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Investigation data obtained at 14 days after applied second time indicated that the efficacy of Zn thiazole 20% SC applied at

锌是噻二类有机锌杀菌剂,对水稻细菌性病害有较好的防治效果。

The kind of three antimoulds including thiazole species,organo-metallic compounds and imidazole species were applied in the research of a polysulfide sealant .

选用了噻类、有机金属络合物、咪类3种防霉剂应用于聚硫密封剂,考察了聚硫密封剂的防霉效果,并研究了不同防霉剂对密封剂工艺性能和力学性能的影响。

Results show that, by using thionyl chloride and N,N-dimethyl formamide as chlorinating reagent and dichloromethane as solvent and taking -15℃ as reaction temperature, Z-iomer crystals with pale white color and stable to temperature can be obtained with an overall yield of 70%.

以2-(2-氨基噻-4-基)-2-甲氧亚氨基乙酸为原料,经盐酸化、氯代等反应合成了Z-2-(2-氨基噻-4-基)-2-甲氧亚氨基乙酰氯盐酸盐;氯代时以用亚硫酰氯和N,N-二甲基甲酰胺的混合物代替五氯化磷作氯化剂,并考察了温度和溶剂对氯代产物中Z-异构体和E-异构体收率的影响。

Objective: Design and synthesis of novel triazole antifungal derivatives based on the structure of fluconazole.

目的:以氟康为先导化合物,设计合成新的三醇类化合物,并研究其抗真菌活性。

Triazole is an interesting moiety, which plays an important role in biological activity. In recent years, many efforts have been paid to develop 1,2,3-triazole derivatives on the basis of many lead compounds with various pharmacological activities, and quite a few successful examples have been seen. Unfortunately, in contrast with 1,2,4-triazole, 1,2,3-triazole has only a few ways to be prepared.

1,2,3-三氮类化合物所具有的广泛生物活性正受到人们的日益重视,在已有的和新开发的各类药物中常可见1,2,3-三氮的结构,而以它为药效基团改良各种先导化合物取得成功的例子也屡见不鲜。

Abstract〕Itraconazole is a triazole antifungal agent that has a broad spectrum activity.

摘要〕伊曲康是三类广谱抗真菌药。

Some approved aneugens Trip terygiuwlIypogaucum (evelHutch, colchicine, thiabendazole, a tropine sulfate,d-ubocurarine was added into the reactive system respectively and the changes of their absorption values were taken down during different periods under the conditions of 37 0C and 350nm .

本研究通过多步聚合和解聚合反应从猪脑中分离纯化微管蛋白,建立微管蛋白的体外聚合和解聚合反应平衡体系,并将已证实的非整倍体诱发剂(昆明山海棠根部水抽提物、2-(4′-噻)苯丙咪、硫酸阿托品、d-筒箭毒碱)分别加入此反应平衡体系中,于37℃、350nm条件下,记录此体系不同时期的吸光值变化,与阳性对照物和溶剂对照处理平衡体系后的吸光值在相同时间点作比较,以此评估这几类非整倍体诱发剂对离体条件下的微管蛋白聚合的影响,寻求这几类非整倍体诱发剂是否可通过抑制微管蛋白聚合作用途径而诱发非整倍体。

Objective: To evaluate the efficacy and safety of rebeprazole and pantoprazole in treating duodenal ulceration.

目的:评价雷贝拉和泮托拉治疗十二指肠溃疡的临床疗效及其安全性。

In ^1H NMR spectra of cyclodextrin modified by 2-amino-1,3,4-thiadiazole, it was found that the chemical shift of thiadiazole ring shifted to upfield due to diamagnetic shielding effect caused by cyclodextrin.

由于环糊精的屏蔽效应,在2-氨基-1,3,4-噻二修饰β-环糊精的^1H NMR中,修饰产物中的噻二质严发生了高场位移。

Levamisole hydrochloride, the ramification of imidazole, is a broad-spectrum medicine against wireworm.

本论文所研究的盐酸左旋咪,又名驱虫净,是咪的一个衍生物。

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However, as the name(read-only memory)implies, CD disks cannot be written onorchanged in any way.

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