JP2006509801A - 新規mch受容体アンタゴニスト - Google Patents
新規mch受容体アンタゴニスト Download PDFInfo
- Publication number
- JP2006509801A JP2006509801A JP2004559142A JP2004559142A JP2006509801A JP 2006509801 A JP2006509801 A JP 2006509801A JP 2004559142 A JP2004559142 A JP 2004559142A JP 2004559142 A JP2004559142 A JP 2004559142A JP 2006509801 A JP2006509801 A JP 2006509801A
- Authority
- JP
- Japan
- Prior art keywords
- biphenyl
- carboxylic acid
- ethylsulfanylmethyl
- phenoxy
- alkyl
- 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.)
- Withdrawn
Links
- 0 C(C1)C2N1*=C2 Chemical compound C(C1)C2N1*=C2 0.000 description 8
- NCTVJZZCBNDOOB-UHFFFAOYSA-N CCOC(c(cc1)ccc1-c1cccc(CSCCOc2ccccc2)c1)=O Chemical compound CCOC(c(cc1)ccc1-c1cccc(CSCCOc2ccccc2)c1)=O NCTVJZZCBNDOOB-UHFFFAOYSA-N 0.000 description 1
- IIXXRUDYYUINQJ-UHFFFAOYSA-N CCOC(c1cc(-c2ccc(CSCCO)cc2)ccc1)=O Chemical compound CCOC(c1cc(-c2ccc(CSCCO)cc2)ccc1)=O IIXXRUDYYUINQJ-UHFFFAOYSA-N 0.000 description 1
- ZXMLJRDQSDGZAD-UHFFFAOYSA-N CCOC(c1ccccc1-c1ccc(CSCCOc2ccccc2)cc1)=O Chemical compound CCOC(c1ccccc1-c1ccc(CSCCOc2ccccc2)cc1)=O ZXMLJRDQSDGZAD-UHFFFAOYSA-N 0.000 description 1
- WFBDWTZOYPUBQZ-UHFFFAOYSA-N CN(C)CCCNC=O Chemical compound CN(C)CCCNC=O WFBDWTZOYPUBQZ-UHFFFAOYSA-N 0.000 description 1
- WUPJWBCAEKWGDY-UHFFFAOYSA-N CN(C)CCNC(c(cc1)ccc1-c1c(CSCCOc2ccccc2)cccc1)=O Chemical compound CN(C)CCNC(c(cc1)ccc1-c1c(CSCCOc2ccccc2)cccc1)=O WUPJWBCAEKWGDY-UHFFFAOYSA-N 0.000 description 1
- DLMBMQNMBCWDEE-UHFFFAOYSA-N CN(C)CCNC(c(cc1)ccc1-c1cc(CSCCOc2ccccc2)ccc1)=O Chemical compound CN(C)CCNC(c(cc1)ccc1-c1cc(CSCCOc2ccccc2)ccc1)=O DLMBMQNMBCWDEE-UHFFFAOYSA-N 0.000 description 1
- IZKADXKYGNXDBR-UHFFFAOYSA-N CN(C)CCNC(c1ccccc1-c1cc(/[O]=C(\C(O)=O)/O)c(CSCCOc2ccccc2)cc1)=O Chemical compound CN(C)CCNC(c1ccccc1-c1cc(/[O]=C(\C(O)=O)/O)c(CSCCOc2ccccc2)cc1)=O IZKADXKYGNXDBR-UHFFFAOYSA-N 0.000 description 1
- LEUBZGIKQCNSLF-UHFFFAOYSA-N CN(C)CCNC(c1ccccc1-c1cc(CSCCOc2ccccc2)ccc1)=O Chemical compound CN(C)CCNC(c1ccccc1-c1cc(CSCCOc2ccccc2)ccc1)=O LEUBZGIKQCNSLF-UHFFFAOYSA-N 0.000 description 1
- XHNDTOIDDFTOSR-MUUNZHRXSA-N C[C@@]1(CSCCOc2ccccc2)C=CC(c(cccc2)c2C(NCCCN(C)C)=O)=CC1 Chemical compound C[C@@]1(CSCCOc2ccccc2)C=CC(c(cccc2)c2C(NCCCN(C)C)=O)=CC1 XHNDTOIDDFTOSR-MUUNZHRXSA-N 0.000 description 1
- XKQXLVJSIBNOIB-JOCHJYFZSA-N C[C@H](C=C(C=C1C(NCCCN(C)C)=O)c2c(CSCCOc3ccccc3)cccc2)C1=C Chemical compound C[C@H](C=C(C=C1C(NCCCN(C)C)=O)c2c(CSCCOc3ccccc3)cccc2)C1=C XKQXLVJSIBNOIB-JOCHJYFZSA-N 0.000 description 1
- DVTVIARLMYRPDW-UHFFFAOYSA-N OC(c1cccc(-c2c(CNCCOc3ccccc3)cccc2)c1)=O Chemical compound OC(c1cccc(-c2c(CNCCOc3ccccc3)cccc2)c1)=O DVTVIARLMYRPDW-UHFFFAOYSA-N 0.000 description 1
- KLOFYERXNUPFDL-UHFFFAOYSA-N OC(c1ccccc1-c1c(CSCCOc2ccccc2)cccc1)=O Chemical compound OC(c1ccccc1-c1c(CSCCOc2ccccc2)cccc1)=O KLOFYERXNUPFDL-UHFFFAOYSA-N 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N c1ccccc1 Chemical compound c1ccccc1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/60—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton with the carbon atom of at least one of the carboxyl groups bound to nitrogen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Diabetes (AREA)
- Ophthalmology & Optometry (AREA)
- Pulmonology (AREA)
- Urology & Nephrology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Child & Adolescent Psychology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US43270102P | 2002-12-11 | 2002-12-11 | |
