JP5564257B2 - 新規副溝バインダー - Google Patents

新規副溝バインダー Download PDF

Info

Publication number
JP5564257B2
JP5564257B2 JP2009529767A JP2009529767A JP5564257B2 JP 5564257 B2 JP5564257 B2 JP 5564257B2 JP 2009529767 A JP2009529767 A JP 2009529767A JP 2009529767 A JP2009529767 A JP 2009529767A JP 5564257 B2 JP5564257 B2 JP 5564257B2
Authority
JP
Japan
Prior art keywords
methyl
amino
pyrrol
carbonyl
ethenyl
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
Application number
JP2009529767A
Other languages
English (en)
Japanese (ja)
Other versions
JP2010505757A5 (enExample
JP2010505757A (ja
Inventor
アベダウン・カラフ
コリン・サックリング
ロジャー・ワイ
Original Assignee
ユニヴァースティ オブ ストラスクライド
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.)
Filing date
Publication date
Application filed by ユニヴァースティ オブ ストラスクライド filed Critical ユニヴァースティ オブ ストラスクライド
Publication of JP2010505757A publication Critical patent/JP2010505757A/ja
Publication of JP2010505757A5 publication Critical patent/JP2010505757A5/ja
Application granted granted Critical
Publication of JP5564257B2 publication Critical patent/JP5564257B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

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
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10—Antimycotics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00—Antiparasitic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00—Antiparasitic agents
    • A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
    • A61P33/06—Antimalarials
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Epidemiology (AREA)
  • Virology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Pyrrole Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
JP2009529767A 2006-09-30 2007-09-28 新規副溝バインダー Expired - Fee Related JP5564257B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0619325.4 2006-09-30
GBGB0619325.4A GB0619325D0 (en) 2006-09-30 2006-09-30 New compounds
PCT/GB2007/003698 WO2008038018A1 (en) 2006-09-30 2007-09-28 Novel minor groove binders

Publications (3)

Publication Number Publication Date
JP2010505757A JP2010505757A (ja) 2010-02-25
JP2010505757A5 JP2010505757A5 (enExample) 2010-12-09
JP5564257B2 true JP5564257B2 (ja) 2014-07-30

Family

ID=37434989

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009529767A Expired - Fee Related JP5564257B2 (ja) 2006-09-30 2007-09-28 新規副溝バインダー

Country Status (10)

Country Link
US (1) US8012967B2 (enExample)
EP (1) EP2066627B1 (enExample)
JP (1) JP5564257B2 (enExample)
CN (1) CN101589024B (enExample)
CA (1) CA2664847C (enExample)
DK (1) DK2066627T3 (enExample)
ES (1) ES2443720T3 (enExample)
GB (2) GB0619325D0 (enExample)
PL (1) PL2066627T3 (enExample)
WO (1) WO2008038018A1 (enExample)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9072535B2 (en) 2011-05-27 2015-07-07 Ethicon Endo-Surgery, Inc. Surgical stapling instruments with rotatable staple deployment arrangements
WO2011150156A2 (en) * 2010-05-26 2011-12-01 Sunovion Pharmaceuticals Inc. Heteroaryl compounds and methods of use thereof
CZ305332B6 (cs) * 2013-10-25 2015-08-05 Univerzita Karlova v Praze, Farmaceutická fakulta v Hradci Králové Použití derivátů pyrazinu a jejich isosterů jako sloučenin vážících se do malého žlábku DNA
CN105732583B (zh) * 2016-03-25 2018-05-04 苏州麦迪耐斯医药科技有限公司 一种治疗脑胶质母细胞瘤的靶向化合物
CN109715637B (zh) 2016-07-22 2022-04-05 百时美施贵宝公司 葡萄糖激酶激活剂及其使用方法
WO2018047148A1 (en) 2016-09-12 2018-03-15 Novartis Ag Compounds for the inhibition of mirna
JP7477858B2 (ja) * 2020-03-05 2024-05-02 国立大学法人電気通信大学 急性tリンパ芽球性白血病若しくはリンパ腫、又は急性骨髄性白血病治療用医薬組成物
GB202114032D0 (en) 2021-09-30 2021-11-17 Univ Strathclyde Antivirals
GB202206931D0 (en) 2022-05-12 2022-06-29 Univ Strathclyde Compounds
CN115109113B (zh) * 2022-05-31 2023-06-27 上海应用技术大学 一种胆固醇类衍生物有机凝胶因子及其制备方法和应用
CN116514698A (zh) * 2023-04-10 2023-08-01 佛山奕安赛医药科技有限公司 一种沃诺拉赞中间体的制备方法及其应用

