β- and γ-diketones and γ-hydroxyketones as Wnt/β-catenin signaling pathway activators
US-9303010-B2 · Apr 5, 2016 · US
US9795550B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9795550-B2 |
| Application number | US-201514831456-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 20, 2015 |
| Priority date | Aug 20, 2014 |
| Publication date | Oct 24, 2017 |
| Grant date | Oct 24, 2017 |
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The present disclosure relates to compounds, cosmetic or dermopharmaceutical compositions comprising the same, and methods for using the compounds or compositions for treating, protecting, and/or improving the condition and/or aesthetic appearance of skin, for example, treating, preventing, ameliorating, reducing and/or eliminating fine lines and/or wrinkles of skin, or improving the appearance of fine lines and/or or wrinkles of skin comprising application of the compounds or compositions disclosed. In some embodiments, the compounds useful in the methods described herein include compounds of Formula I: or a dermatologically acceptable salt thereof.
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What is claimed is: 1. A method for improving the aesthetic appearance of a subject's skin, the method comprising administering to the subject an effective amount of a compound of Formula I, or a dermatologically acceptable salt thereof: wherein: Ring A is a 7-12 membered heteroaryl, with the proviso that a carbon atom on the ring is attached to the carbonyl carbon; Ring B is phenyl; R 1 is a substituent attached to Ring A and is independently selected at each occurrence from the group consisting of unsubstituted —C 1-6 alkyl, —C 1-3 haloalkyl, halide, —OR 3 , and CN; R 2 is a substituent attached to Ring B and is independently selected at each occurrence from the group consisting of unsubstituted —C 1-6 alkyl, —CH 2 OH, —CH 2 N(R 3b ) 2 , —C 1-3 haloalkyl, halide, —OR 3 , and CN; each R 3 is independently selected from the group consisting of H, unsubstituted —C 1-6 alkyl, and —C 1-3 haloalkyl; each R 3b is independently selected from the group consisting of H and unsubstituted —C 1-3 alkyl; each n is 0 to 10; and each m is 0 to 5. 2. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of: or a dermatologically acceptable salt thereof. 3. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of: or a dermatologically acceptable salt thereof. 4. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of: or a dermatologically acceptable salt thereof. 5. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of: or a dermatologically acceptable salt thereof. 6. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of: or a dermatologically acceptable salt thereof. 7. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of: or a dermatologically acceptable salt thereof. 8. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of: or a dermatologically acceptable salt thereof. 9. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of: or a dermatologically acceptable salt thereof. 10. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of: or a dermatologically acceptable salt thereof. 11. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of: or a dermatologically acceptable salt thereof. 12. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of: or a dermatologically acceptable salt thereof. 13. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of: or a dermatologically acceptable salt thereof. 14. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of: or a dermatologically acceptable salt thereof. 15. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of: or a dermatologically acceptable salt thereof. 16. The method of claim 1 , wherein the compound of Formula I is selected from the group consisting of:
containing fluorine · CPC title
containing heterocyclic compounds · CPC title
with more than one nitrogen as the only hetero atom · CPC title
Preparations for dry skin · CPC title
having six membered rings · CPC title
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