IPC분류정보
국가/구분 |
United States(US) Patent
등록
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국제특허분류(IPC7판) |
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출원번호 |
US-0648254
(2000-08-25)
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발명자
/ 주소 |
- Innis, Michael A.
- Reinhard, Christoph J.
- Zuckermann, Ronald N.
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출원인 / 주소 |
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대리인 / 주소 |
Gorthey, LeeAnnCollier, Steven W.Blackburn, Robert P.
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인용정보 |
피인용 횟수 :
26 인용 특허 :
39 |
초록
▼
Chimeric oligonucleotide of the formula 5'-W-X1-Y-X2-Z-3', where W represents a 5'-O-alkyl nucleotide, each of X1and X2represents a block of seven to twelve phosphodiester-linked 2'-O-alkyl ribonucleotides, Y represents a block of five to twelve phosphorothioate-linked deoxyribonucleotides, and Z re
Chimeric oligonucleotide of the formula 5'-W-X1-Y-X2-Z-3', where W represents a 5'-O-alkyl nucleotide, each of X1and X2represents a block of seven to twelve phosphodiester-linked 2'-O-alkyl ribonucleotides, Y represents a block of five to twelve phosphorothioate-linked deoxyribonucleotides, and Z represents a blocking group effective to block nuclease activity at the 3' end of the oligonucleotide, are described. These compounds exhibit high resistance to endo- and exonucleases, high sequence specificity, and the ability to activate RNAse H, as evidenced by efficient and long-lasting suppression of target mRNA. The oligonucleotides are preferably transfected into cells in formulations containing a lipid-peptoid conjugate carrier molecule of the formula L-linker-[N(CH2CH2NH2)CH2(C=O)--N(CH2CH2R)CH2(C=O)--N(CH2CH2R)CH2(C=O)]3--NH2, where L is a lipid moiety, including a steroid, and each group R is independently selected from alkyl, aminoalkyl, and aralkyl.
대표청구항
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1. A composition comprising a chimeric oligonucleotide having the structure: 5'-W-X1-Y-X2-Z-3', wherein: W represents a 5'-O-alkyl nucleotide; each of X1and X2represents a block of seven to twelve phosphodiester-linked 2'-O-alkyl ribonucleotides; Y represents a block of five to twelve phosphor
1. A composition comprising a chimeric oligonucleotide having the structure: 5'-W-X1-Y-X2-Z-3', wherein: W represents a 5'-O-alkyl nucleotide; each of X1and X2represents a block of seven to twelve phosphodiester-linked 2'-O-alkyl ribonucleotides; Y represents a block of five to twelve phosphorothioate-linked deoxyribonucleotides; and Z represents a blocking group effective to block nuclease activity at the 3' end of the oligonucleotide in a pharmaceutically acceptable vehicle. 2. The composition of claim 1, wherein the vehicle includes a lipid-cationic peptoid conjugate of the formula: L-linker-[N(CH2CH2NH2)CH2(C=O)--N(CH2CH2R)CH2(C=O)--N(CH2CH2R)CH2(C=O)]3--NH2 where L is selected from a lipid moiety comprising at least one fatty alkyl or alkenyl chain between about 8 and 24 carbon atoms in length and a steroid; each group R is independently selected from alkyl, aminoalkyl, and aralkyl, and the linker is selected from the group consisting of a direct bond, an oligopeptide, a substantially linear alkyl chain from 2 to about 30 bonds in length, and a substantially linear chain from 2 to about 30 bonds in length consisting of alkyl bonds and one or more linkages selected from the group consisting of ester, amide, carbonate, carbamate, disulfide, peptide, and ether. 3. The composition of claim 2, wherein the linker is from 3 to about 15 bonds in length. 4. The composition of claim 2, wherein said fatty alkyl or alkenyl chain is between about 14 and 24 carbon atoms in length. 5. The composition of claim 2, wherein L is a phospholipid group, having two fatty alkyl or alkenyl chains between about 8 and 24 carbon atoms in length. 6. The composition of claim 2, wherein L is a cholesteryl group. 7. The composition of claim 2, wherein R is isopropyl or 4-methoxyphenyl.
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