CL2014000365A1 - Compuesto 4-(8-metoxi-1-((r)-1-metoxipropan-2-il)-2-(tetrahidro-2h-piran-4-il)-1h-imidazo[4,5-c]quinolin-7-il)-3,5-dimetilisoxazol, inhibidor de brodominio; composicion farmaceutica; producto farmaceutico; procedimiento de tratamiento; y su uso para tratar una afeccion autoinmune y/o inflamatoria cronica y cancer, entre otras. - Google Patents

Compuesto 4-(8-metoxi-1-((r)-1-metoxipropan-2-il)-2-(tetrahidro-2h-piran-4-il)-1h-imidazo[4,5-c]quinolin-7-il)-3,5-dimetilisoxazol, inhibidor de brodominio; composicion farmaceutica; producto farmaceutico; procedimiento de tratamiento; y su uso para tratar una afeccion autoinmune y/o inflamatoria cronica y cancer, entre otras.

Info

Publication number: CL2014000365A1
Authority: CL; Chile
Prior art keywords: brodominium; dimethylisoxazole; methoxypropan; quinolin; imidazo
Prior art date: 2011-08-17

Application number

CL2014000365A

Other languages

English (en)

Inventor

Emmanuel Hubert Demont

Katherine Louise Jones

Robert J Watson

Original Assignee

Glaxosmithkline Llc

Priority date (The priority date 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 date listed.)

2011-08-17

Filing date

2014-02-13

Publication date

2014-07-11

2014-02-13 Application filed by Glaxosmithkline Llc filed Critical Glaxosmithkline Llc

2014-07-11 Publication of CL2014000365A1 publication Critical patent/CL2014000365A1/es

Links

HYPXHDJBILNWLI-CQSZACIVSA-N 4-[8-methoxy-1-[(2r)-1-methoxypropan-2-yl]-2-(oxan-4-yl)imidazo[4,5-c]quinolin-7-yl]-3,5-dimethyl-1,2-oxazole Chemical compound COC1=CC2=C3N([C@H](C)COC)C(C4CCOCC4)=NC3=CN=C2C=C1C=1C(C)=NOC=1C HYPXHDJBILNWLI-CQSZACIVSA-N 0.000 title 1
206010028980 Neoplasm Diseases 0.000 title 1
230000001363 autoimmune Effects 0.000 title 1
201000011510 cancer Diseases 0.000 title 1
230000001684 chronic effect Effects 0.000 title 1
150000001875 compounds Chemical class 0.000 title 1
230000004968 inflammatory condition Effects 0.000 title 1
239000003112 inhibitor Substances 0.000 title 1
239000008194 pharmaceutical composition Substances 0.000 title 1
239000000825 pharmaceutical preparation Substances 0.000 title 1
229940127557 pharmaceutical product Drugs 0.000 title 1

Classifications

- 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
- A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
- 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
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
- 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
- A61P37/00—Drugs for immunological or allergic disorders
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
- 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
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (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)
General Chemical & Material Sciences (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Chemical Kinetics & Catalysis (AREA)
Immunology (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Nutrition Science (AREA)
Physiology (AREA)
Hematology (AREA)
Oncology (AREA)
Transplantation (AREA)
Pain & Pain Management (AREA)
Rheumatology (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

CL2014000365A 2011-08-17 2014-02-13 Compuesto 4-(8-metoxi-1-((r)-1-metoxipropan-2-il)-2-(tetrahidro-2h-piran-4-il)-1h-imidazo[4,5-c]quinolin-7-il)-3,5-dimetilisoxazol, inhibidor de brodominio; composicion farmaceutica; producto farmaceutico; procedimiento de tratamiento; y su uso para tratar una afeccion autoinmune y/o inflamatoria cronica y cancer, entre otras. CL2014000365A1 (es)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GBGB1114103.3A GB201114103D0 (en)	2011-08-17	2011-08-17	Novel compounds

Publications (1)

Publication Number	Publication Date
CL2014000365A1 true CL2014000365A1 (es)	2014-07-11

Family

ID=44764570

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CL2014000365A CL2014000365A1 (es)	2011-08-17	2014-02-13	Compuesto 4-(8-metoxi-1-((r)-1-metoxipropan-2-il)-2-(tetrahidro-2h-piran-4-il)-1h-imidazo[4,5-c]quinolin-7-il)-3,5-dimetilisoxazol, inhibidor de brodominio; composicion farmaceutica; producto farmaceutico; procedimiento de tratamiento; y su uso para tratar una afeccion autoinmune y/o inflamatoria cronica y cancer, entre otras.

