PE20100561A1 - Derivados de piridazina como agentes inhibidores de esteaorilcoa desaturasa - Google Patents
Derivados de piridazina como agentes inhibidores de esteaorilcoa desaturasaInfo
- Publication number
- PE20100561A1 PE20100561A1 PE2010000343A PE2010000343A PE20100561A1 PE 20100561 A1 PE20100561 A1 PE 20100561A1 PE 2010000343 A PE2010000343 A PE 2010000343A PE 2010000343 A PE2010000343 A PE 2010000343A PE 20100561 A1 PE20100561 A1 PE 20100561A1
- Authority
- PE
- Peru
- Prior art keywords
- alkyl
- pyridazine
- piperazin
- amide
- desaturase
- Prior art date
Links
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical class C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 title abstract 2
- 230000002401 inhibitory effect Effects 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 101000874179 Homo sapiens Syndecan-1 Proteins 0.000 abstract 2
- 102100035721 Syndecan-1 Human genes 0.000 abstract 2
- 150000001408 amides Chemical class 0.000 abstract 2
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 102000034570 NR1 subfamily Human genes 0.000 abstract 1
- 108020001305 NR1 subfamily Proteins 0.000 abstract 1
- -1 PYRIDAZINE-3-CARBOXYL (2-CYCLOPROPYL-ETHYL) AMIDE Chemical compound 0.000 abstract 1
- 102000003728 Peroxisome Proliferator-Activated Receptors Human genes 0.000 abstract 1
- 108090000029 Peroxisome Proliferator-Activated Receptors Proteins 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Substances 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 150000002632 lipids Chemical class 0.000 abstract 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-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
- C07D237/20—Nitrogen atoms
-
- 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
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
- A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
-
- 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
- A61P3/06—Antihyperlipidemics
-
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/12—Antidiuretics, e.g. drugs for diabetes insipidus
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-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
- C07D237/22—Nitrogen and oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-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
- C07D237/24—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Diabetes (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Endocrinology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Child & Adolescent Psychology (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
REFERIDA A COMPUESTOS DERIVADOS DE PIRIDAZINA DE FORMULA (Ia), DONDE X E Y SON 1; W ES C(O)NR1, NR1C(O), ENTRE OTROS; V ES C(O), C(O)O, C(S), ENTRE OTROS; R1 ES H, ALQUILO C1-C6, ALQUILO C2-C6, ENTRE OTROS; R2 ES ALQUILO C1-C12, ALQUENILO C2-C12, ENTRE OTROS; R3 ES ALQUILO C1-C12, ALQUENILO C2-C12, ALCOXI C1-C12, ENTRE OTROS; R4 Y R5 SON H, FLUORO, CLORO, METILO, METOXI, ENTRE OTROS; R6, R6a, R7, R7a, R8, R8a, R9 Y R9a SON H O ALQUILO C1-C3; R10 ES H O ALQUILO C1-C3; R12 ES H O ALQUILO C1-C6. SON COMPUESTOS PREFERIDOS: ACIDO 6-[4-(2-ETILBUTIRIL)PIPERAZIN-1-IL]PIRIDAZINA-3-CARBOXILICO(2-CICLOPROPILETIL)AMIDA, ACIDO 