MA33181B1 - Dérivés de pyrrolo [2,3-b]pyridine pour l'inhibition des kinases raf - Google Patents
Dérivés de pyrrolo [2,3-b]pyridine pour l'inhibition des kinases rafInfo
- Publication number
- MA33181B1 MA33181B1 MA34228A MA34228A MA33181B1 MA 33181 B1 MA33181 B1 MA 33181B1 MA 34228 A MA34228 A MA 34228A MA 34228 A MA34228 A MA 34228A MA 33181 B1 MA33181 B1 MA 33181B1
- Authority
- MA
- Morocco
- Prior art keywords
- pyrrolo
- pyridine
- difluoro
- carbonyl
- phenyl
- Prior art date
Links
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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Urology & Nephrology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Enzymes And Modification Thereof (AREA)
Abstract
L'INVENTION CONCERNE LE PROPANE-1-ACIDE SULFONIQUE {2,4-DIFLUORO-3-[5-(2-MÉTHOXY-PYRIMIDINE-5-YL)-1H-PYRROLO[2,3-B]PYRIDINE-3-CARBONYL]-PHÉNYL}-AMIDE, LE PROPANE-1-ACIDE SULFONIQUE [3-(5-CYANO-1H-PYRROLO[2,3-B]PYRIDINE-3-CARBONYL)-2,4-DIFLUORO-PHÉNYL]-AMIDE,LE PROPANE-1-ACIDE SULFONIQUE [3-(5-CYANO-1H-PYRROLO[2,3-B]PYRIDINE-3-CARBONYL)-2-FLUORO-PHÉNYL]-AMIDE, LE N-[3-(5-CYANO-1H-PYRROLO[2,3-B] PYRIDINE-3-CARBONYL)-2,4-DIFLUORO-PHÉNYL]-2,5-DIFLUORO-BENZÈNESULFONAMIDE,LE N-[3-(5-CYANO-1H-PYRROLO[2,3-B] PYRIDINE-3-CARBONYL)-2,4-DIFLUORO-PHÉNYL]-3-FLUORO-BENZÈNESULFONAMIDE, LE PYRROLIDINE-1-ACIDE SULFONIQUE [3-(5-CYANO-1H-PYRROLO[2,3-B] PYRIDINE-3-CARBONYL)-2,4-DIFLUORO-PHÉNYL]-AMIDE, LE N,N-DIMÉTHYLAMINO-ACIDE SULFONIQUE [3-(5-CYANO-1H-PYRROLO[2,3-B]PYRIDINE-3-CARBONYL)-2,4-DIFLUORO-PHÉNYL]-AMIDE, ET LEURS SELS, LEURS FORMULATIONS, LEURS CONJUGUÉS, LEURS DÉRIVÉS, LEURS FORMES ET LEURS UTILISATIONS. DANS CERTAINS ASPECTS ET MODES DE RÉALISATION, LES COMPOSÉS SELON L'INVENTION OU LEURS SELS, LEURS FORMULATIONS, LEURS CONJUGUÉS, LEURS DÉRIVÉS, ET LEURS FORMES SONT ACTIFS SUR AU MOINS UNE PROTÉINE KINASE RAF. L'INVENTION CONCERNE ÉGALEMENT LEURS PROCÉDÉS D'UTILISATION POUR TRAITER DES MALADIES ET DES ÉTATS, Y COMPRIS DES MALADIES ET ÉTATS ASSOCIÉS À L'ACTIVITÉ DES PROTÉINES KINASES RAF, NOTAMMENT LE MÉLANOME, LE GLIOME, LE CANCER COLORECTAL, LE CANCER DE LA THYROÏDE, LE CANCER DU POUMON, LE CANCER DE L'OVAIRE, LE CANCER DE LA PROSTATE, ET LE CANCER DU TRACTUS BILIAIRE.
