CL2008003847A1 - Compuestos derivados de 6-fenilpirazin-2-carboxamida y 6-fenilpirazin-2-carbotioamida, inhibidores de dgat-1; composicion farmaceutica; y su uso en el tratamiento de la diabetes mellitus y obesidad. - Google Patents
Compuestos derivados de 6-fenilpirazin-2-carboxamida y 6-fenilpirazin-2-carbotioamida, inhibidores de dgat-1; composicion farmaceutica; y su uso en el tratamiento de la diabetes mellitus y obesidad.Info
- Publication number
- CL2008003847A1 CL2008003847A1 CL2008003847A CL2008003847A CL2008003847A1 CL 2008003847 A1 CL2008003847 A1 CL 2008003847A1 CL 2008003847 A CL2008003847 A CL 2008003847A CL 2008003847 A CL2008003847 A CL 2008003847A CL 2008003847 A1 CL2008003847 A1 CL 2008003847A1
- Authority
- CL
- Chile
- Prior art keywords
- phenylpyrazine
- dgat
- obesity
- treatment
- pharmaceutical composition
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D241/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Child & Adolescent Psychology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Compuestos derivados de amidas y tioamidas heterocíclicas, antagonistas del receptor dgat-1; composición farmacéutica; procedimiento de preparación; y su uso en el tratamiento de diabetes mellitus y obesidad.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1539707P | 2007-12-20 | 2007-12-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2008003847A1 true CL2008003847A1 (es) | 2009-11-27 |
Family
ID=40427160
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2008003847A CL2008003847A1 (es) | 2007-12-20 | 2008-12-19 | Compuestos derivados de 6-fenilpirazin-2-carboxamida y 6-fenilpirazin-2-carbotioamida, inhibidores de dgat-1; composicion farmaceutica; y su uso en el tratamiento de la diabetes mellitus y obesidad. |
Country Status (23)
| Country | Link |
|---|---|
| US (2) | US7994179B2 (es) |
| EP (1) | EP2234978B1 (es) |
| JP (1) | JP5662803B2 (es) |
| KR (1) | KR20100099738A (es) |
| CN (1) | CN101932562B (es) |
| AR (1) | AR069802A1 (es) |
| AU (1) | AU2008339570B2 (es) |
| BR (1) | BRPI0821274A2 (es) |
| CA (1) | CA2707660A1 (es) |
| CL (1) | CL2008003847A1 (es) |
| CO (1) | CO6290685A2 (es) |
| CR (1) | CR11518A (es) |
| DO (1) | DOP2010000192A (es) |
| EA (1) | EA201001015A1 (es) |
| EC (1) | ECSP10010274A (es) |
| ES (1) | ES2535083T3 (es) |
| IL (1) | IL206045A0 (es) |
| NI (1) | NI201000108A (es) |
| NZ (1) | NZ586104A (es) |
| PE (1) | PE20091682A1 (es) |
| TW (1) | TW200932235A (es) |
| WO (1) | WO2009081195A1 (es) |
| ZA (1) | ZA201003979B (es) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20070087096A (ko) * | 2004-12-14 | 2007-08-27 | 아스트라제네카 아베 | Dgat 억제제로서의 옥사디아졸 유도체 |
| US7749997B2 (en) | 2005-12-22 | 2010-07-06 | Astrazeneca Ab | Pyrimido [4,5-B] -Oxazines for use as DGAT inhibitors |
