ECSP099571A - Derivados pirazólicos como inhibidores de la 11-beta-hsd1 - Google Patents
Derivados pirazólicos como inhibidores de la 11-beta-hsd1Info
- Publication number
- ECSP099571A ECSP099571A EC2009009571A ECSP099571A ECSP099571A EC SP099571 A ECSP099571 A EC SP099571A EC 2009009571 A EC2009009571 A EC 2009009571A EC SP099571 A ECSP099571 A EC SP099571A EC SP099571 A ECSP099571 A EC SP099571A
- Authority
- EC
- Ecuador
- Prior art keywords
- pirazolic
- hsd1
- inhibitors
- beta
- derivatives
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000005764 inhibitory process Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or 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
- C07D231/18—One oxygen or sulfur atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/38—Drugs for disorders of the endocrine system of the suprarenal hormones
- A61P5/46—Drugs for disorders of the endocrine system of the suprarenal hormones for decreasing, blocking or antagonising the activity of glucocorticosteroids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
-
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or 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
-
- 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
- C07D403/06—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 only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Diabetes (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Un compuesto de la fórmula (I): y sales farmacéuticamente aceptables de este donde los grupos variables se definen en la presente; y también se describe su uso en la inhibición de la 11ßHSD1, procesos para prepararlos y composiciones farmacéuticas que los comprenden.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US88933607P | 2007-02-12 | 2007-02-12 | |
| US98573507P | 2007-11-06 | 2007-11-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP099571A true ECSP099571A (es) | 2009-09-29 |
Family
ID=39438215
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EC2009009571A ECSP099571A (es) | 2007-02-12 | 2009-08-11 | Derivados pirazólicos como inhibidores de la 11-beta-hsd1 |
Country Status (23)
| Country | Link |
|---|---|
| US (2) | US7816391B2 (es) |
| EP (2) | EP2292228A1 (es) |
| JP (1) | JP2010518063A (es) |
| KR (1) | KR20090108726A (es) |
| CN (1) | CN102503891A (es) |
| AR (1) | AR065300A1 (es) |
| AU (1) | AU2008215976B2 (es) |
| BR (1) | BRPI0808450A2 (es) |
| CA (1) | CA2676154A1 (es) |
| CL (1) | CL2008000422A1 (es) |
| CO (1) | CO6220949A2 (es) |
| EC (1) | ECSP099571A (es) |
| IL (1) | IL200047A0 (es) |
| MX (1) | MX2009008506A (es) |
| NZ (1) | NZ578568A (es) |
| PE (2) | PE20120355A1 (es) |
| RU (2) | RU2462456C2 (es) |
| SA (1) | SA08290055B1 (es) |
| SG (1) | SG177892A1 (es) |
| TW (1) | TW200836719A (es) |
| UY (1) | UY30912A1 (es) |
| WO (1) | WO2008099145A1 (es) |
| ZA (1) | ZA201000838B (es) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2630665C (en) | 2005-11-21 | 2011-03-15 | Shionogi & Co., Ltd. | Heterocyclic compound having inhibitory activity on 11-.beta.-hydroxysteroid dehydrogenase type i |
| TW200827346A (en) * | 2006-11-03 | 2008-07-01 | Astrazeneca Ab | Chemical compounds |
| TW200836719A (en) | 2007-02-12 | 2008-09-16 | Astrazeneca Ab | Chemical compounds |
| WO2008142986A1 (ja) | 2007-05-18 | 2008-11-27 | Shionogi & Co., Ltd. | I型11βヒドロキシステロイド脱水素酵素阻害活性を有する含窒素複素環誘導体 |
| KR101158191B1 (ko) | 2007-07-17 | 2012-06-19 | 에프. 호프만-라 로슈 아게 | 11b-하이드록시스테로이드 탈수소효소의 억제제 |
