JP5072602B2 - Mch受容体アンタゴニストとしてのチアゾロピリジノン誘導体 - Google Patents
Mch受容体アンタゴニストとしてのチアゾロピリジノン誘導体 Download PDFInfo
- Publication number
- JP5072602B2 JP5072602B2 JP2007546991A JP2007546991A JP5072602B2 JP 5072602 B2 JP5072602 B2 JP 5072602B2 JP 2007546991 A JP2007546991 A JP 2007546991A JP 2007546991 A JP2007546991 A JP 2007546991A JP 5072602 B2 JP5072602 B2 JP 5072602B2
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- alkyl
- chloro
- thiazolo
- methoxy
- 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.)
- Expired - Fee Related
Links
- FEAQWPDZSFYJSG-UHFFFAOYSA-N CC(C)[Si+](C(C)C)(C(C)C)N(CC1)c(cc2)c1cc2N(CCc1c2[s]c(-c(cc3)ccc3Cl)n1)C2=O Chemical compound CC(C)[Si+](C(C)C)(C(C)C)N(CC1)c(cc2)c1cc2N(CCc1c2[s]c(-c(cc3)ccc3Cl)n1)C2=O FEAQWPDZSFYJSG-UHFFFAOYSA-N 0.000 description 1
- WRNGADURHULTCJ-UHFFFAOYSA-N CC(C)[Si+](C(C)C)(C(C)C)N(CCc1c2)c1ccc2[N+]([O-])=O Chemical compound CC(C)[Si+](C(C)C)(C(C)C)N(CCc1c2)c1ccc2[N+]([O-])=O WRNGADURHULTCJ-UHFFFAOYSA-N 0.000 description 1
- QFSMGOXFJZEISJ-UHFFFAOYSA-N CC1(C)OC(C)(C)CN(CCO)C1 Chemical compound CC1(C)OC(C)(C)CN(CCO)C1 QFSMGOXFJZEISJ-UHFFFAOYSA-N 0.000 description 1
- ZOVTYAMQLZVMDU-UHFFFAOYSA-N CN(C)CCCOc(ccc(N(CCc1c2[s]c(-c(cc3)ccc3Cl)n1)C2=O)c1)c1OC Chemical compound CN(C)CCCOc(ccc(N(CCc1c2[s]c(-c(cc3)ccc3Cl)n1)C2=O)c1)c1OC ZOVTYAMQLZVMDU-UHFFFAOYSA-N 0.000 description 1
- GIBVENMRXKZTPM-UHFFFAOYSA-N CN(C1CCN(C)CC1)c1nc(cc(cc2)N)c2[o]1 Chemical compound CN(C1CCN(C)CC1)c1nc(cc(cc2)N)c2[o]1 GIBVENMRXKZTPM-UHFFFAOYSA-N 0.000 description 1
- ZUJHMOJGLZQVRS-UHFFFAOYSA-N CN(CCOc(c(OC)c1)ccc1N(CCc1c2[s]c(-c(cc3)ccc3Cl)n1)C2=O)C1CCCCC1 Chemical compound CN(CCOc(c(OC)c1)ccc1N(CCc1c2[s]c(-c(cc3)ccc3Cl)n1)C2=O)C1CCCCC1 ZUJHMOJGLZQVRS-UHFFFAOYSA-N 0.000 description 1
- OUEXNKFTUUQUPB-UHFFFAOYSA-N COC(COc(cc1)ccc1NC(c1c(CCO)nc(-c2ccccc2)[s]1)=O)OC Chemical compound COC(COc(cc1)ccc1NC(c1c(CCO)nc(-c2ccccc2)[s]1)=O)OC OUEXNKFTUUQUPB-UHFFFAOYSA-N 0.000 description 1
- VWFLTPMGJLTXMU-UHFFFAOYSA-N COc(cc(cc1)N(CCc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)c1OCc1c[nH]cn1 Chemical compound COc(cc(cc1)N(CCc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)c1OCc1c[nH]cn1 VWFLTPMGJLTXMU-UHFFFAOYSA-N 0.000 description 1
- DJPGJWARKQIVBZ-UHFFFAOYSA-N COc1cc(N(CCc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)ccc1C#CCN1CCCC1 Chemical compound COc1cc(N(CCc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)ccc1C#CCN1CCCC1 DJPGJWARKQIVBZ-UHFFFAOYSA-N 0.000 description 1
- QKEPINVDFDMOKF-UHFFFAOYSA-N COc1cc(N(CCc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)ccc1O Chemical compound COc1cc(N(CCc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)ccc1O QKEPINVDFDMOKF-UHFFFAOYSA-N 0.000 description 1
- XZOIEVTYYSWZAI-UHFFFAOYSA-N COc1cc(N(CCc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)ccc1OCCN1CCOCC1 Chemical compound COc1cc(N(CCc2c3[s]c(-c(cc4)ccc4Cl)n2)C3=O)ccc1OCCN1CCOCC1 XZOIEVTYYSWZAI-UHFFFAOYSA-N 0.000 description 1
- IDKQBMBADBCOLZ-UHFFFAOYSA-N Cc(c1c2)c(C)[n](CCN3CCCC3)c1ccc2N(CCc1c2[s]c(-c(cc3)ccc3Cl)n1)C2=O Chemical compound Cc(c1c2)c(C)[n](CCN3CCCC3)c1ccc2N(CCc1c2[s]c(-c(cc3)ccc3Cl)n1)C2=O IDKQBMBADBCOLZ-UHFFFAOYSA-N 0.000 description 1
- CPDULACRVICLJO-UHFFFAOYSA-N N=Cc(cc(cc1)NC(c2c(CCO)nc(-c(cc3)ccc3Cl)[s]2)=O)c1NCCN1CCCC1 Chemical compound N=Cc(cc(cc1)NC(c2c(CCO)nc(-c(cc3)ccc3Cl)[s]2)=O)c1NCCN1CCCC1 CPDULACRVICLJO-UHFFFAOYSA-N 0.000 description 1