| EP2004607B1 (en) | 2006-03-31 | 2011-10-19 | Novartis AG | (4-(4-[6-(trifluoromethyl-pyridin-3-ylamino)-N-containing-heteroaryl]-phenyl)-cyclohexyl)-acetic acid derivatives and pharmaceutical uses thereof |
| NZ572586A (en) | 2006-05-30 | 2011-03-31 | Astrazeneca Ab | Substituted 5-phenylamino-1,3,4-oxadiazol-2-ylcarbonylamino-4-phenoxy-cyclohexane carboxylic acid as inhibitors of acetyl coenzyme a diacylglycerol acyltransferase |
| CA2651663A1 (en) * | 2006-05-30 | 2007-12-06 | Astrazeneca Ab | Chemical compounds |
| MX2008015725A (es) * | 2006-06-08 | 2009-02-13 | Astrazeneca Ab | Benzimidazolas y su uso para el tratamiento de diabetes. |
| TW200808773A (en) | 2006-06-23 | 2008-02-16 | Abbott Lab | Cyclopropyl amine derivatives |
| US9108948B2 (en) | 2006-06-23 | 2015-08-18 | Abbvie Inc. | Cyclopropyl amine derivatives |
| CN101827842A (zh) * | 2007-08-17 | 2010-09-08 | 阿斯利康(瑞典)有限公司 | 作为dgat抑制剂的噁二唑衍生物 |
| AR066169A1 (es) | 2007-09-28 | 2009-07-29 | Novartis Ag | Derivados de benzo-imidazoles, utiles para trastornos asociados con la actividad de dgat |
| CN102395572A (zh) * | 2008-12-19 | 2012-03-28 | 阿斯利康(瑞典)有限公司 | 1,3,4-噁二唑衍生物及其治疗糖尿病的用途 |
| US9186353B2 (en) | 2009-04-27 | 2015-11-17 | Abbvie Inc. | Treatment of osteoarthritis pain |
| KR20120037939A (ko) | 2009-06-19 | 2012-04-20 | 아스트라제네카 아베 | Dgat1의 억제제로서 피라진 카르복사미드 |
| MX2012005281A (es) | 2009-11-05 | 2012-06-19 | Fibrostatin S L | Inhibicion de gpbp utilizando peptidomimeticos q2. |
| US8431575B2 (en) | 2010-02-18 | 2013-04-30 | Transtech Pharma, Inc. | Phenyl-heteroaryl derivatives and methods of use thereof |
| WO2012037258A1 (en) | 2010-09-16 | 2012-03-22 | Abbott Laboratories | Processes for preparing 1,2-substituted cyclopropyl derivatives |
| WO2012064569A1 (en) * | 2010-11-08 | 2012-05-18 | Merck Sharp & Dohme Corp. | Imidazole derivatives |
| MX2013013732A (es) * | 2011-05-23 | 2014-02-27 | Janssen Pharmaceutica Nv | Derivados de bifenilo utiles como antagonistas del receptor de glucagon. |
| WO2012165398A1 (ja) * | 2011-05-30 | 2012-12-06 | 第一三共株式会社 | シクロアルキルオキシビアリール型化合物 |
| WO2013068328A1 (en) * | 2011-11-07 | 2013-05-16 | Intervet International B.V. | Bicyclo [2.2.2] octan-1-ylcarboxylic acid compounds as dgat-1 inhibitors |
| WO2013074387A1 (en) * | 2011-11-14 | 2013-05-23 | Merck Sharp & Dohme Corp. | Imidazole derivatives |
| CN104245696A (zh) * | 2012-02-07 | 2014-12-24 | 凯诺斯医药公司 | 作为1型二酰基甘油o-酰基转移酶的抑制剂的化合物 |
| ES2624291T3 (es) * | 2012-04-27 | 2017-07-13 | Novartis Ag | Inhibidores cíclicos del enlace éter de DGAT1 |
| EP3763367A1 (en) | 2012-12-06 | 2021-01-13 | Celgene Quanticel Research, Inc. | Pyridine-pyrazole derivatives as histone demethylase inhibitors |
