MX2011009034A - Formas de profarmaco de inhibidores de cinasa y su uso en la terapia. - Google Patents
Formas de profarmaco de inhibidores de cinasa y su uso en la terapia.Info
- Publication number
- MX2011009034A MX2011009034A MX2011009034A MX2011009034A MX2011009034A MX 2011009034 A MX2011009034 A MX 2011009034A MX 2011009034 A MX2011009034 A MX 2011009034A MX 2011009034 A MX2011009034 A MX 2011009034A MX 2011009034 A MX2011009034 A MX 2011009034A
- Authority
- MX
- Mexico
- Prior art keywords
- aromatic
- kinase inhibitor
- compounds
- ntr
- reductively
- 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
- A61K31/41—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
- 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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines 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
- A61K31/495—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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/94—Nitrogen atoms
-
- 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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- 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
- C07D401/14—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 three or more hetero 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
- C07D403/12—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 chain containing hetero atoms as chain links
-
- 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
- C07D403/14—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 three or more hetero rings
-
- 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
- C07D405/14—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 three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La invención proporciona compuestos de profármaco novedosos que comprenden un inhibidor de cinasa y un iniciador de nitroheterociclo aromático o nitrocarbocjclo aromático de fragmentación activado reductivamente, donde el compuesto lleva una carga positiva. En modalidades preferidas, los compuestos son de la Fórmula I: donde: X es cualquier contraión con carga negativa; R1 es un grupo de la fórmula -(CH2)nTr, donde Tr es un nitroheterociclo aromático o nitrocarbociclo aromático y -(CH2)nTr actúa como un iniciador de fragmentación activado reductivamente; y n es un número entero de 0 a 6; R2, R3 y R4 se pueden seleccionar cada uno independientemente de grupos alifáticos o aromáticos de un inhibidor de amina cinasa terciaria (R2) (R3) (R4)N, o dos de R2, R3 y R4 pueden formar un anillo de amina heterocíclico, alifático o aromático de un inhibidor de cinasa, o uno de R2, R3 y R4 puede estar ausente y dos de R2, R3 y R4 pueden formar un anillo de amina heterocíclico, aromático de un inhibidor de cinasa. Los compuestos de la invención son útiles en el tratamiento de enfermedades proliferativas tal como el cáncer.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NZ57549009 | 2009-03-11 | ||
NZ57945809 | 2009-09-02 | ||
NZ58117009 | 2009-11-12 | ||
PCT/NZ2010/000040 WO2010104406A1 (en) | 2009-03-11 | 2010-03-11 | Prodrug forms of kinase inhibitors and their use in therapy |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2011009034A true MX2011009034A (es) | 2011-09-22 |
