JP5833010B2 - 抗癌剤としてのピラゾロピリジン誘導体 - Google Patents
抗癌剤としてのピラゾロピリジン誘導体 Download PDFInfo
- Publication number
- JP5833010B2 JP5833010B2 JP2012533621A JP2012533621A JP5833010B2 JP 5833010 B2 JP5833010 B2 JP 5833010B2 JP 2012533621 A JP2012533621 A JP 2012533621A JP 2012533621 A JP2012533621 A JP 2012533621A JP 5833010 B2 JP5833010 B2 JP 5833010B2
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- aryl
- aromatic
- group
- alkoxy
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Fee Related
Links
- 0 CCOC(c1c(-c2c[n]c3c2cccc3)c(c(*)n[n]2)c2nc1-c1ccccc1)=O Chemical compound CCOC(c1c(-c2c[n]c3c2cccc3)c(c(*)n[n]2)c2nc1-c1ccccc1)=O 0.000 description 7
- RRFNWGMAKPDEEH-UHFFFAOYSA-N CCOC(c(c(-c1ccccc1)nc1c2c(N)n[nH]1)c2-c(cc1)ccc1OC)=O Chemical compound CCOC(c(c(-c1ccccc1)nc1c2c(N)n[nH]1)c2-c(cc1)ccc1OC)=O RRFNWGMAKPDEEH-UHFFFAOYSA-N 0.000 description 1
- YYFFEPUCAKVRJX-UHFFFAOYSA-N Fc1ccc(cc[nH]2)c2c1 Chemical compound Fc1ccc(cc[nH]2)c2c1 YYFFEPUCAKVRJX-UHFFFAOYSA-N 0.000 description 1
- ATROVGYMTQXFPV-UHFFFAOYSA-N N#CCC(c(cc(cc[nH]1)c1c1)c1F)=O Chemical compound N#CCC(c(cc(cc[nH]1)c1c1)c1F)=O ATROVGYMTQXFPV-UHFFFAOYSA-N 0.000 description 1
- PUMDULYJJANIOC-UHFFFAOYSA-N N#Cc(c(-c1ccccc1)nc1c2c(-c(cc3)ccc3Cl)n[nH]1)c2-c(cc1)ccc1Cl Chemical compound N#Cc(c(-c1ccccc1)nc1c2c(-c(cc3)ccc3Cl)n[nH]1)c2-c(cc1)ccc1Cl PUMDULYJJANIOC-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0957140 | 2009-10-13 | ||
| FR0957140A FR2951172B1 (fr) | 2009-10-13 | 2009-10-13 | Derives pyrazolopyridines en tant qu'agent anticancereux |
| US25428509P | 2009-10-23 | 2009-10-23 | |
| US61/254,285 | 2009-10-23 | ||
| PCT/EP2010/065346 WO2011045344A1 (en) | 2009-10-13 | 2010-10-13 | Pyrazolopyridine derivatives as anticancer agent |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013507425A JP2013507425A (ja) | 2013-03-04 |
| JP2013507425A5 JP2013507425A5 (https=) | 2013-11-07 |
| JP5833010B2 true JP5833010B2 (ja) | 2015-12-16 |
Family
ID=42112290
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012533621A Expired - Fee Related JP5833010B2 (ja) | 2009-10-13 | 2010-10-13 | 抗癌剤としてのピラゾロピリジン誘導体 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US8889711B2 (https=) |
| EP (1) | EP2488519B1 (https=) |
| JP (1) | JP5833010B2 (https=) |
| FR (1) | FR2951172B1 (https=) |
| WO (1) | WO2011045344A1 (https=) |
Families Citing this family (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
| DE102011105469A1 (de) * | 2011-06-24 | 2012-12-27 | Merck Patent Gmbh | 7-Azaindolderivate |
| WO2013045413A1 (en) * | 2011-09-27 | 2013-04-04 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
| US10138235B2 (en) | 2011-12-14 | 2018-11-27 | Sanofi | Pyrazolopyridine derivatives, preparation process therefor and therapeutic use thereof |
| FR2984325A1 (fr) * | 2011-12-14 | 2013-06-21 | Sanofi Sa | Derives de pyrazolopyridine, leur procede de preparation et leur application en therapeutique |
| FR2985257B1 (fr) * | 2011-12-28 | 2014-02-14 | Sanofi Sa | Composes dimeres agonistes des recepteurs des fgfs (fgfrs), leur procede de preparation et leur application en therapeutique |
| CN103214470A (zh) * | 2012-01-18 | 2013-07-24 | 杨更亮 | 酮类与吲哚衍生物反应合成的新型抗癌化合物 |
| WO2013167403A1 (en) * | 2012-05-09 | 2013-11-14 | Sanofi | Substituted 6-(4-hydroxy-phenyl)-1h-pyrazolo[3,4-b]pyridine derivatives as kinase inhibitors |
