IL235978B - Oligonucleotide synthesis method utilizing liquid support in high dispersive phase - Google Patents

Oligonucleotide synthesis method utilizing liquid support in high dispersive phase

Info

Publication number
IL235978B
IL235978B IL235978A IL23597814A IL235978B IL 235978 B IL235978 B IL 235978B IL 235978 A IL235978 A IL 235978A IL 23597814 A IL23597814 A IL 23597814A IL 235978 B IL235978 B IL 235978B
Authority
IL
Israel
Prior art keywords
synthesis method
oligonucleotide synthesis
phase support
highly dispersible
dispersible liquid
Prior art date
Application number
IL235978A
Other languages
English (en)
Hebrew (he)
Other versions
IL235978A0 (en
Original Assignee
Hokkaido System Science Co Ltd
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 Hokkaido System Science Co Ltd filed Critical Hokkaido System Science Co Ltd
Publication of IL235978A0 publication Critical patent/IL235978A0/en
Publication of IL235978B publication Critical patent/IL235978B/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • C07H21/04Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with deoxyribosyl as saccharide radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H1/00Processes for the preparation of sugar derivatives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H1/00Processes for the preparation of sugar derivatives
    • C07H1/02Phosphorylation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H1/00Processes for the preparation of sugar derivatives
    • C07H1/02Phosphorylation
    • C07H1/04Introducing polyphosphoric acid radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • C07H19/06Pyrimidine radicals
    • C07H19/073Pyrimidine radicals with 2-deoxyribosyl as the saccharide radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • C07H21/02Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids with ribosyl as saccharide radical
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Saccharide Compounds (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
IL235978A 2012-05-30 2014-11-27 Oligonucleotide synthesis method utilizing liquid support in high dispersive phase IL235978B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2012/063921 WO2013179412A1 (ja) 2012-05-30 2012-05-30 高分散性液相支持体を用いたオリゴヌクレオチド合成法

Publications (2)

Publication Number Publication Date
IL235978A0 IL235978A0 (en) 2015-02-01
IL235978B true IL235978B (en) 2018-02-28

Family

ID=49672666

Family Applications (1)

Application Number Title Priority Date Filing Date
IL235978A IL235978B (en) 2012-05-30 2014-11-27 Oligonucleotide synthesis method utilizing liquid support in high dispersive phase

Country Status (7)

