AR089945A1 - DERIVADOS DE FURO[3,2-B] Y TIENO[3,2-B]PIRIDINA COMO MODULADORES DE TBK1 E IKKe - Google Patents
DERIVADOS DE FURO[3,2-B] Y TIENO[3,2-B]PIRIDINA COMO MODULADORES DE TBK1 E IKKeInfo
- Publication number
- AR089945A1 AR089945A1 ARP130100402A ARP130100402A AR089945A1 AR 089945 A1 AR089945 A1 AR 089945A1 AR P130100402 A ARP130100402 A AR P130100402A AR P130100402 A ARP130100402 A AR P130100402A AR 089945 A1 AR089945 A1 AR 089945A1
- Authority
- AR
- Argentina
- Prior art keywords
- cyy
- nyy
- het1
- denotes
- hal
- Prior art date
Links
- 101000665442 Homo sapiens Serine/threonine-protein kinase TBK1 Proteins 0.000 title abstract 2
- 102100038192 Serine/threonine-protein kinase TBK1 Human genes 0.000 title abstract 2
- 101100452374 Mus musculus Ikbke gene Proteins 0.000 title 1
- -1 tetrahidropirazolilo Chemical group 0.000 abstract 5
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000003725 azepanyl group Chemical group 0.000 abstract 1
- 235000010290 biphenyl Nutrition 0.000 abstract 1
- 239000004305 biphenyl Substances 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 1
- 125000003016 chromanyl group Chemical group O1C(CCC2=CC=CC=C12)* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000005959 diazepanyl group Chemical group 0.000 abstract 1
- 125000005052 dihydropyrazolyl group Chemical group N1(NCC=C1)* 0.000 abstract 1
- 125000004925 dihydropyridyl group Chemical group N1(CC=CC=C1)* 0.000 abstract 1
- 125000005054 dihydropyrrolyl group Chemical group [H]C1=C([H])C([H])([H])C([H])([H])N1* 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002883 imidazolyl group Chemical group 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 125000000842 isoxazolyl group Chemical group 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000004193 piperazinyl group Chemical group 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 1
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 abstract 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 abstract 1
- 125000005942 tetrahydropyridyl group Chemical group 0.000 abstract 1
- 125000000335 thiazolyl group Chemical group 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 125000000169 tricyclic heterocycle group Chemical group 0.000 abstract 1
Classifications
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- 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
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
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- 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
- A61K31/436—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 six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
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- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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- 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
- A61K31/5365—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 ortho- or peri-condensed with heterocyclic ring systems
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- 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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- 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
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- C07D407/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- 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