Family Cites Families (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1886481A (en) * 1927-11-07 1932-11-08 Soc Of Chemical Ind Unilaterally acylated diamines and process of making same
DE2331444A1 (de) 1973-06-20 1975-01-23 Hoechst Ag Neue styryl-benzoxazole, verfahren zu deren herstellung und ihre verwendung als optische aufhellungsmittel
US4665181A (en) 1984-05-17 1987-05-12 Pennwalt Corporation Anti-inflammatory phthalazinones
CA1308516C (en) * 1987-07-06 1992-10-06 The Governors Of The University Of Alberta Oligopeptide anticancer and antiviral agents
IL90337A0 (en) 1988-05-24 1989-12-15 Pfizer Aromatic and heterocyclic carboxamide derivatives as antineoplastic agents
US4919199A (en) * 1989-01-13 1990-04-24 The Atlantic Group, Inc. Multiple locking stake for tube bundle
FR2656608B1 (fr) 1989-12-28 1992-04-24 Roussel Uclaf Nouvelles polyamines benzoylees, leur procede de preparation et leur application comme fongicides.
US5273991A (en) * 1992-07-29 1993-12-28 Research Corporation Technologies, Inc. Imidazole-containing compositions and methods of use thereof analogs of distamycin
IT1263089B (it) * 1993-04-26 1996-07-24 Menarini Farma Ind Composti pirrol-amidinici, processi di preparazione e composizioni farmaceutiche che li contengono.
US5698674A (en) * 1994-04-13 1997-12-16 The Regents Of The University Of California Triheterocyclic peptides capable of binding the minor and major grooves of DNA
GB9416005D0 (en) * 1994-08-08 1994-09-28 Erba Carlo Spa Peptidic compounds analogous to distamycin a and process for their preparation
US5637621A (en) * 1994-11-14 1997-06-10 Nzym, Inc. Methods and compositions for treating Botrytis infections
US5801155A (en) * 1995-04-03 1998-09-01 Epoch Pharmaceuticals, Inc. Covalently linked oligonucleotide minor grove binder conjugates
US5767142A (en) * 1996-03-20 1998-06-16 Rutgers, The State University Of New Jersey Trisbenzimidazoles useful as topoisomerase I inhibitors
GB9516943D0 (en) * 1995-08-18 1995-10-18 Cancer Soc Auckland Div Nz Inc Novel cyclopropylindoles and their secoprecursors,and their use as prodrugs
JP2000503999A (ja) 1996-02-02 2000-04-04 フアルマシア・エ・アツプジヨン・エツセ・ピー・アー ジスタマイシン誘導体、その調製方法、および抗腫瘍および抗ウイルス剤としてのその使用
JP2001513759A (ja) * 1996-02-26 2001-09-04 カリフォルニア・インスティチュート・オブ・テクノロジー 二本鎖dnaの副溝において結合する改良されたポリアミド
US6506906B1 (en) * 1996-02-26 2003-01-14 California Institute Of Technology Preparation and use of bifunctional molecules having DNA sequence binding specificity
US6143901A (en) 1996-07-31 2000-11-07 Genesoft, Inc. Complex formation between dsDNA and pyrrole imidazole polyamides
US6635417B1 (en) * 1996-07-31 2003-10-21 California Institute Of Technology Complex formation between DSDNA and oligomer of cyclic heterocycles
US6090947A (en) * 1996-02-26 2000-07-18 California Institute Of Technology Method for the synthesis of pyrrole and imidazole carboxamides on a solid support
US5770617A (en) 1996-03-20 1998-06-23 Rutgers, The State University Of New Jersey Terbenzimidazoles useful as antifungal agents
CA2255703A1 (en) * 1996-05-31 1997-12-04 Dale L. Boger Analogs of cc-1065 and the duocarmycins
WO1998002441A2 (en) * 1996-07-12 1998-01-22 Ariad Pharmaceuticals, Inc. Non immunosuppressive antifungal rapalogs
JP2002515057A (ja) * 1996-08-01 2002-05-21 カリフォルニア・インスティチュート・オブ・テクノロジー ポリアミドdna結合リガンドによる遺伝子発現の阻害
GB9623522D0 (en) 1996-11-11 1997-01-08 Pharmacia & Upjohn Spa Benzoheterocycle distamycin derivatives process for preparing them and their use as antitumour and antiviral agents
