IP Library Granted Patent US 7,053,199
Granted Patent B2
US 7,053,199 · App. 10/363,057 · Granted May 30, 2006

Nucleoside analogs and oligonucleotide derivatives containing these analogs

Assignee: Takeshi Imanishi
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Quick Facts
Patent No.
US 7,053,199
App. No.
10/363,057
Granted
May 30, 2006
Kind
B2
Abstract

Nucleoside analogues expressed by the following general formula where B represents an aromatic base having carbonyl oxygen at the 2-position, or a 2-hydroxyphenyl group, or oligonucleotide derivatives containing one or more of the nucleoside analogues are provided. The oligonucleotide derivatives are triplex-forming oligonucleotide derivatives which bind specifically to target double-stranded DNA with high affinity in the antigene method to form triplexes, and can thereby control and inhibit the expression of relevant genes efficiently, and which show high resistance to nucleases.

Claims (16)

1. Nucleoside analogues expressed by the following general formula (I)

where B represents a substituent selected from substituents expressed by the following general formulas

where J, K, L and Q are identical or different, and each denote —H, a lower alkyl, —OH, or —NH 2 , 1, m and p independently denote an integer of 1 to 4, and n denotes an integer of 1 or 2,

X and Y are identical or different, and each represent hydrogen, an alkyl group, an alkenyl group, an alkinyl group, a cycloalkyl group, an aralkyl group, an aryl group, an acyl group, or a silyl group,

or amidite derivatives thereof.

2. Nucleoside analogues or amidite derivatives thereof according to claim 1 , wherein B represents a substituent expressed by any one of the following general formulas

where J, K, L, l, m, X and Y are as defined above.

3. Nucleoside analogues or amidite derivatives thereof according to claim 1 , wherein B represents a substituent expressed by the following general formula

where Q, p, X and Y are as defined above.

4. Nucleoside analogues according to claim 1 , 2 or 3 , wherein X and Y are each hydrogen.

5. Amidite derivative according to claim 1 , 2 or 3 , wherein X is 4,4′-dimethoxytrityl (DMTr), and Y is a 2-cyanoethoxy(diisopropylamino)phosphino group (amidite group).

6. Nucleoside analogues according to claim 1 or 2 , wherein B is a substituted or unsubstituted 2-oxopyridyl or a substituted or unsubstituted isoquinoline.

7. Nucleoside analogues according to claim 6 , wherein B is selected from 2-oxopyridyl, 5-methyl-2-oxopyridyl, 4-hydroxy-2-oxopyridyl, and isoquinolin-1-one.

8. Nucleoside analogues according to claim 7 , wherein B is 2-oxopyridyl.

9. Nucleoside analogues according to claim 1 or 3 , wherein B is 2-hydroxyphenyl.

10. Oligonucleotide or polynucleotide derivatives having one or more of the nucleoside analogues according to any one of claims 1 to 3 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 20, 2004
From: OBIKA, SATOSHI
To: IMANISHI, TAKESHI
Reel/Frame 015587/0709 →
Priority Claims (1)
JP 2000-259290 · Aug 29, 2000 · national
Continuity (1)
Related Publication 20040192918A1 · Sep 30, 2004