| KR20100126306A (ko) * | 2008-02-04 | 2010-12-01 | 아스트라제네카 아베 | 4-[4-(2-(아다만틸카르바모일)-5-tert-부틸-피라졸-1-일]벤조산의 신규한 결정형 |
| JP2011518216A (ja) * | 2008-04-22 | 2011-06-23 | アストラゼネカ アクチボラグ | 置換ピリミジン−5−カルボキサミド |
| EP2391607A1 (en) * | 2009-01-30 | 2011-12-07 | AstraZeneca AB | Novel process for preparing carboxy-containing pyrazoleamido compounds 597 |
| EP2243479A3 (en) | 2009-04-20 | 2011-01-19 | Abbott Laboratories | Novel amide and amidine derivates and uses thereof |
| US8871208B2 (en) * | 2009-12-04 | 2014-10-28 | Abbvie Inc. | 11-β-hydroxysteroid dehydrogenase type 1 (11β-HSD1) inhibitors and uses thereof |
| WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| GB201004301D0 (en) * | 2010-03-15 | 2010-04-28 | Syngenta Participations Ag | Process |
| EP2582709B1 (de) | 2010-06-18 | 2018-01-24 | Sanofi | Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen |
| US8530413B2 (en) | 2010-06-21 | 2013-09-10 | Sanofi | Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments |
| TW201221505A (en) | 2010-07-05 | 2012-06-01 | Sanofi Sa | Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament |
| TW201215387A (en) | 2010-07-05 | 2012-04-16 | Sanofi Aventis | Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament |
| TW201215388A (en) | 2010-07-05 | 2012-04-16 | Sanofi Sa | (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments |
| JP5605104B2 (ja) * | 2010-09-10 | 2014-10-15 | セントラル硝子株式会社 | ピラゾール化合物の製造方法 |
| US9012657B2 (en) | 2011-06-22 | 2015-04-21 | Central Glass Company, Limited | Method for producing pyrazole compound |
| JP5915004B2 (ja) * | 2011-06-22 | 2016-05-11 | セントラル硝子株式会社 | ピラゾール化合物の製造方法 |
| WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| WO2013045413A1 (en) | 2011-09-27 | 2013-04-04 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| JP2015129094A (ja) * | 2012-04-16 | 2015-07-16 | 大日本住友製薬株式会社 | アリールアミノピラゾール誘導体 |
| CN111148734B (zh) * | 2017-08-28 | 2023-01-06 | 中国医学科学院药物研究所 | 吡咯-2-甲酰胺类化合物及其制备方法和用途 |
Family Cites Families (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GR66581B (es) | 1978-02-21 | 1981-03-27 | Delalande Sa | |
| US4816391A (en) * | 1984-02-29 | 1989-03-28 | Syntex (U.S.A.) Inc. | Amine stabilized aminoglycoside formulations |
| US4734418A (en) | 1984-12-14 | 1988-03-29 | Mitsui Petrochemical Industries, Ltd. | Quinazoline compounds and antihypertensives |
| HU225917B1 (en) | 1999-09-16 | 2007-12-28 | Tanabe Seiyaku Co | Pyrimidine and pyrazine derivatives, pharmaceutical compositions containing them and their use |
| US7273868B2 (en) | 2000-04-28 | 2007-09-25 | Tanabe Seiyaku Co., Ltd. | Pyrazine derivatives |
| AU2001288623A1 (en) | 2000-09-05 | 2002-03-22 | Tularik, Inc. | Fxr modulators |
| NZ526003A (en) | 2000-10-20 | 2005-09-30 | Biocryst Pharm Inc | Biaryl compounds as serine protease inhibitors |
| SE0102764D0 (sv) | 2001-08-17 | 2001-08-17 | Astrazeneca Ab | Compounds |
| JP2005528395A (ja) | 2002-04-05 | 2005-09-22 | ザ ユニバーシティ オブ エディンバラ | 組成物 |
| TW200503994A (en) | 2003-01-24 | 2005-02-01 | Novartis Ag | Organic compounds |
| WO2004076420A1 (ja) | 2003-02-26 | 2004-09-10 | Banyu Pharmaceutical Co., Ltd. | ヘテロアリールカルバモイルベンゼン誘導体 |
| EP1618090A1 (en) * | 2003-04-11 | 2006-01-25 | Novo Nordisk A/S | 11ß-HYDROXYSTEROID DEHYDROGENASE TYPE 1 ACTIVE COMPOUNDS |
| WO2005016877A2 (en) | 2003-08-07 | 2005-02-24 | Merck & Co., Inc. | Pyrazole carboxamides as inhibitors of 11-beta-hydroxysteroid dehydrogenase-1 |
