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INHIBITEURS DE LA PROTEASE D'ASPARTYLE HETEROCYCLIQUES
专利权人:
SCHERING CORPORATION;PHARMACOPEIA, LLC
发明人:
ZHU, ZHAONING,MCKITTRICK, BRIAN,SUN, ZHONG-YUE,YE, YUANZAN C.,VOIGT, JOHANNES H.,STRICKLAND, COREY,SMITH, ELIZABETH M.,STAMFORD, ANDREW,GREENLEE, WILLIAM J.,MAZZOLA, ROBERT D., JR.,CALDWELL, JOHN,CUMM
申请号:
CA2678958
公开号:
CA2678958C
申请日:
2008.02.20
申请国别(地区):
CA
年份:
2014
代理人:
摘要:
Disclosed are compounds of the formula (I) or a stereoisomer, tautomer, or pharmaceutically acceptable salt or solvate thereof, wherein W is a bond, -C(=S)-, -S(O)-, -S(O)2-, -C(=O)-, -O-, -C(R6)(R7)-, -N(R5)- or -C(=N(R5))-; X is -O-, -N(R5)- or -C(R6)(R7)-; provided that when X is -O-, U is not -O-, -S(O)-, -S(O)2-, -C(=O)- or -C(=NR5)-; U is a bond, -S(O)-, -S(O)2-, -C(O)-, -O-, -P(O)(OR15)-, -C(=NR5)-, -(C(R6)(R7))b- or -N(R5)-; wherein b is 1 or 2; provided that when W is -S(O)-, -S(O)2-, -O-, or -N(R5)-, U is not -S(O)-, -S(O)2-, -O-, or -N(R5)-; provided that when X is -N(R5)- and W is -S(O)-, -S(O)2-, -O-, or -N(R5)-, then U is not a bond; and R1, R2, R3, R4, R5, R6, and R7 are as defined in the specification; and pharmaceutical compositions comprising the compounds of formula (I). 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. 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 m1 agonist or m2 antagonist.
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中国工程科技知识中心
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http://www.ckcest.cn/home/

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