PT818460E - Sintese em fase solida de oligonucleotidos - Google Patents
Sintese em fase solida de oligonucleotidosInfo
- Publication number
- PT818460E PT818460E PT97111426T PT97111426T PT818460E PT 818460 E PT818460 E PT 818460E PT 97111426 T PT97111426 T PT 97111426T PT 97111426 T PT97111426 T PT 97111426T PT 818460 E PT818460 E PT 818460E
- Authority
- PT
- Portugal
- Prior art keywords
- alkyl
- groups
- alkoxy
- protected
- optionally
- Prior art date
Links
- 108091034117 Oligonucleotide Proteins 0.000 title abstract 2
- JLCPHMBAVCMARE-UHFFFAOYSA-N [3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[3-[[3-[[3-[[3-[[3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-[[5-(2-amino-6-oxo-1H-purin-9-yl)-3-hydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxyoxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(6-aminopurin-9-yl)oxolan-2-yl]methoxy-hydroxyphosphoryl]oxy-5-(4-amino-2-oxopyrimidin-1-yl)oxolan-2-yl]methyl [5-(6-aminopurin-9-yl)-2-(hydroxymethyl)oxolan-3-yl] hydrogen phosphate Polymers Cc1cn(C2CC(OP(O)(=O)OCC3OC(CC3OP(O)(=O)OCC3OC(CC3O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c3nc(N)[nH]c4=O)C(COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3COP(O)(=O)OC3CC(OC3CO)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3ccc(N)nc3=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cc(C)c(=O)[nH]c3=O)n3cc(C)c(=O)[nH]c3=O)n3ccc(N)nc3=O)n3cc(C)c(=O)[nH]c3=O)n3cnc4c3nc(N)[nH]c4=O)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)n3cnc4c(N)ncnc34)O2)c(=O)[nH]c1=O JLCPHMBAVCMARE-UHFFFAOYSA-N 0.000 title 1
- 230000015572 biosynthetic process Effects 0.000 title 1
- 239000007790 solid phase Substances 0.000 title 1
- 238000003786 synthesis reaction Methods 0.000 title 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 239000002773 nucleotide Substances 0.000 abstract 3
- 125000003729 nucleotide group Chemical group 0.000 abstract 3
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 abstract 2
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 238000010511 deprotection reaction Methods 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 230000000269 nucleophilic effect Effects 0.000 abstract 2
- 239000007787 solid Substances 0.000 abstract 2
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000005336 allyloxy group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000000371 nucleobase group Chemical group 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- -1 p-nitrophenylethyl Chemical group 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000006245 phosphate protecting group Chemical group 0.000 abstract 1
- 238000010532 solid phase synthesis reaction Methods 0.000 abstract 1
- 125000001424 substituent group Chemical group 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
- 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
-
- 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)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19627898A DE19627898A1 (de) | 1996-07-11 | 1996-07-11 | Festphasensynthese von Oligonucleotiden |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PT818460E true PT818460E (pt) | 2003-06-30 |
Family
ID=7799510
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PT97111426T PT818460E (pt) | 1996-07-11 | 1997-07-07 | Sintese em fase solida de oligonucleotidos |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US5936077A (https=) |
| EP (1) | EP0818460B1 (https=) |
| JP (1) | JP4435878B2 (https=) |
| AT (1) | ATE231162T1 (https=) |
| AU (1) | AU716391B2 (https=) |
| CA (1) | CA2210031C (https=) |
| DE (2) | DE19627898A1 (https=) |
| DK (1) | DK0818460T3 (https=) |
| ES (1) | ES2188826T3 (https=) |
| NO (1) | NO317853B1 (https=) |
| PT (1) | PT818460E (https=) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6274725B1 (en) * | 1998-06-02 | 2001-08-14 | Isis Pharmaceuticals, Inc. | Activators for oligonucleotide synthesis |