Country Link
US (1) US9284344B2 (cg-RX-API-DMAC10.html)
EP (1) EP2857412B1 (cg-RX-API-DMAC10.html)
DK (1) DK2857412T3 (cg-RX-API-DMAC10.html)
IL (1) IL235978B (cg-RX-API-DMAC10.html)
IN (1) IN2014DN10144A (cg-RX-API-DMAC10.html)
SG (1) SG11201407967TA (cg-RX-API-DMAC10.html)
WO (1) WO2013179412A1 (cg-RX-API-DMAC10.html)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101881596B1 (ko) 2008-12-02 2018-07-24 웨이브 라이프 사이언시스 재팬 인코포레이티드 인 원자 변형된 핵산의 합성 방법
BR112012000828A8 (pt) 2009-07-06 2017-10-10 Ontorii Inc Novas pró-drogas de ácido nucleico e métodos de uso das mesmas
WO2012039448A1 (ja) 2010-09-24 2012-03-29 株式会社キラルジェン 不斉補助基
BR112014001244A2 (pt) 2011-07-19 2017-02-21 Wave Life Sciences Pte Ltd métodos para a síntese de ácidos nucléicos funcionalizados
JP6237237B2 (ja) * 2012-02-17 2017-11-29 味の素株式会社 塩基部保護オリゴヌクレオチド
US8846885B2 (en) 2012-02-17 2014-09-30 Ajinomoto Co., Inc. Oligonucleotide with protected base
BR112015000723A2 (pt) 2012-07-13 2017-06-27 Shin Nippon Biomedical Laboratories Ltd adjuvante de ácido nucléico quiral
RU2015104762A (ru) 2012-07-13 2018-08-31 Уэйв Лайф Сайенсес Лтд. Хиральный контроль
BR112015000784A8 (pt) 2012-07-13 2018-04-03 Wave Life Sciences Japan Grupo auxiliar assimétrico
WO2015108047A1 (ja) 2014-01-15 2015-07-23 株式会社新日本科学 免疫誘導活性を有するキラル核酸アジュバンド及び免疫誘導活性剤
WO2015108048A1 (ja) 2014-01-15 2015-07-23 株式会社新日本科学 抗腫瘍作用を有するキラル核酸アジュバンド及び抗腫瘍剤
WO2015108046A1 (ja) 2014-01-15 2015-07-23 株式会社新日本科学 抗アレルギー作用を有するキラル核酸アジュバンド及び抗アレルギー剤
WO2015107425A2 (en) 2014-01-16 2015-07-23 Wave Life Sciences Pte. Ltd. Chiral design
CN108350018A (zh) 2015-11-17 2018-07-31 日产化学工业株式会社 寡核苷酸的制造方法
EP3398955A4 (en) * 2015-12-16 2019-10-16 Ajinomoto Co., Inc. OLIGONUCLEOTIDE MANUFACTURING METHOD AND NUCLEOSIDE, NUCLEOTIDE OR OLIGONUCLEOTIDE
JPWO2017111137A1 (ja) * 2015-12-22 2018-10-18 味の素株式会社 オリゴヌクレオチドの製造方法
WO2020166705A1 (ja) 2019-02-15 2020-08-20 味の素株式会社 オリゴヌクレオチドの製造方法
EP3916000A4 (en) 2019-02-28 2022-03-23 FUJIFILM Corporation PROCESS FOR PREPARING A PEPTIDE COMPOUND, PROTECTING REAGENT AND AROMATIC HETEROCYCLIC COMPOUND
CA3131772A1 (en) 2019-02-28 2020-09-03 Fujifilm Corporation Method for producing peptide compound, protecting group-forming reagent, and condensed polycyclic aromatic hydrocarbon compound
JP7632276B2 (ja) * 2019-03-28 2025-02-19 味の素株式会社 ホスホロチオエート化部位を有するオリゴヌクレオチドの製造方法
JP2022531876A (ja) * 2019-05-08 2022-07-12 バイオジェン・エムエイ・インコーポレイテッド オリゴヌクレオチドの収束液相合成
JPWO2021039935A1 (cg-RX-API-DMAC10.html) * 2019-08-29 2021-03-04
AU2021247043A1 (en) 2020-03-31 2022-10-27 Janssen Biopharma, Inc. Synthesis of oligonucleotides and related compounds
FR3111896A1 (fr) * 2020-06-24 2021-12-31 Strainchem Procédés de synthèses en solution de macromolécules à partir d’unités de dérivés de glucides
CN113583069B (zh) * 2021-09-09 2023-06-06 北京大学 核苷磷脂类化合物及其化学合成方法和在核酸递送中的应用
WO2024083746A1 (en) 2022-10-17 2024-04-25 Bachem Holding Ag Method and composition for oligonucleotide synthesis
WO2024137756A1 (en) * 2022-12-23 2024-06-27 Hongene Biotech Corporation Compounds and methods for liquid phase oligonucleotide synthesis
EP4678626A1 (en) 2023-03-06 2026-01-14 Spera Pharma, Inc. Long-chain alkenyloxy-substituted benzoyl derivative and oligonucleotide synthesis method using same
WO2025082632A1 (en) 2023-10-16 2025-04-24 Bachem Holding Ag Method and composition for oligonucleotide synthesis

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7094943B2 (en) 1998-04-27 2006-08-22 Hubert Köster Solution phase biopolymer synthesis
JP2003002895A (ja) 2001-05-30 2003-01-08 Tokyo Inst Of Technol 核酸の合成法
JP4963665B2 (ja) 2007-11-27 2012-06-27 株式会社ミツバ 扁平型コミュテータ及びその製造方法
JP5548852B2 (ja) 2009-05-29 2014-07-16 国立大学法人東京農工大学 疎水性基結合ヌクレオシド、疎水性基結合ヌクレオシド溶液、及び疎水性基結合オリゴヌクレオチド合成方法
CN103476784B (zh) 2011-05-17 2017-05-24 味之素株式会社 制备寡核苷酸的方法
JP6237237B2 (ja) * 2012-02-17 2017-11-29 味の素株式会社 塩基部保護オリゴヌクレオチド

Also Published As

Publication number Publication date
DK2857412T3 (en) 2017-04-03
IL235978A0 (en) 2015-02-01
EP2857412B1 (en) 2017-01-11
US20150112053A1 (en) 2015-04-23
EP2857412A1 (en) 2015-04-08
WO2013179412A1 (ja) 2013-12-05
IN2014DN10144A (cg-RX-API-DMAC10.html) 2015-08-21
EP2857412A4 (en) 2015-10-21
US9284344B2 (en) 2016-03-15
SG11201407967TA (en) 2015-01-29

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