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; 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."/> ETOMIDATE ANALOGUES WITH IMPROVED PHARMACOKINETIC AND PHARMACODYNAMIC PROPERTIES
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ETOMIDATE ANALOGUES WITH IMPROVED PHARMACOKINETIC AND PHARMACODYNAMIC PROPERTIES

机译:具有改善的药动学和药动学性质的依托咪酯类似物

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; 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.
机译:本发明涉及式(I)的化合物: <图像文件=“ IMGA0001.GIF” he =“ 54” imgContent =“ chem” imgFormat =“ GIF” wi =“ 67” /> 其中R 1 是L 1 C(O)OT或L 1 C(O)OL 2 C( O)OT; R 2 是取代或未取代的C 1 -C 10 烷基,C 2 -C 10 烯基或C 2 -C 10 炔基或R 1 ; n是0至5的整数;每个R 3 独立地为卤素或R 2 ; L 1 和L 2 各自独立地为键,取代或未取代的C 1 -C 10 亚烷基, C 2 -C 10 亚烯基,或C 2 -C 10 亚炔基; T为H,为取代或未取代的C 1 -C 10 烷基,C 2 -C 10 烯基或C 2 -C 10 炔基,硝基苯酚或环丙基。本发明还涉及包含式(I)的化合物和药学上可接受的载体的药物组合物,并且涉及通过施用这种药物组合物在哺乳动物中提供麻醉的方法。

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