Applications Claiming Priority (8)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15940209P | 2009-03-11 | 2009-03-11 | |
| US15939509P | 2009-03-11 | 2009-03-11 | |
| US15939009P | 2009-03-11 | 2009-03-11 | |
| US15940009P | 2009-03-11 | 2009-03-11 | |
| US15939209P | 2009-03-11 | 2009-03-11 | |
| US15939609P | 2009-03-11 | 2009-03-11 | |
| US15940609P | 2009-03-11 | 2009-03-11 | |
| PCT/US2010/026816 WO2010104945A1 (fr) | 2009-03-11 | 2010-03-10 | Dérivés de pyrrolo [2, 3-b] pyridine pour l'inhibition des kinases raf |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MA33181B1 true MA33181B1 (fr) | 2012-04-02 |
Family
ID=42199540
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA34228A MA33181B1 (fr) | 2009-03-11 | 2010-03-10 | Dérivés de pyrrolo [2,3-b]pyridine pour l'inhibition des kinases raf |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US8901301B2 (fr) |
| EP (1) | EP2406259A1 (fr) |
| JP (1) | JP2012520307A (fr) |
| KR (1) | KR101663339B1 (fr) |
| CN (1) | CN102421776A (fr) |
| AR (1) | AR075812A1 (fr) |
| AU (1) | AU2010224245B2 (fr) |
| BR (1) | BRPI1011515A2 (fr) |
| CA (1) | CA2755045A1 (fr) |
| CO (1) | CO6620074A2 (fr) |
| CR (1) | CR20110476A (fr) |
| EC (1) | ECSP11011313A (fr) |
| MA (1) | MA33181B1 (fr) |
| MX (1) | MX2011009489A (fr) |
| MY (1) | MY161861A (fr) |
| NI (1) | NI201100168A (fr) |
| NO (1) | NO20111241A1 (fr) |
| PE (1) | PE20120184A1 (fr) |
| RU (1) | RU2011141123A (fr) |
| SG (2) | SG174257A1 (fr) |
| TW (1) | TW201036973A (fr) |
| WO (1) | WO2010104945A1 (fr) |
| ZA (1) | ZA201106599B (fr) |
Families Citing this family (61)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008063888A2 (fr) | 2006-11-22 | 2008-05-29 | Plexxikon, Inc. | Composés modulant l'activité de c-fms et/ou de c-kit et utilisations associées |
| JP2010533729A (ja) | 2007-07-17 | 2010-10-28 | プレキシコン,インコーポレーテッド | キナーゼ調節のための化合物と方法、及びそのための適応 |
| US8158636B2 (en) | 2008-05-19 | 2012-04-17 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| EP2356116A1 (fr) | 2008-11-20 | 2011-08-17 | OSI Pharmaceuticals, Inc. | Pyrroloý2,3-b¨-pyridines et pyrroloý2,3-b¨-pyrazines substituées |
| CA2738573C (fr) | 2009-04-03 | 2013-02-19 | F. Hoffmann-La Roche Ag | Compositions et utilisations associees |
| JP2013510166A (ja) | 2009-11-06 | 2013-03-21 | プレキシコン インコーポレーテッド | キナーゼ調節のための化合物、方法およびその適用 |
| EP2501236B1 (fr) | 2009-11-18 | 2017-03-29 | Plexxikon Inc. | Dérivés de la benzènesulfonamide de N-[2-fluoro-3-(4-amino-7H-pyrrolo[2,3-d]pyrimidine-5-carbonyl)-phényl]-4- en tant que modulateurs de la kinase du protein Raf pour le traitement du cancer |
| CA2784393A1 (fr) | 2009-12-23 | 2011-06-30 | Plexxikon, Inc. | Composes et methodes pour la modulation des kinases, et leurs indications |
| TWI510487B (zh) | 2010-04-21 | 2015-12-01 | Plexxikon Inc | 用於激酶調節的化合物和方法及其適應症 |
| US20130072495A1 (en) | 2010-05-14 | 2013-03-21 | OSI Pharmaceuticals, LLC | Fused bicyclic kinase inhibitors |
| AR081039A1 (es) | 2010-05-14 | 2012-05-30 | Osi Pharmaceuticals Llc | Inhibidores biciclicos fusionados de quinasa |
