化合物

The antioxidative action may involve trapping the initiating radicals generated by AAPH in the bulk phase, inhibiting the propagating lipid peroxyl radicals on the surface of micelles and regeneratingα-tocopherol by reducing theα-tocopheroxyl radical.

在均相溶液中，这些化合物单独使用时都是很好的抗氧化剂，但是只有杨梅树素产生了抑制期，其他化合物均降低了引发速率。

It was indi-cated that compound Ⅳ and Ⅴ possess antitumor activity. The〓 of 〓 and 〓 was 7.85 and 7.45 μg/mL respectively to〓 compound Ⅳ,Ⅴ and Ⅶ show pesticidal activity. The inhibi-tory effect of compound Ⅶ(2) was 1OO% to Barnyardgrass,and 100% to Rice Sheath Blight.

表明化合物Ⅳ、Ⅴ具有一定的抗癌活性（如Ⅳ(1)及Ⅴ(2)，对人白血病细胞株〓的〓分别为7.85和7.45ug／ml，化合物Ⅳ、Ⅴ及Ⅷ具有一定的农药活性（如Ⅷ(2)在50ppm时对水稻纹枯菌的抑制率为100%，对稗草的抑制率（100ppm为100%。

Pharmaceutical compositions comprise an effective amount of the instant compounds, either alone, or in combination with one or more therapeutically active compounds, and a pharmaceutically acceptable carrier.

药物组合物包含有效量的单独的或与一种或多种治疗活性化合物组合的本发明化合物，以及药物可接受载体。

Searching for specific ligand to a certain recepter or enzyme in human body from secondary metabolities of plants, animals and microorganisms, Optimization of lead compound under certain theory or hypothesis, and synthesis methodology investigation of pharmaceutically active compound are all tasks of medicinal chemistry.

药物化学的研究领域十分宽广，既有从动物、植物、微生物的次生代谢产物中寻找与人体内特异性的受体、酶的激动剂或拮抗剂，又有在理论、假想指导下的先导化合物的优化，以及生理活性化合物的合成方法学研究。

The compounds of the formula I are valuable pharmacologically active compounds.

式I的化合物是有价值的药物活性化合物。

Tetra-O-benzyl-D-glucose reacted with bromine to give glucosylbromide. It reacted with hydroxyl phenyl acetonitrile or hydroxyl benzaldehyde to give substituted ph- enylacetonitrile or substituted benzaldehyde.11 New stilbenes were synthesized possessing 2,3,4,6-tetra-O-benzyl-D-glucoside by condensation reaction with pheny lacetonitrile or benzaldehyde, which had potential biological activity and would be sieved in the future.

由2，3，4，6-四芐氧基葡萄糖作为中间体，首先制备出的溴代糖和含有羟基的苯甲醛和苯乙反应制备出含有糖的取代苯甲醛和取代苯乙，再和简单的苯乙或苯甲醛缩合反应生成11种具有潜在的生物活性且含有2，3，4，6-四芐氧基葡萄糖的类化合物，这些新化合物有待于进一步进行药理活性筛选。

Hydrazine compounds including hydrazine, phenylhydrazine, semicarbazide and isoniazid were separated and determined by capillary electrophoresis with a poly modified microdisk carbon fiber electrode.

肼类化合物的毛细管区带电泳/聚谷氨酸修饰碳纤维微盘阵列电极安培检测以电聚合方法制备了聚谷氨酸修饰碳纤维微盘阵列电极，研究了肼、苯肼、氨基脲及异烟肼等肼类化合物在该电极上的电催化氧化。

All the compounds were isolated from the plant for the first time and 1 and 3 were obtained from the plants of Phlomis for the first time.

所有化合物均为首次从该植物中分得，其中化合物1和3为首次从该属植物中分得。

A phomopsis compound, a relative preparation method and an application relate two compounds.

拟茎点菌素化合物及其制备方法和应用，涉及两种化合物。

The preparation method comprises seed cultivation of phomopsis hzla01-1, fermentation of phomopsis hzla01-1, extraction of phomopsis compound and refining phomopsis compound.

拟茎点属hzla01-1的种子培养，拟茎点属hzla01-1的发酵培养，拟茎点菌素化合物的提取，拟茎点菌素化合物的精制。

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。