Antisense design
View Patent ↗A novel class of pharmaceuticals which comprises a Locked Nucleic Acid (LNA) which can be used in antisense therapy. These novel oligonucleotides have improved antisense properties. The novel oligonucleotides are composed of at least one LNA selected from beta-D-thio/amino-LNA or alpha-L-oxy/thio/amino-LNA. The oligonucleotides comprising LNA may also include DNA and/or RNA nucleotides.
1. A gapmer oligonucleotide 12 26 nucleotide units in length of formula A-B-C-D, wherein:
A represents a sequence of locked nucleotide units;
B represents a sequence of at least 6 continuous DNA nucleotide units;
C represents a locked nucleotide unit or a sequence of locked nucleotide units;
D represents a non-locked nucleotide unit or a sequence of non-locked nucleotide units,
wherein the non-locked nucleotide unit of region D is a 2′ substituted non-locked nucleotide, wherein the 2′ substituent is selected from the group consisting of halogen or C 1 -C 9 alkoxy.
2. The gapmer oligonucleotide according to claim 1 , wherein at least one of the locked nucleotide units of regions A and/or C is a nucleotide of formula:
wherein X is O; one of the H's in (CH 2 )n is replaced with a C 1-6 alkyl substituent; n is 1; and Base is independently selected from the group consisting of cytosine, methyl cytosine, uracil, thymine, adenine and guanine.
3. The gapmer oligonucleotide according to claim 2 , wherein one of the H's in (CH 2 )n is replaced with methyl.
4. The gapmer oligonucleotide according to claim 1 wherein at least one of the internucleoside linkages is a phosphorothioate linkage.
5. The gapmer oligonucleotide of claim 1 wherein all of the internucleotide linkages are phosphorothioate linkages.
6. The gapmer oligonucleotide according to claim 2 wherein at least one of the internucleotide linkages is a phosphorothioate linkages.
7. The gapmer oligonucleotide according to claim 2 wherein all of the internucleotide linkages are phosphorothioate linkages.
8. The gapmer oligonucleotide of claim 1 wherein in the central region B is 8-12 DNA nucleotides.
9. The gapmer oligonucleotide of claim 2 wherein in the central region B is 8-12 DNA nucleotides.
10. The gapmer oligonucleotide of claim 1 , wherein region A has a length of 2-6 nucleotide units and region C has a length of 1-5 nucleotide units and region D has a length of 1-3 nucleotide units.
11. The gapmer oligonucleotide of claim 2 , wherein region A has a length of 2-6 nucleotide units and region C has a length of 1-5 nucleotide units and region D has a length of 1-3 nucleotide units.
12. The gapmer oligonucleotide of claim 1 , wherein region A has a length of 3-5 nucleotide units and region C has a length of 2-4 nucleotide units and region D has a length of 1-2 nucleotide units.
13. The gapmer oligonucleotide of claim 2 , wherein region A has a length of 3-5 nucleotide units and region C has a length of 2-4 nucleotide units and region D has a length of 1-2 nucleotide units.
14. The gapmer oligonucleotide of claim 1 , wherein the gapmer oligonucleotide has a length of 12-21 nucleotide units.
15. The gapmer oligonucleotide of claim 2 , wherein the gapmer oligonucleotide has a length of 12-21 nucleotide units.
16. The gapmer oligonucleotide of claim 1 , wherein the gapmer oligonucleotide has a length of 15-17 nucleotide units.
17. The gapmer oligonucleotide of claim 2 , wherein the gapmer oligonucleotide has a length of 15-17 nucleotide units.
18. The gapmer oligonucleotide of claim 1 , wherein the gapmer oligonucleotide has a length of 13, 14, 15, 16, 17 or 18 nucleotide units.
19. The gapmer oligonucleotide of claim 2 , wherein the gapmer oligonucleotide has a length of 13, 14, 15, 16, 17 or 18 nucleotide units in length.