AP2015008236A0 - Azaindole derivatives which acht as PI3K inhibitors - Google Patents
Azaindole derivatives which acht as PI3K inhibitorsInfo
- Publication number
- AP2015008236A0 AP2015008236A0 AP2015008236A AP2015008236A AP2015008236A0 AP 2015008236 A0 AP2015008236 A0 AP 2015008236A0 AP 2015008236 A AP2015008236 A AP 2015008236A AP 2015008236 A AP2015008236 A AP 2015008236A AP 2015008236 A0 AP2015008236 A0 AP 2015008236A0
- Authority
- AP
- ARIPO
- Prior art keywords
- acht
- pi3k inhibitors
- azaindole derivatives
- azaindole
- derivatives
- Prior art date
Links
- 239000012828 PI3K inhibitor Substances 0.000 title 1
- 125000005334 azaindolyl group Chemical class N1N=C(C2=CC=CC=C12)* 0.000 title 1
- 229940043441 phosphoinositide 3-kinase inhibitor Drugs 0.000 title 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
- C07D491/107—Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
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- 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
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- A—HUMAN NECESSITIES
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- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- 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
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- 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
- A61K31/52—Purines, e.g. adenine
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- 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
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- 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
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- A—HUMAN NECESSITIES
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- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- A—HUMAN NECESSITIES
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- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
- C07D473/16—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two nitrogen atoms
-
- 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
-
- 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
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Transplantation (AREA)
- Otolaryngology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261670116P | 2012-07-10 | 2012-07-10 | |
| PCT/US2013/049612 WO2014011568A1 (fr) | 2012-07-10 | 2013-07-08 | Dérivés d'azaindole agissant comme inhibiteur de pi3k |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AP2015008236A0 true AP2015008236A0 (en) | 2015-01-31 |
Family
ID=48795966
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AP2015008236A AP2015008236A0 (en) | 2012-07-10 | 2013-07-08 | Azaindole derivatives which acht as PI3K inhibitors |
Country Status (26)
| Country | Link |
|---|---|
| US (2) | US8835420B2 (fr) |
| EP (1) | EP2872507A1 (fr) |
| JP (1) | JP2015522074A (fr) |
| KR (1) | KR20150031334A (fr) |
| CN (1) | CN104619708A (fr) |
| AP (1) | AP2015008236A0 (fr) |
| AR (1) | AR092347A1 (fr) |
| AU (1) | AU2013288895A1 (fr) |
| BR (1) | BR112015000386A2 (fr) |
| CA (1) | CA2878502A1 (fr) |
| CO (1) | CO7280475A2 (fr) |
| CR (1) | CR20150056A (fr) |
| DO (1) | DOP2015000002A (fr) |
| EA (1) | EA201590183A1 (fr) |
| HK (1) | HK1210771A1 (fr) |
| IL (1) | IL236535A0 (fr) |
| MA (1) | MA37831B1 (fr) |
| MX (1) | MX2015000107A (fr) |
| NZ (1) | NZ704160A (fr) |
| PE (1) | PE20150754A1 (fr) |
| PH (1) | PH12015500063B1 (fr) |
| SG (1) | SG11201500063UA (fr) |
| TN (1) | TN2015000005A1 (fr) |
| TW (1) | TW201414734A (fr) |
| UY (1) | UY34893A (fr) |
| WO (1) | WO2014011568A1 (fr) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LT2718270T (lt) | 2011-06-10 | 2022-08-10 | Merck Patent Gmbh | Pirimidino ir piridino junginių, turinčių btk inhibitorinį aktyvumą, kompozicijos ir gamybos būdai |
| WO2015106014A1 (fr) * | 2014-01-09 | 2015-07-16 | Takeda Pharmaceutical Company Limited | Dérivés d'azaindole |
| AR099052A1 (es) | 2014-01-09 | 2016-06-29 | Takeda Pharmaceuticals Co | Derivados de azaindol |