Family
ID=42728538
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2011009034A MX2011009034A (es) | 2009-03-11 | 2010-03-11 | Formas de profarmaco de inhibidores de cinasa y su uso en la terapia. |
Country Status (13)
Country | Link |
---|---|
US (2) | US9073916B2 (es) |
EP (2) | EP3031807A1 (es) |
JP (1) | JP5793428B2 (es) |
KR (1) | KR20110130468A (es) |
CN (2) | CN105541836A (es) |
AU (1) | AU2010221818A1 (es) |
BR (1) | BRPI1011505A2 (es) |
CA (1) | CA2754808C (es) |
IL (1) | IL214626A0 (es) |
MX (1) | MX2011009034A (es) |
NZ (2) | NZ595206A (es) |
RU (1) | RU2011141121A (es) |
WO (1) | WO2010104406A1 (es) |
Families Citing this family (36)
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AU2006210572B2 (en) | 2005-02-03 | 2011-08-04 | The General Hospital Corporation | Method for treating gefitinib resistant cancer |
AU2006311877A1 (en) | 2005-11-04 | 2007-05-18 | Wyeth Llc | Antineoplastic combinations with mTOR inhibitor, herceptin, and/orHKI-272 |
US8022216B2 (en) | 2007-10-17 | 2011-09-20 | Wyeth Llc | Maleate salts of (E)-N-{4-[3-chloro-4-(2-pyridinylmethoxy)anilino]-3-cyano-7-ethoxy-6-quinolinyl}-4-(dimethylamino)-2-butenamide and crystalline forms thereof |
KR20180128078A (ko) | 2008-06-17 | 2018-11-30 | 와이어쓰 엘엘씨 | Hki-272 및 비노렐빈을 함유하는 항신생물성 조합물 |
NZ590464A (en) | 2008-08-04 | 2012-10-26 | Wyeth Llc | Antineoplastic combinations of the 4-anilino-3-cyanoquinoline neratinib and capecitabine |
US9073916B2 (en) | 2009-03-11 | 2015-07-07 | Auckland Uniservices Limited | Prodrug forms of kinase inhibitors and their use in therapy |
HUE061640T2 (hu) | 2009-04-06 | 2023-07-28 | Wyeth Llc | Gyógykezelési rendszer mellrákhoz neratinib alkalmazásával |
NZ598144A (en) * | 2009-09-02 | 2014-01-31 | Auckland Uniservices Ltd | Kinase inhibitors, prodrug forms thereof and their use in therapy |
CN102558185B (zh) * | 2010-12-09 | 2016-02-10 | 中国科学院上海药物研究所 | 吡啶并吡咯三嗪化合物、其制备方法和用途 |
CN102838590B (zh) * | 2011-06-21 | 2014-07-09 | 苏州迈泰生物技术有限公司 | 氨基喹唑啉衍生物及其在制备抗恶性肿瘤药物中的用途 |
CN104203242B (zh) * | 2012-04-04 | 2017-03-15 | 杭州德润玉成生物科技有限公司 | 取代的喹啉类作为布鲁顿酪氨酸激酶抑制剂 |
CN105796569A (zh) * | 2012-09-10 | 2016-07-27 | 杨子娇 | 化合物在制备防治青光眼病的药物中的用途 |
CN105796562A (zh) * | 2012-09-10 | 2016-07-27 | 杨子娇 | 化合物在制备防治青光眼病的药物中的用途 |
CN103664797A (zh) * | 2012-09-25 | 2014-03-26 | 杨子娇 | 一类治疗房角狭窄的化合物及其用途 |
CN103655576A (zh) * | 2012-09-25 | 2014-03-26 | 杨子娇 | 一类治疗房角狭窄的化合物及其用途 |
CN103724349A (zh) * | 2012-10-11 | 2014-04-16 | 韩冰 | 一类治疗脑性瘫痪的化合物及其用途 |
CN102952095A (zh) * | 2012-10-19 | 2013-03-06 | 盛世泰科生物医药技术(苏州)有限公司 | 一种2-羧酸乙酯-5-溴甲基噻唑的合成方法 |
CN103787986A (zh) * | 2012-10-31 | 2014-05-14 | 韩冰 | 一类治疗干眼症的化合物及其用途 |
CN103784456A (zh) * | 2012-10-31 | 2014-05-14 | 韩冰 | 一类治疗干眼症的化合物及其用途 |
CN103804304A (zh) * | 2012-11-01 | 2014-05-21 | 韩冰 | 一类治疗神经退行性疾病的化合物及其用途 |
CN103804305A (zh) * | 2012-11-05 | 2014-05-21 | 韩文毅 | 一类治疗湿疹的化合物及其用途 |
CN103804306A (zh) * | 2012-11-12 | 2014-05-21 | 韩文毅 | 一类治疗糖尿病的化合物及其用途 |
BR112015022785A2 (pt) * | 2013-03-14 | 2017-07-18 | Epizyme Inc | composto; composição farmacêutica; kit ou artigo farmacêutico embalado; método de inibição de uma arginina metil transferase (rmt); método de modulação da expressão genética; método de modulação da transcrição; e método de tratamento de um distúrbio mediado por rmt |
