Methods, compounds, and compositions for delivering 1,3-propanedisulfonic acid
AssigneeBellus Health Inc.
InventorsXianqi Kong, Nigel Levens, Abderrahim Bouzide, Stephane Ciblat, Richard Frenette, Johanne Renaud
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Abstract
The invention relates to methods, compounds, and compositions for delivering 1,3-propanedisulfonic acid (1,3PDS) in a subject, preferably a human subject. The invention encompasses compounds that will yield or generate 1,3PDS, either in vitro or in vivo. The invention also relates to sulfonate ester prodrugs of 1,3PDS as well as Gemini dimmers and oligomers of 1,3PDS for the prevention or treatment of associated diseases and conditions.
Claims34
A compound of Formula I:
- wherein,
- R1 is selected from OR3, —NHC(O)R5, —NHC(NH)NHR5, —NH(C5-C10heteroaryl) or a nitrogen atom part of a mono or bicyclic heteroaryl having from 5 to 10 ring members;
- R2 is selected from OR4, —NHC(O)R5, —NHC(NH)NHR5, —NH(C5-C10heteroaryl) or a nitrogen atom part of a mono or bicyclic heteroaryl having from 5 to 10 ring members, or R1 is a covalent bond and R2 is selected from O, NH, NC(O)R5, NC(NH)NHR5, and N(C5-C10heteroaryl) when R1 and R2 are taken together with their adjacent atoms to form a heterocycle;
- R3 is selected from hydrogen and a substituted or unsubstituted group selected from C1-C12alkyl, C2-C12alkenyl, C2-C12alkynyl, C3-C15cycloalkyl, C3-C15heterocycloalkyl, C6-C15aryl, and C5-C15heteroaryl;
- R4 is a substituted or unsubstituted group selected from C1-C12alkyl, C2-C12alkenyl, C2-C12alkynyl, C3-C15cycloalkyl, C3-C15heterocycloalkyl, C6-C15aryl, and C5-C15heteroaryl;
- and
- R5 is selected from hydrogen and a substituted or unsubstituted group selected from C1-C12alkyl, C2-C12alkenyl, C2-C12alkynyl, C3-C15cycloalkyl, C3-C15heterocycloalkyl, C6-C15aryl, and C5-C15heteroaryl;
- or a pharmaceutically acceptable salt or solvate thereof.
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Dependencies are inferred from the claim text.