Guanylhydrazone salts, compositions, processes of making and methods of using
The invention relates to pharmaceutically acceptable salts of guanylhydrazone-containing compounds, for example, Semapimod. The invention also relates to pharmaceutically acceptable compositions comprising the salts and methods for their use.
1. A pharmaceutically acceptable salt, comprising the following compound:
as a salt of at least one pharmaceutically acceptable acid selected from the group consisting of compounds having the following formulas:
wherein each C* independently represents a potentially chiral carbon that can be in either the D or L enantiomeric configuration,
wherein each R is independently unsubstituted or substituted and selected from the group consisting of Y—, Y—O—, Y—S—, Y—SO 2 —, (Y) 2 —N—SO 2 —, Y—(C═O)—, Y—(C═O)—O—, YO—(C═O)—, (Y) 2 —N—, Y—(C═O)—(Y—N)—, (Y—(C═O)) 2 —N—, Y—(SO 2 )—(Y—N)—, or (Y—(SO 2 )) 2 —N—; each Y being independently selected from the group consisting of hydrogen, carboxyl, halo, hydroxyl, thiol, nitro, amine, NC—, (C 1 –C 6 )alkyl, (C 3 –C 6 )cycloalkyl, (C 2 –C 6 )alkenyl, (C 3 –C 6 )cycloalkenyl, (C 2 –C 6 )alkynyl, (C 3 –C 6 )cycloalkynyl, (C 1 –C 6 )alkoxy, (C 5 –C 7 )aryl, (C 3 –C 5 )heteroaryl, and (C 3 –C 5 )heterocyclic; wherein each of the aforesaid (C 1 –C 6 )alkyl, (C 3 –C 6 )cycloalkyl, (C 2 –C 6 )alkenyl, (C 3 –C 6 )cycloalkenyl, (C 2 –C 6 )alkynyl, (C 3 –C 6 )cycloalkynyl, (C 1 –C 6 )alkoxy, (C 5 –C 7 )aryl, (C 3 –C 5 )heteroaryl, and (C 3 –C 5 )heterocyclic substituents may be substituted or unsubstituted;
wherein two independently chosen Y alkyl-containing groups may be taken together with any nitrogen atom to which they are attached to form a three to twelve membered cyclic, heterocyclic or heteroaryl ring;
and wherein in the compound having the formula VII, L is a diradical moiety selected from the group consisting of (C 1 –C 20 )alkyl, (C 3 –C 20 )cycloalkyl, (C 2 –C 20 )alkenyl, (C 3 –C 20 )cycloalkenyl, (C 2 –C 20 )alkynyl, (C 3 –C 20 )cycloalkynyl, (C 1 –C 20 )alkoxy/thiol, (C 3 –C 20 )aryl, (C 3 –C 15 )heteroaryl, (C 3 –C 15 )heterocyclic and (C 3 –C 20 )cycloalkyl; wherein each of the aforesaid (C 1 –C 20 )alkyl, (C 3 –C 20 )cycloalkyl, (C 2 –C 20 )alkenyl, (C 3 –C 20 )cycloalkenyl, (C 2 –C 20 )alkynyl, (C 3 –C 20 )cycloalkynyl, (C 1 –C 20 )alkoxy/thiol, (C 3 –C 20 )aryl, (C 3 –C 1 5 )heteroaryl, (C 3 –C 15 )heterocyclic and (C 3 –C 20 )cycloalkyl diradical moieties may be substituted or unsubstituted.
2. The salt of claim 1 , wherein the pharmaceutically acceptable acid has the following formula:
3. The salt of claim 1 , wherein the pharmaceutically acceptable acid has the following formula:
4. The salt of claim 1 , wherein the pharmaceutically acceptable acid has the following formula:
5. The salt of claim 1 , wherein the pharmaceutically acceptable acid has the following formula:
6. The salt of claim 1 , wherein the pharmaceutically acceptable acid has the following formula:
7. The salt of claim 1 , wherein the pharmaceutically acceptable acid has one of the following formulas:
8. The salt of claim 1 , wherein the pharmaceutically acceptable acid has the following formula:
9. A pharmaceutically acceptable composition, comprising the salt of claim 1 in contact with at least one pharmaceutically acceptable carrier.