6-[4-(3,3,3-TRIFLUORO-2-METIL-2-TRIFLUOROMETILPROPIONIL)PIPERAZIN-1-IL]PIRIDAZINA-3-CARBOXILICO(2-CICLOPROPILETIL)AMIDA, ACIDO 6-[4-(4,4,4-TRIFLUORO-3-TRIFLUOROMETILBUT-2-ENOIL)-PIPERAZIN-1-IL]PIRIDAZINA-3-CARBOXILICO(2-CICLOPROPIL-ETIL)AMIDA, ENTRE OTROS. DICHOS COMPUESTOS SON INHIBIDORES DE ESTEAORIL-COA DESATURASA (SDC), PREFERENTEMENTE, SDC1 Y SON UTILES EN EL TRATAMIENTO DE ENFERMEDADES RELACIONADAS CON LOS NIVELES ELEVADOS DE LIPIDOS, ENFERMEDADES CARDIOVASCULARES, DIABETES, OBESIDAD, SINDROME METABOLICO, ENTRE OTROS
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/055,034 US7754711B2 (en) | 2003-07-30 | 2005-02-09 | Pyridazine derivatives and their use as therapeutic agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20100561A1 true PE20100561A1 (es) | 2010-08-25 |
Family
ID=36646207
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2006000153A PE20061065A1 (es) | 2005-02-09 | 2006-02-09 | Derivados de piridazina como agentes inhibidores de esteaoril-coa desaturasa |
| PE2010000343A PE20100561A1 (es) | 2005-02-09 | 2006-02-09 | Derivados de piridazina como agentes inhibidores de esteaorilcoa desaturasa |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2006000153A PE20061065A1 (es) | 2005-02-09 | 2006-02-09 | Derivados de piridazina como agentes inhibidores de esteaoril-coa desaturasa |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US7754711B2 (es) |
| EP (1) | EP1851205B1 (es) |
| JP (1) | JP5114212B2 (es) |
| CN (2) | CN102600162A (es) |
| AR (1) | AR052902A1 (es) |
| AT (1) | ATE553096T1 (es) |
| AU (2) | AU2006212763A1 (es) |
| BR (1) | BRPI0606817A2 (es) |
| CA (1) | CA2597069C (es) |
| ES (1) | ES2385577T3 (es) |
| GT (1) | GT200600045A (es) |
| MX (1) | MX2007009593A (es) |
| MY (1) | MY141939A (es) |
| PE (2) | PE20061065A1 (es) |
| TW (1) | TWI320316B (es) |
| WO (1) | WO2006086447A2 (es) |
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| US20050119251A1 (en) * | 2001-12-21 | 2005-06-02 | Jian-Min Fu | Nicotinamide derivatives and their use as therapeutic agents |
| US7759348B2 (en) * | 2003-07-30 | 2010-07-20 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives and their use as therapeutic agents |
| AR051090A1 (es) * | 2004-09-20 | 2006-12-20 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como inhibidores de la estearoil-coa desaturasa |
| AR051093A1 (es) * | 2004-09-20 | 2006-12-20 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como inhibidores de estearoil-coa desaturasa |
| CN101090724A (zh) * | 2004-09-20 | 2007-12-19 | 泽农医药公司 | 用于抑制人硬脂酰CoA去饱和酶的吡啶衍生物 |
| US7547698B2 (en) * | 2004-09-20 | 2009-06-16 | Xenon Pharmaceuticals Inc. | Bicyclic heterocyclic derivatives and their use as inhibitors of stearoyl-coadesaturase (SCD) |
| MX2007003332A (es) * | 2004-09-20 | 2007-06-05 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como inhibidores de estearoil-coa-desaturasa. |
| AU2005286728A1 (en) * | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as mediators of stearoyl-CoA desaturase |
| EP1830837B1 (en) | 2004-09-20 | 2013-09-04 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives for the treatment of diseases mediated by stearoyl-coa desaturase enzymes |
