PE20091682A1 - Compuestos de carbamoilo como inhibidores de dgat1 190 - Google Patents
Compuestos de carbamoilo como inhibidores de dgat1 190Info
- Publication number
- PE20091682A1 PE20091682A1 PE2008002123A PE2008002123A PE20091682A1 PE 20091682 A1 PE20091682 A1 PE 20091682A1 PE 2008002123 A PE2008002123 A PE 2008002123A PE 2008002123 A PE2008002123 A PE 2008002123A PE 20091682 A1 PE20091682 A1 PE 20091682A1
- Authority
- PE
- Peru
- Prior art keywords
- ring
- trans
- phenyl
- alkyl
- dgat1
- Prior art date
Links
- -1 CARBAMOYL COMPOUNDS Chemical class 0.000 title abstract 6
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 102100036869 Diacylglycerol O-acyltransferase 1 Human genes 0.000 title 1
- 101000927974 Homo sapiens Diacylglycerol O-acyltransferase 1 Proteins 0.000 title 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 150000001924 cycloalkanes Chemical class 0.000 abstract 2
- KKFDJZZADQONDE-UHFFFAOYSA-N (hydridonitrato)hydroxidocarbon(.) Chemical class O[C]=N KKFDJZZADQONDE-UHFFFAOYSA-N 0.000 abstract 1
- 208000008589 Obesity Diseases 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 235000020824 obesity Nutrition 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- IPEHBUMCGVEMRF-UHFFFAOYSA-N pyrazinecarboxamide Chemical compound NC(=O)C1=CN=CC=N1 IPEHBUMCGVEMRF-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Child & Adolescent Psychology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE CARBAMOILO DE FORMULA (I) DONDE A ES 2,6-PIRAZINDIILO, 3,5-PIRIDINDIILO O 2,6-PIRIDINDIILO OPCIONALMENTE SUSTITUIDOS CON ALQUILO(C1-C3), ALQUENILO(C2-C3), ENTRE OTROS; X ES =O O =S; B ES 1,4-FENILENO, FURANDIILO, TIOFENDIILO, ENTRE OTROS; Y1 ES UNA UNION DIRECTA ENTRE EL ANILLO B Y EL ANILLO C, -O-, -S-, ENTRE OTROS; Y2 ES -(CH2)r- DONDE r ES 2 O 3; C ES CICLOALCANO(C4-C6), BICICLOALCANO(C7-C10), TRICICLOALCANO(C8-C12), ENTRE OTROS; L ES UNA UNION DIRECTA CON EL ANILLO C, -O-, -S- O -NH-; Z ES OH, CARBOXI, -CONRbRc, DONDE Rb Y Rc SON CADA UNO H O ALQUILO(C1-C4); RA1 Y RA2 SON CADA UNO H, ALQUILO(C1-C4) O JUNTOS PUEDEN FORMAR UN ANILLO ESPIROALQUILO(C3-C6); n ES 0 O 1; p ES DE 0 A 2. SON COMPUESTOS PREFERIDOS: ACIDO {TRANS-4-[4-(6-CARBAMOIL-3,5-DIMETILPIRAZIN-2-IL)FENIL]CICLOHEXIL}ACETICO, 3,5-DIMETIL-6-[4-(TRANS-4-{2-[(METILSULFONIL)AMINO]-2-OXOETIL}CICLOHEXIL)FENIL]PIRAZIN-2-CARBOXAMIDA, 6-{4-[TRANS-4-(2-AMINO-2-OXOETIL)CICLOHEXIL]FENIL}-3,5-DIMETILPIRAZIN-2-CARBOXAMIDA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA DIACILGLICEROL ACILTRANSFERASA (DGAT1) SIENDO UTILES PARA EL TRATAMIENTO DE DIABETES MELLITUS, 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 |
|---|---|
| PE20091682A1 true PE20091682A1 (es) | 2009-12-04 |
Family
ID=40427160
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2008002123A PE20091682A1 (es) | 2007-12-20 | 2008-12-18 | Compuestos de carbamoilo como inhibidores de dgat1 190 |
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 |
|---|---|---|---|---|
| JP2008523133A (ja) | 2004-12-14 | 2008-07-03 | アストラゼネカ アクチボラグ | Dgat阻害剤としてのオキサジアゾール誘導体 |
| US7749997B2 (en) | 2005-12-22 | 2010-07-06 | Astrazeneca Ab | Pyrimido [4,5-B] -Oxazines for use as DGAT inhibitors |
| EP2301923B1 (en) | 2006-03-31 | 2016-06-08 | Novartis AG | Pyridine derivatives as dgat inhibitors |
