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ANALOGUES DE L'ETOMIDATE QUI N'INHIBENT PAS LA SYNTHESE DE STEROIDES CORTICOSURRENAUX
专利权人:
THE GENERAL HOSPITAL CORPORATION;THE BRIGHAM AND WOMEN'S HOSPITAL, INC.
发明人:
RAINES, DOUGLAS E.,FORMAN, STUART A.,MILLER, KEITH W.,HUSAIN, SYED S.,CUNY, GREGORY D.,COTTEN, JOSEPH F.
申请号:
CA2767112
公开号:
CA2767112C
申请日:
2010.07.08
申请国别(地区):
CA
年份:
2018
代理人:
摘要:
The invention is directed to compounds according to formula (I): where R1 is L1C(O)OT or L1C(O)OL2C(O)OT; R2 is a substituted or unsubstituted C1-C10 alkyl, C2-C10 alkenyl, or C2-C10 alkynyl, or R1; n is an integer from 0 to 5; each R3 is independently halogen or R2; R4 and R5 are independently H, halogen, CN or CF3; L1 and L2 are each independently a bond, a substituted or unsubstituted C1-C10 alkylene, C2-C10 alkenylene, or C2-C10 alkynylene; and T is H, a substituted or unsubstituted C1-C10 alkyl, C2-C10 alkenyl, or C2-C10 alkynyl, nitrophenol, or cyclopropyl. The invention is also directed to a pharmaceutical composition comprising a compound according to formula (I) and a pharmaceutically acceptable carrier, and to methods for providing anesthesia in mammals by administering such a pharmaceutical composition.
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中国工程科技知识中心
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