Critical
Publication of JP5635727B2 publication Critical patent/JP5635727B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2007543041A 2004-10-07 2005-10-06 チアゾリルmglur5アンタゴニスト及びそれらの使用のための方法 Expired - Fee Related JP5635727B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US61680504P 2004-10-07 2004-10-07
US60/616,805 2004-10-07
PCT/US2005/035921 WO2007050050A2 (en) 2004-10-07 2005-10-06 Thiazolyl mglur5 antagonists and methods for their use

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2014184615A Division JP2015013885A (ja) 2004-10-07 2014-09-10 チアゾリルmglur5アンタゴニスト及びそれらの使用のための方法

Publications (3)

Publication Number Publication Date
JP2008516004A JP2008516004A (ja) 2008-05-15
JP2008516004A5 true JP2008516004A5 (enExample) 2014-10-30
JP5635727B2 JP5635727B2 (ja) 2014-12-03

Family

ID=37968242

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2007543041A Expired - Fee Related JP5635727B2 (ja) 2004-10-07 2005-10-06 チアゾリルmglur5アンタゴニスト及びそれらの使用のための方法
JP2014184615A Pending JP2015013885A (ja) 2004-10-07 2014-09-10 チアゾリルmglur5アンタゴニスト及びそれらの使用のための方法

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2014184615A Pending JP2015013885A (ja) 2004-10-07 2014-09-10 チアゾリルmglur5アンタゴニスト及びそれらの使用のための方法

Country Status (9)

Country Link
US (3) US7879882B2 (enExample)
EP (2) EP1893608B1 (enExample)
JP (2) JP5635727B2 (enExample)
CN (1) CN101223166B (enExample)
AT (1) ATE520692T1 (enExample)
AU (1) AU2005336513B2 (enExample)
CA (1) CA2583572C (enExample)
ES (1) ES2369783T3 (enExample)
WO (1) WO2007050050A2 (enExample)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5635727B2 (ja) 2004-10-07 2014-12-03 メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. チアゾリルmglur5アンタゴニスト及びそれらの使用のための方法
US8349852B2 (en) 2009-01-13 2013-01-08 Novartis Ag Quinazolinone derivatives useful as vanilloid antagonists
TW201124391A (en) * 2009-10-20 2011-07-16 Lundbeck & Co As H 2-substituted-ethynylthiazole derivatives and uses of same
AR080056A1 (es) 2010-02-01 2012-03-07 Novartis Ag Derivados de ciclohexil-amida como antagonistas de los receptores de crf
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
JP5748777B2 (ja) 2010-02-02 2015-07-15 ノバルティス アーゲー Crf受容体アンタゴニストとしてのシクロヘキシルアミド誘導体
US8420661B2 (en) 2010-04-13 2013-04-16 Hoffmann-La Roche Inc. Arylethynyl derivatives
US8772300B2 (en) * 2011-04-19 2014-07-08 Hoffmann-La Roche Inc. Phenyl or pyridinyl-ethynyl derivatives
KR101576343B1 (ko) * 2011-04-26 2015-12-09 에프. 호프만-라 로슈 아게 피라졸리딘-3-온 유도체
CA2829170C (en) * 2011-04-26 2019-02-26 F. Hoffmann-La Roche Ag Ethynyl derivatives as positive allosteric modulators of the mglur5
EP2953933A1 (en) 2013-02-07 2015-12-16 Merck Patent GmbH Substituted acetylene derivatives and their use as positive allosteric modulators of mglur4
UA116023C2 (uk) * 2013-07-08 2018-01-25 Ф. Хоффманн-Ля Рош Аг Етинільні похідні як антагоністи метаботропного глутаматного рецептора
WO2015188368A1 (en) 2014-06-13 2015-12-17 Merck Sharp & Dohme Corp. Pyrrolo[2,3-c]pyridines as imaging agents for neurofibrilary tangles
JP6603334B2 (ja) 2015-06-03 2019-11-06 エフ.ホフマン−ラ ロシュ アーゲー エチニル誘導体
RU2020105929A (ru) 2017-08-04 2021-09-06 Скайхоук Терапьютикс, Инк. Способы и композиции для модулирования сплайсинга
JP7603592B2 (ja) 2019-02-05 2024-12-20 スカイホーク・セラピューティクス・インコーポレーテッド スプライシングを調節するための方法および組成物
EP3920926A4 (en) 2019-02-05 2022-10-19 Skyhawk Therapeutics, Inc. Methods and compositions for modulating splicing
WO2020163544A1 (en) 2019-02-06 2020-08-13 Skyhawk Therapeutics, Inc. Methods and compositions for modulating splicing
CN119638696A (zh) 2019-02-06 2025-03-18 斯基霍克疗法公司 用于调节剪接的方法和组合物

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7365074B2 (en) 1999-08-31 2008-04-29 Merck & Co., Inc. Pyridazine, pyrimidine and pyrazine ethyne compounds
US6774138B2 (en) 1999-08-31 2004-08-10 Merck & Co., Inc. Thiazolyl(pyridyl)ethyne compounds
JP4815083B2 (ja) * 1999-08-31 2011-11-16 メルク・シャープ・エンド・ドーム・コーポレイション 複素環化合物およびそれの使用方法
US7462619B2 (en) 1999-08-31 2008-12-09 Merck & Co., Inc. Pyridazine, pyrimidine and pyrazine ethyne compounds
US6956049B1 (en) 1999-08-31 2005-10-18 Merck & Co., Inc. Methods of modulating processes mediated by excitatory amino acid receptors
US6551270B1 (en) 2000-08-30 2003-04-22 Snowden Pencer, Inc. Dual lumen access port
US6903005B1 (en) 2000-08-30 2005-06-07 Micron Technology, Inc. Method for the formation of RuSixOy-containing barrier layers for high-k dielectrics
EP1556142A4 (en) * 2002-10-24 2006-11-08 Merck & Co Inc ALKYN DERIVATIVES AS TRACERS FOR THE METABOTROPE GLUTAMATE RECEPTOR BINDING
JP5635727B2 (ja) * 2004-10-07 2014-12-03 メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. チアゾリルmglur5アンタゴニスト及びそれらの使用のための方法

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