| ES2749679T3 (es) | 2014-10-22 | 2020-03-23 | Bristol Myers Squibb Co | Compuestos de pirrolotriazina amina sustituidos como inhibidores de PI3k |
| WO2016064957A1 (fr) | 2014-10-22 | 2016-04-28 | Bristol-Myers Squibb Company | Composés amine hétéroaryles bicycliques utilisés comme inhibiteurs de la pi3k |
| US9997391B2 (en) * | 2015-10-19 | 2018-06-12 | QROMIS, Inc. | Lift off process for chip scale package solid state devices on engineered substrate |
| LT3371165T (lt) * | 2015-11-04 | 2022-05-10 | Merck Patent Gmbh | Btk inhibitorius, naudojamas vėžiui gydyti |
| NZ741294A (en) * | 2015-11-17 | 2023-07-28 | Merck Patent Gmbh | Methods for treating multiple sclerosis using pyrimidine and pyridine compounds with btk inhibitory activity |
| CA3124815A1 (en) | 2016-03-05 | 2017-09-14 | Hangzhou Zhengxiang Pharmaceuticals Co., Ltd. | Quinoline analogs as phosphatidylinositol 3-kinase inhibitors |
| US10755986B2 (en) * | 2016-03-29 | 2020-08-25 | QROMIS, Inc. | Aluminum nitride based Silicon-on-Insulator substrate structure |
| CN107964018A (zh) * | 2016-10-19 | 2018-04-27 | 中国人民解放军军事医学科学院毒物药物研究所 | 取代嘌呤酮类衍生物及其医药用途 |
| WO2020224626A1 (fr) * | 2019-05-08 | 2020-11-12 | 浙江同源康医药股份有限公司 | Composé utilisé comme inhibiteur de kinase et son application |
| CN112794851B (zh) * | 2021-01-26 | 2022-08-23 | 复旦大学 | 3-(吡啶-3基)-7-氮杂吲哚衍生物PI3Kδ抑制剂及其制备方法与应用 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR0166088B1 (ko) | 1990-01-23 | 1999-01-15 | . | 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도 |
| US5376645A (en) | 1990-01-23 | 1994-12-27 | University Of Kansas | Derivatives of cyclodextrins exhibiting enhanced aqueous solubility and the use thereof |
| GB9518953D0 (en) | 1995-09-15 | 1995-11-15 | Pfizer Ltd | Pharmaceutical formulations |
| GB9711643D0 (en) | 1997-06-05 | 1997-07-30 | Janssen Pharmaceutica Nv | Glass thermoplastic systems |
| US6187777B1 (en) | 1998-02-06 | 2001-02-13 | Amgen Inc. | Compounds and methods which modulate feeding behavior and related diseases |
| US6667300B2 (en) | 2000-04-25 | 2003-12-23 | Icos Corporation | Inhibitors of human phosphatidylinositol 3-kinase delta |
| MXPA02010618A (es) | 2000-04-25 | 2004-05-05 | Icos Corp | Inhibidores de fosfatidilinositol 3-quinasa delta. |
| US20020183292A1 (en) | 2000-10-31 | 2002-12-05 | Michel Pairet | Pharmaceutical compositions based on anticholinergics and corticosteroids |
| US6806272B2 (en) | 2001-09-04 | 2004-10-19 | Boehringer Ingelheim Pharma Kg | Dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions |
| US7348337B2 (en) | 2002-05-28 | 2008-03-25 | Bristol-Myers Squibb Company | Indole, azaindole and related heterocyclic 4-alkenyl piperidine amides |
| US6900206B2 (en) | 2002-06-20 | 2005-05-31 | Bristol-Myers Squibb Company | Indole, azaindole and related heterocyclic sulfonylureido piperazine derivatives |
| US6861422B2 (en) | 2003-02-26 | 2005-03-01 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Dihydropteridinones, processes for preparing them and their use as pharmaceutical compositions |
| DE602004027288D1 (en) | 2003-09-08 | 2010-07-01 | Aventis Pharma Inc | Thienopyrazole |
| BRPI0417323A (pt) | 2003-12-22 | 2007-03-27 | Memory Pharm Corp | indóis, 1h-indazóis, 1,2-benzisoxazóis, e 1,2-benzisotiazóis, composto, composição farmacêutica e usos dos mesmos |
| JP2007534692A (ja) | 2004-04-22 | 2007-11-29 | メモリー・ファーマシューティカルズ・コーポレイション | インドール、1h−インダゾール、1,2−ベンズイソキサゾール、1,2−ベンゾイソチアゾール、ならびにその調製および使用 |
| GB0415364D0 (en) | 2004-07-09 | 2004-08-11 | Astrazeneca Ab | Pyrimidine derivatives |
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| DE102004058337A1 (de) | 2004-12-02 | 2006-06-14 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Verfahren zur Herstellung von annelierten Piperazin-2-on Derivaten |
| FR2878849B1 (fr) | 2004-12-06 | 2008-09-12 | Aventis Pharma Sa | Indoles substitues, compositions les contenant, procede de fabrication et utilisation |
| JP2010501537A (ja) | 2006-08-24 | 2010-01-21 | アストラゼネカ アクチボラグ | 増殖性障害の治療に有用なモルホリノピリミジン誘導体 |