Country Status (38)

Country	Link
US (4)	US9067936B2 (es)
EP (2)	EP3150601A1 (es)
JP (1)	JP6059723B2 (es)
KR (1)	KR20140064878A (es)
CN (1)	CN103889984B (es)
AR (1)	AR087545A1 (es)
AU (1)	AU2012296914B2 (es)
BR (1)	BR112014003681A8 (es)
CA (1)	CA2843537A1 (es)
CL (1)	CL2014000365A1 (es)
CO (1)	CO6862151A2 (es)
CR (1)	CR20140076A (es)
CY (1)	CY1118370T1 (es)
DK (1)	DK2744809T3 (es)
DO (1)	DOP2014000031A (es)
EA (1)	EA023374B1 (es)
ES (1)	ES2609857T3 (es)
GB (1)	GB201114103D0 (es)
HR (1)	HRP20161674T1 (es)
HU (1)	HUE030106T2 (es)
IL (1)	IL230489A (es)
IN (1)	IN2014CN00568A (es)
JO (1)	JO3187B1 (es)
LT (1)	LT2744809T (es)
ME (1)	ME02589B (es)
MX (1)	MX350597B (es)
MY (1)	MY170729A (es)
PE (1)	PE20141406A1 (es)
PH (1)	PH12014500379A1 (es)
PL (1)	PL2744809T3 (es)
PT (1)	PT2744809T (es)
RS (1)	RS55560B1 (es)
SI (1)	SI2744809T1 (es)
SM (2)	SMT201700005T1 (es)
TW (1)	TWI558704B (es)
UA (1)	UA110838C2 (es)
UY (1)	UY34264A (es)
WO (1)	WO2013024104A1 (es)

