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浏览/检索结果: 共13条，第1-10条 帮助 限定条件 发表日期：2014    专题：大连理工大学    第一署名单位    第一作者单位    通讯作者单位     已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 The interaction between organic phosphate ester and p53: An integrated experimental and in silico approach 期刊论文 7th International Conference on Marine Pollution and Ecotoxicology, 2014, 卷号: 85, 页码: 516-521 作者:  Li, Fei;  Li, Renmin;  Yang, Xianhai;  You, Liping;  Zhao, Jianmin 收藏  |  浏览/下载：9/0  |  提交时间：2019/12/09 Organophosphate flame retardants (OPFRs) p53  Docking  Quantitative structure-activity relationship (QSAR)  Binding affinity  Multiple linear regression (MLR)   Discovery of Potent HDAC Inhibitors Based on Chlamydocin with Inhibitory Effects on Cell Migration 期刊论文 CHEMMEDCHEM, 2014, 卷号: 9, 页码: 627-637 作者:  Wang, Shimiao;  Li, Xiaohui;  Wei, Yingdong;  Xiu, Zhilong;  Nishino, Norikazu 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/09 cell migration  chlamydocin analogues  cyclic tetrapeptides  docking  HDAC inhibitors   Structural Analysis for Colchicine Binding Site-Targeted ATCAA Derivatives as Melanoma Antagonists 期刊论文 MEDICINAL CHEMISTRY, 2014, 卷号: 10, 页码: 277-286 作者:  Zhang, Jiawei;  Li, Feng;  Li, Yan;  Guo, Yangyang;  Wang, Jinghui 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/09 3D-QSAR  colchicine binding site  docking  melanoma cancer antagonists   Insight into the Structural Features of Pyrazolopyrimidine- and Pyrazolopyridine-based B-Raf(V600E) Kinase Inhibitors by Computational Explorations 期刊论文 CHEMICAL BIOLOGY & DRUG DESIGN, 2014, 卷号: 83, 页码: 643-655 作者:  Li, Yan;  Han, Chunxiao;  Wang, Jinghui;  Yang, Yinfeng;  Zhang, Jingxiao 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/09 B-Raf(V600E) kinase  Pyrazolopyrimidine- and pyrazolopyridine-based inhibitors  3D-QSAR  docking  md   Exploring unsymmetrical dyads as efficient inhibitors against the insect beta-N-acetyl-D-hexosaminidase OfHex2 期刊论文 BIOCHIMIE, 2014, 卷号: 97, 页码: 152-162 作者:  Chen, Qi;  Guo, Peng;  Xu, Lin;  Liu, Tian;  Qian, Xuhong 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/09 beta-N-Acetyl-D-hexosaminidase  Enzyme inhibitors  Molecular docking  Naphthalimide  Tryptophan fluorescence titration   Insight into the binding mode and the structural features of the pyrimidine derivatives as human A(2A) adenosine receptor antagonists 期刊论文 BIOSYSTEMS, 2014, 卷号: 115, 页码: 13-22 作者:  Zhang, Lihui;  Liu, Tianjun;  Wang, Xia;  Wang, Jinan;  Li, Guohui 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/09 Pyrimidine derivatives  Human A(2A) adenosine receptor  Molecular docking  Molecular dynamics  Thermodynamic analysis  3D-QSAR   Structural insight into the binding complex: beta-arrestin/CCR5 complex 期刊论文 JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 2014, 卷号: 32, 页码: 866-875 作者:  Stambouli, Nejla;  Dridi, Mehdi;  Wei, Ning-Ning;  Jlizi, Asma;  Bouraoui, Abderahmen 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/09 CCR5  docking  normal mode analysis  beta-arrestin  HIV  molecular dynamics   A comparison of various optimization algorithms of protein-ligand docking programs by fitness accuracy 期刊论文 JOURNAL OF MOLECULAR MODELING, 2014, 卷号: 20, 页码: - 作者:  Guo, Liyong;  Yan, Zhiqiang;  Zheng, Xiliang;  Hu, Liang;  Yang, Yongliang 收藏  |  浏览/下载：13/0  |  提交时间：2019/12/09 Protein-ligand docking  AutoDock software  Optimization algorithms  Evolutionary algorithms (EAs)  Particle swarm optimizations (PSOs)   Exploring details about structure requirements based on novel CGRP receptor antagonists urethanamide, aspartate, succinate and pyridine derivatives by in silico methods 期刊论文 JOURNAL OF MOLECULAR STRUCTURE, 2014, 卷号: 1074, 页码: 294-301 作者:  Li, Yan;  He, Haoran;  Wang, Jinghui;  Han, Chunxiao;  Feng, Jiaqi 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/09 Migraine  CGRP receptor antagonist  3D-QSAR  Molecular docking   Profiling the Interaction Mechanism of Quinoline/Quinazoline Derivatives as MCHR1 Antagonists: An in Silico Method 期刊论文 INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2014, 卷号: 15, 页码: 15475-15502 作者:  Wu, Mingwei;  Li, Yan;  Fu, Xinmei;  Wang, Jinghui;  Zhang, Shuwei 收藏  |  浏览/下载：7/0  |  提交时间：2019/12/09 MCHR1  3D-QSAR  molecular docking  MD simulation