Tamamura, H <br/><br/>
Conformational study of a highly specific CXCR4 inhibitor, T140, disclosing the close proximity of its intrinsic pharmacophores associated with strong anti-HIV activity.  [electronic resource] 

 -  Bioorganic & medicinal chemistry letters  Feb 2001 
 - 359-62 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0960-894X 
<br/><br/><label>Standard No.: </label>10.1016/s0960-894x(00)00664-8  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Anti-HIV Agents--chemistry<br/>Computer Simulation<br/>Models, Molecular<br/>Molecular Conformation<br/>Nuclear Magnetic Resonance, Biomolecular<br/>Oligopeptides--chemistry<br/>Protein Structure, Secondary<br/>Receptors, CXCR4--antagonists & inhibitors<br/>Structure-Activity Relationship