Mu, F <br/><br/>
Design, synthesis, and biological evaluation of a series of lavendustin A analogues that inhibit EGFR and Syk tyrosine kinases, as well as tubulin polymerization.  [electronic resource] 

 -  Journal of medicinal chemistry  Feb 2001 
 - 441-52 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0022-2623 
<br/><br/><label>Standard No.: </label>10.1021/jm000387g  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Antineoplastic Agents--chemical synthesis<br/>Biopolymers<br/>Cell-Free System<br/>Drug Screening Assays, Antitumor<br/>Enzyme Inhibitors--chemical synthesis<br/>Enzyme Precursors--antagonists & inhibitors<br/>ErbB Receptors--antagonists & inhibitors<br/>Humans<br/>Inhibitory Concentration 50<br/>Intracellular Signaling Peptides and Proteins<br/>Mice<br/>Phenols--chemical synthesis<br/>Phosphorylation<br/>Protein-Tyrosine Kinases--antagonists & inhibitors<br/>Structure-Activity Relationship<br/>Syk Kinase<br/>Tubulin--chemistry<br/>Tumor Cells, Cultured