Optimized S-Trityl-l-cysteine-Based Inhibitors of Kinesin Spindle Protein with Potent in Vivo Antitumor Activity in Lung Cancer Xenograft Models-Reference-Cited by-同舟云学术

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Optimized S-Trityl-l-cysteine-Based Inhibitors of Kinesin Spindle Protein with Potent in Vivo Antitumor Activity in Lung Cancer Xenograft Models

Published:2013-02-27 Issue:5 Volume:56 Page:1878-1893
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Good James A. D.¹,Wang Fang¹,Rath Oliver¹,Kaan Hung Yi Kristal¹,Talapatra Sandeep K.¹,Podgórski Dawid¹²,MacKay Simon P.²,Kozielski Frank¹

Affiliation:

1. Molecular Motors Laboratory, The Beatson Institute for Cancer Research, Garscube Estate, Switchback Road, Glasgow G61 1BD, Scotland, U.K.

2. Strathclyde Institute of Pharmacy and Biomedical Sciences, 161 Cathedral Street, University of Strathclyde, Glasgow G4 0RE, Scotland, U.K.

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm3014597

Reference76 articles.

1. Kinesins and cancer

2. Kinesin superfamily motor proteins and intracellular transport

3. Elucidating the functionality of kinesins: An overview of small molecule inhibitors

4. Mitotic spindle organization by a plus-end-directed microtubule motor

5. Phosphorylation by p34cdc2 regulates spindle association of human Eg5, a kinesin-related motor essential for bipolar spindle formation in vivo

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