Receptor–Ligand Interaction-Based Virtual Screening for Novel Eg5/Kinesin Spindle Protein Inhibitors-Reference-Cited by-同舟云学术

Receptor–Ligand Interaction-Based Virtual Screening for Novel Eg5/Kinesin Spindle Protein Inhibitors

Published:2012-03-01 Issue:6 Volume:55 Page:2561-2573
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Nagarajan Shanthi¹²,Skoufias Dimitrios A.³,Kozielski Frank⁴,Pae Ae Nim¹²

Affiliation:

1. Neuro-Medicine Center, Life Sciences Division, Korea Institute of Science and Technology, PO Box 131, Cheongryang, Seoul 130-650, Republic of Korea

2. School of Science, Korea University of Science and Technology, 52 Eoeun dongYuseong-gu, Daejeon 305-333, Republic of Korea

3. Institute for Structural Biology (CEA-CNRS-UJF), 41 rue Jules Horowitz, 38027 Grenoble Cedex 1, France,

4. The Beatson Institute for Cancer Research, Garscube Estate, Switchback Road, Bearsden, Glasgow, G61 1BD, Scotland, U.K.

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm201290v

Reference73 articles.

1. Analysis of the kinesin superfamily: insights into structure and function

2. Pathway of ATP Hydrolysis by Monomeric Kinesin Eg5

3. Targeting the Kinesin Spindle Protein: Basic Principles and Clinical Implications

4. A bipolar kinesin

5. The bipolar mitotic kinesin Eg5 moves on both microtubules that it crosslinks

Cited by 36 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Design, synthesis and biological activity evaluation of novel inhibitors targeting TNKS2, based on docking, virtual screening and molecular dynamics simulation studies;Molecular Physics;2024-04-12

2. Synthesis, biological evaluation and molecular docking of thiazole hydrazone derivatives grafted with indole as novel tubulin polymerization inhibitors;Journal of Molecular Structure;2024-04

3. Discovery of potential scaffolds for glutaminyl cyclase inhibitors: Virtual screening, synthesis, and evaluation;Bioorganic & Medicinal Chemistry;2024-01

4. Application of an “inhalation by design” approach to the identification and in-vitro evaluation of novel purine based PI3Kδ inhibitors;European Journal of Medicinal Chemistry;2023-06

5. Role of KSP Inhibitors as Anti-Cancer Therapeutics: An Update;Anti-Cancer Agents in Medicinal Chemistry;2022-08