| ATE492541T1 (de) | 2006-05-30 | 2011-01-15 | Astrazeneca Ab | Substituierte 5-phenylamino-1,3,4-oxadiazol-2- ylcarbonylamino-4-phenoxycyclohexancarbonsäuren als inhibitoren von acetylcoenzym-a- diacylglycerolacyltransferase |
| US8003676B2 (en) * | 2006-05-30 | 2011-08-23 | Astrazeneca Ab | 1,3,4-oxadiazole derivatives as DGAT1 inhibitors |
| CN101460492A (zh) * | 2006-06-08 | 2009-06-17 | 阿斯利康(瑞典)有限公司 | 苯并咪唑及其治疗糖尿病的用途 |
| SG173312A1 (en) | 2006-06-23 | 2011-08-29 | Abbott Lab | Cyclopropyl amine derivatives as histamin h3 receptor modulators |
| US9108948B2 (en) | 2006-06-23 | 2015-08-18 | Abbvie Inc. | Cyclopropyl amine derivatives |
| MX2010001848A (es) * | 2007-08-17 | 2010-03-10 | Astrazeneca Ab | Derivados de oxadiazol como inhibidores de diacilglicerolaciltrans ferasa (dgat). |
| AR066169A1 (es) | 2007-09-28 | 2009-07-29 | Novartis Ag | Derivados de benzo-imidazoles, utiles para trastornos asociados con la actividad de dgat |
| JP2012512860A (ja) * | 2008-12-19 | 2012-06-07 | アストラゼネカ アクチボラグ | 1,3,4−オキサジアゾール誘導体および糖尿病を処置するそれらの使用 |
| US9186353B2 (en) | 2009-04-27 | 2015-11-17 | Abbvie Inc. | Treatment of osteoarthritis pain |
| CA2764013A1 (en) * | 2009-06-19 | 2010-12-23 | Astrazeneca Ab | Pyrazine carboxamides as inhibitors of dgat1 |
| ES2523118T3 (es) | 2009-11-05 | 2014-11-21 | Fibrostatin, S.L. | Inhibición de GPBP utilizando peptidomiméticos de Q2 |
| EP2536283B8 (en) * | 2010-02-18 | 2015-11-04 | vTv Therapeutics LLC | 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 |
| WO2012162409A1 (en) * | 2011-05-23 | 2012-11-29 | Janssen Pharmaceutica Nv | Biphenyl derivatives useful as glucagon receptor antagonists |
| 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 |
| AU2013254307B2 (en) * | 2012-04-27 | 2016-05-26 | Novartis Ag | Cyclic bridgehead ether DGAT1 inhibitors |
| 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 |
| CA2931313C (en) | 2013-11-21 | 2022-04-05 | Marquette University | Substituted (4'-hydroxyphenyl)cycloalkane compounds and uses thereof as selective agonists of the estrogen receptor beta isoform |
| ES2881706T3 (es) * | 2014-03-12 | 2021-11-30 | Astrazeneca Ab | Método de tratamiento de las afecciones de la piel |
| AR109179A1 (es) * | 2016-08-19 | 2018-11-07 | Pfizer | Inhibidores de diacilglicerol aciltransferasa 2 |
| CA3101064A1 (en) * | 2018-06-21 | 2019-12-26 | 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 |
| AU2019387370A1 (en) | 2018-11-30 | 2021-06-10 | Nuvation Bio Inc. | Pyrrole and pyrazole compounds and methods of use thereof |
| JP7406566B2 (ja) * | 2019-04-17 | 2023-12-27 | イクシェル ファーマ エルエルシー | フマル酸モノメチルのプロドラッグ |
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 |
| 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 |
| 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 |
| US20030167483A1 (en) | 1998-06-24 | 2003-09-04 | Farese Robert V. | Diacylglycerol O-acyltransferase |
| WO2000058491A1 (en) | 1999-03-25 | 2000-10-05 | The Kitasato Institute | Novel substances kf-1040t4a, kf-1040t4b, kf-1040t5a and kf-1040t5b and process for producing the 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 |
| PT1425014E (pt) | 2001-08-31 | 2007-03-30 | Sanofi Aventis Deutschland | Derivados diarilcicloalquilo, processo para a sua preparação como activadores de ppar |
