Sirtuin modulating compounds
Provided herein are novel sirtuin-modulating compounds and methods of use thereof. The sirtuin-modulating compounds may be used for increasing the lifespan of a cell, and treating and/or preventing a wide variety of diseases and disorders including, for example, diseases or disorders related to aging or stress, diabetes, obesity, neurodegenerative diseases, cardiovascular disease, blood clotting disorders, inflammation, cancer, and/or flushing as well as diseases or disorders that would benefit from increased mitochondrial activity. Also provided are compositions comprising a sirtuin-modulating compound in combination with another therapeutic agent.
1. A compound represented by Structural Formula (V):
or a salt thereof.
2. The compound of claim 1 , wherein the compound is a free base.
3. The compound of claim 1 , wherein the compound is a salt.
4. A pharmaceutical composition comprising a compound or a pharmaceutically acceptable salt of claim 1 and a pharmaceutically acceptable carrier.
5. The composition of claim 4 , wherein the pharmaceutical composition is pyrogen-free.
6. The composition of claim 4 , further comprising an additional active agent.
7. A method for treating insulin resistance, a metabolic syndrome, diabetes, or complications thereof, or for increasing insulin sensitivity in a subject, comprising administering to a subject in need thereof a therapeutically effective amount of at least one pharmaceutical composition of claim 4 .
8. The method of claim 7 , wherein said compound increases at least one of the level or activity of a sirtuin protein.
9. The method of claim 8 , wherein the compound increases deacetylase activity of the sirtuin protein.
10. The method of claim 8 , wherein the sirtuin protein is a mammalian protein.
11. The method of claim 8 , wherein the sirtuin protein is human SIRT1.
12. The method of claim 8 , wherein the compound does not substantially have one or more of the following activities: inhibition of PI3-kinase, inhibition of aldoreductase, inhibition of tyrosine kinase, transactivation of EGFR tyrosine kinase, coronary dilation, or spasmolytic activity, at concentrations of the compound that are effective for increasing the deacetylation activity of a SIRT1 and/or SIRT3 protein.