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- 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
- A61K31/4355—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 oxygen as a ring hetero atom
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- A61K31/4365—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 having sulfur as a ring hetero atom, e.g. ticlopidine
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Abstract
Los compuestos de la fórmula (1) en donde X denota O ó S; R¹ denota O(CYY)ₙHet¹, NY(CYY)ₙHet¹, O(CYY)ₙCyc o NY(CYY)ₙCyc; R² denota H, Hal, A, OY, NYY, O(CYY)ₘNYY, O(CYY)ₙHet², NY(CYY)ₘNYY, NY(CYY)ₙHet², Ar o Het²; Het¹ denota dihidropirrolilo, pirrolidinilo, tetrahidroimida-zolilo, dihidropirazolilo, tetrahidropirazolilo, tetrahidropiranilo, dihidropiridilo, tetrahidropiridilo, piperidinilo morfolinilo, hexahidropiridazinilo, hexahidropirimidinilo [1,3]dioxolanilo 2-oxa-6-aza-espiro[3,3]heptanilo, azepanilo, diazepanilo, tetrahidrofuranilo, furilo, tienilo, pirrolilo, imidazolilo, pirazolilo, oxazolilo, isoxazolilo, tiazolilo, piridilo, pirimidinilo, cromanilo o piperazinilo, cada uno de los cuales no está sustituido o está mono- o disustituido Hal, CN, A, COOA, OY, S(O)ₙA, S(O)ₙAr y/u =O (oxígeno del carbonilo); Het² denota un heterociclo saturado, insaturado o aromático mono-, bi- o tricíclico que tiene 1 a 4 átomos de N, O y/o S, que puede no estar sustituido o que puede estar mono-, di-, tri-, tetra- o penta-sustituido con Hal, A, (CYY)ₚ-OY, -(CYY)ₚ-NYY, (CYY)ₚ-Het¹, NO₂, CN, (CYY)ₚ-COOY, CO-NYY, NY-COA, NY-SO₂A, SO₂-NYY, S(O)ₙA, -CO-Het¹, O(CYY)ₚ-NYY, -O(CYY)ₚ-Het¹, NH-COOA, NH-CO-NYY, NH-COO-(CYY)ₚ-NYY, NH-COO-(CYY)ₚ-Het¹, NH-CO-NH-(CYY)ₚ-NYY, NH-CO-NH(CYY)ₚ-Het¹, OCO-NH-(CYY)ₚ-NYY, OCO-NH-(CYY)ₚ-Het¹, CHO, COA, =S, =NY y/u =O; Ar denota fenilo, naftilo o bifenilo, cada uno de los cuales no está sustituido o que está mono-, di- o trisustituido con Hal, A, (CYY)ₚ-OY, (CYY)ₚ-NYY, (CYY)ₚ-Het¹, NO₂, CN, (CYY)ₚ-COOY, CO(CYY)ₚNH₂, CO-NYA, CONY(CYY)ₘNYCOOA, NY-COA, NY-SO₂A, SO₂-NYY, S(O)ₙA, CO-Het¹, O(CYY)ₚ-NYY, O(CYY)ₚ-Het¹, NH-COOA, NH-CO-NYY, NH-COO-(CYY)ₚ-NYY, NH-COO-(CYY)ₚ-Het¹, NH-CO-NH-(CYY)ₚ-NYY, NH-CO-NH(CYY)ₚ-Het¹, OCO-NH-(CYY)ₚ-NYY, OCO-NH-(CYY)ₚ-Het¹, CHO, CONY(CYY)ₚHet¹, CONH(CYY)ₚNHCOA y/o COA; Y denota H o alquilo C₁₋₄; A denota alquilo C₁₋₁₀ no ramificado o ramificado, en donde 1 - 7 átomos de H pueden estar reemplazados por F y/o Cl y/o en donde uno o dos grupos no adyacentes CH y/o CH₂ pueden estar reemplazados por O y/o N; Cyc denota cicloalquilo C₃₋₇, que no está sustituido o que está monosustituido con Hal, CN o A; Hal denota F, CI. Br o I; n denota 0, 1, ó 2; m denota 1, 2 ó 3; p denota 0,1, 2, 3 ó 4; y sus sales, tautómeros y estereoisómeros farmacéuticamente aceptables, incluyendo sus mezclas en todas las proporciones. Son inhibidores de TBK1 e lKKe y se pueden emplear, inter alia, para el tratamiento de cáncer y enfermedades inflamatorias.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
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Families Citing this family (17)
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| GB201303109D0 (en) | 2013-02-21 | 2013-04-10 | Domainex Ltd | Novel pyrimidine compounds |
| TW201613916A (en) * | 2014-06-03 | 2016-04-16 | Gilead Sciences Inc | TANK-binding kinase inhibitor compounds |
