ES2591129T3 - Tienopirimidinas - Google Patents
Tienopirimidinas Download PDFInfo
- Publication number
- ES2591129T3 ES2591129T3 ES13725935.4T ES13725935T ES2591129T3 ES 2591129 T3 ES2591129 T3 ES 2591129T3 ES 13725935 T ES13725935 T ES 13725935T ES 2591129 T3 ES2591129 T3 ES 2591129T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- nr6r7
- group
- cycloalkyl
- alkoxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—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
- A61K31/495—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
- 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
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- 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
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines 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
- A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Engineering & Computer Science (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Immunology (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Un compuesto de fórmula general (I): **Fórmula** en la que: R1 representa un grupo seleccionado de: -C(>=O)O-R3, -C(>=O)N(H)R3, -C(>=O)NR3R4; R2a, R2b, R2c, R2d representan, independientemente entre sí, un átomo de hidrógeno o un grupo seleccionado de: alquil C1-C3-, alcoxi C1-C3-, halo-, hidroxi-, haloalquil C1-C3-, haloalcoxi C1-C3-, ciano-, -N(H)R5, -NR5R4; R3 representa un átomo de hidrógeno o un grupo seleccionado de: alquil C1-C6-, alquenil C2-C6-, alquinil C2-C6-, -(CH2)q-(cicloalquilo C3-C7), -(CH2)q-O-(cicloalquilo C3-C7), -(CH2)q-(cicloalquenilo C4-C7), -(CH2)q-O- (cicloalquenilo C4-C7), -(CH2)q-(heterocicloalquilo de 3 a 10 miembros), -(CH2)q-O-(heterocicloalquilo de 3 a 10 miembros), -(CH2)q-(heterocicloalquenilo de 4 a 10 miembros), -(CH2)q-O-(heterocicloalquenilo de 4 a 10 miembros), -(CH2)q-arilo, -(CH2)q-O-arilo, -(CH2)q-heteroarilo, -(CH2)q-O-heteroarilo; estando dicho grupo opcionalmente sustituido, una o más veces, de forma idéntica o diferente, con un sustituyente seleccionado de: halo-, hidroxi-, oxo- (O>=), ciano-, nitro-, alquil C1-C6-, alquenil C2-C6-, alquinil C2-C6-, haloalquil C1-C6-, alcoxi C1-C6-, haloalcoxi C1-C6-, hidroxialquil C1-C6-, alcoxi C1-C6-alquil C1-C6-, -(CH2)q-arilo, -(CH2)q-heteroarilo, -(CH2)q-(cicloalquilo C3-C7), -(CH2)q-(heterocicloalquilo de 3 a 10 miembros), haloalcoxi C1-C6-alquil C1-C6-, R5-O- , -C(>=O)R5, -C(>=O)O-R5, -OC(>=O)R5, -N(H)C(>=O)R5, -N(R4)C(>=O)R5, -N(H)C(>=O)NR5R4, -N(R4)C(>=O)NR5R4, -N(H)R5, -NR5R4, -C(>=O)N(H)R5, -C(>=O)NR5R4, R4-S-, R4-S(>=O), R4-S(>=O)2, -N(H)S(>=O)R4, -N(R4)S(>=O)R4, -S(>=O)N(H)R5, -S(>=O)NR5R4, -N(H)S(>=O)2R4, -N(R4)S(>=O)2R4, -S(>=O)2N(H)R5, -S(>=O)2NR5R4, -S(>=O)(>=NR5)R4, S(>=O)(>=NR4)R5, -N>=S(>=O)(R5)R4; o cuando dos sustituyentes están presentes en posición orto el uno con el otro en un anillo arilo o heteroarilo, dichos dos sustituyentes forman juntos un puente: *O(CH2)pO*, *NH(C(>=O))NH*, en los que * representa el punto de unión a dicho anillo arilo o heteroarilo; R4 representa un grupo seleccionado de: alquil C1-C6-, alquenil C2-C6-, alquinil C2-C6-, haloalquil C1-C6-, hidroxialquil C1-C6-, alcoxi C1-C6-alquil C1-C6-; o NR3R4 juntos representan un grupo heterocicloalquilo de 3 a 10 miembros o un heterocicloalquenilo de 4 a 10 miembros; que está opcionalmente sustituido, una o más veces, de forma idéntica o diferente, con