CL2013003105A1 - Compuestos de microarn que comprende secuencias de nucleósidos modificados, inhibidores de mir-21; usos de los compuestos para modular la actividad de mir -21 y para preparar un medicamento para tratar fibrosis, heridas o cancer - Google Patents
Compuestos de microarn que comprende secuencias de nucleósidos modificados, inhibidores de mir-21; usos de los compuestos para modular la actividad de mir -21 y para preparar un medicamento para tratar fibrosis, heridas o cancerInfo
- Publication number
- CL2013003105A1 CL2013003105A1 CL2013003105A CL2013003105A CL2013003105A1 CL 2013003105 A1 CL2013003105 A1 CL 2013003105A1 CL 2013003105 A CL2013003105 A CL 2013003105A CL 2013003105 A CL2013003105 A CL 2013003105A CL 2013003105 A1 CL2013003105 A1 CL 2013003105A1
- Authority
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- Prior art keywords
- compounds
- mir
- nucleosides
- wounds
- cancer
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 5
- 125000003835 nucleoside group Chemical class 0.000 title abstract 5
- 108091062762 miR-21 stem-loop Chemical class 0.000 title abstract 3
- 108091041631 miR-21-1 stem-loop Chemical class 0.000 title abstract 3
- 108091044442 miR-21-2 stem-loop Chemical class 0.000 title abstract 3
- 206010016654 Fibrosis Diseases 0.000 title abstract 2
- 206010028980 Neoplasm Diseases 0.000 title abstract 2
- 206010052428 Wound Diseases 0.000 title abstract 2
- 208000027418 Wounds and injury Diseases 0.000 title abstract 2
- 201000011510 cancer Diseases 0.000 title abstract 2
- 239000003814 drug Substances 0.000 title abstract 2
- 230000000694 effects Effects 0.000 title abstract 2
- 230000004761 fibrosis Effects 0.000 title abstract 2
- 229940079593 drug Drugs 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 239000002777 nucleoside Substances 0.000 abstract 6
- YIMATHOGWXZHFX-WCTZXXKLSA-N (2r,3r,4r,5r)-5-(hydroxymethyl)-3-(2-methoxyethoxy)oxolane-2,4-diol Chemical compound COCCO[C@H]1[C@H](O)O[C@H](CO)[C@H]1O YIMATHOGWXZHFX-WCTZXXKLSA-N 0.000 abstract 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 Chemical class 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 abstract 1
- 239000005549 deoxyribonucleoside Substances 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 150000003833 nucleoside derivatives Chemical class 0.000 abstract 1
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- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
- C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
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- C12N2310/3231—Chemical structure of the sugar modified ring structure having an additional ring, e.g. LNA, ENA
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Abstract
La invención describe compuestos que comprenden oligonucleótidos modificados porque el tiene la estructura seleccionada desde: TEMeCE AEAECSAETECSAEGETECsTEGEAEUSAEAEGECSTEAE, TEMeC AACSATCSAGTCsTGAUSAAGCSTAE AECS ATCSAGTCS TGAUSAAGCSTAE AECSAETECSAEGETECSTEGEAEUSAEAEGECSTEAE, AEMeCSATMeCSAGTMeCSTGATSAAGEMeCSTAE, AECSATCSAGTCSTGAuSAAGCSTAS, y AEMeCSATMeCSAGTMeCSTGATSAAGMeCSTAs, En donde los nucleosidos que no se encuentran seguidos por un subíndice indican beta-D-desoxirribonucleósidos, nucleósidos seguidos por un subíndice "E" indican nucleósidos 2'-O-metoxietil (2'-MOE), nucleósidos seguidos por un subíndice "S" indican nucleósidos S-etilo limitado (S-cET) y el superíndice"Me" indica un grupo 5-metil en la base nucleósido. Así también, el invento está relacionado con: una composición con los compuestos, un método para inhibir la actividad de miR-21 y usos de los compuestos porque sirven para preparar un medicamento para tratar entre otras enfermedades, fibrosis, heridas o cáncer.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161478767P | 2011-04-25 | 2011-04-25 | |
| US201161565779P | 2011-12-01 | 2011-12-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2013003105A1 true CL2013003105A1 (es) | 2014-08-01 |
Family
ID=46025979
