We present a controlled quantum dialogue scheme by using W states.
我们提出了一个基于W态的控制量子对话方案。
tPSODock:A program for molecular docking using chemscore method and two - layer particle swarm optimization;
tPSODock:基于化学得分函数和两层粒子群算法的计算机分子对接程序
Drug molecular docking design based on optimal conformation search;
药物分子对接中的构象搜索策略
A novel anti-influenza drug:molecular docking of trihydroxymethoxyflavone;
新型抗流感病毒药物——三羟基甲氧基黄酮分子对接的研究
Prediction of the Interaction of HIV-1 Integrase and Inhibitor Aurintricarboxylic Acid Using Docking;
用分子对接方法预测HIV-1整合酶与金精三羧酸抑制剂的相互作用
QSAR and docking studies on a new series of diaryl-substituted-1,2,4-trizole de-rivatives COX-2 inhibitors;
新型二芳基取代-1，2，4-三唑类化合物的抗炎构效关系和分子对接研究
Binding Mode Study of Streptolydigin, an HIV-1 Protease Inhibitor via Docking Methodology;
HIV-1蛋白酶抑制剂—利迪链菌素的分子对接研究
Separation and Detection of Synthetic Food Colors by Ion-pair High-performance Liquid Chromatography;
离子对高效液相色谱法对人工合成色素的分离和测定
Quantitative determination of fosfomycin calcium and its related substances by ion-pair HPLC method;
用离子对-HPLC法测定磷霉素钙及其有关物质的含量
Study on the Determination of the L-carnitine Tablets by Ion-pair RP-HPLC;
离子对RP-HPLC法测定左卡尼汀片剂的含量
Thermodynamics of Ion pair of [MgSO_4]~0 in i-PrOH Water Mixed Solvent;
在i-PrOH-H_2O混合溶剂中硫酸镁离子对缔合热力学研究
A kind of reaction intermediate ion pair Q~(+-)OR(Q~+=PhCH_2N~+(C_2H_5)_3, R=CH_3, C_2H_5) was separated by the use of quaternary ammonium salts as phase transfer catalysts (PTC).
应用苄基三乙基氯化胺作相转移催化剂,在氢氧化钠水溶液和醇中反应,分离出一种反应中间体离子对Q~+-OR(Q~+=(?)—CH_2(?)(C_2H_5)_3,R=CH_3,C_2H_5)。
OBJECTIVE To establish a ion pair RP HPLC method for the determination of gemcitabine in human plasma METHODS Samples were prepared by protein precipitation.
目的 建立使用离子对反相高效液相色谱测定吉西他滨血药浓度的方法。
A Quantum and Docking Study of Substituted Deoxyuridines;
取代脱氧脲苷的量子化学计算及分子对接
3D-QSAR and docking study of a series of 16α-substituted estradiol derivatives;
16α取代雌二醇衍生物的三维定量构效关系和分子对接研究
Based on the reported crystal structure of complexes of the enzyme ketol-acid reductoisomerase (KARI), 279 molecules were obtained with predicted high affinity for KARI from MDL/ACD 3D-database searching, using program DOCK 4.
以酮醇酸还原异构酶KARI复合物 0 165nm高分辨率晶体结构为基础 ,采用DOCK 4 0分子对接程序通过MDL/ACD三维数据库搜寻 ,找到了 2 79个与KARI结合能较低的小分子 ,讨论了能量打分较高分子同靶酶的作用模式 。