| WO2012075327A1 (fr) | 2010-12-02 | 2012-06-07 | University Of Pittsburgh-Of The Commonwealth System Of Higher Education | Méthodes de traitement d'une tumeur au moyen d'un anticorps qui se lie spécifiquement à grp94 |
| PE20141360A1 (es) * | 2011-02-07 | 2014-10-13 | Plexxikon Inc | Compuestos y metodos para la modulacion de quinasas e indicaciones para los mismos. |
| WO2012149547A1 (fr) * | 2011-04-28 | 2012-11-01 | Duke University | Procédés de traitement d'hémoglobinopathies |
| CA2836474A1 (fr) | 2011-05-17 | 2012-11-22 | Plexxikon Inc. | Modulation de kinase et indications pour celle-ci |
| US9988687B2 (en) * | 2011-09-20 | 2018-06-05 | The George Washington Univeristy | Companion diagnostics for cancer and screening methods to identify companion diagnostics for cancer based on splicing variants |
| US9249110B2 (en) | 2011-09-21 | 2016-02-02 | Neupharma, Inc. | Substituted quinoxalines as B-raf kinase inhibitors |
| US20130172375A1 (en) * | 2011-12-13 | 2013-07-04 | Hoffmann-La Roche Inc. | Pharmaceutical composition |
| US9358235B2 (en) | 2012-03-19 | 2016-06-07 | Plexxikon Inc. | Kinase modulation, and indications therefor |
| US9150570B2 (en) * | 2012-05-31 | 2015-10-06 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
| US20150182490A1 (en) | 2012-06-26 | 2015-07-02 | Del Mar Pharmaceuticals | Methods for treating tyrosine-kinase-inhibitor-resistant malignancies in patients with genetic polymorphisms or ahi1 dysregulations or mutations employing dianhydrogalactitol, diacetyldianhydrogalactitol, dibromodulcitol, or analogs or derivatives thereof |
| TWI601725B (zh) | 2012-08-27 | 2017-10-11 | 加拓科學公司 | 取代的氮雜吲哚化合物及其鹽、組合物和用途 |
| JP6318156B2 (ja) | 2012-09-06 | 2018-04-25 | プレキシコン インコーポレーテッドPlexxikon Inc. | キナーゼをモジュレートするための化合物および方法、ならびにその指標 |
| US9861685B2 (en) | 2012-11-20 | 2018-01-09 | Duke University | Methods of treating hemoglobinopathies |
| ME03000B (fr) | 2012-12-21 | 2018-10-20 | Plexxikon Inc | Composés et procédés pour la modulation de kinase, et indications associées |
| US20140303121A1 (en) | 2013-03-15 | 2014-10-09 | Plexxikon Inc. | Heterocyclic compounds and uses thereof |
| CN105073747B (zh) | 2013-03-15 | 2017-06-06 | 普莱希科公司 | 杂环化合物及其应用 |
| CN105492011A (zh) | 2013-04-08 | 2016-04-13 | 丹尼斯·M·布朗 | 不理想给药化学化合物的治疗增效 |
| RU2015149937A (ru) | 2013-05-30 | 2017-07-06 | Плексксикон Инк. | Соединения для модулирования киназы и показания к их применению |
| WO2015108907A2 (fr) | 2014-01-14 | 2015-07-23 | Dana-Farber Cancer Institute, Inc. | Compositions et méthodes pour l'identification, l'évaluation, la prévention, et le traitement d'un mélanome à l'aide d'isoformes de pd-l1 |
| US9771369B2 (en) | 2014-03-04 | 2017-09-26 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| ES2774177T3 (es) | 2014-09-15 | 2020-07-17 | Plexxikon Inc | Compuestos heterocíclicos y usos de estos |
| US20170248603A1 (en) | 2014-10-06 | 2017-08-31 | Dana-Farber Cancer Institute, Inc. | Angiopoiten-2 biomarkers predictive of anti-immune checkpoint response |
| US10160755B2 (en) | 2015-04-08 | 2018-12-25 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| CN112574196A (zh) | 2015-05-06 | 2021-03-30 | 普莱希科公司 | 调节激酶的1H-吡咯并[2,3-b]吡啶衍生物的合成 |
| SMT202000535T1 (it) | 2015-05-06 | 2020-11-10 | Plexxikon Inc | Forme solide di composto modulante chinasi |