| PCT/US2003/037071 WO2004052848A1 (en) | 2002-12-11 | 2003-12-03 | Novel mch receptor antagonists |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006509801A true JP2006509801A (ja) | 2006-03-23 |
| JP2006509801A5 JP2006509801A5 (https=) | 2006-12-28 |
Family
ID=32507985
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004559142A Withdrawn JP2006509801A (ja) | 2002-12-11 | 2003-12-03 | 新規mch受容体アンタゴニスト |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US7132456B2 (https=) |
| EP (1) | EP1572637A1 (https=) |
| JP (1) | JP2006509801A (https=) |
| CN (1) | CN1726189A (https=) |
| AU (1) | AU2003302925A1 (https=) |
| BR (1) | BR0316948A (https=) |
| CA (1) | CA2509042A1 (https=) |
| MX (1) | MXPA05006272A (https=) |
| WO (1) | WO2004052848A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008026614A1 (en) * | 2006-08-30 | 2008-03-06 | Semiconductor Energy Laboratory Co., Ltd. | Method for synthesizing anthracene derivative and anthracene derivative, light emitting element, light emitting device, electronic device |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7329656B2 (en) | 2004-10-08 | 2008-02-12 | H. Lundbeck A/S | Arylthiobenzylpiperidine derivatives |
| US7446204B2 (en) | 2004-10-08 | 2008-11-04 | H. Lundbeck A/S | Amino substituted aryloxybenzylpiperidine derivatives |
| WO2006066174A1 (en) * | 2004-12-17 | 2006-06-22 | Eli Lilly And Company | Thiazolopyridinone derivates as mch receptor antagonists |
| KR101356093B1 (ko) | 2005-03-28 | 2014-01-27 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 안트라센 유도체, 발광소자용 재료, 발광소자, 발광장치 및전자기기 |
| US7731377B2 (en) * | 2006-03-21 | 2010-06-08 | Semiconductor Energy Laboratory Co., Ltd. | Backlight device and display device |
| US7772162B2 (en) | 2006-03-27 | 2010-08-10 | Board Of Regents, The University Of Texas System | Use of fluorocarbon surfactants to improve the productivity of gas and gas condensate wells |
| US20070225176A1 (en) * | 2006-03-27 | 2007-09-27 | Pope Gary A | Use of fluorocarbon surfactants to improve the productivity of gas and gas condensate wells |
| EP2418202B1 (en) | 2006-03-31 | 2014-01-29 | Novartis AG | (4-[4-[5-(substituted amino)-pyridin-2-yl]phenyl]-cyclohexyl)-acetic acid derivatives as DGAT inhibitors |
| WO2008021849A2 (en) | 2006-08-09 | 2008-02-21 | Smithkline Beecham Corporation | Novel compounds as antagonists or inverse agonists at opioid receptors |
| US9353309B2 (en) * | 2007-03-23 | 2016-05-31 | Board Of Regents, The University Of Texas System | Method for treating a formation with a solvent |
| US7723722B2 (en) | 2007-03-23 | 2010-05-25 | Semiconductor Energy Laboratory Co., Ltd. | Organic compound, anthracene derivative, and light-emitting element, light-emitting device, and electronic device using anthracene derivative |
| RU2453690C2 (ru) * | 2007-03-23 | 2012-06-20 | Борд Оф Риджентс, Зе Юниверсити Оф Техас Систем | Способ обработки углеводородной формации |
| US20080286445A1 (en) * | 2007-05-17 | 2008-11-20 | Semiconductor Energy Laboratory Co., Ltd. | Composition, and method of fabricating light-emitting element |
| AR066169A1 (es) * | 2007-09-28 | 2009-07-29 | Novartis Ag | Derivados de benzo-imidazoles, utiles para trastornos asociados con la actividad de dgat |
