HN2008000792A - Compuesto de cinamida biciclico - Google Patents
Compuesto de cinamida biciclicoInfo
- Publication number
- HN2008000792A HN2008000792A HN2008000792A HN2008000792A HN2008000792A HN 2008000792 A HN2008000792 A HN 2008000792A HN 2008000792 A HN2008000792 A HN 2008000792A HN 2008000792 A HN2008000792 A HN 2008000792A HN 2008000792 A HN2008000792 A HN 2008000792A
- Authority
- HN
- Honduras
- Prior art keywords
- bicycle
- cinamide
- composite
- compound
- present
- Prior art date
Links
- 239000002131 composite material Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 239000004480 active ingredient Substances 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 239000008177 pharmaceutical agent Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
-
- 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
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Neurosurgery (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
LA PRESENTE INVENCION SE REFIERE A UN COMPUESTO DE CINAMIDA BICICLICO Y UN AGENTE FARMACEUTICO QUE COMPRENDE EL COMPUESTO COMO UN INGREDIENTE ACTIVO. MAS ESPECIFICAMENTE, LA PRESENTE INVENCION SE REFIERE A UN COMPUESTO DE CINAMIDA BICICLICO NO PEPTIDICO Y UN INHIBIDOR DE PRODUCCION DE AMILOIDE
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2005337963 | 2005-11-24 | ||
| JP2006205538 | 2006-07-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HN2008000792A true HN2008000792A (es) | 2010-09-17 |
Family
ID=38067057
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HN2008000792A HN2008000792A (es) | 2005-11-24 | 2008-05-23 | Compuesto de cinamida biciclico |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US8048878B2 (es) |
| EP (1) | EP1953158B1 (es) |
| JP (1) | JP5178203B2 (es) |
| KR (1) | KR101296239B1 (es) |
| AR (1) | AR057915A1 (es) |
| AU (1) | AU2006317468B2 (es) |
| BR (1) | BRPI0618890A2 (es) |
| CA (1) | CA2629512C (es) |
| CR (1) | CR9983A (es) |
| EA (1) | EA014427B1 (es) |
| EC (1) | ECSP088466A (es) |
| ES (1) | ES2394364T3 (es) |
| GE (1) | GEP20115172B (es) |
| HN (1) | HN2008000792A (es) |
| MA (1) | MA29968B1 (es) |
| ME (1) | ME00040B (es) |
| MY (1) | MY144596A (es) |
| NO (1) | NO20082805L (es) |
| NZ (1) | NZ568422A (es) |
| PE (1) | PE20071029A1 (es) |
| PL (1) | PL1953158T3 (es) |
| RS (1) | RS20080242A (es) |
| SA (1) | SA06270432B1 (es) |
| TW (1) | TWI370130B (es) |
| WO (1) | WO2007060821A1 (es) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI335816B (en) | 2004-05-26 | 2011-01-11 | Eisai R&D Man Co Ltd | Cinnamide compound |
| DE602005019602D1 (de) | 2004-10-26 | 2010-04-08 | Eisai R&D Man Co Ltd | Amorphe form einer zimtsäureamidverbindung |
| TWI370130B (en) | 2005-11-24 | 2012-08-11 | Eisai R&D Man Co Ltd | Two cyclic cinnamide compound |
| AU2006317457B2 (en) | 2005-11-24 | 2011-09-08 | Eisai R & D Management Co., Ltd. | Morpholine type cinnamide compound |
| US7482345B2 (en) * | 2005-12-05 | 2009-01-27 | Meng-Hsin Chen | P38 kinase inhibiting agents |
| TWI378091B (en) | 2006-03-09 | 2012-12-01 | Eisai R&D Man Co Ltd | Multi-cyclic cinnamide derivatives |
| US7737141B2 (en) * | 2006-07-28 | 2010-06-15 | Eisai R&D Management Co., Ltd. | Prodrug of cinnamide compound |