| JP5149009B2 (ja) * | 2004-09-20 | 2013-02-20 | ゼノン・ファーマシューティカルズ・インコーポレイテッド | ヒトステアロイル−CoAデサチュラーゼを阻害するためのピリダジン誘導体 |
| MX2007003325A (es) * | 2004-09-20 | 2007-06-05 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como inhibidores estearoil-coa-desaturasa. |
| EP2029138A1 (en) * | 2005-06-03 | 2009-03-04 | Xenon Pharmaceuticals Inc. | Aminothiazole derivatives as human stearoyl-coa desaturase inhibitors |
| CN101506203B (zh) | 2006-08-24 | 2013-10-16 | 诺瓦提斯公司 | 治疗代谢病、心血管病和其他病症的作为硬脂酰辅酶a脱饱和酶(scd)抑制剂的2-(吡嗪-2-基)-噻唑和2-(1h-吡唑-3-基)-噻唑衍生物及相关化合物 |
| WO2008029266A1 (en) * | 2006-09-08 | 2008-03-13 | Glenmark Pharmaceuticals S.A. | Stearoyl coa desaturase inhibitors |
| WO2008046226A1 (en) * | 2006-10-20 | 2008-04-24 | Merck Frosst Canada Ltd. | Azacycloalkane derivatives as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
| AU2007323193A1 (en) * | 2006-11-20 | 2008-05-29 | Glenmark Pharmaceuticals S.A. | Acetylene derivatives as Stearoyl CoA Desaturase inhibitors |
| TW200826936A (en) | 2006-12-01 | 2008-07-01 | Merck Frosst Canada Ltd | Azacycloalkane derivatives as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
| AR064965A1 (es) | 2007-01-26 | 2009-05-06 | Merck Frosst Canada Inc | Derivados de azacicloalcanos como inhibidores de estearoil - coenzima a delta -9 desaturasa |
| US8575167B2 (en) | 2007-02-06 | 2013-11-05 | Takeda Pharmaceutical Company Limited | Spiro compounds having stearoyl-CoA desaturase action |
| ES2571533T3 (es) * | 2007-04-27 | 2016-05-25 | Purdue Pharma Lp | Antagonistas de TRPV1 y usos de los mismos |
| WO2008157844A1 (en) * | 2007-06-21 | 2008-12-24 | Forest Laboratories Holdings Limited | Novel piperazine derivatives as inhibitors of stearoyl-coa desaturase |
| WO2009037542A2 (en) | 2007-09-20 | 2009-03-26 | Glenmark Pharmaceuticals, S.A. | Spirocyclic compounds as stearoyl coa desaturase inhibitors |
| WO2010075356A1 (en) * | 2008-12-23 | 2010-07-01 | Forest Laboratories Holdings Limited | Novel piperazine derivatives as inhibitors of stearoyl-coa desaturase |
| AU2010215035B2 (en) | 2009-02-17 | 2014-06-12 | Merck Canada Inc. | Novel spiro compounds useful as inhibitors of stearoyl-coenzyme A delta-9 desaturase |
| WO2011011872A1 (en) | 2009-07-28 | 2011-02-03 | Merck Frosst Canada Ltd. | Novel spiro compounds useful as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
| JP2011057661A (ja) * | 2009-08-14 | 2011-03-24 | Bayer Cropscience Ag | 殺虫性カルボキサミド類 |
| WO2011030312A1 (en) | 2009-09-10 | 2011-03-17 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | NOVEL INHIBITORS OF STEAROYL-CoA-DESATURASE-1 AND THEIR USES |
| ES2620528T3 (es) | 2011-06-22 | 2017-06-28 | Purdue Pharma Lp | Antagonistas de TRPV1 que incluyen un sustituyente dihidroxi y usos de los mismos |
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| CN110637015B (zh) | 2017-03-15 | 2024-04-02 | 奥加诺沃公司 | 法尼醇x受体激动剂及其用途 |
| JP7174709B2 (ja) | 2017-03-15 | 2022-11-17 | メタクリン,インク. | ファルネソイドx受容体アゴニストおよびその使用 |
| US11873298B2 (en) | 2017-10-24 | 2024-01-16 | Janssen Pharmaceutica Nv | Compounds and uses thereof |
| AU2019238326B2 (en) | 2018-03-23 | 2025-03-06 | Janssen Pharmaceutica Nv | Compounds and uses thereof |
