Compounds for the treatment of pathologies associated with aging and degenerative disorders
The present invention relates to methods of inhibiting one or more signs of aging and/or degenerative disorder in a subject in need of such treatment, which comprise administering, to the subject, an effective amount of one or more of the compounds as set forth herein. “Inhibiting a sign of aging or degenerative disorder” means reducing the risk of occurrence, delaying the onset, slowing the progression, and/or reducing the severity and/or manifestation, of a sign of aging or degenerative disorder, and includes, but is not limited to, preventing the occurrence, development or progression of a sign of aging or degenerative disorder.
1. A method of treating epidermal atrophy, epidermal hyperpigmentation, rhytid, or photoaging of the skin in a subject in need of such treatment, comprising administering, to the subject, an effective amount of a compound having a structure selected from the group consisting of Formula 1, Formula 2, and Formula 3, wherein the Formula 1 has the following structure:
wherein X is
wherein R 1 of Formula 1 is selected from a group consisting of C 1 -C 6 straight or branched-chain alkyl, optionally including a phenyl (C 6 H 5 ) group, that optionally is methyl-, hydroxyl- or fluoro-substituted,
R 2 of Formula 1 is selected from a group consisting of H, and C 1 -C 6 straight or branched-chain alkyl,
R 4 of Formula 1, is selected from a group consisting of H, C 1 -C 6 straight or branched-chain alkyl, optionally including a phenyl (C 6 H 5 ) group, that optionally is methyl-, hydroxyl- or fluoro-substituted,
wherein R 3 of Formula 1 is —NH—R 5 , —O—R 5 or —CH 2 —R 5 , wherein R 5 is an —N—O. or —N—OH containing group,
wherein R of Formula 1 is —C(O)—R 6 or —C(O)O—R 6 , wherein R 6 is C 1 -C 6 straight or branched-chain alkyl optionally comprising one or more phenyl (—C 6 H 5 ) groups, and that optionally are methyl-, ethyl-, hydroxyl- or fluoro-substituted;
wherein Formula 2 has the following structure:
wherein R1 of Formula 2 is selected from C 1 -C 6 straight or branched-chain alkyl, optionally including a phenyl (C 6 H 5 ) group which optionally is methyl-, hydroxyl- or fluoro-substituted, R3 of Formula 2 is selected from H, or C 1 -C 6 straight or branched-chain alkyl,
R2 of Formula 2, is selected from H, C 1 -C 6 straight or branched-chain alkyl, optionally including a phenyl (C 6 H 5 ) group which optionally is methyl-, hydroxyl- or fluoro-substituted,
wherein R4 of Formula 2 is an —N—O. or —N—OH containing group, wherein R of Formula 2 is —C(O)—R5 or —C(O)O—R5, wherein R5 is C 1 -C 6 straight or branched-chain alkyl, optionally comprising one or more phenyl (—C 6 H 5 ) groups, and that optionally are methyl-, ethyl-, hydroxyl- or fluoro-substituted;
wherein Formula 3 has the following structure
wherein R1, R2 and R3 of Formula 3 are, independently, selected from C 1 -C 6 straight or branched-chain alkyl, optionally including a phenyl (C 6 H 5 ) group, that optionally is methyl-, hydroxyl- or fluoro-substituted,
wherein R4 of Formula 3 is an —N—O. or —N—OH containing group,
wherein R of Formula 3 is —C(O)—R5 or —C(O)O—R5, wherein R5 is C 1 -C 6 straight or branched-chain alkyl, optionally comprising one or more phenyl (—C 6 H 5 ) groups, and that optionally are methyl-, ethyl-, hydroxyl- or fluoro-substituted.
2. The method of claim 1 , wherein R 5 of Formula 1 is TEMPO (2,2,6,6-Tetramethyl-4-piperindine 1-oxyl).
3. The method of claim 1 , wherein R5 of Formula 1 is TEMPOL (4-Hydroxy-TEMPO).
4. The method of claim 1 , wherein R4 of Formula 2 is TEMPO (2,2,6,6-Tetramethyl-4-piperindine 1-oxyl).
5. The method of claim 4 , wherein Formula 2 has one structure selected from the group consisting of
6. The method of claim 1 , wherein R4 of Formula 3 is TEMPO (2,2,6,6-Tetramethyl-4-piperindine 1-oxyl).
7. The method of claim 6 , wherein Formula 3 has one structure selected from the group consisting of
8. The method of claim 1 , wherein the compound is:
9. The method of claim 1 , wherein the method increases proliferation of keratinocytes in the subject.
10. The method of claim 1 , wherein R 1 , R 2 and R 4 of Formula 1 are each independently selected from methyl, ethyl, propyl, butyl, t-butyl, pentyl, hexyl, benzyl, hydroxybenzyl, phenyl or hydroxyphenyl.
11. The method of claim 1 , wherein R of Formula 1 is —C(O)O-t-butyl or —C(O)O-benzyl.
12. The method of claim 1 , wherein epidermal atrophy is treated.