| TW200848054A (en) * | 2007-02-28 | 2008-12-16 | Eisai R&D Man Co Ltd | Two cyclic oxomorpholine derivatives |
| CN101809016A (zh) * | 2007-06-01 | 2010-08-18 | 先灵公司 | γ-分泌酶调节剂 |
| JP5121346B2 (ja) * | 2007-08-07 | 2013-01-16 | 国立大学法人 長崎大学 | 光学活性プロリンエステル誘導体およびn−ホルミル光学活性プロリン誘導体の製造方法 |
| US7935815B2 (en) * | 2007-08-31 | 2011-05-03 | Eisai R&D Management Co., Ltd. | Imidazoyl pyridine compounds and salts thereof |
| JP5433418B2 (ja) | 2007-08-31 | 2014-03-05 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 多環式化合物 |
| RU2010131008A (ru) | 2007-12-26 | 2012-02-10 | ЭЙСАЙ Ар энд Ди МЕНЕДЖМЕНТ КО., ЛТД. (JP) | Способ получения 4-(замещенный фенил)гексагидропиридо[2, 1-c][1, 4]оксазин-6-она |
| ES2428716T3 (es) | 2008-02-22 | 2013-11-11 | F. Hoffmann-La Roche Ag | Moduladores de beta-amiloide |
| WO2010040661A1 (en) | 2008-10-09 | 2010-04-15 | F. Hoffmann-La Roche Ag | Modulators for amyloid beta |
| CA2742317A1 (en) * | 2008-11-06 | 2010-05-14 | Schering Corporation | Gamma secretase modulators |
| EP2356124A1 (en) * | 2008-11-06 | 2011-08-17 | Schering Corporation | Gamma secretase modulators |
| KR101293421B1 (ko) | 2008-11-10 | 2013-08-05 | 에프. 호프만-라 로슈 아게 | 헤테로사이클릭 감마 분비효소 조절제 |
| AU2009314049B2 (en) * | 2008-11-13 | 2015-03-05 | Merck Sharp & Dohme Corp. | Gamma secretase modulators |
| US8703954B2 (en) | 2009-02-26 | 2014-04-22 | Eisai R&D Management Co., Ltd. | Salt of tetrahydrotriazolopyridine derivative and crystal thereof |
| TW201035101A (en) | 2009-02-26 | 2010-10-01 | Eisai R&D Man Co Ltd | Nitrogen-containing fused heterocyclic compound |
| JP2012176901A (ja) * | 2009-09-25 | 2012-09-13 | Eisai R & D Management Co Ltd | 新規ベンゾニトリル化合物およびその製造方法 |
| US8486967B2 (en) | 2010-02-17 | 2013-07-16 | Hoffmann-La Roche Inc. | Heteroaryl substituted piperidines |
| CA2802477A1 (en) * | 2010-06-15 | 2011-12-22 | Eisai R&D Management Co., Ltd. | Agent for treating hcv infection |
| JP6095208B2 (ja) * | 2012-12-04 | 2017-03-15 | 学校法人慶應義塾 | 環化化合物の製造方法、及び、環化化合物を含有する溶液の発光方法 |
| DK3552017T3 (da) * | 2016-12-09 | 2022-05-16 | Denali Therapeutics Inc | Forbindelser, der er anvendelige som ripk1-inhibitorer |
| MX2019013642A (es) | 2017-05-17 | 2020-07-20 | Denali Therapeutics Inc | Compuestos, composiciones y metodos. |
| KR20220079878A (ko) * | 2019-10-07 | 2022-06-14 | 디.이. 쇼우 리서치, 엘엘씨 | Kv1.3 칼륨 셰이커 채널 차단제로서의 아릴 헤테로비시클릭 화합물 |
Family Cites Families (66)
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| US4508718A (en) | 1984-01-16 | 1985-04-02 | Warner-Lambert Company | Cardiotonic and antihypertensive oxadiazinone compounds |
| DE3689506D1 (de) | 1985-10-09 | 1994-02-17 | Shell Int Research | Neue Acrylsäureamide. |
| US4783463A (en) | 1985-10-23 | 1988-11-08 | Rorer Pharmaceutical Corporation | Pyridyl-pyridazinone and pyridyl-pyrazolinone compounds and their use in the treatment of congestive heart failure |
| DE3541716A1 (de) | 1985-11-26 | 1987-05-27 | Celamerck Gmbh & Co Kg | Neue acrylsaeureamide |
| FI91754C (fi) | 1986-12-02 | 1994-08-10 | Tanabe Seiyaku Co | Analogiamenetelmä lääkeaineena käyttökelpoisen imidatsolijohdannaisen valmistamiseksi |
| IT1205834B (it) * | 1987-04-22 | 1989-03-31 | Elbart | Derivati tiodiossolanici ad attivita' mucolitica a procedimento per la loro preparazione |