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| US20230078764A1 (en) * | 2019-03-22 | 2023-03-16 | Yumanity Therapeutics, Inc. | Compounds and uses thereof |
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| TWI345974B (en) * | 2003-07-30 | 2011-08-01 | Xenon Pharmaceuticals Inc | Pyridazine derivatives and their use in the inhibition of stearoyl-coa desaturase |
| ES2386353T3 (es) | 2003-07-30 | 2012-08-17 | Xenon Pharmaceuticals Inc. | Derivados de piridazina y su uso como agentes terapéuticos |
| MX2007003325A (es) * | 2004-09-20 | 2007-06-05 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como inhibidores estearoil-coa-desaturasa. |
| CA2615045A1 (en) * | 2005-07-20 | 2007-01-25 | Merck Frosst Canada Ltd. | Heteroaromatic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
-
2005
- 2005-02-09 US US11/055,034 patent/US7754711B2/en not_active Expired - Fee Related
-
2006
- 2006-02-07 GT GT200600045A patent/GT200600045A/es unknown
- 2006-02-08 JP JP2007555182A patent/JP5114212B2/ja not_active Expired - Fee Related
- 2006-02-08 AT AT06748193T patent/ATE553096T1/de active
- 2006-02-08 AU AU2006212763A patent/AU2006212763A1/en not_active Abandoned
- 2006-02-08 MY MYPI20060535A patent/MY141939A/en unknown
- 2006-02-08 ES ES06748193T patent/ES2385577T3/es active Active
- 2006-02-08 CA CA2597069A patent/CA2597069C/en not_active Expired - Fee Related
- 2006-02-08 WO PCT/US2006/004389 patent/WO2006086447A2/en not_active Ceased
- 2006-02-08 BR BRPI0606817-0A patent/BRPI0606817A2/pt not_active IP Right Cessation
- 2006-02-08 EP EP06748193A patent/EP1851205B1/en not_active Not-in-force
- 2006-02-08 CN CN201210057740XA patent/CN102600162A/zh active Pending
- 2006-02-08 CN CNA2006800097087A patent/CN101160289A/zh active Pending
- 2006-02-08 MX MX2007009593A patent/MX2007009593A/es active IP Right Grant
- 2006-02-09 PE PE2006000153A patent/PE20061065A1/es not_active Application Discontinuation
- 2006-02-09 PE PE2010000343A patent/PE20100561A1/es not_active Application Discontinuation
- 2006-02-09 AR ARP060100466A patent/AR052902A1/es unknown
- 2006-02-09 TW TW095104384A patent/TWI320316B/zh not_active IP Right Cessation
-
2010
- 2010-10-06 AU AU2010227003A patent/AU2010227003B2/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| JP5114212B2 (ja) | 2013-01-09 |
| WO2006086447A3 (en) | 2007-04-05 |
| TWI320316B (en) | 2010-02-11 |
| BRPI0606817A2 (pt) | 2009-07-14 |
| GT200600045A (es) | 2006-09-13 |
| ES2385577T3 (es) | 2012-07-26 |
| CN101160289A (zh) | 2008-04-09 |
| AU2010227003B2 (en) | 2012-06-14 |
| JP2008530098A (ja) | 2008-08-07 |
| AU2006212763A1 (en) | 2006-08-17 |
| PE20061065A1 (es) | 2006-12-01 |
| ATE553096T1 (de) | 2012-04-15 |
| US7754711B2 (en) | 2010-07-13 |
| AR052902A1 (es) | 2007-04-11 |
| WO2006086447A2 (en) | 2006-08-17 |
| CA2597069A1 (en) | 2006-08-17 |
| EP1851205B1 (en) | 2012-04-11 |
| CN102600162A (zh) | 2012-07-25 |
| US20060009459A1 (en) | 2006-01-12 |
| TW200638935A (en) | 2006-11-16 |
| EP1851205A2 (en) | 2007-11-07 |
| MY141939A (en) | 2010-07-30 |
| MX2007009593A (es) | 2007-10-16 |
| CA2597069C (en) | 2011-09-20 |
| AU2010227003A1 (en) | 2010-10-28 |
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