abstract |
The present invention provides the following formula (formula (I)): Where, for example, X is C or N; n is 1-10; each L is independently a 5-12 membered heteroaryl containing at least 2 nitrogen atoms; Or a pharmaceutically acceptable salt thereof. The present compounds are useful as histone deacetylase (HDAC) inhibitors. That is, the compounds of the present invention can be used in methods of treating diseases associated with overexpression of HDAC. |