Imaging histone deacetylases with a radiotracer using positron emission tomography
US-2016271276-A1 · Sep 22, 2016 · US
US11207431B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11207431-B2 |
| Application number | US-201816603746-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 11, 2018 |
| Priority date | Apr 11, 2017 |
| Publication date | Dec 28, 2021 |
| Grant date | Dec 28, 2021 |
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Provided herein are compounds useful for binding to one or more histone deacetylase enzymes (HDACs). The present application further provides radiolabeled compounds useful as a radiotracer for position emission tomography imaging of HDAC. Methods for prepared unlabeled and labeled compounds, diagnostic methods, and methods of treating diseases associated HDAC are also provided.
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What is claimed is: 1. A compound, which is selected from the group consisting of: or a pharmaceutically acceptable salt thereof. 2. A pharmaceutical composition, comprising a compound of claim 1 , or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable carrier. 3. A method of inhibiting an activity of a histone deacetylase (HDAC) enzyme, comprising contacting the HDAC enzyme with a compound of claim 1 , or a pharmaceutically acceptable salt thereof. 4. The method of claim 3 , wherein the histone deacetylase (HDAC) enzyme is HDAC6. 5. The method of claim 3 , wherein the compound selectively inhibits HDAC6 over one or more of HDAC1, HDAC2, HDAC3, HDAC4, HDAC5, HDAC7, HDAC8, HDAC9, HDAC10, and HDAC11. 6. The compound of claim 1 , which is: or a pharmaceutically acceptable salt thereof. 7. The compound of claim 1 , which is: or a pharmaceutically acceptable salt thereof.
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