Resist composition and patterning process
US-2017351177-A1 · Dec 7, 2017 · US
US9283230B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9283230-B2 |
| Application number | US-201113984841-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 15, 2011 |
| Priority date | Feb 11, 2011 |
| Publication date | Mar 15, 2016 |
| Grant date | Mar 15, 2016 |
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The invention relates to compounds of general formula (I): wherein: each of R 1 and R 9 is independently selected from: —H, C 1-4 alkyl, C 2-4 alkenyl, and halogenated C 1-4 alkyl; each of R 3NA and R 3NB is independently selected from: —H, C 1-4 alkyl, C 2-4 alkenyl, and halogenated C 1-4 alkyl; each of R7NA and R7NB is independently selected from: —H, C 1-4 alkyl, C 2-4 alkenyl, and halogenated C 1-4 alkyl; and wherein: each of R A and R B is independently selected from: C 1-4 alkyl, halogenated C 1-4 alkyl, and C 6-10 aryl; or R A and R B are linked to form a group selected from: C 1-6 alkylene and C 6-10 arylene; and pharmaceutically acceptable salts thereof, which are useful in the treatment of, for example, Alzheimer's disease. In other aspects the invention also relates to novel formulations of 3,7-diamino-10H-phenothiazinium salts.
Opening claim text (preview).
The invention claimed is: 1. A method of treating a tauopathy comprising administering to a subject in need thereof the compound of the following formula: or a pharmaceutically acceptable salt, solvate, or hydrate thereof. 2. The method of claim 1 , wherein the tauopathy is Alzheimer's disease (AD), Pick's disease, progressive supranuclear palsy (PSP), frontotemporal dementia (FTD), FTD with parkinsonism linked to chromosome 17 (FTDP 17), frontotemporal lobar degeneration (FTLD) syndromes; disinhibition-dementia-parkinsonism-amyotrophy complex (DDPAC), pallido-ponto-nigral degeneration (PPND), Guam-ALS syndrome, pallido nigro luysian degeneration (PNLD), cortico-basal degeneration (CBD), dementia with argyrophilic grains (AgD), dementia pugilistica (DP) or chronic traumatic encephalopathy (CTE), Down's syndrome (DS), dementia with Lewy bodies (DLB), subacute sclerosing panencephalitis (SSPE), Niemann-Pick disease, type C (NPC), Sanfilippo syndrome type B, mucopolysaccharidosis III B (MPS III B)), or myotonic dystrophies (DM), DM1 or DM2. 3. The method of claim 2 , wherein the tauopathy is Alzheimer's disease. 4. The method of claim 2 , wherein the tauopathy is PSP. 5. The method of claim 2 , wherein the tauopathy is FTD, FTDP-17, or FTLD.
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