| FI902321A7 (fi) | 1989-05-19 | 1990-11-20 | Eisai Co Ltd | Buteenihappojohdannaiset |
| JPH03206042A (ja) | 1990-01-06 | 1991-09-09 | Takeda Chem Ind Ltd | 降圧剤 |
| ES2100943T3 (es) * | 1990-02-08 | 1997-07-01 | Eisai Co Ltd | Derivado de bencenosulfonamida. |
| AU680870B2 (en) | 1993-04-28 | 1997-08-14 | Astellas Pharma Inc. | New heterocyclic compounds |
| GB9402807D0 (en) | 1994-02-14 | 1994-04-06 | Xenova Ltd | Pharmaceutical compounds |
| EP0784612A1 (en) | 1994-10-04 | 1997-07-23 | Fujisawa Pharmaceutical Co., Ltd. | Urea derivatives and their use as acat-inhibitors |
| JPH08283219A (ja) | 1995-04-07 | 1996-10-29 | Eisai Co Ltd | アラルキルアミノアルキルアミド誘導体 |
| ES2175404T3 (es) | 1996-05-10 | 2002-11-16 | Icos Corp | Derivados de carbolina. |
| BR9710752A (pt) | 1996-07-22 | 1999-08-17 | Monsanto Co | Inbidores de metaloprotease de sulfonamida de tiol |
| WO1998024785A1 (en) | 1996-12-02 | 1998-06-11 | Fujisawa Pharmaceutical Co., Ltd. | Indole-urea derivatives with 5-ht antagonist properties |
| AU6520098A (en) | 1997-03-31 | 1998-10-22 | Takeda Chemical Industries Ltd. | Azole compounds, their production and their use |
| JP3108997B2 (ja) | 1997-03-31 | 2000-11-13 | 武田薬品工業株式会社 | アゾール化合物、その製造法および用途 |
| TW379224B (en) | 1997-12-02 | 2000-01-11 | Fujisawa Pharmaceutical Co | Urea derivatives |
| NZ505515A (en) * | 1997-12-31 | 2003-03-28 | Univ Kansas | Water soluble prodrugs of secondary and tertiary amine containing drugs and methods of making thereof |
| GB9816984D0 (en) | 1998-08-05 | 1998-09-30 | Smithkline Beecham Plc | Novel compounds |
| US6235728B1 (en) * | 1999-02-19 | 2001-05-22 | Bristol-Myers Squibb Company | Water-soluble prodrugs of azole compounds |
| WO2000050391A1 (en) | 1999-02-26 | 2000-08-31 | Merck & Co., Inc. | Novel sulfonamide compounds and uses thereof |
| WO2000051981A1 (en) | 1999-03-04 | 2000-09-08 | Nortran Pharmaceuticals Inc. | Aminocycloalkyl cinnamide compounds for arrhythmia and as analgesics and anesthetics |
| WO2001068585A1 (en) | 2000-03-14 | 2001-09-20 | Fujisawa Pharmaceutical Co., Ltd. | Novel amide compounds |
| US20010051642A1 (en) * | 2000-04-17 | 2001-12-13 | Kyunghye Ahn | Method for treating Alzheimer's disease |
| CA2405170A1 (en) | 2000-04-24 | 2001-11-01 | Merck Frosst Canada & Co. | Method of treatment using phenyl and biaryl derivatives as prostaglandin e inhibitors and compounds useful therefore |
| HUP0400570A3 (en) * | 2000-12-04 | 2004-09-28 | Hoffmann La Roche | Phenylethenyl or phenylethinyl heteroaril derivatives as glutamate receptor antagonists, their use, process for their preparation and pharmaceutical compositions containing them |
| GB0108770D0 (en) * | 2001-04-06 | 2001-05-30 | Eisai London Res Lab Ltd | Inhibitors |
| WO2003022273A1 (en) | 2001-09-13 | 2003-03-20 | Boehringer Ingelheim Pharmaceuticals, Inc. | Methods of treating cytokine mediated diseases |
| DE60220424T2 (de) | 2001-09-14 | 2008-03-06 | Novo Nordisk A/S | NEUE LIGANDEN FÜR DIE HisB10 Zn2+ STELLEN DES INSULIN-HEXAMERS IN DER R-KONFORMATION |
| US7582657B2 (en) * | 2001-12-10 | 2009-09-01 | Amgen Inc. | Vanilloid receptor ligands and their use in treatments |