| US8962660B2 (en) * | 2013-03-14 | 2015-02-24 | Bristol-Myers Squibb Company | Oxabicyclo [2.2.2] acid GPR120 modulators |
| CN105308026B (zh) * | 2013-07-09 | 2018-12-21 | 东曹株式会社 | 具有金刚烷基的环状吖嗪化合物、制造方法、以及以该化合物作为构成成分的有机电致发光元件 |
| JP6431538B2 (ja) * | 2013-11-21 | 2018-11-28 | マーケット ユニバーシティー | エストロゲン受容体ベータアイソフォームの選択的アゴニストとしての置換(4’−ヒドロキシフェニル)シクロアルカン化合物およびその使用 |
| WO2015136275A1 (en) * | 2014-03-12 | 2015-09-17 | Astrazeneca Ab | Method of treating skin conditions |
| AR109179A1 (es) * | 2016-08-19 | 2018-11-07 | Pfizer | Inhibidores de diacilglicerol aciltransferasa 2 |
| SG11202011549RA (en) * | 2018-06-21 | 2020-12-30 | Dermavant Sciences GmbH | Topical formulations of dgat1 inhibitors and their methods of use |
| EP3590927A1 (en) | 2018-07-05 | 2020-01-08 | Bayer Animal Health GmbH | Novel compounds for controlling arthropods |
| WO2020113094A1 (en) | 2018-11-30 | 2020-06-04 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| WO2020214693A1 (en) * | 2019-04-17 | 2020-10-22 | Ixchel Pharma, Llc | Prodrugs of monomethyl fumarate |
Family Cites Families (80)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3245989A (en) | 1962-12-15 | 1966-04-12 | Acraf | 3-aminophenyl-5-aminoloweralkyl-1, 2, 4-oxadiazoles |
| US4983731A (en) | 1989-03-17 | 1991-01-08 | Nebraska Department Of Economic Development | Separation and purification of sugar esters |
| US5491172A (en) | 1993-05-14 | 1996-02-13 | Warner-Lambert Company | N-acyl sulfamic acid esters (or thioesters), N-acyl sulfonamides, and N-sulfonyl carbamic acid esters (or thioesters) as hypercholesterolemic agents |
| IL109431A (en) | 1993-05-14 | 2001-01-11 | Warner Lambert Co | Pharmaceutical compositions containing n-acyl sulfamic acid esters (or thioesters), n-acyl sulfonamides, and n-sulfonyl carbamic acid esters (or thioesters), for regulating plasma cholesterol concentration, and certain such novel compounds |
| US20030167483A1 (en) | 1998-06-24 | 2003-09-04 | Farese Robert V. | Diacylglycerol O-acyltransferase |
| US6608185B1 (en) | 1999-03-25 | 2003-08-19 | Kitasato Institute | Substances KF-1040T4A,KF-1040T4B, KF-1040T5A, and KF-1040T5B, and process for producing same |
| TW518218B (en) | 1999-05-27 | 2003-01-21 | Merck Patent Gmbh | Pharmaceutical compositions comprising 1-[4-(5-cyanoindol-3-yl)butyl]-4-(2-carbamoylbenzofuran-5-yl)piperazine or its physiologically acceptable salts for use in the treatment of sub-type anxiety disorders |
| GB0021670D0 (en) | 2000-09-04 | 2000-10-18 | Astrazeneca Ab | Chemical compounds |
| CA2369967A1 (en) | 2001-02-12 | 2002-08-12 | Joseph Anthony Cornicelli | Methods of treating nuclear factor-kappa b mediated diseases and disorders |
| JP2002284741A (ja) | 2001-03-23 | 2002-10-03 | Kitasato Inst:The | ローズリピン誘導体 |
