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covalent相关的网络例句

查询词典 covalent

与 covalent 相关的网络例句 [注:此内容来源于网络,仅供参考]

To create covalent bonds where the sticky ends have hybridized, an enzyme called ligase is required.

要在粘性末端已经发生杂交的地方形成共价键,还需要一种称为连接酶的酶。

To create covalent bonds where the sticky ends have hybridized, an enzyme called ligase is required.

要在粘性末端已经发生杂交的地方形成共价键,还需要一种称为连接酶连接酶的酶。

In this paper, the stable Au complexes are classified according to the coordination atoms and their characteristic structure. The recent development of the researches on the antitumor activity of Au complexes including the structure-activity relationship, biological targets and the mechanisms of action are reviewed. The structure of the coordination ligand and the leaving group have great impact on the in vitro cytotoxicity of the Au complex. Many physical and biological methods are introduced to study the interaction between the Au complexes and the suspected bio-target, such as DNA, protein, mitochondrion, thio-containing biomolecules, etc. The interaction modes (intercalating, electrostatic interaction, covalent bonding, etc.) are focused to illustrate the reason for the antitumor activity of Au complexes.

本文按配位原子的不同总结了稳定三价金配合物的结构特征,按其生物活性的构效关系、生物靶点和作用机制综述了三价金配合物抗肿瘤活性研究的最新成果:配体的结构特点以及离去基团对三价金配合物的体外细胞毒性影响较大;介绍了用于检测三价金配合物与可能的生物靶分子之间的相互作用的多种物理和生物学方法,重点关注了相互作用的模式,如嵌入/静电吸引/共价结合等,并解释了三价金配合物抗肿瘤活性的原因。

In this paper, the stable Au complexes are classified according to the coordination atoms and their structural characteristics. The recent development of the researches on the antitumor activity of Au complexes including the structure-activity relationships, biological targets and the mechanisms of action are reviewed. The structure of the coordination ligand and the leaving group have great impact on the in vitro cytotoxicity of the Au complex. Many physical and biological methods are introduced to study the interaction between the Au complexe and the suspected bio-target, such as DNA, protein, mitochondrion, thio-containing biomolecules, etc. The interaction modes (intercalating, electrostatic interaction, covalent bonding, etc.) are focused to illustrate the reason for the antitumor activity of Au complexes.

本文按配位原子的不同总结了稳定三价金配合物的结构特征,按其生物活性的构效关系、生物靶点和作用机制综述了三价金配合物抗肿瘤活性研究的最新成果:配体的结构特点以及离去基团对三价金配合物的体外细胞毒性影响较大;介绍了用于检测三价金配合物与可能的生物靶分子之间相互作用的多种物理和生物学方法,重点关注了相互作用的模式,如嵌入/静电吸引/共价结合等,并解释了三价金配合物抗肿瘤活性的原因。

The specific inhibitor of DNA methylation that is available currently is 5-Aza-2'-deoxycytidine (5Aza-dc), which forms a covalent bond with the DNA methyltransferase, thus, limiting the number of free DMT molecules for methylating DNA and then decreasing its biology activity.

目前研究较多的甲基化抑制剂是胞苷类似物5-氮杂-2'-脱氧胞苷(5-Aza-2'-deoxycytidine, 5Aza-dc)。5Aza-dc的作用机制是与DNA甲基转移酶共价结合,降低酶的生物活性。

The high polarizing power polarizes all but the smallest anions producing covalent character

高极化能力极化所有但最小的那些负离子产生共价特性。

It shows that with the content increase of modified nano-silica in the butyl rubber, the portions of covalent bond interaction increases, overall crosslink density of vulcanizes increases, chemistry crosslink density of vulcanizes increases and reaches its maximum when the content is 2.0%, then followed by a slow decrease.

研究了纳米二氧化硅用量对硫化胶力学性能的影响,随着纳米二氧化硅填充量的增加,结合橡胶中共价键作用的贡献增加,硫化胶总交联密度增加,化学交联密度在填充量2.0%时增至最大然后缓慢降低。

Sc. I am interested in the covalent modification of carbon nanotubes and atom transfer radical polymerization ATRP on the nanoscale materials surface.

2005年毕业于曲阜师范大学,目前主要研究方向是碳纳米管的共价键修饰和纳米尺度的原子转移自由基聚合。

"There are no practical natural sources of simple covalent amides, but the peptides and proteins in living systems are long chains with peptide bonds, which are amide linkages."

简单的有机共价醯胺没有实际的天然来源,然而生命系统中的和蛋白质都是些带键的长链,这些都是醯胺链接。

"There are no practical natural sources of simple covalent amides, but the peptides and proteins in living systems are long chains with peptide bonds, which are amide linkage s."

简单的有机共价醯胺没有实际的天然来源,然而生命系统中的和蛋白质都是些带键的长链,这些都是醯胺链接。

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