- ZLPPXBYGAJAUJR-UHFFFAOYSA-N Nc(cc1)cc(Cl)c1OCCN1CCCC1 Chemical compound Nc(cc1)cc(Cl)c1OCCN1CCCC1 ZLPPXBYGAJAUJR-UHFFFAOYSA-N 0.000 description 1
- VKDVFUSENKSPEY-UHFFFAOYSA-N Nc1ccc2[n](CCN3CCCC3)ccc2c1 Chemical compound Nc1ccc2[n](CCN3CCCC3)ccc2c1 VKDVFUSENKSPEY-UHFFFAOYSA-N 0.000 description 1
- SJWSZTXWVAMNOJ-UHFFFAOYSA-N O=C(c1c(CC2)nc(-c(cc3)ccc3Cl)[s]1)N2c(cc1)cc2c1[n](Cc1ncccc1)cc2 Chemical compound O=C(c1c(CC2)nc(-c(cc3)ccc3Cl)[s]1)N2c(cc1)cc2c1[n](Cc1ncccc1)cc2 SJWSZTXWVAMNOJ-UHFFFAOYSA-N 0.000 description 1
- UQWFIKHNWUNXCV-UHFFFAOYSA-N OCCc1c(C(Nc(cc2Cl)ccc2OCCN2CCCC2)=O)[s]c(-c(cc2)ccc2Cl)n1 Chemical compound OCCc1c(C(Nc(cc2Cl)ccc2OCCN2CCCC2)=O)[s]c(-c(cc2)ccc2Cl)n1 UQWFIKHNWUNXCV-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
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- 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
-
- 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
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P1/12—Antidiarrhoeals
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- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- 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
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- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
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- A—HUMAN NECESSITIES
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- A61P25/08—Antiepileptics; Anticonvulsants
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P25/20—Hypnotics; Sedatives
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
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- 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
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P27/06—Antiglaucoma agents or miotics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- A—HUMAN NECESSITIES
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Ophthalmology & Optometry (AREA)
- Endocrinology (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Anesthesiology (AREA)
- Rheumatology (AREA)
- Emergency Medicine (AREA)
- Vascular Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Gynecology & Obstetrics (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US63714304P | 2004-12-17 | 2004-12-17 | |
| US60/637,143 | 2004-12-17 | ||
| PCT/US2005/045866 WO2006066174A1 (en) | 2004-12-17 | 2005-12-16 | Thiazolopyridinone derivates as mch receptor antagonists |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2008524250A JP2008524250A (ja) | 2008-07-10 |
| JP2008524250A5 JP2008524250A5 (https=) | 2009-01-22 |
| JP5072602B2 true JP5072602B2 (ja) | 2012-11-14 |
Family
ID=36123161
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007546991A Expired - Fee Related JP5072602B2 (ja) | 2004-12-17 | 2005-12-16 | Mch受容体アンタゴニストとしてのチアゾロピリジノン誘導体 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US7902356B2 (https=) |
| EP (1) | EP1828207B1 (https=) |
| JP (1) | JP5072602B2 (https=) |
| CN (1) | CN101080411B (https=) |
| AT (1) | ATE446962T1 (https=) |
| AU (1) | AU2005316314B2 (https=) |
| BR (1) | BRPI0519124A2 (https=) |
| CA (1) | CA2589695A1 (https=) |
| DE (1) | DE602005017423D1 (https=) |
| ES (1) | ES2333243T3 (https=) |
| MX (1) | MX2007007227A (https=) |
| WO (1) | WO2006066174A1 (https=) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2582327A1 (en) | 2004-10-01 | 2006-04-13 | Takao Suzuki | 2-arylcarboxamide-nitrogeneous heterocycle compound |