halo-, hidroxi-, ciano-, nitro-, alquil C1-C6-, haloalquil C1-C6-, alcoxi C1-C6-, haloalcoxi C1-C6-, hidroxialquil C1-C6-, alcoxi C1-C6- alquil C1-C6-, R6R7N-alquil C1-C6-, haloalcoxi C1-C6-alquil C1-C6-, alquenil C2-C6-, alquinil C2-C6-, -(CH2)q-cicloalquilo C3-C7, -(CH2)q-arilo, -(CH2)q-heteroarilo, R5-O-, -C(>=O)R5, -C(>=O)O-R5, -OC(>=O)R5, -N(H)C(>=O)R5, -N(R4)C(>=O)R5, -N(H)C(>=O)NR6R7, -N(R5)C(>=O)NR6R7, -N(H)R5, -NR6R7, -C(>=O)N(H)R5, -C(>=O)NR6R7, R5-S-, R5-S(>=O), R5-S(>=O)2, -N(H)S(>=O)R5, -N(R5)S(>=O)R6, -S(>=O)N(H)R5, -S(>=O)NR6R7, -N(H)S(>=O)2R5, -N(R5)S(>=O)2R6, -S(>=O)2N(H)R6, -S(>=O)2NR6R7, -S(>=O)(>=NR5)R6, S(>=O)(>=NR5)R6, -N>=S(>=O)(R5)R6; en el que dichos grupos alquil C1-C6-, -(CH2)q-cicloalquilo C3-C7, -(CH2)q-arilo o -(CH2)q-heteroarilo están opcionalmente sustituidos, una o más veces, de forma idéntica o diferente, con halo-, hidroxi-, oxo- (O>=), ciano-, nitro-, alquil C1-C6-, haloalquil C1-C6-, alcoxi C1-C6-, haloalcoxi C1-C6-, hidroxialquil C1-C6-, alcoxi C1-C6-alquil C1-C6-, R6R7N-alquil C1-C6-, haloalcoxi C1-C6-alquil C1-C6-, alquenil C2-C6-, alquinil C2-C6-, R5-O-, -C(>=O)R5, -C(>=O)-R5, -OC(>=O)R5, -N(H)C(>=O)R5, -N(R4)C(>=O)R5, -N(H)C(>=O)NR6R7, -N(R5)C(>=O)NR6R7, -N(H)R5, -NR6R7, -C(>=O)N(H)R5, -C(>=O)NR6R7, R5-S-, R5-S(>=O), R5-S(>=O)2, -N(H)S(>=O)R5, -N(R5)S(>=O)R6, -S(>=O)N(H)R5, -S(>=O)NR5R6, -N(H)S(>=O)2R5, -N(R5)S(>=O)2R6, -S(>=O)2N(H)R6, -S(>=O)2NR5R6, -S(>=O)(>=NR5)R6, S(>=O)(>=NR5)R6, -N>=S(>=O)(R5)R6; R5 representa un átomo de hidrógeno, un grupo alquil C1-C6- o un cicloalquil C3-C7-; R6 representa un átomo de hidrógeno, un grupo alquil C1-C6- o un cicloalquil C3-C7-; R7 representa un átomo de hidrógeno, un grupo alquil C1-C6- o un cicloalquil C3-C7-; o NR6R7 juntos representan un grupo heterocicloalquilo de 3 a 10 miembros o un heterocicloalquenilo de 4 a 10 miembros; p representa un número entero de 1 o 2; q representa un número entero de 0, 1, 2 o 3; o un tautómero, un N-óxido, un hidrato, un solvato o una sal farmacéuticamente aceptable del mismo, o una mezcla del mismo.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12168670 | 2012-05-21 | ||
| EP12168670 | 2012-05-21 | ||
| EP13153607 | 2013-02-01 | ||
| EP13153607 | 2013-02-01 | ||
| PCT/EP2013/060233 WO2013174744A1 (en) | 2012-05-21 | 2013-05-17 | Thienopyrimidines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2591129T3 true ES2591129T3 (es) | 2016-11-25 |
Family
ID=48537948
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES13725935.4T Active ES2591129T3 (es) | 2012-05-21 | 2013-05-17 | Tienopirimidinas |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US9540392B2 (es) |
| EP (1) | EP2852596B1 (es) |
| JP (1) | JP6234444B2 (es) |
| CN (1) | CN104507950B (es) |
| AR (1) | AR091093A1 (es) |
| CA (1) | CA2873975A1 (es) |
| ES (1) | ES2591129T3 (es) |
| HK (1) | HK1206723A1 (es) |
| UY (1) | UY34817A (es) |
| WO (1) | WO2013174744A1 (es) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2852595B1 (en) | 2012-05-21 | 2016-06-22 | Bayer Pharma Aktiengesellschaft | Substituted benzothienopyrimidines |
| TW201412740A (zh) | 2012-09-20 | 2014-04-01 | Bayer Pharma AG | 經取代之吡咯并嘧啶胺基苯并噻唑酮 |
| JP2016506944A (ja) | 2013-02-01 | 2016-03-07 | バイエル・ファルマ・アクティエンゲゼルシャフト | 置換ピラゾロピリミジニルアミノ−インダゾール |
| CN105189518A (zh) * | 2013-02-01 | 2015-12-23 | 拜耳制药股份公司 | 取代的噻吩并吡啶和其药物用途 |
| HK1220972A1 (zh) | 2013-03-06 | 2017-05-19 | Bayer Pharma Aktiengesellschaft | 取代的噻唑并嘧啶 |