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2013003105A CL2013003105A1 (es) | 2011-04-25 | 2013-10-25 | Compuestos de microarn que comprende secuencias de nucleósidos modificados, inhibidores de mir-21; usos de los compuestos para modular la actividad de mir -21 y para preparar un medicamento para tratar fibrosis, heridas o cancer |
Country Status (30)
| Country | Link |
|---|---|
| US (7) | US9181547B2 (es) |
| EP (3) | EP2702155B9 (es) |
| JP (2) | JP6320292B2 (es) |
| KR (2) | KR20190063482A (es) |
| CN (3) | CN113151272A (es) |
| AU (4) | AU2012249851B2 (es) |
| BR (1) | BR112013027187A2 (es) |
| CA (2) | CA2833615C (es) |
| CL (1) | CL2013003105A1 (es) |
| CO (1) | CO6821889A2 (es) |
| CY (1) | CY1120304T1 (es) |
| DK (2) | DK2702155T3 (es) |
| EA (1) | EA025894B1 (es) |
| ES (2) | ES2868950T3 (es) |
| HR (2) | HRP20170557T2 (es) |
| HU (2) | HUE054129T2 (es) |
| IL (3) | IL229032B (es) |
| LT (2) | LT2702155T (es) |
| MX (5) | MX393138B (es) |
| MY (2) | MY187685A (es) |
| NZ (1) | NZ717921A (es) |
| PH (1) | PH12013502199A1 (es) |
| PL (2) | PL3211082T3 (es) |
| PT (2) | PT3211082T (es) |
| RS (1) | RS61775B1 (es) |
| SG (1) | SG194636A1 (es) |
| SI (2) | SI3211082T1 (es) |
| TW (2) | TWI698445B (es) |
| UA (1) | UA115652C2 (es) |
| WO (1) | WO2012148952A1 (es) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2857881A1 (en) | 2004-11-12 | 2006-12-28 | Asuragen, Inc. | Methods and compositions involving mirna and mirna inhibitor molecules |
| DK2702155T3 (en) * | 2011-04-25 | 2017-05-01 | Regulus Therapeutics Inc | MICRO-RNA COMPOUNDS AND METHODS FOR MODULATING MIR-21 ACTIVITY |
| US9193971B2 (en) * | 2012-04-10 | 2015-11-24 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | Methods for the treatment of nonalcoholic steatohepatitis |
| NZ630591A (en) | 2012-04-25 | 2017-02-24 | Regulus Therapeutics Inc | Microrna compounds and methods for modulating mir-21 activity |
| UA116639C2 (uk) | 2012-10-09 | 2018-04-25 | Рег'Юлес Терап'Ютікс Інк. | Способи лікування синдрому альпорта |
| CA2889044A1 (en) | 2012-11-15 | 2014-05-22 | Roche Innovation Center Copenhagen A/S | Anti apob antisense conjugate compounds |
| SG10201803157XA (en) | 2013-05-01 | 2018-05-30 | Regulus Therapeutics Inc | Microrna compounds and methods for modulating mir-122 |
| US9994846B2 (en) | 2013-10-25 | 2018-06-12 | Regulus Therapeutics Inc. | MicroRNA compounds and methods for modulating miR-21 activity |
| KR101625755B1 (ko) | 2013-11-18 | 2016-05-30 | 울산대학교 산학협력단 | ｍｉＲＮＡ 스폰지 및 이의 용도 |
| CA2935426C (en) * | 2014-01-30 | 2023-07-25 | F. Hoffmann-La Roche Ag | Polyoligomer compound with biocleavable conjugates for reducing or inhibiting expression of a nucleic acid target |
| CN105734127A (zh) * | 2016-02-29 | 2016-07-06 | 上海中医药大学 | miR-21-3p在制备用于检测早期急性肾损伤的试剂中的用途 |
| WO2017187426A1 (en) | 2016-04-29 | 2017-11-02 | Aptamir Therapeutics, Inc. | Inhibition of mir-22 mirna by apt-110 |
| AU2017368050A1 (en) | 2016-11-29 | 2019-06-20 | Puretech Lyt, Inc. | Exosomes for delivery of therapeutic agents |
| FI3684949T3 (fi) | 2017-09-22 | 2024-07-17 | Univ Washington | Solumolekyylien kombinatorinen in situ -leimaaminen |
| CN108148911B (zh) * | 2018-03-02 | 2019-11-05 | 广州医科大学附属第二医院 | miR-582在制备前列腺癌骨转移的诊断、预后试剂盒及药物中的应用 |
| JP7279081B2 (ja) | 2018-05-08 | 2023-05-22 | レグルス セラピューティクス インコーポレイテッド | Ｍｉｒ－１２２を調節するためのマイクロｒｎａ化合物及び方法 |
| CN110747266A (zh) * | 2018-07-23 | 2020-02-04 | 深圳先进技术研究院 | miR-21和miR-21拮抗剂在抑制预防/治疗1型糖尿病中的应用 |
| CN109880907A (zh) * | 2019-03-26 | 2019-06-14 | 中国人民解放军第八一医院 | 一种肝癌细胞侵袭转移的分子机制研究方法 |
| US11965162B2 (en) | 2020-04-16 | 2024-04-23 | The Johns Hopkins University | MicroRNA and inhibitors thereof and methods of treatment |
| WO2022165092A1 (en) * | 2021-01-29 | 2022-08-04 | Angion Biomedica Corp. | Methods for treatment of fibrotic diseases |
| WO2025110217A1 (ja) * | 2023-11-22 | 2025-05-30 | 国立大学法人東海国立大学機構 | 嚢胞性腎疾患の予防及び／又は治療剤 |
| CN120505413A (zh) * | 2025-07-15 | 2025-08-19 | 湖南工程学院 | 一种基于引物交换反应和G-四链体检测AKI相关miRNA的探针体系及方法 |
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| CZ296262B6 (cs) | 1998-05-22 | 2006-02-15 | Boys Town National Research Hospital | Farmaceutický prostredek |
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