| US10829484B2 (en) | 2015-07-28 | 2020-11-10 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| HK1255102A1 (zh) | 2015-09-21 | 2019-08-02 | Plexxikon Inc. | 杂环化合物及其应用 |
| US9938273B2 (en) | 2015-12-07 | 2018-04-10 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| US10160747B2 (en) | 2016-03-16 | 2018-12-25 | Plexxikon Inc. | Compounds and methods for kinase modulation, and indications therefor |
| TW201815766A (zh) | 2016-09-22 | 2018-05-01 | 美商普雷辛肯公司 | 用於ido及tdo調節之化合物及方法以及其適應症 |
| JP7193460B2 (ja) | 2016-12-23 | 2022-12-20 | プレキシコン インコーポレーテッド | Cdk8調節およびその適応症のための化合物および方法 |
| US11040027B2 (en) | 2017-01-17 | 2021-06-22 | Heparegenix Gmbh | Protein kinase inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death |
| WO2018175311A1 (fr) | 2017-03-20 | 2018-09-27 | Plexxikon Inc. | Formes cristallines de l'acide 4-(1-(1,1-di(pyridin-2-yl)éthyl)-6-(3,5-diméthylisoxazol-4-yl)-1h- pyrrolo[3,2-b]pyridin-3-yl)benzoïque inhibiteur de bromodomaine |
| WO2018226846A1 (fr) | 2017-06-07 | 2018-12-13 | Plexxikon Inc. | Composés et procédés de modulation de kinase |
| BR112019028235B1 (pt) | 2017-07-25 | 2024-04-30 | Plexxikon, Inc. | Composições e seus métodos de preparação |
| US10717735B2 (en) | 2017-10-13 | 2020-07-21 | Plexxikon Inc. | Solid forms of a compound for modulating kinases |
| CA3080197C (fr) | 2017-10-27 | 2023-12-19 | Plexxikon Inc. | Formulation d'un compose modulant les kinases |
| AU2019216264B2 (en) | 2018-01-31 | 2023-08-31 | Heparegenix Gmbh | Protein kinase MKK4 inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death |
| US11149011B2 (en) | 2018-03-20 | 2021-10-19 | Plexxikon Inc. | Compounds and methods for IDO and TDO modulation, and indications therefor |
| GB201809460D0 (en) * | 2018-06-08 | 2018-07-25 | Crt Pioneer Fund Lp | Salt form |
| WO2019243315A1 (fr) | 2018-06-21 | 2019-12-26 | Heparegenix Gmbh | Inhibiteurs de protéine kinase tricycliques pour favoriser la régénération du foie ou réduire ou prévenir la mort des hépatocytes |
| SG11202012732UA (en) | 2018-07-16 | 2021-02-25 | Heparegenix Gmbh | Protein kinase inhibitors for promoting liver regeneration or reducing or preventing hepatocyte death |
| JP7636646B2 (ja) | 2019-04-09 | 2025-02-27 | オプナ バイオ ソシエテ アノニム | Ep300またはcbpの調節のための縮合アジンおよびその適応 |
| JP7629442B2 (ja) | 2019-07-29 | 2025-02-13 | ヘパリジェニックス ゲーエムベーハー | 肝臓再生を促進または肝細胞死を縮減もしくは防止するためのヘテロアリール置換ピラゾロ-ピリジンタンパク質キナーゼ阻害剤 |
| WO2021113625A1 (fr) | 2019-12-06 | 2021-06-10 | Plexxikon Inc. | Composés et procédés de modulation de cd73 et leurs indications |
| CA3164361A1 (fr) | 2020-01-15 | 2021-07-22 | Heparegenix Gmbh | Derives de 3-benzoyl-1h-pyrrolo[2,3-b]pyridine utilises en tant qu'inhibiteurs de mkk4 pour le traitement de maladies du foie |
| JP7842698B2 (ja) | 2020-04-23 | 2026-04-08 | オプナ バイオ ソシエテ アノニム | Cd73調節のための化合物及び方法並びにそれらの表示 |
| AU2021263383A1 (en) | 2020-04-29 | 2022-11-24 | Plexxikon Inc. | Synthesis of heterocyclic compounds |
| WO2021255212A1 (fr) | 2020-06-19 | 2021-12-23 | F. Hoffmann-La Roche Ag | Agents de dégradation de braf |
