Substituted bridged urea analogs as sirtuin modulators
US-2017355697-A1 · Dec 14, 2017 · US
US2018228808A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2018228808-A1 |
| Application number | US-201615580419-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jun 3, 2016 |
| Priority date | Jun 8, 2015 |
| Publication date | Aug 16, 2018 |
| Grant date | — |
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Use of H3K9me3 modulation for enhancing cognitive function and treating anxiety related disorders is presented. A composition is administered to the subject comprising a therapeutically effective amount of a SUV39H1 inhibitor comprising analogs of ETP69. The therapeutically effective amount is effective in treating cognitive dysfunction in aging and age-related disorders.
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What is claimed is: 1 . A method of reversing cognition loss in an animal subject in need thereof, the method comprising: selecting an animal subject with cognitive loss; and administering a therapeutically effective amount of a SUV39H1 inhibitor compound to said animal subject, wherein said therapeutically effective amount comprises single dosing for acute treatment and repeated dosing for chronic treatment. 2 . A method of reversing cognition loss in a patient in need thereof, the method comprising: selecting a patient with loss of memory function; and administering to the patient a therapeutically effective amount of a SUV39H1 inhibitor compound together with a pharmaceutical cognitive enhancer, wherein said therapeutically effective amount comprises single dosing for acute treatment and repeated dosing for chronic treatment. 3 . The method of claim 2 , wherein the cognitive enhancer is a cholinesterase inhibitor. 4 . The method of claim 3 , wherein the cholinesterase inhibitor is selected from a group comprising tacrine, donepezil, rivastigmine, and galantamine. 5 . The method of claim 2 , wherein the cognitive enhancer is an NMDA antagonist or an NMDA agonist. 6 . The method of claim 2 , wherein the cognitive enhancer is an ampakine. 7 . The method of claim 2 , wherein the cognitive enhancer is a BZD/GABA receptor complex modulator. 8 . The method of claim 2 , wherein the cognitive enhancer is a serotonin antagonist. 9 . The method of claim 2 , wherein the cognitive enhancer is a nicotinic class compound. 10 . The method of claim 2 , wherein the cognitive enhancer is a muscarinic class compound. 11 . The method of claim 2 , wherein the cognitive enhancer is a PDE inhibitor. 12 . The method of claim 2 , wherein the cognitive enhancer is a G protein class compound. 13 . The method of claim 2 , wherein the cognitive enhancer is a channel modulator. 14 . The method of claim 2 , wherein the cognitive enhancer is an immunotherapeutic class compound. 15 . The method of claim 2 , wherein the cognitive enhancer is an anti-amyloid or amyloid lowering agent. 16 . The method of claim 2 , wherein the cognitive enhancer is a statin or a PPARS modulator. 17 . A method of enhancing cognition in a subject in need thereof, the method comprising: selecting a subject in need of memory enhancement; and administering to the subject a therapeutically effective amount of a SUV39H1 inhibitor compound together with a lifestyle cognitive enhancer. 18 . The method of claim 17 , wherein the cognitive enhancer is physical exercise. 19 . The method of claim 17 , wherein the cognitive enhancer is mental exercise. 20 . The method of claim 17 , wherein the cognitive enhancer is dietary supplement. 21 . The method of claim 20 , wherein the supplement is an antioxidant. 22 . The method of claim 20 , wherein the supplement is a mitochondrial function enhancer. 23 . The method of claim 20 , wherein the supplement is caffeine. 24 . The method of claim 20 , wherein the supplement is omega-3. 25 . The method of claim 20 , wherein the supplement is Docosahexaenoic acid (DHA). 26 . A method of treatment, prevention or alleviation of a cognitive dysfunction of a living animal subject, including a human, the method comprising: selecting a living animal subject with signs of cognitive loss; and administering to such living animal subject a therapeutically effective amount of a SUV39H1 inhibitor compound. 27 . A method of treatment and alleviation of anxiety related disorders in an animal subject in need thereof, the method comprising: selecting an animal subject with anxiety related disorder; and administering a therapeutically effective amount of a SUV39H1 inhibitor compound to said animal subject, wherein said therapeutically effective amount comprises single dosing for acute treatment and repeated dosing for chronic treatment.
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