Derivatized oligonucleotides having improved uptake and other properties
First Claim
1. A compound comprising a plurality of linked nucleosides, wherein:
- at least one of the nucleosides is a 2′
-deoxy′
-2′
-fluoro, 2′
-O—
C1–
C20-alkyl, 2′
-O—
C2–
C20-alkenyl, 2′
-O—
C2–
C20-alkynyl, 2′
-S—
C1–
C20-alkyl, 2′
-S—
C2–
C20-alkenyl, 2′
-S—
C2–
C20-alkynyl, 2′
-NH—
C1–
C20-alkyl, 2′
-NH—
C2–
C20-alkenyl, or 2′
-NH—
C2–
C20-alkynyl nucleoside; and
at least one of the nucleosides is a 5′
-O-terminal nucleoside having a non-aromatic lipophilic molecule linked to the 5′
-O-position of the nucleoside, provided that the compound does not include sulfamate or sulfamide internucleotide linkages.
3 Assignments
0 Petitions
Accused Products
Abstract
Linked nucleosides having at least one functionalized nucleoside that bears a substituent such as a steroid molecule, a reporter molecule, a non-aromatic lipophilic molecule, a reporter enzyme, a peptide, a protein, a water soluble vitamin, a lipid soluble vitamin, an RNA cleaving complex, a metal chelator, a porphyrin, an alkylator, a pyrene, a hybrid photonuclease/intercalator, or an aryl azide photo-crosslinking agent exhibit increased cellular uptake and other properties. The substituent can be attached at the 2′-position of the functionalized nucleoside via a linking group. If at least a portion of the remaining liked nucleosides are 2′-deoxy-2′-fluoro, 2′-O-methoxy, 2′-O-ethoxy, 2′-O-propoxy, 2′-O-aminoalkoxy or 2′-O-allyloxy nucleosides, the substituent can be attached via a linking group at any of the 3′ or the 5′ positions of the nucleoside or on the heterocyclic base of the nucleoside or on the inter-nucleotide linkage linking the nucleoside to an adjacent nucleoside.
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Citations
6 Claims
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1. A compound comprising a plurality of linked nucleosides, wherein:
-
at least one of the nucleosides is a 2′
-deoxy′
-2′
-fluoro, 2′
-O—
C1–
C20-alkyl, 2′
-O—
C2–
C20-alkenyl, 2′
-O—
C2–
C20-alkynyl, 2′
-S—
C1–
C20-alkyl, 2′
-S—
C2–
C20-alkenyl, 2′
-S—
C2–
C20-alkynyl, 2′
-NH—
C1–
C20-alkyl, 2′
-NH—
C2–
C20-alkenyl, or 2′
-NH—
C2–
C20-alkynyl nucleoside; andat least one of the nucleosides is a 5′
-O-terminal nucleoside having a non-aromatic lipophilic molecule linked to the 5′
-O-position of the nucleoside, provided that the compound does not include sulfamate or sulfamide internucleotide linkages. - View Dependent Claims (2)
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3. A compound comprising a plurality of linked nucleosides, wherein:
-
at least one of the nucleosides is a 2′
-deoxy′
-2′
-fluoro, 2′
-O—
C1–
C20-alkyl, 2′
-O—
C2–
C20-alkenyl, 2′
-O—
C2–
C20-alkynyl, 2′
-S—
C1–
C20-alkyl, 2′
-S—
C2–
C20-alkenyl, 2′
-S—
C2–
C20-alkynyl, 2′
-NH—
C1–
C20-alkyl, 2′
-NH—
C2–
C20-alkenyl, or 2′
-NH—
C2–
C20-alkynyl nucleoside; andat least one of the nucleosides is a 5′
-O-terminal nucleoside having a non-aromatic molecule linked to the 5′
-O-position of the nucleoside, provided that the compound does not include sulfamate or sulfamide internucleotide linkages. - View Dependent Claims (4)
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5. A compound comprising a plurality of linked nucleosides, wherein:
-
at least one of the nucleosides is a 2′
-deoxy′
-2′
-fluoro, 2′
-O—
C1–
C20-alkyl, 2′
-O—
C2–
C20-alkenyl, 2′
-O—
C2–
C20-alkynyl, 2′
-S—
C1–
C20-alkyl, 2′
-S—
C2–
C20-alkenyl, 2′
-S—
C2–
C20-alkynyl, 2′
-NH—
C1–
C20-alkyl, 2′
-NH—
C2–
C20-alkenyl, or 2′
-NH—
C2–
C20-alkynyl nucleoside; andat least one of the nucleosides is a 5′
-O-terminal nucleoside having a lipophilic molecule linked to the 5′
-position of the nucleoside, provided that the compound does not include sulfamate or sulfamide internucleotide linkages. - View Dependent Claims (6)
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Specification