CN103108871B - 17α-羟化酶/C17,20-裂合酶抑制剂 - Google Patents
17α-羟化酶/C17,20-裂合酶抑制剂 Download PDFInfo
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- CN103108871B CN103108871B CN201180044494.8A CN201180044494A CN103108871B CN 103108871 B CN103108871 B CN 103108871B CN 201180044494 A CN201180044494 A CN 201180044494A CN 103108871 B CN103108871 B CN 103108871B
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- Prior art keywords
- alkyl
- pyridin
- methyl
- mmol
- dihydro
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- 0 CC(C)c1c(*)c(*)c(*)nc1 Chemical compound CC(C)c1c(*)c(*)c(*)nc1 0.000 description 22
- PGVNIXQJEXNZHE-UHFFFAOYSA-N CC(C(C(CCN)C=C1)C=C1C#N)=O Chemical compound CC(C(C(CCN)C=C1)C=C1C#N)=O PGVNIXQJEXNZHE-UHFFFAOYSA-N 0.000 description 1
- PXSYKFKOKXYQRH-UHFFFAOYSA-N Cc(ccc(CCN)c1)c1OC Chemical compound Cc(ccc(CCN)c1)c1OC PXSYKFKOKXYQRH-UHFFFAOYSA-N 0.000 description 1
- BWYHGEQTCVTNFQ-UHFFFAOYSA-N Cc1c(CCO)ccnc1 Chemical compound Cc1c(CCO)ccnc1 BWYHGEQTCVTNFQ-UHFFFAOYSA-N 0.000 description 1
- ZSZCXAOQVBEPME-UHFFFAOYSA-N NCCc(cc1)ccc1Br Chemical compound NCCc(cc1)ccc1Br ZSZCXAOQVBEPME-UHFFFAOYSA-N 0.000 description 1
- HMFOBPNVAAAACP-UHFFFAOYSA-N NCCc1ccc(C(F)(F)F)cc1 Chemical compound NCCc1ccc(C(F)(F)F)cc1 HMFOBPNVAAAACP-UHFFFAOYSA-N 0.000 description 1
- XXHSKGGPLKGDJR-UHFFFAOYSA-N O=C(C(C(CC1)C=C2F)C=C2Cl)N1C1=C=[N]=CCC1C(F)(F)F Chemical compound O=C(C(C(CC1)C=C2F)C=C2Cl)N1C1=C=[N]=CCC1C(F)(F)F XXHSKGGPLKGDJR-UHFFFAOYSA-N 0.000 description 1
- PWZBFAAVBDWGRS-UHFFFAOYSA-N O=C(C(C1)C(CC2)=CC=C1C(F)(F)F)N2c1c[n]ccc1C1CC1 Chemical compound O=C(C(C1)C(CC2)=CC=C1C(F)(F)F)N2c1c[n]ccc1C1CC1 PWZBFAAVBDWGRS-UHFFFAOYSA-N 0.000 description 1
- RDNZDMDLRIQQAX-UHFFFAOYSA-N O=C(CCN1)CC1=O Chemical compound O=C(CCN1)CC1=O RDNZDMDLRIQQAX-UHFFFAOYSA-N 0.000 description 1
- ZZXDILUZKNPOER-UHFFFAOYSA-N O=C(c1cc(C(F)(F)F)ccc1CC1)N1c1c(C(F)(F)F)ccnc1 Chemical compound O=C(c1cc(C(F)(F)F)ccc1CC1)N1c1c(C(F)(F)F)ccnc1 ZZXDILUZKNPOER-UHFFFAOYSA-N 0.000 description 1
- RAIRXYJWCATZKS-UHFFFAOYSA-N O=C1NCCC2=C1CC=CC=C2 Chemical compound O=C1NCCC2=C1CC=CC=C2 RAIRXYJWCATZKS-UHFFFAOYSA-N 0.000 description 1
- OWIVTJUGQKUQAQ-UHFFFAOYSA-N O=C1NCCC2C1=CC(C(F)(F)F)=CC2 Chemical compound O=C1NCCC2C1=CC(C(F)(F)F)=CC2 OWIVTJUGQKUQAQ-UHFFFAOYSA-N 0.000 description 1
- RTSIUKMGSDOSTI-SNAWJCMRSA-N OC(/C=C/c1cc(F)ccc1)=O Chemical compound OC(/C=C/c1cc(F)ccc1)=O RTSIUKMGSDOSTI-SNAWJCMRSA-N 0.000 description 1
- IEXXHNKQVORYBK-UHFFFAOYSA-N OC(C(C1)C(CC2)CC=C1C(F)(F)F)N2c1cnccc1CN1CCCC1 Chemical compound OC(C(C1)C(CC2)CC=C1C(F)(F)F)N2c1cnccc1CN1CCCC1 IEXXHNKQVORYBK-UHFFFAOYSA-N 0.000 description 1
- CMNQIVHHHBBVSC-UHFFFAOYSA-N Oc1c(CCNC2=O)c2ccc1 Chemical compound Oc1c(CCNC2=O)c2ccc1 CMNQIVHHHBBVSC-UHFFFAOYSA-N 0.000 description 1
- MXWBZSYBKZEXLK-UHFFFAOYSA-N [O-][N+](C#Cc1cc2ccccc2cc1)=O Chemical compound [O-][N+](C#Cc1cc2ccccc2cc1)=O MXWBZSYBKZEXLK-UHFFFAOYSA-N 0.000 description 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
- A61K31/473—Quinolines; Isoquinolines ortho- or peri-condensed with carbocyclic ring systems, e.g. acridines, phenanthridines
-
