MA38393A3 - Composés hétéroaryle et utilisations associées - Google Patents
Composés hétéroaryle et utilisations associéesInfo
- Publication number
- MA38393A3 MA38393A3 MA38393A MA38393A MA38393A3 MA 38393 A3 MA38393 A3 MA 38393A3 MA 38393 A MA38393 A MA 38393A MA 38393 A MA38393 A MA 38393A MA 38393 A3 MA38393 A3 MA 38393A3
- Authority
- MA
- Morocco
- Prior art keywords
- protein kinase
- heteroaryl compounds
- related uses
- compositions
- carcinomas
- Prior art date
Links
- 125000001072 heteroaryl group Chemical group 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 201000009030 Carcinoma Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 102000001253 Protein Kinase Human genes 0.000 abstract 1
- 229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 abstract 1
- 125000000151 cysteine group Chemical group N[C@@H](CS)C(=O)* 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 108060006633 protein kinase Proteins 0.000 abstract 1
- 239000003909 protein kinase inhibitor Substances 0.000 abstract 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- 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
- 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
- C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
- C07D239/80—Oxygen atoms
-
- 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
- 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)
- 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)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Neurology (AREA)
- Gastroenterology & Hepatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Epidemiology (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Abstract
L'invention concerne des composés utiles comme inhibiteurs de protéines kinases, contenant un reste de cystéine dans le site de liaison atp. L'invention concerne également des compositions pharmaceutiquement acceptables comprenant des quantités thérapeutiquement efficaces d'un ou de plusieurs composés inhibiteurs de protéines kinases, ainsi que des méthodes d'utilisation de ces compositions dans le traitement de cancers et de carcinomes.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14305361 | 2014-03-13 | ||
| PCT/US2014/029270 WO2014144737A1 (fr) | 2013-03-15 | 2014-03-14 | Composés hétéroaryle et utilisations associées |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| MA38393A3 true MA38393A3 (fr) | 2018-05-31 |
| MA38393B1 MA38393B1 (fr) | 2018-11-30 |
Family
ID=50390019
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MA38393A MA38393B1 (fr) | 2014-03-13 | 2014-03-14 | Composés hétéroaryle et utilisations associées |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US9663524B2 (fr) |
| EP (1) | EP2968337B1 (fr) |
| JP (1) | JP6576325B2 (fr) |
| KR (1) | KR102219695B1 (fr) |
| CN (2) | CN111793068A (fr) |
| AU (1) | AU2014228746B2 (fr) |
| BR (1) | BR112015022191A8 (fr) |
| EA (1) | EA036160B1 (fr) |
| MA (1) | MA38393B1 (fr) |
| MX (1) | MX374558B (fr) |
| PE (1) | PE20151776A1 (fr) |
| SG (1) | SG11201507478VA (fr) |
| WO (1) | WO2014144737A1 (fr) |
Families Citing this family (71)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2012088266A2 (fr) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Imidazopyridazines et benzimidazoles substitués en tant qu'inhibiteurs de fgfr3 |
| GB201204384D0 (en) | 2012-03-13 | 2012-04-25 | Univ Dundee | Anti-flammatory agents |