| ES2881195T3 (es) | 2014-09-26 | 2021-11-29 | Gilead Sciences Inc | Derivados de aminotriazina útiles como compuestos inhibidores de quinasas que se unen a TANK |
| CN108473478A (zh) * | 2015-06-29 | 2018-08-31 | 默克专利有限公司 | TBK/IKKε抑制剂化合物及其用途 |
| JP2019500368A (ja) | 2015-12-17 | 2019-01-10 | ギリアード サイエンシーズ, インコーポレイテッド | Tank結合キナーゼ阻害剤化合物 |
| EP3390387B1 (en) | 2015-12-18 | 2021-11-17 | Bayer Pharma Aktiengesellschaft | Heteroarylbenzimidazole compounds |
| WO2017207534A1 (en) | 2016-06-03 | 2017-12-07 | Bayer Pharma Aktiengesellschaft | Substituted heteroarylbenzimidazole compounds |
| DE102016113714A1 (de) | 2016-07-26 | 2018-02-01 | Rosa Karl | Transfektionsverfahren mit nicht-viralen Genliefersystemen |
| GB201702947D0 (en) | 2017-02-23 | 2017-04-12 | Domainex Ltd | Novel compounds |
| BR112020007549A2 (pt) | 2017-10-17 | 2020-09-24 | Merck Patent Gmbh | compostos inibidores de pirimidina tbk/ikképsilon e uso dos mesmos |
| US10722514B2 (en) * | 2017-11-13 | 2020-07-28 | Rapt Therapeutics, Inc. | Ubiquitin-specific-processing protease 7 (USP7) modulators and uses thereof |
| WO2020068600A1 (en) * | 2018-09-24 | 2020-04-02 | Rapt Therapeutics, Inc. | Ubiquitin-specific-processing protease 7 (usp7) modulators and uses thereof |
| KR102658602B1 (ko) | 2018-10-31 | 2024-04-19 | 길리애드 사이언시즈, 인코포레이티드 | Hpk1 억제 활성을 갖는 치환된 6-아자벤즈이미다졸 화합물 |
| SG11202103839UA (en) | 2018-10-31 | 2021-05-28 | Gilead Sciences Inc | Substituted 6-azabenzimidazole compounds as hpk1 inhibitors |
| US11453681B2 (en) | 2019-05-23 | 2022-09-27 | Gilead Sciences, Inc. | Substituted eneoxindoles and uses thereof |
| WO2024033281A1 (en) | 2022-08-09 | 2024-02-15 | Merck Patent Gmbh | Furo pyrimidine derivates |
| WO2024033280A1 (en) | 2022-08-09 | 2024-02-15 | Merck Patent Gmbh | Furopyridin and furopyrimidin, inhibitors of pi4k, for use in the treatment of parasite infection and malaria |
Family Cites Families (27)
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| US5747469A (en) | 1991-03-06 | 1998-05-05 | Board Of Regents, The University Of Texas System | Methods and compositions comprising DNA damaging agents and p53 |
| GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
| CN1125817C (zh) | 1996-02-13 | 2003-10-29 | 曾尼卡有限公司 | 作为vegf抑制剂的喹唑啉衍生物 |
| JP4464466B2 (ja) | 1996-03-05 | 2010-05-19 | アストラゼネカ・ユーケイ・リミテッド | 4―アニリノキナゾリン誘導体 |
| GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
| GB9714249D0 (en) | 1997-07-08 | 1997-09-10 | Angiogene Pharm Ltd | Vascular damaging agents |
| US6187777B1 (en) * | 1998-02-06 | 2001-02-13 | Amgen Inc. | Compounds and methods which modulate feeding behavior and related diseases |
| GB9900334D0 (en) | 1999-01-07 | 1999-02-24 | Angiogene Pharm Ltd | Tricylic vascular damaging agents |
| GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
| GB9904387D0 (en) | 1999-02-25 | 1999-04-21 | Pharmacia & Upjohn Spa | Antitumour synergistic composition |
| CA2406979A1 (en) | 2000-05-31 | 2001-12-06 | Astrazeneca Ab | Indole derivatives with vascular damaging activity |
| CA2410562A1 (en) | 2000-07-07 | 2002-01-31 | Angiogene Pharmaceuticals Limited | Colchinol derivatives as angiogenesis inhibitors |
| JP2004502766A (ja) | 2000-07-07 | 2004-01-29 | アンギオジェン・ファーマシューティカルズ・リミテッド | 血管損傷剤としてのコルヒノール誘導体 |
| TWI319387B (en) * | 2002-04-05 | 2010-01-11 | Astrazeneca Ab | Benzamide derivatives |