| BR0215182A (pt) | 2001-12-20 | 2004-10-19 | Bristol Myers Squibb Co | Derivados de (alfa)- (n-sulfonamido) acetamida como inibidores de (beta)-amilóide |
| JP2003206280A (ja) | 2001-12-28 | 2003-07-22 | Takeda Chem Ind Ltd | ビアリール化合物およびその用途 |
| WO2003062206A2 (en) | 2002-01-23 | 2003-07-31 | Arena Pharmaceuticals, Inc. | Small molecule modulators of the 5-ht2a serotonin receptor useful for the prophylaxis and treatment of disorders related thereto |
| GB0207436D0 (en) | 2002-03-28 | 2002-05-08 | Glaxo Group Ltd | Novel compounds |
| MXPA04011472A (es) * | 2002-05-22 | 2005-02-14 | Amgen Inc | Derivados de amino-piridina, piridina y piridazina para usarse como ligandos del receptor vaniloide para el tratamiento del dolor. |
| PT2527315E (pt) * | 2002-05-31 | 2014-06-24 | Proteotech Inc | Compostos, composições e métodos para o tratamento de doenças da amiloide e sinucleínopatias tais como doença de alzheimer, diabetes do tipo 2, e doença de parkinson |
| US7459476B2 (en) * | 2002-06-27 | 2008-12-02 | Elan Pharmaceuticals, Inc. | Methods for treating Alzheimer's disease using hydroxyethylene compounds containing a heterocyclic amide bond isostere |
| HRP20050022A2 (en) * | 2002-07-12 | 2006-03-31 | Sanofi-Aventis Deutschland Gmbh | Heterocyclically substituted benzoylureas, method for their production and their use as medicaments |
| US6900354B2 (en) | 2002-07-15 | 2005-05-31 | Hoffman-La Roche Inc. | 3-phenyl-propionamido, 3-phenyl-acrylamido and 3-phenyl-propynamido derivatives |
| CA2514363A1 (en) | 2003-02-12 | 2004-08-26 | Transtech Pharma, Inc. | Substituted azole derivatives as therapeutic agents |
| BRPI0410348A (pt) | 2003-05-14 | 2006-05-30 | Torreypines Therapeutics Inc | compostos e usos dos mesmos na modulação de amilóide-beta |
| CA2536954C (en) * | 2003-08-29 | 2012-11-27 | Exelixis, Inc. | C-kit modulators and methods of use |
| GEP20084571B (en) | 2003-12-22 | 2008-12-25 | Pfizer | Triazole derivatives as vasopressin antagonists |
| WO2005072731A1 (en) | 2004-01-29 | 2005-08-11 | X-Ceptor Therapeutics, Inc. | 3-phenyl-n- ((1, 3, 4) thiadiazol-2-yl) -acrylamide derivatives and related compounds as modulators of estrogen-related receptors for the treatment of e.g. cancer, rheumatoid arthritis or neurological disorders |
| EP1730118A1 (en) | 2004-02-12 | 2006-12-13 | Transtech Pharma, Inc. | Substituted azole derivatives, compositions, and methods of use |
| TWI335816B (en) * | 2004-05-26 | 2011-01-11 | Eisai R&D Man Co Ltd | Cinnamide compound |
| WO2006018662A2 (en) | 2004-08-16 | 2006-02-23 | Prosidion Limited | Aryl urea derivatives for treating obesity |
| DE602005019602D1 (de) | 2004-10-26 | 2010-04-08 | Eisai R&D Man Co Ltd | Amorphe form einer zimtsäureamidverbindung |
| US20060241038A1 (en) | 2005-04-20 | 2006-10-26 | Eisai Co., Ltd. | Therapeutic agent for Abeta related disorders |
| WO2007034282A2 (en) | 2005-09-19 | 2007-03-29 | Pfizer Products Inc. | Diaryl-imidazole compounds condensed with a heterocycle as c3a receptor antagonists |
| JPWO2007058304A1 (ja) * | 2005-11-18 | 2009-05-07 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | シンナミド化合物の塩またはそれらの溶媒和物 |
| EP1950211A4 (en) * | 2005-11-18 | 2011-08-31 | Eisai R&D Man Co Ltd | PROCESS FOR PREPARING A CINEMA ACID AMID DERIVATIVE |
