类并

On the basis of summarizing the rationales for various kinds of delivery systems and comparing their merits and demerits, four novel types of hydrophobically modified hydrogels cross-linked with azobenzene were designed and synthesized.

本文在总结各类传递系统的设计原理、比较其优缺点的基础上，设计并合成了四类疏水改性的偶氮苯交联凝胶。

From the aspect of urban and rural integrative "Modern Cadastration" management style,the paper discusses the differences from traditional cadastral alterations,introduces right alteration s,land use alterations and history backdate of "Modern Cadastration" alterations.

本文从城乡一体化"现代地籍"管理方式的角度，探讨了有别于传统方式的现代地籍变更模式，并详细介绍了"现代地籍"变更中的权属变更、地类变更和历史回溯。

This thesis consists of two parts. The first one was that boundary value problem was discrete with five point difference method. Three kinds of memory formats were studied, which were full matrix, half band width and row compress sparse. Full matrix memory format and half band width memory format first was contrasted. The results show that half band width has efficiency in space. Then the algebraic system of finite element method was solved by Gauss-Seidel iteration method to popular row compress sparse memory format.

本论文由两部分组成，第1部分针对边值问题，用5点差分格式进行离散，并对离散矩阵这类大型稀疏矩阵，研究了系数矩阵的3种存储格式的优劣，即：满矩阵存储格式、半带宽存储格式和按行压缩稀疏存储格式，首先我们将满矩阵存储方式和半带宽存储格式进行了对比，迭代法的数值实验表明：利用半带宽存储的矩阵在空间运算方面具有高效性；然后针对目前数值实验中流行的按行压缩稀疏存储格式，实现了有限元离散代数系统的迭代法的求解。

The objective was to study the target of benzimidazole carbamate drugs against Cysticerci cellulosae and give theoretical basis for type evolution and new drug design.

研究苯并咪唑氨基甲酸酯类抗囊药物对猪带绦虫囊尾蚴的作用靶点，为药物的类型衍化和新药开发提供理论依据。

EDTB metal complexes in which contained four benzimidazole groups have distorted octahedron geometry structure because of rigidity of EDTB.

本文的研究手段基于常规的方法，目的是探讨多苯并咪唑类化合物与金属配合后的结构特征，对SOD模拟活性的影响。

On the basis of synthesis of the H+/K+-ATPase inhibitor omeprazole,seven benzimidazole derivatives were synthesized for the first time,and their structures were identified by 1H-NMR、MS and elementary analysis.

设计合成了7个未见文献报道的苯并咪唑类衍生物，经质谱、核磁共振氢谱和元素分析确定了结构。

We developed a simple and efficient method for the synthesis of benzimidazole derivatives in water. Imidazolium salt grafted iodobenzene diacetate containing double features of ionic liquid and iodobenzene diacetate was synthesized.

报道了一种简便高效的苯并咪唑类衍生物的水相合成新方法，合成了兼具离子液体和二醋酸碘苯双重特点的咪唑盐二醋酸碘苯。

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。

Using comparative molecular field analysis and comparative molecular similarity indices analysis, three dimensional structure-activity relationship (3D-QSAR) studies were carried out on a series of benzofuran N-myristoyl transferase inhibitors.

采用比较分子力场分析法和比较分子相似性指数分析法，系统地研究了40个苯并呋喃类N-肉蔻酰基转移酶抑制剂的三维定量构效关系。

AbstractUsing comparative molecular field analysis and comparative molecular similarity indices analysis, three dimensional structureactivity relationship(3D-QSAR) studies were carried out on a series of benzofuran N-myristoyl transferase inhibitors.

摘要采用比较分子力场分析法和比较分子相似性指数分析法，系统地研究了40个苯并呋喃类N-肉豆蔻酰基转移酶抑制剂的三维定量构效关系。

Do you know, i need you to come back

你知道吗，我需要你回来

Yang yinshu、Wang xiangsheng、Li decang,The first discovery of haemaphysalis conicinna.

1〕 杨银书，王祥生，李德昌。安徽省首次发现嗜群血蜱。