US6251933B1 (en) * 1996-12-13 2001-06-26 The Cancer Research Campaign Technology Limited Seco precursors of cyclopropylindolines and their use as prodrugs
JP2001510057A (ja) * 1997-07-17 2001-07-31 ティーエム テクノロジーズ, インク. 核酸の融解温度を調節する方法及び組成
JPH11189594A (ja) 1997-12-25 1999-07-13 Mitsui Chem Inc アクリル酸誘導体を側鎖にもつピロリルベンズイミダゾール誘導体
US6008247A (en) * 1998-02-27 1999-12-28 The University Of North Carolina At Chapel Hill 2,4-bis[(4-amidino)phenyl]furans as anti-Pneumocystis carinii agents
ES2198139T3 (es) * 1998-08-20 2004-01-16 The University Of North Carolina At Chapel Hill Compuestos de dibenzotiofeno y procedimientos de uso de los mismos.
GB9818730D0 (en) * 1998-08-27 1998-10-21 Univ Portsmouth Collections of compounds
ES2260570T3 (es) * 1998-08-27 2006-11-01 Spirogen Limited Pirrolobenziodiazepinas dimericas.
GB9818731D0 (en) * 1998-08-27 1998-10-21 Univ Portsmouth Compounds
JP2002524503A (ja) * 1998-09-17 2002-08-06 ザ・ユニヴァーシティ・オヴ・ノース・キャロライナ・アト・チャペル・ヒル 二陽イオン分子の抗真菌活性
GB9908828D0 (en) * 1999-04-16 1999-06-16 Univ Reading The Compounds
CA2377902A1 (en) * 1999-07-08 2001-01-18 The University Of North Carolina At Chapel Hill Novel prodrugs for antimicrobial amidines
AU7381600A (en) 1999-09-17 2001-04-17 Genelabs Technologies, Inc. Covalently linked dimeric dna binding molecules
JP2003519623A (ja) * 1999-12-20 2003-06-24 ザ ユニバーシティ オブ ノース カロライナ アット チャペル ヒル Dna小溝結合剤としてのジアミジン化合物
JP2001181279A (ja) 1999-12-28 2001-07-03 Mitsui Chemicals Inc ベンゾフラニルピロールカルボキシアミド誘導体
ATE362940T1 (de) * 2000-03-16 2007-06-15 Genesoft Inc Geladene verbindungen mit einer nukleinsäure- bindenden einheit sowie deren verwendungen
AU2001262974A1 (en) 2000-05-03 2001-11-12 The Scripps Research Institute Dna alkylating agent and activation thereof
WO2001096313A1 (en) 2000-06-14 2001-12-20 The Scripps Research Institute Distamycin a analogs
EP1294713A2 (en) 2000-06-27 2003-03-26 Genelabs Technologies, Inc. Compounds possessing antibacterial, antifungal or antitumor activity
GB0015904D0 (en) 2000-06-28 2000-08-23 Hoffmann La Roche Inhibitors of HPV E1 helicase enzyme
AU2001282070A1 (en) * 2000-07-11 2002-01-21 Universite De Geneve Linked, sequence-specific DNA-binding molecules
DE60115265T2 (de) * 2000-09-19 2006-08-10 Lee, Moses, Holland Zusammensetzungen und verfahren zur verwendung achiraler analoge von cc-1065 und den duocarmycinen
AU2002310764A1 (en) 2001-05-21 2002-12-03 Universite De Geneve Sequence-specific dna binding compounds and their use in targeting telomeres and other dna sequences
AU2002312370A1 (en) 2001-06-13 2002-12-23 Roland W. Burli Antipathogenic benzamide compounds
CA2450625A1 (en) 2001-06-13 2002-12-19 Genesoft Pharmaceuticals, Inc. Isoquinoline compounds having antiinfective activity
JP2003089652A (ja) 2001-09-20 2003-03-28 Meiji Seika Kaisha Ltd 抗口腔カンジダ症組成物
US20030187026A1 (en) * 2001-12-13 2003-10-02 Qun Li Kinase inhibitors
GB0130868D0 (en) * 2001-12-24 2002-02-06 Univ Strathclyde New compounds
WO2003070450A1 (en) 2002-02-21 2003-08-28 Riken High-strength film of polyhydroxyalkanoic acid and process for producing the same
AU2003217782A1 (en) 2002-02-27 2003-09-09 The Government Of The United States Of America, Representated By The Secretary, Deparment Of Health Dna-binding polyamide drug conjugates
AU2003213836A1 (en) 2002-03-11 2003-09-29 Epoch Biosciences, Inc. Negatively charged minor groove binders
US7470717B2 (en) 2003-07-30 2008-12-30 Kyowa Hakko Kogyo Co., Ltd. Indazole derivatives