| RS58514B1 (sr) | 2012-06-13 | 2019-04-30 | Incyte Holdings Corp | Supstituisana triciklična jedinjenja kao inhibitori fgfr |
| HK1207375A1 (en) | 2012-06-14 | 2016-01-29 | Daiichi Sankyo Company, Limited | Piperidinylpyrazolopyridine derivative |
| EP2867236B1 (en) | 2012-06-29 | 2017-06-14 | Pfizer Inc | Novel 4-(substituted-amino)-7h-pyrrolo[2,3-d]pyrimidines as lrrk2 inhibitors |
| US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| US9045477B2 (en) | 2013-03-15 | 2015-06-02 | Epizyme, Inc. | Substituted 6,5-fused bicyclic heteroaryl compounds |
| US9776996B2 (en) | 2013-03-15 | 2017-10-03 | Epizyme, Inc. | Substituted 6,5-fused bicyclic heteroaryl compounds |
| PH12015502383B1 (en) | 2013-04-19 | 2023-02-03 | Incyte Holdings Corp | Bicyclic heterocycles as fgfr inhibitors |
| EP3083618B1 (en) | 2013-12-17 | 2018-02-21 | Pfizer Inc | Novel 3,4-disubstituted-1h-pyrrolo[2,3-b]pyridines and 4,5-disubstituted-7h-pyrrolo[2,3-c]pyridazines as lrrk2 inhibitors |
| WO2016012896A1 (en) | 2014-07-24 | 2016-01-28 | Pfizer Inc. | Pyrazolopyrimidine compounds |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| WO2016115272A1 (en) | 2015-01-13 | 2016-07-21 | Vanderbilt University | Benzothiazole and benzisothiazole-substituted compounds as mglur4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
| US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| TWI712601B (zh) | 2015-02-20 | 2020-12-11 | 美商英塞特公司 | 作為fgfr抑制劑之雙環雜環 |
| WO2016205460A1 (en) * | 2015-06-16 | 2016-12-22 | Nantbioscience, Inc. | Polycyclic derivatives targeting ral gtpases and their therapeutical applications |
| BR112018000808A2 (pt) | 2015-07-16 | 2018-09-04 | Array Biopharma Inc | compostos de pirazolo[1,5-a]piridina substituída como inibidores de ret cinase |
| RU2722149C1 (ru) | 2015-09-14 | 2020-05-27 | Пфайзер Инк. | Новые производные имидазо[4,5-c] хинолинов и имидазо[4,5-c][1,5] нафтиридинов в качестве ингибиторов LRRK2 |
| KR102482673B1 (ko) * | 2016-07-05 | 2022-12-30 | 광저우 맥시노벨 파마수티컬스 씨오., 엘티디. | 방향족 아세틸렌 또는 방향족 에틸렌계 화합물, 그의 중간체, 제조 방법, 약물 조성물 및 용도 |
| TWI752098B (zh) | 2016-10-10 | 2022-01-11 | 美商亞雷生物製藥股份有限公司 | 作為ret激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物 |
| TWI704148B (zh) | 2016-10-10 | 2020-09-11 | 美商亞雷生物製藥股份有限公司 | 作為ret激酶抑制劑之經取代吡唑并[1,5-a]吡啶化合物 |
| WO2018136661A1 (en) | 2017-01-18 | 2018-07-26 | Andrews Steven W | SUBSTITUTED PYRAZOLO[1,5-a]PYRAZINE COMPOUNDS AS RET KINASE INHIBITORS |
| AR111473A1 (es) * | 2017-04-19 | 2019-07-17 | Sumitomo Chemical Co | Método para la preparación de compuesto de piridina |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| AU2018312349A1 (en) | 2017-08-01 | 2020-02-06 | Theravance Biopharma R&D Ip, Llc | Pyrazolo and triazolo bicyclic compounds as JAK kinase inhibitors |
| CN109988144B (zh) | 2017-12-29 | 2024-07-05 | 广州再极医药科技有限公司 | 芳香乙烯或芳香乙基类衍生物、其制备方法、中间体、药物组合物及应用 |
| US11472802B2 (en) | 2018-01-18 | 2022-10-18 | Array Biopharma Inc. | Substituted pyrazolyl[4,3-c]pyridine compounds as RET kinase inhibitors |
| EP3740490A1 (en) | 2018-01-18 | 2020-11-25 | Array Biopharma, Inc. | Substituted pyrazolo[3,4-d]pyrimidine compounds as ret kinase inhibitors |
| JP7060694B2 (ja) | 2018-01-18 | 2022-04-26 | アレイ バイオファーマ インコーポレイテッド | Retキナーゼ阻害剤としての置換ピロロ[2,3-d]ピリミジン化合物 |
| AU2019262579B2 (en) | 2018-05-04 | 2024-09-12 | Incyte Corporation | Salts of an FGFR inhibitor |
