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filingDate 2006-06-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8e8eb3ce76bf3b12a3f2ce93b5f7780c
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publicationDate 2010-06-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2194047-A1
titleOfInvention Preparation and use of aspartyl protease inhibitors
abstract Disclosed are compounds of the formula In nor a stereoisomer, tautomer, or pharmaceutically acceptable salt or solvate thereof, wherein nA is a bond; nX is -N(R 1 )- or -C(R 6 )(R 7 )-; nY is -S(O) 2 -, -C(=O)-, or -C(R 6' R 7' )-; n ------ is a single or double bond nand R, R 1 , R 2 , R 3 , R 4 , R 3' , R 4' , R 5 , R 6 , R 6' , R 7 and R 7' are as defined in the specification; and pharmaceutical compositions comprising the compounds of formula I. n Also disclosed is the method of inhibiting aspartyl protease, and in particular, the methods of treating cardiovascular diseases, cognitive and neurodegenerative diseases, and the methods of inhibiting of Human Immunodeficiency Virus, plasmepins, cathepsin D and protozoal enzymes. n Also disclosed are methods of treating cognitive or neurodegenerative diseases using the compounds of formula I in combination with a cholinesterase inhibitor or a muscarinic antagonist.
priorityDate 2005-06-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 594.