hydrophobic [,haidrə'fəubik]

hydrophobic的基本解释

adj.

恐水病的, 狂犬病的, 患恐水病的

与hydrophobic相关的网络例句 [注：此内容来源于网络，仅供参考]

The experimental results show that hydrophobic association increases obviously with increasing polymer concentration, hydrophobe content, hydrophobic side chain length and temperature. The Critical aggregate concentration of P(AM/NaAA/C_8AM) with different hydrophobic content is 1.5-3g/L. Strong ass...

结果表明，随聚合物浓度、疏水单体摩尔分数、疏水侧链长和温度的增加，疏水缔合作用增强；不同疏水单体含量的P(AM/NaAA/C8AM)的临界缔合浓度为1.5~3.0 g/L；表面活性剂十二烷基硫酸钠与P(AM/NaAA/C8AM)发生了强烈的疏水相互作用，形成混合胶束，得到SDS的临界胶束浓度为8×10-3 mol/L；由于聚合物链上羧基的存在，使其具有良好的 pH敏感性，随 pH值的增大，P(AM/NaAA/C8AM)的疏水缔合作用呈现先减弱后恒定再增强的变化。

The experimental results show that hydrophobic association increases obviously with increasing polymer concentration, hydrophobe content, hydrophobic side chain length and temperature. The Critical aggregate concentration of P (AM/NaAA/C8AM) with different hydrophobic content is 1.5~3g/L. Strong association between surfactant sodium dodecyl sulfate and P (AM/NaAA/C8AM) occurs through the formation of mixed micelles. The CMC of SDS is 8×10^(-3)mol/L. Moreover, because of the presence of-COOH group, the terpolymers have pH-responsive characterization. The hydrophobical association changes greatly with increasing pH.

结果表明，随聚合物浓度、疏水单体摩尔分数、疏水侧链长和温度的增加，疏水缔合作用增强；不同疏水单体含量的P(AM/NaAA/C8AM)的临界缔合浓度为1.5~3.0g/L；表面活性剂十二烷基硫酸钠与P(AM/NaAA/C8AM)发生了强烈的疏水相互作用，形成混合胶束，得到SDS的临界胶束浓度为8×l0^(-3)mol/L；由于聚合物链上羟基的存在，使其具有良好的pH敏感性，随pH值的增大，P(AM/NaAA/C8AM)的疏水缔合作用呈现先减弱后恒定再增强的变化。

From the calculations, it can be found that the van der Waals interactions, the hydrophobic interactions, as well as the H-bonding interactions are crucial for the ligand binding. The 4-phenylamino group can produce strong van der Waals adn hydrophobic interactions with the nonpolar side chains of the residues deep in the binding cleft. The R^1 and R^2 substituents on the bicyclic chromophore can also produce strong van der Waals and hydrophobic interactions with the residues located at the exterior part of the binding pocket. Moreover, the two N atoms of the quinazoline can form H-bonds with EGFR, which will produce significant contribution to biological activities. The calculated nonbonded interactions between anilinoquinazolines and EGFR, as well as the information obtained from the predicted complexes, can interpret the structure-activities of the inhibitors well, which can afford us important information for structure-based drug design.

从模拟结果得到的抑制剂和靶酶之间的相互作用模式表明范德华相互作用、疏水相互作用以及氢键相互作用对抑制剂的活性都有重要的影响，抑制剂的苯胺部分位于活性口袋的底部，能够与受体残基的非极性侧链产生很强的范德华和疏水相互作用，抑制剂双环上的取代基团也能和活性口袋外部的部分残基形成一定的范德华和疏水性相互作用，而抑制剂喹唑啉环上的氮原子能和周围的残基形成较强的氢键相互作用，对抑制剂的活性有较大的影响，计算得到抑制剂和靶酶之间的非键相互作用能以及抑制剂和靶酶之间的相互作用信息能够很好地解释抑制剂活性和结构的关系，为全新抑制剂的设计提供了重要的结构信息。

与hydrophobic相关的网络解释 [注：此内容来源于网络，仅供参考]

hydrophobic colloid：疏水胶体

hydrophilite 氯钙石 | hydrophobic colloid 疏水胶体 | hydrophobic radical 疏水基

hydrophobic colloid：疏水性胶体

hydrophilic fiber 亲水性纤维 | hydrophobic colloid 疏水性胶体 | hydroseparator 水力分离器

hydrophobic colloid：憎水胶体;疏水胶体

hydrophilic colloid 亲水胶体 | hydrophobic colloid 憎水胶体;疏水胶体 | hydroscopic coefficient 吸湿系数

hydrophobic：疏水的

一般认为[5],在高温条件下经H2处理后的活性炭表面产生了疏水的(hydrophobic)变化. 从图上可以看出,在相同的实验条件下Nc/H950吸附最少量的水(<1mmol/g),并且在整个吸附过程中没有突跃变化. 近年来在催化研究领域carbon作为催化剂或催化剂载体正日益得到新的重视,

hydrophobic：疏水性

而利用X光绕射技术则可获取蛋白质活化部位的完整资讯,包含其位置、距离、氢键性(hydrogen-bonded)、疏水性(hydrophobic)及静电性(electrostatic),作为最佳化修饰化合物的参考分析资料.