Also Published As

Publication number Publication date
US8012967B2 (en) 2011-09-06
ES2443720T3 (es) 2014-02-20
EP2066627B1 (en) 2013-10-23
WO2008038018A1 (en) 2008-04-03
US20100016311A1 (en) 2010-01-21
DK2066627T3 (da) 2014-01-27
CN101589024B (zh) 2014-01-01
GB2455479C (en) 2012-05-16
GB0619325D0 (en) 2006-11-08
GB2455479B (en) 2009-10-28
EP2066627A1 (en) 2009-06-10
PL2066627T3 (pl) 2014-05-30
GB2455479A (en) 2009-06-17
HK1138281A1 (en) 2010-08-20
JP2010505757A (ja) 2010-02-25
CA2664847C (en) 2014-12-02
CA2664847A1 (en) 2008-04-03
CN101589024A (zh) 2009-11-25
GB0906908D0 (en) 2009-06-03

Similar Documents

Publication Publication Date Title
EP2066627B1 (en) Novel minor groove binders
WO2002100832A1 (en) Isoquinoline compounds having antiinfective activity
WO2002100852A1 (en) Benzothiophene compounds having antiinfective activity
US20070270386A1 (en) Selective inhibitors of rock protein kinase and uses thereof
CN102574818A (zh) Apaf-1抑制剂化合物
EP1444228A2 (en) Substituted heteroarylalkanoic acids and their use as aldose reductase inhibitors
JP2010174023A (ja) Dna副溝結合化合物
JP2003529584A (ja) Bax阻害剤としての医薬として活性なピロリジン誘導体
TR201906325T4 (tr) Tetrazolon sübstitüeli dihidropiridinon MGAT2 inhibitörleri.
KR20170012559A (ko) P53-mdm2 단백질-단백질 상호작용 억제제로서 1,1'',2,5''-테트라하이드로스피로[인돌-3,2''-피롤]-2,5''-디온계를 포함하는 화합물
Viger et al. Exploring the limits of benzimidazole DNA-binding oligomers for the hypoxia inducible factor (HIF) site
US9868731B2 (en) Indole amide compound as inhibitor of necrosis
JP2011088847A (ja) 三環性化合物およびその用途
Fowler et al. Synthesis of fluorescent enone derived α-amino acids
NZ577031A (en) Substituted pyrrole derivatives and their use as HMG-CO inhibitors
WO2021161084A1 (en) N-(4-fluorophenyl)-5-phenyl-[1,2,4] triazolo [1,5-a] pyridine-2-carboxamide derivatives and their synthesis thereof
Khalaf et al. Synthesis and antimicrobial activity of some netropsin analogues
Chortani et al. Design and synthesis of novel N-benzyl-2, 5-dihydro-1 H-pyrrole-linked benzopyrimidine conjugates as antimicrobial agents: study combining in vitro and in silico analysis
WO2011057477A1 (zh) 四肽类似物及其制备和应用
HK1138281B (en) Minor groove binders
CN110357878B (zh) 1,3-二氢-2H-吡咯并[3,2-b]吡啶-2-酮衍生物及其医药用途
WO2026078729A1 (en) N-functionalized indole compounds as antimicrobial agents and process for preparation thereof

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20100927

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20100927

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20121218

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20121221

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20130313

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20130321

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20130621

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20131008

A601 Written request for extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A601

Effective date: 20131217

A602 Written permission of extension of time

Free format text: JAPANESE INTERMEDIATE CODE: A602

Effective date: 20131225

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20140328

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: 20140520

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20140616

R150 Certificate of patent or registration of utility model

Ref document number: 5564257

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

R250 Receipt of annual fees

Free format text: JAPANESE INTERMEDIATE CODE: R250

LAPS Cancellation because of no payment of annual fees