| TW201605867A (zh) * | 2013-11-20 | 2016-02-16 | 拜耳製藥公司 | 噻吩并嘧啶 |
| CA2944103A1 (en) | 2014-05-07 | 2015-11-12 | Evotec International Gmbh | Sulfoximine substituted quinazolines for pharmaceutical compositions |
| JP2017519737A (ja) * | 2014-05-26 | 2017-07-20 | バイエル・ファルマ・アクティエンゲゼルシャフト | 置換テトラヒドロピリドチエノピリミジン |
| EP3149003A1 (en) * | 2014-05-27 | 2017-04-05 | Bayer Pharma Aktiengesellschaft | Benzothiadiazolamines |
| JO3705B1 (ar) | 2014-11-26 | 2021-01-31 | Bayer Pharma AG | إندازولات مستبدلة جديدة، عمليات لتحضيرها، مستحضرات دوائية تحتوي عليها واستخدامها في إنتاج أدوية |
| CU20170086A7 (es) * | 2014-12-19 | 2017-11-07 | Bayer Pharma AG | Pirazolpiridinaminas como inhibidores de mknk1 y mknk2 |
| CA2982984C (en) | 2015-04-20 | 2023-10-17 | Effector Therapeutics, Inc. | Inhibitors of immune checkpoint modulators for use in treating cancer and infections |
| TW201701879A (zh) | 2015-04-30 | 2017-01-16 | 拜耳製藥公司 | Irak4抑制劑組合 |
| EP3195865A1 (de) | 2016-01-25 | 2017-07-26 | Bayer Pharma Aktiengesellschaft | Kombinationen von irak4 inhibitoren und btk inhibitoren |
| WO2017025491A1 (en) * | 2015-08-12 | 2017-02-16 | F. Hoffmann-La Roche Ag | Bace1 inhibitors |
| WO2017081003A1 (en) * | 2015-11-12 | 2017-05-18 | Bayer Pharma Aktiengesellschaft | Substituted pyrazolopyridinamines |
| US20170191136A1 (en) | 2015-12-31 | 2017-07-06 | Effector Therapeutics, Inc. | Mnk biomarkers and uses thereof |
| US10435396B2 (en) | 2016-03-03 | 2019-10-08 | Bayer Pharma Aktiegesellschaft | 2-substituted indazoles, methods for producing same, pharmaceutical preparations that contain same, and use of same to produce drugs |
| EP3219329A1 (en) | 2016-03-17 | 2017-09-20 | Bayer Pharma Aktiengesellschaft | Combinations of copanlisib |
| RU2743170C2 (ru) | 2016-06-01 | 2021-02-15 | Байер Энимал Хелс Гмбх | Замещенные индазолы, пригодные для лечения и предупреждения аллергических и/или воспалительных заболеваний у животных |
| AU2017273771B2 (en) | 2016-06-01 | 2022-09-29 | Bayer Pharma Aktiengesellschaft | Use of 2-substituted indazoles for the treatment and prophylaxis of autoimmune diseases |
Family Cites Families (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5023252A (en) | 1985-12-04 | 1991-06-11 | Conrex Pharmaceutical Corporation | Transdermal and trans-membrane delivery of drugs |
| US5011472A (en) | 1988-09-06 | 1991-04-30 | Brown University Research Foundation | Implantable delivery system for biological factors |
| US5444038A (en) | 1992-03-09 | 1995-08-22 | Zeneca Limited | Arylindazoles and their use as herbicides |
| US6849638B2 (en) | 2001-04-30 | 2005-02-01 | Bayer Pharmaceuticals Corporation | 4-amino-5,6-substituted thiopheno [2,3-d] pyrimidines, pharmaceutical compositions containing the same, and their use in the treatment or prevention of pde7b-mediated diseases and conditions |
| WO2005010008A1 (en) | 2003-07-24 | 2005-02-03 | Bayer Pharmaceuticals Corporation | Substituted tetrahydrobenzothienopyrimidinamine compounds useful for treating hyper-proliferative disorders |
| US20080269238A1 (en) | 2004-04-01 | 2008-10-30 | Takeda Pharmaceutical Company Limited | Thiazolopyrimidine Derivative |
| EP1899353A1 (en) | 2005-06-22 | 2008-03-19 | DeveloGen Aktiengesellschaft | Thienopyrimidines for pharmaceutical compositions |
| JP2007084494A (ja) | 2005-09-22 | 2007-04-05 | Oncorex Inc | Pim−1活性阻害剤 |