| TWI370130B (en) | 2005-11-24 | 2012-08-11 | Eisai R&D Man Co Ltd | Two cyclic cinnamide compound |
| US20070117839A1 (en) * | 2005-11-24 | 2007-05-24 | Eisai R&D Management Co., Ltd. | Two cyclic cinnamide compound |
| AU2006317457B2 (en) * | 2005-11-24 | 2011-09-08 | Eisai R & D Management Co., Ltd. | Morpholine type cinnamide compound |
| TWI378091B (en) * | 2006-03-09 | 2012-12-01 | Eisai R&D Man Co Ltd | Multi-cyclic cinnamide derivatives |
| WO2007102580A1 (ja) | 2006-03-09 | 2007-09-13 | Eisai R & D Management Co., Ltd. | 多環式シンナミド誘導体 |
| US7737141B2 (en) | 2006-07-28 | 2010-06-15 | Eisai R&D Management Co., Ltd. | Prodrug of cinnamide compound |
| US8183276B2 (en) | 2007-02-08 | 2012-05-22 | Christian Fischer | Therapeutic agents |
| WO2008137102A2 (en) | 2007-05-04 | 2008-11-13 | Torreypines Therapeutics, Inc. | Methods of modulating amyloid beta and compounds useful therefor |
| CN101809019A (zh) | 2007-05-07 | 2010-08-18 | 先灵公司 | γ分泌酶调节剂 |
| MX2009012163A (es) * | 2007-05-11 | 2009-12-01 | Hoffmann La Roche | Hetarilanilinas como moduladores para beta-amiloide. |
| WO2008156580A1 (en) | 2007-06-13 | 2008-12-24 | Merck & Co., Inc. | Triazole derivatives for treating alzheimer's disease and related conditions |
| JP2010535762A (ja) | 2007-08-06 | 2010-11-25 | シェーリング コーポレイション | ガンマセクレターゼモジュレーター |
-
2006
- 2006-10-27 TW TW095139718A patent/TWI370130B/zh not_active IP Right Cessation
- 2006-11-01 RS RSP-2008/0242A patent/RS20080242A/sr unknown
- 2006-11-01 ES ES06822806T patent/ES2394364T3/es active Active
- 2006-11-01 PL PL06822806T patent/PL1953158T3/pl unknown
- 2006-11-01 CA CA2629512A patent/CA2629512C/en not_active Expired - Fee Related
- 2006-11-01 EA EA200801417A patent/EA014427B1/ru not_active IP Right Cessation
- 2006-11-01 BR BRPI0618890-7A patent/BRPI0618890A2/pt not_active IP Right Cessation
- 2006-11-01 WO PCT/JP2006/321877 patent/WO2007060821A1/ja not_active Ceased
- 2006-11-01 ME MEP-2008-49A patent/ME00040B/me unknown
- 2006-11-01 NZ NZ568422A patent/NZ568422A/en not_active IP Right Cessation
- 2006-11-01 KR KR1020087014992A patent/KR101296239B1/ko not_active Expired - Fee Related
- 2006-11-01 JP JP2007546389A patent/JP5178203B2/ja not_active Expired - Fee Related
- 2006-11-01 MY MYPI20081628A patent/MY144596A/en unknown
- 2006-11-01 AU AU2006317468A patent/AU2006317468B2/en not_active Ceased
- 2006-11-01 EP EP06822806A patent/EP1953158B1/en active Active
- 2006-11-01 GE GEAP200610709A patent/GEP20115172B/en unknown
- 2006-11-20 AR ARP060105075A patent/AR057915A1/es not_active Application Discontinuation
- 2006-11-21 PE PE2006001479A patent/PE20071029A1/es not_active Application Discontinuation
- 2006-11-22 SA SA6270432A patent/SA06270432B1/ar unknown
-
2008
- 2008-05-16 CR CR9983A patent/CR9983A/es not_active Application Discontinuation
- 2008-05-20 MA MA30952A patent/MA29968B1/fr unknown
- 2008-05-22 EC EC2008008466A patent/ECSP088466A/es unknown
- 2008-05-23 HN HN2008000792A patent/HN2008000792A/es unknown
- 2008-06-19 NO NO20082805A patent/NO20082805L/no not_active Application Discontinuation
-
2009
- 2009-03-13 US US12/403,565 patent/US8048878B2/en not_active Expired - Fee Related
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