| DE10223273A1 (de) | 2002-05-24 | 2003-12-04 | Aventis Pharma Gmbh | Diarylcycloalkylderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| CA2458210C (en) | 2001-08-31 | 2011-09-20 | Aventis Pharma Deutschland Gmbh | Diaryl cycloalkyl derivatives, method for producing the same and the use thereof as ppar-activators |
| CN100491371C (zh) * | 2001-11-01 | 2009-05-27 | 詹森药业有限公司 | 用作糖原合酶激酶3β抑制剂(GSK3抑制剂)的杂芳胺化合物 |
| US20090286791A1 (en) | 2001-11-27 | 2009-11-19 | Takeda Pharmaceutical Company Limited | Amide Compounds |
| FR2840301B1 (fr) | 2002-05-29 | 2007-03-23 | Sanofi Synthelabo | Derives de phenyl-cyclohexyl-propanolamine, leur preparation et leur applicaton en therapeutique |
| JPWO2004007472A1 (ja) | 2002-07-10 | 2005-11-17 | 小野薬品工業株式会社 | Ccr4アンタゴニストおよびその医薬用途 |
| CN1304371C (zh) | 2002-07-12 | 2007-03-14 | 塞诺菲-安万特德国有限公司 | 杂环取代的苯甲酰脲、其药物和制备药物的用途 |
| JP4164645B2 (ja) | 2002-08-09 | 2008-10-15 | 株式会社大塚製薬工場 | Dgat阻害剤 |
| CA2495903A1 (en) | 2002-08-23 | 2004-03-04 | University Of Connecticut | Novel biphenyl and biphenyl-like cannabinoids |
| US6875784B2 (en) | 2002-10-09 | 2005-04-05 | Pharmacia & Upjohn Company | Antimibicrobial [3.1.0.] bicyclic oxazolidinone derivatives |
| AU2003287178A1 (en) | 2002-10-10 | 2004-05-04 | Smithkline Beecham Corporation | Chemical compounds |
| CA2514473C (en) | 2002-11-22 | 2008-05-27 | Japan Tobacco Inc. | Fused bicyclic nitrogen-containing heterocycles |
| KR101076018B1 (ko) | 2003-01-08 | 2011-10-21 | 유니버시티 오브 워싱톤 | 항균제 |
| WO2004089927A1 (en) | 2003-04-07 | 2004-10-21 | Cortical Pty Ltd | Novel methods for the treatment of inflammatory diseases |
| AR044152A1 (es) | 2003-05-09 | 2005-08-24 | Bayer Corp | Derivados de alquilarilo, metodo de preparacion y uso para el tratamiento de la obesidad |
| CA2525547C (en) | 2003-05-14 | 2012-07-03 | Torreypines Therapeutics, Inc. | Compounds and uses thereof in modulating amyloid beta |
| WO2005013907A2 (en) | 2003-08-07 | 2005-02-17 | Japan Tobacco Inc. | Pyrrolo[1,2-b]pyridazine derivatives |
| JPWO2005023771A1 (ja) | 2003-09-05 | 2006-11-02 | 小野薬品工業株式会社 | ケモカインレセプターアンタゴニストおよびその医薬用途 |
| US20050143464A1 (en) | 2003-09-22 | 2005-06-30 | Use-Techno Corporation | Insulin secretion potentiator |
| BRPI0415500A (pt) | 2003-10-17 | 2007-04-10 | Incyte Corp | hidroxamatos cìclicos substituìdos como inibidores de metaloproteinases de matriz |
| GB0325192D0 (en) | 2003-10-29 | 2003-12-03 | Astrazeneca Ab | Method of use |
| WO2005046670A1 (en) | 2003-11-11 | 2005-05-26 | The Skinny Drink Company | Composition for prevention and treatment of obesity, cardiovascular and coronary artery disease |
| JP2005206492A (ja) | 2004-01-21 | 2005-08-04 | Sankyo Co Ltd | スルホンアミド化合物 |
| CA2554455A1 (en) | 2004-01-30 | 2005-08-11 | Japan Tobacco Inc. | Anorectic |