| AU2008331558A1 (en) * | 2007-11-30 | 2009-06-11 | 3M Innovative Properties Company | Methods for improving the productivity of oil producing wells |
| CN102089282A (zh) * | 2008-07-08 | 2011-06-08 | 株式会社半导体能源研究所 | 咔唑衍生物、发光元件用材料、发光元件以及发光装置 |
| EP2166001B1 (en) * | 2008-09-19 | 2011-07-20 | Semiconductor Energy Laboratory Co., Ltd. | Carbazole Derivative and Method for Producing the Same |
| EP2348857B1 (en) | 2008-10-22 | 2016-02-24 | Merck Sharp & Dohme Corp. | Novel cyclic benzimidazole derivatives useful anti-diabetic agents |
| US8329914B2 (en) | 2008-10-31 | 2012-12-11 | Merck Sharp & Dohme Corp | Cyclic benzimidazole derivatives useful as anti-diabetic agents |
| 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 |
| SG192941A1 (en) | 2011-02-25 | 2013-09-30 | Merck Sharp & Dohme | Novel cyclic azabenzimidazole derivatives useful as anti-diabetic agents |
| RU2015106909A (ru) | 2012-08-02 | 2016-09-27 | Мерк Шарп И Доум Корп. | Антидиабетические трициклические соединения |
| KR20150118158A (ko) | 2013-02-22 | 2015-10-21 | 머크 샤프 앤드 돔 코포레이션 | 항당뇨병 비시클릭 화합물 |
| WO2014139388A1 (en) | 2013-03-14 | 2014-09-18 | Merck Sharp & Dohme Corp. | Novel indole derivatives useful as anti-diabetic agents |
| WO2015051496A1 (en) | 2013-10-08 | 2015-04-16 | Merck Sharp & Dohme Corp. | Antidiabetic tricyclic compounds |
| KR102844041B1 (ko) | 2016-02-26 | 2025-08-11 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 유기 화합물, 발광 소자, 발광 장치, 전자 기기, 및 조명 장치 |
| US11072602B2 (en) | 2016-12-06 | 2021-07-27 | Merck Sharp & Dohme Corp. | Antidiabetic heterocyclic compounds |
| EP3558298B1 (en) | 2016-12-20 | 2026-03-11 | Merck Sharp & Dohme LLC | Antidiabetic spirochroman compounds |
| BR102018007822A2 (pt) | 2017-04-20 | 2018-11-06 | Gilead Sciences, Inc. | composto, métodos para inibir pd-1, pd-l1 e/ou interação de pd-1/pd-l1 e para tratamento de câncer, composição farmacêutica, e, kit para tratamento de ou prevenção de câncer ou uma doença ou condição |
| CR20200347A (es) | 2018-02-13 | 2020-09-23 | Gilead Sciences Inc | Inhibidores pd-1/pd-l1 |
| TWI712412B (zh) | 2018-04-19 | 2020-12-11 | 美商基利科學股份有限公司 | Pd‐1/pd‐l1抑制劑 |
| SG11202012425QA (en) | 2018-07-13 | 2021-01-28 | Gilead Sciences Inc | Pd-1/pd-l1 inhibitors |
| WO2020086556A1 (en) | 2018-10-24 | 2020-04-30 | Gilead Sciences, Inc. | Pd-1/pd-l1 inhibitors |
| US12421331B2 (en) | 2023-11-09 | 2025-09-23 | Chevron Phillips Chemical Company Lp | Systems and methods for chromium catalyst activation |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3535330A (en) * | 1968-04-29 | 1970-10-20 | Sandoz Ag | 2,6-diphenyl - 4 - (p-(dilower-alkyl amino lower - alkoxy)phenyl)pyridines and derivatives thereof |
| US3928449A (en) * | 1969-04-03 | 1975-12-23 | Sandoz Ag | Aminoalkoxy-terphenyls and the salts thereof |
| LU78484A1 (de) * | 1977-11-10 | 1979-06-13 | Ciba Geigy Ag | Verfahren zur herstellung von benzoxazolyl-phenyl-stilbenen |
| DE2752361A1 (de) * | 1977-11-24 | 1979-06-07 | Troponwerke Gmbh & Co Kg | Neue indolderivate, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel |
| EP1218336A2 (en) * | 1999-09-20 | 2002-07-03 | Takeda Chemical Industries, Ltd. | Melanin concentrating hormone antagonist |
-
2003
- 2003-12-03 EP EP03812783A patent/EP1572637A1/en not_active Withdrawn
- 2003-12-03 MX MXPA05006272A patent/MXPA05006272A/es unknown
