Apoptosis-inducing agents for the treatment of cancer and immune and autoimmune diseases
US-9156856-B2 · Oct 13, 2015 · US
US8987335B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-8987335-B2 |
| Application number | US-201213586603-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 15, 2012 |
| Priority date | Aug 15, 2011 |
| Publication date | Mar 24, 2015 |
| Grant date | Mar 24, 2015 |
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In one aspect, the invention relates to substituted (E)-N′-(1-phenylethylidene)benzohydrazide analogs, derivatives thereof, and related compounds, which are useful as inhibitors of lysine-specific histone demethylase, including LSD1; synthetic methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of using the compounds and compositions to treat disorders associated with dysfunction of the LSD1. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.
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What is claimed is: 1. A compound selected from the group consisting of: or a pharmaceutically acceptable salt thereof. 2. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 1 and a pharmaceutically acceptable carrier. 3. A compound having a structure represented by a formula: or a pharmaceutically acceptable salt thereof. 4. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 3 and a pharmaceutically acceptable carrier. 5. A compound having a structure represented by a formula: or a pharmaceutically acceptable salt thereof. 6. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 5 and a pharmaceutically acceptable carrier. 7. A compound having a structure represented by a formula: or a pharmaceutically acceptable salt thereof. 8. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 7 and a pharmaceutically acceptable carrier.
having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil · CPC title
having four-membered rings, e.g. azetidine · CPC title
Sulfur atoms · CPC title
with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings · CPC title
having no double bonds between ring members or between ring members and non-ring members · CPC title
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