Complex of nucleic acid medicine and multibranched lipid
The purpose of the present invention is to provide novel complexes that improve the effect of nucleic acid medicines. Provided is a complex in which a multibranched lipid(s) binds through a linker to a strand of an oligonucleotide comprising a nucleic acid medicine having suppressing activity of the target gene expression.
1. A complex, comprising:
an oligonucleotide having suppressing activity of a target gene expression;
a linker; and
a lipid binding through the linker to the oligonucleotide and comprising a group of formula
wherein
A 11 is substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl or a group of formula:
A 1 to A 10 and A 16 to A 17 are each independently a bond, substituted or unsubstituted alkylene, substituted or unsubstituted alkenylene, or substituted or unsubstituted alkynylene,
when A 1 and A 2 or A 16 and A 17 are substituted or unsubstituted alkylene, substituted or unsubstituted alkenylene, or substituted or unsubstituted alkynylene, any carbon atom of A 1 and any carbon atom of A 2 , or any carbon atom of A 16 and any carbon atom of A 17 taken together may form substituted aromatic carbocycle or substituted non-aromatic carbocycle, Y 1 to Y 7 are each independently a bond or O,
X 1 , X 3 and X 6 are each independently NR 1 C(═O), C(═O)NR 1 , R 2 C(═O)NR 1 or NR 1 C(═O)R 2 ,
X 2 , X 4 , X 5 and X 7 are each independently a bond, NR 3 C(═O), C(═O)NR 3 , R 4 C(═O)NR 3 , NR 3 C(═O)R 4 or S—S,
R 2 and R 4 are each independently O or NR 5 ,
R 1 , R 3 and R 5 are each independently hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, or substituted or unsubstituted alkynyl,
A 12 and A 14 are substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted alkynyl, or a group comprising a fat-soluble compound,
A 13 , A 15 , A 20 and A 21 are each independently substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, or substituted or unsubstituted alkynyl, and
m, n, p, q, r, s and t are each independently 1 or 2,
provided that a substituent for the alkyls, alkenyls, alkynyls, alkylenes, alkenylenes and alkynylenes is halogen, hydroxy, carboxy, amino, imino, formyl, formyloxy, carbamoyl, sulfamoyl, sulfanyl, sulfino, sulfo, thioformyl, thiocarboxy, dithiocarboxy, thiocarbamoyl, cyano, nitro, nitroso, azide, hydrazino, ureide, amidino, guanidino, trialkylsilyl, aromatic carbocyclyl, non-aromatic carbocyclyl, non-aromatic heterocyclyl, non-aromatic heterocyclyl, aromatic carbocyclylcarbonyl, non-aromatic carbocyclylcarbonyl, aromatic heterocyclylcarbonyl or non-aromatic heterocyclylcarbonyl, and the substituent is unsubstituted or comprises one or more substituents selected from Group α consisting of hydroxy, alkyl, alkyloxy, mercapto, alkylthio, amino, alkylamino and halogen, and
wherein the linker is a group of formula
wherein
L 0 binds to the oligonucleotide and L 6 binds to the lipid,
L 0 is a bond, a nucleotide linker or a non-nucleotide linker, and
L 1 is a group of formula
wherein
Z are each independently O or S,
R 6 are each independently hydroxy, alkyl or alkyloxy,
L 2 and L 4 are each independently a bond or substituted or unsubstituted C1 to C20 alkylene,
L 3 are each independently C(═O)NR 7 , NR 8 C(═O), or S—S, wherein R 7 is hydrogen or substituted or unsubstituted alkyl and R 8 is hydrogen, substituted or unsubstituted alkyl or R 8 and a carbon atom in alkylene of L 2 taken together may form substituted or unsubstituted nitrogen-containing ring,
L 5 are each independently a bond, substituted or unsubstituted C1 to C20 alkylene, C(═O)NR 9 , NR 9 C(═O), NR 9 , O, or substituted or unsubstituted non-aromatic heterocyclyl,
R 9 is each independently hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, or substituted or unsubstituted alkynyl,
u is 1 or 2, and
L 6 is a bond or an amino acid linker.
2. The complex of claim 1 , wherein, in the lipid,
A 1 to A 5 and Y 1 to Y 5 are a bond,
A 6 to A 10 are each independently a bond, substituted or unsubstituted alkylene, substituted or unsubstituted alkenylene, or substituted or unsubstituted alkynylene,
X 1 to X 5 are NHC(═O), and
n, p, q and r are 1.
3. The complex of claim 1 , wherein A 11 and A 13 are C6 to C30 alkyl.
4. The complex of claim 1 , wherein the lipid binds at the 3′-end and/or 5′-end of the oligonucleotide.
5. A complex of one of formulas (C-2) to (C-7)
wherein
OL is an oligonucleotide having suppressing activity of a target gene expression,
5′ represents that the oligonucleotide binds at the 5′-end of the oligonucleotide,
3′ represents that the oligonucleotide binds at the 3′-end of the oligonucleotide,
Z 1-1 is O or S,
L 0-1 is a bond, a nucleotide linker or a non-nucleotide linker,
L 5-1 is a bond, NH or O,
L 6-1 is a bond or an amino acid linker,
LI is a lipid comprising a group of one of formulas (LI-1) to (LI-9)
wherein
A 1-1 is a bond or methylene,
A 2-1 is C1 to C4 straight alkylene,
A 11-1 is C7 to C23 straight or branched alkyl, and
A 12-1 is C3 to C23 straight or branched alkyl or alkenyl, a group comprising a fat-soluble compound, or a group of formula
wherein A 13-1 , A 14-1 and A 15-1 are C9 to C13 straight alkyl,
wherein
A 20-1 and A 21-1 is C13 straight alkyl, and
A 12-2 is C15 straight alkyl or a group comprising a fat-soluble compound,
wherein
A 11-2 is C15 straight alkyl, and
A 12-3 is C1 to C4 straight alkyl substituted with amino,
wherein
A 20-2 and A 21-2 are C13 straight alkyl, and
A 12-4 is C4 straight alkyl substituted with amino,
wherein A 11-3 and A 12-5 are C15 straight alkyl,
wherein
A 11-4 is C14 straight alkyl, and
A 12-6 is C6 to C12 straight alkyl.
6. A pharmaceutical composition, comprising:
the complex of claim 1 .
7. The complex of claim 2 , wherein A 11 and A 13 are C6 to C30 alkyl.
8. The complex of claim 2 , wherein the lipid binds at the 3′-end and/or 5′-end of the oligonucleotide.
9. The complex of claim 3 , wherein the lipid binds at the 3′-end and/or 5′-end of the oligonucleotide.
10. A pharmaceutical composition, comprising:
the complex of claim 2 .
11. A pharmaceutical composition, comprising:
the complex of claim 3 .
12. A pharmaceutical composition, comprising:
the complex of claim 4 .
13. A pharmaceutical composition, comprising:
the complex of claim 5 .
14. The complex of claim 7 , wherein the lipid binds at the 3′-end and/or 5′-end of the oligonucleotide.
15. The complex of claim 1 , wherein the lipid binds at the 3′-end and 5′-end of the oligonucleotide.
16. The complex of claim 1 , wherein the lipid binds at the 3′-end of the oligonucleotide.
17. The complex of claim 1 , wherein the lipid binds at the 5′-end of the oligonucleotide.
18. A pharmaceutical composition, comprising:
the complex of claim 15 .
19. A pharmaceutical composition, comprising:
the complex of claim 16 .
20. A pharmaceutical composition, comprising:
the complex of claim 17 .