Gill, Sumandeep K <br/><br/>
Structure-based design of novel benzoxazinorifamycins with potent binding affinity to wild-type and rifampin-resistant mutant Mycobacterium tuberculosis RNA polymerases.  [electronic resource] 

 -  Journal of medicinal chemistry  Apr 2012 
 - 3814-26 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1520-4804 
<br/><br/><label>Standard No.: </label>10.1021/jm201716n  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Antibiotics, Antitubercular--chemical synthesis<br/>Benzoxazines--chemical synthesis<br/>DNA-Directed RNA Polymerases--metabolism<br/>Drug Design<br/>Drug Resistance, Bacterial<br/>Mice<br/>Mycobacterium tuberculosis--drug effects<br/>Rifampin--pharmacology<br/>Rifamycins--chemical synthesis