- 2003-12-03 CA CA002509042A patent/CA2509042A1/en not_active Abandoned
- 2003-12-03 JP JP2004559142A patent/JP2006509801A/ja not_active Withdrawn
- 2003-12-03 US US10/536,053 patent/US7132456B2/en not_active Expired - Fee Related
- 2003-12-03 BR BR0316948-0A patent/BR0316948A/pt not_active Application Discontinuation
- 2003-12-03 WO PCT/US2003/037071 patent/WO2004052848A1/en not_active Ceased
- 2003-12-03 AU AU2003302925A patent/AU2003302925A1/en not_active Abandoned
- 2003-12-03 CN CNA2003801059746A patent/CN1726189A/zh active Pending
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008026614A1 (en) * | 2006-08-30 | 2008-03-06 | Semiconductor Energy Laboratory Co., Ltd. | Method for synthesizing anthracene derivative and anthracene derivative, light emitting element, light emitting device, electronic device |
| US8183793B2 (en) | 2006-08-30 | 2012-05-22 | Semiconductor Energy Laboratory Co., Ltd. | Method for synthesizing anthracene derivative and anthracene derivative, light emitting element, light emitting device, electronic device |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2004052848A1 (en) | 2004-06-24 |
| US7132456B2 (en) | 2006-11-07 |
| BR0316948A (pt) | 2005-10-18 |
| EP1572637A1 (en) | 2005-09-14 |
| AU2003302925A1 (en) | 2004-06-30 |
| CN1726189A (zh) | 2006-01-25 |
| CA2509042A1 (en) | 2004-06-24 |
| MXPA05006272A (es) | 2005-08-19 |
| US20060052449A1 (en) | 2006-03-09 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2006509801A (ja) | 新規mch受容体アンタゴニスト | |
| RU2345983C2 (ru) | Гетероциклические соединения и способы применения | |
| US9133122B2 (en) | Amide compounds, compositions and uses thereof | |
| US10179781B2 (en) | Sodium channel modulators for the treatment of pain | |
| US6399631B1 (en) | Carbazole neuropeptide Y5 antagonists | |
| US20140243324A1 (en) | Use of hematopoietic growth factor mimetics | |
| US20060111357A1 (en) | Quinoline compounds for use in mch receptor related disorders | |
| HRP20050108A2 (hr) | Indolinfenilsulfonamidni derivati | |
| BG108487A (bg) | Заместени с триамид индоли, бензофурани и бензотиофени като инхибитори на микрозомния триглицерид пренасящ протеин (mtp) и/или секрецията на аполипопротеин б (аро в) | |
| KR20170048588A (ko) | 바이사이클릭 화합물 | |
| JP2004525175A (ja) | チオヒダントイン及び糖尿病治療のためのその使用 | |
| JP2010520877A (ja) | Ppar活性化合物 | |
| JP2009507079A (ja) | Ppar活性化合物 | |
| KR20190003686A (ko) | 인돌아민 2,3-디옥시게나제의 억제제 및 그의 사용 방법 | |
| JP2016504282A (ja) | ジヒドロピラゾールgpr40モジュレーター | |
| US20070149514A1 (en) | Indole-phenylsulfonamide derivatives used as ppar-delta activating compounds | |
| JP2007510629A (ja) | 新規mch受容体アンタゴニスト | |
| PT2094684E (pt) | 1,5-difenil-3-piridinilamino-1,5-di-hidro-pirrolidin-2-ona como modulador de receptores cb1 | |
| US20090099199A1 (en) | Organic compounds | |
| KR20100135248A (ko) | 인돌리논 화합물 | |
| JP7185633B2 (ja) | 7員アザ複素環を含有するデルタ-オピオイド受容体調節化合物、その使用方法及び製造方法 | |
| JP2007501195A (ja) | 二環式インドリンスルホンアミド誘導体 | |
| WO2007069671A1 (ja) | 二環式複素環化合物 | |
| JP2007501196A (ja) | Ppar−デルタ調節因子としてのインドリンスルファニル酸アミド化合物 | |
| KR20080023758A (ko) | 비만 및 관련 질환의 치료를 위한 신규한 아미노산 유도체 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20061110 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20061110 |
|
| A761 | Written withdrawal of application |
Free format text: JAPANESE INTERMEDIATE CODE: A761 Effective date: 20090114 |