JP2006504761A5 - - Google Patents

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Publication number
JP2006504761A5
JP2006504761A5 JP2004547576A JP2004547576A JP2006504761A5 JP 2006504761 A5 JP2006504761 A5 JP 2006504761A5 JP 2004547576 A JP2004547576 A JP 2004547576A JP 2004547576 A JP2004547576 A JP 2004547576A JP 2006504761 A5 JP2006504761 A5 JP 2006504761A5
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JP
Japan
Prior art keywords
chloro
alkyl
phenyl
acetamide
phenoxy
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.)
Pending
Application number
JP2004547576A
Other languages
English (en)
Japanese (ja)
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JP2006504761A (ja
Filing date
Publication date
Priority claimed from DE10250743A external-priority patent/DE10250743A1/de
Application filed filed Critical
Publication of JP2006504761A publication Critical patent/JP2006504761A/ja
Publication of JP2006504761A5 publication Critical patent/JP2006504761A5/ja
Pending legal-status Critical Current

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JP2004547576A 2002-10-31 2003-10-28 Mch拮抗活性を有する新規アミド化合物及びこれらの化合物を含む薬物 Pending JP2006504761A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10250743A DE10250743A1 (de) 2002-10-31 2002-10-31 Neue Amid-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel
PCT/EP2003/011933 WO2004039764A1 (de) 2002-10-31 2003-10-28 Neue amid-verbindungen mit mch-antagonistischer wirkung und diese verbindungen enthaltende arzneimittel

Publications (2)

Publication Number Publication Date
JP2006504761A JP2006504761A (ja) 2006-02-09
JP2006504761A5 true JP2006504761A5 (enExample) 2009-10-08

Family

ID=32115015

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2004547576A Pending JP2006504761A (ja) 2002-10-31 2003-10-28 Mch拮抗活性を有する新規アミド化合物及びこれらの化合物を含む薬物

Country Status (24)

Country Link
EP (1) EP1558567B1 (enExample)
JP (1) JP2006504761A (enExample)
KR (1) KR20050065654A (enExample)
CN (1) CN1708476A (enExample)
AR (1) AR041735A1 (enExample)
AT (1) ATE434601T1 (enExample)
AU (1) AU2003285306A1 (enExample)
BR (1) BR0315797A (enExample)
CA (1) CA2504207C (enExample)
CO (1) CO5570698A2 (enExample)
DE (2) DE10250743A1 (enExample)
EA (1) EA009040B1 (enExample)
EC (1) ECSP055765A (enExample)
ES (1) ES2327329T3 (enExample)
HR (1) HRP20050383A2 (enExample)
MX (1) MXPA05002865A (enExample)
NO (1) NO20050745L (enExample)
PE (1) PE20040785A1 (enExample)
PL (1) PL376256A1 (enExample)
RS (1) RS20050330A (enExample)
TW (1) TW200412936A (enExample)
UY (1) UY28051A1 (enExample)
WO (1) WO2004039764A1 (enExample)
ZA (1) ZA200501164B (enExample)

Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7592373B2 (en) 2003-12-23 2009-09-22 Boehringer Ingelheim International Gmbh Amide compounds with MCH antagonistic activity and medicaments comprising these compounds
FR2866880A1 (fr) * 2004-02-27 2005-09-02 Oreal Para-phenylenediamine secondaire n-alkylaminee ortho-et/ou meta-substituee, composition de teinture des fibres keratiniques contenant une telle para-phenylenediamine, procedes mettant en oeuvre cette composition et utilisations
US7605176B2 (en) 2004-03-06 2009-10-20 Boehringer Ingelheim International Gmbh β-ketoamide compounds with MCH antagonistic activity
JP2006076990A (ja) * 2004-03-12 2006-03-23 Bayer Cropscience Ag 殺虫性ベンゼンジカルボキサミド類
US7524862B2 (en) 2004-04-14 2009-04-28 Boehringer Ingelheim International Gmbh Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds
DE102004017934A1 (de) 2004-04-14 2005-11-03 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue Alkin-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel
BRPI0716579A2 (pt) 2006-08-25 2013-10-08 Boehringer Ingelheim Int Derivados de piridona com atividade antagonista ao mch e medicamentos que compreendem estes compostos
WO2008069611A1 (en) * 2006-12-08 2008-06-12 Korea Research Institute Of Chemical Technology N-phenylamide derivative, process for the preparation thereof, and composition for preventing or treating ischemic diseases comprising same
WO2008071646A1 (en) 2006-12-11 2008-06-19 Boehringer Ingelheim International Gmbh New pyridazine derivatives with mch antagonistic activity and medicaments comprising these compounds
AR073049A1 (es) * 2008-08-07 2010-10-13 Bayer Cropscience Sa Derivados fungicidas de oxialquilamida
US8410284B2 (en) 2008-10-22 2013-04-02 Merck Sharp & Dohme Corp Cyclic benzimidazole derivatives useful as anti-diabetic agents
EP2362731B1 (en) 2008-10-31 2016-04-06 Merck Sharp & Dohme Corp. Novel cyclic benzimidazole derivatives useful anti-diabetic agents
US9452980B2 (en) * 2009-12-22 2016-09-27 Hoffmann-La Roche Inc. Substituted benzamides
JP2013520502A (ja) 2010-02-25 2013-06-06 メルク・シャープ・エンド・ドーム・コーポレイション 有用な抗糖尿病薬である新規な環状ベンズイミダゾール誘導体
US9079880B2 (en) * 2010-07-07 2015-07-14 Boehringer Ingelheim International Gmbh Rho kinase inhibitors
EP2583965B1 (en) * 2010-07-15 2017-01-25 Takeda Pharmaceutical Company Limited Heterocyclic ring compound
SG192941A1 (en) 2011-02-25 2013-09-30 Merck Sharp & Dohme Novel cyclic azabenzimidazole derivatives useful as anti-diabetic agents
CA2842364A1 (en) * 2011-07-29 2013-02-07 Karyopharm Therapeutics, Inc. Nuclear transport modulators and uses thereof
ES2655645T3 (es) 2011-07-29 2018-02-21 Karyopharm Therapeutics, Inc. Moduladores de transporte nuclear que contienen hidrazida y usos de los mismos
CA2868484A1 (en) 2012-03-28 2013-10-03 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Salicylic acid derivatives useful as glucocerebrosidase activators
PL3404027T3 (pl) 2012-05-09 2020-09-21 Biogen Ma Inc. Modulatory transportu jądrowego i ich zastosowania
WO2014022528A1 (en) 2012-08-02 2014-02-06 Merck Sharp & Dohme Corp. Antidiabetic tricyclic compounds
JP2016516004A (ja) 2013-02-22 2016-06-02 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. 抗糖尿病二環式化合物
EP2970119B1 (en) 2013-03-14 2021-11-03 Merck Sharp & Dohme Corp. Novel indole derivatives useful as anti-diabetic agents
WO2014144772A1 (en) 2013-03-15 2014-09-18 Karyopharm Therapeutics Inc. Methods of promoting wound healing using crm1 inhibitors
LT3010892T (lt) 2013-06-21 2019-04-10 Karyopharm Therapeutics Inc. 1,2,4-triazolai kaip branduolio transporto moduliatoriai ir jų panaudojimas
DK3013796T3 (da) 2013-06-27 2020-03-16 Lg Chemical Ltd Biarylderivater som gpr120-agonister
WO2015051496A1 (en) 2013-10-08 2015-04-16 Merck Sharp & Dohme Corp. Antidiabetic tricyclic compounds
DK3180331T3 (da) 2014-08-15 2022-09-12 Karyopharm Therapeutics Inc Polymorfer af selinexor
CN105439914B (zh) * 2014-09-17 2017-07-11 复旦大学 4‑氨酰基苯氧乙酰胺类化合物及其药物用途
CA2970011C (en) * 2014-12-24 2021-08-03 Lg Chem, Ltd. Biaryl derivative as gpr120 agonist
JP6533997B2 (ja) * 2014-12-26 2019-06-26 株式会社ヤクルト本社 Znf143阻害活性を有する化合物およびその利用
EP3397633A1 (en) 2015-12-31 2018-11-07 Karyopharm Therapeutics, Inc. Nuclear transport modulators and uses thereof
MA43530A (fr) 2015-12-31 2018-11-07 Karyopharm Therapeutics Inc Modulateurs de transport nucléaire et leurs utilisations
JP6814814B2 (ja) 2016-03-17 2021-01-20 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft Taarのアゴニストとしての活性を有する5−エチル−4−メチル−ピラゾール−3−カルボキサミド誘導体
WO2018098472A1 (en) 2016-11-28 2018-05-31 Karyopharm Therapeutics Inc. Crm1 inhibitors for treating epilepsy
WO2018106518A1 (en) 2016-12-06 2018-06-14 Merck Sharp & Dohme Corp. Antidiabetic heterocyclic compounds
WO2018118670A1 (en) 2016-12-20 2018-06-28 Merck Sharp & Dohme Corp. Antidiabetic spirochroman compounds
US20220315545A1 (en) 2019-07-10 2022-10-06 Bayer Aktiengesellschaft Process of preparing 2-(phenylimino)-1,3-thiazolidin-4-ones
US20240174680A1 (en) 2021-01-29 2024-05-30 Cedilla Therapeutics, Inc. Cdk2 inhibitors and methods of using the same
US12053459B2 (en) 2021-06-26 2024-08-06 Cedilla Therapeutics, Inc. CDK2 inhibitors and methods of using the same

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Publication number Priority date Publication date Assignee Title
EP1100495A4 (en) * 1998-07-28 2002-09-25 Smithkline Beecham Corp PROPENAMIDES AS CCR5 MODULATORS
US7115750B1 (en) * 1999-09-20 2006-10-03 Takeda Pharmaceutical Company Limited Melanin concentrating hormone antagonist
JP2004504303A (ja) * 2000-07-05 2004-02-12 シナプティック・ファーマスーティカル・コーポレーション 選択的メラニン凝集ホルモン−1(mch1)受容体アンタゴニストおよびその使用
US20030022891A1 (en) * 2000-12-01 2003-01-30 Anandan Palani MCH antagonists and their use in the treatment of obesity
AR036939A1 (es) * 2001-10-25 2004-10-13 Schering Corp Antagonistas de la hormona de concentracion de melanina (mch) composiciones farmaceuticas, un proceso para su elaboracion y el uso de dichos compuestos, solos o en combinacion, para la elaboracion de un medicamento para el tratamiento de obesidad

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