| WO2006001463A1 (ja) | 2004-06-23 | 2006-01-05 | Ono Pharmaceutical Co., Ltd. | S1p受容体結合能を有する化合物およびその用途 |
| CA2572874A1 (en) | 2004-07-02 | 2006-01-12 | Sankyo Company Limited | Urea derivative |
| WO2006019020A1 (ja) | 2004-08-16 | 2006-02-23 | Sankyo Company, Limited | 置換されたウレア化合物 |
| WO2006044775A2 (en) | 2004-10-15 | 2006-04-27 | Bayer Pharmaceuticals Corporation | Preparation and use of biphenyl-4-yl-carbonylamino acid derivatives for the treatment of obesity |
| WO2006054370A1 (en) | 2004-11-16 | 2006-05-26 | Use-Techno Corporation | Gluconeogenesis inhibiting agent |
| KR20070087096A (ko) | 2004-12-14 | 2007-08-27 | 아스트라제네카 아베 | Dgat 억제제로서의 옥사디아졸 유도체 |
| JPWO2006082952A1 (ja) | 2005-02-01 | 2008-06-26 | 武田薬品工業株式会社 | アミド化合物 |
| EP1848687A1 (en) | 2005-02-07 | 2007-10-31 | F. Hoffmann-Roche AG | Inhibitors of diacylglycerol acyltransferase (dgat) |
| EP1874317A4 (en) | 2005-04-19 | 2011-10-26 | Bayer Healthcare Llc | PREPARATION AND USE OF ARYL ALKYL ACID DERIVATIVES IN THE TREATMENT OF OBESITY |
| MX2007013939A (es) | 2005-05-10 | 2008-01-11 | Hoffmann La Roche | Inhibidores de diacilglicerol aciltransferasa. |
| MX2007015759A (es) | 2005-06-11 | 2008-02-21 | Astrazeneca Ab | Derivados de oxadiazol como inhibidores de diacilglicerol aciltransferasa (dgat). |
| WO2007007588A1 (ja) | 2005-07-08 | 2007-01-18 | Ono Pharmaceutical Co., Ltd. | 平面性を有する環状基を母核とする化合物 |
| US20100016295A1 (en) | 2005-07-29 | 2010-01-21 | Bayer Healthcare Llc | Preparation and Use of Biphenyl Amino Acid Derivatives for the Treatment of Obesity |
| JP2007131584A (ja) | 2005-11-11 | 2007-05-31 | Sankyo Co Ltd | 新規ベンゾオキサゾール誘導体 |
| AU2006316560B2 (en) | 2005-11-28 | 2011-06-16 | Madrigal Pharmaceuticals, Inc. | Inhibitors of diacyglycerol acyltransferase (DGAT) |
| JP2007191471A (ja) | 2005-12-21 | 2007-08-02 | Sankyo Co Ltd | ウレア誘導体を含有する医薬 |
| US7749997B2 (en) | 2005-12-22 | 2010-07-06 | Astrazeneca Ab | Pyrimido [4,5-B] -Oxazines for use as DGAT inhibitors |
| WO2007074753A1 (ja) | 2005-12-27 | 2007-07-05 | Daiichi Sankyo Company, Limited | 置換されたウレア誘導体を含有する医薬 |
| EP2004607B1 (en) * | 2006-03-31 | 2011-10-19 | Novartis AG | (4-(4-[6-(trifluoromethyl-pyridin-3-ylamino)-N-containing-heteroaryl]-phenyl)-cyclohexyl)-acetic acid derivatives and pharmaceutical uses thereof |
| ES2435115T3 (es) | 2006-04-21 | 2013-12-18 | Eli Lilly And Company | Derivados de bifenilamida-lactama como inhibidores de 11-beta-hidroxiesteroide deshidrogenasa 1 |
| WO2007137107A2 (en) | 2006-05-19 | 2007-11-29 | Abbott Laboratories | Inhibitors of diacylglycerol o-acyltransferase type 1 enzyme |
| WO2007137103A2 (en) | 2006-05-19 | 2007-11-29 | Abbott Laboratories | Inhibitors of diacylglycerol o-acyltransferase type 1 enzyme |
| CA2651663A1 (en) | 2006-05-30 | 2007-12-06 | Astrazeneca Ab | Chemical compounds |