| WO2007059905A2 (en) | 2005-11-25 | 2007-05-31 | Develogen Aktiengesellschaft | Thienopyrimidines treating inflammatory diseases |
| US7982035B2 (en) | 2007-08-27 | 2011-07-19 | Duquesne University Of The Holy Spirit | Tricyclic compounds having antimitotic and/or antitumor activity and methods of use thereof |
| JP5562865B2 (ja) | 2007-12-17 | 2014-07-30 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Trpv1のイミダゾロ−、オキサゾロ−、及びチアゾロピリミジン・モジュレーター |
| CA2722220C (en) | 2008-04-30 | 2016-06-07 | National Health Research Institutes | Fused bicyclic pyrimidine compounds as aurora kinase inhibitors |
| AU2009286734A1 (en) * | 2008-08-26 | 2010-03-04 | Boehringer Ingelheim International Gmbh | Thienopyrimidines for pharmaceutical compositions |
| PH12012501693A1 (en) | 2010-02-26 | 2012-11-05 | Boehringer Ingelheim Int | 4 - [cycloalkyloxy (hetero) arylamino] thieno [2,3 - d] pyrimidines having mnkl/mnk2 inhibiting activity for pharmaceutical compositions |
| EP2539344B1 (en) | 2010-02-26 | 2014-10-15 | Boehringer Ingelheim International GmbH | Halogen or cyano substituted thieno[2,3-d]pyrimidines having mnk1/ mnk2 inhibiting activity for pharmaceutical compositions |
| BR112012021453A2 (pt) | 2010-02-26 | 2017-02-21 | Boehringer Ingelheim Int | tienopirimidina, sua composição farmacêutica e seu uso |
| UY33241A (es) | 2010-02-26 | 2011-09-30 | Boehringer Ingelheim Int | ?Tienopirimidinas que contienen heterocicloalquilo para composiciones farmacéuticas?. |
| EP2852595B1 (en) | 2012-05-21 | 2016-06-22 | Bayer Pharma Aktiengesellschaft | Substituted benzothienopyrimidines |
| TW201412740A (zh) | 2012-09-20 | 2014-04-01 | Bayer Pharma AG | 經取代之吡咯并嘧啶胺基苯并噻唑酮 |
| CN104781260A (zh) | 2012-09-26 | 2015-07-15 | 拜耳制药股份公司 | 用于治疗过度增殖性障碍的取代的吲唑-吡咯并嘧啶 |
| US20150252047A1 (en) | 2012-09-26 | 2015-09-10 | Bayer Pharma Aktiengesellschaft | Substituted indazol-pyrrolopyrimidines useful in the treatment of hyperproliferative diseases |
| JP2016506944A (ja) | 2013-02-01 | 2016-03-07 | バイエル・ファルマ・アクティエンゲゼルシャフト | 置換ピラゾロピリミジニルアミノ−インダゾール |
| HK1220972A1 (zh) | 2013-03-06 | 2017-05-19 | Bayer Pharma Aktiengesellschaft | 取代的噻唑并嘧啶 |
-
2013
- 2013-05-17 ES ES13725935.4T patent/ES2591129T3/es active Active
- 2013-05-17 EP EP13725935.4A patent/EP2852596B1/en not_active Not-in-force
- 2013-05-17 CA CA2873975A patent/CA2873975A1/en not_active Abandoned
- 2013-05-17 US US14/403,151 patent/US9540392B2/en not_active Expired - Fee Related
- 2013-05-17 WO PCT/EP2013/060233 patent/WO2013174744A1/en not_active Ceased
- 2013-05-17 HK HK15107190.6A patent/HK1206723A1/xx unknown
- 2013-05-17 CN CN201380038580.7A patent/CN104507950B/zh not_active Expired - Fee Related
- 2013-05-17 JP JP2015513117A patent/JP6234444B2/ja not_active Expired - Fee Related
- 2013-05-20 AR ARP130101735 patent/AR091093A1/es unknown
- 2013-05-21 UY UY0001034817A patent/UY34817A/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| JP6234444B2 (ja) | 2017-11-22 |
| EP2852596A1 (en) | 2015-04-01 |
| CN104507950A (zh) | 2015-04-08 |
| EP2852596B1 (en) | 2016-06-22 |
| JP2015517545A (ja) | 2015-06-22 |
| WO2013174744A1 (en) | 2013-11-28 |
| CA2873975A1 (en) | 2013-11-28 |
| HK1206723A1 (en) | 2016-01-15 |
| US20150133425A1 (en) | 2015-05-14 |
| CN104507950B (zh) | 2017-03-22 |
| US9540392B2 (en) | 2017-01-10 |
| UY34817A (es) | 2013-12-31 |
| AR091093A1 (es) | 2015-01-14 |
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