| HRP20241288T1 (hr) | 2018-05-04 | 2024-12-06 | Incyte Corporation | Čvrsti oblici fgfr inhibitora i postupci za njihovu proizvodnju |
| CN112996794A (zh) | 2018-09-10 | 2021-06-18 | 阿雷生物药品公司 | 作为ret激酶抑制剂的稠合杂环化合物 |
| CN113498352A (zh) | 2019-01-23 | 2021-10-12 | 施万生物制药研发Ip有限责任公司 | 作为jak抑制剂的咪唑并[1,5-a]吡啶、1,2,4-三唑并[4,3-a]吡啶和咪唑并[1,5-a]吡嗪 |
| US11628162B2 (en) | 2019-03-08 | 2023-04-18 | Incyte Corporation | Methods of treating cancer with an FGFR inhibitor |
| US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| WO2021067374A1 (en) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| CA3157361A1 (en) | 2019-10-14 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| WO2021076728A1 (en) | 2019-10-16 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| CA3163875A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| JP7832891B2 (ja) | 2019-12-04 | 2026-03-18 | インサイト・コーポレイション | Fgfr阻害剤の誘導体 |
| US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| TW202246259A (zh) * | 2021-01-29 | 2022-12-01 | 瑞士商赫孚孟拉羅股份公司 | 吡唑醯胺衍生物 |
| WO2022221170A1 (en) | 2021-04-12 | 2022-10-20 | Incyte Corporation | Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent |
| US11939331B2 (en) | 2021-06-09 | 2024-03-26 | Incyte Corporation | Tricyclic heterocycles as FGFR inhibitors |
| CA3220155A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| CN119968359A (zh) * | 2022-09-29 | 2025-05-09 | 英矽智能科技知识产权有限公司 | Tead抑制剂及其使用方法 |
| WO2025190406A1 (en) * | 2024-03-15 | 2025-09-18 | Insilico Medicine Ip Limited | Tead inhibitor combinations and uses thereof |
| WO2025209524A1 (en) * | 2024-04-03 | 2025-10-09 | Insilico Medicine Ip Limited | Crystalline tead inhibitor and uses thereof |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE84533T1 (de) * | 1985-12-13 | 1993-01-15 | American Cyanamid Co | Neue kondensierte pyridinverbindungen, zwischenverbindungen fuer die herstellung und ihre verwendung als herbizide wirkstoffe. |
| US4822799A (en) * | 1988-01-27 | 1989-04-18 | Sandoz Pharm. Corp. | Pyrazolopyridine analogs of mevalonolactone and derivatives thereof useful for inhibiting cholesterol biosynthesis in mammals |
| WO2003068773A1 (en) * | 2002-02-12 | 2003-08-21 | Glaxo Group Limited | Pyrazolopyridine derivatives |
| AU2003250539A1 (en) | 2002-08-07 | 2004-02-25 | Mitsubishi Pharma Corporation | Dihydropyrazolopyridine compounds |
| US20040142978A1 (en) * | 2002-12-12 | 2004-07-22 | Pharmacia Corporation | Aminocyanopyridine inhibitors of mitogen activated protein kinase-activated protein kinase-2 |
| US7468376B2 (en) * | 2003-02-27 | 2008-12-23 | Palau Pharma, S.A. | Pyrazolopyridine derivates |
| EP1648455A4 (en) * | 2003-07-23 | 2009-03-04 | Exelixis Inc | MODULATORS OF ALK PROTEIN (ANAPLASTIC LYMPHOMA KINASE) AND METHODS OF USE |
| DE602005011286D1 (en) * | 2004-07-05 | 2009-01-08 | Astellas Pharma Inc | Pyrazolopyridinderivate |
| KR101011958B1 (ko) * | 2005-08-25 | 2011-01-31 | 에프. 호프만-라 로슈 아게 | p38 MAP 키나아제 저해제로서의 융합형 피라졸 |
| WO2009006580A1 (en) * | 2007-07-05 | 2009-01-08 | Cv Therapeutics, Inc. | Optionally condensed dihydropyridine, dihydropyrimidine and dihydropyrane derivatives acting as late sodium channel blockers |
| US20100113415A1 (en) * | 2008-05-29 | 2010-05-06 | Rajapakse Hemaka A | Epha4 rtk inhibitors for treatment of neurological and neurodegenerative disorders and cancer |
-
2009