| LT3495367T (lt) | 2012-06-13 | 2021-02-25 | Incyte Holdings Corporation | Pakeistieji tricikliniai junginiai, kaip fgfr inhibitoriai |
| NZ703495A (en) | 2012-07-11 | 2018-02-23 | Blueprint Medicines Corp | Inhibitors of the fibroblast growth factor receptor |
| WO2014026125A1 (fr) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Dérivés de pyrazine en tant qu'inhibiteurs de fgfr |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| JP6576325B2 (ja) | 2013-03-15 | 2019-09-18 | セルジーン シーエーアール エルエルシー | ヘテロアリール化合物およびそれらの使用 |
| CA2907243C (fr) | 2013-03-15 | 2021-12-28 | Celgene Avilomics Research, Inc. | Composes de dihydropyrimidopyrimidinones substitues et leurs compositions pharmaceutiques utilisees en tant qu'inhibiteur du gene fgfr4 |
| US9321786B2 (en) | 2013-03-15 | 2016-04-26 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
| LT2986610T (lt) | 2013-04-19 | 2018-04-10 | Incyte Holdings Corporation | Bicikliniai heterociklai, kaip fgfr inhibitoriai |
| SMT201800379T1 (it) | 2013-10-18 | 2018-09-13 | Eisai R&D Man Co Ltd | Inibitori di fgfr4 della pirimidina |
| BR112016008276B1 (pt) | 2013-10-25 | 2021-03-02 | Novartis Ag | derivados bicíclicos de piridila fundidos ao anel, seus usos e seu intermediário, e composição farmacêutica |
| DK3395814T3 (da) | 2013-10-25 | 2022-07-04 | Blueprint Medicines Corp | Hæmmere af fibroblastvækstfaktorreceptoren |
| WO2015108992A1 (fr) | 2014-01-15 | 2015-07-23 | Blueprint Medicines Corporation | Composés hétérobicycliques et leur utilisation en tant qu'inhibiteurs du récepteur fgfr4 |
| US10287268B2 (en) | 2014-07-21 | 2019-05-14 | Dana-Farber Cancer Institute, Inc. | Imidazolyl kinase inhibitors and uses thereof |
| DK3172213T3 (da) | 2014-07-21 | 2021-12-13 | Dana Farber Cancer Inst Inc | Makrocykliske kinasehæmmere og anvendelser deraf |
| WO2016023014A2 (fr) | 2014-08-08 | 2016-02-11 | Dana-Farber Cancer Institute, Inc. | Utilisations d'inhibiteurs de kinases inductibles par un sel (sik) |
| WO2016054483A1 (fr) | 2014-10-03 | 2016-04-07 | Novartis Ag | Utilisation de dérivés pyridyle bicycliques à anneaux fusionnés en tant qu'inhibiteurs de fgfr4 |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| SG11201706287PA (en) | 2015-02-20 | 2017-09-28 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
| WO2016134294A1 (fr) * | 2015-02-20 | 2016-08-25 | Incyte Corporation | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| US9802917B2 (en) | 2015-03-25 | 2017-10-31 | Novartis Ag | Particles of N-(5-cyano-4-((2-methoxyethyl)amino)pyridin-2-yl)-7-formyl-6-((4-methyl-2-oxopiperazin-1-yl)methyl)-3,4-dihydro-1,8-naphthyridine-1(2H)-carboxamide |
| CA2976766A1 (fr) | 2015-03-25 | 2016-09-29 | Novartis Ag | Derives n-heterocycliques formyles utilises en tant qu'inhibiteurs de fgfr4 |
| CN107660200B (zh) | 2015-04-14 | 2022-01-11 | 卫材R&D管理有限公司 | 结晶fgfr4抑制剂化合物和其用途 |
| EP3454898B1 (fr) | 2016-05-10 | 2021-11-10 | Eisai R&D Management Co., Ltd. | Associations médicamenteuses permettant de réduire la viabilité et/ou la prolifération cellulaire |
| KR20180002053A (ko) * | 2016-06-28 | 2018-01-05 | 한미약품 주식회사 | 신규한 헤테로시클릭 유도체 화합물 및 이의 용도 |
| AU2017291812B2 (en) | 2016-07-05 | 2023-12-14 | Dana-Farber Cancer Institute, Inc. | Bicyclic urea kinase inhibitors and uses thereof |
| US11241435B2 (en) | 2016-09-16 | 2022-02-08 | The General Hospital Corporation | Uses of salt-inducible kinase (SIK) inhibitors for treating osteoporosis |
