JPWO2019168687A5 - - Google Patents
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- Publication number
- JPWO2019168687A5 JPWO2019168687A5 JP2020568663A JP2020568663A JPWO2019168687A5 JP WO2019168687 A5 JPWO2019168687 A5 JP WO2019168687A5 JP 2020568663 A JP2020568663 A JP 2020568663A JP 2020568663 A JP2020568663 A JP 2020568663A JP WO2019168687 A5 JPWO2019168687 A5 JP WO2019168687A5
- Authority
- JP
- Japan
- Prior art keywords
- oligonucleotide
- nucleotides
- length
- oligonucleotide according
- antisense strand
- 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.)
- Granted
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- 108091034117 Oligonucleotide Proteins 0.000 claims description 78
- 125000003729 nucleotide group Chemical group 0.000 claims description 52
- 239000002773 nucleotide Substances 0.000 claims description 51
- 230000000692 anti-sense effect Effects 0.000 claims description 37
- 108091081021 Sense strand Proteins 0.000 claims description 33
- 102100039264 Glycogen [starch] synthase, liver Human genes 0.000 claims description 17
- 101001036117 Homo sapiens Glycogen [starch] synthase, liver Proteins 0.000 claims description 17
- 230000000295 complement effect Effects 0.000 claims description 14
- OVRNDRQMDRJTHS-KEWYIRBNSA-N N-acetyl-D-galactosamine Chemical group CC(=O)N[C@H]1C(O)O[C@H](CO)[C@H](O)[C@@H]1O OVRNDRQMDRJTHS-KEWYIRBNSA-N 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 8
- 238000012986 modification Methods 0.000 claims description 7
- 230000004048 modification Effects 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 108020004999 messenger RNA Proteins 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 claims description 2
- MSWZFWKMSRAUBD-GASJEMHNSA-N 2-amino-2-deoxy-D-galactopyranose Chemical compound N[C@H]1C(O)O[C@H](CO)[C@H](O)[C@@H]1O MSWZFWKMSRAUBD-GASJEMHNSA-N 0.000 claims 1
- 230000002440 hepatic effect Effects 0.000 description 4
- 239000003446 ligand Substances 0.000 description 4
- 208000007345 glycogen storage disease Diseases 0.000 description 3
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 108091023037 Aptamer Proteins 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 208000032008 Glycogen storage disease due to glycogen debranching enzyme deficiency Diseases 0.000 description 1
- 241000332595 Grouper sleepy disease iridovirus Species 0.000 description 1
- 206010019629 Hepatic adenoma Diseases 0.000 description 1
- 206010019668 Hepatic fibrosis Diseases 0.000 description 1
- 206010019708 Hepatic steatosis Diseases 0.000 description 1
- 208000002404 Liver Cell Adenoma Diseases 0.000 description 1
- OVRNDRQMDRJTHS-CBQIKETKSA-N N-Acetyl-D-Galactosamine Chemical compound CC(=O)N[C@H]1[C@@H](O)O[C@H](CO)[C@H](O)[C@@H]1O OVRNDRQMDRJTHS-CBQIKETKSA-N 0.000 description 1
- MBLBDJOUHNCFQT-UHFFFAOYSA-N N-acetyl-D-galactosamine Natural products CC(=O)NC(C=O)C(O)C(O)C(O)CO MBLBDJOUHNCFQT-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZTWTYVWXUKTLCP-UHFFFAOYSA-L ethenyl-dioxido-oxo-$l^{5}-phosphane Chemical compound [O-]P([O-])(=O)C=C ZTWTYVWXUKTLCP-UHFFFAOYSA-L 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 201000004543 glycogen storage disease III Diseases 0.000 description 1
- 208000011460 glycogen storage disease due to glucose-6-phosphatase deficiency type IA Diseases 0.000 description 1
- 150000002337 glycosamines Chemical class 0.000 description 1
- 201000002735 hepatocellular adenoma Diseases 0.000 description 1
- 206010073071 hepatocellular carcinoma Diseases 0.000 description 1
- 231100000844 hepatocellular carcinoma Toxicity 0.000 description 1
- 206010020718 hyperplasia Diseases 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 230000024121 nodulation Effects 0.000 description 1
- 229920001184 polypeptide Polymers 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201862637574P | 2018-03-02 | 2018-03-02 | |
US62/637,574 | 2018-03-02 | ||
PCT/US2019/018189 WO2019168687A1 (fr) | 2018-03-02 | 2019-02-15 | Compositions et méthodes pour inhiber l'expression de gys2 |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2021517826A JP2021517826A (ja) | 2021-07-29 |