| DE10223273A1 (de) | 2002-05-24 | 2003-12-04 | Aventis Pharma Gmbh | Diarylcycloalkylderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| EA010859B1 (ru) * | 2001-11-01 | 2008-12-30 | Янссен Фармацевтика Н.В. | Гетероариламины - производные пиримидина и пиридазина в качестве ингибиторов гликогенсинтаза-киназы 3-бета (ингибиторов gsk3) |
| WO2008011131A2 (en) | 2006-07-21 | 2008-01-24 | 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 |
| WO2004007472A1 (ja) | 2002-07-10 | 2004-01-22 | Ono Pharmaceutical Co., Ltd. | Ccr4アンタゴニストおよびその医薬用途 |
| AU2003249937A1 (en) | 2002-07-12 | 2004-02-02 | Sanofi-Aventis Deutschland Gmbh | Heterocyclically substituted benzoylureas, method for their production and their use as medicaments |
| 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 |
| WO2004032882A2 (en) | 2002-10-10 | 2004-04-22 | Smithkline Beecham Corporation | Chemical compounds |
| NZ539952A (en) | 2002-11-22 | 2008-05-30 | Japan Tobacco Inc | Fused bicyclic nitrogen-containing heterocyclic compounds for treating diabetes, obesity and syndrome X |
| ES2387803T3 (es) | 2003-01-08 | 2012-10-02 | Novartis Vaccines And Diagnostics, Inc. | Agentes antibacterianos |
| EP1611120A4 (en) | 2003-04-07 | 2008-04-23 | Cortical Pty Ltd | NEW M THODES 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 |
| US7244739B2 (en) | 2003-05-14 | 2007-07-17 | 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 |
| WO2005023771A1 (ja) | 2003-09-05 | 2005-03-17 | Ono Pharmaceutical Co., Ltd. | 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 |
| JP4820299B2 (ja) | 2003-11-11 | 2011-11-24 | ザ スキニー ドリンク カンパニー | 肥満、心臓血管疾患及び冠状動脈疾患の予防及び治療のための組成物 |
| JP2005206492A (ja) | 2004-01-21 | 2005-08-04 | Sankyo Co Ltd | スルホンアミド化合物 |
| JP2007519605A (ja) | 2004-01-30 | 2007-07-19 | 日本たばこ産業株式会社 | 食欲抑制薬 |
| EP1760071A4 (en) | 2004-06-23 | 2008-03-05 | Ono Pharmaceutical Co | COMPOUND WITH S1P RECEPTOR BINDING ABILITY AND USE THEREOF |
| US20070249620A1 (en) | 2004-07-02 | 2007-10-25 | Hitoshi Kurata | Urea Derivative |
| WO2006019020A1 (ja) | 2004-08-16 | 2006-02-23 | Sankyo Company, Limited | 置換されたウレア化合物 |
| ES2357015T3 (es) | 2004-10-15 | 2011-04-15 | Bayer Healthcare Llc | Preparación y uso de derivados bifenil-4-ilcarbonilaminoácido para el tratamiento de la obesidad. |
| WO2006054370A1 (en) | 2004-11-16 | 2006-05-26 | Use-Techno Corporation | Gluconeogenesis inhibiting agent |
| JP2008523133A (ja) | 2004-12-14 | 2008-07-03 | アストラゼネカ アクチボラグ | Dgat阻害剤としてのオキサジアゾール誘導体 |
| WO2006082952A1 (ja) | 2005-02-01 | 2006-08-10 | Takeda Pharmaceutical Company Limited | アミド化合物 |
| KR100883694B1 (ko) | 2005-02-07 | 2009-02-12 | 에프. 호프만-라 로슈 아게 | 디아실글리세롤 아실트랜스퍼라제 억제제 |
| AU2006236155A1 (en) | 2005-04-19 | 2006-10-26 | Bayer Pharmaceuticals Corporation | Aryl alkyl acid derivatives for and use thereof |
| KR100910440B1 (ko) | 2005-05-10 | 2009-08-04 | 에프. 호프만-라 로슈 아게 | 다이아실글리세롤 아실트랜스퍼레이즈 억제제 |
| 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 |
| EP2301923B1 (en) | 2006-03-31 | 2016-06-08 | Novartis AG | Pyridine derivatives as dgat inhibitors |
| CN101541747B (zh) | 2006-04-21 | 2012-11-14 | 伊莱利利公司 | 作为11-β-羟基甾族化合物脱氢酶1的抑制剂的联苯基酰胺内酰胺衍生物 |
| 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 |
| ATE492541T1 (de) | 2006-05-30 | 2011-01-15 | Astrazeneca Ab | Substituierte 5-phenylamino-1,3,4-oxadiazol-2- ylcarbonylamino-4-phenoxycyclohexancarbonsäuren als inhibitoren von acetylcoenzym-a- diacylglycerolacyltransferase |