| AU2021327375A1 (en) | 2020-08-21 | 2023-03-16 | Opna Bio SA | Combinational drug anticancer therapies |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20140070676A (ko) | 2002-09-06 | 2014-06-10 | 인설트 테라페틱스, 인코퍼레이티드 | 공유결합된 치료제 전달을 위한 사이클로덱스트린-기초 중합체 |
| MY153898A (en) * | 2005-06-22 | 2015-04-15 | Plexxikon Inc | Compounds and methods for kinase modulation, and indications therefor |
| PE20121126A1 (es) * | 2006-12-21 | 2012-08-24 | Plexxikon Inc | Compuestos pirrolo [2,3-b] piridinas como moduladores de quinasa |
-
2010
- 2010-03-10 AR ARP100100731A patent/AR075812A1/es unknown
- 2010-03-10 AU AU2010224245A patent/AU2010224245B2/en active Active
- 2010-03-10 WO PCT/US2010/026816 patent/WO2010104945A1/fr not_active Ceased
- 2010-03-10 EP EP10708681A patent/EP2406259A1/fr not_active Withdrawn
- 2010-03-10 MA MA34228A patent/MA33181B1/fr unknown
- 2010-03-10 RU RU2011141123/04A patent/RU2011141123A/ru unknown
- 2010-03-10 PE PE2011001620A patent/PE20120184A1/es not_active Application Discontinuation
- 2010-03-10 SG SG2011063914A patent/SG174257A1/en unknown
- 2010-03-10 CN CN2010800206771A patent/CN102421776A/zh active Pending
- 2010-03-10 KR KR1020117023712A patent/KR101663339B1/ko not_active Expired - Fee Related
- 2010-03-10 SG SG10201402977WA patent/SG10201402977WA/en unknown
- 2010-03-10 BR BRPI1011515A patent/BRPI1011515A2/pt not_active Application Discontinuation
- 2010-03-10 MY MYPI2011004233A patent/MY161861A/en unknown
- 2010-03-10 US US12/721,496 patent/US8901301B2/en active Active
- 2010-03-10 JP JP2011554147A patent/JP2012520307A/ja not_active Withdrawn
- 2010-03-10 MX MX2011009489A patent/MX2011009489A/es not_active Application Discontinuation
- 2010-03-10 CA CA2755045A patent/CA2755045A1/fr not_active Abandoned
- 2010-03-10 TW TW099106990A patent/TW201036973A/zh unknown
-
2011
- 2011-08-09 EC EC2011011313A patent/ECSP11011313A/es unknown
- 2011-09-06 CR CR20110476A patent/CR20110476A/es unknown
- 2011-09-08 ZA ZA2011/06599A patent/ZA201106599B/en unknown
- 2011-09-09 NI NI201100168A patent/NI201100168A/es unknown
- 2011-09-12 CO CO11117856A patent/CO6620074A2/es not_active Application Discontinuation
- 2011-09-13 NO NO20111241A patent/NO20111241A1/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| PE20120184A1 (es) | 2012-03-28 |
| BRPI1011515A2 (pt) | 2016-03-29 |
| CO6620074A2 (es) | 2013-02-15 |
| CR20110476A (es) | 2012-01-04 |
| KR20110125670A (ko) | 2011-11-21 |
| WO2010104945A1 (fr) | 2010-09-16 |
| AR075812A1 (es) | 2011-04-27 |
| US8901301B2 (en) | 2014-12-02 |
| NI201100168A (es) | 2012-01-11 |
| TW201036973A (en) | 2010-10-16 |
| US20100286178A1 (en) | 2010-11-11 |
| NO20111241A1 (no) | 2011-09-28 |
| KR101663339B1 (ko) | 2016-10-06 |
| AU2010224245B2 (en) | 2016-07-21 |
| ECSP11011313A (es) | 2011-10-31 |
| MX2011009489A (es) | 2011-10-11 |
| RU2011141123A (ru) | 2013-04-20 |
| JP2012520307A (ja) | 2012-09-06 |
| SG174257A1 (en) | 2011-10-28 |
| CA2755045A1 (fr) | 2010-09-16 |
| ZA201106599B (en) | 2014-02-26 |
| AU2010224245A1 (en) | 2011-09-29 |
| CN102421776A (zh) | 2012-04-18 |
| EP2406259A1 (fr) | 2012-01-18 |
| SG10201402977WA (en) | 2014-09-26 |
| MY161861A (en) | 2017-05-15 |
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