Families Citing this family (56)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AR084070A1 (es)	2010-12-02	2013-04-17	Constellation Pharmaceuticals Inc	Inhibidores del bromodominio y usos de los mismos
US9249161B2 (en)	2010-12-02	2016-02-02	Constellation Pharmaceuticals, Inc.	Bromodomain inhibitors and uses thereof
EP2705039B1 (en)	2011-05-04	2017-07-26	Constellation Pharmaceuticals, Inc.	Bromodomain inhibitors and uses thereof
US9328117B2 (en)	2011-06-17	2016-05-03	Constellation Pharmaceuticals, Inc.	Bromodomain inhibitors and uses thereof
GB201114103D0 (en) *	2011-08-17	2011-09-28	Glaxosmithkline Llc	Novel compounds
TWI602820B (zh)	2012-06-06	2017-10-21	星宿藥物公司	溴域抑制劑及其用途
US9624244B2 (en)	2012-06-06	2017-04-18	Constellation Pharmaceuticals, Inc.	Benzo [B] isoxazoloazepine bromodomain inhibitors and uses thereof
US9073878B2 (en)	2012-11-21	2015-07-07	Zenith Epigenetics Corp.	Cyclic amines as bromodomain inhibitors
WO2014080291A2 (en)	2012-11-21	2014-05-30	Rvx Therapeutics Inc.	Biaryl derivatives as bromodomain inhibitors
US9271978B2 (en)	2012-12-21	2016-03-01	Zenith Epigenetics Corp.	Heterocyclic compounds as bromodomain inhibitors
JP2016512524A (ja)	2013-03-11	2016-04-28	アッヴィ・インコーポレイテッド	ブロモドメイン阻害剤
JP6401773B2 (ja)	2013-03-11	2018-10-10	ザリージェンツオブザユニヴァシティオブミシガン	Ｂｅｔブロモドメイン阻害剤およびこれを用いる治療方法
EP2970285B1 (en)	2013-03-11	2019-04-17	AbbVie Inc.	Fused tetracyclic bromodomain inhibitors
US9227985B2 (en) *	2013-03-15	2016-01-05	Incyte Corporation	Tricyclic heterocycles as bet protein inhibitors
TWI530499B (zh)	2013-03-28	2016-04-21	吉李德科學股份有限公司	作為溴結構域（ｂｒｏｍｏｄｏｍａｉｎ）抑制劑之苯並咪唑酮衍生物類
WO2015004533A2 (en)	2013-06-21	2015-01-15	Zenith Epigenetics Corp.	Novel substituted bicyclic compounds as bromodomain inhibitors
SG11201510409QA (en)	2013-06-21	2016-01-28	Zenith Epigenetics Corp	Novel bicyclic bromodomain inhibitors
EP3019502B1 (en)	2013-07-08	2017-05-17	Incyte Holdings Corporation	Tricyclic heterocycles as bet protein inhibitors
AU2014298051B2 (en)	2013-07-31	2018-11-15	Zenith Epigenetics Ltd.	Novel quinazolinones as bromodomain inhibitors
WO2015049629A1 (en) *	2013-10-01	2015-04-09	Piramal Enterprises Limited	Imidazoquinoline compounds as bromodomain inhibitors
US9399640B2 (en)	2013-11-26	2016-07-26	Incyte Corporation	Substituted pyrrolo[2,3-c]pyridines and pyrazolo[3,4-c]pyridines as BET protein inhibitors
WO2015081189A1 (en)	2013-11-26	2015-06-04	Incyte Corporation	Bicyclic heterocycles as bet protein inhibitors
US9309246B2 (en)	2013-12-19	2016-04-12	Incyte Corporation	Tricyclic heterocycles as BET protein inhibitors
JP2017511801A (ja)	2014-02-28	2017-04-27	ザリージェンツオブザユニヴァシティオブミシガン	ＢＥＴブロモドメイン阻害剤としての９Ｈ−ピリミド［４，５−ｂ］インドールおよび関連類似体
MY180775A (en)	2014-04-23	2020-12-09	Incyte Corp	1h-pyrrolo[2,3-c]pyridin-7(6h)-ones and pyrazolo[3,4-c]pyridin-7(6h)-ones as inhibitors of bet proteins
PL3157928T3 (pl)	2014-06-20	2019-07-31	Constellation Pharmaceuticals, Inc.	Krystaliczne postacie 2-((4S)-6-(4-chlorofenylo)-1-metylo-4H-benzo[ c]izoksazolo-[4,5-e]azepin-4-ylo)acetamidu
US9527864B2 (en)	2014-09-15	2016-12-27	Incyte Corporation	Tricyclic heterocycles as BET protein inhibitors
WO2016087942A1 (en)	2014-12-01	2016-06-09	Zenith Epigenetics Corp.	Substituted pyridines as bromodomain inhibitors
WO2016087936A1 (en)	2014-12-01	2016-06-09	Zenith Epigenetics Corp.	Substituted pyridinones as bromodomain inhibitors
CN107207474B (zh)	2014-12-11	2021-05-07	恒翼生物医药科技(上海)有限公司	被取代的杂环作为溴结构域抑制剂
CA2966450A1 (en)	2014-12-17	2016-06-23	Olesya KHARENKO	Inhibitors of bromodomains
CA2974153A1 (en)	2015-02-03	2016-08-11	Trillium Therapeutics Inc.	Fluorinated imidazo[4,5-c]quinoline derivatives as inhibitors of bromodomain containing proteins
US10307407B2 (en)	2015-02-27	2019-06-04	The Regents Of The University Of Michigan	9H-pyrimido [4,5-B] indoles as BET bromodomain inhibitors
GB201504689D0 (en) *	2015-03-19	2015-05-06	Glaxosmithkline Ip Dev Ltd	Chemical compounds
GB201504694D0 (en)	2015-03-19	2015-05-06	Glaxosmithkline Ip Dev Ltd	Covalent conjugates
WO2016186453A1 (en) *	2015-05-20	2016-11-24	Kainos Medicine, Inc.	Quinoline derivatives as bromodomain inhibitors
WO2016196065A1 (en)	2015-05-29	2016-12-08	Genentech, Inc.	Methods and compositions for assessing responsiveness of cancers to bet inhibitors
WO2016199943A1 (en) *	2015-06-11	2016-12-15	Takeda Pharmaceutical Company Limited	Heterocyclic compounds
EP3334717B1 (en)	2015-08-11	2020-07-01	Neomed Institute	Aryl-substituted dihydroquinolinones, their preparation and their use as pharmaceuticals
WO2017024406A1 (en)	2015-08-11	2017-02-16	Neomed Institute	N-substituted bicyclic lactams, their preparation and their use as pharmaceuticals
CA2994478C (en)	2015-08-12	2023-10-03	Neomed Institute	Substituted benzimidazoles, their preparation and their use as pharmaceuticals
WO2017066876A1 (en)	2015-10-21	2017-04-27	Neomed Institute	Substituted imidazopyridines, their preparation and their use as pharmaceuticals
WO2017075377A1 (en)	2015-10-29	2017-05-04	Incyte Corporation	Amorphous solid form of a bet protein inhibitor
WO2017127930A1 (en)	2016-01-28	2017-08-03	Neomed Institute	Substituted [1,2,4]triazolo[4,3-a]pyridines, their preparation and their use as pharmaceuticals
JP6967522B2 (ja)	2016-02-15	2021-11-17	ザリージェンツオブザユニヴァシティオブミシガン	Ｂｅｔブロモドメイン阻害剤としての融合１，４−オキサゼピンおよび関連類似体
JP7037500B2 (ja)	2016-04-06	2022-03-16	ザリージェンツオブザユニヴァシティオブミシガン	Ｍｄｍ２タンパク質分解剤
AU2017246453A1 (en)	2016-04-06	2018-11-08	The Regents Of The University Of Michigan	Monofunctional intermediates for ligand-dependent target protein degradation
AU2017250076B2 (en)	2016-04-12	2021-07-22	The Regents Of The University Of Michigan	Bet protein degraders
KR102643344B1 (ko)	2016-06-20	2024-03-07	인사이트 코포레이션	Bet 저해제의 결정질 고체 형태
CN110062759B (zh)	2016-09-13	2022-05-24	密执安大学评议会	作为bet蛋白降解剂的稠合的1,4-氧氮杂䓬
ES2857743T3 (es)	2016-09-13	2021-09-29	Univ Michigan Regents	1,4-diazepinas fusionadas como degradadores de proteína BET
US11046709B2 (en)	2017-02-03	2021-06-29	The Regents Of The University Of Michigan	Fused 1,4-diazepines as BET bromodomain inhibitors
US11267822B2 (en)	2017-09-13	2022-03-08	The Regents Of The University Of Michigan	BET bromodomain protein degraders with cleavable linkers
CN108033957A (zh) *	2018-01-09	2018-05-15	中国药科大学	一种喹啉类BET bromodomain抑制剂及其制备方法和用途
US11833155B2 (en)	2020-06-03	2023-12-05	Incyte Corporation	Combination therapy for treatment of myeloproliferative neoplasms
WO2022132049A1 (en) *	2020-12-17	2022-06-23	National University Of Singapore	Treating cancers using bet inhibitors

