Synthetic studies on mitotic kinesin Eg5 inhibitors: Synthesis and structure–activity relationships of novel 2,4,5-substituted-1,3,4-thiadiazoline derivatives-Reference-Cited by-同舟云学术

Synthetic studies on mitotic kinesin Eg5 inhibitors: Synthesis and structure–activity relationships of novel 2,4,5-substituted-1,3,4-thiadiazoline derivatives

Published:2014-08 Issue:16 Volume:24 Page:3961-3963
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Yamamoto Junichiro^ORCID,Amishiro Nobuyoshi,Kato Kazuhiko,Ohta Yoshihisa,Ino Yoji,Araki Mitsuharu,Tsujita Tetsuya,Okamoto Seiho,Takahashi Takeshi,Kusaka Hideaki,Akinaga Shiro,Yamashita Yoshinori,Nakai Ryuichiro,Murakata Chikara

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference7 articles.

1. Microtubules as a target for anticancer drugs

2. Kinetochore Localization of Murine Bub1 Is Required for Normal Mitotic Timing and Checkpoint Response to Spindle Damage

3. Past and future of the mitotic spindle as an oncology target

4. Targeting the Kinesin Eg5 to Monitor siRNA Transfection in Mammalian Cells

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