咪唑

The medicine had been reported treatment of pulmonary acariasis were arsenical, Pyquiton, however our studies confirmed the high treatment value of Metronidazole.

为了筛选治疗肠螨病的有效药物，我们将30例典型的肠螨病患者随机分为4组，用双盲法分别给予伊维菌素、甲硝哒唑、丙硫咪唑、吡喹酮4种药物进行治疗。

Research results show that 25% Amistar SC could be used safely on Fuji, New Red Star, Beidou, Australian Green Apple, but it is harmful to Gala. Amistar has a great control effect on apple powdery mildew, apple scab and apple Alternaria leaf spot. The control effect works from 80% to 90% when it is used with 1:2000 to 1:3000 dilutions in field.

结果表明，25% Amistar SC除对嘎啦品种有药害外，对红富士、新红星、北斗、澳州青苹等6个骨干品种均无任何不良影响，使用安全；同时，25%阿米西达SC对苹果白粉病、黑星病及斑点落叶病等3种主要病害均具有显著防治效果，使用浓度1：2000~1：2500，防治效果为80%~90%；在广谱性和防效上显著优於目前生产上推广的常规性的苯并咪唑类、三唑类及代森类的杀菌剂品种。

Rabeprazole is contraindicated in patients with known hypersensitiity to rabeprazole, substituted benzimidazole or to any component of the formulation.

对雷贝拉唑敏感性高的病人禁用，代之以苯并咪唑或者任何同类组分

K-ATPase is the last passageway of gastric acid secretion.On the basis of synthesis of the H+K-ATPase inhibitor pantoprazole,twelve benzimidazole derivatives were synthesized for the first time,and their structures were proved by IR,1H-NMR and elementary analysis.

摘 要 H+/K+-ATP酶是胃酸分泌的最后环节，在合成H+/K+-ATP酶抑制剂泮托拉唑的基础上，设计合成了12个未见文献报道的苯并咪唑类衍生物，经红外光谱、核磁共振氢谱和元素分析确定了结构。

In this thesis, the emphasis is on the research of synthesis of a novel chiral imidazolium salt and application of chiral/achiral imidazolium salt in catalytic benzoin condensations.

本文致力于手性咪唑鎓盐离子液体的合成及手性/非手性咪哗基催化安息香缩合反应的研究。

Undergoing elective surgery were randomly divided intothree groups acˉcording to the method of the induction of general anesthesia,i.e GroupⅠ（n=13）:intravenous induction:midazolam0.03mg/kg,fentanyl3μg/kg ,etomidate0.3mg/kg,vecuronium1mg and succinylcholine1.5mg/kg;GroupⅡ（n=13）:orolaryngeal lignocaine spray combined with intravenous induction,lignocaine administered just before the inducˉtion of anesthesia;GroupⅢ（n=13）:epidural block combined with general anesthesia,2%lignocaine3ml adminˉistered via epidural catheter before the induction.

组Ⅰ为单纯经静脉全麻诱导组，麻醉用药为咪唑安定0.03mg/kg、芬太尼3μg/kg 、依托咪酯0.3mg/kg、维库溴铵1mg和琥珀胆碱1.5mg/kg；组Ⅱ为诱导即刻咽喉部喷雾表麻加经静脉全麻诱导组；组Ⅲ为硬膜外阻滞加经静脉全麻诱导组。

However, coadministration of midazolam and etomidate and sufentail for induction is the least impaction on blood pressure and heart rate.

但是，咪唑安定、依托咪酯复合舒芬太尼进行麻醉诱导时对病人的血压和心率影响最小。

Their tribological properties in paraffin and water were investigated with a four-ball test machine, the results shown that the thiadiazole derivatives and the imidazoline borates have better friction reduction and antiwear properties, and the thiadiazole derivatives also have excellent extreme pressure properties in water.

通过在四球摩擦磨损试验机上评价上述两类衍生物分散在液体石腊及水中的抗磨减摩性能，首次发现噻二唑及咪唑啉衍生物在水中也有较好的抗磨减摩性能，且噻二唑衍生物在水中具有良好的极压性能。

The best of them were 4c and 8d which exhibited 87% and 89% inhibition of Penicilium digitatum . And benzothieno[3,2-d]imidazol[1,2-a]pyrimidin-2,5(1H, 3H)-diones or benzothieno[3,2-d][1,2,4]triazol[1,5-a]pyrimidin-10(3H)-one only exhibited moderate inhibition.

而苯并噻吩并[3，2-d]嘧啶-4(3H)-酮和苯并噻吩并[3，2-d]咪唑并[1，2-a]嘧啶-2，5(1H，3H)-二酮以及苯并噻吩并[3，2-d][1，2，4]三唑[1，5-a]嘧啶-10(3H)-酮衍生物以及三唑醇衍生物均只表现出中等的抑制率。

And benzothieno[3,2-d]imidazol[1,2-a]pyrimidin-2,5(1H, 3H)-diones or benzothieno[3,2-d][1,2,4]triazol[1,5-a]pyrimidin-10(3H)-one only exhibited moderate inhibition.

而苯并噻吩并[3，2-d]嘧啶-4(3H)-酮和苯并噻吩并[3，2-d]咪唑并[1，2-a]嘧啶-2，5(1H，3H)-二酮以及苯并噻吩并[3，2-d][1，2，4]三唑[1，5-a]嘧啶-10(3H)-酮衍生物以及三唑醇衍生物均只表现出中等的抑制率。

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。