| WO2018055503A1 (fr) | 2016-09-20 | 2018-03-29 | Novartis Ag | Combinaison comprenant un antagoniste de pd-1 et un inhibiteur de fgfr4 |
| US11229643B2 (en) | 2016-11-02 | 2022-01-25 | Novartis Ag | Combinations of FGFR4 inhibitors and bile acid sequestrants |
| US10968220B2 (en) * | 2016-12-19 | 2021-04-06 | Abbisko Therapeutics Co., Ltd. | FGFR4 inhibitor, preparation method therefor and pharmaceutical use thereof |
| BR112019017741A2 (pt) | 2017-02-28 | 2020-04-07 | Dana Farber Cancer Inst Inc | usos de pirimidopirimidinonas como inibidores de sik |
| CN108503593B (zh) * | 2017-02-28 | 2021-04-27 | 暨南大学 | 2-氨基嘧啶类化合物及其应用 |
| US11174255B2 (en) * | 2017-05-15 | 2021-11-16 | University Of Houston System | Pyrido[2,3-d]pyrimidin-7-ones and related compounds as inhibitors of protein kinases |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| WO2019015593A1 (fr) * | 2017-07-19 | 2019-01-24 | 江苏奥赛康药业股份有限公司 | Composé de pyrimidopyridone ou pyridopyridone et utilisation correspondante |
| CN109384790B (zh) * | 2017-08-08 | 2022-05-10 | 药捷安康(南京)科技股份有限公司 | 成纤维细胞生长因子受体抑制剂及其用途 |
| CN109745325B (zh) * | 2017-11-08 | 2022-02-15 | 上海翰森生物医药科技有限公司 | Fgfr4抑制剂、其制备方法和用途 |
| CN110386921A (zh) * | 2018-04-23 | 2019-10-29 | 南京药捷安康生物科技有限公司 | 成纤维细胞生长因子受体抑制剂化合物 |
| ES3061844T3 (en) | 2018-05-04 | 2026-04-07 | Incyte Corp | Salts of an fgfr inhibitor |
| MX2020011718A (es) | 2018-05-04 | 2021-02-15 | Incyte Corp | Formas solidas de un inhibidor de receptores del factor de crecimiento de fibroblastos (fgfr) y procesos para prepararlas. |
| CN111868058B (zh) * | 2018-05-25 | 2023-06-13 | 上海和誉生物医药科技有限公司 | 一种fgfr抑制剂、其制备方法和在药学上的应用 |
| CN110577524B (zh) * | 2018-06-07 | 2022-01-28 | 北京大学深圳研究生院 | 一种激酶选择性抑制剂 |
| CN111936493B (zh) * | 2018-06-19 | 2023-05-26 | 上海和誉生物医药科技有限公司 | 一种高选择性FGFRi抑制剂及其制备方法和应用 |
| US12351576B2 (en) | 2018-09-14 | 2025-07-08 | Abbisko Therapeutics Co., Ltd. | FGFR inhibitor, preparation method therefor and application thereof |
| US20230065740A1 (en) | 2018-12-28 | 2023-03-02 | Spv Therapeutics Inc. | Cyclin-dependent kinase inhibitors |
| WO2020177067A1 (fr) | 2019-03-05 | 2020-09-10 | Bioardis Llc | Dérivés aromatiques, procédés de préparation et utilisations médicales de ceux-ci |
| US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
| JP7378488B2 (ja) * | 2019-03-08 | 2023-11-13 | ショウヤオ ホールディングス(ベイジン) カンパニー, リミテッド | Fgfr4キナーゼ阻害剤、その製造方法及び用途 |
| US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| US12122767B2 (en) | 2019-10-01 | 2024-10-22 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| TWI891666B (zh) | 2019-10-14 | 2025-08-01 | 美商英塞特公司 | 作為fgfr抑制劑之雙環雜環 |
| US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| KR102333854B1 (ko) | 2019-10-24 | 2021-12-06 | 한국과학기술연구원 | 단백질 키나아제 저해 활성을 갖는 신규한 피리디닐트리아진 유도체 및 이를 포함하는 암의 예방, 개선 또는 치료용 약학 조성물 |
| GB201915828D0 (en) * | 2019-10-31 | 2019-12-18 | Cancer Research Tech Ltd | Compounds, compositions and therapeutic uses thereof |
| WO2021108803A1 (fr) | 2019-11-26 | 2021-06-03 | Theravance Biopharma R&D Ip, Llc | Composés de pyrimidine pyridinone fusionnés en tant qu'inhibiteurs de jak |
| WO2021113462A1 (fr) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Dérivés d'un inhibiteur de fgfr |
| CA3163875A1 (fr) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Heterocycles tricycliques en tant qu'inhibiteurs de fgfr |