| NZ572586A (en) | 2006-05-30 | 2011-03-31 | Astrazeneca Ab | Substituted 5-phenylamino-1,3,4-oxadiazol-2-ylcarbonylamino-4-phenoxy-cyclohexane carboxylic acid as inhibitors of acetyl coenzyme a diacylglycerol acyltransferase |
| EP2035397A1 (en) | 2006-06-06 | 2009-03-18 | Astra Zeneca AB | Chemical compounds |
| MX2008015725A (es) | 2006-06-08 | 2009-02-13 | Astrazeneca Ab | Benzimidazolas y su uso para el tratamiento de diabetes. |
| GB0611507D0 (en) | 2006-06-10 | 2006-07-19 | Astrazeneca Ab | Chemical compounds |
| GB0611506D0 (en) | 2006-06-10 | 2006-07-19 | Astrazeneca Ab | Chemical compounds |
| GB0611552D0 (en) | 2006-06-12 | 2006-07-19 | Astrazeneca Ab | Chemical compounds |
| WO2008011130A2 (en) | 2006-07-21 | 2008-01-24 | Takeda Pharmaceutical Company Limited | Amide compounds |
| US7569590B2 (en) | 2006-09-19 | 2009-08-04 | Bristol-Myers Squibb Company | Use of thianecarboxamides as dgat inhibitors |
| KR100811100B1 (ko) | 2006-09-27 | 2008-03-06 | 한국생명공학연구원 | 벤즈아졸 유도체를 유효성분으로 함유하는 대사성 질환예방 및 치료용 약학적 조성물 |
| KR100795462B1 (ko) | 2006-09-27 | 2008-01-16 | 한국생명공학연구원 | 인돌 유도체, 이의 제조방법 및 이를 유효성분으로함유하는 대사성 질환 예방 및 치료용 약학적 조성물 |
| WO2008042925A1 (en) | 2006-10-04 | 2008-04-10 | Bristol-Myers Squibb Company | Cyclic derivatives as modulators of chemokine receptor activity |
| EP2074096B1 (en) | 2006-10-04 | 2012-06-27 | F. Hoffmann-La Roche AG | 3-pyridinecarboxamide and 2-pyrazinecarboxamide derivatives as hdl-cholesterol raising agents |
| WO2008046216A1 (en) | 2006-10-18 | 2008-04-24 | Methylgene, Inc. | Kinase inhibitors and uses thereof |
| AR063311A1 (es) | 2006-10-18 | 2009-01-21 | Novartis Ag | Compuestos organicos |
| EP2081892A4 (en) | 2006-11-17 | 2014-03-05 | Donald F Weaver | COMPOUNDS AND METHOD FOR THE TREATMENT OF PROTEIN DISAPPEARANCE |
| JP2010511058A (ja) | 2006-11-29 | 2010-04-08 | アボット・ラボラトリーズ | ジアシルグリセロールo−アシルトランスフェラーゼ1型酵素の阻害薬 |
| KR20090098877A (ko) | 2006-12-11 | 2009-09-17 | 노파르티스 아게 | 심근 허혈의 예방 또는 치료 방법 |
| WO2008099221A1 (en) | 2007-02-15 | 2008-08-21 | Prosidion Limited | Amide and urea derivatives for the treatment of metabolic diseases |
| GB0707662D0 (en) | 2007-04-20 | 2007-05-30 | Astrazeneca Ab | Chemical compounds |
| RU2497816C2 (ru) | 2007-04-30 | 2013-11-10 | Эббви Инк. | Ингибиторы фермента диацилглицерин о-ацилтрансферазы типа 1 |
| US8058299B2 (en) | 2007-05-22 | 2011-11-15 | Via Pharmaceuticals, Inc. | Diacylglycerol acyltransferase inhibitors |
| JP2010132590A (ja) | 2008-12-03 | 2010-06-17 | Astellas Pharma Inc | オキサジアゾール化合物 |
| CN102395572A (zh) | 2008-12-19 | 2012-03-28 | 阿斯利康(瑞典)有限公司 | 1,3,4-噁二唑衍生物及其治疗糖尿病的用途 |
-
2008
- 2008-12-18 JP JP2010538918A patent/JP5662803B2/ja not_active Expired - Fee Related