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB9004781D0 (en)	1990-03-02	1990-04-25	Glaxo Group Ltd	Device
GB0211649D0 (en)	2002-05-21	2002-07-03	Novartis Ag	Organic compounds
EP1590348A1 (en)	2002-12-20	2005-11-02	3M Innovative Properties Company	Aryl / hetaryl substituted imidazoquinolines
CN1901958B (zh)	2003-11-03	2011-03-09	葛兰素集团有限公司	流体分配装置
JP2007511575A (ja)	2003-11-21	2007-05-10	ノバルティスアクチエンゲゼルシャフト	タンパク質キナーゼ阻害剤としての１ｈ−イミダゾキノリン誘導体
CA2597446A1 (en)	2005-02-11	2006-08-31	Coley Pharmaceutical Group, Inc.	Substituted imidazoquinolines and imidazonaphthyridines
WO2007035935A1 (en)	2005-09-23	2007-03-29	Coley Pharmaceutical Group, Inc.	METHOD FOR 1H-IMIDAZO[4,5-c]PYRIDINES AND ANALOGS THEREOF
CN101330916A (zh)	2005-12-16	2008-12-24	科勒制药集团公司	经取代的咪唑并喹啉、咪唑并萘啶和咪唑并吡啶、其组合物及其方法
JP2008156311A (ja)	2006-12-26	2008-07-10	Institute Of Physical & Chemical Research	Ｂｒｄ２ブロモドメイン結合剤
US8476260B2 (en)	2007-12-28	2013-07-02	Mitsubishi Tanabe Pharma Corporation	Antitumor agent
GB0919434D0 (en) *	2009-11-05	2009-12-23	Glaxosmithkline Llc	Novel compounds
GB0919423D0 (en) *	2009-11-05	2009-12-23	Glaxosmithkline Llc	Novel compounds
SI2496582T1 (sl) *	2009-11-05	2016-04-29	Glaxosmithkline Llc Corporation Service Company	Benzodiazepinski inhibitor bromodomene
GB0919432D0 (en) *	2009-11-05	2009-12-23	Glaxosmithkline Llc	Use
GB201106799D0 (en) *	2011-04-21	2011-06-01	Glaxosmithkline Llc	Novel compounds
GB201114103D0 (en)	2011-08-17	2011-09-28	Glaxosmithkline Llc	Novel compounds