- 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
- A61K31/4365—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
-
- 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
- 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
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine 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
- A61K31/495—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
-
- 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
- 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
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
- 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
- C07D471/12—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 three hetero rings
- C07D471/14—Ortho-condensed systems
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN2719CH2010 | 2010-09-16 | ||
| IN2719/CHE/2010 | 2010-09-16 | ||
| PCT/EP2011/065965 WO2012035078A1 (en) | 2010-09-16 | 2011-09-14 | 17α-HYDROXYLASE/C17,20-LYASE INHIBITORS |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN103108871A CN103108871A (zh) | 2013-05-15 |
| CN103108871B true CN103108871B (zh) | 2014-09-10 |
Family
ID=44719880
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201180044494.8A Expired - Fee Related CN103108871B (zh) | 2010-09-16 | 2011-09-14 | 17α-羟化酶/C17,20-裂合酶抑制剂 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8946260B2 (https=) |
| EP (1) | EP2627648A1 (https=) |
| JP (1) | JP2013537210A (https=) |
| CN (1) | CN103108871B (https=) |
| WO (1) | WO2012035078A1 (https=) |
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|---|---|---|---|---|
| AU2012249421B9 (en) | 2011-04-28 | 2015-10-22 | Novartis Ag | 17alpha-hydroxylase/C17,20-lyase inhibitors |
| BR112014013136B1 (pt) * | 2011-11-30 | 2020-05-26 | F. Hoffmann-La Roche Ag | Novos derivados de dihidroisoquinolina-1-ona biciclicos |
| CN103958478B (zh) * | 2011-11-30 | 2017-08-01 | 霍夫曼-拉罗奇有限公司 | 双环二氢异喹啉‑1‑酮衍生物 |
| AR092742A1 (es) | 2012-10-02 | 2015-04-29 | Intermune Inc | Piridinonas antifibroticas |
| UA111305C2 (uk) | 2012-12-21 | 2016-04-11 | Пфайзер Інк. | Конденсовані лактами арилу та гетероарилу |
| CN104370925A (zh) * | 2013-01-24 | 2015-02-25 | 韩冰 | 一类蛋白酶抑制剂及其制备方法和用途 |
| CN104370926A (zh) * | 2013-01-24 | 2015-02-25 | 韩冰 | 一类具有神经保护作用的化合物及其制备方法和用途 |
| CN103086945A (zh) * | 2013-01-24 | 2013-05-08 | 张家港威胜生物医药有限公司 | 一种重要医药化工中间体色胺合成工艺 |
| CN104370938A (zh) * | 2013-01-24 | 2015-02-25 | 韩冰 | 一类降低眼压的化合物及其制备方法和用途 |
| JP6581970B2 (ja) * | 2013-05-27 | 2019-09-25 | エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft | 新規3,4−ジヒドロ−2h−イソキノリン−1−オン及び2,3−ジヒドロ−イソインドール−1−オン化合物 |
| WO2014191338A1 (en) * | 2013-05-27 | 2014-12-04 | F. Hoffmann-La Roche Ag | New 3,4-dihydro-2h-isoquinoline-1-one and 2,3-dihydro-isoindol-1-one compounds |
| SI3004076T1 (sl) * | 2013-05-27 | 2020-02-28 | F. Hoffmann-La Roche Ag | Novi spojini 3,4-dihidro-2H-izokinolin-1-on in 2,3-dihidro-izoindol-1-on |
| JO3368B1 (ar) | 2013-06-04 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 6، 7- ثاني هيدرو بيرازولو [5،1-a] بيرازين- 4 (5 يد)- اون واستخدامها بصفة منظمات تفارغية سلبية لمستقبلات ميجلور 2 |