| CA2639910A1 (en) | 2006-01-25 | 2007-08-02 | Synta Pharmaceuticals Corp. | Thiazole and thiadiazole compounds for inflammation and immune-related uses |
| MX2008015662A (es) * | 2006-06-08 | 2009-01-12 | Lilly Co Eli | Nuevos receptores antagonistas de la hormona concentradora de melanina (mch). |
| CN101558075A (zh) * | 2006-12-14 | 2009-10-14 | 伊莱利利公司 | 5-[4-(氮杂环丁烷-3-基氧基)-苯基]-2-苯基-5H-噻唑并[5,4-c]吡啶-4-酮衍生物及其作为MCH受体拮抗剂的用途 |
| US8198307B2 (en) * | 2007-05-11 | 2012-06-12 | Korea Research Institute Of Chemical Technology | Imidazole derivatives having aryl piperidine substituent, method for preparation thereof and pharmaceutical compositions containing same |
| DE102007028925A1 (de) | 2007-06-22 | 2008-12-24 | Saltigo Gmbh | Verfahren zur Herstellung von 2-Phenoxyacetalen und den daraus korrespondierenden 2-Phenoxycarbaldehyden |
| US20090076275A1 (en) * | 2007-09-19 | 2009-03-19 | David Robert Bolin | Diacylglycerol acyltransferase inhibitors |
| WO2010024258A1 (ja) | 2008-08-29 | 2010-03-04 | 塩野義製薬株式会社 | Pi3k阻害活性を有する縮環アゾール誘導体 |
| KR20120101551A (ko) | 2009-12-18 | 2012-09-13 | 얀센 파마슈티카 엔.브이. | Mglur5 수용체의 알로스테릭 조절자로서 바이사이클릭 티아졸 |
| CA2782950A1 (en) | 2009-12-18 | 2011-06-23 | Janssen Pharmaceutica Nv | Bicyclic thiazoles as allosteric modulators of mglur5 receptors |
| US8895737B2 (en) | 2010-07-16 | 2014-11-25 | Shashank Shekhar | Process for preparing antiviral compounds |
| BR112013001138A2 (pt) | 2010-07-16 | 2016-07-05 | Abbvie Inc | ligantes de fosfina para reações catalíticas |
| US8975443B2 (en) | 2010-07-16 | 2015-03-10 | Abbvie Inc. | Phosphine ligands for catalytic reactions |
| US9255074B2 (en) | 2010-07-16 | 2016-02-09 | Abbvie Inc. | Process for preparing antiviral compounds |
| CN102532123B (zh) * | 2010-12-29 | 2016-03-09 | 中国医学科学院药物研究所 | 噻唑-5-甲酰胺化合物、及其制法和药物组合物与用途 |
| WO2012109573A1 (en) * | 2011-02-11 | 2012-08-16 | Purdue Research Foundation | Substituted thiazoles for use as antiviral agents |
| CN104350059B (zh) * | 2012-03-27 | 2016-12-07 | 拜耳知识产权有限责任公司 | 具有除草和杀虫活性的噻唑并吡啶酮 |
| EP2848621A4 (en) * | 2012-05-10 | 2016-06-01 | Takeda Pharmaceutical | AROMATIC RING CONNECTION |
| FI3805233T3 (fi) | 2014-01-13 | 2024-04-17 | Aurigene Oncology Ltd | N-(5-(3-hydroksipyrrolidin-1-yyli)-2-morfolinooksatsolo[4,5-b]pyridin-6-yyli)-2-(2-metylipyridin-4-yyli)okatsoli-karboksamidin (r)- (s)-enantiomeerit irak4-estäjänä syövän hoitoon |
| US20150252022A1 (en) * | 2014-03-10 | 2015-09-10 | Innov17 Llc | Retinoic acid receptor-related orphan receptor modulators and uses thereof |
| US20150252051A1 (en) * | 2014-03-10 | 2015-09-10 | Innov17 Llc | Retinoic acid receptor-related orphan receptor modulators and uses thereof |
| BR112018000624A2 (pt) * | 2015-07-15 | 2018-09-18 | Aurigene Discovery Technologies Limited | compostos de indazol e azaindazol como inibidores de irak-4 |
| NZ746901A (en) * | 2016-03-11 | 2023-06-30 | Ac Immune Sa | Bicyclic compounds for diagnosis and therapy |
| DK3600270T3 (da) | 2017-03-31 | 2023-07-10 | Aurigene Oncology Ltd | Forbindelser og sammensætninger til behandling af hæmatologiske lidelser |
| CA3079628A1 (en) | 2017-10-31 | 2019-05-09 | Curis, Inc. | Compounds and compositions for treating hematological disorders |
| CN109928939A (zh) * | 2019-02-27 | 2019-06-25 | 上海卡洛化学有限公司 | 一种2,2,6,6-四甲基吗啉的制备方法 |