JPWO2019168687A5 true JPWO2019168687A5 (fr) | 2022-02-24 |
JP7453921B2 JP7453921B2 (ja) | 2024-03-21 |
Family
ID=67805080
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2020568663A Active JP7453921B2 (ja) | 2018-03-02 | 2019-02-15 | Gys2発現を阻害するための組成物及び方法 |
Country Status (9)
Country | Link |
---|---|
US (2) | US11572562B2 (fr) |
EP (1) | EP3740247A4 (fr) |
JP (1) | JP7453921B2 (fr) |
KR (1) | KR20200127211A (fr) |
CN (1) | CN112055598A (fr) |
CA (1) | CA3092092A1 (fr) |
IL (1) | IL277058A (fr) |
MX (1) | MX2020009072A (fr) |
WO (1) | WO2019168687A1 (fr) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20200127211A (ko) | 2018-03-02 | 2020-11-10 | 다이서나 파마수이티컬, 인크. | Gys2 발현을 억제하기 위한 조성물 및 방법 |
CN113795581A (zh) * | 2019-05-03 | 2021-12-14 | 迪克纳制药公司 | 具有缩短的有义链的双链核酸抑制剂分子 |
WO2022223515A2 (fr) * | 2021-04-19 | 2022-10-27 | Novo Nordisk A/S | Compositions et procédés pour inhiber l'expression de l'élément 3 du groupe h de la sous-famille 1 de récepteur nucléaire (nr1h3) |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20030004122A1 (en) * | 1997-11-05 | 2003-01-02 | Leonid Beigelman | Nucleotide triphosphates and their incorporation into oligonucleotides |
US6436703B1 (en) | 2000-03-31 | 2002-08-20 | Hyseq, Inc. | Nucleic acids and polypeptides |
EP2305813A3 (fr) * | 2002-11-14 | 2012-03-28 | Dharmacon, Inc. | SIRNA fonctionnel et hyperfonctionnel |
US20050119210A1 (en) * | 2003-05-20 | 2005-06-02 | Xiaobing Be | Compositions and methods for diagnosing and treating cancers |
US20060078902A1 (en) * | 2004-04-15 | 2006-04-13 | Michaeline Bunting | Method and compositions for RNA interference |
EP1752536A4 (fr) * | 2004-05-11 | 2008-04-16 | Alphagen Co Ltd | Polynucleotide provoquant l'interference rna et procede de regulation d'expression genetique avec l'usage de ce dernier |
US8278287B2 (en) * | 2008-04-15 | 2012-10-02 | Quark Pharmaceuticals Inc. | siRNA compounds for inhibiting NRF2 |
JP2012504389A (ja) | 2008-09-22 | 2012-02-23 | ダイセルナ ファーマシューティカルズ, インコーポレイテッド | 修飾を有するdsRNAによる遺伝子発現の特異的な阻害のための組成物および方法 |
WO2010105372A1 (fr) | 2009-03-20 | 2010-09-23 | Protiva Biotherapeutics, Inc. | Compositions et procedes d'inactivation de l'expression du virus de l'hepatite c |
EP2764007A4 (fr) | 2011-10-05 | 2015-05-06 | Protiva Biotherapeutics Inc | Compositions et procédés permettant de réprimer l'expression de l'aldéhyde déshydrogénase |
US10351854B2 (en) * | 2014-10-10 | 2019-07-16 | Dicerna Pharmaceuticals, Inc. | Therapeutic inhibition of lactate dehydrogenase and agents therefor |
EP3569711B1 (fr) * | 2014-12-15 | 2021-02-03 | Dicerna Pharmaceuticals, Inc. | Acides nucléiques à double brin modifiés par ligands |
US10689647B2 (en) | 2015-05-08 | 2020-06-23 | Dicerna Pharmaceuticals, Inc. | Methods and compositions for the specific inhibition of antithrombin 3 (AT3) by double-stranded RNA |
EP3416689B1 (fr) * | 2016-02-18 | 2023-01-18 | CRISPR Therapeutics AG | Matériel et procédés de traitement d'une immunodéficience combinée grave (scid) ou d'un syndrome d'omenn |
CN111448316A (zh) * | 2017-12-22 | 2020-07-24 | 罗氏创新中心哥本哈根有限公司 | 新的硫代亚磷酰胺 |
KR20200127211A (ko) | 2018-03-02 | 2020-11-10 | 다이서나 파마수이티컬, 인크. | Gys2 발현을 억제하기 위한 조성물 및 방법 |
-
2019
- 2019-02-15 KR KR1020207027734A patent/KR20200127211A/ko not_active Application Discontinuation
- 2019-02-15 JP JP2020568663A patent/JP7453921B2/ja active Active
- 2019-02-15 US US16/977,152 patent/US11572562B2/en active Active
- 2019-02-15 WO PCT/US2019/018189 patent/WO2019168687A1/fr active Application Filing
- 2019-02-15 MX MX2020009072A patent/MX2020009072A/es unknown
- 2019-02-15 EP EP19760244.4A patent/EP3740247A4/fr active Pending
- 2019-02-15 CN CN201980029587.XA patent/CN112055598A/zh active Pending
- 2019-02-15 CA CA3092092A patent/CA3092092A1/fr active Pending
-
2020
- 2020-08-31 IL IL277058A patent/IL277058A/en unknown
-
2023
- 2023-01-18 US US18/156,177 patent/US20230365974A1/en active Pending
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