| JP4364120B2 (ja) * | 2002-06-06 | 2009-11-11 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | 置換3−アミノ−チエノ[2,3−b]ピリジン−2−カルボン酸アミド化合物、その製造方法及び使用 |
| US7276519B2 (en) * | 2002-11-25 | 2007-10-02 | Wyeth | Thieno[3,2-b]pyridine-6-carbonitriles and thieno[2,3-b]pyridine-5-carbonitriles as protein kinase inhibitors |
| SE0203754D0 (sv) | 2002-12-17 | 2002-12-17 | Astrazeneca Ab | New compounds |
| JP2008524134A (ja) * | 2004-12-17 | 2008-07-10 | エフ.ホフマン−ラ ロシュ アーゲー | Gaba−bアロステリックエンハンサーとしてのチエノ−ピリジン誘導体 |
| WO2007129044A1 (en) | 2006-05-03 | 2007-11-15 | Astrazeneca Ab | Thiazole derivatives and their use as anti-tumour agents |
| WO2009030890A1 (en) | 2007-09-03 | 2009-03-12 | University Court Of The University Of Dundee | Pyrimidine compounds for the treatment of cancer, septic shock and/or primary open angle glaucoma |
| WO2009053737A2 (en) | 2007-10-25 | 2009-04-30 | Astrazeneca Ab | Pyridine and pyrazine derivatives useful in the treatment of cell proliferative disorders |
| US20100056524A1 (en) | 2008-04-02 | 2010-03-04 | Mciver Edward Giles | Compound |
| GB0903759D0 (en) | 2009-03-04 | 2009-04-15 | Medical Res Council | Compound |
| BR112012004843A2 (pt) * | 2009-09-03 | 2019-09-24 | Allergan Inc | compostos como moduladores de tirosina cinase |
| KR20120114224A (ko) * | 2009-10-12 | 2012-10-16 | 마이렉시스 인코포레이티드 | Ikk 엡실론 및/또는 tbk1의 억제제로서의 아미노-피리미딘 화합물 |
| GB201012105D0 (en) * | 2010-07-19 | 2010-09-01 | Domainex Ltd | Novel pyrimidine compounds |
| JP5789300B2 (ja) * | 2010-08-27 | 2015-10-07 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | フロピリジン誘導体 |
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2013
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- 2013-01-03 HR HRP20161578TT patent/HRP20161578T1/hr unknown
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- 2013-01-03 PT PT137001921T patent/PT2812337T/pt unknown
- 2013-01-03 RS RS20161082A patent/RS55388B1/sr unknown
- 2013-01-03 RU RU2014136366A patent/RU2622034C2/ru not_active IP Right Cessation
- 2013-01-03 SG SG11201404630UA patent/SG11201404630UA/en unknown
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Also Published As
| Publication number | Publication date |
|---|---|
| KR20140120371A (ko) | 2014-10-13 |
| JP2015510511A (ja) | 2015-04-09 |
| HRP20161578T1 (hr) | 2016-12-30 |
| AU2013218354B2 (en) | 2017-01-19 |
| ES2606637T3 (es) | 2017-03-24 |
| CA2863985C (en) | 2020-08-11 |
| US9045493B2 (en) | 2015-06-02 |
| US20150005284A1 (en) | 2015-01-01 |
| PT2812337T (pt) | 2016-12-14 |
| CA2863985A1 (en) | 2013-08-15 |
| IL233981A (en) | 2016-09-29 |
| BR112014017762A8 (pt) | 2017-07-11 |
| JP6138831B2 (ja) | 2017-05-31 |
| RU2622034C2 (ru) | 2017-06-09 |
| HK1202550A1 (zh) | 2015-10-02 |
| RS55388B1 (sr) | 2017-03-31 |
| PL2812337T3 (pl) | 2017-01-31 |
| DK2812337T3 (en) | 2016-11-07 |
| HUE032203T2 (en) | 2017-08-28 |
| LT2812337T (lt) | 2016-11-25 |
| AU2013218354A1 (en) | 2014-09-25 |
| BR112014017762A2 (es) | 2017-06-20 |
| ZA201406581B (en) | 2015-12-23 |
| SI2812337T1 (sl) | 2017-01-31 |
| MX2014009173A (es) | 2014-08-27 |
| MX350112B (es) | 2017-08-28 |
| CN104093722B (zh) | 2016-07-27 |
| CN104093722A (zh) | 2014-10-08 |
| SG11201404630UA (en) | 2014-09-26 |
| EP2812337A1 (en) | 2014-12-17 |
| RU2014136366A (ru) | 2016-03-27 |
| EP2812337B1 (en) | 2016-09-07 |
| WO2013117285A1 (en) | 2013-08-15 |
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