6386-80-7Relevant articles and documents
SPIRO-OXADIAZOLINE COMPOUNDS AS AGONISTS OF α-7-NICOTINIC ACETYLCHOLINE RECEPTORS
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Paragraph 00400-00401, (2015/05/19)
The present invention relates to novel spiro-oxadiazoline compounds that are suitable as agonists or partial agonists of a7-nAChR, and pharmaceutical compositions of the same, methods of preparing these compounds and compositions, and the use of these compounds and compositions in methods of maintaining, treating and/or improving cognitive function. In particular, methods of administering a spiro-oxadiazoline cx7-nAChR agonist or partial agonist, to a patient in need thereof, for example a patient with a cognitive deficiency and/or a desire to enhance cognitive function, that may derive a benefit therefrom.
SUBSTITUTED TRIAZOLE AND IMIDAZOLE COMPOUNDS
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Page/Page column 61, (2014/06/24)
The invention is concerned with the compounds of formula (I): and pharmaceutically acceptable salts thereof. In addition, the present invention relates to methods of manufacturing and using the compounds of formula (I) as well as pharmaceutical compositions containing such compounds. The compounds of formula (I) are LMP7 inhibitors and may be useful in treating associated inflammatory diseases and disorders such as, for example, rheumatoid arthritis, lupus and irritable bowel disease.
N-ALKOXYALKYL-N,N-DIALKYLAMINE DERIVATIVES OR SALTS THEREOF, AND REMEDIES FOR NERVE DEGENERATION DISEASES CONTAINING THE SAME
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Example 16'(3), (2008/06/13)
An N-alkoxyalkyl-N,N-dialkylamine derivative represented by the following general formula [1]: wherein the ring D represents a 5- or 6-membered heterocyclic ring or hydrocarbon ring; R3 and R4, which are the same or different, represent an unsubstituted or substituted alkyl, cycloalkyl or aralkyl group; and R1, R2, R5, R6, R7, R8, m and n are as defined in the specification, or a salt thereof has an anti-hypoxic activity, a nerve-protecting activity and a nerve regeneration promoting activity and is useful for the treatment of neurodegenerative diseases.
Studies in sulfur heterocycles. Part 12. Use of 5,6-dihydrobenzo[b]-thiophen-7(4H)-one in the synthesis of condensed sulfur heterocycles
Samanta, Subhendu Sekhar,Ghosh, Sukhen Chandra,De, Asish
, p. 3673 - 3677 (2007/10/03)
Readily available 5,6-dihydrobenzo[b]thiophen-7(4H)-one has been used as a convenient intermediate for the synthesis of several condensed heterocyclic systems and substituted benzo[b]thiophenes.
5-[Substituted bicyclic aryl or heteroaryl]cyclohexane-1,3-dione herbicides
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, (2008/06/13)
The invention concerns novel compounds of the formula I STR1 wherein: A is selected from CH and N; B is selected from oxygen, sulfur, CH2 and the group N-Z wherein Z is selected from the group consisting of hydrogen, alkyl, alkenyl, alkynyl, cy