| AU4965499A (en) | 1998-07-09 | 2000-02-01 | Biocept, Inc. | Method of using an improved peptide nucleic acid universal library to optimize dna sequence hybridation |
| DE19842164B4 (de) * | 1998-09-15 | 2004-06-03 | Deutsches Krebsforschungszentrum Stiftung des öffentlichen Rechts | Verfahren zur Qualitätskontrolle beim Aufbau von Oligomerrastern |
| US6175001B1 (en) * | 1998-10-16 | 2001-01-16 | The Scripps Research Institute | Functionalized pyrimidine nucleosides and nucleotides and DNA's incorporating same |
| US6465628B1 (en) | 1999-02-04 | 2002-10-15 | Isis Pharmaceuticals, Inc. | Process for the synthesis of oligomeric compounds |
| US6887990B1 (en) | 1999-02-05 | 2005-05-03 | Amersham Biosciences Corp | Method for deprotecting oligonucleotides |
| ATE312841T1 (de) * | 2001-03-08 | 2005-12-15 | Applera Corp | Verfahren zum entschützen von oligonukleotide |
| WO2006025154A1 (ja) * | 2004-08-30 | 2006-03-09 | Gifu University | 修飾オリゴヌクレオチド |
| DE102006016473A1 (de) * | 2005-12-08 | 2007-06-14 | Continental Teves Ag & Co. Ohg | Druckregelventil |
| CA2721969C (en) * | 2008-04-24 | 2016-06-07 | Girindus America, Inc. | Process for the manufacture of oligonucleotides |
| US9708360B2 (en) | 2013-09-30 | 2017-07-18 | Geron Corporation | Phosphorodiamidate backbone linkage for oligonucleotides |
| WO2017066782A1 (en) * | 2015-10-16 | 2017-04-20 | Modernatx, Inc. | Hydrophobic mrna cap analogs |
| WO2017066797A1 (en) | 2015-10-16 | 2017-04-20 | Modernatx, Inc. | Trinucleotide mrna cap analogs |
| SI3362461T1 (sl) | 2015-10-16 | 2022-05-31 | Modernatx, Inc. | Analogi kape MRNA z modificirano fosfatno povezavo |
| CA3033867A1 (en) | 2016-08-17 | 2018-02-22 | Solstice Biologics, Ltd. | Polynucleotide constructs |
| US11597744B2 (en) | 2017-06-30 | 2023-03-07 | Sirius Therapeutics, Inc. | Chiral phosphoramidite auxiliaries and methods of their use |
| KR20190090301A (ko) | 2018-01-24 | 2019-08-01 | 에스티팜 주식회사 | 신규한 뉴클레오사이드 또는 뉴클레오타이드 유도체 및 이들의 용도 |
| CN115772201B (zh) * | 2021-09-08 | 2024-11-26 | 苏州金唯智生物科技有限公司 | 一种固相合成rna的后处理方法及其应用 |
| CN117362370B (zh) * | 2023-12-07 | 2024-03-05 | 北京百力格生物科技有限公司 | 核苷亚磷酰胺单体及其制备方法和应用 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR930016437A (ko) * | 1992-01-22 | 1993-08-26 | 귀틀라인, 슈미트 | 올리고뉴클레오티드 유사체, 이의 제조방법 및 용도 |
| US5623068A (en) * | 1994-03-07 | 1997-04-22 | Beckman Instruments, Inc. | Synthesis of DNA using substituted phenylacetyl-protected nucleotides |
-
1996
- 1996-07-11 DE DE19627898A patent/DE19627898A1/de not_active Withdrawn
-
1997
- 1997-07-07 PT PT97111426T patent/PT818460E/pt unknown
- 1997-07-07 DK DK97111426T patent/DK0818460T3/da active
- 1997-07-07 ES ES97111426T patent/ES2188826T3/es not_active Expired - Lifetime
- 1997-07-07 DE DE59709128T patent/DE59709128D1/de not_active Expired - Lifetime
- 1997-07-07 AT AT97111426T patent/ATE231162T1/de active
- 1997-07-07 EP EP97111426A patent/EP0818460B1/de not_active Expired - Lifetime
- 1997-07-09 AU AU28552/97A patent/AU716391B2/en not_active Ceased
- 1997-07-10 JP JP18514297A patent/JP4435878B2/ja not_active Expired - Fee Related
- 1997-07-10 CA CA002210031A patent/CA2210031C/en not_active Expired - Fee Related
- 1997-07-10 NO NO19973217A patent/NO317853B1/no not_active IP Right Cessation
- 1997-07-11 US US08/893,614 patent/US5936077A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JP4435878B2 (ja) | 2010-03-24 |
| DE19627898A1 (de) | 1998-01-15 |
| ATE231162T1 (de) | 2003-02-15 |
| CA2210031A1 (en) | 1998-01-11 |
| AU2855297A (en) | 1998-01-22 |
| NO317853B1 (no) | 2004-12-20 |
| EP0818460B1 (de) | 2003-01-15 |
| NO973217L (no) | 1998-01-12 |
| CA2210031C (en) | 2008-04-22 |
| EP0818460A3 (de) | 1999-02-24 |
| ES2188826T3 (es) | 2003-07-01 |
| AU716391B2 (en) | 2000-02-24 |
| JPH1072486A (ja) | 1998-03-17 |
| US5936077A (en) | 1999-08-10 |
| DK0818460T3 (da) | 2003-05-05 |
| DE59709128D1 (de) | 2003-02-20 |
| NO973217D0 (no) | 1997-07-10 |
| EP0818460A2 (de) | 1998-01-14 |
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