| US8003676B2 (en) | 2006-05-30 | 2011-08-23 | Astrazeneca Ab | 1,3,4-oxadiazole derivatives as DGAT1 inhibitors |
| JP2009539816A (ja) | 2006-06-06 | 2009-11-19 | アストラゼネカ アクチボラグ | 化学化合物 |
| CN101460492A (zh) | 2006-06-08 | 2009-06-17 | 阿斯利康(瑞典)有限公司 | 苯并咪唑及其治疗糖尿病的用途 |
| GB0611506D0 (en) | 2006-06-10 | 2006-07-19 | Astrazeneca Ab | Chemical compounds |
| GB0611507D0 (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 |
| US8354432B2 (en) | 2006-10-04 | 2013-01-15 | Bristol-Myers Squibb Company | Cyclic derivatives as modulators of chemokine receptor activity |
| AU2007304365A1 (en) | 2006-10-04 | 2008-04-10 | 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 |
| WO2008058402A1 (en) | 2006-11-17 | 2008-05-22 | Queen's University At Kingston | Compounds and methods for treating protein folding disorders |
| NZ597247A (en) | 2006-11-29 | 2013-06-28 | Abbott Lab | Inhibitors of diacylglycerol O-acylotransferase type 1 enzyme |
| BRPI0720023A2 (pt) | 2006-12-11 | 2018-09-04 | Novartis Ag | método para prevenir ou tratar isquemia do miocárdio por inibição da enzima dgat1 com um inibidor de dgat1 |
| US20100093733A1 (en) | 2007-02-15 | 2010-04-15 | Prosidion Limited | Amide and urea derivatives for the treatment of metabolic diseases |
| GB0707662D0 (en) | 2007-04-20 | 2007-05-30 | Astrazeneca Ab | Chemical compounds |
| KR20100017508A (ko) | 2007-04-30 | 2010-02-16 | 아보트 러보러터리즈 | 디아실글리세롤 o-아실트랜스퍼라제 타입 1 효소의 억제제 |
| 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 |
| JP2012512860A (ja) | 2008-12-19 | 2012-06-07 | アストラゼネカ アクチボラグ | 1,3,4−オキサジアゾール誘導体および糖尿病を処置するそれらの使用 |
-
2008
- 2008-12-18 WO PCT/GB2008/051199 patent/WO2009081195A1/en not_active Ceased
- 2008-12-18 PE PE2008002123A patent/PE20091682A1/es not_active Application Discontinuation
- 2008-12-18 CN CN2008801259853A patent/CN101932562B/zh not_active Expired - Fee Related
- 2008-12-18 NZ NZ586104A patent/NZ586104A/en not_active IP Right Cessation
- 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 AU AU2008339570A patent/AU2008339570B2/en not_active Expired - Fee Related
- 2008-12-18 BR BRPI0821274A patent/BRPI0821274A2/pt not_active IP Right Cessation
- 2008-12-18 EA EA201001015A patent/EA201001015A1/ru unknown
- 2008-12-18 CA CA2707660A patent/CA2707660A1/en not_active Abandoned
- 2008-12-18 TW TW097149460A patent/TW200932235A/zh unknown
- 2008-12-18 KR KR1020107016252A patent/KR20100099738A/ko not_active Withdrawn
- 2008-12-18 JP JP2010538918A patent/JP5662803B2/ja not_active Expired - Fee Related
- 2008-12-18 ES ES08865783.8T patent/ES2535083T3/es active Active
- 2008-12-19 US US12/339,349 patent/US7994179B2/en not_active Expired - Fee Related
- 2008-12-19 CL CL2008003847A patent/CL2008003847A1/es unknown
-
2010
- 2010-05-27 IL IL206045A patent/IL206045A0/en unknown
- 2010-06-03 ZA ZA2010/03979A patent/ZA201003979B/en unknown
- 2010-06-18 NI NI201000108A patent/NI201000108A/es unknown
- 2010-06-18 CR CR11518A patent/CR11518A/es not_active Application Discontinuation
- 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 |
|---|---|
| CN101932562A (zh) | 2010-12-29 |
| ZA201003979B (en) | 2011-11-30 |
| EP2234978A1 (en) | 2010-10-06 |
| CN101932562B (zh) | 2013-06-12 |