| EP1670787B1 (en) | 2003-09-11 | 2012-05-30 | iTherX Pharma, Inc. | Cytokine inhibitors |
| GB0327761D0 (en) | 2003-11-29 | 2003-12-31 | Astrazeneca Ab | Compounds |
| MXPA06007077A (es) | 2003-12-19 | 2006-08-23 | Pfizer | Derivados de bencenosulfonilamino-piridin-2-ilo y compuestos relacionados como inhibidores de 11-beta-hidroxi esteroide deshidrogenasa tipo 1 para el tratamiento de diabetes y obesidad. |
| JP2007536369A (ja) | 2004-05-06 | 2007-12-13 | ファイザー・インク | プロリン及びモルホリン誘導体の新規化合物 |
| TW200600086A (en) | 2004-06-05 | 2006-01-01 | Astrazeneca Ab | Chemical compound |
| JP4809339B2 (ja) | 2004-06-28 | 2011-11-09 | エフ.ホフマン−ラ ロシュ アーゲー | ピリミジン誘導体 |
| WO2006048750A2 (en) | 2004-11-02 | 2006-05-11 | Pfizer Inc. | Novel compounds of substituted and unsubstituted adamantyl amides |
| EP1809290A2 (en) | 2004-11-03 | 2007-07-25 | Vertex Pharmaceuticals Incorporated | Pyrimidine derivatives as ion channel modulators and methods of use |
| CN103242192B (zh) | 2005-01-05 | 2016-05-04 | Abbvie公司 | 11-β-羟甾类脱氢酶1型酶的抑制剂 |
| ATE519744T1 (de) | 2005-04-05 | 2011-08-15 | Hoffmann La Roche | 1h-pyrazol-4-carbonsäure-amide, deren herstellung und verwendung als 11-beta-hydroxysteroid- dehydrogenase-hemmer |
| DK1868999T3 (da) | 2005-04-06 | 2009-08-17 | Hoffmann La Roche | Pyridin-3-carboxamidderivater som omvendte CB1-agonister |
| WO2006106423A2 (en) | 2005-04-07 | 2006-10-12 | Pfizer Inc. | Amino sulfonyl derivatives as inhibitors of human 11-.beta.-hydrosysteroid dehydrogenase |
| EP2527337A1 (en) | 2005-04-14 | 2012-11-28 | Bristol-Myers Squibb Company | Inhibitors of 11-beta hydroxysteroid dehydrogenase type I |
| EP1891069A1 (en) | 2005-05-24 | 2008-02-27 | AstraZeneca AB | 2-phenyl substituted imidazol [4,5b]pyridine/ pyrazine and purine derivatives as glucokinase modulators |
| US8952176B2 (en) | 2005-06-07 | 2015-02-10 | Shionogi & Co., Ltd. | Heterocyclic compound having type I 11 β hydroxysteroid dehydrogenase inhibitory activity |
| AU2006255944B2 (en) * | 2005-06-08 | 2010-03-04 | Japan Tobacco Inc. | Heterocyclic compound |
| EP1893609B1 (en) | 2005-06-16 | 2009-11-18 | Pfizer, Inc. | N-(pyridin-2-yl)-sulfonamide derivatives |
| US7642259B2 (en) | 2005-07-09 | 2010-01-05 | Astrazeneca Ab | Heteroaryl benzamide derivatives for use as GLK activators in the treatment of diabetes |
| EP1915367A1 (en) | 2005-08-09 | 2008-04-30 | AstraZeneca AB | Heteroarylcarbamoylbenzene derivatives for the treatment of diabetes |
| EP1951707A1 (en) | 2005-11-01 | 2008-08-06 | Janssen Pharmaceutica N.V. | Substituted pyrrolones as allosteric modulators of glucokinase |
| WO2007052843A1 (ja) | 2005-11-04 | 2007-05-10 | Takeda Pharmaceutical Company Limited | 複素環アミド化合物およびその用途 |
| CA2630665C (en) * | 2005-11-21 | 2011-03-15 | Shionogi & Co., Ltd. | Heterocyclic compound having inhibitory activity on 11-.beta.-hydroxysteroid dehydrogenase type i |
| KR20080091503A (ko) | 2006-01-31 | 2008-10-13 | 인사이트 코포레이션 | 아미도 화합물 및 약제로서의 이의 용도 |
| HRP20151078T1 (hr) * | 2006-03-22 | 2015-11-20 | F. Hoffmann - La Roche Ag | Pirazoli kao 11-beta-hsd-1 |
| AU2007236049A1 (en) | 2006-04-07 | 2007-10-18 | High Point Pharmaceuticals, Llc | 11beta-hydroxysteroid dehydrogenase type 1 active compounds |
| RU2008146591A (ru) | 2006-04-27 | 2010-06-10 | Зольвай Фармасьютиклз Гмбх (De) | Применение модуляторов каннабиноидного рецептора свх в качестве модуляторов калиевых каналов |