- 2009-10-13 FR FR0957140A patent/FR2951172B1/fr not_active Expired - Fee Related
-
2010
- 2010-10-13 US US13/500,757 patent/US8889711B2/en not_active Expired - Fee Related
- 2010-10-13 WO PCT/EP2010/065346 patent/WO2011045344A1/en not_active Ceased
- 2010-10-13 EP EP10770774.7A patent/EP2488519B1/en not_active Not-in-force
- 2010-10-13 JP JP2012533621A patent/JP5833010B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US20120245170A1 (en) | 2012-09-27 |
| JP2013507425A (ja) | 2013-03-04 |
| US8889711B2 (en) | 2014-11-18 |
| FR2951172A1 (fr) | 2011-04-15 |
| EP2488519A1 (en) | 2012-08-22 |
| EP2488519B1 (en) | 2015-06-10 |
| WO2011045344A1 (en) | 2011-04-21 |
| FR2951172B1 (fr) | 2014-09-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5833010B2 (ja) | 抗癌剤としてのピラゾロピリジン誘導体 | |
| CN103534254B (zh) | 作为抗肿瘤剂的三环和四环吡唑并[3,4-b]吡啶化合物 | |
| WO2022223025A1 (zh) | 杂环类衍生物抑制剂、其制备方法和应用 | |
| AU2006297948B2 (en) | Novel imidazo [4,5 -b] pyridine derivatives as inhibitors of glycogen synthase kinase 3 for use in the treatment of dementia and neurodegenerative disorders | |
| ES3030549T3 (en) | Compounds useful as inhibitors of atr kinase | |
| CN113454082B (zh) | 咪唑并吡啶基化合物及其用于治疗神经退行性疾病的用途 | |
| JP6151919B2 (ja) | ヘタリールアミノナフチリジン | |
| CZ2003683A3 (cs) | Chinolinonové deriváty | |
| JP2019514938A (ja) | イソキノリン−3イル−カルボキサミドならびにその調製および使用の方法 | |
| BRPI1007018B1 (pt) | Composto ligante de receptores de adenosina, composição farmacêutica, e, uso de um composto. | |
| JP2004513134A (ja) | Hivインテグラーゼ阻害薬として有用なアザ−およびポリアザ−ナフタレニルケトン類 | |
| JP2008534664A (ja) | 置換複素環およびchk1、pdk1及びpak阻害剤としてのそれらの使用 | |
| JP2013533318A (ja) | ヘテロアリールおよびその使用 | |
| TWI508968B (zh) | 用於治療呼吸道融合性病毒感染的化合物 | |
| JP5937201B2 (ja) | 2−アミノ−3−(イミダゾール−2−イル)ピリジン−4−オン誘導体及びvegf受容体キナーゼ阻害剤としてのその使用 | |
| CN106459060A (zh) | 作为磷酸二酯酶10a抑制剂的稠合的三唑衍生物 | |
| KR20060017865A (ko) | 환상 3급 아민 화합물 | |
| JP2024500841A (ja) | cGASと関連する病態の処置に有用なピロロ[3.2-b]ピリジン誘導体 | |
| KR20150074007A (ko) | 3,4-이치환된 1h-피라졸 및 4,5-이치환된 티아졸 syk 억제제 | |
| JP6605624B2 (ja) | 新規なヘテロ環化合物、その製造方法およびこれを含む薬学的組成物 | |
| AU2020367204A1 (en) | Derivatives of 4-(imidazo[1,2-a]pyridin-3-yl)-N-(pyridin-3-yl) pyrimidin-2- amine for treating proliferative diseases and conditions | |
| TW202342013A (zh) | 雜環化合物、其組成物及用其進行治療之方法 | |
| CA2578841A1 (en) | Inhibitors of the hiv integrase enzyme | |
| CN118307518A (zh) | 多环类parp选择性抑制剂 | |
| BR112020008640B1 (pt) | Composto derivado de dihidropiridina, composição farmacêutica, produto de combinação e uso do composto |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130920 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20130920 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20140821 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20141014 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20150114 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20150216 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20150316 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20150320 |
|
| TRDD | Decision of grant or rejection written | ||
| A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20151002 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20151028 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 5833010 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
| LAPS | Cancellation because of no payment of annual fees |