[4-(Imidazol-1-yl)thiazol-2-yl]phenylamines. A Novel Class of Highly Potent Colchicine Site Binding Tubulin Inhibitors: Synthesis and Cytotoxic Activity on Selected Human Cancer Cell Lines-Reference-Cited by-同舟云学术

[4-(Imidazol-1-yl)thiazol-2-yl]phenylamines. A Novel Class of Highly Potent Colchicine Site Binding Tubulin Inhibitors: Synthesis and Cytotoxic Activity on Selected Human Cancer Cell Lines

Published:2006-08-29 Issue:19 Volume:49 Page:5769-5776
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Mahboobi Siavosh¹,Sellmer Andreas¹,Höcher Heymo¹,Eichhorn Emerich¹,Bär Thomas¹,Schmidt Mathias¹,Maier Thomas¹,Stadlwieser Josef F.¹,Beckers Thomas L.¹

Affiliation:

1. Department of Pharmaceutical Chemistry I, University of Regensburg, D-93040 Regensburg, Germany, and Therapeutic Area Oncology and Enabling Technologies, ALTANA Pharma AG, D-78467 Konstanz, Germany

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm060545p

Reference27 articles.

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