SG11201407967TA - Oligonucleotide synthesis method using highly dispersible liquid-phase support - Google Patents
Oligonucleotide synthesis method using highly dispersible liquid-phase supportInfo
- Publication number
- SG11201407967TA SG11201407967TA SG11201407967TA SG11201407967TA SG11201407967TA SG 11201407967T A SG11201407967T A SG 11201407967TA SG 11201407967T A SG11201407967T A SG 11201407967TA SG 11201407967T A SG11201407967T A SG 11201407967TA SG 11201407967T A SG11201407967T A SG 11201407967TA
- Authority
- SG
- Singapore
- Prior art keywords
- synthesis method
- acid
- phase support
- hydrophobic
- highly dispersible
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 4
- 239000007791 liquid phase Substances 0.000 title abstract 3
- 238000002515 oligonucleotide synthesis Methods 0.000 title abstract 2
- 239000002777 nucleoside Substances 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000001165 hydrophobic group Chemical group 0.000 abstract 3
- 239000007858 starting material Substances 0.000 abstract 3
- 108091034117 Oligonucleotide Proteins 0.000 abstract 2
- 150000003833 nucleoside derivatives Chemical class 0.000 abstract 2
- -1 nucleoside phosphoramidite compound Chemical class 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 230000008878 coupling Effects 0.000 abstract 1
- 238000010168 coupling process Methods 0.000 abstract 1
- 238000005859 coupling reaction Methods 0.000 abstract 1
- 239000012530 fluid Substances 0.000 abstract 1
- 239000012454 non-polar solvent Substances 0.000 abstract 1
- 238000001668 nucleic acid synthesis Methods 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 230000002194 synthesizing effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
- C07H1/02—Phosphorylation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
- C07H1/02—Phosphorylation
- C07H1/04—Introducing polyphosphoric acid radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
- C07H19/073—Pyrimidine radicals with 2-deoxyribosyl as the saccharide radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
- C07H21/02—Compounds 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H21/00—Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
- C07H21/04—Compounds 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
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design 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)
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 (1)
| Publication Number | Publication Date |
|---|---|
| SG11201407967TA true SG11201407967TA (en) | 2015-01-29 |
Family
ID=49672666
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SG11201407967TA SG11201407967TA (en) | 2012-05-30 | 2012-05-30 | Oligonucleotide synthesis method using highly dispersible liquid-phase support |
Country Status (7)
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2015151857A (ru) | 2008-12-02 | 2019-01-15 | Уэйв Лайф Сайенсес Джапан, Инк. | Способ синтеза модифицированных по атому фосфора нуклеиновых кислот |
| SG10201403841QA (en) | 2009-07-06 | 2014-09-26 | Ontorii Inc | Novel nucleic acid prodrugs and methods of use thereof |
| DK2620428T3 (da) | 2010-09-24 | 2019-07-01 | Wave Life Sciences Ltd | Asymmetrisk hjælpegruppe |
| DK2734208T3 (en) | 2011-07-19 | 2017-06-19 | Wave Life Sciences Ltd | PROCEDURES FOR SYNTHESIS OF FUNCTIONALIZED NUCLEIC ACIDS |
| EP3296306B1 (en) * | 2012-02-17 | 2022-11-09 | Ajinomoto Co., Inc. | Base-protected oligonucleotide |
| US8846885B2 (en) | 2012-02-17 | 2014-09-30 | Ajinomoto Co., Inc. | Oligonucleotide with protected base |
| AU2013287630B2 (en) | 2012-07-13 | 2017-05-25 | Shin Nippon Biomedical Laboratories, Ltd. | Chiral nucleic acid adjuvant |
| SG10201912895PA (en) | 2012-07-13 | 2020-02-27 | Wave Life Sciences Ltd | Chiral control |
| US9598458B2 (en) | 2012-07-13 | 2017-03-21 | Wave Life Sciences Japan, Inc. | Asymmetric auxiliary group |
| US10149905B2 (en) | 2014-01-15 | 2018-12-11 | Shin Nippon Biomedical Laboratories, Ltd. | Chiral nucleic acid adjuvant having antitumor effect and antitumor agent |
| US10144933B2 (en) | 2014-01-15 | 2018-12-04 | Shin Nippon Biomedical Laboratories, Ltd. | Chiral nucleic acid adjuvant having immunity induction activity, and immunity induction activator |
| US10322173B2 (en) | 2014-01-15 | 2019-06-18 | Shin Nippon Biomedical Laboratories, Ltd. | Chiral nucleic acid adjuvant having anti-allergic activity, and anti-allergic agent |