WO2014172482A1 (en) * | 2013-04-17 | 2014-10-23 | Robert Alfred Volkmann | Compounds for treatment of pain |
US10072018B2 (en) | 2013-04-17 | 2018-09-11 | Biopharma Works | Compounds for treatment of pain |
CN107892684B (zh) * | 2013-07-18 | 2020-05-26 | 锦州奥鸿药业有限责任公司 | 喹唑啉衍生物及其药物组合物,以及作为药物的用途 |
JP6769962B2 (ja) | 2014-12-03 | 2020-10-14 | オークランド ユニサービシーズ リミティド | 癌治療のためのキナーゼ阻害剤プロドラッグ |
US20160376239A1 (en) * | 2015-06-29 | 2016-12-29 | Ontogenesis, Llc | N-Acylalkyl Prodrugs of Multi-Tyrosine Kinase Inhibitors and Methods of Use |
EP3589634A4 (en) * | 2017-03-03 | 2020-08-12 | Auckland Uniservices Limited | FGFR KINASE INHIBITORS AND PHARMACEUTICAL USES |
CN107569491A (zh) * | 2017-08-30 | 2018-01-12 | 杭州科兴生物化工有限公司 | 一种星孢菌素类化合物的应用 |
WO2019051155A1 (en) | 2017-09-08 | 2019-03-14 | The Regents Of The University Of Colorado, A Body Corporate | COMPOUNDS, COMPOSITIONS AND METHODS FOR TREATING OR PREVENTING HER INDUCED PHARMACORE-RESISTANT CANCERS |
WO2019125184A1 (en) | 2017-12-19 | 2019-06-27 | Auckland Uniservices Limited | Use of biomarker in cancer therapy |
WO2019169065A2 (en) * | 2018-02-28 | 2019-09-06 | The Regents Of The University Of Colorado, A Body Corporate | Wee1 kinase inhibitors and methods of treating cancer using the same |
US20220289707A1 (en) * | 2019-07-03 | 2022-09-15 | The Regents Of The University Of Colorado, A Body Corporate | Amp-activated protein kinase inhibitors and methods of making and using the same |
WO2021127456A1 (en) | 2019-12-19 | 2021-06-24 | Rain Therapeutics Inc. | Methods of inhibiting epidermal growth factor receptor proteins |
WO2022006412A2 (en) | 2020-07-02 | 2022-01-06 | The Regents Of The University Of Colorado, A Body Corporate | Conjugates of ampk inhibitors and protac degraders and related uses |
Family Cites Families (19)
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WO1997007101A1 (en) | 1995-08-18 | 1997-02-27 | Auckland Uniservices Limited | Radiation-activated cytotoxin therapy |
IL126351A0 (en) | 1996-04-12 | 1999-05-09 | Warner Lambert Co | Irreversible inhibitors of tyrosine kinases |
ZA986732B (en) | 1997-07-29 | 1999-02-02 | Warner Lambert Co | Irreversible inhibitiors of tyrosine kinases |
TW436485B (en) * | 1997-08-01 | 2001-05-28 | American Cyanamid Co | Substituted quinazoline derivatives |
US6251912B1 (en) | 1997-08-01 | 2001-06-26 | American Cyanamid Company | Substituted quinazoline derivatives |
US6288082B1 (en) | 1998-09-29 | 2001-09-11 | American Cyanamid Company | Substituted 3-cyanoquinolines |
US6297258B1 (en) | 1998-09-29 | 2001-10-02 | American Cyanamid Company | Substituted 3-cyanoquinolines |
US6355636B1 (en) | 1999-04-21 | 2002-03-12 | American Cyanamid Company | Substituted 3-cyano-[1.7],[1.5], and [1.8] naphthyridine inhibitors of tyrosine kinases |
US7019012B2 (en) | 2000-12-20 | 2006-03-28 | Boehringer Ingelheim International Pharma Gmbh & Co. Kg | Quinazoline derivatives and pharmaceutical compositions containing them |
ES2279361T3 (es) | 2003-04-16 | 2007-08-16 | F. Hoffmann-La Roche Ag | Derivados de (6-(fenoxi)-pirido-3,4-dipirimidin-2-il)-amina como inhibidores de p38 kinasa para el tratamiento de estados inflamatorios tal como artritis reumatoide. |