| JP2024513227A (ja) | 2021-04-05 | 2024-03-22 | ハリア・セラピューティクス・インコーポレイテッド | Nek7阻害剤 |
| KR20240004476A (ko) | 2021-04-08 | 2024-01-11 | 쿠리스 인코퍼레이션 | 암 치료를 위한 병용 요법 |
| US20250177382A1 (en) | 2021-04-22 | 2025-06-05 | Halia Therapeutics, Inc. | Nek7 inhibitors |
| CN115403456B (zh) * | 2022-09-22 | 2023-11-17 | 成都大学 | 一种合成爱德万甜中间体3-羟基-4-甲氧基苯丙醛的方法 |
| CN119592965B (zh) * | 2024-12-10 | 2025-09-26 | 西安交通大学 | 一种基于电合成的羟基酮类化合物的制备方法及其制备的羟基酮类化合物 |
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| JPH0867678A (ja) * | 1993-11-10 | 1996-03-12 | Takeda Chem Ind Ltd | 複素環アミド化合物、その製造法および剤 |
| US7229986B2 (en) * | 2000-05-16 | 2007-06-12 | Takeda Pharmaceutical Company Ltd. | Melanin-concentrating hormone antagonist |
| JP2002371059A (ja) * | 2000-05-16 | 2002-12-26 | Takeda Chem Ind Ltd | メラニン凝集ホルモン拮抗剤 |
| GB0124627D0 (en) | 2001-10-15 | 2001-12-05 | Smithkline Beecham Plc | Novel compounds |
| SE0202134D0 (sv) * | 2002-07-08 | 2002-07-08 | Astrazeneca Ab | Therapeutic agents |
| EP1572637A1 (en) | 2002-12-11 | 2005-09-14 | Eli Lilly And Company | Novel mch receptor antagonists |
| US20040214856A1 (en) * | 2003-04-23 | 2004-10-28 | Pfizer Inc | Cannabinoid receptor ligands and uses thereof |
| WO2005047293A1 (en) | 2003-11-07 | 2005-05-26 | Neurocrine Biosciences, Inc. | Melanin-concentrating hormone receptor antagonists and compositions and methods related thereto |
| MX2007007226A (es) * | 2004-12-17 | 2007-08-21 | Lilly Co Eli | Antagonistas receptores novedosos de hormona concentradora de melanina (mch). |
| EP1987020B1 (en) | 2006-02-15 | 2012-10-03 | Sanofi | Azacyclyl-substituted aryldihydroisoquinolinones, process for their preparation and their use as medicaments |
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- 2005-12-16 US US11/721,079 patent/US7902356B2/en not_active Expired - Fee Related
- 2005-12-16 EP EP05854554A patent/EP1828207B1/en not_active Expired - Lifetime
- 2005-12-16 WO PCT/US2005/045866 patent/WO2006066174A1/en not_active Ceased
- 2005-12-16 JP JP2007546991A patent/JP5072602B2/ja not_active Expired - Fee Related
- 2005-12-16 MX MX2007007227A patent/MX2007007227A/es active IP Right Grant
- 2005-12-16 ES ES05854554T patent/ES2333243T3/es not_active Expired - Lifetime
- 2005-12-16 CN CN2005800431124A patent/CN101080411B/zh not_active Expired - Fee Related
- 2005-12-16 AU AU2005316314A patent/AU2005316314B2/en not_active Ceased
- 2005-12-16 AT AT05854554T patent/ATE446962T1/de not_active IP Right Cessation
- 2005-12-16 BR BRPI0519124-6A patent/BRPI0519124A2/pt not_active IP Right Cessation
- 2005-12-16 CA CA002589695A patent/CA2589695A1/en not_active Abandoned
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Also Published As
| Publication number | Publication date |
|---|---|
| CN101080411A (zh) | 2007-11-28 |
| JP2008524250A (ja) | 2008-07-10 |
| AU2005316314B2 (en) | 2011-06-23 |
| MX2007007227A (es) | 2007-08-21 |
| AU2005316314A1 (en) | 2006-06-22 |
| US7902356B2 (en) | 2011-03-08 |
| WO2006066174A1 (en) | 2006-06-22 |
| CN101080411B (zh) | 2011-11-02 |
| EP1828207A1 (en) | 2007-09-05 |
| ATE446962T1 (de) | 2009-11-15 |
| DE602005017423D1 (de) | 2009-12-10 |
| EP1828207B1 (en) | 2009-10-28 |
| US20090233919A1 (en) | 2009-09-17 |
| ES2333243T3 (es) | 2010-02-18 |
| BRPI0519124A2 (pt) | 2008-12-23 |
| CA2589695A1 (en) | 2006-06-22 |
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