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
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JP2007543041A
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English (en)
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JP2008516004A (ja
JP5635727B2 (ja
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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
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Description

実施例18に対し、カルシウムフラックス及び結合アッセイの比較的高い値を、IPアッセイのアッセイ結果につり合う(実施例110中で報告どおり)ことに注意する。

Claims (2)

  1. 式:
    Figure 2008516004

    の化合物又は医薬的に許容されるその塩及び医薬上許容される賦形剤を含む経口投与に適した医薬組成物であって、前記化合物又はその塩が放射性同位体を含まない前記医薬組成物。
  2. 錠剤、カプセル又は分散性粉剤若しくは顆粒剤の形態である、請求項1に記載の医薬組成物。
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 Active 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 (ja) 2014-10-30
JP5635727B2 JP5635727B2 (ja) 2014-12-03

Family

ID=37968242

Family Applications (2)

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JP2007543041A Active 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)

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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 (ja)
EP (2) EP2380889B1 (ja)
JP (2) JP5635727B2 (ja)
CN (1) CN101223166B (ja)
AT (1) ATE520692T1 (ja)
AU (1) AU2005336513B2 (ja)
CA (1) CA2583572C (ja)
ES (1) ES2369783T3 (ja)
WO (1) WO2007050050A2 (ja)

Families Citing this family (17)

* 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
JP2013518085A (ja) 2010-02-01 2013-05-20 ノバルティス アーゲー CRF−1受容体アンタゴニストとしてのピラゾロ[5,1b]オキサゾール誘導体
WO2011092293A2 (en) 2010-02-01 2011-08-04 Novartis Ag Cyclohexyl amide derivatives as crf receptor antagonists
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
UA113625C2 (xx) * 2011-04-26 2017-02-27 Похідні піразолідин-3-ону
CA2829170C (en) * 2011-04-26 2019-02-26 F. Hoffmann-La Roche Ag Ethynyl derivatives as positive allosteric modulators of the mglur5
US9879004B2 (en) 2013-02-07 2018-01-30 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
PE20180358A1 (es) 2015-06-03 2018-02-21 Hoffmann La Roche Derivados de etinilo
BR122020005073A2 (pt) 2017-08-04 2020-10-13 Skyhawk Therapeutics, Inc. Composto, composição farmacêutica e uso do composto
KR20210135241A (ko) 2019-02-05 2021-11-12 스카이호크 테라퓨틱스, 인코포레이티드 스플라이싱을 조절하는 방법 및 조성물
WO2020163544A1 (en) 2019-02-06 2020-08-13 Skyhawk Therapeutics, Inc. Methods and compositions for modulating splicing

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6956049B1 (en) * 1999-08-31 2005-10-18 Merck & Co., Inc. Methods of modulating processes mediated by excitatory amino acid receptors
US7365074B2 (en) * 1999-08-31 2008-04-29 Merck & Co., Inc. Pyridazine, pyrimidine and pyrazine ethyne compounds
EP1214303A1 (en) * 1999-08-31 2002-06-19 Merck & Co., Inc. Heterocyclic compounds and methods of use thereof
US6774138B2 (en) 1999-08-31 2004-08-10 Merck & Co., Inc. Thiazolyl(pyridyl)ethyne compounds
US7462619B2 (en) * 1999-08-31 2008-12-09 Merck & Co., Inc. Pyridazine, pyrimidine and pyrazine ethyne compounds
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
AU2003285957A1 (en) * 2002-10-24 2004-05-13 Merck & Co., Inc. Alkyne derivatives as tracers for metabotropic 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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