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US 2024/0392289 A1Published application
Ligand conjugates for delivery of therapeutically active agents
AssigneeHepagene Therapeutics (HK) Limited
InventorsXiaodong Xu, Cheng Mo, Shijia Chen
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Abstract
The present invention discloses compounds of Formula (I) as novel ligand conjugates, and use thereof for delivering therapeutically active agents. The compounds of the present invention have the advantages for in vitro and/or in vivo delivery of therapeutically active agents, e.g., iRNA agents.
Claims34
A compound having the structure shown in Formula (I)
- or a pharmaceutically acceptable salt or solvate thereof, wherein
- A and B, for each occurrence, are each independently O, N(RN), or S;
- RN is H or C1-6 alkyl;
- X and W, for each occurrence, are each independently H, a protecting group, a phosphate group, a phosphodiester group, an activated phosphate group, an activated phosphite group, a phosphoramidite, a solid support, —P(Z′)(Z″)O-nucleoside, —P(Z′)(Z″)O-oligonucleotide, a lipid, a PEG, a steroid, a polymer, a nucleotide, a nucleoside, an oligonucleotide, or a therapeutically active agent;
- Z′ and Z″ are each independently O or S;
- L is a covalent linker;
- Z is a carbohydrate mimetic or a disaccharide, trisaccharide, or oligosaccharide;
- each Y is independently -L′-T;
- each T is independently a ligand selected from the group consisting of carbohydrate ligands, polypeptide ligands, and lipophile ligands;
- each L′ is independently a covalent linker;
- and
- p and q are each independently 1, 2, 3, 4, or 5.
9 more elements
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-28. (canceled)
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-45. (canceled)
Dependencies are inferred from the claim text.