- 2008-12-18 ES ES08865783.8T patent/ES2535083T3/es active Active
- 2008-12-18 AR ARP080105523A patent/AR069802A1/es not_active Application Discontinuation
- 2008-12-18 EP EP08865783.8A patent/EP2234978B1/en active Active
- 2008-12-18 CN CN2008801259853A patent/CN101932562B/zh not_active Expired - Fee Related
- 2008-12-18 BR BRPI0821274A patent/BRPI0821274A2/pt not_active IP Right Cessation
- 2008-12-18 PE PE2008002123A patent/PE20091682A1/es not_active Application Discontinuation
- 2008-12-18 WO PCT/GB2008/051199 patent/WO2009081195A1/en not_active Ceased
- 2008-12-18 AU AU2008339570A patent/AU2008339570B2/en not_active Expired - Fee Related
- 2008-12-18 EA EA201001015A patent/EA201001015A1/ru unknown
- 2008-12-18 NZ NZ586104A patent/NZ586104A/en not_active IP Right Cessation
- 2008-12-18 TW TW097149460A patent/TW200932235A/zh unknown
- 2008-12-18 CA CA2707660A patent/CA2707660A1/en not_active Abandoned
- 2008-12-18 KR KR1020107016252A patent/KR20100099738A/ko not_active Withdrawn
- 2008-12-19 CL CL2008003847A patent/CL2008003847A1/es unknown
- 2008-12-19 US US12/339,349 patent/US7994179B2/en not_active Expired - Fee Related
-
2010
- 2010-05-27 IL IL206045A patent/IL206045A0/en unknown
- 2010-06-03 ZA ZA2010/03979A patent/ZA201003979B/en unknown
- 2010-06-18 CR CR11518A patent/CR11518A/es not_active Application Discontinuation
- 2010-06-18 NI NI201000108A patent/NI201000108A/es unknown
- 2010-06-18 EC EC2010010274A patent/ECSP10010274A/es unknown
- 2010-06-18 DO DO2010000192A patent/DOP2010000192A/es unknown
- 2010-06-21 CO CO10074457A patent/CO6290685A2/es not_active Application Discontinuation
-
2011
- 2011-05-05 US US13/101,926 patent/US20120108602A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| AU2008339570B2 (en) | 2012-04-12 |
| EP2234978A1 (en) | 2010-10-06 |
| JP5662803B2 (ja) | 2015-02-04 |
| EP2234978B1 (en) | 2015-02-25 |
| US20120108602A1 (en) | 2012-05-03 |
| WO2009081195A1 (en) | 2009-07-02 |
| US7994179B2 (en) | 2011-08-09 |
| ES2535083T3 (es) | 2015-05-05 |
| AR069802A1 (es) | 2010-02-17 |
| CN101932562A (zh) | 2010-12-29 |
| EA201001015A1 (ru) | 2011-02-28 |
| AU2008339570A1 (en) | 2009-07-02 |
| CO6290685A2 (es) | 2011-06-20 |
| BRPI0821274A2 (pt) | 2017-06-13 |
| NZ586104A (en) | 2012-02-24 |
| IL206045A0 (en) | 2010-11-30 |
| ZA201003979B (en) | 2011-11-30 |
| NI201000108A (es) | 2012-05-14 |
| US20090298853A1 (en) | 2009-12-03 |
| CR11518A (es) | 2010-07-15 |
| ECSP10010274A (es) | 2010-07-30 |
| CA2707660A1 (en) | 2009-07-02 |
| KR20100099738A (ko) | 2010-09-13 |
| JP2011507823A (ja) | 2011-03-10 |
| DOP2010000192A (es) | 2010-07-15 |
| PE20091682A1 (es) | 2009-12-04 |
| CN101932562B (zh) | 2013-06-12 |
| TW200932235A (en) | 2009-08-01 |
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