查询词典 chlordiazepoxide

This paper describes an effective method for determining chlordiazepoxide.

本文介绍一种可有效地测定氯氮艹卓含量的方法。

It is based on the greatly enhancive effect of chlordiazepoxide on the chemiluminescence reaction between luminol and hydrogen peroxide in the flow system.

研究了氯氮卓在luminol-H2O2-NaOH体系中的化学发光行为，在选定的最佳实验条件下，测定了氯氮卓浓度与化学发光强度的关系。

A trademark used for preparations of chlordiazepoxide hydrochloride .

他的书以言及生动的时事问题而增添了风趣。

A trademark used for preparations of chlordiazepoxide hydrochloride.

以氨水分子中的氮原子的振动频率为基础的原子钟。

Drugs can be used in small doses of olfactory agents, or Chlordiazepoxide 5 ~ 10 mg, 1 or 2 times daily in order to reduce muscle tension in breathing, increase the training effect.

药物方面可使用小剂量嗅剂，或利眠宁5～10毫克，每日1～2次，以减轻肌肉、呼吸紧张，增加训练效果。

The increase in chemiluminescence intensity was linearly proportional to the chlordiazepoxide concentration in the range from 1.11×10^(-11) to 8.35×l0^(-10) mol/L.

结果表明：在1.11×10^(-11)~8.35×10^(-10)mol/L内氯氮卓浓度与发光信号成线性关系，检出限为4.79×10^(-12)mol/L，重复测定11次的相对标准偏差为2.49%Cs=3.34×10^

The method is simple and rapid, it has been applied for the determination of chlordiazepoxide raw materials with satisfactory results.

太原理工大学化学工程与技术学院太原030024 (李彦威；魏文珑；王志忠)；山西大学校医院太原030006王晋辉

Injection of vitamin D3: a monthly 2-30 IU3, a lack of vitamin B1 caused夜啼available Vitamin B1 10 mg oral, 1 times daily. 4, night waking, sleep panic disorder, can cause a nightmare夜啼, if necessary, a short period of time to give stability and 1.25-2.5mg or Chlordiazepoxide 2.5-5mg, every time, even served a few nights.

3维生素D3针剂：每月一次20至30万IU3、缺乏维生素B1引起夜啼，可用维生素B1 10毫克口服，每日1次。4、夜醒、睡惊症、梦魇均可引起夜啼，必要时可短时间给予安定1.25—2.5mg或利眠宁2.5—5mg，每晚一次，连服数晚。

"Chlordiazepoxide:a benzodiazepine drug, CHClNO, whose hydrochloride is used as an antianxiety drug and in the treatment of chronic alcoholism and alcohol withdrawal."

甲氨二氮，利眠宁：一种苯二氮？镇静药，CHClNO，其氢氯化物成分用作抗忧虑剂，并可用作慢性酒精中毒的治疗和戒酒。

In clinical. acetylcholinesterase inhibitors reduce the breakdown of synaptic acetylcholine, have been modestly effective in improving the cognitive deficits of Alzheimer's disease.The goal of this work is to determine enzyme kinetics and mechanisms of acetylcholinesterase and butyrlcholinesterase inhibition by five cardiovascular drugs, lovastatin, simvastatin, amlodipine besylate, nifedipine, and hydralazine hydrochloride, and two benzodiazepines, diazepam and chlordiazepoxide hydrochloride. All drugs in this study are reversible mixed-type inhibitors of acetylcholinesterase and butyrylcholinesterase. The pKi values for acetylcholinesterase and butyrylcholinesterase inhibition by the cardiovascular drugs are linearly correlated with the molecular weights of the drugs with the slopes of 0.005 and 0.0021, respectively. Therefore, van der Waals' interactions between acetylcholinesterase and the cardiovascular drugs are stronger than those between butyrylcholinesterase and the drugs. This is probably due to a smaller active site gorge and a more significant peripheral anionic substrate binding site of acetylcholinesterase than those of butyrylcholinesterase.

本研究之目的系决定乙醯胆碱酯酵素和丁醯胆碱酯酵素被五种心脏血管药物lovastatin， simvastatin， amlodipine besylate， nifedipine、hydralazine hydrochloride和两种benzodiazepines：diazepam和Chlordiazepoxide hydrochloride的抑制作用之动力学及机转，这些药物都是乙醯胆碱酯酵素和丁醯胆碱酯酵素的可逆性、混合型之抑制剂，实验结果显示，五种心血管药物对於乙醯胆碱酯酵素及丁醯胆碱酯酵素抑制之pKi值和药物之分子量呈直线之关系，斜率分别为0.005及0.0021因此丁醯胆碱酯酵素，与心血管药物间之凡德瓦作用（van der Waals' ）比乙醯胆碱酯酵素与心血管药物间者弱，这可能原因是丁醯胆碱酯酵素之活性区域比乙醯胆碱酯酵素之活性区域更宽广，但丁醯胆碱酯酵素之周边阴离子区域不及乙醯胆碱酯酵素之周边阴离子区域者明显重要，由於五种心血管药物对於乙醯胆碱酯酵素和丁醯胆碱酯酵素抑制之pKi值存在著线性关系表示此种抑制作用系经过共同之反应机理。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。