| US20100022589A1 (en) | 2006-07-27 | 2010-01-28 | Mccoull William | Pyridine-3-carboxamide compounds and their use for inhibiting 11-beta-hydroxysteroid dehydrogenase |
| TW200827346A (en) | 2006-11-03 | 2008-07-01 | Astrazeneca Ab | Chemical compounds |
| TW200836719A (en) | 2007-02-12 | 2008-09-16 | Astrazeneca Ab | Chemical compounds |
| WO2008142986A1 (ja) | 2007-05-18 | 2008-11-27 | Shionogi & Co., Ltd. | I型11βヒドロキシステロイド脱水素酵素阻害活性を有する含窒素複素環誘導体 |
| KR101158191B1 (ko) | 2007-07-17 | 2012-06-19 | 에프. 호프만-라 로슈 아게 | 11b-하이드록시스테로이드 탈수소효소의 억제제 |
| EA201000701A1 (ru) | 2007-11-06 | 2010-12-30 | Астразенека Аб | 4-[4-(2-адамантилкарбамоил)-5-трет-бутилпиразол-1-ил]бензойная кислота-465 |
| KR20100126306A (ko) | 2008-02-04 | 2010-12-01 | 아스트라제네카 아베 | 4-[4-(2-(아다만틸카르바모일)-5-tert-부틸-피라졸-1-일]벤조산의 신규한 결정형 |
| JP2011518216A (ja) | 2008-04-22 | 2011-06-23 | アストラゼネカ アクチボラグ | 置換ピリミジン−5−カルボキサミド |
| EP2391607A1 (en) | 2009-01-30 | 2011-12-07 | AstraZeneca AB | Novel process for preparing carboxy-containing pyrazoleamido compounds 597 |
| AR078673A1 (es) | 2009-10-20 | 2011-11-23 | Astrazeneca Ab | Pirimidinas sustituidas con adamantiliminocarbonilo como inhibidores de 11-b-hsd1 826 |
-
2008
- 2008-02-05 TW TW097104688A patent/TW200836719A/zh unknown
- 2008-02-08 CL CL2008000422A patent/CL2008000422A1/es unknown
- 2008-02-09 SA SA8290055A patent/SA08290055B1/ar unknown
- 2008-02-11 RU RU2009133259/04A patent/RU2462456C2/ru not_active IP Right Cessation
- 2008-02-11 SG SG2011091865A patent/SG177892A1/en unknown
- 2008-02-11 CA CA002676154A patent/CA2676154A1/en not_active Abandoned
- 2008-02-11 PE PE2012000020A patent/PE20120355A1/es not_active Application Discontinuation
- 2008-02-11 JP JP2009548741A patent/JP2010518063A/ja active Pending
- 2008-02-11 EP EP10183055A patent/EP2292228A1/en not_active Withdrawn
- 2008-02-11 MX MX2009008506A patent/MX2009008506A/es not_active Application Discontinuation
- 2008-02-11 WO PCT/GB2008/000454 patent/WO2008099145A1/en not_active Ceased
- 2008-02-11 KR KR1020097018195A patent/KR20090108726A/ko not_active Ceased
- 2008-02-11 AU AU2008215976A patent/AU2008215976B2/en not_active Ceased
- 2008-02-11 BR BRPI0808450-5A patent/BRPI0808450A2/pt not_active IP Right Cessation
- 2008-02-11 NZ NZ578568A patent/NZ578568A/en not_active IP Right Cessation
- 2008-02-11 EP EP08702088A patent/EP2124937A1/en not_active Withdrawn
- 2008-02-11 AR ARP080100584A patent/AR065300A1/es not_active Application Discontinuation
- 2008-02-11 PE PE2008000295A patent/PE20090649A1/es not_active Application Discontinuation
- 2008-02-11 CN CN2011102665044A patent/CN102503891A/zh active Pending
- 2008-02-12 UY UY30912A patent/UY30912A1/es not_active Application Discontinuation
- 2008-10-28 US US12/259,562 patent/US7816391B2/en not_active Expired - Fee Related
-
2009
- 2009-07-23 IL IL200047A patent/IL200047A0/en unknown
- 2009-08-11 EC EC2009009571A patent/ECSP099571A/es unknown
- 2009-08-12 CO CO09084454A patent/CO6220949A2/es not_active Application Discontinuation
-
2010
- 2010-02-04 ZA ZA2010/00838A patent/ZA201000838B/en unknown
- 2010-09-09 US US12/878,416 patent/US8344016B2/en not_active Expired - Fee Related
-
2012
- 2012-06-20 RU RU2012125372/04A patent/RU2012125372A/ru not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AR065300A1 (es) | 2009-05-27 |
| PE20090649A1 (es) | 2009-06-26 |
| CN102503891A (zh) | 2012-06-20 |
| TW200836719A (en) | 2008-09-16 |
| AU2008215976B2 (en) | 2011-11-24 |
| SG177892A1 (en) | 2012-02-28 |
| RU2009133259A (ru) | 2011-03-20 |