| AU2015207773B2 (en) | 2014-01-16 | 2021-06-17 | Wave Life Sciences Ltd. | Chiral design |
| WO2017086397A1 (ja) | 2015-11-17 | 2017-05-26 | 日産化学工業株式会社 | オリゴヌクレオチドの製造方法 |
| WO2017104836A1 (ja) * | 2015-12-16 | 2017-06-22 | 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 |
| 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 |
| KR20210121181A (ko) | 2019-02-28 | 2021-10-07 | 후지필름 가부시키가이샤 | 펩타이드 화합물의 제조 방법, 보호기 형성용 시약, 및 방향족 복소환 화합물 |
| 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 |
| CN119143828A (zh) * | 2019-05-08 | 2024-12-17 | 渤健马萨诸塞州股份有限公司 | 寡核苷酸的汇聚液相合成 |
| 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 |
| MX2022012255A (es) | 2020-03-31 | 2023-01-11 | Janssen Biopharma Inc | Sintesis de oligonucleotidos y compuestos relacionados. |
| 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 |
| US12180140B2 (en) | 2022-12-23 | 2024-12-31 | 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)
| 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 |
| US9029528B2 (en) | 2011-05-17 | 2015-05-12 | Ajinomoto Co., Inc. | Solution-based method of making oligonucleotides via phosphoramidite coupling |
| EP3296306B1 (en) | 2012-02-17 | 2022-11-09 | Ajinomoto Co., Inc. | Base-protected oligonucleotide |
-
2012
- 2012-05-30 WO PCT/JP2012/063921 patent/WO2013179412A1/ja active Application Filing
- 2012-05-30 US US14/404,562 patent/US9284344B2/en active Active
- 2012-05-30 EP EP12877844.6A patent/EP2857412B1/en active Active
- 2012-05-30 IN IN10144DEN2014 patent/IN2014DN10144A/en unknown
- 2012-05-30 DK DK12877844.6T patent/DK2857412T3/en active
- 2012-05-30 SG SG11201407967TA patent/SG11201407967TA/en unknown
-
2014
- 2014-11-27 IL IL235978A patent/IL235978B/en active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| EP2857412B1 (en) | 2017-01-11 |
| US9284344B2 (en) | 2016-03-15 |
| EP2857412A4 (en) | 2015-10-21 |
| IL235978A0 (en) | 2015-02-01 |
| IL235978B (en) | 2018-02-28 |
| WO2013179412A1 (ja) | 2013-12-05 |
| EP2857412A1 (en) | 2015-04-08 |
| IN2014DN10144A (enrdf_load_stackoverflow) | 2015-08-21 |
| US20150112053A1 (en) | 2015-04-23 |
| DK2857412T3 (en) | 2017-04-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SG11201407967TA (en) | Oligonucleotide synthesis method using highly dispersible liquid-phase support | |
| SG11201808721YA (en) | Cell-free production of ribonucleic acid | |
| SG11201806400XA (en) | Replicative transposon system | |
| SG11201900635QA (en) | Chimeric antigen receptors targeting bcma and methods of use thereof | |
| SG11201807252QA (en) | Anti-lag-3 antibodies | |
| SG11201808622SA (en) | Chimeric receptors to flt3 and methods of use thereof | |
| SG11201908325PA (en) | Process for the preparation of glucuronide drug-linkers and intermediates thereof | |
| SG11201909710XA (en) | Indole ahr inhibitors and uses thereof | |
| SG11201807069XA (en) | Nucleic acid sequencing method and system employing enhanced detection of nucleotide-specific ternary complex formation | |
| SG11201804997XA (en) | Process for preparing non-cariogenic, sustained energy release juice | |
| SG11201408297XA (en) | Porous graphene oxide materials | |
| SG11201803169WA (en) | Cellulase variants and polynucleotides encoding same | |
| SG11201901077RA (en) | Anti-tigit antibodies, anti-pvrig antibodies and combinations thereof | |
| SG11201809344QA (en) | Process for synthesizing 2-hydroxy-6-((2-(1-isopropyl-1h-pyrazol-5-yl)-pyridin-3-yl)methoxy)benzaldehyde | |
| SG11201810600WA (en) | Fxr (nr1h4) modulating compounds | |
| SG11201808457PA (en) | Icos ligand variant immunomodulatory proteins and uses thereof | |
| SG11201807187XA (en) | Binding members to pd-l1 | |
| SG11201900772YA (en) | Gene editing of car-t cells for the treatment of t cell malignancies with chimeric antigen receptors | |
| SG11201404936YA (en) | Channel plate heat transfer system | |
| SG11201805166PA (en) | Light-mediated polymerase chain reaction amplification and product detection system and methods of use | |
| SG11201908899WA (en) | An alcoholic beverage | |
| SG11201406438WA (en) | Alkoxylation catalyst, method for producing catalyst, and method for producing fatty acid alkyl ester alkoxylate using catalyst | |
| SG11201407117TA (en) | Composition for repairing cartilage tissue, method for producing same, and use thereof | |
| SG11201407540TA (en) | Methods of growing uniform, large-scale, multilayer graphene films | |
| SG11201408198QA (en) | Jumper tube locking assembly and method |