2011
- 2011-08-17 GB GBGB1114103.3A patent/GB201114103D0/en not_active Ceased
2012
- 2012-08-15 TW TW101129613A patent/TWI558704B/zh not_active IP Right Cessation
- 2012-08-15 EP EP16192662.1A patent/EP3150601A1/en not_active Withdrawn
- 2012-08-15 US US14/237,905 patent/US9067936B2/en not_active Expired - Fee Related
- 2012-08-15 CA CA2843537A patent/CA2843537A1/en not_active Abandoned
- 2012-08-15 JO JOP/2012/0229A patent/JO3187B1/ar active
- 2012-08-15 CN CN201280040092.5A patent/CN103889984B/zh not_active Expired - Fee Related
- 2012-08-15 WO PCT/EP2012/065918 patent/WO2013024104A1/en not_active Ceased
- 2012-08-15 PT PT127480283T patent/PT2744809T/pt unknown
- 2012-08-15 JP JP2014525437A patent/JP6059723B2/ja not_active Expired - Fee Related
- 2012-08-15 IN IN568CHN2014 patent/IN2014CN00568A/en unknown
- 2012-08-15 EP EP12748028.3A patent/EP2744809B1/en active Active
- 2012-08-15 PH PH1/2014/500379A patent/PH12014500379A1/en unknown
- 2012-08-15 MX MX2014001834A patent/MX350597B/es active IP Right Grant
- 2012-08-15 SI SI201230818A patent/SI2744809T1/sl unknown
- 2012-08-15 SM SM20170005T patent/SMT201700005T1/it unknown
- 2012-08-15 AR ARP120102987A patent/AR087545A1/es unknown
- 2012-08-15 DK DK12748028.3T patent/DK2744809T3/en active
- 2012-08-15 BR BR112014003681A patent/BR112014003681A8/pt not_active Application Discontinuation
- 2012-08-15 PL PL12748028T patent/PL2744809T3/pl unknown
- 2012-08-15 AU AU2012296914A patent/AU2012296914B2/en not_active Ceased
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- 2012-08-15 RS RS20170014A patent/RS55560B1/sr unknown
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- 2012-08-15 HU HUE12748028A patent/HUE030106T2/en unknown
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- 2012-08-15 KR KR1020147007082A patent/KR20140064878A/ko not_active Ceased
- 2012-08-15 UA UAA201400590A patent/UA110838C2/uk unknown
2014
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- 2014-01-21 CO CO14011125A patent/CO6862151A2/es not_active Application Discontinuation
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2015
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2016
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2017
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Also Published As

Publication number	Publication date
JO3187B1 (ar)	2018-03-08
CN103889984A (zh)	2014-06-25
US9861627B2 (en)	2018-01-09
CY1118370T1 (el)	2017-06-28
PH12014500379A1 (en)	2021-07-12
DOP2014000031A (es)	2014-06-01
KR20140064878A (ko)	2014-05-28
AU2012296914B2 (en)	2016-03-03
CA2843537A1 (en)	2013-02-21
PL2744809T3 (pl)	2017-08-31
MY170729A (en)	2019-08-27
IL230489A0 (en)	2014-03-31
US20170157113A1 (en)	2017-06-08
RS55560B1 (sr)	2017-05-31
MX2014001834A (es)	2014-02-27
US20150315184A1 (en)	2015-11-05
PE20141406A1 (es)	2014-10-25
ES2609857T3 (es)	2017-04-24
CR20140076A (es)	2014-03-19
TWI558704B (zh)	2016-11-21
DK2744809T3 (en)	2017-01-23
HRP20161674T1 (hr)	2017-01-27
BR112014003681A2 (pt)	2017-03-01
CO6862151A2 (es)	2014-02-10
SI2744809T1 (sl)	2017-01-31
SMT201700005B (it)	2017-03-08
US9610284B2 (en)	2017-04-04
EA023374B1 (ru)	2016-05-31
TW201323424A (zh)	2013-06-16
CN103889984B (zh)	2016-01-13
NZ620263A (en)	2016-04-29
MX350597B (es)	2017-09-11
EP2744809A1 (en)	2014-06-25
SMT201700005T1 (it)	2017-03-08
LT2744809T (lt)	2016-12-27
BR112014003681A8 (pt)	2018-01-23
HUE030106T2 (en)	2017-04-28
UY34264A (es)	2013-04-05
IL230489A (en)	2016-07-31
EP2744809B1 (en)	2016-10-12
JP2014521735A (ja)	2014-08-28
EA201490200A1 (ru)	2014-07-30
ME02589B (me)	2017-06-20
UA110838C2 (uk)	2016-02-25
EP3150601A1 (en)	2017-04-05
AU2012296914A1 (en)	2014-02-13
US20140171462A1 (en)	2014-06-19
PT2744809T (pt)	2017-01-06
US20160317529A1 (en)	2016-11-03
AR087545A1 (es)	2014-04-03
JP6059723B2 (ja)	2017-01-11
IN2014CN00568A (es)	2015-04-03
WO2013024104A1 (en)	2013-02-21
GB201114103D0 (en)	2011-09-28
US9067936B2 (en)	2015-06-30
US9416130B2 (en)	2016-08-16

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