盐酸利多卡因

盐酸利多卡因

盐酸利多卡因(无水的);利多卡因盐酸盐;2-二乙氨基-N-2,6-二甲苯基乙酰胺氮盐酸盐;盐酸利多卡因;N-(2,6-二甲苯基)-2-(二乙氨基)乙酰胺盐酸盐;利多卡因盐酸;盐酸利多卡因(N-(2,6-二甲苯基)-2-(二乙氨基)乙酰胺盐酸盐、2-二乙氨基-N-2,6-二甲苯基乙酰胺氮盐酸盐、克拉维酸锂、利多卡因盐酸盐);盐酸利多卡因原料药

lidocaine hydrochloride

LIGNOCAINE HYDROCHLORIDE;LIDOCAINE HYDROCHLORIDE;LIDOCAINE HCL;Lidocaine hydrochloride CP2000,BP98;a-(diethylamino)-26-acetoxylidideHCl;a-(diethylamino)-26-acetoxylididehydrochloride;Acetamide, 2-(diethylamino)-N-(2,6-dimethylphenyl)-, monohydrochloride 2-(diethylamino)-n-(2,6-dimethylphenyl)-acetamid monohydrochloride alpha-diethylamino-2,6-acetoxylidine hydrochloride anestacon hydrochloride duncaine hydrochloride;2-(Diethylamino)-N-(2,6-dimethylphenyl)-acetamide hydrochloride

200-803-8

C14H23ClN2O

270.8

InChI=1/C14H22N2O.ClH/c1-5-16(6-2)10-13(17)15-14-11(3)8-7-9-12(14)4;/h7-9H,5-6,10H2,1-4H3,(H,15,17);1H

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-80-82°C

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盐酸利多卡因具有穿透性强、弥散性强、起效快的特点，麻醉效能2倍与普鲁卡因，而毒性为1。用药后5分钟即可出现麻醉作用，麻醉作用可持续1～1.5小时，比普鲁卡因长50%。吸收后可抑制中枢神经系统，并能抑制心室自律性，缩短不应期，可用作控制室性心动过速，治疗室性早搏、室性心动过速和心室颤动等心律失常症状。对心脏本身疾患或强心苷所引起的心律失常都有效，对室上性心动过速则效果不佳。本品作用快，持续时间短，口服无效，常作为静脉注射给药。###局部麻醉药，抗心律失常药，用于各种麻醉及快速性室性心律失常

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