Abulwerdi, Fardokht A <br/><br/>
3-Substituted-N-(4-hydroxynaphthalen-1-yl)arylsulfonamides as a novel class of selective Mcl-1 inhibitors: structure-based design, synthesis, SAR, and biological evaluation.  [electronic resource] 

 -  Journal of medicinal chemistry  May 2014 
 - 4111-33 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1520-4804 
<br/><br/><label>Standard No.: </label>10.1021/jm500010b  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Antineoplastic Agents--chemical synthesis<br/>Cell Line, Tumor<br/>Drug Design<br/>Humans<br/>Myeloid Cell Leukemia Sequence 1 Protein--antagonists & inhibitors<br/>Structure-Activity Relationship<br/>Sulfonamides--chemical synthesis<br/>bcl-2 Homologous Antagonist-Killer Protein--physiology<br/>bcl-2-Associated X Protein--physiology