| MX382781B (es) | 2014-04-02 | 2025-03-13 | Intermune Inc | Piridinonas anti-fibroticas. |
| EP3157915B1 (en) | 2014-06-17 | 2019-02-27 | Pfizer Inc | Substituted dihydroisoquinolinone compounds |
| US9657015B2 (en) | 2014-07-31 | 2017-05-23 | Boehringer Ingelheim International Gmbh | Substituted bicyclic dihydropyrimidinones and their use as inhibitors of neutrophil elastase activity |
| JOP20150179B1 (ar) | 2014-08-01 | 2021-08-17 | Janssen Pharmaceutica Nv | مركبات 6 ، 7 ثاني هيدرو بيرازولو [ 1، 5 الفا ] بيرازين – 4 (5 يد) – اون واستخدامها كمنظمات الوسترية سلبية لمستقبلات ملجور 2 |
| JOP20150177B1 (ar) | 2014-08-01 | 2021-08-17 | Janssen Pharmaceutica Nv | مركبات 6 ، 7 ثاني هيدرو بيرازولو [ 1، 5 الفا ] بيرازين – 4 (5 يد) – اون واستخدامها كمنظمات الوسترية سلبية لمستقبلات ملجور 2 |
| JP6861154B2 (ja) | 2014-12-03 | 2021-04-21 | ヤンセン ファーマシューティカ エヌ.ベー. | 放射標識されたmGluR2 PETリガンド |
| AU2015357167B2 (en) | 2014-12-03 | 2020-06-25 | Janssen Pharmaceutica Nv | 6,7-dihydropyrazolo(1,5-alpha)pyrazin-4(5H)-one compounds and their use as negative allosteric modulators of mGluR2 receptors |
| MA41140A (fr) * | 2014-12-12 | 2017-10-17 | Cancer Research Tech Ltd | Dérivés de 2,4-dioxo-quinazoline-6-sulfonamide en tant qu'inhibiteurs de la parg |
| MA41179A (fr) | 2014-12-19 | 2017-10-24 | Cancer Research Tech Ltd | Composés inhibiteurs de parg |
| LT3389727T (lt) | 2015-12-18 | 2020-10-12 | Janssen Pharmaceutica Nv | Radioaktyviai pažymėti mglur2/3 pet ligandai |
| EA037941B1 (ru) | 2015-12-18 | 2021-06-09 | Янссен Фармацевтика Нв | ЛИГАНДЫ mGluR2/3 ДЛЯ PET, МЕЧЕННЫЕ РАДИОАКТИВНЫМИ ИЗОТОПАМИ |
| CN105541712B (zh) * | 2016-01-08 | 2018-10-09 | 山东金城医药集团股份有限公司 | 索利那新中间体的制备方法 |
| CN108264509B (zh) * | 2016-12-30 | 2021-05-04 | 复旦大学 | 取代的苯并噻吩并[2,3-c]四氢吡啶衍生物及其制备方法和用途 |
| CN109071448B (zh) * | 2017-01-22 | 2020-03-17 | 福建广生堂药业股份有限公司 | Ask1抑制剂及其制备方法和应用 |
| CN108929228A (zh) * | 2018-07-09 | 2018-12-04 | 上海华堇生物技术有限责任公司 | 一种3-甲氧基-β-硝基苯乙烯的新制备方法 |
| CN108586259A (zh) * | 2018-07-09 | 2018-09-28 | 上海华堇生物技术有限责任公司 | 一种2-甲氧基-β-硝基苯乙烯的新制备方法 |
| CN108929229A (zh) * | 2018-07-10 | 2018-12-04 | 上海华堇生物技术有限责任公司 | 一种4-氯-β-硝基苯乙烯的新制备方法 |
| CN114410727B (zh) * | 2022-01-25 | 2023-09-19 | 山东诺明康药物研究院有限公司 | 一种克拉考特酮的制备方法 |
| AR128846A1 (es) | 2022-03-23 | 2024-06-19 | Ideaya Biosciences Inc | Compuestos de indazol sustituidos con piperazina como inhibidores de parg |
| CN117229284B (zh) * | 2023-11-10 | 2024-02-06 | 上海泽德曼医药科技有限公司 | 三环稠杂环类化合物、其制备方法及其在医药上的应用 |
| CN119751453B (zh) * | 2025-01-13 | 2025-10-10 | 浙江工业大学 | 一种n-n轴手性异喹啉酮衍生物的制备方法 |
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- 2011-09-14 WO PCT/EP2011/065965 patent/WO2012035078A1/en not_active Ceased
- 2011-09-14 CN CN201180044494.8A patent/CN103108871B/zh not_active Expired - Fee Related
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| Publication number | Publication date |
|---|---|
| JP2013537210A (ja) | 2013-09-30 |
| US8946260B2 (en) | 2015-02-03 |
| EP2627648A1 (en) | 2013-08-21 |
| WO2012035078A1 (en) | 2012-03-22 |
| US20140045872A1 (en) | 2014-02-13 |
| CN103108871A (zh) | 2013-05-15 |
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