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| WO2008157179A2 (fr) | 2007-06-12 | 2008-12-24 | Genentech, Inc. | Azaindoles n-substitués et procédés d'utilisation |
| CA2695583A1 (fr) | 2007-08-13 | 2009-02-19 | Metabasis Therapeutics, Inc. | Nouveaux activateurs de glucokinase |
| WO2010036380A1 (fr) | 2008-09-26 | 2010-04-01 | Intellikine, Inc. | Inhibiteurs hétérocycliques de kinases |
| WO2010129467A1 (fr) | 2009-05-04 | 2010-11-11 | Plexxikon, Inc. | Composés et procédés pour inhiber la rénine, et indications associées |
| US8754089B2 (en) | 2009-06-25 | 2014-06-17 | Amgen Inc. | Heterocyclic compounds and their uses |
| UY32743A (es) * | 2009-06-25 | 2010-12-31 | Amgen Inc | Compuestos heterocíclicos y sus usos |
| EP2448938B9 (fr) | 2009-06-29 | 2015-06-10 | Incyte Corporation | Pyrimidinones comme inhibiteurs de pi3k |
| WO2012148548A1 (fr) | 2011-02-25 | 2012-11-01 | Takeda Pharmaceutical Company Limited | Oxazinoptéridines et oxazonoptéridinones n-substituées |
| AR099052A1 (es) * | 2014-01-09 | 2016-06-29 | Takeda Pharmaceuticals Co | Derivados de azaindol |
-
2013
- 2013-07-05 TW TW102124297A patent/TW201414734A/zh unknown
- 2013-07-05 UY UY0001034893A patent/UY34893A/es not_active Application Discontinuation
- 2013-07-08 AP AP2015008236A patent/AP2015008236A0/xx unknown
- 2013-07-08 CA CA2878502A patent/CA2878502A1/fr not_active Abandoned
- 2013-07-08 JP JP2015521701A patent/JP2015522074A/ja active Pending
- 2013-07-08 WO PCT/US2013/049612 patent/WO2014011568A1/fr not_active Ceased
- 2013-07-08 HK HK15111423.7A patent/HK1210771A1/xx unknown
- 2013-07-08 KR KR20157003555A patent/KR20150031334A/ko not_active Withdrawn
- 2013-07-08 BR BR112015000386A patent/BR112015000386A2/pt not_active Application Discontinuation
- 2013-07-08 US US13/937,081 patent/US8835420B2/en not_active Expired - Fee Related
- 2013-07-08 EP EP13737976.4A patent/EP2872507A1/fr not_active Withdrawn
- 2013-07-08 EA EA201590183A patent/EA201590183A1/ru unknown
- 2013-07-08 AU AU2013288895A patent/AU2013288895A1/en not_active Abandoned
- 2013-07-08 MA MA37831A patent/MA37831B1/fr unknown
- 2013-07-08 PE PE2015000013A patent/PE20150754A1/es not_active Application Discontinuation
- 2013-07-08 NZ NZ704160A patent/NZ704160A/en not_active IP Right Cessation
- 2013-07-08 SG SG11201500063UA patent/SG11201500063UA/en unknown
- 2013-07-08 MX MX2015000107A patent/MX2015000107A/es unknown
- 2013-07-08 AR ARP130102427A patent/AR092347A1/es unknown
- 2013-07-08 CN CN201380043657.XA patent/CN104619708A/zh active Pending
-
2014
- 2014-08-04 US US14/451,254 patent/US20140343033A1/en not_active Abandoned
- 2014-12-31 IL IL236535A patent/IL236535A0/en unknown
-
2015
- 2015-01-07 DO DO2015000002A patent/DOP2015000002A/es unknown
- 2015-01-07 TN TNP2015000005A patent/TN2015000005A1/fr unknown
- 2015-01-09 PH PH12015500063A patent/PH12015500063B1/en unknown
- 2015-02-04 CO CO15021949A patent/CO7280475A2/es unknown
- 2015-02-06 CR CR20150056A patent/CR20150056A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PH12015500063A1 (en) | 2015-03-02 |
| BR112015000386A2 (pt) | 2017-06-27 |
| JP2015522074A (ja) | 2015-08-03 |
| DOP2015000002A (es) | 2015-04-15 |
| IL236535A0 (en) | 2015-02-26 |
| UY34893A (es) | 2014-02-28 |
| TN2015000005A1 (en) | 2016-06-29 |
| AU2013288895A1 (en) | 2015-02-12 |
| HK1210771A1 (zh) | 2016-05-06 |
| CA2878502A1 (fr) | 2014-01-16 |
| EP2872507A1 (fr) | 2015-05-20 |
| US20140018344A1 (en) | 2014-01-16 |
| MX2015000107A (es) | 2015-04-14 |
| PH12015500063B1 (en) | 2015-03-02 |
| SG11201500063UA (en) | 2015-03-30 |
| EA201590183A1 (ru) | 2015-06-30 |
| US8835420B2 (en) | 2014-09-16 |
| MA37831A1 (fr) | 2018-02-28 |
| KR20150031334A (ko) | 2015-03-23 |
| NZ704160A (en) | 2017-01-27 |
| PE20150754A1 (es) | 2015-05-15 |
| WO2014011568A1 (fr) | 2014-01-16 |
| US20140343033A1 (en) | 2014-11-20 |
| TW201414734A (zh) | 2014-04-16 |
| CO7280475A2 (es) | 2015-05-29 |
| CN104619708A (zh) | 2015-05-13 |
| CR20150056A (es) | 2015-05-25 |
| AR092347A1 (es) | 2015-04-15 |
| MA37831B1 (fr) | 2018-09-28 |
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