| KR102382613B1 (ko) * | 2020-01-15 | 2022-04-06 | 한국과학기술연구원 | 단백질 키나아제 저해 활성을 갖는 7-아미노-3,4-디히드로피리미도피리미딘-2-온 유도체 및 이를 포함하는 치료용 약학 조성물 |
| US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| CA3213379A1 (fr) * | 2021-03-26 | 2022-09-29 | Weiqiang Zhan | Inhibiteur de fgfr4 heterocyclique bicyclique, composition pharmaceutique, preparation le comprenant, et utilisation associee |
| TW202304459A (zh) | 2021-04-12 | 2023-02-01 | 美商英塞特公司 | 包含fgfr抑制劑及nectin-4靶向劑之組合療法 |
| EP4352060A1 (fr) | 2021-06-09 | 2024-04-17 | Incyte Corporation | Hétérocycles tricycliques utiles en tant qu'inhibiteurs de fgfr |
| JP2024522189A (ja) | 2021-06-09 | 2024-06-11 | インサイト・コーポレイション | Fgfr阻害剤としての三環式ヘテロ環 |
| CN113527311B (zh) * | 2021-08-23 | 2022-05-06 | 中南大学湘雅医院 | Fgfr4抑制剂、组合物及其在药物制备中的用途 |
| WO2023039828A1 (fr) * | 2021-09-17 | 2023-03-23 | Nutshell Biotech (Shanghai) Co., Ltd. | Composés cycliques fusionnés utiles en tant qu'inhibiteurs de tyrosine kinases fgfr4 |
| CN113912602B (zh) * | 2021-10-14 | 2023-05-05 | 温州医科大学 | 一种2-氧代-1,2-二氢-1,6-萘啶-7-基类化合物及其制备方法和用途 |
| WO2024199388A1 (fr) * | 2023-03-29 | 2024-10-03 | 微境生物医药科技(上海)有限公司 | Composé agissant comme inhibiteur de myt1 |
| EP4509142A1 (fr) | 2023-08-16 | 2025-02-19 | Ona Therapeutics S.L. | Fgfr4 comme cible dans le traitement du cancer |
| CN120775123A (zh) * | 2025-09-12 | 2025-10-14 | 怀化市恒渝新材料有限公司 | 一种光引发剂制备方法、光引发剂及其应用 |
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-
2014
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- 2014-03-14 CN CN202010661205.XA patent/CN111793068A/zh active Pending
- 2014-03-14 EA EA201591420A patent/EA036160B1/ru not_active IP Right Cessation
- 2014-03-14 MX MX2015011514A patent/MX374558B/es active IP Right Grant
- 2014-03-14 EP EP14763001.6A patent/EP2968337B1/fr active Active
- 2014-03-14 KR KR1020157029048A patent/KR102219695B1/ko not_active Expired - Fee Related
- 2014-03-14 US US14/776,373 patent/US9663524B2/en active Active
- 2014-03-14 CN CN201480016170.7A patent/CN105307657B/zh not_active Expired - Fee Related
- 2014-03-14 WO PCT/US2014/029270 patent/WO2014144737A1/fr not_active Ceased
- 2014-03-14 AU AU2014228746A patent/AU2014228746B2/en not_active Ceased
- 2014-03-14 SG SG11201507478VA patent/SG11201507478VA/en unknown
- 2014-03-14 PE PE2015002022A patent/PE20151776A1/es unknown
- 2014-03-14 MA MA38393A patent/MA38393B1/fr unknown
- 2014-03-14 BR BR112015022191A patent/BR112015022191A8/pt active Search and Examination
Also Published As
| Publication number | Publication date |
|---|---|
| EP2968337A1 (fr) | 2016-01-20 |
| EA201591420A1 (ru) | 2016-02-29 |
| CN105307657B (zh) | 2020-07-10 |
| CN105307657A (zh) | 2016-02-03 |
| AU2014228746A1 (en) | 2015-09-10 |
| EA036160B1 (ru) | 2020-10-08 |
| WO2014144737A1 (fr) | 2014-09-18 |
| BR112015022191A2 (pt) | 2017-10-10 |
| US20160046634A1 (en) | 2016-02-18 |
| AU2014228746B2 (en) | 2018-08-30 |
| EP2968337A4 (fr) | 2016-10-19 |
| US9663524B2 (en) | 2017-05-30 |
| KR20150131237A (ko) | 2015-11-24 |
| MX374558B (es) | 2025-03-06 |
| JP6576325B2 (ja) | 2019-09-18 |
| KR102219695B1 (ko) | 2021-02-25 |
| MA38393B1 (fr) | 2018-11-30 |
| PE20151776A1 (es) | 2015-12-11 |
| BR112015022191A8 (pt) | 2018-01-23 |
| JP2016519673A (ja) | 2016-07-07 |
| SG11201507478VA (en) | 2015-10-29 |
| EP2968337B1 (fr) | 2021-07-21 |
| MX2015011514A (es) | 2016-08-11 |
| CN111793068A (zh) | 2020-10-20 |
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