US7399865B2 (en) | 2003-09-15 | 2008-07-15 | Wyeth | Protein tyrosine kinase enzyme inhibitors |
DE10349113A1 (de) | 2003-10-17 | 2005-05-12 | Boehringer Ingelheim Pharma | Verfahren zur Herstellung von Aminocrotonylverbindungen |
UA85706C2 (en) | 2004-05-06 | 2009-02-25 | Уорнер-Ламберт Компани Ллси | 4-phenylaminoquinazolin-6-yl amides |
GB0421294D0 (en) | 2004-09-24 | 2004-10-27 | Angiogene Pharm Ltd | Bioreductively-activated prodrugs |
DK1948180T3 (da) * | 2005-11-11 | 2013-05-27 | Boehringer Ingelheim Int | Kombinationsbehandling af cancer omfattende EGFR/HER2 inhibitorer |
CN101003514A (zh) | 2006-01-20 | 2007-07-25 | 上海艾力斯医药科技有限公司 | 喹唑啉衍生物、其制备方法及用途 |
WO2008039087A2 (en) | 2006-09-29 | 2008-04-03 | Auckland Uniservices Limited | Indoline derivatives and uses thereof |
WO2008151253A1 (en) * | 2007-06-04 | 2008-12-11 | Threshold Pharmaceuticals, Inc. | Hypoxia activated prodrugs of antineoplastic agents |
US9073916B2 (en) | 2009-03-11 | 2015-07-07 | Auckland Uniservices Limited | Prodrug forms of kinase inhibitors and their use in therapy |
-
2010
- 2010-03-11 US US13/138,429 patent/US9073916B2/en active Active
- 2010-03-11 RU RU2011141121/04A patent/RU2011141121A/ru not_active Application Discontinuation
- 2010-03-11 NZ NZ595206A patent/NZ595206A/en unknown
- 2010-03-11 JP JP2011553972A patent/JP5793428B2/ja active Active
- 2010-03-11 CN CN201610031117.5A patent/CN105541836A/zh active Pending
- 2010-03-11 AU AU2010221818A patent/AU2010221818A1/en not_active Abandoned
- 2010-03-11 EP EP16150071.5A patent/EP3031807A1/en not_active Withdrawn
- 2010-03-11 CN CN2010800114500A patent/CN102348708A/zh active Pending
- 2010-03-11 EP EP10751067.9A patent/EP2406262B1/en active Active
- 2010-03-11 KR KR1020117023889A patent/KR20110130468A/ko not_active Application Discontinuation
- 2010-03-11 MX MX2011009034A patent/MX2011009034A/es unknown
- 2010-03-11 BR BRPI1011505A patent/BRPI1011505A2/pt not_active IP Right Cessation
- 2010-03-11 CA CA2754808A patent/CA2754808C/en active Active
- 2010-03-11 NZ NZ620000A patent/NZ620000A/en unknown
- 2010-03-11 WO PCT/NZ2010/000040 patent/WO2010104406A1/en active Application Filing
-
2011
- 2011-08-11 IL IL214626A patent/IL214626A0/en unknown
-
2015
- 2015-06-04 US US14/731,309 patent/US20160002222A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
US20160002222A1 (en) | 2016-01-07 |
WO2010104406A1 (en) | 2010-09-16 |
IL214626A0 (en) | 2011-09-27 |
KR20110130468A (ko) | 2011-12-05 |
RU2011141121A (ru) | 2013-04-20 |
AU2010221818A1 (en) | 2011-10-06 |
EP2406262A1 (en) | 2012-01-18 |
EP3031807A1 (en) | 2016-06-15 |
US20120077811A1 (en) | 2012-03-29 |
US9073916B2 (en) | 2015-07-07 |
CN102348708A (zh) | 2012-02-08 |
NZ595206A (en) | 2014-02-28 |
JP2012520295A (ja) | 2012-09-06 |
CA2754808C (en) | 2019-01-08 |
EP2406262B1 (en) | 2016-02-17 |
CN105541836A (zh) | 2016-05-04 |
NZ620000A (en) | 2015-07-31 |
WO2010104406A8 (en) | 2011-10-06 |
CA2754808A1 (en) | 2010-09-16 |
JP5793428B2 (ja) | 2015-10-14 |
BRPI1011505A2 (pt) | 2016-03-22 |
EP2406262A4 (en) | 2012-06-20 |
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