Treprostinil derivative compounds and methods of using same
Compounds represented by formulae I, II, III, and IV including pro-drugs for treprostinil and prostacyclin analogs. Uses include treatment of pulmonary hypertension (PH) or pulmonary arterial hypertension (PAH). The structures of the compounds can be adapted to the particular application for a suitable treatment dosage. Transdermal applications can be used.
1. A compound represented by Formula II:
wherein:
R 2 is selected from the group consisting of H and P 2 ;
R 20 , R 21 , R 22 , R 23 , R 24 , R 25 , R 26 , R 27 , R 28 , R 29 , R 30 , R 31 , R 32 , R 33 , R 34 , R 35 , and R 36 are independently selected from the group consisting of H and deuterium;
L 1 is selected from the group consisting of —O-alkylene-C(O)—, —O-alkylene-OC(O)—, and a bond; and
P 2 is selected from the group consisting of:
wherein:
m is 1, 2, 3, or 4;
R 14 and R 15 are independently in each occurrence selected from the group consisting of H, alkyl, cycloalkyl, alkylcycloalkyl, haloalkyl, heteroalkyl, substituted alkyl, aryl, heteroaryl, arylalkyl, heteroarylalkyl, substituted aryl, substituted heteroaryl, substituted arylalkyl, and substituted heteroarylalkyl; or
R 14 and R 15 taken together with the atom(s) to which they are attached optionally form a 5- to 7-membered ring which incorporates one or two ring heteroatoms chosen from N, O, and S, and which is unsubstituted or substituted with 1, 2, or 3 substituents independently selected from the group consisting of halo, methyl, and methoxy;
R 16 and R 17 are independently H or alkyl; or
R 16 and R 17 taken together with the atom to which they are attached optionally form a 3- to 6-membered ring; and
R 18 and R 19 are independently in each occurrence selected from the group consisting of hydrogen and alkyl, wherein the alkyl is unsubstituted or substituted with 1 substituent selected from the group consisting of halo, hydroxy, alkoxy, amino, thio, methylthio, —C(O)OH, —C(O)O-(alkyl), —CONH 2 , aryl, and heteroaryl, wherein the aryl or heteroaryl is unsubstituted or substituted with a substituent selected from the group consisting of alkyl, halo, haloalkyl, hydroxy, alkoxy, and haloalkoxy; or
R 14 and R 18 taken together with the atoms to which they are attached optionally form a 5- to 7-membered ring; or
R 14 and R 19 taken together with the atoms to which they are attached optionally form a 5- to 7-membered ring;
or an enantiomer or a pharmaceutically acceptable salt thereof.
2. The compound of claim 1 , wherein R 20 , R 21 , R 22 , R 23 , R 24 , R 25 , R 26 , R 27 , R 28 , R 29 , R 30 , R 31 , R 32 , R 33 , R 34 , R 35 , and R 36 are H.
3. The compound of claim 1 , wherein at least one of R 20 , R 21 , R 22 , R 23 , R 24 , R 25 , R 26 , R 27 , R 28 , R 29 , R 30 , R 31 , R 32 , R 33 , R 34 , R 35 , and R 36 is deuterium.
4. The compound of claim 1 , wherein L 1 is —O-alkylene-C(O)—.
5. The compound of claim 1 , wherein L 1 is —O-alkylene-OC(O)—.
6. The compound of claim 1 , wherein L 1 is a bond.
7. The compound of claim 1 , wherein the alkylene group is a C 1 -C 5 alkylene group.
8. The compound of claim 1 , wherein the alkylene group is a C 1 alkylene group.
9. A compound represented by Formula IV:
wherein:
R 1 is selected from the group consisting of H and P 2 ;
R 20 , R 21 , R 22 , R 23 , R 24 , R 25 , R 26 , R 27 , R 28 , R 29 , R 30 , R 31 , R 32 , R 33 , R 34 , R 35 , and R 36 are independently selected from the group consisting of H and deuterium;
L 1 is selected from the group consisting of —O-alkylene-C(O)—, —O-alkylene-OC(O)—, and a bond;
P 2 is selected from the group consisting of:
wherein:
m is 1, 2, 3, or 4;
R 14 and R 15 are independently in each occurrence selected from the group consisting of H, alkyl, cycloalkyl, alkylcycloalkyl, haloalkyl, heteroalkyl, substituted alkyl, aryl, heteroaryl, arylalkyl, heteroarylalkyl, substituted aryl, substituted heteroaryl, substituted arylalkyl, and substituted heteroarylalkyl; or
R 14 and R 15 taken together with the atom(s) to which they are attached optionally form a 5- to 7-membered ring which incorporates one or two ring heteroatoms chosen from N, O, and S, and which is unsubstituted or substituted with 1, 2, or 3 substituents independently selected from the group consisting of halo, methyl, and methoxy;
R 16 and R 17 are independently H or alkyl; or
R 16 and R 17 taken together with the atom to which they are attached optionally form a 3- to 6-membered ring; and
R 18 and R 19 are independently in each occurrence selected from the group consisting of hydrogen and alkyl, wherein the alkyl is unsubstituted or substituted with 1 substituent selected from the group consisting of halo, hydroxy, alkoxy, amino, thio, methylthio, —C(O)OH, —C(O)O-(alkyl), —CONH 2 , aryl, and heteroaryl, wherein the aryl or heteroaryl is unsubstituted or substituted with a substituent selected from the group consisting of alkyl, halo, haloalkyl, hydroxy, alkoxy, and haloalkoxy; or
R 14 and R 18 taken together with the atoms to which they are attached optionally form a 5- to 7-membered ring; or
R 14 and R 19 taken together with the atoms to which they are attached optionally form a 5- to 7-membered ring;
or an enantiomer or a pharmaceutically acceptable salt thereof.
10. The compound of claim 9 , wherein the compound is represented by Formula IVA:
wherein L 1 and R 1 are defined as in claim 9 .
11. A composition comprising a compound of claim 1 or 9 and one or more pharmaceutically acceptable excipients.
12. The composition of claim 11 , which is formulated for transdermal delivery.
13. A method of treating pulmonary hypertension, comprising administering to a subject in need of treatment a therapeutically effective amount of a compound of claim 1 or 9 or a pharmaceutically acceptable salt thereof.
14. The method of claim 13 , wherein the pulmonary hypertension is pulmonary arterial hypertension.
15. The method of claim 13 , wherein the compound is administered transdermally.