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 (enExample)
EP (1) EP2857412B1 (enExample)
DK (1) DK2857412T3 (enExample)
IL (1) IL235978B (enExample)
IN (1) IN2014DN10144A (enExample)
SG (1) SG11201407967TA (enExample)
WO (1) WO2013179412A1 (enExample)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010064146A2 (en) 2008-12-02 2010-06-10 Chiralgen, Ltd. Method for the synthesis of phosphorus atom modified nucleic acids
CA2767253A1 (en) 2009-07-06 2011-01-13 Ontorii, Inc. Novel nucleic acid prodrugs and methods of use thereof
WO2012039448A1 (ja) 2010-09-24 2012-03-29 株式会社キラルジェン 不斉補助基
CN103796657B (zh) 2011-07-19 2017-07-11 波涛生命科学有限公司 合成官能化核酸的方法
US8846885B2 (en) 2012-02-17 2014-09-30 Ajinomoto Co., Inc. Oligonucleotide with protected base
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
CA2879066C (en) 2012-07-13 2019-08-13 Shin Nippon Biomedical Laboratories, Ltd. Chiral nucleic acid adjuvant
WO2014010250A1 (en) 2012-07-13 2014-01-16 Chiralgen, Ltd. Asymmetric auxiliary group
JP6453212B2 (ja) 2012-07-13 2019-01-16 ウェイブ ライフ サイエンシズ リミテッドWave Life Sciences Ltd. キラル制御
JPWO2015108048A1 (ja) 2014-01-15 2017-03-23 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
JPWO2015108046A1 (ja) 2014-01-15 2017-03-23 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
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
KR20230152178A (ko) 2014-01-16 2023-11-02 웨이브 라이프 사이언시스 리미티드 키랄 디자인
TWI729028B (zh) * 2015-11-17 2021-06-01 日商日產化學工業股份有限公司 寡核苷酸的製造方法
JP7027889B2 (ja) * 2015-12-16 2022-03-02 味の素株式会社 オリゴヌクレオチドの製造方法、およびヌクレオシド、ヌクレオチドまたはオリゴヌクレオチド
WO2017111137A1 (ja) * 2015-12-22 2017-06-29 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
WO2020175472A1 (ja) 2019-02-28 2020-09-03 富士フイルム株式会社 ペプチド化合物の製造方法、保護基形成用試薬、及び、縮合多環芳香族炭化水素化合物
WO2020175473A1 (ja) 2019-02-28 2020-09-03 富士フイルム株式会社 ペプチド化合物の製造方法、保護基形成用試薬、及び、芳香族複素環化合物
EP3950698A4 (en) * 2019-03-28 2023-01-25 Ajinomoto Co., Inc. METHOD OF PREPARING AN OLIGONUCLEOTIDE WITH PHOSPHOROTHIOATE SITE
MA55891A (fr) 2019-05-08 2022-03-16 Ajinomoto Kk Synthèses en phase liquide convergente d'oligonucléotides
WO2021039935A1 (ja) * 2019-08-29 2021-03-04 富士フイルム株式会社 核酸化合物の製造方法、及び、核酸化合物
WO2021198883A1 (en) 2020-03-31 2021-10-07 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
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
WO2012157723A1 (ja) 2011-05-17 2012-11-22 味の素株式会社 オリゴヌクレオチドの製造方法
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
US20150112053A1 (en) 2015-04-23
EP2857412A4 (en) 2015-10-21
DK2857412T3 (en) 2017-04-03
US9284344B2 (en) 2016-03-15
SG11201407967TA (en) 2015-01-29
WO2013179412A1 (ja) 2013-12-05
EP2857412B1 (en) 2017-01-11
IN2014DN10144A (enExample) 2015-08-21
EP2857412A1 (en) 2015-04-08
IL235978A0 (en) 2015-02-01

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