| CA2676154A1 (en) | 2008-08-21 |
| NZ578568A (en) | 2012-01-12 |
| MX2009008506A (es) | 2009-10-12 |
| EP2292228A1 (en) | 2011-03-09 |
| CL2008000422A1 (es) | 2009-01-02 |
| BRPI0808450A2 (pt) | 2014-08-12 |
| EP2124937A1 (en) | 2009-12-02 |
| AU2008215976A1 (en) | 2008-08-21 |
| US8344016B2 (en) | 2013-01-01 |
| RU2012125372A (ru) | 2013-12-27 |
| ZA201000838B (en) | 2010-10-27 |
| SA08290055B1 (ar) | 2012-09-26 |
| IL200047A0 (en) | 2010-04-15 |
| UY30912A1 (es) | 2008-09-30 |
| RU2462456C2 (ru) | 2012-09-27 |
| US7816391B2 (en) | 2010-10-19 |
| JP2010518063A (ja) | 2010-05-27 |
| CO6220949A2 (es) | 2010-11-19 |
| PE20120355A1 (es) | 2012-05-17 |
| WO2008099145A1 (en) | 2008-08-21 |
| US20110224273A1 (en) | 2011-09-15 |
| US20090221663A1 (en) | 2009-09-03 |
| KR20090108726A (ko) | 2009-10-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ECSP099571A (es) | Derivados pirazólicos como inhibidores de la 11-beta-hsd1 | |
| CO6321254A2 (es) | Pirimidin -5-carboxamidas sustituidas 281 | |
| UY31069A1 (es) | Nuevos derivados de imidazoquinola, composiciones conteniendolos, proceso de preparacion y aplicaciones | |
| CR11518A (es) | Compuestos de carbamoilo como inhibidores de dgat1 190 | |
| PA8791801A1 (es) | Compuestos de pirazol | |
| ECSP109856A (es) | Derivados de oxadiazol y su uso como potenciadores de los receptores metabotrópicos de glutamato - 842 | |
| DOP2010000183A (es) | Derivados de itazol usados como inhibidores de pi 3-cinasa | |
| CR20120283A (es) | Inhibidor de bromodominio de benzodiazepina | |
| UY30444A1 (es) | Derivados de pirimidina, procesos para su preparacinn, composiciones farmaccuticos y usos de los mismos. | |
| ECSP099721A (es) | Inhibidores de cinasa p70 s6 | |
| ECSP10010272A (es) | Derivados bis-(sulfonilamino) para uso en terapia | |
| UY31906A (es) | Derivados de n-cicloalquil-3-fenilnicotinamida que inhiben pgds, sus composiciones, su uso para el tratamiento por ejemplo de afecciones alérgicas y respiratorias. | |
| CO6290656A2 (es) | Derivados heterociclicos de urea y metodos de uso de los mismos -211 | |
| UY32158A (es) | Derivados heterociclicos y metodos de uso de los mismos | |
| UY31639A1 (es) | Derivados de amida espirocíclica de fórmula i, sales farmacéuticamente aceptables, composiciones farmacéuticas conteniéndolas, procesos de preparación y aplicaciones | |
| DOP2009000200A (es) | Derivados de 2-amino-5,7-dihidro-6h-pirrolo[3,4-d] pimiridina como inhibidores hsp-90 para tratar el cancer | |
| ECSP088700A (es) | Acidos 4-fenil-tiazol-5-carboxilicos y amidas de acidos 4-fenil-tiazol-5-carboxilicos como inhibidores de la plk1 | |
| UY31905A (es) | Derivados de benzoxazinona, procesos de preparación, composiciones farmacéuticas conteniéndolos y aplicaciones. | |
| SV2010003752A (es) | Derivados de urea heterociclicos para el tratamiento de infecciones bacterianas | |
| UY32954A (es) | PIRIMIDINAS SUSTITUIDAS CON ADAMANTILIMINOCARBONILO COMO INHIBIDORES DE 11-ß-HSD1 826?. | |
| UY32674A (es) | Derivados heterociclicos de la urea y sus metodos de empleo | |
| DOP2010000155A (es) | Derivados de pirazol como inhibidores de 5-lo | |
| UY29896A1 (es) | Nuevos derivados de cromano, composiciones farmacéuticas conteniéndolos, procesos de preparación y aplicaciones | |
| UY30417A1 (es) | Derivados de aril y heteroaril-etil-acilguanidina,su preparacion y su aplicacion en terapeutica | |
| ECSP13012372A (es) | Nuevos derivados 1,4-diazepanos, inhibidores de pde-5. |