| DOP2010000192A (es) | 2010-07-15 |
| WO2009081195A1 (en) | 2009-07-02 |
| CA2707660A1 (en) | 2009-07-02 |
| JP5662803B2 (ja) | 2015-02-04 |
| AU2008339570A1 (en) | 2009-07-02 |
| ECSP10010274A (es) | 2010-07-30 |
| JP2011507823A (ja) | 2011-03-10 |
| EA201001015A1 (ru) | 2011-02-28 |
| CL2008003847A1 (es) | 2009-11-27 |
| AR069802A1 (es) | 2010-02-17 |
| IL206045A0 (en) | 2010-11-30 |
| ES2535083T3 (es) | 2015-05-05 |
| EP2234978B1 (en) | 2015-02-25 |
| NI201000108A (es) | 2012-05-14 |
| US7994179B2 (en) | 2011-08-09 |
| US20120108602A1 (en) | 2012-05-03 |
| NZ586104A (en) | 2012-02-24 |
| TW200932235A (en) | 2009-08-01 |
| US20090298853A1 (en) | 2009-12-03 |
| BRPI0821274A2 (pt) | 2017-06-13 |
| CO6290685A2 (es) | 2011-06-20 |
| KR20100099738A (ko) | 2010-09-13 |
| AU2008339570B2 (en) | 2012-04-12 |
| CR11518A (es) | 2010-07-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PE20091682A1 (es) | Compuestos de carbamoilo como inhibidores de dgat1 190 | |
| PE20141700A1 (es) | Compuestos de 2-(2,4,5-anilino sustituido) pirimidina | |
| PE20091816A1 (es) | Inhibidores de bace | |
| PE20070593A1 (es) | Compuestos pirrolopirimidina como inhibidores de syk | |
| PE20160654A1 (es) | Compuestos de inhibidor de autotaxina | |
| PE20061490A1 (es) | Derivados de ciclohexanosulfonilo como inhibidores del transportador de glicina glyt1 | |
| RU2010145171A (ru) | Аналоги галихондрина в | |
| NZ607845A (en) | Besylate salt of a btk inhibitor | |
| NZ700778A (en) | Crystalline forms of 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-{ 6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl} -1-methyl-urea and salts thereof. | |
| PE20140630A1 (es) | Derivados de acido 3-fenilpropionico ramificados y su uso | |
| TR201904655T4 (tr) | Piridilaminoasetik asit bileşiği. | |
| AR078944A1 (es) | Inhibidores de n1-pirazoloespirocetona acetil-coa carboxilasa | |
| PE20142083A1 (es) | Derivados de anilina, su preparacion y su aplicacion terapeutica | |
| PE20080888A1 (es) | COMPUESTOS HETEROCICLICOS COMO INHIBIDORES DE LA ACIL-TRANSFERASA DE ACIL-CoA-DIACIL-GLICEROL 1 (DGAT1) | |
| MX2009009492A (es) | Compuestos organicos biciclicos adecuados para el tratamiento de condiciones inflamatorias o alergicas. | |
| NZ596826A (en) | Polycyclic antagonists of lysophosphatidic acid receptors | |
| PE20090601A1 (es) | Derivados de piridin-il-oxi-piridinas como inhibidores de alk5 | |
| PE20140826A1 (es) | Compuestos sustituidos fungicidas de 2-[2-halogenalquil-4-(fenoxi)-fenil]-1-[1,2,4]triazol-1-il-etanol | |
| NO20082610L (no) | Trihydrokloridformer av et dihydropteridonderivat og metoder for fremstilling | |
| PE20080659A1 (es) | Benzotriazoles como moduladores de quinasas | |
| PE20091456A1 (es) | Nuevas formas cristalinas de acido 4-[4-(2-adamantilcarbamoil)-5-tert-butil-pirazol-1-il]benzoico- 471 | |
| PE20071254A1 (es) | Derivados de sulfonamidas como agentes moduladores de los receptores de orexina y su preparacion | |
| NZ606700A (en) | Process for manufacturing dihydropteridinones and intermediates thereof | |
| PE20121529A1 (es) | Compuestos derivados de piridopirimidina como inhibidores de pde4 | |
| NZ596431A (en) | Liquid formulations of salts of 1-[2-(2,4-dimethylphenylsulfanyl)phenyl]piperazine |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC | Refusal |